Sunday, January 26, 2020
The Physiological Healing Process Of Soft Tissue Biology Essay
The Physiological Healing Process Of Soft Tissue Biology Essay It is imperative, as a sports therapist, to understand the process of soft tissue repair to develop a safe and effective management plan for clients injury problems. Understanding this, allows us to decide what modalities or interventions to apply. If certain therapy techniques or inappropriate exercises are applied, it can lead to further problems in the healing stages. A therapist cannot change the time is takes to heal an injury but can certainly make the stages more effective. There are four stages of healing that will be discussed in more detail later on in the essay. In the event of an injury, the process of healing that follows depends on the extent of the injury and the approximation of the wound sites stump ends. There are two types of tissue healing; primary and secondary intention. Healing by primary intention commonly occurs in minor wounds wherein the tissue separation is small and a bridge of cells bind the ends of the wound together, resulting in a small line of scar tissue. Healing by secondary intention occurs in more severe wounds, where the stump ends cannot be bridged as they are too far apart. The wound heals by producing tissue from around the wound to fill the space created by the wound. This can occur in second degree sprains where ligament tissue is torn and not surgically repaired. Secondary intention healing takes longer than primary and also results in a larger scar. Healing can be described as a continuum of changing events. There are four common stages to healing; bleeding, inflammation, proliferation and re-modelling. All the stages overlap considerably and are not separate. Figure 1 healing phases Diagram to illustrate the four stages of healing (Watson, 2009) Figure 1 shows a basic overview of the four stages. The phases are shown individually, but in reality, they are overlapped. Some events associated with one phase act as stimulant for the next phase. The first stage of soft tissue repair is bleeding. As a result of soft tissue damage; blood vessels are damaged as well. The severity of the bleeding depends upon the vascularity of the tissue involved. Muscles have a more increased vascularity than ligaments. This stage lasts around 6 to 8 hours depending on the tissue involved. The main focus of a sports therapists management would be to rest. It would be advisable to use crutches, stopping any weight bearing activity, as bleeding can start if the wound opens up again. A compression bandage could be considered to delay the onset of the inflammation phase. Restricting the intake of alcohol, aspirins and medications could be beneficial for the patient as these can thin the blood considerably. Once the body has moved into the haemostasis stage, bleeding will stop and the repair phase moves into the inflammation stage. The second stage of healing is inflammation. The shift from bleeding to inflammation is not clear, as there may be some bleeding in the start of the inflammation phase. Houglum (2005) identifies that there are five cardinal signs to inflammation; heat, redness, swelling, pain and loss of function. This is a normal and necessary process to healing and can take up to 2 to 3 days. The stage can be initiated by numerous events such as trauma, mechanical irritation and thermal or chemical insult. Houglum (2005, p.37) states that During inflammation, the injury is contained and stabilized and debris removed. There are two elements to the inflammatory events that occur in parallel; vascular and cellular. The vascular phase consists of close interaction between cells and chemicals, the process of chemotaxis taking place causing vascular permeability. Vascular permeability allows cells and chemicals that are in the blood stream to enter the injury site and perform their functions to heal the tissue. It is initially caused by histamine, a local hormone that is released by cells that enter the area due to which blood vessels get larger and leaker. As a result of this unwanted fluids and waste material are cleared. Histamine is a short lived hormone and its function is carried on by serotin and kinins. Kinins presence at the injury site is also short term and is followed by prostaglandin formation. There are two prostaglandins, one continuing the vascular permeability and one attracts leukocytes to the injury site. These prostaglandins stimulate repair or the damaged site and stimulate the stage into proliferation. As a result of vasodilation and vasopermeability there is an increase in f low volume, an increase in hydrostatic pressure and swelling. The other phase of the inflammation stage is cellular events where there is a migration of various cells to the injured area. Platelets release phospholipids which effectively stop the bleeding by stimulating a clotting mechanism. According to Houglum (2005, p. 38) Platelets also bind to the collagen fiber stumps that were exposed by the injury. Platelets can also release substances such as fibronectin, growth factors and fibrogen. Watson (2009) suggests that following the bleeding phase, fibrin and fibronectin form a solid layer that helps the adhesion of various cells, like a plug stopping the bleeding. As the healing stage progresses, the plug is replaced by type III collagen. Leakage from the blood vessels is stopped by the fibrin plug, which compromises their ability to remove the extra fluid from the area. However, later on fibrinolysin is released allowing drainage of excess fluid from the area. Within the first few hours of injury, white blood cells such as neutrophils, eosinophils and basophils start to remove debris from the site. As these are short lived, they are replaced by monocytes and macrophages. These exhibit a strong phagocytic activity that is responsible for the tissue debridement that takes place. Houglum (2005) argues that inflammation can become harmful if it is prolonged, further than the normal healing time. Generally an injury should be passed through to acute inflammation and then to healing. Conversely, if acute inflammation is interrupted there can be a negative effect and as a result the injury can move into chronic inflammation. Chronic inflammation will result in a pus formation consisting of dead white blood cells. Failure of the body to deal with the initial insult is where healing fails to take place. As a result of this healing by fibrosis takes place where scar tissue is formed. The goal of a sports therapist would be to facilitate inflammation but minimizing it (Houglum, 2005). This would be accomplished by applying initial first aid using the price principles. Protection via bandages and supports to the injury would be applied to reduce the likeliness of further bleeding or swelling. Brukner and Khan (2007) suggest that rest, with the use of crutches for lower limb injury and a sling for upper limb, will help reduce the metabolic requirement around the injury site. Ice can slow down nerve conduction, which slows down the rate pain gets to the spinal cord, effectively reducing the pain sensation. Ice would also increase vasospasm, reducing uncontrolled swelling around the injury. Brukner and Khan (2007) also advise that compression and elevation reduce swelling around the area and can decrease the effect of hydrostatic pressure which helps to reduce pain around the site. Hands off techniques such as active movements in a pain free range can beneficial. Inflammation takes place in an anaerobic environment. After the macrophages clean up the injury site they recruit and activate other cells that start through anaerobic respiration where lactic acid is produced. Lactic acid stimulates the next stage of tissue repair named proliferation. The third stage of soft tissue repair is proliferation, the true phase of healing, when bleeding has completely stopped. Watson (2009) suggests that it is the restoration of tissue continuity with the deposition of repair tissue. The stage of proliferation has a rapid onset of 24 to 48 hours but takes much longer to reach its peak reactivity, between 2 to 3 weeks. If the tissue is more vascular, it will take a shorter time in reaching peak proliferation production. There are two fundamental processes involved in the repair which are fibroplasia and angiogenesis. The migration of fibroblasts is principally responsible for the development of new capillaries and extracellular matrix. A production of substances made by the fibroblasts will make up a matrix of collagen, proteoglycans and elastin which are required for vital scar tissue formation and proliferation. This migration to the injured site, allows fibroblasts to lay down collagen type III. Although, the fibre structure of type III collagen is weak, it helps provide the wounds primary tensile strength. It can be easily torn if too much stress is applied. Alongside fibroplasia, a process called angiogenesis takes place. Watson (2009) states à ¢Ã¢â ¬Ã ¦capillaries in the region of the tissue damage bud and grow towards the repair zone. Blood flow through the region is re-established, providing oxygen and nutrients while removing metabolic waste products. Oxygen is essential for many of the repair processes, but more importantly for collagen production. This process of tissue maturation continues into the remodelling phase. To facilitate the proliferation stage, a sports therapist should apply heat to increase the blood flow to the area, effectively bringing more oxygen to the injury site and allowing more collagen production. Houglum (2005) believes ultrasound promotes collagen and myofibroblast production. Ultrasound would facilitate the proliferation phase as there is an increased need of collagen and myofibroblasts. Brukner and Khan (2007) claim that proprioceptive work such as joint awareness and positional sense can help enhance general coordination which will help facilitate strength and endurance exercises required in the next stage. Nutritional support such as whey proteins and vitamin c can speed up the healing process. Various authors (Houglum, 2005 and Watson, 2009) identify that the remodelling stage normally starts at the peak of proliferation around 2-3 weeks and can last up to 18 months. Wound contraction starts and type III collagen are converted to type I, to stabilise and restore the injury site. As there is more type I collagen, it becomes more insoluble and less resistant to damage. Collagen fibres produce more cross links as fluid is reduced in the area, strengthening the structure of the scar. Eventually this cross linking becomes the major source of the scars tensile strength. The large numbers of capillaries produced in the proliferation phase are no longer needed and start to retreat. Fibroblasts migrated from the previous stage will also reduce. Visible changes can be seen, with the cellular changes taking place including the loss of scars red colour changing to white and then evening out with natural skin tone. Therapeutic interventions to facilitate the remodelling phase can be a range of exercises and deep tissue work. These can help the arrangement of collagen fibres. Houglum (2005, p.43) claims that: When collagen fibers are aligned in an organized, parallel fashion, collagen can form the greatest number of cross links and thereby possess optimal strength. In this organised arrangement, function and mobility is at its greatest degree and properly applied forces can enhance it. Khan and Scott (2009, p. 249) in their report confirm that: The benefits of loading include improved alignment of regenerating myotubes, faster and more complete regeneration, and minimisation of atrophy of surrounding myotubes. Physical stress is an important component in the development of quality tissue repair. With this in mind, resistance training can be considered. Brukner and Khan (2007) suggest that resistance training may stimulate collagen synthesis. Strength and power training such as squats, dead lifts, compounds lifts that use more than one joint will increase the strength not only in the wounded area but the overall body. Sports specific exercises and complex training can also help in this stage. Brukner and Khan (2007) identify that stretching will promote a flexible strong scar. These interventions can speed up the conversion of type III collagen fibres into type I. General factors that delay the healing process are age, protein deficiency, low vitamin c levels, steroids and NSAIDs and temperature when low. The local factors known to delay healing are a poor blood supply, adhesion to bone or other underlying tissue, continued inflammation, drying of the wound and excessive movement can restart inflammation. Bleeding, inflammation, proliferation and remodelling are the four stages of soft tissue repair that are distinct but overlapping. From a sports therapists perspective it is important we apply therapeutic intervention at the right time and the appropriate management in order to facilitate the repair process avoiding delays by entering the chronic inflammation phase. Each athlete or client has different post injury sporting goals, level of skill and degrees of competitiveness, which all influence the rehabilitation programme. Therapeutic exercise must be administered carefully without causing harm to the healing tissues if rehabilitation programs are to be successful.
Saturday, January 18, 2020
English Language Anxiety Essay
English as all know is the international communication language which plays a great role in many important aspects of a society. In Malaysia, English as a second language after Malay language, is not only used in terms of education system, but is extensively used in inter-cultural communication and professions such as law, medicine, engineering and of course business. In this era of increasing globalization, Malaysia will have to face with tighter and rigid competition from other foreign countries. In accordance to that, Malaysian students will have to get themselves ready for the upcoming circumstances especially those involving the usage of English. Malaysian students have been learning English continuously for at least 11 years starting from primary school till secondary school before enrolling themselves into a third-level education. English has been a compulsory subject for students in Malaysia in which they need to pass in all the major examinations in Malaysia such as UPSR, PMR and SPM. In higher education, English is used more expressively as entire main and core subjects such as medical, law, algebra and business use English as the principal language. Whether it is a local university or a private one, English has become the main source of commandment other than becoming a subject in the curriculum. To exemplify, universities which use English as the medium of language such as International Islamic Universities Malaysia (IIUM), which has been an English-medium university since it was first established in 1983, require its students to pass a standard level of English before enrolling into the university. The students will be tested again during their orientation week on English language by undergoing an English Placement Test ( EPT). Students who gain level 6 and below will be placed in English classes till they have reached the standard of exemption. These English classes are necessary as all the subjects taught are in English. These efforts show the importance of English in education. After graduation, students who are proficient in English will have a better future as they will be easily employed by multinational companies. One of the jobââ¬â¢s specifications in Malaysia is to have soft skills especially the ability to communicate in good English. Furthermore, job interviews nowadays are also conducted in English. Here it is clear that, in order to have better chances in future, one must have full confidence in using English language. Nonetheless, English is not the first language for most Malaysian students. Most Malaysian students use their own mother language, for example Malay language, Mandarin and Tamil when communicating with family and friends. This will cause their English language skills to rot if it is continuously being practiced which will later on lead to anxiety in the process of learning English. After a minimum of 11 years of studying English in both the primary and secondary schools, students in the Centre for Foundation Studies ( CFS), IIUM still have difficulties in using the language effectively. For example, a study by Mohd Hilmi Bin Hamzah ( 2007) in CFS, ââ¬Å"in Semester 1, 2006/2007, more than 40% of the students taking first level English obtained grade ââ¬Å"Dâ⬠in their papers, while only 5% of them obtained an ââ¬Å"Aâ⬠â⬠. This shows that the students have not yet mastered the language before entering the university. The writer added that despite of having English Intensive Class Programme and extra classes by individual English lecturers, the level of English proficiency remains dissatisfactory. With the increasing usage of English globally, it is really necessary to find out the factors which may hinder English language learning. One of the factors which has not been paid attention to is language learning anxiety. ââ¬Å"Anxiety is a major factor that affects second/foreign language learningâ⬠( Mohammad Javad Riasati, 2011). He also states that levels of anxiety differ from one individual to another but is always present. Most of todayââ¬â¢s education and economy uses English as the language of commandment. For that reason, it is really important to find out the factors which affect anxiety and ways to reduce it to increase the performance of an English language learner. Different students have different proficiency levels in English language skills namely reading, writing, listening and speaking. With that reason, different students will also encounter different levels of anxiety for all those skills. One student may feel more anxious in speaking while the other in writing. As all of these four skills are needed to be mastered in order to be proficient in English, even by losing confidence in only one of it might cause difficulties in carrying out tasks in both education and job. This study will help both the educators and learners of English language in CFS, IIUM. The teachers will get information about the factors causing anxiety among students. They will also be given information on the rank of studentsââ¬â¢ anxiety in possessing the 4 language skills namely writing, listening, reading and speaking so that the teachers will consider about which one of these 4 language skills should be given more attention to. Last but not least, the findings of this study will help both the students and teachers to design a suitable strategy on ways to reduce anxiety in order to increase the performance of mastering English language. This study specifically addresses the following 3 research questions: 1) Which language skill namely writing, listening, speaking and reading creates the highest anxiety level among students in CFS, IIUM? 2) What are the factors that are probable to cause anxiety? 3) What are the ways used by the students to reduce anxiety? The objectives of this study are as follows: 1) To identify specific language skill in which students in CFS, IIUM feel most anxious. 2) To identify the factors which are more probable to cause anxiety. 3) To identify the ways students use to reduce anxiety. According to Hansen (1977), anxiety is ââ¬Å"an experience of general uneasiness, a sense of foreboding, a feeling of tensionâ⬠(p. 91). Anxiety is a type of psychological phenomena and ranges from mixture of open views of behavioral attribution. Due to anxietyââ¬â¢s impact on the studentsââ¬â¢ performance in learning English as a second language, it has been continuously studied by many researchers. Learning a second language will cause awareness among the learners that they are using a language which they have not yet mastered to communicate (Toth, 2011). This phenomenon will lead to many upcoming problems the learners have to face in using English as they have not completely accepted a second language as a part of their lives. This is according to Cohen and Norst ( 1989) ââ¬Å" language and self/identity are so closely bound, if indeed they are not one and the same thing, that a perceived attack on one is an attack on the otherâ⬠(p. 76). This will somehow lead students of English learners to feel less enjoyable during their class. Few studies conducted about the factors that affect anxiety are communication apprehension ( McCroskey, 1970), fear of negative evaluation ( Watson & Friend, 1969) and test anxiety ( Sarason, 1978). Communication apprehension for example is the difficulty in understanding teacherââ¬â¢s instructions, negative evaluation for example is the fear of correction and last but not least, example of test anxiety is the fear of failing in the class. According to Young ( n.d.), language anxiety is caused by ââ¬Å" (a) personal and interpersonal Anxiety, (b) learner beliefs about language learning, (c) instructor beliefs about language teaching, (d) instructor-learner interactions, (e) classroom procedures and (f) language testingâ⬠( Mohammad Javad Riasati, 2011, p.908). The 4 language skills namely writing, speaking, reading and writing plays vital role in helping students to attain proficiency in English Language. A study of anxiety in learning English as a foreign language by Wilson (2006) and Mohd Hilmi Bin Hamzah (2007) have included the findings on language skills. Wilson (2006) states that ââ¬Å"â⬠¦anxiety might exert a deleterious influence on language achievement and equally intuitively, that poor language achievement might arouse even more anxietyâ⬠(p. 25). In Wilsonââ¬â¢s (2006) research, although a four-skills approach is used (taking in listening, speaking, writing and reading) the oral skill was emphasized. This shows that most students are afraid of speaking English as a second language during class. In his study, Young (1991) interviewed Krashen who stated that teachers often expect new students to perform beyond their expectations which increases the level of anxiety among students. This will further discourage the students to use English in their lives. ââ¬Å" A students who believes that one must never say anything in English until it can be said correctly will probably avoid speaking most of the timeâ⬠( Khairi Izwan Abdullah and Nurul Lina Bt. Abdul Rahman, n.d.). An arouse of language anxiety from different language skills such as writing, listening, reading, speaking and grammar have further been studied by Brantmeier (2005), Hussein Elkafaifi (2005), Greyersen and Horwitz (2002) and Casado (2001). This will lead the learners to perform poorly especially in speaking. The feeling of anxiety needs to be treated to avoid students that have been affected by this problem to be carried away into some other serious problems. In some studies, it was found that anxiety levels were highest during the early stages of language learning and lessened at an advanced level. This has been concluded by MacIntyre and Gardner (1991, p.111), ââ¬Å"an experience and proficiency increase, anxiety declines in a fairly consistent mannerâ⬠. This means that if students keep on practicing all the language skills of English by reading books, listening to English songs, writing blogs and communicating in English continuously, they will be able to overcome the feelings of anxiety and will perform better. Methodology The main purpose of this study is to investigate the level of English learning Anxiety among the students of Centre for Foundation Studies (CFS), International Islamic University Malaysia (IIUM). A population from CFS, IIUM was chosen to identify the specific language skills in which students in CFS, IIUM feel most anxious, the factors which are more probable to cause anxiety and the ways the students use to reduce anxiety. Data for this research was collected through a set of questionnaire. This research employed the use of questionnaire research methodology. The instrument used to collect the data was a questionnaire containing nine questions. The questionnaire was passed to thirty students of the CFS, IIUM randomly where its scope of distribution was not limited on a certain course, level of study, age or gender. To ensure that the questions were fully understood by the students, a brief introduction about the topic was provided at the top of each questionnaire.
Friday, January 10, 2020
Prevalence of Escherichia Coli on Money
PREVALENCE OF ESCHERICHIA COLI ON PHILIPPINE PESO BILL WITHIN THE VICINITY OF ILOILO CITY 2012-2013 A Research Paper Presented to The Faculty College of Medical Laboratory Science Department Central Philippine University Iloilo City In Partial Fulfillment of the Requirement for the Research 1 JUSTINE GRACE G. JIMENEA ISAAC JAMES T. LEDESMA MAJA HANNAH LOU L. LOJA ROBERTO R. MANALO JR. JIRAH L. PEDROSA MARCH 2013 CHAPTER 1 INTRODUCTION Background of the Study A classic characteristic of human parasitic and bacterial agents is the evolution of routes for transmission pathogens to susceptible hosts.The environment plays a critical role in transmission to humans, with many environmental materials serving as vehicles. Microbial contaminants may be transmitted directly, through hand-to-hand contact, or indirectly, via food or other inanimate objects like fomites. (Rote, et al. , 2010) According to Umeh, et al (2007), Contamination of objects by pathogenic microorganism is much a public hea lth concern as contaminated materials can be sources of transmitting pathogens. Items that pass from hand to hand are likely to be contaminated with disease causing microorganisms especially if handled with unclean hands or kept in dirty surroundings.Ahmed, et al (2010) pointed out that paper currency is widely exchanged for goods and services in most countries worldwide. Paper currencies are widely used and each currency is exchanged many times during the time it circulates. If some of these paper money are contaminated with pathogenic bacteria, there is a potential to spread these microorganism. Pope, et al (2002) mentioned, since bacteria, have been shown to spread from person to person via contact with fomites paper money, therefore, presents a particular risk of public health.Paper currency is commonly and routinely passed among individuals. Thus bacteria could be spread on the surface of paper currency. Paper currency, as asserted by Oyero, et al (2007) can be contaminated by droplets during coughing, sneezing, touching with previously contaminated hands or other materials and placement on dirty surface. Paper currency is commonly handled by various categories of people during transaction. The possibility that paper currency might act as environmental vehicles for the transmission of potential pathogenic microorganisms was suggested in 1970s.Various pathogens related with throat infection, pneumonia, tonsillitis, peptic ulcers, urino-genital tract infection, gastroenteritis and lung abscess had been reported. (Pope, et al. , 2002) The money which may get contaminated during production, storage, after production and during use are always in circulation. Numerous research on currency in several countries indicated bacterial contamination. A study in Bangladesh reported thatEscherichia coli (58%),Klebsiella(50%), Staphylococcus aureus(25%), Salmonella (15%), Bacillus (9%), Pseudomonas (7%) and Vibrio cholera (5%) were recovered from Bangladesh Paper Currenc y Notes (Taka). Ahmed, et al,. 2010) In another study carried out in Nigeria, the bacteria isolated E. coli (80%), Aerobacter (59%), Salmonella (40. 9%), yeast cells (36. 4%), Streptococcus fecalis(31. 8%), Staphylococcus aureus( 27. 3%) and the coagulase negative staphylococci (18. 2%). (Umeh, et al. , 2007) A similar study was also conducted in Nepal and reported thatStaphylococcusaureus, S. Epidermidis, Streptococcus pyogenes, Klebsiella pneumonia, Salmonella choleraesius, E. coli, Enterobacteraerogenesand cloaceaewere isolated from paper money of Nepal. (Lamichhane, et al. 2009) In another study in India, 100% of the currency notes of Indian upee were contaminated with bacteria. Mainly three species including E. coli, Proteus spp. And Staphylococcus aureuswere isolated. (Bhat, et al. , 2010) In another study in India, currency samples of different denominations from different occupational groups were evaluated for isolation of microbial contaminants and Staphylococcus aureu, E. coli, Bacillus spp. , Klebsiella spp. , Proteus mirablisand fungus like Aspergillusnigerand Fusariumwere isolated from these paper currency notes. (Rote, et al. 2010) Although, a lot of studies on the microbiological status of paper currency have been carried out elsewhere, data on the microbial contamination of the Peso (Philippine currency) is scanty. In order to know the prevalence of Escherichia coli on Philippine Peso bill within the vicinity of Iloilo City in the year 2012-2013, this study is to be conducted. General Objectives What is the prevalence rate of E. coli contamination on the Philippine peso bill of Public Utility Jeepney (PUJ)? Specific Objectives 1. ) What is the prevalence rate of E. coli contamination on the 20 peso bill? . ) What is the prevalence rate of E. coli contamination on the 50 peso bill? 3. ) What is the prevalence rate of E. coli contamination on the 100 peso bill? Research Paradigm Independent variableDependent variable Location:Public Utility Jeepn ey (PUJ)Value:20 PHP50 PHP100 PHP| Prevalence rate of Escherichia coli contamination| Figure 1. Schematic Diagram of the Study Definition of Terms To provide clarity and understanding, the following terms were defined conceptually and operationally. Bacteria- are minute, unicellular organisms that reproduce by binary fission.They are considered prokaryotes due to the absence of nuclear membrane. They possess both DNA and RNA. They sensitive to penicillins, tetracycline and chloramphenicol. (Moraleta, Review of Microbiology) In the study, the bacteria is the E. coli to be identified. Escherichia coli- or E. coli is a bacterium that is commonly found in the gut of humans and other warm-blooded animals. While most strains are harmless, some can cause severe foodborne disease. E. colià infection is usually transmitted through consumption of contaminated water or food, such as undercooked meat products and raw milk.Symptoms of disease include abdominal cramps and diarrhoea, which may b e bloody. Fever and vomiting may also occur. Most patients recover within 10 days, although in a few cases the disease may become life-threatening. (WHO, 2012) As used in this study,E. coli is the subject of the study and it is isolated in the surfaces different peso bill. Contamination-The act or process ofà contaminating; pollution; defilement; taint; also, that which contaminates. (http://www. merriam-webster. com/) In this study, contamination refers how high or low E. oli bacteria level is found on the surface of the peso bill. Denomination-a value or size of a series of values or sizes. (http://www. merriam-webster. com/) As used in thisstudy, 20, 50, 100 are used as denomination. Paper bill- (often known as aà bill,à paper moneyà or simply aà note) is a type ofnegotiable instrumentà known as aà promissory note, made by aà bank, payable to the bearer on demand. (http://en. wikipedia. org) In this study, paper bill was tested for the presence or absence of E. co li. Philippine peso- is the currency of theà Philippines.The peso is usually denoted by the symbol ââ¬Å"? ââ¬Å". Other ways of writing the Philippine peso sign are ââ¬Å"PHPâ⬠, ââ¬Å"PhPâ⬠, ââ¬Å"Phpâ⬠, and/or ââ¬Å"Pâ⬠. (http://www. wikipedia. org/) As used in this study, Philippine peso paper bill was tested for the presence of E. coli. Public Utility Jeepney (PUJ)- are the most popular means ofà public transportationà in the Philippines. (http://www. wikipedia. org/) In this study, this is the location of the Philippine peso billwhere the E. coli is to be isolated. Significance of the Study The result of the study will benefit the following:Department of Health. May provide information on how to properly handle and care for money to prevent the risk of Escherichia coli contamination from hand-to-hand communication. The Medical Researchers. They may use this study as reference for future studies especially in the prevention of the deadly disease c aused by Escherichia coli on the circulating money. Commercial Banks. They may have an idea that Escherichia coli can inhabit the paper bill and cause such disease. Hence, they will come up bacteria-free money. Jeepney Drivers.May help them in protecting their selves from being the courier of contaminated money from one person to another. The public. The result will provide information and awareness about money contaminated by Escherichia coli circulates, and find ways in preventing disease and reduce mortality. Future researcher. The result of the study may also be used by other future researcher as a reference or basis for future researcher or investigation. Scope and Limitation of the Study This study aims to determine the prevalence of Escherichia coli contamination on Philippine peso bill within the vicinity of Iloilo City.A total of 45 paper currency of denominations, fifteen paper currencies of each: 20 PhP, 50 PhP and 100 PhP in circulation were randomly collected in 15 jeep neys at different times. Coins were excluded from the study. Paper currencies were gathered from Jaro-CPU Public Utility Jeepney (PUJ) from CPU to Iloilo City route and vice versa. This study is conducted during the month of March until May in the year 2013. Persons handling the bill were asked to deposit them in sterile polyethylene bags, sealed and taken to the Medical Laboratory Science Research Laboratory of Central Philippine University, for analysis. CHAPTER 2REVIEW OF RELATED LITERATURE AND STUDIES This chapter deals with the related literature and studies relevant to the study of Escherichia coli contamination on paper money bills. Money in the form of notes or coins is handled by everyone, and ââ¬Ëdirty' money (money contaminated with pathogenic microorganisms) is always in circulation. Contamination may occur during production, during storage after production, and during use. Microorganisms on the skin can be transferred from cashiers, salespeople and the general public to the currency notes that they handle. Contamination from the anal region, wounds, nasal secretions and aerosols enerated by sneezing and coughing are potential sources of transfer of microorganisms to currency notes during handling. Staphylococcus epidermidis, Pseudomonas aeruginosaà andà Klebsiellaaerogenesà have been reported to survive well on the skin,and are known to be transferred from fabrics to hand as well as from hand to fabrics. (Tswana, 2000) Items that are passed from hand to hand are likely to be contaminated with disease-causing bacteria particularly if carried with unclear hands, or kept in a dirty environment. Similarly, paper currency is widely exchanged for goods and services in countries worldwide.Currency contamination with pathogenic bacteria is of much public health concern as contaminated materials can be sources of serious pathogens. Paper currency, therefore presents a particular risk to public health, since they go in circulation and contaminate t he hands of others transmitting pathogenic organisms in the process. (Uneke&Ogbu, 2007) Pathogenic bacteria that may survive on the currency banknotes may serve as a potential source of enteropathogens causing food poisoning because food vendors handle and serve food and at the same time handle currency banknotes as they sell. Cardoenet al. , 2009; Lamichhaneet al. , 2009) The incidence of food poisoning is on the increase worldwide, although it is estimated that only 10% of cases are reported ââ¬â just the tip of the iceberg. Money bill play a major role in transmission of pathogenic bacteria. Some mathematical models have been developed to help understand the movements of currency and how this might contribute to the global spread of disease. One of the main sources of pathogenic or food-poisoning bacteria is people. People commonly carry these bacteria in their nose, mouth, wounds and intestines, and on their skin.There are several reports of the occurrence of microorganisms, in particular bacteria, on cash ââ¬â banknotes and coins. A study in the US showed that only 6% of banknotes tested were free from microbial contamination. Dirty money Modern banknotes are made from a special blend of 75% cotton and 25% linen with small segments of fibre, so ââ¬Ëpaperââ¬â¢ money is something of a misnomer. The ââ¬Ëpaperââ¬â¢ is referred to as the substrate during the manufacturing process; this is an appropriate name as bacteria require a substrate for growth.The cotton/linen/fibre combinations of banknotes produce a strong bond and do not pull apart, unlike the fibres of ordinary paper. The average life span of a low denomination paper banknote is about 24 months. In the early 1980s, an American Bank developed polyethylene fibres for use as currency and they are still in use in some Central American countries. Non-fibrous, non-porous, polymer banknotes, developed by the Reserve Bank of Australia, were first issued as currency in 1988. The banknotes were made from biaxially oriented polypropylene that made them more durable, with security features that rendered them difficult to counterfeit. Aidoo, 2011) Various routes are known that lead to the contamination of paper bill. Handling of it results in the transfer of bacteria from money onto hands or from hands onto money. Individuals who cough or sneeze into their hands can easily transfer bacteria onto currency when they handle it. Viruses may also be transmitted when infected people touch surfaces, such as banknotes, that are then touched by others. In the hospitality and catering industry, it is unacceptable for staff to use one hand to handle food and the other to handle money.Food, either cooked or uncooked, may contain bacteria which can be transferred either directly or indirectly through a medium such as a work surface onto currency. This may occur particularly with street food, mobile food vendors and in retail outlets at the counter. Obviously, the transfer of pathoge nic bacteria to food that is ready to be eaten and that requires no further heat treatment could have serious consequences. Should money be handled between hand washing and food handling, then it is equally important to repeat the process of hand washing before handling high-risk food.Wallets, purses, cash registers and other ââ¬Ëclosedââ¬â¢ environments are conducive for microbial growth because they create warm and moist conditions. Transfer of micro-organisms from one banknote to another in such closed environments may also be common. (Aidoo, 2011) Money on which pathogenic microorganisms might survive represents an often overlooked reservoir for enteric disease (Michaels, 2002). In most parts of the developed world, there is a popular belief that the simultaneous handling of food and money contributes to the incidence of food-related public health incidents (Food Science Australia [FSA], 2000).It goes without saying that bacteria are everywhere in the environment and most of these microbes are harmless to humans. Should germs on money worry us? Surprisingly, studies of bacteria on money are scarce. In 1972 a study in the Journal of the American Medical Association studied bacteria from 200 coins and bills and found harmful germs like fecal bacteria and Staphylococcus aureus on 13 percent of coins and 42 percent of notes. The study concluded: ââ¬Å"Money is truly dirty. â⬠(http://christophreilly. hubpages. com/) Micro-organisms commonly associated with banknotes include Staphylococcus aureus, ? haemolytic Streptococcus, Enterobacter spp. , Acinetobacter spp. , Pseudomonas spp. , Bacillusspp. , Escherichia coli, Salmonella spp. , viruses, yeasts and moulds. Some of these bacteria are pathogenic, while others may cause opportunistic infections. The predominant, recurrent pathogenic bacteria found on banknotes are S. aureus, Bacillus spp. and Escherichia spp. Many members of the Enterobacteriaceae are found in the gut of animals and humans, and th eir presence in food or on inanimate objects and surfaces is a good indicator of poor hygiene.Members of the genera Enterobacter, Escherichia and Klebsiella isolated from banknotes may not themselves cause serious illness; however, their isolation from money may indicate the presence of other pathogenic organisms. Escherichia coliis an important member of the faecal coliform group and its presence on banknotes is of public health concern, especially as some strains can of course cause serious illness. Species of the Gram-negative genus Pseudomonas, which can cause serious opportunistic infections, have also been isolated from banknotes.S. aureus is the predominant bacterium present on the surface of banknotes and it is also a common cause of food poisoning. This organism is indicative of poor standards of hygiene particularly during food handling and/or preparation. Many people in the adult population carry S. aureus on their skin, in their nasal cavity, and in septic cuts, boils an d spots. Coagulase-positive S. aureus is readily isolated from banknotes and the toxins it produces may cause toxic shock syndrome. It has also been implicated in pneumonia.Streptococci are part of the normal microflora in the mouth, skin, intestine and upper respiratory tract of humans. Although many streptococcal species are non-pathogenic, some have been implicated in meningitis and pneumonia. Bacillus spp. are spore-formers and can withstand harsh, adverse conditions, such as drying. Some species, for example Bacillus cereus, cause two types of food poisoning: diarrhoeal (heat-labile toxin) and emetic (heat-stable toxin). (Aidoo, 2011) The surface of ââ¬Ëpaperââ¬â¢ banknotes is not smooth, but irregular, and can harbour many different types of microorganisms.The two main factors that determine the occurrence of bacteria on currency are (i) the material that the banknotes are made from and (ii) the age of the banknote. Bacteria have enormous capabilities to allow them to su rvive in adverse conditions. Two of the most important strategies for survival are their ability to adhere to surfaces and the ability to form biofilms (multicellular aggregates). Members of some genera, such as Bacillus, may form spores and can survive attached to banknotes for many years. Formation of a biofilm or a spore is controlled by genetic activity of the bacterium.Bacterial cells on banknotes are measured by the number of colony-forming units (c. f. u. ) per cm2 of banknote. A banknote may contain up to 106c. f. u. cmââ¬â2, whilst a coin may have up to 103c. f. u. cmââ¬â2. Studies have shown that polymer-based banknotes often have a relatively low bacterial count compared with the cotton-based ââ¬Ëpaperââ¬â¢ banknotes. This may be due to various physicochemical parameters of polymers. For example, a negatively charged and hydrophilic synthetic polymer would adversely affect bacterial attachment. (Vriesekoop et. al. , 2010) Escherichia coli, also known as E. o li is a Gram-negative, rod-shaped bacterium that is commonly found in the lower intestine of warm-blooded organisms (endotherms). Most E. coli strains are harmless, but some types can cause serious food poisoning in humans, and are occasionally responsible for food contamination. (CDC National Center for Emerging and Zoonotic Infectious Diseases, 2012) The harmless strains are part of the normal flora of the gut, and can benefit their hosts by producing vitamin K2, and by preventing the establishment of pathogenic bacteria within the intestine. (Hudault et al. , 2001).Fecalââ¬âoral transmission is the major route through which pathogenic strains of the bacterium cause disease. Cells are able to survive outside the body for a limited amount of time, which makes them ideal indicator organisms to test environmental samples for fecal contamination. There is, however, a growing body of research that has examined environmentally persistent E. coli which can survive for extended period s outside of the host. (Ishii &Sadowsky, 2008) Escherichia coli (or E. coli) is the most prevalent infecting organism in the family of gram-negative bacteria known as enterobacteriaceae.E. coli is often referred to as the best or most-studied free-living organism. More than 700 serotypes of E. coli have been identified. The ââ¬Å"Oâ⬠and ââ¬Å"Hâ⬠antigens on the bacteria and their flagella distinguish the different serotypes. Indeed, some E. coli are beneficial, while some cause infections other than gastrointestinal infections, such as urinary tract infections. The E. coli that are responsible for the numerous reports of contaminated foods and beverages are those that produce Shiga toxin, so called because the toxin is virtually identical to that produced by Shigelladysenteria type 1. Eisenstein et al, 2000) Strains of E. coli that causes diarrhea in man â⬠¢ Enteropathogenic E. coli (EPEC) ââ¬â causes diarrhea, but the molecular mechanisms of colonization and a etiology are different. EPEC lack fimbriae, ST and LT toxins, but they use an adhesin known as intimin to bind host intestinal cells. This virotype has an array of virulence factors that are similar to those found in Shigella, and may possess a shiga toxin. Adherence to the intestinal mucosa causes a rearrangement of actin in the host cell, causing significant deformation. EPEC cells are moderately invasive (i. . they enter host cells) and elicit an inflammatory response. A change in intestinal cell ultrastructure due to ââ¬Å"attachment and effacementâ⬠is likely the prime cause of diarrhea in those afflicted with EPEC. (University of Wisconsinââ¬âMadison Department of Bacteriology, 2007) â⬠¢ Enterotoxigenic E. coli (ETEC) ââ¬â Enterotoxigenic Escherichia coli, or ETEC, is the name given to a group of E. coli that produce special toxins which stimulate the lining of the intestines causing them to secrete excessive fluid, thus producing diarrhea. (cdc. gov, 2004) à ¢â¬ ¢ Enteroinvasive E. oli (EIEC) ââ¬â this infection causes a syndrome that is identical to Shigellosis, with profuse diarrhea and high fever. EIEC are highly invasive, and they utilize adhesin proteins to bind to and enter intestinal cells. They produce no toxins, but severely damage the intestinal wall through mechanical cell destruction. ( Lan et al, 2004). â⬠¢ Enteroaggregative E. coli (EAEC) ââ¬â is a subgroup of diarrhoeagenic E. coli (DEC) that during the past decade has received increasing attention as a cause of watery diarrhea, which is often persistent. EAEC have been isolated from children and adults worldwide.As well as sporadic cases, outbreaks of EAEC-caused diarrhea have been described. (sgmjournals. org, 2003) â⬠¢ Diffusely adherent E. coli (DAEC) ââ¬â may cause disease in immunologically naive or malnourished children. Discrepancies among epidemiological studies could be explained by age-dependent susceptibility to diarrhea or by the use of a n inappropriate detection method such as DNA probing. The current prospective case-control study was done to determine the role of DAEC strains as a cause of acute diarrhea in northeastern Brazil, where childhood diarrhea is endemic. ( M. M. Levine. 1990) â⬠¢ Shiga toxin-producing E. oli (STEC) ââ¬â Some strains of E. coli produce a toxin called Shiga toxin that causes diarrhea and can lead to severe illness. These Shiga toxin-producing E. coli are sometimes called STEC (pronounced ââ¬Å"S-TECK). STEC can be spread from cattle and other animals to people through raw or undercooked meat, unpasteurized milk, or through contact with an infected animal. People can also get infected by consuming contaminated water, raw produce or unpasteurized juice or cider. Foods can become contaminated with bacteria from manure in the field or from raw beef or raw beef juices in the kitchen.People with STEC who do not wash hands well after a bowel movement can spread it to others. (kingcounty . gov, 2005) The genera Escherichia and Salmonella diverged around 102 million years ago, which coincides with the divergence of their hosts: the former being found in mammals and the latter in birds and reptiles. This was followed by a split of the escherichian ancestor into five species (E. albertii, E. coli, E. fergusonii, E. hermannii and E. vulneris. ) The last E. coli ancestor split between 20 and 30 million years ago. ( Lecointre et al. 2007) In 1885, a German pediatrician, Theodor Escherich, first discovered this species isolated from the feces of newborns and called it Bacterium coli commune due to the fact it is found in the colon and early classifications of Prokaryotes placed these in a handful of genera based on their shape and motility (at that time Ernst Haeckel's classification of Bacteria in the kingdom Monera was in place). Bacterium coli was the type species of the now invalid genus Bacterium when it was revealed that the former type species (ââ¬Å"Bacterium tril oculareâ⬠) was missing.Following a revision of Bacteria it was reclassified as Bacillus coli by Migula in 1895 and later reclassified in the newly created genus Escherichia, named after its original discoverer. ( Castellani and Chalmers, 2009) The genus belongs in a group of bacteria informally known as ââ¬Å"coliformsâ⬠, and is a member of the Enterobacteriaceae family (ââ¬Å"the entericsâ⬠) of the Gammaproteobacteria. (Garrity, 2005) Escherichia coli encompass an enormous population of bacteria that exhibit a very high degree of both genetic and phenotypic diversity. Genome sequencing of a large number of isolates of E. oli and related bacteria shows that a taxonomic reclassification would be desirable. However, this has not been done, largely due to its medical importance and E. coli remains one of the most diverse bacterial species: only 20% of the genome is common to all strains. (Lukjancenko et. al. , 2010) In fact, from the evolutionary point of view, the mem bers of genus Shigella (S. dysenteriae, S. flexneri, S. boydii, S. sonnei) should be classified as E. coli strains, a phenomenon termed taxa in disguise. Similarly, other strains of E. coli (e. g. he K-12 strain commonly used in recombinant DNA work) are sufficiently different that they would merit reclassification. (Lan; Reeves, 2002) A strain is a sub-group within the species that has unique characteristics that distinguish it from other strains. These differences are often detectable only at the molecular level; however, they may result in changes to the physiology or lifecycle of the bacterium. For example, a strain may gain pathogenic capacity, the ability to use a unique carbon source, the ability to take upon a particularecological niche or the ability to resist antimicrobial agents. Different strains of E. oli are often host-specific, making it possible to determine the source of fecal contamination in environmental samples. For example, knowing which E. coli strains are pre sent in a water sample allows researchers to make assumptions about whether the contamination originated from a human, another mammal or a bird. (Feng et. al. , 2002) The bacteria normally adhere to the mucus or the epithelium on the wall of the intestines, and a single strain can last for months or years. E. coli is one of the most studied and best understood organism, but the organism's role and how it colonizes isn't very well understood.Freter's Nutrient-Niche theory best describes E. coli's role: The ecological functions of E. coli depend on the nutrient availability within the intestines of the host organism. Since there are so many different nutrients that can be found within the intestines, it is said that they contain a balanced ecosystem because there are so many different nutrient-defined functions where the E. coli colonize. This is dependent on the preferred nutrient for that particular population occupying the niche. E. coli can also be found outside of the body in fae cally-contaminated environments such as water or mud. (bioweb. wlax. edu, 2008) The optimal growth of E. coli occurs at 37 degrees Celsius but some laboratory strains can multiply at temperatures of up to 49 degrees C. Growth can be driven by aerobic or anaerobic respiration. (answers. ask. com, 2010) As E. coli is part of the common micro? ora in the large intestine, it is accustomed to a pH of 7-8. As glucose is absorbed in the small intestine, the E. coli would be used to low concentrations. However, as glucose is its energy source, if excess glucose were available for consumption, it would be expected that the E. coli would utilise it and grow at a faster rate.Salt (NaCl) is absorbed in the colon, so the amount of salt that the E. coli is exposed to depends on how much salt is consumed by the host organism. However, because of the mechanism of osmosis, extremely high levels as well as complete absence of salt could be lethal to E. coli bacteria. (APUA, 2007 How Antibiotics Work ââ¬â the Mechanism of Action , Alliance for the Prudent Use of Antibiotics,) You get an E. coli infection by coming into contact with the feces of humans or animals. This can happen when you drink water or eat food that has been contaminated by feces. Healthwise, 2011) E. coli infection can cause human illness when E. coli is ingested through various modes of transmission, including through food and water sources, animal-to-human contact, and person-to-person contact. (Clark, 2012) And according to the (Centers for Disease Control and Prevention) CDC, the transmission of these bacteria to humans may occur in the following manner: â⬠¢Meat, such as beef from cows, may become contaminated when organisms are accidently mixed in with beef, especially when it is ground. Meat contaminated with E. coli does not smell and looks normal.It is important to thoroughly cook the beef. â⬠¢Infection may occur after swimming in or drinking water that has been contaminated with E. coli. â ⬠¢Person-to-person contact in families and in child-care and other institutional-care centers are also places where the transmission of the bacteria can occur. However, the CDC also indicates the way E. coli is transmitted may change over time. (medicalcenter. osu. edu, 2006) To help avoid food poisoning and prevent infection, handle food safely. Cook meat well, wash fruits and vegetables before eating or cooking them, and avoid unpasteurized milk and juices.You can also get the infection by swallowing water in a swimming pool contaminated with human waste. (nlm. nih. gov, 2012) Pathogenic Escherichia coli, or E. coli, is believed to mostly live in the intestines of cattle. Certain serotypes of E. coli have also been found in the intestines of chickens, sheep, and pigs. (Clark, 2012) E. coli in food E. coli can get into meat during processing. If the infected meat is not cooked to 160à °F (71à °C), the bacteria can survive and infect you when you eat the meat. This is the most common way people become infected with E. coli.Any food that has been in contact with raw meat can also become infected. Other foods that can be infected with E. coli include: Raw milk or dairy products. Bacteria can spread from a cow's udders to its milk. Check the labels on dairy products to make sure they contain the word ââ¬Å"pasteurized. â⬠This means the food has been heated to destroy bacteria. Raw fruits and vegetables, such as lettuce, alfalfa sprouts, or unpasteurized apple cider or other unpasteurized juices that have come in contact with infected animal feces. E. coli in water Human or animal feces infected with E. oli sometimes get into lakes, pools, and water supplies. People can become infected when a contaminated city or town water supply has not been properly treated with chlorine or when people accidentally swallow contaminated water while swimming in a lake, pool, or irrigation canal. E. coli from person-to-person contact The bacteria can also spread from o ne person to another, usually when an infected person does not wash his or her hands well after a bowel movement. E. coli can spread from an infected person's hands to other people or to objects. Person-to-person transmission of E. oli occurs through a fecal-oral route, and is particularly common among infants and young children due to their unrefined hygienic practices. Person-to-person transmission of E. coli has also been known to occur between infected individuals and their caregivers, and between infected handlers of certain objects. (WebMD, 2010) In a study entitled ââ¬Å"Microbial Contamination in 20-Peso Banknotes in Monterrey, Mexicoâ⬠, the banknotes came from various sources, including banks, toll booths, convenience stores, restaurants, cafeterias, and yogurt stores, among others.Samples were randomly obtained and banknotes were placed in a sterile polyethylene bag. The bag was sealed and the sample was taken to the laboratory. All currency banknotes were in good ph ysical condition. Each banknote was placed in 5-mL sterile saline for 24 hours. A sterile, cotton-tipped swab was briefly introduced in the saline and the swab was seeded with a portion of the saline homogenized in blood agar plates and incubated for 48 hours at 37à °C in aerobic conditions. Plates were then examined for bacterial growth and the colonies underwent Gram stain.Gram-negative colonies were grown on Eosin methylene blue agar plates and identified with the Crystal Identification System (Becton Dickinson). Gram-positive cocci were grown on azide agar plates and identified by conventional biochemical tests. Identification of yeasts was performed with CHROMagar Candida (Becton Dickinson). Of the 70 currency banknotes on which bacteriological analysis was conducted, 48 (69%) were found to be contaminated with several microbial species (Table 1).Sixteen species isolates were obtained from the banknotes: 14 bacterial species (four [23%] Gram positive and 10 [63%] Gram negative ) and two (13%) yeast species. The most prevalent species observed was Candida kruseii (19 banknotes, 27%) followed by Burkholderiacepacia (nine banknotes, 13%). Of the 70 banknotes included, 22 (31%) showed no growth. Four bills (5. 7%) yielded bacteria considered pathogenic to healthy hosts and the other 44 contaminated bills (63%) yielded bacteria considered potentially pathogenic to hospitalized or immunocompromised hosts.Additionally, 11 bills showed more than one microbial species. Pope and co-authors analyzed 68 $1 bills collected from a school and a grocery store and found that five (7%) were contaminated with pathogenic bacteria, 59 (87%) were contaminated with opportunistic pathogens, and just four (6%) were free of bacteria (Pope et al. , 2002). Unlike the study by Pope and co-authors, in our study 31% of the banknotes were negative. Our results are similar to a previous publication (Abrams; Waterman, 1972), in which 70% of banknotes were contaminated with bacteria.Of the se banknotes, 60% contained pathogens, including S. aureus, E. coli, and P. aeruginosa. Medical personnel seem to play an important role in contamination of paper currency, since it has been reported that 13% of coins and 42% of currency collected from laboratory personnel were contaminated with S. aureus, E. coli, Klebsiella sp. , and Proteus mirabilis (Abrams; Waterman, 1972). Additionally, the culture of 100 banknotes and 102 coins collected from medical personnel showed that 3% of coins and 11% of banknotes were contaminated with opportunistic pathogens (KhinNwe et al. 1989). In our study, we did not include banknotes collected in any hospital, but banknotes collected near hospital facilities were contaminated with opportunistic pathogens such as B. cepacia and A. baumannii. Uneke and Ogbu assessed the potential of Nigerian currency notes to act as environmental vehicles for the transmission of pathogenic parasites and bacteria. Currency notes obtained from four major cities in Nigeria were evaluated according to standard techniques. Fifty-four (21. 6 percent [95 percent CI: 16. 50-26. 0]) of the first batch of 250 notes, which underwent parasitological analysis, were contaminated with enteric parasites; 133 (53. 2 percent [95 percent CI: 47. 02-59. 39]) of the second batch of 250 notes, which underwent bacteriological analysis, were found to be contaminated with bacteria. Parasites that were isolated from the notes included Ascarislumbricoides (8. 0 percent), Enterobiusvermicularis (6. 8 percent), Trichuristrichiura (2. 8 percent), and Taenia species (4. 0 percent). Bacteria that were isolated were Streptococcus species (21. percent), Staphylococcus species (12. 8 percent), Escherichia coli (13. 2 percent), and Bacillus species (5. 6 percent). Among dirty/mutilated currency notes, parasite contamination and bacterial contamination were both significantly (p ; . 05) more pervasive (30. 6 percent and 73. 8 percent, respectively) than they were among clean a nd mint currency notes. Lower-denomination notes were more likely to be contaminated than were higher-denomination notes, although the difference was not statistically significant (p ; . 05).Parasite contamination and bacteria contamination were both most frequent in notes obtained from butchers and beggars. These results suggest that currency notes may be contaminated, especially with bacteria and enteric parasites, and may serve as sources of infection. The possibility that currency notes might act as environmental vehicles for the transmission of potential pathogenic microorganisms was suggested in the 1970s (Abrams; Waterman, 1972). Paper currency is widely exchanged for goods and services in countries worldwide.It is used for every type of commerce, from buying milk at a local store to trafficking in sex and drugs. All this trade is hard on currency, with lower-denomination notes receiving the most handling because they are exchanged many times (Gadsby, 1998). Although paper cu rrency is made to take abuse (up to 4,000 folds in each direction) in most parts of the world, including in Nigeria (where paper currency is a rugged mix of 75 percent cotton and 25 percentlinen), it lasts less than a few years in circulation (Gadsby, 1998).The average U. S. dollar, for instance-like most currency notes worldwide-lasts a mere 18 months (Gadsby). Paper currency also provides a large surface area as a breeding ground for pathogens (Podhajny, 2004). Oddly, publications regarding the degree to which paper money is contaminated with bacteria are few and far between, as the authors found when they conducted a Medline search in December 2005 (Abrams; Waterman, 1972; El-Dars; Hassan, 2005; Goktas;Oktay, 1992; Jiang ; Doyle, 1999; Khin et al. 1989; Michaels, 2002; Pope et al. , 2002; Singh et al. , 2002; Xu et al. , 2005). Furthermore, the search found no documented study of the parasitological status of currency notes (as of December 2005). Scientific information on the con tamination of money by microbial agents is also lacking in most developing countries in sub-Saharan Africa, including Nigeria. This dearth of information may have contributed to the absence of public health policies or legislation on currency usage, handling, and circulation in many parts of Africa.Although the studies done in the United States and Australia have had no major impact on policies or legislation on currency handling and circulation in those countries, they have fostered a higher level of public awareness about the potential for currency contamination by microorganisms (Dow Jones News, 1998; FSA, 2000; Michaels; Jiang ; Doyle; Pope et al. ). In the United States, a whole division of the Department of Treasury deals with what is termed ââ¬Å"mutilated currency,â⬠and the department Web site boasts many examples of beleaguered, burned, buried, water-damaged money (Siddique, 2003).Isolation of various bacterial contaminants from the currency notes was performed via s tandard techniques described previously (Gilchrist, 1993; Singh et al. , 2002). Briefly, a sterile, cotton-tipped swab moistened with sterile physiological saline was used to swab both sides of the currency note. The swabs were directly inoculated on blood agar and MacConkey agar. The pairs of inoculated media were incubated aerobically at 35-37à °C for 24 hours and then examined for bacterial growth according to standard protocol described previously (Cheesbrough, 2000).The authors isolated bacteria by assessing colony characteristics and Gram reaction, and by conducting catalase and coagulase tests; hemolysis, sugar fermentation, and other biochemical tests, including tests for indole production, citrate utilization, and urase activity; triple sugar iron (TSI) agar tests (for glucose, sucrose, and lactose fermentation); gas and hydrogen sulfide production tests; and oxidase tests, according to protocols described previously (Cheesbrough). Bacteria were identified but were not qua ntified.Microbial contaminants can be transmitted directly by hand-to-hand contact or indirectly via food or inanimate objects like banknotes and doorknobs or other objects that come into contact with multiple human hands. Banknotes may be contaminated during storage and exchange, with lower-denomination banknotes receiving the most handling and therefore more contamination (Abrams; Waterman, 1972). In general, a greater number of bacteria have been reported on banknotes than on coins. Banknotes are an excellent transport medium for different types of microorganisms because they are commonly passed among individuals.Thus, handling money may be a route for transmission of infections (Xu et al. , 2005). We analyzed a sample of 70 20peso bills to isolate and identify bacteria or yeast that may be present on the surface of these banknotes. A recent study that included 1,280 banknotes from 10 countries, including Mexico, reported that pathogens could only be isolated after enrichment and their mere presence did not appear to be alarming (Vriesekoop et al. , 2010). The authors discussed that the presence of bacteria on banknotes is influenced by the material used for the banknotes (polymer based vs. otton based) and the age of the banknotes. They stated that the average number of bacteria encountered on the polymer banknotes was approximately 25% of that found on cotton-based banknotes (Vriesekoop et al. , 2010). That study showed a lower percentage of contamination in Mexican banknotes in comparison to banknotes from China, the U. S. , the UK, and the Netherlands, among others. We analyzed only polymer-based banknotes in good condition, but the presence of contamination was detected in most banknotes analyzed without any enrichment procedure.In that study, the only contaminations detected in Mexican banknotes were E. coli, S. aureus, and a low percentage of Bacillus cereus, which were interpreted as an indicator of poor hygiene, background microorganism, and the ab ility of spore-forming bacteria to persist on banknotes, respectively. In our study, we detected S. aureus and Bacillus spp. but we did not detect E. coli. It is important to point out that the 10-country study included currencies obtained only from food outlets and for this reason the results from that study and ours cannot strictly be compared. Source: Microbial Contamination in 20-Peso Banknotes in Monterrey, Mexico Rocha-Gamez, Judith; Tejeda-Villarreal, Paula Nelly, QCB; Macias-Cardenas, Patricia; Canizales-Oviedo, Jorge; Garza-Gonzalez, Elvira; et al. Journal of Environmental Health 75. 2 (Sep 2012): 20-3. ) In another study, entitled ââ¬Å"Potential for Parasite and Bacterial Transmission by Paper Currency in Nigeriaâ⬠, Bacteria that were isolated were Streptococcus species (21. 6 percent), Staphylococcus species (12. 8 percent), Escherichia coli (13. 2 percent), and Bacillus species (5. 6 percent).Among dirty/mutilated currency notes, parasite contamination and bacteri al contamination were both significantly (p ; . 05) more pervasive (30. 6 percent and 73. 8 percent, respectively) than they were among clean and mint currency notes. Lower-denomination notes were more likely to be contaminated than were higher-denomination notes, although the difference was not statistically significant (p ; . 05). Personal hygiene to reduce risk of infection is recommended. Microbial contaminants may be transmitted either directly, through hand-to-hand contact, or indirectly, via food or other inanimate objects.These routes of transmission are of great importance in the health of many populations in developing countries, where the frequency of infection is a general indication of local hygiene and environmental sanitation levels. (Cooper, 1991). Paper currency is widely exchanged for goods and services in countries worldwide. It is used for every type of commerce, from buying milk at a local store to trafficking in sex and drugs. All this trade is hard on currency , with lower-denomination notes receiving the most handling because they are exchanged many times (Gadsby, 1998).Bacteriological analysis indicated that 133 (53. 2 percent, [95 percent CI: 47. 02-57. 39]) of the second batch of 250 notes were contaminated with bacteria: 37 (52. 9 percent) of the 70 clean notes and 96 (73. 8 percent) of the 130 dirty/mutilated notes. Neither parasite ova nor bacteria were found on the mint notes. Contamination was related to denomination of currency. Contamination with bacteria was most prevalent among the N5 notes (62. 2 percent) and least prevalent among the N500 notes (32. 0 percent). Contamination was also related to the physical condition of the currency.The dirty/mutilated notes also had the highest prevalence of bacterial contamination (73. 8 percent). Among the clean notes, 52. 9 percent were contaminated with bacteria. Chi-square analysis indicated a statistically significant association between bacterial contamination and currency condition (? ^sup 2^ = 79. 030, df = 2, p;. 05). In the study reported here, a random approach was adopted for currency sampling; whatever money was provided was collected. The implication is that the majority of the people are exposed to dirty notes.In Nigeria, poor-currency-handling culture is widespread, and there is indiscriminate abuse of currency notes. A great majority of the populace does not carry money in wallets, and squeezing of currency notes is a common occurrence. Women, especially among the unenlightened, often place money underneath their brassieres, while men place theirs in their socks. These activities not only enhance currency contamination but may also increase the risk of infection from contaminated notes. The situation is further compounded by the inability of the Nigerian government to consistently withdraw old, worn-out, and mutilated notes from circulation.The presence of damaged currency notes and the failure to consistently withdraw them from circulation are comm on phenomena in many parts of Africa and Asia (Gadsby, 1998; Podhajny, 2004). The persistence of damaged or terribly mutilated notes in active circulation (some so damaged that they can no longer be stuck together) could elevate their contributory role in transmission of some pathogens, thereby constituting potential public health hazard. ( Source: Uneke, C. and Ogbu, O. Potential for parasite and bacteria transmission by paper currency in Nigeria. J Environ Health, 69 (2007) 54ââ¬â60. (1)) CHAPTER 3RESEARCH DESIGN AND METHODOLOGY Purpose of the Study The purpose of the study is to determine the prevalence of E. coli contamination on Philippine Peso bill on Public Utility jeepney (PUJ), specifically on: twenty (20), fifty (50), one hundred (100) pesos. Subjects of the study The subject of the study is the fifteen (15) Public Utility Jeepney drivers routing Jaro-CPU and City Proper bound. On each driver, three (3) Philippine Peso bill samples with amounts: 20, 50 and 100 are to b e collected. Data Gathering 45 peso bills are to be used as sample and will be collected on the month of March 2013 at around 10:00 ââ¬â 11:00 in the morning.The samples will be taken randomly from 15 Public Utility Jeepney (PUJ) of Jaro ââ¬â Cpu Route. In each jeepney, three(3) different values: 20, 50, and 100 Php are to be taken and tested, so the total number of samples is 45. The samples collected will be placed in a sealable plastic container, so as to preserve the contaminants on the peso bill. The paper bill will be brought immediately to Central Philippine University, particularly at the Medical Laboratory Science Department Research Lab for confirmatory testing of E. coli. Preparation of Laboratory Materials Needed The following are needed to conduct our study: . ) Sterile cotton swab ââ¬â will be used in obtaining the possible contaminant on the surface of the paper bill. b. )Eosin Methylene Blue Agar ââ¬â will be used in the confirmatory test for the pres ence of E. coli The following are the apparatus needed for our study: a. )Petri Dish b. )Alcohol Lamp c. )Oven All of the enumerated materials above will be borrowed from the stockroom of Medical Laboratory Science Department. A letter of permission was given to the stockroom coordinator for authorized use of the materials stated above. Eosin Methylene Blue Agar (EMB) Procedure: 1.Using a sterile cotton swab, swab on the surface of the peso bill then streak it onto an EMB agar. 2. Incubate plates at 35oC for twenty-four(24) hours. 3. After 24 hours, observe the plate as follows: The colonies developing on EMB agar plates may be divides as: Typical ââ¬â nucleated with or without metallic sheen Atypical ââ¬â opaque, pink mucoid, non-nucleated Negative ââ¬â no growth or clear watery, or clear colonies Interpretation of Data Philippine peso paper bill that will give a negative reaction on the EMB agar plate is considered not contaminated with E. coli and is safe for everyday domestic use.There will be no growth or clear watery or clear colonies. On the other hand, water sample that yielded a positive result in E. coli analysis is considered to be contaminated with E. coli bacteria and is not safe. There would be a typical nucleated with or without metallic sheen. Central Philippine University Jaro, Iloilo City College of Arts and Sciences __________________ __________________ __________________ __________________ Sir/Madam, We, the 3rd yearBachelor in Medical Laboratory Science students of Central Philippine University who are currently enrolled in the subject Research is conducting a study entitled Prevalence of E. oli in Philippine Peso Bill. This is a requirement for the completion of the subject in Research 1. In line withthis, we are respectfully requesting you to be one of the respondents of our study by exchanging such peso bills: 20, 50 and 100 respectively that has been collected as commuterââ¬â¢s fare. We need this data for the completion of this study. Your positive response to this request is highly appreciated. Thank you and God bless. Respectfully yours, JUSTINE GRACE JIMENEA ISAAC JAMES LEDESMA MAJA HANNAH LOU LOJA ROBERTO MANALO Jr. JIRAH PEDROSA Researchers Noted by: DR. MA. CORAZON PORRAS Research Adviser BibliographyAbel, Andrew;à Bernanke, Benà (2005). ââ¬Å"7â⬠. Macroeconomics(5th ed. ). Pearson. pp. 266ââ¬â269. ISBNà 0-201-32789-9. Ahmed, S. U. , S. Parveen, T. Nasreen and B. Feroza, 2010. Evaluation of The Microbial Contamination of Bangladesh Paer Currency Notes (Taka) in Circulation. Advances in Biological Res. , 4 (5):266-271. Aidoo, Kofi (2011). Microbiology Today Answers. ask. com/Health/Diseases/how_does_e_coli_grow, 2010 Bernstein, Peter,à A Primer on Money and Banking, and Gold, Wiley, 2008 edition, pp29-39 Bhat, B. , S. Bhat, K. Asawa and A. Agarwal, 2010. An assessment of oral health risk associated with handling of currency notes. Int. J.Dntal Clinics, 2(3): 14-16. Bioweb. uw lax. edu/bio203/s2008/moder_just/habitat. htm, 2008 Boyle, Davidà (2006). The Little Money Book. The Disinformation Company. pp. 37. ISBNà 978-1-932857-26-9. British Royal Mint. Retrieved 2007-09-02. ââ¬Å"Legal Tender Guidelinesâ⬠. Cardoen, S. ,VanHuffel, X. , Berkvens, D. , Quoilin, S. , Ducoffre, G. , Saegerman, C. , Speybroeck, N. , Imberechts, H. , Herman, L. , Ducatelle, R. , and Dierick, K. Evidence-based semi quantitative methodology for prioritization of food borne zoonoses. Food borne Pathog. Dis. , 6 (2009) 1083-1096. (2) CDC National Center for Emerging and Zoonotic Infectious Diseases. Escherichia coliâ⬠. Retrieved 2012-10-02. Christophreilly. hubpages. com Castellani (A. ) and Chalmers(A. J. ): Manual of Tropical Medicine, 3rd ed. , Williams Wood and Co. , New York, 2009 Eisenstein, Barry and Zaleznik, Dori, ââ¬Å"Enterobacteriiaceae,â⬠in Mandell, Douglas, & Bennettââ¬â¢s Principles and Practice of Infectious Diseases, Fifth Edition, Chap. 206, pp. 2294-2310, 2000 Federal Institute for Risk Assessment. 30 June 2011. ââ¬Å"Samen von BockshornkleemithoherWahrscheinlichkeitfur EHEC O104:H4 Ausbruchverantwortlichà in English: Fenugreek seeds with high probability for EHEC O104: H4 responsible outbreakâ⬠à (in German) (PDF).BundesinstitutfurRisikobewertung (BfR)à in English. Retrieved 17 July 2011.. Feng P, Weagant S, Grant, M (2002-09-01). ââ¬Å"Enumeration ofà Escherichia colià and the Coliform Bacteriaâ⬠. Bacteriological Analytical Manual (8th ed. ). FDA/Center for Food Safety & Applied Nutrition. Retrieved 2007-01-25. Freeman, David. ââ¬Å"Change For a Hundred. â⬠à Popular Mechanics,à January 1996, pp. 72-73. Garrity, George M, ed. (July 26, 2005) [1984(Williams & Wilkins)]. The Gammaproteobacteria. Bergey's Manual of Systematic Bacteriology. 2Bà (2nd ed. ). New York: Springer. pp. 1108.ISBNà 978-0-387-24144-9. British Library no. GBA561951. Geschickter, J. ââ¬Å"Making Money. â⬠à National Geographic World,à November 2005, pp. 30-33. Goetzmann, William N. ; K. Geert Rouwenhorst (1 August 2005). The Origins of Value: The Financial Innovations that Created Modern Capital Markets. Oxford University Press. p. 94. ISBNà 978-0-19-517571-4. ââ¬Å"The Mongols adopted the Jin and Song practice of issuing paper money, and the earliest European account of paper money is the detailed description given by Marco Polo, who claimed to have served at the court of the Yuan dynasty rulers. Greco T. H. Money: Understanding and Creating Alternatives to Legal Tender, White River Junction, Vt: Chelsea Green Publishing (2001). ISBN 1-890132-37-3 Headrick , Daniel R. (1 April 2009). Technology: A World History. Oxford University Press. p. 85. ISBNà 978-0-19-988759-0. Hudault S, Guignot J, Servin AL (July 2001). ââ¬Å"Escherichia colià strains colonizing the gastrointestinal tract protect germ-free mice againstà Salmonella typhimuriumà infectionâ⬠. Gutà 49à (1) :47-55. doi:10. 1136/gut. 49. 1. 47. PMCà 1728375. PMIDà 11413110. Jmm. sgmjournals. org/content/56/1/4. full, 2003 Kingcounty. ov/healthservices/health/communicable/diseases/ecoli. aspx, 2005 Krugman, Paul ; Wells, Robin,à Economics, Worth Publishers, New York (2006) Lamichhane, J. , S. Adhikary, P. Gautam, R. Maharjan and B. Dhakal, 2009. Risk of handling paper currency in circulation chances of potential bacterial transmittance. Nepal J. Sci and Technol. , 10:161-166. Lan R, Reeves PR (September 2002). ââ¬Å"Escherichia coli in disguise: molecular origins of Shigellaâ⬠. Microbes Infect. 4à (11): 1125ââ¬â32. doi:10. 1016/S1286-4579(02)01637-4. PMIDà 12361912. Lecointre G, Rachdi L, Darlu P, Denamur E (December 2007). Escherichia coli molecular phylogeny using the incongruence length difference testâ⬠. Mol. Biol. Evol. 15à (12): 1685ââ¬â95. PMIDà 9866203. Lukjancenko O, Wassenaar TM, Ussery DW (November 2010). ââ¬Å"Comparison of 61 sequenced Esche richia coli genomesâ⬠. Microb. Ecol. 60à (4): 708ââ¬â20. doi:10. 1007/s00248-010-9717-3. PMCà 2974192. PMIDà 20623278. Mankiw, N. Gregoryà (2007). ââ¬Å"2â⬠. Macroeconomicsà (6th ed. ). New York: Worth Publishers. pp. 22ââ¬â32. ISBNà 0-7167-6213-7. Medicalcenter. osu. edu/patientcare/healthcare_services/infectious_diseases/ecoli/Pages/index. aspx on January 26, 2013 Michaels, B. (2002).Money and serving ready-to-eat food. Food Service Technology, 2(1), 1-3. Mishkin, Frederic S. (2007). The Economics of Money, Banking, and Financial Markets (Alternate Edition). Boston: Addison Wesley. p. 8. ISBNà 0-321-42177-9. Moraleta, Nardito (2007). Review of Microbiology page 91 Nlm. nih. gov/medlineplus/ecoliinfections. html Oyero, O. G. and B. O Emikpe, 2007. Preliminary Investigation on the Microbial Contamination of Nigerian Currency. Int. J. Trop. Med, 2(2):29-32 Pope, T. W. , P. T Ender, W. K Woelk, M. A. Koroscil and T. M. Koroscil, 2002. Bacterial contami nation of paper currency Southern Med.J. , 95:14061410. Rocha-Gamez, Judith; Tejeda-Villarreal, Paula Nelly, QCB; Macias-Cardenas, Patricia; Canizales-Oviedo, Jorge; Garza-Gonzalez, Elvira; et al. , Microbial Contamination in 20-Peso Banknotes in Monterrey, Mexico Journal of Environmental Health 75. 2 (Sep 2012): 20-3. Rote, R. B. , N. G Deogade and M. Kawale, 2010. Isolation, characterization and antibiotic sensitivity of organism from Indian currency Asiatic J. Biotechnology Resources, 3:255-260 Taylor, George Rogers (2007). The Transportation Revolution, 1815ââ¬â1860. New York, Toronto: Rinehart &Co.. ISBNà 978-0-87332-101-3. Thompson,
Thursday, January 2, 2020
Carol Ann Duffy Poems Analysis - 8144 Words
Originally Introduction Memories play a significant role in the poetry of Carol Ann Duffy, particularly her recollections of childhood places and events. The poem ââ¬Å"Originally,â⬠published in The Other Country (1990), draws specifically from memories of Duffys familys move from Scotland to England when she and her siblings were very young. The first-born child, Duffy was just old enough to feel a deep sense of personal loss and fear as she traveled farther and farther away from the only place she had known as ââ¬Å"homeâ⬠and the family neared its alien destination. This sentiment is captured in ââ¬Å"Originally,â⬠in which it is described in the rich detail and defining language of both the child who has had the experience and the adult who recallsâ⬠¦show more contentâ⬠¦The hate name of the racists is sprayed on a brick wall the harshness and unyielding nature of which is symbolic of the mentality of those who do such things. The unfamiliar, snowy weather and artificial neon lights create the impression for the immigrant that the country moved to is coming to bits. This image of fragmentation is, though, not entirely imaginary as he or she has a life splintered from all that is familiar and constantly experiences a sense of alienation. The italicised words at the close of the poem give voice to the immigrant but this only gives away a difficulty with English. The unfinished verbs, Me not know and It like they onlyâ⬠¦ are drawn attention to by Duffy in order that the reader may ponder what it would be like to face the same language problem. The final words of the poem, Imagine that remind us of the opening and there is quite a clear impression that Duffy is adopting an undisguised didactic stance. As a skilled and empowered user of the English language herself she is drawing attention to the lot of those who are marginalised because of their deficiency in its use. Carol Ann Duffyââ¬â¢s Stealing -An Analysis and thoughts.(Part One) This is a cold poem in more ways than one.The subject matter is seasonally icy and so is the tone of the speaker. The insouciant delivery suggestsShow MoreRelatedPoem Analysis: Medusa by Carol Ann Duffy923 Words à |à 4 PagesMedusa by Carol Ann Duffy The poem Medusa explores the theme of jealousy and anger; the poet illustrates this using the extended metaphor of a Greek mythological creature Medusa, whose story describes her as a beautiful maiden that is turned into a hideous creature after being raped by Poseidon. The poet furthermore links this metaphor to the theme of feminism when she describes the women in the poem overpowering the man that hurt her. The language in this poem is quite harsh, emphasising theRead MoreAnalysis Of The Poem War Photographer By Carol Ann Duffy2591 Words à |à 11 PagesPoetry is a way of confronting experiences and the issues it raises for the living. Death is rife during global conflicts and some poets use their craft to show the pain and suffering aspects of death. ââ¬ËWar Photographerââ¬â¢ by Carol Ann Duffy presents peopleââ¬â¢s death through both literal and figurative lexis. It uses the metaphorical lens of a camera to create an opinion about war and the role of media is reporting it humanely. ââ¬ËA Mother in a Refugee Campââ¬â¢ by Chinua Achebe presents the suffering andRead MoreAnalysis of Poems Eurydice and Mrs. Midas by Carol-Ann Duffy1020 Words à |à 5 Pageswoman being seen as an accessory to a man rather than an individual with the capability to think for herself. However, Carol Ann Duffyââ¬â¢s anthology ââ¬ËThe Worldââ¬â¢s Wifeââ¬â¢ seeks to correct the gen der inequalities, with the poems Eurydice and Mrs. Midas portraying strong minded and authoritative females that retell the Greek mythological stories from a womenââ¬â¢s point of view. In both poems Eurydice and Mrs. Midas we are introduced to two women who in mythology have been overshadowed by their more famous husbandsRead MoreAnalysis of Poems Eurydice and Mrs. Midas by Carol-Ann Duffy1005 Words à |à 5 Pageswoman being seen as an accessory to a man rather than an individual with the capability to think for herself. However, Carol Ann Duffyââ¬â¢s anthology ââ¬ËThe Worldââ¬â¢s Wifeââ¬â¢ seeks to correct the gender inequalities, with the poems Eurydice and Mrs. Midas portraying strong minded and authoritative females that retell the Greek mythological stories from a womenââ¬â¢s point of view. In both poems Eurydice and Mrs. Midas we are introduced to two women who in mythology have been overshadowed by their more famous husbandsRead MoreIn Mrs Tilschers Classroom a Poem by Carol Ann Duffy740 Words à |à 3 PagesA poem that highlights the theme of childhood is ââ¬Å"In Mrs Tilscherââ¬â¢s Classâ⬠. It is a thought provoking and nostalgic poem written by Carol Ann Duffy which at first glance seems straightforward by after close examination and analysis reveals to be more complex than originally anticipated. The poem is structured into four stanzas. Each represent a term in the final year of Primary school and highlights a change in mood and atmosphere in parallel with the child. The first half of the poem celebratesRead More Attitude Towards Love in Valentine and The Flea Essay1660 Words à |à 7 PagesThrough Close Analysis of Language, Structure and Theme, Compare and Contrast the Poets Attitude Towards Love in Valentine and The Flea. The two poems Valentine and The Flea are about the two different ways in which the poets portray their views about love, however the poems are still linked in a few ways. The Flea was published in the seventeenth century and was written by John Donne. Valentine was published in 1983 and was written by Carol Ann Duffy. Both poems are addressedRead More Carol Ann Duffys Revision of Masculinist Representations of Female Identity3217 Words à |à 13 PagesCarol Ann Duffys Revision of Masculinist Representations of Female Identity Carol Ann Duffy is one of the freshest and bravest talents to emerge in British poetry ââ¬âany poetry ââ¬â for years, writes Eavan Boland (Duffy, 1994, cover). This courage is manifest in Duffyââ¬â¢s ability and desire to revise masculinist representations of female identity and her engagement with feminine discourse, a concept which, as Sara Mills points out: has moved away from viewing women as simply an oppressed group, asRead MoreEssay on Carol Ann Duffy and Liz Lochhead Explore Memories1137 Words à |à 5 PagesCompare and contrast how Duffy and Lochhead explore memories Both Carol Ann Duffy and Liz Lochhead provide an exploration of their childhood memories, and how these memories have changed and developed with age into analysis of social expectations of men and women in the 1960s. In Duffys poem Litany and Lochheads poem 1953, both poets reflect on their childish perceptions of their parents conformity to social convention. Duffy and Lochhead excellently implement a dramatic monologueRead More Comparison of Stealing and Hitcher Essay1324 Words à |à 6 Pagesbe comparing two poems; Stealing, by Carol Ann Duffy and Hitcher, by Simon Armitage. I will be using several categories in which to structure my comparison, which include style of language and structure. In this piece, I hope to provide in depth analysis into the narrators feelings and the poets techniques. Finally I will be making a summary of my comments in a brief conclusion at the end, which will include my thoughts on both poems. The style of language in these poems have several similaritiesRead MoreA Skittle of Milk2741 Words à |à 11 PagesANALYSIS IN MRS TILSCHERS CLASS ââ¬Å"a skittle of milkâ⬠The metaphor, ââ¬Å"skittle of milk,â⬠is very effective. The inclusion of the detail of, ââ¬Å"milk,â⬠is particularly effective. The white colour of the milk reflects the purity and innocent mind of the persona. Highlighting that Duffy is in her youth and is inexperienced. The comparison of milk bottles to skittles is also effective. It reminds us of games played at school highlighting how innocent the poet was. This shows how enjoyable school was for
Subscribe to:
Posts (Atom)