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MicroBioNet Your Microbiology Universe on the Internet |
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There are curretly five accepted species, E. coli, E. blattae, E. fergusonii, E. hermanii and E. vuneris . They can be differentiated particularly on the basis of the following reactions: Indole, citrate, lysine decarboxylase, growth in KCN and malonate utilization. They frequently produce indole (except E. blattae and E.vulneris ), ferment glucose by the mixed acid fermentation, do not produce H2S, phenylalaninedeaminase or urease, do not utilize citrate as sole carbon source (except some strains of E. blattae , and E. fergusonii. ) Most are motile, ferment a variety of carbohydrates and decarboxylae arginine, lysine and/or ornithine. Most genetic studies have
been done on E. coli . It consists of a single circular DNA molecule
of about 4 x 106 base pairs with a molecular weight of 4 x 109
and a total length of about 1.4mm. Many of the genes have been mapped. E. coli can be subdivided according to their somatic (cell-wall) or O antigens and their flagellar or H antigens. Currently there are over 160 recognized O types and 55 recognized H types making over 8000 possible OH serotypes. There are also capsular and fimbrial antigens. Enterotoxins: Verotoxins or
Shiga-like toxins: E. coli colonise the intestine of virtually all warm blooded animals from shortly after birth, where they are part of the commensal flora. Enteric Infections: Animal Infections: E. coli can be grown very easily on most microbiological media. Generally the production of lactose-fermenting colonies on media containing bile-salts is a strong indication of the presence of E. coli . To isolate dammaged cells (e.g. after antibiotic therapy) may require special media. With E. coli infections it is generally the problem to characterise the pathogenic types among the commensal types. For this very special techniques tailor-made for each type must be applied. For the isolation of E. coli from sites which are normally sterile, but where their presence indicates infection such as blood or urine, there are many standard techniques available. With the emergence of EHEC as important pathogens special media are being developed to identify these from faeces and food. Most commonly used is Sorbitol MacConkey (SMAC) Agar on which some but not all EHEC will appear as non-fermenting colonies while most other E. coli ferment sorbitol. E. coli can not
only survive but acitively grow in many environmental waters. As E. coli
are present in the faeces of humans and most animals their presence has been
used as an indicator of faecal pollution for many years. However, caution
has to be excersised, because E. coli have been isolated from pristine
waters and birds particularly have been associated with causing E. coli
to be present in some waters. Currently methods involving some form of counting
bacteria which give characteristic E.coli biochemical reactions are
the main means by which pollution can be monitored. As E. coli can be grown very easily on simple media and its genetic characteristics have been essentially determined, they have found extensive use as vehicles for the preparation of biological polymers, including polypeptide hormones, proteins, carbohydrates etc. By incorporating into the E. coli genome the genetic information required to produce such substances, it is a simple process to produce these in large amounts. Currently most of the
specific E. coli vaccines are for use agains animal diseases. E.
coli toxins have been used toxoided (made harmless but still antigenic)
and used as vaccines. There are also some studies on the development of compound
toxoids containing immunologically competent components from a number of bacterial
toxins including some of the E. coli toxins. |
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