Literature DB >> 6099090

The population genetics of Escherichia coli.

D L Hartl, D E Dykhuizen.   

Abstract

E. coli is a successful and diverse group of organisms, well defined by DNA hybridization within the Enterobacteriacae and including the closely related organisms Shigella and the Alkalescens-Dispar biogroup. The primary habitat of E. coli is the lower intestinal tract of warm-blooded animals, which is colonized shortly after birth. At any one time, most normal individuals carry several strains of E. coli in their intestinal tract, including a small number of resident clones exhibiting a rate of replacement measured in weeks or months and a much larger number of transient clones that are replaced in a matter of days or weeks. The secondary habitats of E. coli are soil, sediment, and water, where its half life is thought to be only a few days. Pathogenic forms of E. coli are associated with diarrheal diseases, urinary tract infections, neonatal meningitis, nosocomial infections, and in infections of domesticated animals. E. coli populations contain much genetic diversity, more than is found in most eukaryotes. Genetic diversity has been studied from the standpoint of (a) serology with respect to surface antigens, (b) biogrouping with respect to variable characters such as nutritional versatility, antibiotic resistance, and bacteriophage susceptibility, (c) electrophoresis of enzymes of intermediary metabolism or outer membrane proteins, (d) DNA hybridization, (e) restriction-fragment length polymorphisms, (f) DNA sequences, (g) insertion sequences, and (h) plasmids. However identified, strains of E. coli appear to have a wide, but not totally indiscriminate, host range. Aside from genes directly associated with virulence, genetic divergence between pathogenic and nonpathogenic strains, although statistically significant, is not pronounced. Electrophoretic studies indicate that, while some serotypes may represent a single genetic clone almost exclusively, other serotypes may represent two or more genetically unrelated clones. Unrelated clones may therefore converge to the same or very similar serotypes. Electrophoresis has also been used to define three groups of clones among natural isolates, perhaps corresponding to subspecies of E. coli. These groups are worldwide in distribution and have a wide host range. E. coli populations exhibit great linkage disequilibrium, which occurs as highly nonrandom combinations of alleles at different loci. Reproduction is evidently largely asexual, with insufficient genetic recombination to dissipate linkage disequilibrium.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1984        PMID: 6099090     DOI: 10.1146/annurev.ge.18.120184.000335

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  75 in total

Review 1.  Bacteria are different: observations, interpretations, speculations, and opinions about the mechanisms of adaptive evolution in prokaryotes.

Authors:  B R Levin; C T Bergstrom
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

2.  Mutators, population size, adaptive landscape and the adaptation of asexual populations of bacteria.

Authors:  O Tenaillon; B Toupance; H Le Nagard; F Taddei; B Godelle
Journal:  Genetics       Date:  1999-06       Impact factor: 4.562

3.  Inhibition of development of Shiga toxin-converting bacteriophages by either treatment with citrate or amino acid starvation.

Authors:  Bożena Nejman-Faleńczyk; Piotr Golec; Monika Maciąg; Alicja Wegrzyn; Grzegorz Węgrzyn
Journal:  Foodborne Pathog Dis       Date:  2011-11-02       Impact factor: 3.171

4.  Stability and instability in the lysogenic state of phage lambda.

Authors:  John W Little; Christine B Michalowski
Journal:  J Bacteriol       Date:  2010-09-24       Impact factor: 3.490

Review 5.  Clonal dynamics of Escherichia coli in its natural habitat.

Authors:  T S Whittam
Journal:  Antonie Van Leeuwenhoek       Date:  1989       Impact factor: 2.271

6.  Development of goose- and duck-specific DNA markers to determine sources of Escherichia coli in waterways.

Authors:  Matthew J Hamilton; Tao Yan; Michael J Sadowsky
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

7.  Genetic structure of a lotic population of Burkolderia (Pseudomonas) cepacia.

Authors:  M G Wise; L J Shimkets; J V McArthur
Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

8.  Physiological state of Escherichia coli BJ4 growing in the large intestines of streptomycin-treated mice.

Authors:  L K Poulsen; T R Licht; C Rang; K A Krogfelt; S Molin
Journal:  J Bacteriol       Date:  1995-10       Impact factor: 3.490

9.  Genetic characterization of Escherichia coli populations from host sources of fecal pollution by using DNA fingerprinting.

Authors:  Sandra L McLellan; Annette D Daniels; Alissa K Salmore
Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

10.  Identification of a high-virulence clone of type III Streptococcus agalactiae (group B Streptococcus) causing invasive neonatal disease.

Authors:  J M Musser; S J Mattingly; R Quentin; A Goudeau; R K Selander
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

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