Skip to main content
Genetics logoLink to Genetics
. 1981 Jul;98(3):467–490. doi: 10.1093/genetics/98.3.467

Genetic Diversity and Temporal Variation in the E. COLI Population of a Human Host

Dominique A Caugant 1,2, Bruce R Levin 1,2, Robert K Selander 1,2
PMCID: PMC1214454  PMID: 7037535

Abstract

Electrophoretic techniques were employed to study variation in chromosomal genes encoding enzymes and in the distribution of cryptic plasmids in the E. coli population of a human host over an 11-month period. Thirteen of the 15 enzymes studied were polymorphic, and mean genetic diversity per locus was 0.39. Among 550 clones isolated from fecal samples, protein electrophoresis revealed 53 distinct electrophoretic types (ETs). Most ETs appeared on only one or a few days and were considered transients, but two (ET-12 and ET-13) were observed many times over extended periods and represented residents. Complete turnover in the transient ETs in the population occurred in periods of from two weeks to a month. ETs appearing in one month showed no particular genetic similarity to those of the previous month. — All but 4 of the 53 ETs carried one or more "cryptic" plasmids with molecular weights ranging from 1 to 80 megadaltons. With few exceptions, the plasmid composition of each ET was unique. In the course of the 11-month sampling period, there were changes in the plasmid profiles of the resident strains ET-12 and ET-13, and also in the profile of a recurrent strain, ET-2, which was isolated on four days. Modification of the plasmid profile of ET-12 involved the sequential addition of relatively high molecular weight bands. For ET-2 and ET-13, the changes in the plasmid profiles were radical, suggesting invasions of new cell types rather than merely the addition and deletion of plasmids. — The results of this study provide three lines of evidence that recombination plays a minor role in the generation of genetic diversity in the E. coli population of a single host. (1) Several pairs of loci were in strong linkage disequilibrium; compared to a randomly generated array of genotypes, the sample of ETs contained an excess of pairs differing at one or two loci and too many pairs with highly distinctive combinations of electromorphs. (2) In most cases where pairs of ETs differed at a single locus and, therefore, could reasonably have been generated by phage- or plasmid-mobilized gene transfer, the plasmid profiles of the pair members were radically different and/or the potentially transmitted alleles were not present in other ETs in the population. (3) Although ET-12 was abundant, being represented by 252 of the 550 clones sampled, the electrophoretic type most similar to ET-12 different from it at six loci, and ET-12 carried two unique alleles. We conclude that most of the genetic diversity observed in this human host is a consequence of successive invasions of E. coli genotypes.

Full Text

The Full Text of this article is available as a PDF (1.7 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Curtiss R., 3rd Bacterial conjugation. Annu Rev Microbiol. 1969;23:69–136. doi: 10.1146/annurev.mi.23.100169.000441. [DOI] [PubMed] [Google Scholar]
  2. FALKOW S., SCHNEIDER H., BARON L. S., FORMAL S. B. VIRULENCE OF ESCHERICHIA-SHIGELLA GENETIC HYBRIDS FOR THE GUINEA PIG. J Bacteriol. 1963 Dec;86:1251–1258. doi: 10.1128/jb.86.6.1251-1258.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fowler A. V., Zabin I. The amino acid sequence of beta-galactosidase of Escherichia coli. Proc Natl Acad Sci U S A. 1977 Apr;74(4):1507–1510. doi: 10.1073/pnas.74.4.1507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Graham J. B., Istock C. A. Genetic exchange in Bacillus subtilis in soil. Mol Gen Genet. 1978 Nov 9;166(3):287–290. doi: 10.1007/BF00267620. [DOI] [PubMed] [Google Scholar]
  5. Guerry P., LeBlanc D. J., Falkow S. General method for the isolation of plasmid deoxyribonucleic acid. J Bacteriol. 1973 Nov;116(2):1064–1066. doi: 10.1128/jb.116.2.1064-1066.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Guiso N., Ullmann A. Expression and regulation of lactose genes carried by plasmids. J Bacteriol. 1976 Aug;127(2):691–697. doi: 10.1128/jb.127.2.691-697.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Jones R. T., Curtiss R., 3rd Genetic exchange between Escherichia coli strains in the mouse intestine. J Bacteriol. 1970 Jul;103(1):71–80. doi: 10.1128/jb.103.1.71-80.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Levin B. R., Rice V. A. The kinetics of transfer of nonconjugative plasmids by mobilizing conjugative factors. Genet Res. 1980 Jun;35(3):241–259. doi: 10.1017/s0016672300014117. [DOI] [PubMed] [Google Scholar]
  9. Levin B. R., Stewart F. M. The population biology of bacterial plasmids: a priori conditions for the existence of mobilizable nonconjugative factors. Genetics. 1980 Feb;94(2):425–443. doi: 10.1093/genetics/94.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Meyers J. A., Sanchez D., Elwell L. P., Falkow S. Simple agarose gel electrophoretic method for the identification and characterization of plasmid deoxyribonucleic acid. J Bacteriol. 1976 Sep;127(3):1529–1537. doi: 10.1128/jb.127.3.1529-1537.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. SEARS H. J., BROWNLEE I. Further observations on the persistence of individual strains of Escherichia coli in the intestinal tract of man. J Bacteriol. 1952 Jan;63(1):47–57. doi: 10.1128/jb.63.1.47-57.1952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SEARS H. J., BROWNLEE I., UCHIYAMA J. K. Persistence of individual strains of Escherichia coli in the intestinal tract of man. J Bacteriol. 1950 Feb;59(2):293–301. doi: 10.1128/jb.59.2.293-301.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. SEARS H. J., JANES H., SALOUM R., BROWNLEE I., LAMOREAUX L. F. Persistence of individual strains of Escherichia coli in man and dog under varying conditions. J Bacteriol. 1956 Mar;71(3):370–372. doi: 10.1128/jb.71.3.370-372.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Selander R. K., Levin B. R. Genetic diversity and structure in Escherichia coli populations. Science. 1980 Oct 31;210(4469):545–547. doi: 10.1126/science.6999623. [DOI] [PubMed] [Google Scholar]
  15. Stewart F. M., Levin B. R. The Population Biology of Bacterial Plasmids: A PRIORI Conditions for the Existence of Conjugationally Transmitted Factors. Genetics. 1977 Oct;87(2):209–228. doi: 10.1093/genetics/87.2.209. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES