Skip to main content
Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1990 Apr;28(4):742–746. doi: 10.1128/jcm.28.4.742-746.1990

Virulence-related genes in ColV plasmids of Escherichia coli isolated from human blood and intestines.

M E Fernandez-Beros 1, V Kissel 1, H Lior 1, F C Cabello 1
PMCID: PMC267787  PMID: 2185262

Abstract

DNA probes for the colicin V, traT, iss, and iu genes were used in this study of four representative ColV plasmids together with 200 Escherichia coli strains isolated from the stools of patients with diarrhea and 146 E. coli strains isolated from the blood of patients with bacteremia. The study indicated that the ColV plasmids are heterogeneous. Southern and colony hybridization analyses showed that in most of the colicin V-producing intestinal E. coli strains, the colicin V genes are located in the chromosome (14 of 16); in most of the colicin V-producing E. coli strains isolated from the blood, they are located in plasmids (18 of 22). In both intestinal and blood E. coli isolates, the traT, iss, and aerobactin receptor genes were present at similar frequencies, but the frequency of the aerobactin synthesis genes was significantly different. The aerobactin receptor gene was present in 25% of the intestinal E. coli strains that lack the aerobactin synthesis gene. In the blood isolates, the aerobactin synthesis and receptor genes were present at almost equal frequencies. Among the colicin V-producing isolates, the iss, traT, and iu genes were present in 95.5, 86.4, and 90.9% of the blood isolates and in only 68.8, 43.8, and 81.3% of the intestinal isolates, respectively. The ColV plasmids from blood isolates that were tested for the presence of traT, iss, and iu genes were homogeneous and had DNA sequences that hybridized with each of the probes. On the other hand, the two intestinal strains containing ColV genes in a plasmid were heterogeneous in regard to the carriage of these genes. The presence of ColV is not restricted to specific O types.

Full text

PDF
742

Images in this article

Selected References

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

  1. Aguero M. E., de la Fuente G., Vivaldi E., Cabello F. ColV increases the virulence of Escherichia coli K1 strains in animal models of neonatal meningitis and urinary infection. Med Microbiol Immunol. 1989;178(4):211–216. doi: 10.1007/BF00202554. [DOI] [PubMed] [Google Scholar]
  2. Agüero M. E., Aron L., DeLuca A. G., Timmis K. N., Cabello F. C. A plasmid-encoded outer membrane protein, TraT, enhances resistance of Escherichia coli to phagocytosis. Infect Immun. 1984 Dec;46(3):740–746. doi: 10.1128/iai.46.3.740-746.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Agüero M. E., Cabello F. C. Relative contribution of ColV plasmid and K1 antigen to the pathogenicity of Escherichia coli. Infect Immun. 1983 Apr;40(1):359–368. doi: 10.1128/iai.40.1.359-368.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Agüero M. E., Harrison H., Cabello F. C. Increased frequency of ColV plasmids and mannose-resistant hemagglutinating activity in an Escherichia coli K1 population. J Clin Microbiol. 1983 Dec;18(6):1413–1416. doi: 10.1128/jcm.18.6.1413-1416.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Agüero M. E., Reyes L., Prado V., Orskov I., Orskov F., Cabello F. C. Enterotoxigenic Escherichia coli in a population of infants with diarrhea in Chile. J Clin Microbiol. 1985 Oct;22(4):576–581. doi: 10.1128/jcm.22.4.576-581.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bindereif A., Neilands J. B. Cloning of the aerobactin-mediated iron assimilation system of plasmid ColV. J Bacteriol. 1983 Feb;153(2):1111–1113. doi: 10.1128/jb.153.2.1111-1113.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Binns M. M., Davies D. L., Hardy K. G. Cloned fragments of the plasmid ColV,I-K94 specifying virulence and serum resistance. Nature. 1979 Jun 28;279(5716):778–781. doi: 10.1038/279778a0. [DOI] [PubMed] [Google Scholar]
  8. Binns M. M., Mayden J., Levine R. P. Further characterization of complement resistance conferred on Escherichia coli by the plasmid genes traT of R100 and iss of ColV,I-K94. Infect Immun. 1982 Feb;35(2):654–659. doi: 10.1128/iai.35.2.654-659.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Birnboim H. C., Doly J. A rapid alkaline extraction procedure for screening recombinant plasmid DNA. Nucleic Acids Res. 1979 Nov 24;7(6):1513–1523. doi: 10.1093/nar/7.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Darken J., Savage D. C. Influences of conjugal genetic transfer functions of colicin V plasmids on adhesion of Escherichia coli to murine intestinal tissue. Infect Immun. 1987 Oct;55(10):2483–2489. doi: 10.1128/iai.55.10.2483-2489.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gilson L., Mahanty H. K., Kolter R. Four plasmid genes are required for colicin V synthesis, export, and immunity. J Bacteriol. 1987 Jun;169(6):2466–2470. doi: 10.1128/jb.169.6.2466-2470.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hughes V., Le Grice S., Hughes C., Meynell G. G. Two major groups of colicin factors: their molecular weights. Mol Gen Genet. 1978 Feb 16;159(2):219–221. doi: 10.1007/BF00270897. [DOI] [PubMed] [Google Scholar]
  13. Luckey M., Pollack J. R., Wayne R., Ames B. N., Neilands J. B. Iron uptake in Salmonella typhimurium: utilization of exogenous siderochromes as iron carriers. J Bacteriol. 1972 Sep;111(3):731–738. doi: 10.1128/jb.111.3.731-738.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. MacFarren A. C., Clowes R. C. A comparative study of two F-like colicin factors, ColV2 and ColV3, in Escherichia coli K-12. J Bacteriol. 1967 Aug;94(2):365–377. doi: 10.1128/jb.94.2.365-377.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Meynell E., Meynell G. G., Datta N. Phylogenetic relationships of drug-resistance factors and other transmissible bacterial plasmids. Bacteriol Rev. 1968 Mar;32(1):55–83. doi: 10.1128/br.32.1.55-83.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Minshew B. H., Jorgensen J., Swanstrum M., Grootes-Reuvecamp G. A., Falkow S. Some characteristics of Escherichia coli strains isolated from extraintestinal infections of humans. J Infect Dis. 1978 May;137(5):648–654. doi: 10.1093/infdis/137.5.648. [DOI] [PubMed] [Google Scholar]
  17. Moll A., Manning P. A., Timmis K. N. Plasmid-determined resistance to serum bactericidal activity: a major outer membrane protein, the traT gene product, is responsible for plasmid-specified serum resistance in Escherichia coli. Infect Immun. 1980 May;28(2):359–367. doi: 10.1128/iai.28.2.359-367.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Montenegro M. A., Bitter-Suermann D., Timmis J. K., Agüero M. E., Cabello F. C., Sanyal S. C., Timmis K. N. traT gene sequences, serum resistance and pathogenicity-related factors in clinical isolates of Escherichia coli and other gram-negative bacteria. J Gen Microbiol. 1985 Jun;131(6):1511–1521. doi: 10.1099/00221287-131-6-1511. [DOI] [PubMed] [Google Scholar]
  19. Moseley S. L., Huq I., Alim A. R., So M., Samadpour-Motalebi M., Falkow S. Detection of enterotoxigenic Escherichia coli by DNA colony hybridization. J Infect Dis. 1980 Dec;142(6):892–898. doi: 10.1093/infdis/142.6.892. [DOI] [PubMed] [Google Scholar]
  20. Smith H. W., Huggins M. B. Further observations on the association of the colicine V plasmid of Escherichia coli with pathogenicity and with survival in the alimentary tract. J Gen Microbiol. 1976 Feb;92(2):335–350. doi: 10.1099/00221287-92-2-335. [DOI] [PubMed] [Google Scholar]
  21. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  22. Timmis K., Cabello F., Cohen S. N. Utilization of two distinct modes of replication by a hybrid plasmid constructed in vitro from separate replicons. Proc Natl Acad Sci U S A. 1974 Nov;71(11):4556–4560. doi: 10.1073/pnas.71.11.4556. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Vial P. A., Robins-Browne R., Lior H., Prado V., Kaper J. B., Nataro J. P., Maneval D., Elsayed A., Levine M. M. Characterization of enteroadherent-aggregative Escherichia coli, a putative agent of diarrheal disease. J Infect Dis. 1988 Jul;158(1):70–79. doi: 10.1093/infdis/158.1.70. [DOI] [PubMed] [Google Scholar]
  24. Vogelstein B., Gillespie D. Preparative and analytical purification of DNA from agarose. Proc Natl Acad Sci U S A. 1979 Feb;76(2):615–619. doi: 10.1073/pnas.76.2.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Waters V. L., Crosa J. H. DNA environment of the aerobactin iron uptake system genes in prototypic ColV plasmids. J Bacteriol. 1986 Aug;167(2):647–654. doi: 10.1128/jb.167.2.647-654.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Williams P. H., Warner P. J. ColV plasmid-mediated, colicin V-independent iron uptake system of invasive strains of Escherichia coli. Infect Immun. 1980 Aug;29(2):411–416. doi: 10.1128/iai.29.2.411-416.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES