1887

Abstract

Summary

We compared the usefulness of gene probes with standard bioassays to identify diarrhoeagenic amongst isolates from Bangladeshi children under 1 year of age with diarrhoea. isolates were analysed with specific gene probes for localised adhesiveness (LA), diffuse adhesiveness (DA), heat-labile toxin (LT), heat-stable toxin (ST), Shiga-like toxins (SLT I and SLT II), and enteroinvasiveness, and in bioassays for production of enterotoxins and cytotoxins, and for cell adherence. With 1136 isolates from 387 patients, there was general agreement between the two assay methods. When there was disparity, gene-probe-positive isolates gave negative results in the corresponding bioassay. In the HeLa cell adherence assay, 94% of the LA probe-positive isolates and 91.6% of the DA probe-positive isolates gave positive bioassay results for LA and DA respectively. Thirty-six of 39 LT probe-positive isolates and 73 of 86 ST probe-positive isolates gave positive results in the bioassays. Of 28 isolates that gave negative results in the suckling mouse assay but were initially positive with the probe for ST, 15 were later found to hybridise with the cloning vector for the ST probe. Addition of denatured vector DNA at a concentration of 10 g/ml in the hybridisation solution eliminated these false positive results. None of the other probe-positive isolates hybridised with any of the cloning vectors used. The DNA hybridisation assay appeared to be a convenient alternative to bioassays for screening large numbers of isolates in epidemiological investigation.

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1992-01-01
2024-04-20
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References

  1. Levine M. M. Escherichia coli that cause diarrhea: enterotoxigenic, enteropathogenic, enteroinvasive, enterohemorrhagic, and enteroadherent. J Infect Dis 1987; 155:377–389
    [Google Scholar]
  2. Levine M. M., Edelman R. Enteropathogenic Escherichia coli of classic serotypes associated with infant diarrhea: epidemiology and pathogenesis. Epidemiol Rev 1984; 6:31–51
    [Google Scholar]
  3. Mathewson J. J., Johnson P. C., DuPont H. L. A newly recognized cause of travelers’ diarrhea: enteroadherent Escherichia coli. J Infect Dis 1985; 151:471–475
    [Google Scholar]
  4. Dean A. G., Ching Y. C., Williams R. G., Harden L. B. Test for Escherichia coli enterotoxin using infant mice: application in a study of diarrhea in children in Honolulu. J Infect Dis 1972; 125:407–411
    [Google Scholar]
  5. Sack D. A., Sack R. B. Test for enterotoxigenic Escherichia coli using Y1 adrenal cells in miniculture. Infect Immun 1975; 11:334–336
    [Google Scholar]
  6. Gentry M. K., Dalrymple J. M. Quantitative microtiter cytotoxicity assay for shigella toxin. J Clin Microbiol 1980; 12:361–366
    [Google Scholar]
  7. Cravioto A., Gross R. J., Scotland S. M., Rowe B. An adhesive factor found in strains of Escherichia coli belonging to the traditional infantile enteropathogenic serotypes. Curr Microbiol 1979; 3:95–99
    [Google Scholar]
  8. Scaletsky I. C. A., Silva M. L. M., Trabulsi L. R. Distinctive patterns of adherence of enteropathogenic Escherichia coli to HeLa cells. Infect Immun 1984; 45:534–536
    [Google Scholar]
  9. Handl C., Ronnberg B., Nilsson B., Olsson E., Johnsson H., Flock J. I. Enzyme-linked immunosorbent assay for Escherichia coli heat–stable enterotoxin type II. J Clin Microbiol 1988; 26:1555–1560
    [Google Scholar]
  10. Svennerholm A., Holmgren J. Identification of Escherichia coli heat-labile enterotoxin by means of a ganglioside immunosorbent assay (GM-1 ELISA) procedure. Curr Microbiol 1978; 1:19–23
    [Google Scholar]
  11. Moseley S. L., Echeverria P. Seriwatana, J et al., Identification of enterotoxigenic Escherichia coli by colony hybridization using three enterotoxin gene probes. J Infect Dis 1982; 145:863–869
    [Google Scholar]
  12. Boileau C. R., d’Hauteville H. M., Sansonetti P. J. DNA hybridization technique to detect Shigella species and enteroinvasive Escherichia coli. J Clin Microbiol 1984; 20:959–961
    [Google Scholar]
  13. Newland J. W., Neill R. J. DNA probes for Shiga-like toxins I and II and for toxin-converting bacteriophages. J Clin Microbiol 1988; 26:1292–1297
    [Google Scholar]
  14. Nataro J. P., Baldini M. M., Kaper J. B., Black R. E., Bravo N., Levine M. M. Detection of an adherence factor of enteropathogenic Escherichia coli with a DNA probe. J Infect Dis 1985; 152:560–565
    [Google Scholar]
  15. Moseley S. L., Clausen C. R., Smith A. L. A new bacterial adhesin associated with enteritis in infants. Abstracts of the 25th Interscience Conference on Antimicrobial Agents and Chemotherapy American Society for Microbiology: Washington DC; 1985 abstract no 1128
    [Google Scholar]
  16. Bilge S. S., Clausen C. R., Lau W., Moseley S. L. Molecular characterization of a fimbrial adhesin, FI845, mediating diffuse adherence of diarrhea-associated Escherichia coli to HEp-2 cells. J Bacteriol 1989; 171:4281–4289
    [Google Scholar]
  17. Baudry B., Savarino S. J., Vial P., Kaper J. B., Levine M. M. A sensitive and specific DNA probe to identify entero-aggregative Escherichia coli, a recently discovered diarrheal pathogen. J Infect Dis 1990; 161:1249–1251
    [Google Scholar]
  18. Echeverria P., Taylor D. N., Seriwatana J. A comparative study of enterotoxin gene probes and tests for toxin production to detect enterotoxigenic Escherichia coli. J Infect Dis 1986; 153:255–260
    [Google Scholar]
  19. Stoll B. J., Glass R. I., Huq M. I., Khan M. U., Holt J. E., Banu H. Surveillance of patients attending a diarrhoeal disease hospital in Bangladesh. Br Med J 1982; 285:1185–1188
    [Google Scholar]
  20. Moseley S. L., Hardy J. W., Huq M. I., Echeverria P., Falkow S. Isolation and nucleotide sequence determination of a gene encoding a heat-stable enterotoxin of Escherichia coli. Infect Immun 1983; 39:1167–1174
    [Google Scholar]
  21. So M., McCarthy B. Nucleotide sequence of the bacterial transposon Tn 1681 encoding a heat-stable (ST) toxin and its identification in enterotoxigenic Escherichia coli strains. Proc Natl Acad Sci USA 1980; 77:4011–4015
    [Google Scholar]
  22. Gicquelais K. G., Baldini M. M., Martinez J. Practical and economical method for using biotinylated DNA probes with bacterial colony blots to identify diarrhea-causing Escherichia coli. J Clin Microbiol 1990; 28:2485–2490
    [Google Scholar]
  23. Feinberg A. P., Volgelstein B. A technique for radio-labeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 1984; 137:266–267
    [Google Scholar]
  24. Echeverria P., Taylor D. N., Seriwatana J., Brown J. E., Lexomboon U. Examination of colonies and stool blots for detection of enteropathogens by DNA hybridization with eight DNA probes. J Clin Microbiol 1989; 27:331–334
    [Google Scholar]
  25. Maniatis T. Molecular cloning: a laboratory manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory; 1982109–112
    [Google Scholar]
  26. Nataro J. P., Kaper J. B., Robins-Browne R., Prado V., Vial P. A., Levine M. M. Patterns of adherence of diarrheagenic Escherichia coli to HEp-2 cells. Pediatr Infect Dis J 1987; 6:829–831
    [Google Scholar]
  27. Echeverria P., Taylor D. N., Seriwatana J., Moe C. Comparative study of synthetic oligonucleotide and cloned polynucleotide enterotoxin gene probes to identify enterotoxigenic Escherichia coli. J Clin Microbiol 1987; 25:106–109
    [Google Scholar]
  28. Mathewson J. J., Johnson P. C., DuPont H. L., Satterwhite T. K., Winsor D. K. Pathogenicity of enteroadherent Escherichia coli in adult volunteers. J Infect Dis 1986; 154:524–527
    [Google Scholar]
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