Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-04T18:01:57.134Z Has data issue: false hasContentIssue false

The prevalence of Vibrio spp. in drinking water and environmental samples in Vellore South India

Published online by Cambridge University Press:  01 August 1998

C. J. THOMSON
Affiliation:
Department of Medical Microbiology, University of Edinburgh Medical School, Teviot Place, Edinburgh EH8 9AG, UK
M. V. JESUDASON
Affiliation:
Department of Clinical Microbiology, Christian Medical College and Hospital Vellore, Tamil Nadu 632 004, India
V. BALAJI
Affiliation:
Department of Clinical Microbiology, Christian Medical College and Hospital Vellore, Tamil Nadu 632 004, India
B. MALATHI
Affiliation:
Department of Clinical Microbiology, Christian Medical College and Hospital Vellore, Tamil Nadu 632 004, India
U. MUKUNDAN
Affiliation:
Department of Clinical Microbiology, Christian Medical College and Hospital Vellore, Tamil Nadu 632 004, India
S. G. B. AMYES
Affiliation:
Department of Medical Microbiology, University of Edinburgh Medical School, Teviot Place, Edinburgh EH8 9AG, UK
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The prevalence of Vibrio cholerae in drinking water, lakes and sewage outfalls during July and August 1996 in Vellore, India was determined. Drinking water samples were collected on single occasions from 12 sites in different geographic areas of the town where cholera had been reported. Samples of water, plankton and sediment were collected from fixed sites at three lakes on three occasions separated by at least 3 days during the course of the study. Samples from open sewers were taken from two representative sites in four areas of the town. Bacteria isolated from samples were identified by standard biochemical tests and isolated strains of V. cholerae tested for their ability to agglutinate O1 and O139 antisera. Water samples from lakes were also tested for the presence of V. cholerae O1 and O139 by fluorescent antibody staining. Non-O1, non-O139 strains of V. cholerae were detected in 41% of drinking water samples and 100% of water, sediment and plankton samples from the test lakes. Eighty-seven per cent of open sewers sampled contained viable non-O1, non-O139 V. cholerae. Fluorescent antibody staining gave positive results for V. cholerae O1 and O139 for all water samples from the three lake sites. Strains of Aeromonas spp. were isolated from 58% of drinking water samples and from 66% of sediment, 77% of plankton and 55% of water samples from lakes. All open sewers sampled contained Aeromonas spp. PCR amplification employing specific primers demonstrated that none of the non-agglutinating V. cholerae isolates contained the ctx operon. The non-O1, non-O139 V. cholerae isolates showed different patterns of antibiotic resistance to ampicillin, ciprofloxacin, chloramphenicol, tetracycline and trimethoprim.

Type
Research Article
Copyright
© 1998 Cambridge University Press