Detection of
Vibrio cholerae
O1 and O139 in Environmental Water Samples by an Immunofluorescent-Aggregation Assay
-
Published:2010-08-15
Issue:16
Volume:76
Page:5520-5525
-
ISSN:0099-2240
-
Container-title:Applied and Environmental Microbiology
-
language:en
-
Short-container-title:Appl Environ Microbiol
Author:
Wang Duochun1, Xu Xuebin2, Deng Xiaoling3, Chen Changyi2, Li Baisheng3, Tan Hailing3, Wang Haibo1, Tang Song1, Qiu Haiyan1, Chen Jingdiao3, Ke Bixia3, Ke Changwen3, Kan Biao1
Affiliation:
1. State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China 2. Shanghai Municipal Center for Disease Control and Prevention, Shanghai, China 3. Guangdong Province Center for Disease Control and Prevention, Guangzhou, China
Abstract
ABSTRACT
Environmental waters are an important reservoir for
Vibrio cholerae
, and effective surveillance of the pathogen can help to warn of and prevent infection with this potentially fatal pathogen. An immunofluorescent-aggregation (IFAG) assay to detect
V. cholerae
O1 and O139 was established and evaluated with estuarine water samples. The practical application of this assay was compared with the conventional culture method and real-time PCR. The IFAG method had a sensitivity of 10
3
CFU/ml for detection of
V. cholerae
O1 and O139 strains in a suspension containing 10 different species of enterobacterial strains (total, 10
5
CFU/ml). Ten fluorescent bacterial aggregate colonies were randomly picked and tested positive in serum agglutination tests for the
V. cholerae
O1 and O139 strains, showing a high specificity. The enrichment broths of 146 samples of estuarine water were tested, and the percentage positive by the IFAG assay was 19.9% (29/146), which was significantly higher than that of the conventional culture method (10.3%, 15/146;
P
< 0.01) but lower than that of real-time PCR (29.5%, 43/146;
P
< 0.01). The coincidence rates of real-time PCR and IFAG detection were decreased with the reduction of the
V. cholerae
concentration. The IFAG method, with a high specificity and a relatively high sensitivity, may be used for detection and isolation of
V. cholerae
in environmental water samples.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference29 articles.
1. Toxigenic
Vibrio cholerae
in the Aquatic Environment of Mathbaria, Bangladesh 2. Alam, M., M. Sultana, G. B. Nair, A. K. Siddique, N. A. Hasan, R. B. Sack, D. A. Sack, K. U. Ahmed, A. Sadique, H. Watanabe, C. J. Grim, A. Huq, and R. R. Colwell. 2007. Viable but nonculturable Vibrio cholerae O1 in biofilms in the aquatic environment and their role in cholera transmission. Proc. Natl. Acad. Sci. U. S. A.104:17801-17806. 3. Albert, M. J., A. K. Siddique, M. S. Islam, A. S. Faruque, M. Ansaruzzaman, S. M. Faruque, and R. B. Sack. 1993. Large outbreak of clinical cholera due to Vibrio cholerae non-O1 in Bangladesh. Lancet341:704. 4. Barua, D. 1992. History of cholera, p. 1-5. In D. Barua and W. B. Greenough III (ed.), Cholera. Plenum, New York, NY. 5. Bhattacharya, M. K., S. K. Bhattacharya, S. Garg, P. K. Saha, D. Dutta, G. B. Nair, B. C. Deb, and K. P. Das. 1993. Outbreak of Vibrio cholerae non-O1 in India and Bangladesh. Lancet341:1346-1347.
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|