Abstract
An indirect fluorescent-antibody (IFA) technique, which employed adsorbed Behring polyvalent I O antiserum, was used to detect Salmonella spp. in environmental water systems. The IFA method used in this study detected 95% of Salmonella serotypes encountered in human infections in France, with a sensitivity threshold of 7.5 x 10(3) bacteria per ml of wastewater. Specificity was assessed by testing IFA against Salmonella-free seawater and a variety of bacteria other than Salmonella spp. When used to examine raw and chlorinated wastewater over a 2-month period, the IFA method was successful in detecting Salmonella spp. in all 12 of the samples examined, with total numbers determined to be 4.5 x 10(5) to 3.3 x 10(7) salmonellae per 100 ml. In comparison, for the same samples, enumeration by culture, using the most-probable-number technique, was effective in detecting Salmonella spp. in only four of eight raw-water samples and one of four chlorinated water samples tested. Three samples were further tested by using the direct viable count procedure combined with IFA and results showed that 5 to 31.5% of the Salmonella spp. enumerated by this method in chlorinated water were substrate responsive.
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- Brayton P. R., Tamplin M. L., Huq A., Colwell R. R. Enumeration of Vibrio cholerae O1 in Bangladesh waters by fluorescent-antibody direct viable count. Appl Environ Microbiol. 1987 Dec;53(12):2862–2865. doi: 10.1128/aem.53.12.2862-2865.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cabelli V. J., Dufour A. P., Levin M. A., McCabe L. J., Haberman P. W. Relationship of microbial indicators to health effects at marine bathing beaches. Am J Public Health. 1979 Jul;69(7):690–696. doi: 10.2105/ajph.69.7.690. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Camper A. K., McFeters G. A. Chlorine injury and the enumeration of waterborne coliform bacteria. Appl Environ Microbiol. 1979 Mar;37(3):633–641. doi: 10.1128/aem.37.3.633-641.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chaicumpa W., Thin-Inta W., Khusmith S., Tapchaisri P., Echeverria P., Kalambaheti T., Chongsa-Nguan M. Detection with monoclonal antibody of Salmonella typhi antigen 9 in specimens from patients. J Clin Microbiol. 1988 Sep;26(9):1824–1830. doi: 10.1128/jcm.26.9.1824-1830.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fricker C. R. A comparison of isolation procedures for salmonellas from polluted water using two forms of Rappaport's medium. J Appl Bacteriol. 1984 Apr;56(2):305–309. doi: 10.1111/j.1365-2672.1984.tb01351.x. [DOI] [PubMed] [Google Scholar]
- Goepfert J. M., Mann M. E., Hicks R. One-day fluorescent-antibody procedure for detecting salmonellae in frozen and dried foods. Appl Microbiol. 1970 Dec;20(6):977–983. doi: 10.1128/am.20.6.977-983.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAGLUND J. R., AYRES J. C., PATON A. M., KRAFT A. A., QUINN L. Y. DETECTION OF SALMONELLA IN EGGS AND EGG PRODUCTS WITH FLUORESCENT ANTIBODY. Appl Microbiol. 1964 Sep;12:447–450. doi: 10.1128/am.12.5.447-450.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harvey R. W., Price T. H. A comparison of two modifications of Rappaport's enrichment medium (R25 and RV) for the isolation of salmonellas from sewage polluted natural water. J Hyg (Lond) 1983 Dec;91(3):451–458. doi: 10.1017/s0022172400060496. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hobbie J. E., Daley R. J., Jasper S. Use of nuclepore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977 May;33(5):1225–1228. doi: 10.1128/aem.33.5.1225-1228.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kogure K., Simidu U., Taga N. A tentative direct microscopic method for counting living marine bacteria. Can J Microbiol. 1979 Mar;25(3):415–420. doi: 10.1139/m79-063. [DOI] [PubMed] [Google Scholar]
- Kogure K., Simidu U., Taga N., Colwell R. R. Correlation of direct viable counts with heterotrophic activity for marine bacteria. Appl Environ Microbiol. 1987 Oct;53(10):2332–2337. doi: 10.1128/aem.53.10.2332-2337.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LeChevallier M. W., Schiemann D. A., McFeters G. A. Factors contributing to the reduced invasiveness of chlorine-injured Yersinia enterocolitica. Appl Environ Microbiol. 1987 Jun;53(6):1358–1364. doi: 10.1128/aem.53.6.1358-1364.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LeChevallier M. W., Singh A., Schiemann D. A., McFeters G. A. Changes in virulence of waterborne enteropathogens with chlorine injury. Appl Environ Microbiol. 1985 Aug;50(2):412–419. doi: 10.1128/aem.50.2.412-419.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robison B. J., Pretzman C. I., Mattingly J. A. Enzyme immunoassay in which a myeloma protein is used for detection of salmonellae. Appl Environ Microbiol. 1983 Jun;45(6):1816–1821. doi: 10.1128/aem.45.6.1816-1821.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rollins D. M., Colwell R. R. Viable but nonculturable stage of Campylobacter jejuni and its role in survival in the natural aquatic environment. Appl Environ Microbiol. 1986 Sep;52(3):531–538. doi: 10.1128/aem.52.3.531-538.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Roszak D. B., Grimes D. J., Colwell R. R. Viable but nonrecoverable stage of Salmonella enteritidis in aquatic systems. Can J Microbiol. 1984 Mar;30(3):334–338. doi: 10.1139/m84-049. [DOI] [PubMed] [Google Scholar]
- Seyfried P. L., Tobin R. S., Brown N. E., Ness P. F. A prospective study of swimming-related illness. I. Swimming-associated health risk. Am J Public Health. 1985 Sep;75(9):1068–1070. doi: 10.2105/ajph.75.9.1068. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seyfried P. L., Tobin R. S., Brown N. E., Ness P. F. A prospective study of swimming-related illness. II. Morbidity and the microbiological quality of water. Am J Public Health. 1985 Sep;75(9):1071–1075. doi: 10.2105/ajph.75.9.1071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Singh A., Yeager R., McFeters G. A. Assessment of in vivo revival, growth, and pathogenicity of Escherichia coli strains after copper- and chlorine-induced injury. Appl Environ Microbiol. 1986 Oct;52(4):832–837. doi: 10.1128/aem.52.4.832-837.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walsh S. M., Bissonnette G. K. Chlorine-induced damage to surface adhesions during sublethal injury of enterotoxigenic Escherichia coli. Appl Environ Microbiol. 1983 Mar;45(3):1060–1065. doi: 10.1128/aem.45.3.1060-1065.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward B. B., Perry M. J. Immunofluorescent Assay for the Marine Ammonium-Oxidizing Bacterium Nitrosococcus oceanus. Appl Environ Microbiol. 1980 Apr;39(4):913–918. doi: 10.1128/aem.39.4.913-918.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]