USE OF THE POLYMERASE CHAIN-REACTION AND FLUORESCENT-ANTIBODY METHODS FOR DETECTING VIABLE BUT NONCULTURABLE SHIGELLA-DYSENTERIAE TYPE-1 IN LABORATORY MICROCOSMS

被引:63
作者
ISLAM, MS [1 ]
HASAN, MK [1 ]
MIAH, MA [1 ]
SUR, GC [1 ]
FELSENSTEIN, A [1 ]
VENKATESAN, M [1 ]
SACK, RB [1 ]
ALBERT, MJ [1 ]
机构
[1] WALTER REED ARMY INST RES, WASHINGTON, DC 20307 USA
关键词
D O I
10.1128/AEM.59.2.536-540.1993
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Epidemiological studies of shigellosis in Bangladesh have demonstrated that surface-water sources can act as foci of infection. Studies of laboratory microcosms have shown that shigellae become nonculturable but remain viable when exposed to environmental samples of water. The present study was carried out to detect viable but nonculturable Shigella dysenteriae 1 from laboratory microcosms by the polymerase chain reaction and the fluorescent-antibody techniques. S. dysenteriae 1 was inoculated into laboratory microcosms consisting of water samples collected from ponds, lakes, rivers, and drains in Bangladesh. The survival of S. dysenteriae in microcosms was assessed by viable counting on MacConkey agar. After 2 to 3 weeks, S. dysenteriae 1 became nonculturable but remained viable. After 6 weeks, this nonculturable but viable S. dysenteriae 1 was detected by both the polymerase chain reaction and the fluorescent-antibody methods. The viable but nonculturable state of S. dysenteriae 1 demonstrated in this study may be important for understanding the epidemiology of shigellosis.
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页码:536 / 540
页数:5
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