Oligonucleotide probe for the visualization of Escherichia coli/Escherichia fergusonii cells by in situ hybridization:: specificity and potential applications

被引:64
作者
Regnault, B
Martin-Delautre, S
Lejay-Collin, M
Lefèvre, M
Grimont, PAD [1 ]
机构
[1] Inst Pasteur, Aquabiolab, Unite Enterobacteries, F-75724 Paris 15, France
[2] Inst Pasteur, Unite Inserm, U389, F-75724 Paris, France
关键词
Escherichia coli; in situ hybridization; urine; food; water;
D O I
10.1016/S0923-2508(00)00222-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There are several occasions when enumeration of Escherichia coli cells is needed. These include examination of urine specimens and water or food samples. Present methods rely on growth in more or less selective media (colony-forming units on agar or the most probable number method using liquid media). Unfortunately, no really selective medium with 100% efficiency of plating is available for E. coli. A 24-mer oligonucleotide probe (Colinsitu), complementary to a piece of 16S ribosomal ribonucleic acid, has been tested for specifically visualizing E. coli cells by in situ hybridization and epifluorescence microscopy. The fluorescent dye-labeled probe was able to stain cells of E. coli, Shigella spp. and E. fergusonii. Shigella spp. are known to belong to the E. coli genomospecies and E. fergusoni is the nomenspecies closest to E. coli by DNA-DNA hybridization. The probe did not stain any strain of 169 other genomospecies of the family Enterobacteriaceae or of a few other species frequently encountered in the environment. Revivification without cell division allowed the visualization of E. coli cells in contaminated water. In situ hybridization using the Colinsitu probe is a potential tool for the confirmation of (atypical) E. coli in reference centers and the rapid (3-6 h) detection and enumeration of E. coli in urine specimens, contaminated water and food. More work is needed to include in situ hybridization in laboratory routine. (C) 2000 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:521 / 533
页数:13
相关论文
共 32 条
[1]   FLUORESCENT-OLIGONUCLEOTIDE PROBING OF WHOLE CELLS FOR DETERMINATIVE, PHYLOGENETIC, AND ENVIRONMENTAL-STUDIES IN MICROBIOLOGY [J].
AMANN, RI ;
KRUMHOLZ, L ;
STAHL, DA .
JOURNAL OF BACTERIOLOGY, 1990, 172 (02) :762-770
[2]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[3]   DETECTION OF ESCHERICHIA-COLI AND SHIGELLA SPP IN WATER BY USING THE POLYMERASE CHAIN-REACTION AND GENE PROBES FOR UID [J].
BEJ, AK ;
DICESARE, JL ;
HAFF, L ;
ATLAS, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (04) :1013-1017
[4]  
BOTTGER EC, 1989, FEMS MICROBIOL LETT, V53, P171
[5]   ISOLATION OF ANTIGENICALLY HOMOGENEOUS STRAINS OF BACT-COLI-NEAPOLITANUM FROM SUMMER DIARRHOEA OF INFANTS [J].
BRAY, J .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1945, 57 (02) :239-247
[6]   CONFIRMATION OF AEROGENIC STRAINS OF SHIGELLA-BOYDII-13 AND FURTHER STUDY OF SHIGELLA SEROTYPES BY DNA RELATEDNESS [J].
BRENNER, DJ ;
STEIGERWALT, AG ;
WATHEN, HG ;
GROSS, RJ ;
ROWE, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1982, 16 (03) :432-436
[7]   POLYNUCLEOTIDE SEQUENCE RELATEDNESS AMONG SHIGELLA SPECIES [J].
BRENNER, DJ ;
FANNING, GR ;
MIKLOS, GV ;
STEIGERWALT, AG .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1973, 23 (01) :1-7
[8]  
BROSIUS J, 1978, P NATL ACAD SCI USA, V75, P4801, DOI 10.1073/pnas.75.10.4801
[9]   AN IMPROVED DIRECT VIABLE COUNT FOR THE ENUMERATION OF BACTERIA IN MILK [J].
BUCHRIESER, C ;
KASPAR, CW .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1993, 20 (04) :227-237
[10]  
Christensen H, 1999, APPL ENVIRON MICROB, V65, P1753