USE OF SPECIFIC OLIGONUCLEOTIDES FOR DIRECT ENUMERATION OF LISTERIA-MONOCYTOGENES IN FOOD SAMPLES BY COLONY HYBRIDIZATION AND RAPID DETECTION BY PCR

被引:55
作者
BOHNERT, M
DILASSER, F
DALET, C
MENGAUD, J
COSSART, P
机构
[1] INST PASTEUR,GENET MOLEC LISTERIA LAB,F-75724 PARIS 15,FRANCE
[2] LCHA CNEVA,F-75015 PARIS,FRANCE
[3] SOC DNA,F-34831 CLAPIERS,FRANCE
关键词
OLIGONUCLEOTIDE; LISTERIA-MONOCYTOGENES; FOOD; DETECTION; ENUMERATION; PCR; COLONY HYBRIDIZATION; DNA; HLY GENE; SPECIES-SPECIFICITY;
D O I
10.1016/0923-2508(92)90019-K
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two 18-mer oligonucleotides derived from the sequence of hly, the gene coding for listeriolysin O, were shown to be specific for Listeria monocytogenes in the genus Listeria in colony hybridization tests. The oligonucleotides did not hybridize with any of the bacterial species found in food and co-isolated with Listeria on selective media. They were used in colony hybridization tests for enumeration of L. monocytogenes present in food samples after direct plating on selective media plates. In addition, two 24-mer oligonucleotides, each including the sequence of one of the 18-mers, were successfully used for the PCR-based detection of L. monocytogenes bacilli present in food samples after a 48-h enrichment period. Using this technique, as little as 10(2) bacteria per ml of enrichment broth can be detected.
引用
收藏
页码:271 / 280
页数:10
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