A reverse transcriptase polymerase chain reaction assay for the detection of thermophilic Campylobacter spp.

被引:25
|
作者
Sails, AD
Bolton, FJ
Fox, AJ
Wareing, DRA
Greenway, DLA
机构
[1] Royal Preston Hosp, Preston Publ Hlth Lab, Preston PR2 9HG, Lancs, England
[2] Withington Hosp, Manchester Publ Hlth Lab, Manchester M20 2LR, Lancs, England
[3] Univ Cent Lancashire, Dept Appl Biol, Preston PR1 2HE, Lancs, England
关键词
Campylobacter; reverse transcriptase; polymerase chain reaction; viability; mRNA;
D O I
10.1006/mcpr.1998.0184
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel method was developed for the detection of thermophilic enteropathogenic campylobacters based on the detection of mRNA using the reverse transcriptase polymerase chain reaction (RT-PCR). The RNA extraction method, DNase treatment and RT-RCR assay were shown to be specific for mRNA. The assay is specific for the thermophilic campylobacters Campylobacter jejuni, Campylobacter coil and Campylobacter upsaliensis and restriction fragment length polymorphism (RFLP) analysis of the 256 bp amplified product with the restriction endonucleases Alu I, Dde I and Dra I revealed distinct species specific patterns. The assay was applied to the detection of C. jejuni cells killed by heating at 72 degrees C for 5 min and mRNA was detected by RT-PCR immediately after heat killing but became undetectable within 4 h when the cells were held at 37 degrees C. The assay therefore can differentiate between viable and dead cells of C. jejuni. (C) 1998 Academic Press.
引用
收藏
页码:317 / 322
页数:6
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