Nayak Rajesh, Stewart Tabitha M, Nawaz Mohamed S
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, 3900 NCTR Road, Jefferson, AR 72079, USA.
Mol Cell Probes. 2005 Jun;19(3):187-93. doi: 10.1016/j.mcp.2004.11.005.
The objective of this study was to utilize a multiplex PCR assay for concurrent detection of Campylobacter spp. and C. coli or C. jejuni, using probes derived from genes cadF and ceuE and an undefined virulence gene. A total of 97 Campylobacter strains, isolated from turkey litter (n=74), chicken livers (n=15) and clinical (n=8) samples, were speciated using the PCR-based assay. PCR amplification of the isolates identified a 400-bp cadF gene, conserved in Campylobacter species, an 894-bp ceuE gene, specific for C. coli, and a 160-bp oxidoreductase gene, specific for C. jejuni. The approximately 35 kDa cadF adhesion proteins allow Campylobacter to bind to the intestinal epithelial cells and the 37 kDa ceuE lipoproteins are involved in siderophore transport. Sequencing of the 160-bp undefined gene yielded a 67% protein identical match with a gene encoding an oxidoreductase subunit in C. jejuni. The specificity of the assay was validated on 36 non-Campylobacter strains (11 Gram-positive and 25 Gram-negative bacteria). The PCR assay identified 59% of turkey and 47% of chicken isolates as C. jejuni, and 41% of turkey and 53% of chicken isolates as C. coli. All human isolates were identified as C. jejuni. The specificity of this assay to detect C. coli or C. jejuni was 97%.
本研究的目的是利用多重PCR检测法同时检测弯曲杆菌属、大肠弯曲杆菌或空肠弯曲杆菌,使用源自cadF和ceuE基因以及一个未明确的毒力基因的探针。总共97株弯曲杆菌菌株,分别从火鸡垫料(n = 74)、鸡肝(n = 15)和临床样本(n = 8)中分离得到,使用基于PCR的检测法进行鉴定。对分离菌株进行PCR扩增,鉴定出弯曲杆菌属中保守的400 bp cadF基因、大肠弯曲杆菌特有的894 bp ceuE基因以及空肠弯曲杆菌特有的160 bp氧化还原酶基因。约35 kDa的cadF黏附蛋白使弯曲杆菌能够结合到肠道上皮细胞,而37 kDa的ceuE脂蛋白参与铁载体转运。对160 bp未明确基因进行测序,结果显示与空肠弯曲杆菌中一个编码氧化还原酶亚基的基因有67%的蛋白质同源性。该检测法的特异性在36株非弯曲杆菌菌株(11株革兰氏阳性菌和25株革兰氏阴性菌)上得到验证。PCR检测法鉴定出59%的火鸡分离株和47%的鸡分离株为空肠弯曲杆菌,41%的火鸡分离株和53%的鸡分离株为大肠弯曲杆菌。所有人类分离株均鉴定为空肠弯曲杆菌。该检测法检测大肠弯曲杆菌或空肠弯曲杆菌的特异性为97%。