Shams Saeed, Bakhshi Bita, Tohidi Moghadam Tahereh
Department of Medical Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, IR Iran.
Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, IR Iran.
Jundishapur J Microbiol. 2016 Feb 9;9(2):e29645. doi: 10.5812/jjm.29645. eCollection 2016 Feb.
Campylobacteriosis is a zoonotic infectious disease caused by Campylobacter jejuni and C. coli. The cadF gene is considered as a genus-specific gene while other genes are mainly used for discrimination at the species level.
This study aimed to analyze the cadF gene and to develop a duplex PCR assay for simultaneous detection of C. coli and C. jejuni, the two commonly encountered species.
In silico analysis of the cadF gene was carried out by several software and available online tools. A duplex PCR optimized with specific primers was used for detection and differentiation of both species. To evaluate specificity and sensitivity of the test, a panel of different Campylobacter spp. together with several intestinal bacterial pathogens was tested. The limit of detection (LOD) of method was determined using serial dilutions of standard genomes.
The analysis of the full size cadF gene indicated variations in this gene, which can be used to differentiate C. jejuni and C. coli. The duplex PCR designed in this study showed that it could simultaneously detect and differentiate both C. jejuni and C. coli with product sizes of 737 bp and 461 bp, respectively. This assay, with 100% specificity and sensitivity, had a limit of detection (LOD) of about 14 and 0.7 µg/mL for C. jejuni and C. coli, respectively.
In silico analysis of the cadF full-gene showed variations between the two species that can be used as a molecular target for differentiating C. jejuni and C. coli in a single-step duplex-PCR assay with high specificity and sensitivity.
弯曲杆菌病是一种由空肠弯曲杆菌和大肠弯曲杆菌引起的人畜共患传染病。cadF基因被认为是属特异性基因,而其他基因主要用于种水平的鉴别。
本研究旨在分析cadF基因,并开发一种双重PCR检测方法,用于同时检测两种常见的弯曲杆菌——大肠弯曲杆菌和空肠弯曲杆菌。
利用多种软件和在线工具对cadF基因进行电子分析。使用经特异性引物优化的双重PCR检测和区分这两种弯曲杆菌。为评估该检测方法的特异性和敏感性,对一组不同的弯曲杆菌属菌株以及几种肠道细菌病原体进行了检测。通过对标准基因组进行系列稀释来确定该方法的检测限(LOD)。
全长cadF基因分析表明该基因存在变异,可用于区分空肠弯曲杆菌和大肠弯曲杆菌。本研究设计的双重PCR显示,它能够同时检测和区分空肠弯曲杆菌和大肠弯曲杆菌,产物大小分别为737 bp和461 bp。该检测方法具有100%的特异性和敏感性,空肠弯曲杆菌和大肠弯曲杆菌的检测限(LOD)分别约为14和0.7 μg/mL。
cadF全基因的电子分析显示两种弯曲杆菌之间存在变异,可作为分子靶点,在一步双重PCR检测中以高特异性和敏感性区分空肠弯曲杆菌和大肠弯曲杆菌。