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应用实时 PCR 技术快速检测禽肉和屠宰环境样本中的空肠弯曲菌

Rapid identification of Campylobacter jejuni from poultry carcasses and slaughtering environment samples by real-time PCR.

机构信息

Department of Biotechnology, University of Food Technologies, 26 Maritza Blvd, 4002 Plovdiv, Bulgaria.

School of Public Health and Zoonoses, Guru Angad Dev Veterinary and Animal Science University, Ludhiana, India PB-141004.

出版信息

Poult Sci. 2014 Jun;93(6):1587-97. doi: 10.3382/ps.2013-03736.

Abstract

The objective of this study was to develop a real-time PCR assay for rapid identification of Campylobacter jejuni and to apply the method in analyzing samples from poultry processing. A C. jejuni-specific primer set targeting a portion of the C. jejuni hippuricase gene was developed. The specificity of the newly designed primer pair was verified using 5 C. jejuni strains and 20 other bacterial strains. Sensitivity was determined to be as low as 1 genome copy per reaction. A total of 73 samples were collected at different sites along the processing line during 2 visits to a poultry slaughterhouse and were examined by direct plating onto modified charcoal cefoperazone deoxycholate agar or after enrichment in Bolton broth followed by plating on modified charcoal cefoperazone deoxycholate agar. The newly developed real-time PCR assay was used to identify the presumptive colonies as belonging to C. jejuni. A real-time PCR assay targeting 16S ribosomal RNA was also applied to determine Campylobacter spp. prevalence. Results from the real-time PCR analysis indicated considerable variability in Campylobacter contamination, with incidence rates of 72.7 and 27.6% for sampling days A and B, respectively. Campylobacter was isolated from 100% of prescalded and preeviscerated carcasses on sampling day A. In contrast, on sampling day B, the highest number of Campylobacter-positive carcasses was recovered after evisceration (60%). The chilling process significantly reduced (P < 0.05) Campylobacter population, but the percentage of positive samples on sampling day A increased to 80%. All samples collected from the processing environment, except scalding tank 3 and the prechiller and chiller tanks, were 100% positive on day A, whereas no campylobacters were isolated from machinery on sampling day B. Our results revealed the widespread of C. jejuni in poultry processing and proved that the newly developed real-time PCR assay is a simple, specific, and inexpensive method for rapid C. jejuni identification. The newly developed PCR method can be easily used in laboratories for reliable and unambiguous identification of C. jejuni in poultry samples.

摘要

本研究旨在开发一种用于快速鉴定空肠弯曲菌的实时 PCR 检测方法,并将该方法应用于分析家禽加工样本。设计了一组针对空肠弯曲菌 hippuricase 基因部分的空肠弯曲菌特异性引物。新设计的引物对的特异性通过 5 株空肠弯曲菌和 20 株其他细菌菌株得到验证。灵敏度低至每个反应 1 个基因组拷贝。在两次访问家禽屠宰场期间,在加工线上的不同地点共采集了 73 个样本,通过直接在改良的炭头孢哌酮脱氧胆酸盐琼脂上划线或在 Bolton 肉汤中富集后在改良的炭头孢哌酮脱氧胆酸盐琼脂上划线进行检查。使用新开发的实时 PCR 检测方法鉴定推定的菌落是否为空肠弯曲菌。还应用针对 16S 核糖体 RNA 的实时 PCR 检测来确定弯曲菌属的流行率。实时 PCR 分析结果表明,弯曲菌污染的变化很大,采样日 A 和 B 的发生率分别为 72.7%和 27.6%。采样日 A 时,100%的预烫和预剖腹的胴体上分离到空肠弯曲菌。相比之下,在采样日 B 时,在剖腹后回收的空肠弯曲菌阳性胴体数量最多(60%)。冷却过程显著降低了(P<0.05)空肠弯曲菌的种群,但采样日 A 的阳性样本百分比增加到 80%。除了烫池 3 以及预冷器和冷却器外,在加工环境中采集的所有样本在采样日 A 时均为 100%阳性,而在采样日 B 时从机器上没有分离到空肠弯曲菌。我们的结果表明空肠弯曲菌在家禽加工中广泛存在,并证明新开发的实时 PCR 检测方法是一种简单、特异和廉价的空肠弯曲菌快速鉴定方法。新开发的 PCR 方法可方便地用于实验室,用于可靠和明确地鉴定家禽样本中的空肠弯曲菌。

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