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通过多重聚合酶链反应检测和鉴定家禽及家禽产品中弯曲杆菌属、弓形杆菌属和幽门螺杆菌属的食源性病原体。

Detection and identification of food-borne pathogens of the genera Campylobacter, Arcobacter and Helicobacter by multiplex PCR in poultry and poultry products.

作者信息

Neubauer C, Hess M

机构信息

Clinic for Avian, Reptile and Fish Medicine, University of Veterinary Medicine Vienna, Veterinaerplatz 1, 1210 Vienna, Austria.

出版信息

J Vet Med B Infect Dis Vet Public Health. 2006 Oct;53(8):376-81. doi: 10.1111/j.1439-0450.2006.00991.x.

DOI:10.1111/j.1439-0450.2006.00991.x
PMID:17010041
Abstract

The objective of this study was to develop a multiplex polymerase chain reaction (PCR) to detect and differentiate food-borne pathogens of the three genera Campylobacter, Arcobacter and Helicobacter in a single step procedure. One common reverse primer and three genus-specific forward primers were designed by hybridizing to the 16S rRNA of selected reference strains. Besides the species with significance as food-borne pathogens isolated from poultry meat--Campylobacter jejuni, Campylobacter coli, Arcobacter butzleri and Helicobacter pullorum--several other members of these genera were tested to determine the specificity of the designed multiplex PCR. In total, 20 ATCC and NCTC reference strains of Campyobacter, Arcobacter and Helicobacter were used to evaluate the PCR. Specific amplificates were obtained from all thermophilic species of Campylobacter as well as from species of Arcobacter and Helicobacter. No amplification product was obtained from the non-thermophilic Campylobacter, C. hyointestinalis and C. fetus. Furthermore, a total of 43 field strains of the three genera isolated from poultry, pigs, cattle and humans were investigated using this PCR. To confirm the classification of 10 H. pullorum strains the 16S rRNAs were sequenced. The developed PCR is a helpful diagnostic tool to detect and differentiate Campylobacter, Arcobacter and Helicobacter isolated from poultry and poultry products.

摘要

本研究的目的是开发一种多重聚合酶链反应(PCR),以便在一个步骤中检测和区分弯曲杆菌属、嗜冷弧菌属和幽门螺杆菌属这三个属的食源性病原体。通过与选定参考菌株的16S rRNA杂交,设计了一条通用反向引物和三条属特异性正向引物。除了从禽肉中分离出的具有食源性病原体意义 的空肠弯曲菌、结肠弯曲菌、布氏嗜冷弧菌和拉氏幽门螺杆菌等菌种外,还对这些属的其他几个成员进行了测试,以确定所设计的多重PCR的特异性。总共使用了20株弯曲杆菌属、嗜冷弧菌属和幽门螺杆菌属的ATCC和NCTC参考菌株来评估该PCR。从所有嗜热弯曲杆菌菌种以及嗜冷弧菌属和幽门螺杆菌属的菌种中都获得了特异性扩增产物。从非嗜热弯曲杆菌、猪肠弯曲菌和胎儿弯曲菌中未获得扩增产物。此外,使用该PCR对从家禽、猪、牛和人类中分离出的这三个属的总共43株现场菌株进行了研究。为了确认10株拉氏幽门螺杆菌菌株的分类,对其16S rRNA进行了测序。所开发的PCR是一种有助于检测和区分从家禽及家禽产品中分离出的弯曲杆菌属、嗜冷弧菌属和幽门螺杆菌属的诊断工具。

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