Hiett Kelli L, Cox Nelson A, Stern Norman J
United States Department of Agriculture, Agricultural Research Service, Poultry Microbiological Safety Research Unit, Athens, GA 30604-5677, USA.
Avian Dis. 2002 Jan-Mar;46(1):219-23. doi: 10.1637/0005-2086(2002)046[0219:DPCRDO]2.0.CO;2.
A rapid, sensitive, and specific polymerase chain reaction (PCR) assay was developed for the direct detection of Campylobacter in environmental samples from hatcheries. PCR, with a set of primers specific for the Campylobacter flaA short variable region (SVR), detected the presence of Campylobacter in both fluff and eggshell samples; however, a determination of whether the organism was living or dead could not be made. Conventional cultural methods detected no Campylobacter from the same samples. An additional benefit of the direct PCR assay is it allows for the production of a product that can be sequenced to provide further epidemiologic information.
开发了一种快速、灵敏且特异的聚合酶链反应(PCR)检测方法,用于直接检测孵化场环境样本中的弯曲杆菌。使用一组针对弯曲杆菌鞭毛蛋白A短可变区(SVR)的引物进行PCR,可检测绒毛和蛋壳样本中弯曲杆菌的存在;然而,无法确定该微生物是活的还是死的。传统培养方法在相同样本中未检测到弯曲杆菌。直接PCR检测的另一个优点是,它能够产生可进行测序的产物,以提供更多的流行病学信息。