Lund Marianne, Nordentoft Steen, Pedersen Karl, Madsen Mogens
Danish Institute for Food and Veterinary Research (DFVF), Hangovej 2, DK 8200 Arhus N, Denmark.
J Clin Microbiol. 2004 Nov;42(11):5125-32. doi: 10.1128/JCM.42.11.5125-5132.2004.
A real-time PCR assay for detecting thermophilic Campylobacter spp. directly in chicken feces has been developed. DNA was isolated from fecal material by using magnetic beads followed by PCR with a prealiquoted PCR mixture, which had been stored at -18 degrees C. Campylobacter could be detected in less than 4 h, with a detection limit of 100 to 150 CFU/ml, in a fecal suspension. A bacterial internal control was added before DNA extraction to control both DNA isolation and the presence of PCR inhibitors in the samples. The assay was performed on 111 swab samples from a Danish surveillance program and compared to conventional culturing using selective enrichment. There was no statistically significant difference in performance between real-time PCR and culture by selective enrichment, and the diagnostic specificity was 0.96 with an agreement of 0.92. Therefore, the assay should be useful for screening poultry flocks for the presence of Campylobacter.
已开发出一种用于直接检测鸡粪便中嗜热弯曲菌属的实时聚合酶链反应(PCR)检测方法。通过使用磁珠从粪便材料中分离DNA,随后使用预先分装并保存在-18℃的PCR混合物进行PCR。在粪便悬液中,不到4小时即可检测到弯曲菌,检测限为100至150 CFU/ml。在DNA提取前添加细菌内部对照,以控制DNA分离以及样品中PCR抑制剂的存在。对来自丹麦监测项目的111个拭子样本进行了该检测,并与使用选择性富集的传统培养方法进行比较。实时PCR与选择性富集培养在性能上无统计学显著差异,诊断特异性为0.96,一致性为0.92。因此,该检测方法应有助于筛查家禽群中弯曲菌的存在情况。