Phillips N D, La T, Hampson D J
School of Veterinary and Biomedical Sciences, Murdoch University, South Street, Murdoch, Perth, WA 6150, Australia.
Vet Microbiol. 2005 Feb 25;105(3-4):189-98. doi: 10.1016/j.vetmic.2004.10.016. Epub 2004 Dec 21.
A cross-sectional study was conducted on a commercial egg-producing farm with a history of wet litter. A total of 600 fresh caecal faecal samples were obtained from under cages of laying hens in three sheds each containing flocks of approximately 5400 hens. Samples were cultured for intestinal spirochaetes, and growth on the primary isolation plate was observed under a phase contrast microscope and subjected to PCRs specific for the intestinal spirochaetes Brachyspira intermedia and Brachyspira pilosicoli. Spirochaete isolates obtained in pure culture were assessed for their ability to cause haemolysis on blood agar and to produce indole, and were typed using pulsed field gel electrophoresis (PFGE). A 1250 base pair portion of the 16S rRNA gene of three B. intermedia and five unidentified isolates was sequenced, and the sequences compared with those of other Brachyspira species. Overall, 121 (20.2%) of the faecal samples contained spirochaetes as determined by growth on the plate and microscopy. Using PCR on the primary growth from these positive samples, 43 (7.2% overall) were shown to contain B. intermedia, 8 (1.3%) to contain B. pilosicoli, and 70 (11.7%) were PCR negative. Only 24 isolates of B. intermedia and five isolates of unknown species were obtained in pure culture. Comparative analysis of the 16S rRNA gene sequence identified the non-B. intermedia isolates as belonging to the proposed species "Brachyspira pulli". PFGE analysis of the B. intermedia strains identified them as having four major banding patterns. Individual patterns were found in hens from different flocks, suggesting cross-transmission of strains between flocks. No environmental sources of infection were identified. The youngest flock had a significantly lower level of colonisation with B. intermedia than the flock of intermediate age (P = 0.004), suggesting that following initial infection of individual young hens on this farm there was amplification and transmission of infection amongst members of the flock.
对一个有垫料潮湿历史的商业蛋鸡养殖场进行了一项横断面研究。从三个鸡舍的产蛋母鸡笼下共采集了600份新鲜盲肠粪便样本,每个鸡舍约有5400只母鸡。对样本进行肠道螺旋体培养,在相差显微镜下观察初次分离平板上的生长情况,并进行针对中间短螺旋体和结肠短螺旋体的PCR检测。对纯培养获得的螺旋体分离株进行血平板溶血能力和吲哚产生能力评估,并使用脉冲场凝胶电泳(PFGE)进行分型。对3株中间短螺旋体和5株未鉴定分离株的16S rRNA基因的1250个碱基对部分进行测序,并将序列与其他短螺旋体物种的序列进行比较。总体而言,通过平板生长和显微镜检查确定,121份(20.2%)粪便样本含有螺旋体。对这些阳性样本的初次生长物进行PCR检测,结果显示43份(总体7.2%)含有中间短螺旋体,8份(1.3%)含有结肠短螺旋体,70份(11.7%)PCR检测为阴性。仅获得了24株中间短螺旋体分离株和5株未知物种的分离株。16S rRNA基因序列的比较分析确定非中间短螺旋体分离株属于拟议的“鸡短螺旋体”物种。对中间短螺旋体菌株的PFGE分析确定它们有四种主要条带模式。在不同鸡群的母鸡中发现了个体模式,表明菌株在鸡群之间交叉传播。未发现感染的环境来源。最年轻的鸡群中中间短螺旋体的定植水平明显低于中年鸡群(P = 0.004),这表明在该农场个别年轻母鸡初次感染后,感染在鸡群成员中发生了扩增和传播。