Feberwee Anneke, Hampson David J, Phillips Nyree D, La Tom, van der Heijden Harold M J F, Wellenberg Gerard J, Dwars R Marius, Landman Wil J M
Animal Health Service (GD), PO Box 9, 7400 AA Deventer, The Netherlands.
J Clin Microbiol. 2008 Feb;46(2):593-600. doi: 10.1128/JCM.01829-07. Epub 2007 Dec 12.
Cecal samples from laying chickens from 25 farms with a history of decreased egg production, diarrhea, and/or increased feed conversion ratios were examined for anaerobic intestinal spirochetes of the genus Brachyspira. Seventy-three samples positive in an immunofluorescence assay for Brachyspira species were further examined using selective anaerobic culture, followed by phenotypic analysis, species-specific PCRs (for Brachyspira hyodysenteriae, B. intermedia, and B. pilosicoli), and a Brachyspira genus-specific PCR with sequencing of the partial 16S rRNA gene products. Brachyspira cultures were obtained from all samples. Less than half of the isolates could be identified to the species level on the basis of their biochemical phenotypes, while all but four isolates (5.2%) were speciated by using PCR and sequencing of DNA extracted from the bacteria. Different Brachyspira spp. were found within a single flock and also in cultures from single chickens, emphasizing the need to obtain multiple samples when investigating outbreaks of avian intestinal spirochetosis. The most commonly detected spirochetes were the pathogenic species B. intermedia and B. pilosicoli. The presumed nonpathogenic species B. innocens, B. murdochii, and the proposed "B. pulli" also were identified. Pathogenic B. alvinipulli was present in two flocks, and this is the first confirmed report of B. alvinipulli in chickens outside the United States. Brachyspira hyodysenteriae, the agent of swine dysentery, also was identified in samples from three flocks. This is the first confirmed report of natural infection of chickens with B. hyodysenteriae. Experimental infection studies are required to assess the pathogenic potential of these B. hyodysenteriae isolates.
对来自25个养殖场的产蛋鸡盲肠样本进行检测,这些养殖场有产蛋量下降、腹泻和/或饲料转化率增加的病史,检测其中的短螺旋体属厌氧肠道螺旋体。对73份在短螺旋体属免疫荧光检测中呈阳性的样本,进一步采用选择性厌氧培养,随后进行表型分析、种特异性PCR(针对猪痢疾短螺旋体、中间短螺旋体和结肠短螺旋体)以及对部分16S rRNA基因产物进行测序的短螺旋体属特异性PCR。所有样本均获得了短螺旋体培养物。基于生化表型,不到一半的分离株能够鉴定到种水平,而除4株分离株(5.2%)外,所有分离株均通过对细菌提取的DNA进行PCR和测序来鉴定种属。在单个鸡群内以及单只鸡的培养物中都发现了不同的短螺旋体种,这强调了在调查禽肠道螺旋体病暴发时需要采集多个样本。最常检测到的螺旋体是致病种中间短螺旋体和结肠短螺旋体。还鉴定出了推测的非致病种无害短螺旋体、默多克短螺旋体以及提议的“雏鸡短螺旋体”。致病的阿尔文短螺旋体存在于两个鸡群中,这是美国以外地区鸡群中首次确认有阿尔文短螺旋体感染的报告。猪痢疾的病原体猪痢疾短螺旋体也在三个鸡群的样本中被鉴定出来。这是鸡自然感染猪痢疾短螺旋体的首次确认报告。需要进行实验性感染研究来评估这些猪痢疾短螺旋体分离株的致病潜力。