Moore L J, Wassink G J, Green L E, Grogono-Thomas R
School of Clinical Veterinary Science, University of Bristol, Churchill Building, Langford House, Langford, North Somerset BS40 5DU, UK.
Vet Microbiol. 2005 Jun 15;108(1-2):57-67. doi: 10.1016/j.vetmic.2005.01.029. Epub 2005 Mar 31.
Footrot, caused by the strictly anaerobic bacterium Dichelobacter nodosus, is the most common cause of lameness in sheep in Great Britain but problems exist in association with its diagnosis and control. The fastidious nature of D. nodosus means that complex media and several weeks are required for characterisation. An alternative method to simplify and enhance the detection of D. nodosus in clinical samples is therefore highly desirable. In terms of control, anecdotal evidence from the farming community suggests that the commercially available vaccine, based on Australian isolates of D. nodosus, is not widely employed in this country due to its perceived inefficacy. Seven hundred and six isolates, collected from outbreaks in England and Wales, were therefore used to investigate these issues. A 16S rRNA PCR was adapted to detect D. nodosus in clinical material within 1 day of sampling; a 15% increase in detection compared with culture and less than 1% false negatives were achieved. This represents a major advance in the rapid diagnosis of footrot and will be of great value to practitioners and diagnostic laboratories. Bacterial virulence was tested using protease thermostability and zymogram assays, whilst serogrouping was performed by slide agglutination. All isolates demonstrated virulence patterns previously recorded in Australia and all nine serogroups of D. nodosus (A-I) were represented. Serogroup H was predominant. There was, therefore, no evidence for the presence of novel strains of D. nodosus compared with Australia suggesting the need for further investigation into farmers' views on the use of the commercial vaccine in Great Britain.
腐蹄病由严格厌氧的结节拟杆菌引起,是英国绵羊跛足的最常见原因,但在其诊断和控制方面存在问题。结节拟杆菌苛求的特性意味着需要复杂的培养基和数周时间来进行鉴定。因此,非常需要一种简化和增强临床样本中结节拟杆菌检测的替代方法。在控制方面,来自养殖社区的传闻证据表明,基于澳大利亚结节拟杆菌分离株的市售疫苗在该国未被广泛使用,因为人们认为其无效。因此,从英格兰和威尔士的疫情中收集了706株分离株来研究这些问题。采用16S rRNA聚合酶链反应(PCR)在采样后1天内检测临床材料中的结节拟杆菌;与培养法相比,检测率提高了15%,假阴性率不到1%。这代表了腐蹄病快速诊断方面的一项重大进展,对从业者和诊断实验室具有重要价值。使用蛋白酶热稳定性和酶谱分析检测细菌毒力,同时通过玻片凝集进行血清分型。所有分离株均表现出先前在澳大利亚记录的毒力模式,并且代表了结节拟杆菌的所有九个血清群(A - I)。血清群H占主导地位。因此,与澳大利亚相比,没有证据表明存在结节拟杆菌新菌株,这表明需要进一步调查英国农民对使用商业疫苗的看法。