Cagatay Ifakat Tulay, Hickford Jon G H
Agriculture and Life Sciences Division, P.O. Box 84, Lincoln University, Canterbury, New Zealand.
Vet Microbiol. 2005 Dec 20;111(3-4):171-80. doi: 10.1016/j.vetmic.2005.09.010. Epub 2005 Nov 8.
Dichelobacter nodosus, a Gram-negative strict anaerobe, is the essential causative agent of ovine footrot. Despite its worldwide presence, the disease has significant economic impact in those sheep-farming countries with a temperate climate and moderate to high rainfall, such as New Zealand (NZ) and Australia. In this study, we aimed to isolate, identify, and characterize as many D. nodosus strains as possible from NZ farms by using polymerase chain reaction (PCR)-based technology. Understanding the virulence of this bacterium and showing extensive genomic variation in the fimbrial subunit gene (fimA) in different D. nodosus strains was very important to produce serogroup specific and effective vaccine for NZ. More than 100 footrot samples were collected from four different farming regions in NZ. Thousands of primary plates were cultured anaerobically and examined with Gram-staining in order to detect single colonies of D. nodosus. Approximately 500 plates that had potential D. nodosus colonies were subcultured several times to eliminate contaminating colonies until single colonies were obtained. Variable and a part of the conserved regions of the fimbrial subunit gene (fimA) were amplified directly from bacterial DNA extracted from footrot lesions and also from cultured NZ D. nodosus isolates, using the polymerase chain reaction. Different fimA amplimers were analyzed by DNA sequencing. On the basis of DNA sequence analysis, 16 new D. nodosus isolates belonging to eight different serogroups were identified from NZ. These new D. nodosus fimA sequences from NZ were different to previously reported strains and strains used in a commercial vaccine.
结节拟杆菌是一种革兰氏阴性严格厌氧菌,是绵羊腐蹄病的主要致病因子。尽管它在全球范围内存在,但该病在气候温和、降雨适中至高的养羊国家,如新西兰(NZ)和澳大利亚,具有重大的经济影响。在本研究中,我们旨在通过基于聚合酶链反应(PCR)的技术,从新西兰农场分离、鉴定和表征尽可能多的结节拟杆菌菌株。了解这种细菌的毒力,并显示不同结节拟杆菌菌株的菌毛亚基基因(fimA)存在广泛的基因组变异,对于为新西兰生产血清群特异性和有效的疫苗非常重要。从新西兰的四个不同养殖地区收集了100多个腐蹄病样本。数千个原始平板进行厌氧培养,并用革兰氏染色检查,以检测结节拟杆菌的单菌落。大约500个有潜在结节拟杆菌菌落的平板进行了多次传代培养,以消除污染菌落,直到获得单菌落。使用聚合酶链反应,直接从腐蹄病病变中提取的细菌DNA以及培养的新西兰结节拟杆菌分离物中扩增菌毛亚基基因(fimA)的可变区和部分保守区。通过DNA测序分析不同的fimA扩增子。基于DNA序列分析,从新西兰鉴定出16株属于八个不同血清群的新的结节拟杆菌分离物。这些来自新西兰的新的结节拟杆菌fimA序列与先前报道的菌株以及商业疫苗中使用的菌株不同。