Jeon Bo- Young, Je Sungmo, Park Jinhee, Kim Yeun, Lee Eun-Gae, Lee Hyeyoung, Seo Sangkyo, Cho Sang-Nae
Department of Microbiology and the Brain Korea 21 Project for the Medical Sciences, Yonsei University College of Medicine, Seoul 120-752, Korea.
J Vet Sci. 2008 Jun;9(2):145-53. doi: 10.4142/jvs.2008.9.2.145.
Bovine tuberculosis (TB) is a major zoonosis that's caused by Mycobacterium bovis (M. bovis). Being able to detect M. bovis is important to control bovine TB. We applied a molecular technique, the variable number tandem repeat (VNTR) typing method, to identify and distinguish the M. bovis isolates from Gyeonggi-do, Korea. From 2003 to 2004, 59 M. bovis clinical strains were isolated from dairy cattle in Gyeonggi-do, Korea, and these cattle had tuberculosis- like lesions. Twenty-four published MIRUVNTR markers were applied to the M. bovis isolates and ten of them showed allelic diversity. The most discriminatory locus for the M. bovis isolates in Korea was QUB 3336 (h = 0.64). QUB 26 and MIRU 31 also showed high discriminative power (h = 0.35). The allelic diversity by the combination of all VNTR loci was 0.86. Six loci (MIRU 31, ETR-A and QUB-18, -26, -3232, -3336) displayed valuable allelic diversity. Twelve genotypes were identified from the 59 M. bovis isolates that originated from 20 cattle farms that were dispersed throughout the region of Gyenggi-do. Two genotypes [designation index (d.i.) = e, g] showed the highest prevalence (20% of the total farms). For the multiple outbreaks on three farms, two successive outbreaks were caused by the same genotype at two farms. Interestingly, the third outbreak at one farm was caused by both a new genotype and a previous genotype. In conclusion, this study suggests that MIRU-VNTR typing is useful to identify and distinguish the M. bovis isolates from Gyeonggi-do, Korea.
牛结核病(TB)是一种主要的人畜共患病,由牛分枝杆菌(M. bovis)引起。能够检测到牛分枝杆菌对于控制牛结核病很重要。我们应用了一种分子技术,即可变数目串联重复序列(VNTR)分型方法,来鉴定和区分来自韩国京畿道的牛分枝杆菌分离株。2003年至2004年,从韩国京畿道的奶牛中分离出59株牛分枝杆菌临床菌株,这些奶牛有类似结核病的病变。将24个已发表的MIRUVNTR标记应用于牛分枝杆菌分离株,其中10个显示出等位基因多样性。在韩国,对牛分枝杆菌分离株最具鉴别力的位点是QUB 3336(h = 0.64)。QUB 26和MIRU 31也显示出高鉴别力(h = 0.35)。所有VNTR位点组合的等位基因多样性为0.86。六个位点(MIRU 31、ETR-A和QUB-18、-26、-3232、-3336)显示出有价值的等位基因多样性。从分布在京畿道地区的20个奶牛场的59株牛分枝杆菌分离株中鉴定出12种基因型。两种基因型[指定指数(d.i.)= e,g]的流行率最高(占农场总数的20%)。对于三个农场的多次疫情爆发,两个农场的两次连续疫情爆发是由相同基因型引起的。有趣的是,一个农场的第三次疫情爆发是由一种新基因型和一种先前的基因型共同引起的。总之,本研究表明,MIRU-VNTR分型有助于鉴定和区分来自韩国京畿道的牛分枝杆菌分离株。