National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido 080-8555, Japan.
Vet Parasitol. 2012 Mar 23;184(2-4):309-16. doi: 10.1016/j.vetpar.2011.09.021. Epub 2011 Oct 1.
We conducted a molecular epidemiological study on Babesia bovis in Mongolia. Three hundred blood samples collected from cattle grazed in seven different districts were initially screened using a previously established diagnostic polymerase chain reaction (PCR) assay for the detection of B. bovis-specific DNA. Positive samples were then used to amplify and sequence the hyper-variable regions of three B. bovis genes encoding the merozoite surface antigen (MSA)-1, MSA-2b, and MSA-2c. The diagnostic PCR assay detected B. bovis among cattle populations of all districts surveyed (4.4-26.0%). Sequences of each of the three genes were highly homologous among the Mongolian isolates, and found in a single phylogenetic cluster. In particular, a separate branch was formed only by the Mongolian isolates in the MSA-2b gene-based phylogenetic tree. Our findings indicate that effective preventative and control strategies are essential to control B. bovis infection in Mongolian cattle populations, and suggest that a careful approach must be adopted when using immunization techniques.
我们对蒙古的牛巴贝斯虫进行了分子流行病学研究。使用先前建立的用于检测牛巴贝斯虫特异性 DNA 的诊断聚合酶链反应(PCR)检测法,对从七个不同地区放牧的 300 份牛血样进行了初步筛查。阳性样本随后用于扩增和测序编码裂殖子表面抗原(MSA)-1、MSA-2b 和 MSA-2c 的三个牛巴贝斯虫基因的高变区。诊断 PCR 检测法在调查的所有地区的牛群中均检测到了牛巴贝斯虫(4.4-26.0%)。蒙古分离株的三个基因的序列在种系发生上高度同源,且存在于单个系统发育群中。特别是,蒙古分离株在基于 MSA-2b 基因的系统发育树上仅形成了一个单独的分支。我们的研究结果表明,在蒙古牛群中控制牛巴贝斯虫感染需要采取有效的预防和控制策略,并建议在使用免疫技术时必须采取谨慎的方法。