Key Laboratory of Veterinary Parasitology of Gansu Province, State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Science, Xujiaping 1, Lanzhou, Gansu, 730046, PR China.
Parasitology. 2010 May;137(6):927-38. doi: 10.1017/S0031182009991922. Epub 2010 Jan 29.
Babesia sp. BQ1 (Lintan) is a Babesia isolated from sheep infested with Haemaphysalis qinghaiensis in China, and is closely related to B. motasi based on the 18S rRNA gene sequence. In the present study, an ELISA was developed with merozoite antigens of Babesia sp. BQ1 (Lintan) (BQMA) purified from in vitro culture. When the positive threshold was chosen as 30% of the antibodies rate, evaluated with 198 negative sera, the specificity was 95.5%. Except for Babesia sp. Tianzhu, there was no cross-reaction between BQMA and positive sera from Babesia sp. BQ1 (Ningxian)-, Babesia sp. Hebei-, Babesia sp. Xinjiang-, Theileria luwenshuni-, T. uilenbergi-, or Anaplasma ovis-infected sheep, which are the dominant haemoparasites of small ruminants in China. Specific antibodies against Babesia sp. BQ1 (Lintan) were produced 1 or 2 weeks post-infection and a high level of antibodies persisted for more than 8 months in experimentally infected sheep. This ELISA was tested on 974 sera collected from field-grazing sheep in 3 counties of Gansu province, northwestern China to evaluate the seroprevalence of Babesia sp. BQ1 (Lintan) infection and the average positive rate was 66.84%. The feasibility of increasing the specificity of this BQMA-based ELISA, by using some BQMA antigens for serodiagnosis is discussed.
巴贝斯虫 sp. BQ1(宁夏)是从感染青海血蜱的绵羊中分离到的一种巴贝斯虫,根据 18S rRNA 基因序列,与 B. motasi 密切相关。本研究用体外培养的巴贝斯虫 sp. BQ1(宁夏)(BQMA)裂殖子抗原建立了一种 ELISA。当阳性阈值选择为抗体率的 30%时,用 198 份阴性血清进行评估,特异性为 95.5%。除巴贝斯虫 sp. 天祝外,BQMA 与巴贝斯虫 sp. BQ1(宁陕)、巴贝斯虫 sp. 河北、巴贝斯虫 sp. 新疆、吕氏泰勒虫、乌氏泰勒虫或绵羊无浆体感染的阳性血清均无交叉反应,这些是中国小反刍动物的主要血液寄生虫。感染后 1 或 2 周可产生针对巴贝斯虫 sp. BQ1(宁夏)的特异性抗体,在实验感染绵羊中,抗体水平可持续 8 个月以上。该 ELISA 在中国西北部甘肃省 3 个县的 974 份野外放牧绵羊血清中进行了检测,以评估巴贝斯虫 sp. BQ1(宁夏)感染的血清流行率,平均阳性率为 66.84%。讨论了用一些 BQMA 抗原提高基于 BQMA 的 ELISA 特异性的可行性。