机构地区: 华南农业大学兽医学院
出 处: 《中国兽医科学》 2011年第3期245-249,共5页
摘 要: 无菌采集疑似巴贝斯虫感染血样,进行全血基因组DNA的抽提,用保守引物5-22F和1661R进行巴贝斯虫18SrRNA基因的PCR扩增,扩增产物经克隆、测序后,获得大小为1 677bp的核苷酸序列。序列比对和系统发育分析发现,该序列与韦氏巴贝斯虫(AB083374)18SrRNA基因的相似性达100%,而与犬巴贝斯虫(AY072926)、罗氏巴贝斯虫(L19079)和吉氏巴贝斯虫(AF271081)18SrRNA基因的相似性分别为98.0%,95.2%和93.4%。从分子水平证实了韦氏巴贝斯虫在广东宠物犬的存在,同时也对巴贝斯虫的分类进行了讨论。 The 18 S rRNA gene of Babesia was amplified by PCR using a pair of conserved primers(5-22F and 1661R) from canine whole blood genomic DNA extracted from suspected pet dogs in Guangzhou and Foshan.The recombinant plasmids were identified by PCR and the positive clones were sequenced.A 1 677 bp sequence in length was obtained that was identical to the 18 S rRNA gene of Babesia vogeli published previously(AB083374),meanwhile,compared with the 18 S rRNA gene of B.canis(AY072926),B.rossi(L19079) and B.gibsoni(AF271081) available in GenBank,the sequences similarities were 98.0%,95.2% and 93.4%,respectively.We confirmed the prevalence of B.vogeli in pet dogs in China by molecular approach for the first time,and the classification of Babesia was discussed in the present study.