Anifowose Olaoluwa Isaac, Takeet Michael Irewole, Talabi Adewale Oladele, Otesile Ebenezer Babatunde
Department of Veterinary Medicine, College of Veterinary Medicine, Federal University of Agriculture, Abeokuta, Nigeria.
Department of Veterinary Microbiology and Parasitology, College of Veterinary Medicine, Federal University of Agriculture, Abeokuta, Nigeria.
J Parasit Dis. 2020 Jun;44(2):403-410. doi: 10.1007/s12639-020-01218-4. Epub 2020 Apr 8.
Early diagnosis of in cattle is a recipe for effective control of heartwater in ruminants. Hence, we assessed the presence of in the blood of cattle and the engorged by nested PCR. The electrophoresed PCR products obtained after primary and secondary amplifications revealed amplicon sizes of about350 bp and 280 bp respectively, which corresponded with the partial region of pSC20 gene amplified. Sequences obtained had 95-99% homology with those sequences available in GenBank. The prevalence of the in ticks (50%; 126/252) was significantly ( < 0.05) higher than that in cattle blood 23.55% (61/259). The prevalence was significantly ( < 0.05) higher in ticks from adult cattle 51.47% (133/259) than those from the young cattle 44.86% (116/259) and in tick from females 54.55% (141/259) than in ticks from the males 41.38% (107/259). Alignment of autochthonous sequences revealed that the three sequences were polymorphic with two sequences showing similar nucleotides deletion at points 87-91 and 107-108. The phylogenetic trees inferred by ML showed topologies with two autochthonous sequences, one each from cattle blood and tick, clustering together in one clade and the other clustering within those sequences from South Africa and Zimbabwe in another clade. In conclusion, this study revealed a higher prevalence of in engorged than in the blood of infected cattle. Hence, it is suggested that the amplification that targets the pCS20 gene in engorged ticks may be more suitable to determine the carrier status of cattle.
牛的早期诊断是有效控制反刍动物心水病的诀窍。因此,我们通过巢式PCR评估牛血液中以及饱血蜱体内该病原体的存在情况。一次和二次扩增后得到的经电泳的PCR产物显示,扩增子大小分别约为350 bp和280 bp,这与扩增的pSC20基因的部分区域相对应。获得的序列与GenBank中可用的序列具有95 - 99%的同源性。蜱体内该病原体的流行率(50%;126/252)显著高于牛血液中的流行率(23.55%;61/259)(P < 0.05)。成年牛身上蜱的流行率(51.47%;133/259)显著高于幼牛身上蜱的流行率(44.86%;116/259)(P < 0.05),雌性牛身上蜱的流行率(54.55%;141/259)高于雄性牛身上蜱的流行率(41.38%;107/259)。本地序列的比对显示,三个序列具有多态性,其中两个序列在第87 - 91位和107 - 108位显示出相似的核苷酸缺失。最大似然法推断的系统发育树显示,拓扑结构中有两个本地序列,一个来自牛血液,一个来自蜱,聚集在一个分支中,另一个聚集在来自南非和津巴布韦的序列所在的另一个分支中。总之,本研究表明饱血蜱体内该病原体的流行率高于感染牛血液中的流行率。因此,建议针对饱血蜱中pCS20基因的扩增可能更适合确定牛的该病原体携带状态。