Molecular prevalence and distribution of tick-borne bacterial and protozoan pathogens of sheep and goats in Africa: A systematic review and meta-analysis

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Abstract

Tick-borne pathogens (TBPs) are a major impediment to the health, welfare, and production of small ruminants across the world, including Africa. Comprehensive information about the epidemiology of TBPs infecting sheep and goats across Africa is lacking. Therefore, this study was undertaken to determine the prevalence through a meta-analysis of selected TBPs in blood DNA from domestic sheep and goats in Africa obtained using molecular-based methods. The literature review was done according to Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines using five English electronic databases (PubMed, Science Direct, Springer Link, Web of Science, and African Journals Online (AJOL). The search was performed with no restriction in time through to 18th January 2023. Of the 63 full-text articles subjected to eligibility, only 30 articles met the eligibility criteria and were included in the review. The overall pooled prevalence of selected TBPs varied considerably between host species (sheep vs. goats), with Anaplasma ovis (44.50 vs. 48.40%), Ehrlichia ruminantium (5.50 vs. 2.00%), Coxiella burnetii (4.40 vs. 1.70%), Borrelia theileri in sheep (5.20%), Babesia ovis (1.70% vs. 1.90%), Theileria ovis (40.50% vs 10.00%), T. separata (1.00% vs 1.00%) and T. lestoquardi in sheep (8.40%). However, the prevalence of the selected TBPs was generally higher in sheep compared to goats. Several genetic loci were targeted in the characterization of tick-borne pathogens, such as 16S rDNA, groEL, and msp4 for Anaplasma ovis, pCS20 for Ehrlichia ruminantium, Insertion Sequence (IS1111) for Coxiella burnetii, flaB (flagellin) and 16S rRNA for Borrelia theileri, 5.8S rRNA and 18S rRNA for Babesia/Theileria, as well as the utilization of numerous PCR variants including conventional polymerase chain reaction (PCR), nested-PCR, qPCR, Loop-mediated isothermal amplification (LAMP), and reverse line blotting (RLB). In conclusion, A. ovis was the most widely distributed and prevalent TBP affecting small ruminants within the continent. Hence, this warrants adequate attention towards early diagnosis and treatment of infected animals as well as the control of the tick vectors involved in their transmission.
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非洲绵羊和山羊蜱传细菌和原生动物病原体的分子流行率和分布:系统回顾和荟萃分析
蜱媒病原体(TBPs)是包括非洲在内的世界各地小型反刍动物健康、福利和生产的主要障碍。目前缺乏有关非洲绵羊和山羊感染蜱传病原体流行病学的全面信息。因此,本研究通过对使用分子方法从非洲家养绵羊和山羊血液 DNA 中获得的部分 TBPs 进行荟萃分析,以确定其流行率。文献综述是根据系统综述和荟萃分析首选报告项目(PRISMA)指南,利用五个英文电子数据库(PubMed、Science Direct、Springer Link、Web of Science 和 African Journals Online (AJOL))进行的。检索时间不受限制,直至 2023 年 1 月 18 日。在经过资格审查的 63 篇全文文章中,只有 30 篇符合资格标准,被纳入综述。在不同宿主物种(绵羊与山羊)之间,所选 TBPs 的总体汇总流行率差异很大,其中猫鼬疟原虫(44.50% vs. 48.40%)、反刍埃希氏菌(5.50% vs. 2.00%)、烧伤柯西氏菌(4.40 vs. 1.70%)、绵羊 Theileri 波氏杆菌(5.20%)、绵羊巴贝斯虫(1.70% vs. 1.90%)、绵羊 Theileria ovis(40.50% vs. 10.00%)、绵羊 T. separata(1.00% vs. 1.00%)和绵羊 T. lestoquardi(8.40%)。然而,与山羊相比,所选 TBPs 在绵羊中的流行率普遍较高。在确定蜱传病原体的特征时,有几个基因位点是目标位点,如猫疽的 16S rDNA、groEL 和 msp4,反刍埃希氏菌的 pCS20,烧伤克氏菌的插入序列 (IS1111),包柔氏疟原虫的 flaB(鞭毛蛋白)和 16S rRNA,绵羊的 5.8S rRNA 和 18S rRNA。此外,还使用了多种 PCR 方法,包括传统聚合酶链反应(PCR)、巢式 PCR、qPCR、环介导等温扩增(LAMP)和反向印迹法(RLB)。总之,羱羊是非洲大陆分布最广、影响小反刍动物最普遍的 TBP。因此,有必要对受感染动物的早期诊断和治疗给予足够重视,并对参与传播的蜱媒进行控制。
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