Department of Parasitology, College of Veterinary Medicine, Firat University, 23119, Elazig, Turkey.
Department of Parasitology, College of Veterinary Medicine, Firat University, 23119, Elazig, Turkey.
Vet Microbiol. 2018 Apr;217:13-17. doi: 10.1016/j.vetmic.2018.02.026. Epub 2018 Feb 24.
Anaplasma ovis is a widely distributed tick-borne rickettsial pathogen of sheep, goats, and wild ruminants. The aims of this study were to assess the prevalence, associations of Anaplasma ovis in sheep and goats, as well as its genetic diversity based on analysis of the msp1α gene. A total of 416 DNA samples from sheep (n = 236) and goats (n = 180) from four provinces in southeastern Turkey were analyzed by PCR. The overall A. ovis prevalence was 18% (CI 14.4-22.1). The infection rates of A. ovis varied from 15.9% to 21.8% in sampled provinces, and they were not significantly different. There was no difference between Anaplasma ovis infection in sheep (20.3%, CI 15.4-26.0) and goats (15.0%, CI 10.1-21.1) or in infection rate of animals <1 year (21.8%, CI 14.9-30.1) compared to >1 year (16.4%, CI 12.4-21.2). A significant association between A. ovis infection and the presence of Rhipicephalus bursa and Rhipicephalus turanicus was observed (P < 0.05). Prevalence of A. ovis-positive animals was higher in animals showing co-infection with Babesia and Theileria compared to those not co-infected (P < 0.05). The Msp1a amino acid repeats were identified and used for the characterization of A. ovis strains. Forty partial msp1a gene sequences containing the repeated sequences of A. ovis were obtained, and 14 previously undescribed tandem repeats with 33 to 43 amino acids were found. Thirteen A. ovis genotypes were identified based on the structure of Msp1a tandem repeats. The majority of A. ovis isolates exhibited one Msp1a tandem repeat, with a maximum of three. This study revealed the Msp1a could be used as a marker for genotyping A. ovis, and high genetic diversity of A. ovis were found in small ruminants in Turkey.
绵羊无浆体病是一种广泛分布的蜱传立克次氏体病原体,可感染绵羊、山羊和野生反刍动物。本研究旨在评估绵羊和山羊中绵羊无浆体病的流行情况、关联以及基于 msp1α 基因分析的遗传多样性。对来自土耳其东南部四个省份的 416 份绵羊(n=236)和山羊(n=180)的 DNA 样本进行了 PCR 分析。绵羊无浆体病的总感染率为 18%(置信区间 14.4-22.1)。采样省份的绵羊无浆体病感染率从 15.9%到 21.8%不等,但无显著差异。绵羊(20.3%,置信区间 15.4-26.0)和山羊(15.0%,置信区间 10.1-21.1)以及<1 岁(21.8%,置信区间 14.9-30.1)与>1 岁(16.4%,置信区间 12.4-21.2)动物之间的无浆体病感染率无差异。绵羊无浆体病感染与硬蜱和土耳其斯坦璃眼蜱的存在之间存在显著关联(P<0.05)。与未合并感染的动物相比,同时感染巴贝斯虫和泰勒虫的动物中,绵羊无浆体病阳性动物的比例更高(P<0.05)。鉴定了 Msp1a 氨基酸重复序列,并用于鉴定绵羊无浆体病株。获得了包含绵羊无浆体病重复序列的 40 个部分 msp1a 基因序列,发现了 14 个以前未描述的含有 33 到 43 个氨基酸的串联重复。根据 Msp1a 串联重复结构,鉴定了 13 种绵羊无浆体病基因型。大多数绵羊无浆体病分离株显示一个 Msp1a 串联重复,最多有三个。本研究表明 Msp1a 可作为绵羊无浆体病基因分型的标记,并且在土耳其的小反刍动物中发现了绵羊无浆体病的高遗传多样性。