首页> 外文期刊>Veterinary Parasitology >Molecular detection of Babesia bovis and Babesia bigemina in white-tailed deer (Odocoileus virginianus) from Tom Green County in central Texas
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Molecular detection of Babesia bovis and Babesia bigemina in white-tailed deer (Odocoileus virginianus) from Tom Green County in central Texas

机译:得克萨斯州中部汤姆格林县白尾鹿(Odocoileus virginianus)中牛巴贝斯虫和大巴贝斯虫的分子检测

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摘要

Serologic and molecular evidence suggest that white-tailed deer in South Texas and North Mexico carry the agents of bovine babesiosis, Babesia bovis and Babesia bigemina. To determine if white-tailed deer in central Texas, which is outside the known occurrence of the vector tick at this time, harbor these parasites, blood samples from free-ranging and captive white-tailed deer (Odocoileus virginianus) in Tom Green County were tested by polymerase chain reaction (PCR) assays for B. bovis and B. bigemina 18S rDNA. Of the 25 samples tested, three (12%)were positive by nested PCR for B. bovis. This identity was confirmed by sequence analysis of the cloned 18S rDNA PCR product. Further confirmation was made by sequence analysis of the rRNA internal transcribed spacer (ITS) 1, 5.85 rRNA gene, and ITS 2 genomic region in two (representing samples from two different ranches) of the B. bovis positive samples. Three samples were positive by B. bigemina nested PCR, but sequencing of the cloned products confirmed only one animal positive for B. bigemina; Theileria spp. DNA was amplified from the other two animal samples. In addition to Theileria spp., two genotypically unique Babesia species sequences were identified among the cloned sequences produced by the B. bigemina primers in one sample. Phylogenetic analysis showed no separation of the deer B. bovis or B. bigemina 18S rDNA, or deer B. bovis ITS region sequences from those of bovine origin. Clarification of the possible role of white-tailed deer as reservoir hosts in maintaining these important pathogens of cattle is critical to understanding whether or not deer contribute to the epidemiology of bovine babesiosis
机译:血清学和分子学证据表明,南德克萨斯州和北墨西哥的白尾鹿携带了牛巴贝虫病,牛巴贝斯虫和大巴贝斯虫的病原体。为了确定是否在德克萨斯州中部的白尾鹿(目前不在矢量壁虱的发生范围内),藏有这些寄生虫,汤姆格林县散养的圈养白尾鹿(Odocoileus virginianus)的血样牛双歧杆菌和双歧双歧杆菌18S rDNA的聚合酶链反应(PCR)分析测试。在测试的25个样品中,有3个(12%)的牛肝菌通过巢式PCR呈阳性。通过克隆的18S rDNA PCR产物的序列分析证实了这一身份。通过对牛双歧杆菌阳性样品的两个(代表两个不同牧场的样品)rRNA内部转录间隔区(ITS)1、5.85 rRNA基因和ITS 2基因组区域进行序列分析,进一步证实了这一点。通过双歧双歧杆菌巢式PCR,三份样品均为阳性,但是对克隆产物的测序证实只有一只动物对双歧双歧杆菌呈阳性。泰勒虫属从另外两个动物样品中扩增DNA。除了Theileria spp。,在一个样品中,由双歧双歧杆菌引物产生的克隆序列中还鉴定了两个基因型独特的巴贝虫物种序列。系统发育分析表明,没有将牛双歧杆菌或双歧双歧杆菌18S rDNA或牛双歧杆菌ITS区序列与牛起源区分开。弄清白尾鹿作为水库宿主在维持牛这些重要病原体中的可能作用,对于了解鹿是否对牛杆状杆菌病的流行病学至关重要。

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