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检测和多样性的一个假定的新的异构多态脯氨酸-甘氨酸重复(PGR)蛋白在蹄疫病原体Dichelobacter nodosus。

Detection and diversity of a putative novel heterogeneous polymorphic proline-glycine repeat (Pgr) protein in the footrot pathogen Dichelobacter nodosus.

机构信息

Department of Biological Sciences, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK.

出版信息

Vet Microbiol. 2011 Jan 27;147(3-4):358-66. doi: 10.1016/j.vetmic.2010.06.024. Epub 2010 Jul 3.

DOI:10.1016/j.vetmic.2010.06.024
PMID:20655152
Abstract

Dichelobacter nodosus, a Gram-negative anaerobic bacterium, is the essential causative agent of footrot in sheep. Currently, depending on the clinical presentation in the field, footrot is described as benign or virulent; D. nodosus strains have also been classified as benign or virulent, but this designation is not always consistent with clinical disease. The aim of this study was to determine the diversity of the pgr gene, which encodes a putative proline-glycine repeat protein (Pgr). The pgr gene was present in all 100 isolates of D. nodosus that were examined and, based on sequence analysis had two variants, pgrA and pgrB. In pgrA, there were two coding tandem repeat regions, R1 and R2: different strains had variable numbers of repeats within these regions. The R1 and R2 were absent from pgrB. Both variants were present in strains from Australia, Sweden and the UK, however, only pgrB was detected in isolates from Western Australia. The pgrA gene was detected in D. nodosus from tissue samples from two flocks in the UK with virulent footrot and only pgrB from a flock with no virulent or benign footrot for >10 years. Bioinformatic analysis of the putative PgrA protein indicated that it contained a collagen-like cell surface anchor motif. These results suggest that the pgr gene may be a useful molecular marker for epidemiological studies.

摘要

无乳链球菌是一种革兰氏阴性厌氧菌,是绵羊腐蹄病的主要病原体。目前,根据田间的临床表现,腐蹄病被描述为良性或恶性;无乳链球菌菌株也被分为良性或恶性,但这种命名并不总是与临床疾病一致。本研究旨在确定 pgr 基因的多样性,该基因编码一种假定的脯氨酸-甘氨酸重复蛋白(Pgr)。在检查的 100 株无乳链球菌中均存在 pgr 基因,基于序列分析有两种变体,pgrA 和 pgrB。在 pgrA 中,有两个编码串联重复区 R1 和 R2:不同菌株在这些区域内的重复数不同。R1 和 R2 不存在于 pgrB 中。两种变体均存在于来自澳大利亚、瑞典和英国的菌株中,但仅在来自西澳大利亚的分离株中检测到 pgrB。pgrA 基因在来自英国两个具有恶性腐蹄病的羊群的组织样本中被检测到,而在一个没有恶性或良性腐蹄病超过 10 年的羊群中仅检测到 pgrB。对假定的 PgrA 蛋白的生物信息学分析表明,它含有胶原样细胞表面锚定基序。这些结果表明,pgr 基因可能是流行病学研究的有用分子标记。

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