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So close and yet so far – Molecular Microbiology ofCampylobacter fetus subspecies

机译:如此遥远却又如此遥远–分子生物学弯曲杆菌胎儿亚种

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摘要

Campylobacter fetus comprises two subspecies, C. fetus subsp. fetus and C. fetus subsp. venerealis, which are considered emerging pathogens in humans and animals. Comparisons at the genome level have revealed modest subspecies-specific variation; nevertheless, these two subspecies show distinct host and niche preferences. C. fetus subsp. fetus is a commensal and pathogen of domesticated animals that can be transmitted to humans via contaminated food. The clinical features of human infection can be severe, especially in impaired hosts. In contrast, C. fetus subsp. venerealis is a sexually transmitted pathogen essentially restricted to cattle. Infections leading to bovine venereal campylobacteriosis cause substantial economic losses due to abortion and infertility. Recent genome sequencing of the two subspecies has advanced our understanding of C. fetus adaptations through comparative genomics and the identification of subspecies-specific gene regions predicted to be involved in pathogenesis. The most striking difference between the subspecies is the highly subspecies-specific association of a pathogenicityisland in the C. fetus subsp. venerealischromosome. The inserted region encodes a Type 4 secretion system, whichcontributes to virulence properties of this organism in vitro.This review describes the main differences in epidemiological, phenotypic, andmolecular characteristics of the two subspecies and summarizes recent advancestowards understanding the molecular mechanisms of C. fetuspathogenesis.
机译:胎儿弯曲杆菌包括两个亚种,即胎儿弯曲杆菌亚种。胎儿和C.胎儿亚种委内瑞拉,被认为是人和动物中新兴的病原体。在基因组水平上的比较揭示了适度的亚种特异性变异。然而,这两个亚种显示出不同的寄主和利基偏好。 C.胎儿亚种胎儿是家养动物的常见病原体,可以通过被污染的食物传播给人类。人类感染的临床特征可能很严重,尤其是在受损宿主中。相反,C。胎儿亚种。委内瑞拉是一种性传播病原体,基本上只限于牛。导致牛性病性弯曲杆菌病的感染由于流产和不育而造成重大的经济损失。这两个亚种的最新基因组测序已通过比较基因组学和鉴定预计与发病有关的亚种特异基因区域,进一步提高了我们对C.胎儿适应性的了解。亚种之间最显着的差异是致病性与亚种高度相关C.胎儿亚种中的小岛。委内瑞拉人染色体。插入的区域编码4型分泌系统,该系统有助于这种生物体外的毒性特性。这篇综述描述了流行病学,表型和这两个亚种的分子特征并总结了最新进展理解胎儿梭状芽胞杆菌的分子机制发病。

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