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与抗原性和基因上不同的有毒力牛巴贝斯虫菌株的混合感染在寄生虫生命周期的所有阶段都持续存在。

Coinfection with antigenically and genetically distinct virulent strains of Babesia bovis is maintained through all phases of the parasite life cycle.

作者信息

Berens Shawn J, Brayton Kelly A, McElwain Terry F

机构信息

Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA 99164-7040, USA.

出版信息

Infect Immun. 2007 Dec;75(12):5769-76. doi: 10.1128/IAI.00802-07. Epub 2007 Sep 24.

Abstract

Antigenic polymorphism is a defining characteristic of the Babesia bovis variable merozoite surface antigen (VMSA) family. Sequence analysis strongly suggests that recombination between virulent strains contributes to VMSA diversity. While meiosis during the aneuploid stage of the parasite's life cycle in the tick vector Rhipicephalus (Boophilus) microplus is the most probable source of interstrain recombination, there is no definitive evidence that coinfection of the mammalian host or R. microplus ticks with more than one virulent strain occurs. Using allele-specific real-time quantitative PCR, we tested the hypotheses that cattle could support coinfection of two antigenically variant virulent tick-transmissible strains of B. bovis and that R. microplus ticks could acquire and transmit these two divergent strains. The results indicate that both calves and ticks can support virulent B. bovis coinfection through all phases of the hemoparasite's life cycle. Neither strain dominated in either the mammalian or invertebrate host, and larval tick progeny, which could be coinfected individually, were also able to transmit both strains, resulting in virulent babesiosis in recipients. While coinfection of the tick vector provides the context in which allelic antigenic diversity can be generated, recombination of VMSA genes could not be confirmed, suggesting that VMSA allelic changes are slow to accumulate.

摘要

抗原多态性是牛巴贝斯虫可变裂殖子表面抗原(VMSA)家族的一个决定性特征。序列分析有力地表明,强毒株之间的重组促成了VMSA的多样性。虽然在微小扇头蜱(Rhipicephalus (Boophilus) microplus)作为蜱传播媒介的寄生虫生命周期的非整倍体阶段进行减数分裂是菌株间重组最可能的来源,但尚无确凿证据表明哺乳动物宿主或微小扇头蜱会同时感染一种以上的强毒株。我们使用等位基因特异性实时定量PCR,检验了以下假设:牛能够支持两种抗原性不同的牛巴贝斯虫强毒株的蜱传播性感染,微小扇头蜱能够获取并传播这两种不同的菌株。结果表明,犊牛和蜱在血液寄生虫生命周期的各个阶段都能支持牛巴贝斯虫强毒株的混合感染。在哺乳动物宿主或无脊椎动物宿主中,两种菌株都不占优势,单个混合感染的蜱幼虫后代也能够传播这两种菌株,从而在受体中导致强毒性巴贝斯虫病。虽然蜱传播媒介的混合感染为等位基因抗原多样性的产生提供了背景,但无法确认VMSA基因的重组,这表明VMSA等位基因的变化积累缓慢。

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