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Coinfection with Antigenically and Genetically Distinct Virulent Strains of Babesia bovis Is Maintained through All Phases of the Parasite Life Cycle

机译:在寄生虫生命周期的所有阶段都维持与牛和牛的抗原性和遗传性不同的毒株的共感染

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摘要

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.
机译:抗原多态性是牛肝杆菌可变裂殖子表面抗原(VMSA)家族的定义特征。序列分析强烈表明,毒株之间的重组有助于VMSA多样性。尽管the矢量Rhipicephalus(Boophilus)microplus在寄生虫生命周期的非整倍体阶段减数分裂是菌株间重组的最可能来源,但没有确凿的证据表明哺乳动物宿主或R. microplus coin的共感染具有一种以上的毒性。发生应变。使用等位基因特异性实时定量PCR,我们测试了牛可以支持牛分枝杆菌的两个抗原性变异毒力tick传播的菌株的共感染,而微小牛R可以捕获和传播这两个不同株的假说。结果表明,犊牛和tick虫都可以在血液寄生虫生命周期的所有阶段都支持强力牛双歧杆菌的合并感染。两种菌株都不能在哺乳动物或无脊椎动物宿主中占主导地位,而且可以单独感染的幼虫tick子后代也不能传播两种菌株,从而在受体中导致强毒性贝贝病。虽然滴答载体的共转染提供了可产生等位基因抗原多样性的背景,但无法确认VMSA基因的重组,这表明VMSA等位基因变化的积累较慢。

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