Durand Jonas, Jacquet Maxime, Paillard Lye, Rais Olivier, Gern Lise, Voordouw Maarten J
Laboratory of Ecology and Evolution of Parasites, Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland
Laboratory of Ecology and Evolution of Parasites, Institute of Biology, University of Neuchâtel, Neuchâtel, Switzerland.
Appl Environ Microbiol. 2015 Nov;81(22):7740-52. doi: 10.1128/AEM.02296-15. Epub 2015 Aug 28.
Many vector-borne pathogens consist of multiple strains that circulate in both the vertebrate host and the arthropod vector. Characterization of the community of pathogen strains in the arthropod vector is therefore important for understanding the epidemiology of mixed vector-borne infections. Borrelia afzelii and B. garinii are two species of tick-borne bacteria that cause Lyme disease in humans. These two sympatric pathogens use the same tick, Ixodes ricinus, but are adapted to different classes of vertebrate hosts. Both Borrelia species consist of multiple strains that are classified using the highly polymorphic ospC gene. Vertebrate cross-immunity against the OspC antigen is predicted to structure the community of multiple-strain Borrelia pathogens. Borrelia isolates were cultured from field-collected I. ricinus ticks over a period spanning 11 years. The Borrelia species of each isolate was identified using a reverse line blot (RLB) assay. Deep sequencing was used to characterize the ospC communities of 190 B. afzelii isolates and 193 B. garinii isolates. Infections with multiple ospC strains were common in ticks, but vertebrate cross-immunity did not influence the strain structure in the tick vector. The pattern of genetic variation at the ospC locus suggested that vertebrate cross-immunity exerts strong selection against intermediately divergent ospC alleles. Deep sequencing found that more than 50% of our isolates contained exotic ospC alleles derived from other Borrelia species. Two alternative explanations for these exotic ospC alleles are cryptic coinfections that were not detected by the RLB assay or horizontal transfer of the ospC gene between Borrelia species.
许多媒介传播的病原体由多种菌株组成,这些菌株在脊椎动物宿主和节肢动物媒介中循环。因此,对节肢动物媒介中病原体菌株群落进行特征描述,对于理解混合媒介传播感染的流行病学至关重要。阿氏疏螺旋体和加氏疏螺旋体是两种蜱传细菌,可导致人类莱姆病。这两种同域分布的病原体利用同一种蜱——蓖麻硬蜱,但适应不同类别的脊椎动物宿主。这两种疏螺旋体都由多种菌株组成,这些菌株通过高度多态的ospC基因进行分类。预计脊椎动物对OspC抗原的交叉免疫会构建多菌株疏螺旋体病原体的群落结构。在11年的时间里,从野外采集的蓖麻硬蜱中培养出疏螺旋体分离株。使用反向线印迹(RLB)分析法鉴定每个分离株的疏螺旋体种类。采用深度测序对190株阿氏疏螺旋体分离株和193株加氏疏螺旋体分离株的ospC群落进行特征描述。蜱中存在多种ospC菌株感染很常见,但脊椎动物交叉免疫并未影响蜱媒介中的菌株结构。ospC基因座的遗传变异模式表明,脊椎动物交叉免疫对中等分化的ospC等位基因施加了强烈的选择压力。深度测序发现,超过50%的分离株含有源自其他疏螺旋体物种的外来ospC等位基因。对于这些外来ospC等位基因,有两种解释:一是RLB分析法未检测到的隐匿性混合感染,二是ospC基因在疏螺旋体物种之间的水平转移。