Jacquet Maxime, Durand Jonas, Rais Olivier, 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.
Infect Genet Evol. 2015 Dec;36:131-140. doi: 10.1016/j.meegid.2015.09.012. Epub 2015 Sep 16.
Cross-reactive acquired immunity in the vertebrate host induces indirect competition between strains of a given pathogen species and is critical for understanding the ecology of mixed infections. In vector-borne diseases, cross-reactive antibodies can reduce pathogen transmission at the vector-to-host and the host-to-vector lifecycle transition. The highly polymorphic, immunodominant, outer surface protein C (OspC) of the tick-borne spirochete bacterium Borrelia afzelii induces a strong antibody response in the vertebrate host. To test how cross-immunity in the vertebrate host influences tick-to-host and host-to-tick transmission, mice were immunized with one of two strain-specific recombinant OspC proteins (A3, A10), challenged via tick bite with one of the two B. afzelii ospC strains (A3, A10), and infested with xenodiagnostic ticks. Immunization with a given rOspC antigen protected mice against homologous strains carrying the same major ospC group allele but provided little or no cross-protection against heterologous strains carrying a different major ospC group allele. There were cross-immunity effects on the tick spirochete load but not on the probability of host-to-tick transmission. The spirochete load in ticks that had fed on mice with cross-immune experience was reduced by a factor of two compared to ticks that had fed on naive control mice. In addition, strain-specific differences in mouse spirochete load, host-to-tick transmission, tick spirochete load, and the OspC-specific IgG response revealed the mechanisms that determine variation in transmission success between strains of B. afzelii. This study shows that cross-immunity in infected vertebrate hosts can reduce pathogen load in the arthropod vector with potential consequences for vector-to-host pathogen transmission.
脊椎动物宿主中的交叉反应性获得性免疫会引发特定病原体物种不同菌株之间的间接竞争,对于理解混合感染的生态学至关重要。在媒介传播疾病中,交叉反应性抗体可在病原体从媒介到宿主以及从宿主到媒介的生命周期转换过程中减少病原体传播。蜱传螺旋体伯氏疏螺旋体高度多态、具有免疫显性的外膜蛋白C(OspC)可在脊椎动物宿主中诱导强烈的抗体反应。为了测试脊椎动物宿主中的交叉免疫如何影响蜱到宿主以及宿主到蜱的传播,用两种菌株特异性重组OspC蛋白(A3、A10)之一对小鼠进行免疫,通过蜱叮咬用两种伯氏疏螺旋体ospC菌株(A3、A10)之一对小鼠进行攻击,并让其感染异体诊断蜱。用特定的重组OspC抗原进行免疫可保护小鼠免受携带相同主要ospC组等位基因的同源菌株感染,但对携带不同主要ospC组等位基因的异源菌株几乎没有交叉保护作用。交叉免疫对蜱内螺旋体载量有影响,但对宿主到蜱的传播概率没有影响。与以未免疫对照小鼠为食的蜱相比,以具有交叉免疫经验的小鼠为食的蜱内螺旋体载量降低了一半。此外,小鼠螺旋体载量、宿主到蜱的传播、蜱内螺旋体载量以及OspC特异性IgG反应中的菌株特异性差异揭示了决定伯氏疏螺旋体不同菌株传播成功率差异的机制。这项研究表明,受感染脊椎动物宿主中的交叉免疫可降低节肢动物媒介中的病原体载量,这可能会对病原体从媒介到宿主的传播产生影响。