Multi-strain compatibility polymorphism between a parasite and its snail host, a neglected vector of schistosomiasis in Africa

IF 1.7 Q3 PARASITOLOGY
Johannie M. Spaan , Tom Pennance , Martina R. Laidemitt , Nicole Sims , Jewell Roth , Yvonne Lam , Fredrick Rawago , George Ogara , Eric S. Loker , Maurice R. Odiere , Michelle L. Steinauer
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Abstract

Interactions between Schistosoma mansoni and its snail host are understood primarily through experimental work with one South American vector species, Biomphalaria glabrata. However, 90% of schistosomiasis transmission occurs in Africa, where a diversity of Biomphalaria species may serve as vectors. With the long-term goal of determining the genetic and ecological determinants of infection in African snail hosts, we developed genetic models of Biomphalaria sudanica, a principal vector in the African Great Lakes. We determined laboratory infection dynamics of two S. mansoni lines in four B. sudanica lines. We measured the effects of the following variables on infection success and the number of cercariae produced (infection intensity): (i) the combination of parasite and snail line; (ii) the dose of parasites; and (iii) the size of snail at time of exposure. We found one snail line to be almost completely incompatible with both parasite lines, while other snail lines showed a polymorphism in compatibility: compatible with one parasite line while incompatible with another. Interestingly, these patterns were opposite in some of the snail lines. The parasite-snail combination had no significant effect on the number of cercariae produced in a successful infection. Miracidia dose had a strong effect on infection status, in that higher doses led to a greater proportion of infected snails, but had no effect on infection intensity. In one of the snail-schistosome combinations, snail size at the time of exposure affected both infection status and cercarial production in that the smallest size class of snails (1.5–2.9 mm) had the highest infection rates, and produced the greatest number of cercariae, suggesting that immunity increases with age and development. The strongest predictor of the infection intensity was the size of snail at the time of shedding: 1 ​mm of snail growth equated to a 19% increase in cercarial production. These results strongly suggest that infection status is determined in part by the interaction between snail and schistosome genetic lines, consistent with a gene-for-gene or matching allele model. This foundational work provides rationale for determining the genetic interactions between African snails and schistosomes, which may be applied to control strategies.

Abstract Image

非洲血吸虫病的一种被忽视的媒介——寄生虫与其蜗牛宿主之间的多株相容性多态性
曼氏血吸虫与其蜗牛宿主之间的相互作用主要是通过对一种南美媒介物种——光滑生物phalaria glabrata的实验工作来了解的。然而,90%的血吸虫病传播发生在非洲,那里的多种生物phalaria物种可能是传播媒介。为了确定非洲蜗牛宿主感染的遗传和生态决定因素这一长期目标,我们开发了非洲五大湖主要媒介苏丹虫的遗传模型。我们测定了两个曼氏S.mansoni品系和四个苏丹B.sudanica品系的实验室感染动态。我们测量了以下变量对感染成功率和产生尾蚴数量(感染强度)的影响:(i)寄生虫和蜗牛系的组合;(ii)寄生虫的剂量;以及(iii)暴露时蜗牛的大小。我们发现一个蜗牛系与两个寄生虫系几乎完全不相容,而其他蜗牛系在相容性方面表现出多态性:与一个寄生虫系相容,而与另一个不相容。有趣的是,这些模式在一些蜗牛线上是相反的。寄生虫-蜗牛组合对成功感染时产生的尾蚴数量没有显著影响。Miracidia剂量对感染状态有很大影响,因为更高的剂量会导致更大比例的蜗牛感染,但对感染强度没有影响。在一种蜗牛-血吸虫组合中,暴露时的蜗牛大小影响感染状态和尾蚴的产生,因为最小大小的蜗牛类(1.5–2.9毫米)感染率最高,产生的尾蚴数量最多,这表明免疫力随着年龄和发育而增加。感染强度的最强预测因子是脱落时蜗牛的大小:1​蜗牛生长的毫米相当于尾蚴产量增加了19%。这些结果有力地表明,感染状态在一定程度上是由蜗牛和血吸虫遗传系之间的相互作用决定的,这与基因对基因或匹配等位基因模型一致。这项基础性工作为确定非洲蜗牛和血吸虫之间的基因相互作用提供了理论依据,可用于控制策略。
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CiteScore
3.60
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