两栖类寄生虫表现出与时空环境和寄主群落变化的特殊关系。

IF 1 4区 医学 Q4 PARASITOLOGY
Kyle D Gustafson, Vasyl V Tkach, Robert A Newman
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引用次数: 0

摘要

为什么寄生虫会发生在特定地点的特定宿主身上,这是生态和进化寄生虫学家长期以来的一个问题。相遇和兼容性过滤器总结了宿主和寄生虫在接触后发生物理相互作用并建立感染的可能性。相遇过滤器和相容性过滤器不是固定的,在多个地点中,促成过滤器的非生物环境特征和生物群落组成往往在空间和时间上发生变化。非生物变异可能直接影响宿主或寄生虫,特别是具有一个或多个自由生活阶段的寄生虫,而当地生物群落可能会稀释或放大寄生虫的传播。与直接传播的寄生虫不同,复杂生命周期寄生虫使用多个宿主,因此我们假设其生命周期极易受到时空环境变化的影响。我们模拟了后变质林蛙(Rana [Lithobates] sylvatica)和北豹蛙(Rana pipiens)内生蠕虫感染概率与湿地特征、景观组成和当地群落内的anuran物种之间的关系。寄生虫包括以两栖动物为最终宿主(Haematoloechus spp., Glypthelmins quieta .)或中间宿主(Alaria sp., Neodiplostomum sp., echinostomatids和Lechriorchis)的复杂生命周期吸虫和具有直接或间接生命周期的线虫(Cosmocercoides和oswaldocruziia)。虽然我们的研究结果表明,具有复杂和直接生命周期的寄生虫的分布与环境的一些非生物和生物特征相关,但没有普遍的趋势。每种寄生虫的分布与湿地、景观和两栖动物群落变量有其独特的关系,并且大多数物种的总体可预测性较低。一个景观特征——在两栖动物捕获地点附近的湿地数量——通常被包括在豹蛙的顶级模型中,并且可能与最终宿主(如两栖动物、哺乳动物和鸟类)和中间宿主(如蜗牛和齿形动物)如何使用景观有关。任何特定地点的两栖动物群落通常也会影响感染概率,因此其他物种的本地存在往往会降低采样青蛙的感染概率,从而支持景观层面的稀释效应。我们的研究强调,在研究任何给定组成群落的寄生虫流行时,需要考虑时空采样、环境变化和宿主-群落变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AMPHIBIAN PARASITES EXHIBIT IDIOSYNCRATIC RELATIONSHIPS WITH SPATIOTEMPORAL ENVIRONMENTAL AND HOST-COMMUNITY VARIATION.

Why parasites occur in certain hosts in certain locations has been a long-standing question among ecological and evolutionary parasitologists. Encounter and compatibility filters summarize the likelihood that a host and parasite will physically interact and establish an infection upon contact. Encounter and compatibility filters are not fixed and, among multiple locations, the abiotic environmental characteristics and biotic community composition that contribute to the filters often vary spatially and temporally. Abiotic variation may directly affect hosts or parasites-particularly parasites with 1 or more free-living stages-whereas the local biotic community may dilute or amplify parasite transmission. Unlike directly transmitted parasites, complex-life cycle parasites use multiple hosts, thus having life cycles that, we hypothesize, are highly susceptible to the effects of spatiotemporal environmental variation. We modeled infection probability relationships of endohelminths from post-metamorphic wood frogs (Rana [Lithobates] sylvatica) and northern leopard frogs (Rana pipiens) with wetland characteristics, landscape composition, and the anuran species within the local community. Parasites included complex-life cycle trematodes that use amphibians as definitive hosts (Haematoloechus spp., Glypthelmins quieta) or as intermediate hosts (Alaria sp., Neodiplostomum sp., echinostomatids, and Lechriorchis) and nematodes with direct or indirect life cycles (Cosmocercoides and Oswaldocruzia). Although our results demonstrate that distributions of parasites with complex and direct life cycles are correlated with some abiotic and biotic characteristics of the environment, there were few general trends. Each parasite's distribution had its own unique relationship with wetland, landscape, and amphibian-community variables, and there was overall low predictability for most species. One landscape feature-the number of wetlands within the vicinity of the site of amphibian capture-was commonly included in top models for leopard frogs and could be associated with how definitive hosts (e.g., amphibians, mammals, and birds) and intermediate hosts (e.g., snails and odonates) use the landscape. The amphibian community at any given site also commonly affected infection probabilities, such that the local presence of other species tended to reduce infection probabilities in sampled frogs, lending support to the dilution effect at the landscape level. Our research highlights the need to consider spatiotemporal sampling, environmental variation, and host-community variation when studying parasite prevalence in any given component community.

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来源期刊
Journal of Parasitology
Journal of Parasitology 医学-寄生虫学
CiteScore
2.10
自引率
7.70%
发文量
60
审稿时长
2 months
期刊介绍: The Journal of Parasitology is the official peer-reviewed journal of the American Society of Parasitologists (ASP). The journal publishes original research covering helminths, protozoa, and other parasitic organisms and serves scientific professionals in microbiology, immunology, veterinary science, pathology, and public health. Journal content includes original research articles, brief research notes, announcements of the Society, and book reviews. Articles are subdivided by topic for ease of reference and range from behavior and pathogenesis to systematics and epidemiology. The journal is published continuously online with one full volume printed at the end of each year.
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