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原生动物寄生虫(顶复门)在其蚯蚓宿主中的生活史特征的变化和权衡。

Variation and trade-offs in life history traits of the protist parasite (Apicomplexa) in its earthworm host .

机构信息

School of Biological Sciences, Washington State University, Pullman, WA, United States of America.

Department of Biology, University of Vermont, Burlington, VT, United States of America.

出版信息

PeerJ. 2024 Mar 26;12:e17161. doi: 10.7717/peerj.17161. eCollection 2024.

DOI:10.7717/peerj.17161
PMID:38560466
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10979743/
Abstract

The life history of a parasite describes its partitioning of assimilated resources into growth, reproduction, and transmission effort, and its precise timing of developmental events. The life cycle, in contrast, charts the sequence of morphological stages from feeding to the transmission forms. Phenotypic plasticity in life history traits can reveal how parasites confront variable environments within hosts. Within the protist phylum Apicomplexa major clades include the malaria parasites, coccidians, and most diverse, the gregarines (with likely millions of species). Studies on life history variation of gregarines are rare. Therefore, life history traits were examined for the gregarine in its host, the invasive earthworm at three sites in northern Vermont, United States of America. An important value of this system is the short life-span of the hosts, with only seven months from hatching to mass mortality; we were thus able to examine life history variation during the entire life cycle of both host and parasite. Earthworms were collected ( = 968 over 33 sample periods during one host season), then parasites of all life stages were counted, and sexual and transmission stages measured, for each earthworm. All traits varied substantially among individual earthworm hosts and across the sites. Across sites, timing of first appearance of infected earthworms, date when transmission stage (oocysts packed within gametocysts) appeared, date when number of both feeding (trophic) cells and gametocysts were at maximum, and date when 100% of earthworms were infected differed from 2-8 weeks, surprising variation for a short season available for parasite development. The maximal size of mating cells varied among hosts and across sites and this is reflected in the number of oocysts produced by the gametocyst. A negative trade-off was observed for the number of oocysts and their size. Several patterns were striking: (1) Prevalence reached 100% at all sites by mid season, only one to three weeks after parasites first appeared in the earthworms. (2) The number of parasites per host was large, reaching 300 × 10 cells in some hosts, and such high numbers were present even when parasites first appeared in the host. (3) At one site, few infected earthworms produced any oocysts. (4) The transmission rate to reach such high density of parasites in hosts needed to be very high for a microbe, from >0.33% to >34.3% across the three sites. was one of the first protist parasites to have its life cycle described (early 19 century), but these results suggest the long-accepted life cycle of could be incomplete, such that the parasites may be transmitted vertically (within the earthworm's eggs) as well as horizontally (leading to 100% prevalence) and merogony (asexual replication) could be present, not recognized for , leading to high parasitemia even very early in the host's season.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/c325fce661dc/peerj-12-17161-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/b08484862fcd/peerj-12-17161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/133fdbb6ef91/peerj-12-17161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/b108ce39c8e3/peerj-12-17161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/9ca16bf40121/peerj-12-17161-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/c325fce661dc/peerj-12-17161-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/b08484862fcd/peerj-12-17161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/133fdbb6ef91/peerj-12-17161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/b108ce39c8e3/peerj-12-17161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/9ca16bf40121/peerj-12-17161-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e7c/10979743/c325fce661dc/peerj-12-17161-g005.jpg
摘要

寄生虫的生活史描述了其将同化资源分配到生长、繁殖和传播努力中的情况,以及其发育事件的确切时间安排。相比之下,生命周期描绘了从摄食到传播形式的形态阶段的顺序。生活史特征的表型可塑性可以揭示寄生虫如何应对宿主内的可变环境。在原生动物门顶复动物亚门中,主要的类群包括疟原虫、球虫和最多样化的原虫(可能有数百万种)。关于原虫生活史变异的研究很少。因此,在美国佛蒙特州北部的三个地点,对其宿主入侵蚯蚓中的原虫进行了生活史特征研究。该系统的一个重要价值是宿主的生命周期很短,从孵化到大量死亡只有七个月;因此,我们能够在宿主和寄生虫的整个生命周期中研究生活史变异。收集了蚯蚓(在一个宿主季节的 33 个采样期内共收集了 968 条),然后对每条蚯蚓的所有生活阶段的寄生虫进行计数,并测量有性和传播阶段。所有特征在个体蚯蚓宿主之间以及在各个地点之间都有很大差异。在各个地点,感染蚯蚓首次出现的时间、传播阶段(包含配子囊的卵囊)出现的时间、摄食(营养)细胞和配子囊数量达到最大值的时间以及 100%的蚯蚓被感染的时间差异为 2-8 周,对于寄生虫发育的短季节来说,这是惊人的变化。有性细胞的最大尺寸在宿主之间和地点之间存在差异,这反映在配子囊中产生的卵囊数量上。观察到卵囊数量及其大小之间存在负的权衡关系。有几个模式引人注目:(1)在所有地点,寄生虫在蚯蚓中首次出现后一到三周,到季中时,所有地点的患病率都达到了 100%。(2)每个宿主的寄生虫数量很大,在一些宿主中达到 300×10 个细胞,即使在寄生虫首次出现在宿主中时,也存在如此高的数量。(3)在一个地点,很少有感染的蚯蚓产生任何卵囊。(4)为了在宿主中达到如此高的寄生虫密度,微生物的传播率必须非常高,在三个地点的范围从 0.33%到 34.3%。是最早描述其生命周期的原生动物寄生虫之一(19 世纪早期),但这些结果表明,长期以来被接受的生命周期可能不完整,因此寄生虫可能通过垂直传播(在蚯蚓的卵中)以及水平传播(导致 100%的患病率)进行传播,并且可能存在裂殖生殖(无性复制),而这对于原虫来说是未被识别的,导致即使在宿主季节的早期,寄生虫血症也很高。

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