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疟原虫节律性复制可塑性的表型及适应性后果

Phenotypic and fitness consequences of plasticity in the rhythmic replication of malaria parasites.

作者信息

Holland Jacob G, O'Donnell Aidan J, Herbert-Mainero Alejandra, Reece Sarah E

机构信息

Institute of Ecology and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.

Eccles Institute of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2025 Jan 23;380(1918):20230340. doi: 10.1098/rstb.2023.0340.

DOI:10.1098/rstb.2023.0340
PMID:39842485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11753878/
Abstract

The environments that parasites experience within hosts change dramatically over 24 h. How rhythms shape host-parasite-vector interactions is poorly understood owing to the challenges of disentangling the roles of rhythms of multiple interacting species in the context of the complex lifecycles of parasites. Using canonical circadian clock-disrupted hosts, we probe the limits of flexibility in the rhythmic replication of malaria () parasites and quantify the consequences for fitness proxies of both parasite and host. We reveal that parasites alter the duration of their replication rhythm to resonate with host rhythms that have short (21 h) daily T-cycles as accurately as when infecting hosts with 24 h cycles, but appear less capable of extending their replication rhythm in hosts with long (27 h) cycles. Despite matching the period of short T-cycle hosts, parasites are unable to lock to the correct phase, likely leading to lower within-host productivity and a reduction in transmission potential. However, parasites in long T-cycle hosts do not experience substantial fitness costs. Furthermore, T-cycle duration does not affect disease severity in clock-disrupted hosts. Understanding the rhythmic replication of malaria parasites offers the opportunity to interfere with parasite timing to improve health and reduce transmission.This article is part of the Theo Murphy meeting issue issue 'Circadian rhythms in infection and immunity'.

摘要

寄生虫在宿主体内所经历的环境在24小时内会发生巨大变化。由于在寄生虫复杂的生命周期背景下,难以厘清多个相互作用物种的节律作用,因此对于节律如何塑造宿主 - 寄生虫 - 媒介相互作用的了解甚少。我们使用典型的生物钟紊乱宿主,探究疟原虫节律性复制的灵活性极限,并量化对寄生虫和宿主适应性指标的影响。我们发现,寄生虫会改变其复制节律的时长,以便与每日T周期较短(21小时)的宿主节律同步,其精确程度与感染T周期为24小时的宿主时相同,但在T周期较长(27小时)的宿主中,寄生虫似乎不太能够延长其复制节律。尽管与短T周期宿主的周期相匹配,但寄生虫无法锁定到正确的相位,这可能导致宿主体内的繁殖力降低以及传播潜力下降。然而,长T周期宿主中的寄生虫并未经历显著的适应性代价。此外,T周期时长并不影响生物钟紊乱宿主的疾病严重程度。了解疟原虫的节律性复制为干预寄生虫的时间节律以改善健康状况和减少传播提供了机会。本文是西奥·墨菲会议议题“感染与免疫中的昼夜节律”的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/c071ce37a934/rstb.2023.0340.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/9f5e50a2b680/rstb.2023.0340.f001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/073b6edc3722/rstb.2023.0340.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/c071ce37a934/rstb.2023.0340.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/9f5e50a2b680/rstb.2023.0340.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/2cc8f7c225d6/rstb.2023.0340.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/6416a3015d92/rstb.2023.0340.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/073b6edc3722/rstb.2023.0340.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/245b/11753878/c071ce37a934/rstb.2023.0340.f005.jpg

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F1000Res. 2022 Nov 15;11:1323. doi: 10.12688/f1000research.127234.2. eCollection 2022.
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Diurnal biting of malaria mosquitoes in the Central African Republic indicates residual transmission may be "out of control".
中非共和国的疟疾蚊的日间叮咬表明,残留传播可能“失控”。
Proc Natl Acad Sci U S A. 2022 May 24;119(21):e2104282119. doi: 10.1073/pnas.2104282119. Epub 2022 May 16.
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Mistimed malaria parasites re-synchronize with host feeding-fasting rhythms by shortening the duration of intra-erythrocytic development.时机不当的疟原虫通过缩短红内期发育时间与宿主的摄食-禁食节律重新同步。
Parasite Immunol. 2022 Mar;44(3):e12898. doi: 10.1111/pim.12898. Epub 2021 Nov 22.
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The private life of malaria parasites: Strategies for sexual reproduction.疟原虫的私生活:有性生殖策略。
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