边缘疟原虫和类柯西氏杆菌内生体在小蹄甲鱼本体发育过程中的不同嵌套模式

IF 6.1 1区 生物学 Q1 MICROBIOLOGY
Lianet Abuin-Denis , Elianne Piloto-Sardiñas , Apolline Maitre , Alejandra Wu-Chuang , Lourdes Mateos-Hernández , Patrícia Gonzaga Paulino , Yamil Bello , Frank Ledesma Bravo , Anays Alvarez Gutierrez , Rafmary Rodríguez Fernández , Alier Fuentes Castillo , Luis Méndez Mellor , Angélique Foucault-Simonin , Dasiel Obregon , Mario Pablo Estrada-García , Alina Rodríguez-Mallon , Alejandro Cabezas-Cruz
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引用次数: 0

摘要

了解节肢动物媒介微生物组中错综复杂的生态相互作用对于阐明疾病传播动态和制定有效的控制策略至关重要。在这项研究中,我们调查了类柯西氏杆菌内生体(CLE)和边疟原虫在小蹄甲虫幼虫、若虫和成虫阶段的生态作用。我们假设 CLE 会呈现出一种稳定的嵌套模式,反映出与蜱宿主的共同进化,而边缘疟原虫则会呈现出一种受环境因素和宿主免疫反应影响的更加动态的非嵌套模式。我们的研究结果表明,在蜱的所有发育阶段,CLE 都表现出稳定的嵌套模式,这是共同进化的互惠关系的特征。与此相反,A. marginale 的发生率变化不定,但对微生物群落结构有显著影响,这对我们最初关于其非嵌套动态的假设提出了挑战。此外,从共生网络中移除这两种微生物会改变网络拓扑结构,从而强调它们在 R. microplus 微生物群中的核心作用。值得注意的是,在若虫网络中观察到了 CLE 和 A. marginale 之间的竞争性相互作用,这可能反映了 CLE 对病原体转座传播的影响。这些发现揭示了蜱微生物组内复杂的生态动态,并对疾病管理策略产生了影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential nested patterns of Anaplasma marginale and Coxiella-like endosymbiont across Rhipicephalus microplus ontogeny

Understanding the intricate ecological interactions within the microbiome of arthropod vectors is crucial for elucidating disease transmission dynamics and developing effective control strategies. In this study, we investigated the ecological roles of Coxiella-like endosymbiont (CLE) and Anaplasma marginale across larval, nymphal, and adult stages of Rhipicephalus microplus. We hypothesized that CLE would show a stable, nested pattern reflecting co-evolution with the tick host, while A. marginale would exhibit a more dynamic, non-nested pattern influenced by environmental factors and host immune responses. Our findings revealed a stable, nested pattern characteristic of co-evolutionary mutualism for CLE, occurring in all developmental stages of the tick. Conversely, A. marginale exhibited variable occurrence but exerted significant influence on microbial community structure, challenging our initial hypotheses of its non-nested dynamics. Furthermore, in silico removal of both microbes from the co-occurrence networks altered network topology, underscoring their central roles in the R. microplus microbiome. Notably, competitive interactions between CLE and A. marginale were observed in nymphal network, potentially reflecting the impact of CLE on the pathogen transstadial-transmission. These findings shed light on the complex ecological dynamics within tick microbiomes and have implications for disease management strategies.

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来源期刊
Microbiological research
Microbiological research 生物-微生物学
CiteScore
10.90
自引率
6.00%
发文量
249
审稿时长
29 days
期刊介绍: Microbiological Research is devoted to publishing reports on prokaryotic and eukaryotic microorganisms such as yeasts, fungi, bacteria, archaea, and protozoa. Research on interactions between pathogenic microorganisms and their environment or hosts are also covered.
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