面对复杂生命周期和瓶颈的微生物组组成和周转:通过对屎壳郎的研究获得的见解。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2025-01-31 Epub Date: 2024-12-20 DOI:10.1128/aem.01278-24
Joshua A Jones, Irene Garcia Newton, Armin P Moczek
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引用次数: 0

摘要

微生物组的组成和功能在宿主的整个生命周期中经常发生变化,反映了宿主生态位的变化。因此,建立这些关系的机制是宿主生态和进化的重要方面;然而,人们对它们的性质仍然知之甚少。在这里,我们试图研究与屎壳郎复杂生命周期相关的微生物群落,以及宿主生命阶段、性别和环境在决定微生物群聚集方面的相对贡献。我们发现金牛O.金牛是多种微生物群的宿主,这些微生物群在宿主发育过程中经历了剧烈的群落变化,受宿主生命阶段、环境微生物群以及性别(在较小程度上)的影响。与预测相反,我们发现卵和蛹阶段——尽管没有消化道或明确的微生物储存器官——并不限制微生物的维持,而宿主构建的环境,如母体衍生的粪便颗粒或晚期幼虫构建的蛹室,仍然可以作为某些分类群的补充微生物避难所。最后,我们确定了一个可能影响宿主发育和健康的假定核心微生物群的小群落。我们的研究结果为孤立生物组装、维持和调整有益微生物群以应对生命阶段特定需求和挑战的机制提供了重要见解。重要性:随着共生体对宿主生态、进化和发展的影响越来越明显,了解宿主如何促进与这些共生体的相互作用的可靠维持也变得越来越重要。因此,越来越多的工作已经开始确定各种行为和生理机制,这些行为和生理机制支撑着有益共生体在一系列宿主分类群中的选择性定植。然而,具有复杂生命周期的生物,如全代谢昆虫,如何建立和维持关键的共生体仍然知之甚少。考虑到内部和外部宿主形态的剧烈变化,以及饮食和环境中的生态位变化,这是变态的标志,这一点特别有趣。本研究研究了牛头蜣螂(Onthophagus taurus)复杂的生命周期和宿主构建的环境中微生物群的动态变化,这是了解生物如何在整个发育过程中维持和调节其微生物群的有用模型。
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Microbiome composition and turnover in the face of complex lifecycles and bottlenecks: insights through the study of dung beetles.

Microbiome composition and function often change throughout a host's life cycle, reflecting shifts in the ecological niche of the host. The mechanisms that establish these relationships are therefore important dimensions of host ecology and evolution; yet, their nature remains poorly understood. Here, we sought to investigate the microbial communities associated with the complex life cycle of the dung beetle Onthophagus taurus and the relative contributions of host life stage, sex, and environment in determining microbiome assembly. We find that O. taurus plays host to a diverse microbiota that undergo drastic community shifts throughout host development, influenced by host life stage, environmental microbiota, and, to a lesser degree, sex. Contrary to predictions, we found that egg and pupal stages-despite the absence of a digestive tract or defined microbe-storing organs-do not constrain microbial maintenance, while host-constructed environments, such as a maternally derived fecal pellet or the pupal chamber constructed by late larvae, may still serve as complementary microbial refugia for select taxa. Lastly, we identify a small community of putative core microbiota likely to shape host development and fitness. Our results provide important insights into mechanisms employed by solitary organisms to assemble, maintain, and adjust beneficial microbiota to confront life-stage-specific needs and challenges.

Importance: As the influence of symbionts on host ecology, evolution, and development has become more apparent so has the importance of understanding how hosts facilitate the reliable maintenance of their interactions with these symbionts. A growing body of work has thus begun to identify diverse behaviors and physiological mechanisms underpinning the selective colonization of beneficial symbionts across a range of host taxa. Yet, how organisms with complex life cycles, such as holometabolous insects, establish and maintain key symbionts remains poorly understood. This is particularly interesting considering the drastic transformations of both internal and external host morphology, and the ecological niche shifts in diet and environment, that are the hallmark of metamorphosis. This work investigates the dynamic changes of the microbiota associated with the complex life cycle and host-constructed environments of the bull-headed dung beetle, Onthophagus taurus, a useful model for understanding how organisms may maintain and modulate their microbiota across development.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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