比较群落生态学揭示了在可变宿主和环境微生物组中保守的体外寄生虫微生物组

IF 2.3 2区 生物学 Q2 ECOLOGY
Kelly A. Speer, Luis Víquez-R, Winifred F. Frick, Ana Ibarra, Nancy B. Simmons, Katharina Dittmar, Ricardo Sánchez Calderón, Raisa Preciado, Rodrigo Medellín, Marco Tschapka, Simone Sommer, Susan L. Perkins
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引用次数: 0

摘要

微生物群落——与单个动物相关的微生物群落——一直是全球昆虫生物多样性的重要驱动因素,使昆虫能够专注于狭窄、营养缺乏的食物。母系遗传的专性细菌内共生体在提供这些狭窄的饮食生态位所缺少的营养方面的重要性已经在昆虫中得到了很好的研究。然而,我们对昆虫微生物组中非母系遗传细菌组成的过程知之甚少,尽管这些细菌对昆虫的健康、适应性和媒介能力很重要。本研究以蝙蝠的两种专性昆虫体外寄生虫——蝙蝠蝇(Streblidae) Trichobius sphaeronotus和Nycterophilia coxata为研究对象,研究除专性细菌内共生体外,其微生物群是否在地理空间、物种间是保守的或变化的,或者与蝙蝠宿主或洞穴环境的外部微生物群是共变的。我们的研究结果表明,尽管在某些情况下,这些物种以同一蝙蝠个体的血液为食,但体外寄生虫的微生物组是高度保守的,并且对体外寄生虫物种具有特异性。相比之下,我们发现宿主蝙蝠的皮毛微生物组具有很高的地理差异,并且蝙蝠的皮毛微生物组与洞穴微生物组相似。这项研究表明,在维持与宿主和环境不同的特定微生物群方面,食血昆虫体外寄生虫存在限制,可能满足它们的营养需求。考虑到这些细菌中的许多都不是母系遗传的,这项研究为未来研究血食性节肢动物如何在其微生物群中获得和维持细菌奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative Community Ecology Reveals Conserved Ectoparasite Microbiomes Amidst Variable Host and Environment Microbiomes

Comparative Community Ecology Reveals Conserved Ectoparasite Microbiomes Amidst Variable Host and Environment Microbiomes

The microbiome—the community of microorganisms that is associated with an individual animal—has been an important driver of insect biodiversity globally, enabling insects to specialize in narrow, nutrient-deficient diets. The importance of maternally inherited, obligate bacterial endosymbionts in provisioning nutrients missing from these narrow dietary niches has been well studied in insects. However, we know comparatively little about the processes that dictate the composition of non-maternally inherited bacteria in insect microbiomes, despite the importance of these bacteria in insect health, fitness, and vector competence. Here, we used two species of obligate insect ectoparasites of bats, the bat flies (Streblidae) Trichobius sphaeronotus and Nycterophilia coxata, to examine whether the microbiome, beyond obligate bacterial endosymbionts, is conserved or variable across geographic space, between ectoparasite species, or covaries with the external microbiome of their bat hosts or the cave environment. Our results indicate that ectoparasite microbiomes are highly conserved and specific to ectoparasite species, despite these species feeding on the blood of the same bat individuals in some cases. In contrast, we found high geographic variation in the fur microbiome of host bats and that the bat fur microbiome mimics the cave microbiomes. This research suggests that there is a constraint on blood-feeding insect ectoparasites to maintain a specific microbiome distinct from their host and the environment, potentially to meet their nutritional needs. Given that many of these bacteria are not known to be maternally inherited, this research lays the foundation for future examinations of how blood-feeding arthropods acquire and maintain bacteria in their microbiomes.

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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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