Clesson H. V. Higashi, Vilas Patel, Bryan Kamalaker, Rahul Inaganti, Alberto Bressan, Jacob A. Russell, Kerry M. Oliver
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引用次数: 0
摘要
蚜虫体内有九种常见的面共生体,其中大多数介导着一种或多种生态相互作用。Wolbachia pipientis 在其他节肢动物中研究得很透彻,但在蚜虫中的特征还很模糊。在香蕉的全球性害虫 Pentalonia nigronervosa 和 P. caladii 中,最初假定 Wolbachia 与传统的强制性营养共生体 Buchnera 一起发挥共生作用。然而,基因组分析未能支持这一假设。我们在众多种群中取样发现,超过 80% 的 Pentalonia 蚜虫携带有 Wolbachia 的 M 超群菌株(wPni)。Wolbachia缺乏固定性进一步证明了它的临时性地位,而在这些完全无性繁殖的蚜虫中的高感染频率则有力地证明了Wolbachia带来的净适应性益处。我们发现沃尔巴克氏体的存在与食用植物的使用之间没有关联,于是用常见的天敌来挑战感染了沃尔巴克氏体的蚜虫。生物测定显示,沃尔巴克氏体对一种专门的真菌病原体(Pandora neoaphidis)有显著的保护作用,但对普通病原体或寄生虫没有保护作用。在没有敌害挑战的情况下,沃尔巴克氏菌还能提高蚜虫的适应能力。因此,我们首次发现了与蚜虫相关的狼杆菌和 M 超群菌株的明显益处。蚜虫-狼杆菌系统为合并共生的关键模型提供了独特的机会,以更好地了解感染动态和共生体介导表型的基础机制。
Another tool in the toolbox: Aphid-specific Wolbachia protect against fungal pathogens
Aphids harbor nine common facultative symbionts, most mediating one or more ecological interactions. Wolbachia pipientis, well-studied in other arthropods, remains poorly characterized in aphids. In Pentalonia nigronervosa and P. caladii, global pests of banana, Wolbachia was initially hypothesized to function as a co-obligate nutritional symbiont alongside the traditional obligate Buchnera. However, genomic analyses failed to support this role. Our sampling across numerous populations revealed that more than 80% of Pentalonia aphids carried an M-supergroup strain of Wolbachia (wPni). The lack of fixation further supports a facultative status for Wolbachia, while high infection frequencies in these entirely asexual aphids strongly suggest Wolbachia confers net fitness benefits. Finding no correlation between Wolbachia presence and food plant use, we challenged Wolbachia-infected aphids with common natural enemies. Bioassays revealed that Wolbachia conferred significant protection against a specialized fungal pathogen (Pandora neoaphidis) but not against generalist pathogens or parasitoids. Wolbachia also improved aphid fitness in the absence of enemy challenge. Thus, we identified the first clear benefits for aphid-associated Wolbachia and M-supergroup strains specifically. Aphid-Wolbachia systems provide unique opportunities to merge key models of symbiosis to better understand infection dynamics and mechanisms underpinning symbiont-mediated phenotypes.
期刊介绍:
Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens