Characterization of larval gut microbiota of two endoparasitoid wasps associated with their common host, Plutella xylostella (Linnaeus) (Lepidoptera: Plutellidae).

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-10-03 Epub Date: 2024-09-09 DOI:10.1128/spectrum.01208-24
Na-Na Hu, Zi-Qi Wang, Si-Jie Zhang, Zhi-Zhi Wang, Xue-Xin Chen
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Abstract

Insect gut microbes play important roles in digestion, metabolism, development, and environmental adaptation. Parasitoid wasps are one of the most important biological control agents in pest control, while the gut microbial species compositions and the associated functions have been poorly investigated. Two endoparasitoid wasps, Cotesia vestalis and Diadromus collaris, parasitize the larval stage and pupal stage of the diamondback moth, Plutella xylostella, respectively. Using whole-genome shotgun metagenomic sequencing, we characterized the gut microbial composition, diversity, and potential functional roles associated with the two parasitoid wasp larvae. The results reveal that Proteobacteria and Firmicutes are the dominant phyla in the gut of C. vestalis and D. collaris larvae, with Rhizobium and Enterococcus being the dominant genera. The putative microbial functions associated with the two parasitoid wasps might play a virtual role in assisting in consuming the host's nutritional composition. The enriched CAZymes family genes are primarily involved in the degradation and synthesis of chitin. Despite the richness of microbial species and communities, the microbes species and the microbial community structure exhibit significant similarity between the two parasitoid wasps and between the parasitoid wasp and the host P. xylostella. Notably, the prevalence of the genus Enterococcus shared among them suggests a possible link of gut microbes between the host and their associated parasitoids. Our study offers insights into the gut microbe-based interactions between the host and parasitoid wasps for the first time, potentially paving the way for the development of an ecologically friendly biocontrol strategy against the pest P. xylostella.IMPORTANCEEndoparasitoid wasps spend the majority of their lifespan within their host and heavily rely on the host's nutrition for survival. There is limited understanding regarding the composition and physiological impacts of gut microbial communities in parasitoid wasps, particularly during the larval stage, which is directly linked to the host. Based on a thorough characterization of the gut microbe and comprehensive comparative analysis, we found the microbial species of the larval parasitoid wasp Cotesia vestalis and the pupal parasitoid wasp Diadromus collaris were similar, sharing 159 genera and 277 species, as were the microbial community structure. Certain of the dominant microbial strains of the two parasitoid wasps were similar to that of their host Plutella xylostella larvae, revealing host insect may affect the microbial community of the parasitoid wasps. The putative microbial functions associated with the parasitoid wasp larvae play an important role in dietary consumption.

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两种内寄生蜂幼虫肠道微生物群的特征,这两种内寄生蜂与它们的共同宿主--木虱(Plutella xylostella (Linnaeus) )(鳞翅目:木虱科)有关联。
昆虫肠道微生物在消化、新陈代谢、发育和环境适应方面发挥着重要作用。寄生蜂是害虫防治中最重要的生物防治媒介之一,但对其肠道微生物种类组成及其相关功能的研究却很少。两种内寄生蜂 Cotesia vestalis 和 Diadromus collaris 分别寄生于钻石背蛾 Plutella xylostella 的幼虫期和化蛹期。利用全基因组霰弹枪元基因组测序技术,我们鉴定了这两种寄生蜂幼虫的肠道微生物组成、多样性和潜在的功能作用。结果发现,变形菌和固缩菌是 C. vestalis 和 D. collaris 幼虫肠道中的优势菌门,其中根瘤菌和肠球菌是优势菌属。与这两种寄生蜂相关的假定微生物功能可能在协助消耗宿主的营养成分方面发挥了虚拟作用。丰富的 CAZymes 家族基因主要参与几丁质的降解和合成。尽管微生物物种和群落十分丰富,但两种寄生蜂之间以及寄生蜂与寄主木虱之间的微生物物种和微生物群落结构表现出明显的相似性。值得注意的是,寄生蜂和寄生蜂之间都普遍存在肠球菌属,这表明宿主和相关寄生蜂之间可能存在肠道微生物联系。我们的研究首次揭示了宿主与寄生蜂之间基于肠道微生物的相互作用,可能为开发针对害虫 P. xylostella 的生态友好型生物控制策略铺平道路。重要意义内寄生蜂的大部分寿命都在宿主体内度过,严重依赖宿主的营养生存。人们对寄生蜂肠道微生物群落的组成和生理影响了解有限,尤其是在与寄主直接相关的幼虫阶段。基于对肠道微生物的全面描述和综合比较分析,我们发现幼虫寄生蜂 Cotesia vestalis 和蛹寄生蜂 Diadromus collaris 的微生物种类相似,共有 159 属 277 种,微生物群落结构也相似。这两种寄生蜂的某些优势微生物菌株与寄主灰飞虱幼虫的微生物菌株相似,这表明寄主昆虫可能会影响寄生蜂的微生物群落。与寄生蜂幼虫相关的假定微生物功能在食物消耗中发挥了重要作用。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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