The gut microbiome of Helicoverpa armigera enhances immune response to baculovirus infection via suppression of Duox‐mediated reactive oxygen species

Author:

Tian Zhiqiang1ORCID,Guo Xi1,Michaud JP2,Zha Meng1,Zhu Lin1,Liu Xiaoming1ORCID,Liu Xiaoxia1

Affiliation:

1. Department of Entomology MOA Key Laboratory of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University Beijing China

2. Department of Entomology Kansas State University, Agricultural Research Center‐Hays Hays KS USA

Abstract

AbstractBACKGROUNDBaculoviruses such as Helicoverpa armigera nucleopolyhedrovirus (HearNPV) infect their lepidopteran hosts via the larval midgut where they interact with host immune responses and gut microbiota. Here we demonstrate that gut microbiota proliferating in response to HearNPV infection promote larval immune responses which impede the infection process.RESULTSThe microbial load of the larval midgut increased following HearNPV infection, due primarily to increases in Enterococcus spp., whereas most other bacterial genera declined, with Firmicutes replacing Proteobacteria as the dominant phylum. Injection of abdominal prolegs of infected larvae with H2O2 promoted viral infection, diminished microbial abundance, and accelerated larval death, mimicking the effects of HearNPV infection, which up‐regulated dual oxidase (Duox) expression, increasing H2O2 levels in the midgut. Knockdown of Duox with RNAi reduced H2O2 production in the guts of infected larvae, increased bacterial loads, decreased viral replication, and improved larval survival. Germ‐free larvae were more susceptible to HearNPV than control larvae, exhibiting greater expression of Duox, higher levels of H2O2, and lower survival. Replenishment of gut bacteria in germ‐free larvae restored the base‐line immunity to HearNPV observed in normal larvae. Enterococcus spp., Levilactobacillus brevis, and Lactobacillus sp. bacteria were isolated and implicated in immunity restoration via replenishment in germ‐free larvae.CONCLUSIONThese findings illuminate how gut microbiota play important roles in larval defense against oral baculovirus infection, and suggest novel avenues of investigation to enhance the efficacy of baculoviruses and improve control of lepidopteran pests. © 2023 Society of Chemical Industry.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Insect Science,Agronomy and Crop Science,General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3