Molecular mechanism of Enterococcus faecalis-induced phosphine sensitivity in Tribolium castaneum (Coleoptera: Tenebrionidae).

IF 2.2 2区 农林科学 Q1 ENTOMOLOGY
Zhengyan Wang, Haisheng Hu, Zhenzhen Chang, Shan Zhang, Yujie Lu
{"title":"Molecular mechanism of Enterococcus faecalis-induced phosphine sensitivity in Tribolium castaneum (Coleoptera: Tenebrionidae).","authors":"Zhengyan Wang,&nbsp;Haisheng Hu,&nbsp;Zhenzhen Chang,&nbsp;Shan Zhang,&nbsp;Yujie Lu","doi":"10.1093/jee/toad171","DOIUrl":null,"url":null,"abstract":"<p><p>Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) has developed extensive resistance to the fumigant phosphine. Knowledge of the resistance mechanisms offers insight into resistance management. Although several studies have highlighted the positive or negative impacts of symbiotic microbiota on host pesticide resistance, little is known about the association between gut symbionts and host phosphine resistance. To reveal the effect of the gut bacterium, Enterococcus faecalis (Andrewes & Horder) (Lactobacillales: Enterococcaceae), on host phosphine resistance and its underlying mechanism, we investigated mortality, fitness, redox responses, and immune responses of adult T. castaneum when challenged with E. faecalis inoculation and/or phosphine exposure. When T. castaneum was exposed to phosphine, E. faecalis inoculation decreased its survival and female fecundity and aggravated its oxidative stress. Furthermore, E. faecalis inoculation suppressed the expression and activity of superoxide dismutase, catalase, and peroxidase in phosphine-exposed T. castaneum. Enterococcus faecalis inoculation also triggered excessive host immune responses, including the immune deficiency signaling pathway and the dual oxidase-reactive oxygen species system. These findings suggest that E. faecalis likely modulates host phosphine resistance by interfering with the redox system. This provides information for examining the symbiotic function in the insect-microorganism relationship and new avenues for pesticide resistance management.</p>","PeriodicalId":15632,"journal":{"name":"Journal of Economic Entomology","volume":" ","pages":"1820-1829"},"PeriodicalIF":2.2000,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Economic Entomology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1093/jee/toad171","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) has developed extensive resistance to the fumigant phosphine. Knowledge of the resistance mechanisms offers insight into resistance management. Although several studies have highlighted the positive or negative impacts of symbiotic microbiota on host pesticide resistance, little is known about the association between gut symbionts and host phosphine resistance. To reveal the effect of the gut bacterium, Enterococcus faecalis (Andrewes & Horder) (Lactobacillales: Enterococcaceae), on host phosphine resistance and its underlying mechanism, we investigated mortality, fitness, redox responses, and immune responses of adult T. castaneum when challenged with E. faecalis inoculation and/or phosphine exposure. When T. castaneum was exposed to phosphine, E. faecalis inoculation decreased its survival and female fecundity and aggravated its oxidative stress. Furthermore, E. faecalis inoculation suppressed the expression and activity of superoxide dismutase, catalase, and peroxidase in phosphine-exposed T. castaneum. Enterococcus faecalis inoculation also triggered excessive host immune responses, including the immune deficiency signaling pathway and the dual oxidase-reactive oxygen species system. These findings suggest that E. faecalis likely modulates host phosphine resistance by interfering with the redox system. This provides information for examining the symbiotic function in the insect-microorganism relationship and new avenues for pesticide resistance management.

粪肠球菌诱导赤兔Tribolium castaneum磷化氢敏感性的分子机制(鞘翅目:Tenebrionidae)。
赤兔Tribolium castaneum(Herbst)(鞘翅目:Tenebrionidae)对熏蒸剂磷化氢产生了广泛的抗性。对阻力机制的了解为阻力管理提供了见解。尽管几项研究强调了共生微生物群对宿主杀虫剂耐药性的积极或消极影响,但对肠道共生菌与宿主磷化氢耐药性之间的关系知之甚少。为了揭示肠道细菌粪肠球菌(Andrewes&Horder)(乳酸杆菌属:肠球菌科)对宿主磷化氢抗性的影响及其潜在机制,我们研究了成年灰鼠在接种粪肠球菌和/或接触磷化氢时的死亡率、适应性、氧化还原反应和免疫反应。当赤兔暴露于磷化氢时,接种粪肠球菌降低了其存活率和雌性生殖力,并加剧了其氧化应激。此外,接种粪大肠杆菌抑制了磷化氢暴露的赤兔体内超氧化物歧化酶、过氧化氢酶和过氧化物酶的表达和活性。粪肠球菌接种也引发了过度的宿主免疫反应,包括免疫缺陷信号通路和双氧化酶活性氧系统。这些发现表明,粪肠球菌可能通过干扰氧化还原系统来调节宿主对磷化氢的抗性。这为研究昆虫与微生物关系中的共生功能以及农药抗性管理的新途径提供了信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.60
自引率
9.10%
发文量
198
审稿时长
3-6 weeks
期刊介绍: Journal of Economic Entomology the most-cited entomological journal – publishes articles on the economic significance of insects and other arthropods and includes sections on apiculture & social insects, insecticides, biological control, household & structural insects, crop protection, forest entomology, and more. In addition to research papers, Journal of Economic Entomology publishes Reviews, interpretive articles in a Forum section, Short Communications, and Letters to the Editor. The journal is published bimonthly in February, April, June, August, October, and December.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信