Engineering and Functional Expression of the Type III Secretion System in Xenorhabdus: Enhancing Insecticidal Efficacy and Expanding T3SE Libraries

IF 6.2 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY
Xiyin Huang, , , Chen Li, , , Ke Zhang, , , Kunyan Li, , , Jiajie Xie, , , Meifang Quan, , , Yunjun Sun, , , Yibo Hu, , , Liqiu Xia, , and , Shengbiao Hu*, 
{"title":"Engineering and Functional Expression of the Type III Secretion System in Xenorhabdus: Enhancing Insecticidal Efficacy and Expanding T3SE Libraries","authors":"Xiyin Huang,&nbsp;, ,&nbsp;Chen Li,&nbsp;, ,&nbsp;Ke Zhang,&nbsp;, ,&nbsp;Kunyan Li,&nbsp;, ,&nbsp;Jiajie Xie,&nbsp;, ,&nbsp;Meifang Quan,&nbsp;, ,&nbsp;Yunjun Sun,&nbsp;, ,&nbsp;Yibo Hu,&nbsp;, ,&nbsp;Liqiu Xia,&nbsp;, and ,&nbsp;Shengbiao Hu*,&nbsp;","doi":"10.1021/acs.jafc.5c08269","DOIUrl":null,"url":null,"abstract":"<p >Entomopathogenic nematode symbiotic bacteria (EPNB) enhance nematode insecticidal capacity through symbiosis. This study cloned the complete 32-kb type III secretion system (T3SS) gene cluster from <i>Photorhabdus luminescens</i> TT01 using Red/ET recombineering and functionally expressed it in T3SS-deficient <i>Xenorhabdus stockiae</i> HN_xs01. Heterologous T3SS expression significantly enhanced HN_xs01 adhesion and invasion capabilities in CF-203 cells. In <i>Helicoverpa armigera</i> models, the engineered strain induced severe intestinal damage by suppressing antimicrobial peptide expression and demonstrated improved colonization and biocontrol efficacy (LC<sub>50</sub> decreased by 3.7-fold). Crucially, the TT01 derived T3SS mediated delivery of XopA─a novel effector exhibiting YopJ-family homology and characteristic T3SS effector features─into host cells. These findings establish the synthetic biology-driven potential of T3SS and its effectors for biological control applications while providing a mechanistic framework for future research.</p>","PeriodicalId":41,"journal":{"name":"Journal of Agricultural and Food Chemistry","volume":"73 38","pages":"24042–24054"},"PeriodicalIF":6.2000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Agricultural and Food Chemistry","FirstCategoryId":"97","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jafc.5c08269","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Entomopathogenic nematode symbiotic bacteria (EPNB) enhance nematode insecticidal capacity through symbiosis. This study cloned the complete 32-kb type III secretion system (T3SS) gene cluster from Photorhabdus luminescens TT01 using Red/ET recombineering and functionally expressed it in T3SS-deficient Xenorhabdus stockiae HN_xs01. Heterologous T3SS expression significantly enhanced HN_xs01 adhesion and invasion capabilities in CF-203 cells. In Helicoverpa armigera models, the engineered strain induced severe intestinal damage by suppressing antimicrobial peptide expression and demonstrated improved colonization and biocontrol efficacy (LC50 decreased by 3.7-fold). Crucially, the TT01 derived T3SS mediated delivery of XopA─a novel effector exhibiting YopJ-family homology and characteristic T3SS effector features─into host cells. These findings establish the synthetic biology-driven potential of T3SS and its effectors for biological control applications while providing a mechanistic framework for future research.

Abstract Image

Abstract Image

Xenorhabdus III型分泌系统的工程与功能表达:增强杀虫效果,扩大T3SE文库
昆虫病原线虫共生细菌(EPNB)通过共生增强线虫的杀虫能力。本研究利用Red/ET重组克隆了光habdus luminescens TT01中32 kb的III型分泌系统(T3SS)完整基因簇,并在T3SS缺失的Xenorhabdus stockiae HN_xs01中进行了功能表达。异种T3SS表达显著增强了HN_xs01在CF-203细胞中的粘附和侵袭能力。在棉铃虫模型中,工程菌株通过抑制抗菌肽的表达诱导严重的肠道损伤,并显示出更好的定植和生物防治效果(LC50降低3.7倍)。至关重要的是,TT01衍生出T3SS介导的XopA递送到宿主细胞中,XopA是一种具有yopj家族同源性和T3SS效应特征的新型效应物。这些发现奠定了T3SS及其效应物在生物防治应用中的合成生物学驱动潜力,同时为未来的研究提供了机制框架。
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
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
×
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:604180095
Book学术官方微信