Dissemination patterns and functional role of a symbiotic bacteria Stenotrophomonas maltophilia in Phytoseiulus persimilis.

IF 1.8 2区 农林科学 Q2 ENTOMOLOGY
Hong Yan, Endong Wang, Xuenong Xu, Guo-Shu Wei, Bo Zhang
{"title":"Dissemination patterns and functional role of a symbiotic bacteria Stenotrophomonas maltophilia in Phytoseiulus persimilis.","authors":"Hong Yan, Endong Wang, Xuenong Xu, Guo-Shu Wei, Bo Zhang","doi":"10.1007/s10493-024-00982-9","DOIUrl":null,"url":null,"abstract":"<p><p>Symbiotic bacteria play a crucial role in various facets of host biology and physiology. The development and utilization of symbiotic bacteria in insects show promising potential for enhancing their reproduction, temperature tolerance, resistances to pathogens and insecticides. However, limited research has been conducted on symbiotic bacteria in predatory mites. In Phytoseiulus persimilis, we successfully cultivated a strain of Stenotrophomonas maltophilia, which has been noted for its significant contributions to pathogen control, pesticide and toxin resistance, and nutrition provision in some insect species. To explore the effect of S. maltophilia and its potential application on predatory mites, we fed S. maltophilia to P. persimilis and evaluated the transmission dynamics within mite generations. We examined its impacts on predator fitness and resistances to pesticides, pathogens, and starvation. The results showed that the S. maltophilia content in the offspring increased by 12.91 times when gravid mites were fed with the bacterial solution. P. persimilis that consumed prey treated with S. maltophilia showed a 25.20-fold increase in microbial content. Mating with treated males did not affect microbial levels in females. Moreover, S. maltophilia did not cause any discernible effect on the fitness of P. persimilis, including survival, developmental duration, fecundity, and longevity. Notably, it was found to improve P. persimilis survival following exposure to the pathogen Acaricomes phytoseiuli, resulting in a reduction of mortality by 20% compared to the control. This study serves as a foundational step for further utilization of beneficial microbes to improve the efficacy of predatory mite biological control.</p>","PeriodicalId":12088,"journal":{"name":"Experimental and Applied Acarology","volume":"94 1","pages":"11"},"PeriodicalIF":1.8000,"publicationDate":"2024-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Applied Acarology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1007/s10493-024-00982-9","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Symbiotic bacteria play a crucial role in various facets of host biology and physiology. The development and utilization of symbiotic bacteria in insects show promising potential for enhancing their reproduction, temperature tolerance, resistances to pathogens and insecticides. However, limited research has been conducted on symbiotic bacteria in predatory mites. In Phytoseiulus persimilis, we successfully cultivated a strain of Stenotrophomonas maltophilia, which has been noted for its significant contributions to pathogen control, pesticide and toxin resistance, and nutrition provision in some insect species. To explore the effect of S. maltophilia and its potential application on predatory mites, we fed S. maltophilia to P. persimilis and evaluated the transmission dynamics within mite generations. We examined its impacts on predator fitness and resistances to pesticides, pathogens, and starvation. The results showed that the S. maltophilia content in the offspring increased by 12.91 times when gravid mites were fed with the bacterial solution. P. persimilis that consumed prey treated with S. maltophilia showed a 25.20-fold increase in microbial content. Mating with treated males did not affect microbial levels in females. Moreover, S. maltophilia did not cause any discernible effect on the fitness of P. persimilis, including survival, developmental duration, fecundity, and longevity. Notably, it was found to improve P. persimilis survival following exposure to the pathogen Acaricomes phytoseiuli, resulting in a reduction of mortality by 20% compared to the control. This study serves as a foundational step for further utilization of beneficial microbes to improve the efficacy of predatory mite biological control.

共生细菌嗜麦芽窄养单胞菌在persimilis中的传播模式和功能作用。
共生细菌在宿主生物学和生理学的各个方面起着至关重要的作用。昆虫共生细菌的开发和利用在提高昆虫繁殖能力、耐温性、对病原体和杀虫剂的抗性方面显示出良好的潜力。然而,对掠食性螨体内共生细菌的研究有限。在persimilis植物中,我们成功培养了一株嗜麦芽窄养单胞菌,该菌株在某些昆虫的病原控制、农药和毒素抗性以及营养供应方面具有重要贡献。为探讨嗜麦芽假单胞菌对捕食性螨的影响及其应用潜力,本研究向persimilis投喂嗜麦芽假单胞菌,并评价其在螨代内的传播动态。我们研究了它对捕食者适应性和对杀虫剂、病原体和饥饿的抗性的影响。结果表明,用菌液喂养的孕螨子代中嗜麦芽链球菌的含量提高了12.91倍。食用嗜麦芽葡萄球菌处理过的猎物的persimilis的微生物含量增加了25.20倍。与处理过的雄性交配不会影响雌性体内的微生物水平。此外,嗜麦芽葡萄球菌对persimilis的适应性(包括存活、发育持续时间、繁殖力和寿命)没有任何明显的影响。值得注意的是,研究发现,与对照相比,它可以提高persimilis在暴露于病原菌acaricome phytoseiuli后的存活率,导致死亡率降低20%。本研究为进一步利用有益微生物提高捕食性螨生物防治效果奠定了基础。
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
3.90
自引率
9.10%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Experimental and Applied Acarology publishes peer-reviewed original papers describing advances in basic and applied research on mites and ticks. Coverage encompasses all Acari, including those of environmental, agricultural, medical and veterinary importance, and all the ways in which they interact with other organisms (plants, arthropods and other animals). The subject matter draws upon a wide variety of disciplines, including evolutionary biology, ecology, epidemiology, physiology, biochemistry, toxicology, immunology, genetics, molecular biology and pest management sciences.
×
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