{"title":"Interactions Between Endosymbionts <i>Wolbachia</i> and <i>Rickettsia</i> in the Spider Mite <i>Tetranychus turkestani</i>: Cooperation or Antagonism?","authors":"Sha Wang, Xinlei Wang, Ali Basit, Qiancheng Wei, Kedi Zhao, Yiying Zhao","doi":"10.3390/microorganisms13030642","DOIUrl":null,"url":null,"abstract":"<p><p>Maternally inherited endosymbionts are widespread in arthropods, with multiple symbionts commonly co-existing within a single host, potentially competing for or sharing limited host resources and space. <i>Wolbachia</i> and <i>Rickettsia</i>, two maternally-inherited symbionts in arthropods, can co-infect hosts, yet research on their combined impacts on host reproduction and interaction remains scarce. <i>Tetranychus turkestani</i> (Acari: Tetranychidae) is an important agricultural pest mite, characterized by rapid reproduction, a short life cycle, and being difficult to control. <i>Wolbachia</i> and <i>Rickettsia</i> are two major endosymbiotic bacteria present in <i>T. turkestani</i>. This study used diverse parthenogenetic backcross and antibiotic screening to explore the reproductive effects of these two symbionts on <i>T. turkestani</i>. The results show that single <i>Rickettsia</i> infection induced male killing in the amphigenesis of <i>T. turkestani</i>, leading to arrhenotokous embryo death and fewer offspring. Single <i>Wolbachia</i> infection induced strong cytoplasmic incompatibility (CI). During dual infection, CI intensity decreased because <i>Rickettsia</i>'s male-killing effect antagonized the <i>Wolbachia</i>-induced CI. Dual-infected mites had increased oviposition, lower mortality, a higher female-to-male ratio, and more offspring, thus enhancing <i>T. turkestani</i>'s fitness. These findings will be helpful for understanding the nature of host-endosymbiont interactions and the potential for evolutionary conflicts, offering insights into their co-evolutionary relationship.</p>","PeriodicalId":18667,"journal":{"name":"Microorganisms","volume":"13 3","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11946427/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microorganisms","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/microorganisms13030642","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Maternally inherited endosymbionts are widespread in arthropods, with multiple symbionts commonly co-existing within a single host, potentially competing for or sharing limited host resources and space. Wolbachia and Rickettsia, two maternally-inherited symbionts in arthropods, can co-infect hosts, yet research on their combined impacts on host reproduction and interaction remains scarce. Tetranychus turkestani (Acari: Tetranychidae) is an important agricultural pest mite, characterized by rapid reproduction, a short life cycle, and being difficult to control. Wolbachia and Rickettsia are two major endosymbiotic bacteria present in T. turkestani. This study used diverse parthenogenetic backcross and antibiotic screening to explore the reproductive effects of these two symbionts on T. turkestani. The results show that single Rickettsia infection induced male killing in the amphigenesis of T. turkestani, leading to arrhenotokous embryo death and fewer offspring. Single Wolbachia infection induced strong cytoplasmic incompatibility (CI). During dual infection, CI intensity decreased because Rickettsia's male-killing effect antagonized the Wolbachia-induced CI. Dual-infected mites had increased oviposition, lower mortality, a higher female-to-male ratio, and more offspring, thus enhancing T. turkestani's fitness. These findings will be helpful for understanding the nature of host-endosymbiont interactions and the potential for evolutionary conflicts, offering insights into their co-evolutionary relationship.
期刊介绍:
Microorganisms (ISSN 2076-2607) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to prokaryotic and eukaryotic microorganisms, viruses and prions. It publishes reviews, research papers and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.