Molecular Biology of Cytoplasmic Incompatibility Caused by Wolbachia Endosymbionts.

IF 8.5 1区 生物学 Q1 MICROBIOLOGY Annual review of microbiology Pub Date : 2023-09-15 Epub Date: 2023-06-07 DOI:10.1146/annurev-micro-041020-024616
Mark Hochstrasser
{"title":"Molecular Biology of Cytoplasmic Incompatibility Caused by <i>Wolbachia</i> Endosymbionts.","authors":"Mark Hochstrasser","doi":"10.1146/annurev-micro-041020-024616","DOIUrl":null,"url":null,"abstract":"<p><p>Among endosymbiotic bacteria living within eukaryotic cells, <i>Wolbachia</i> is exceptionally widespread, particularly in arthropods. Inherited through the female germline, it has evolved ways to increase the fraction of bacterially infected offspring by inducing parthenogenesis, feminization, male killing, or, most commonly, cytoplasmic incompatibility (CI). In CI, <i>Wolbachia</i> infection of males causes embryonic lethality unless they mate with similarly infected females, creating a relative reproductive advantage for infected females. A set of related <i>Wolbachia</i> bicistronic operons encodes the CI-inducing factors. The downstream gene encodes a deubiquitylase or nuclease and is responsible for CI induction by males, while the upstream product when expressed in females binds its sperm-introduced cognate partner and rescues viability. Both toxin-antidote and host-modification mechanisms have been proposed to explain CI. Interestingly, male killing by either <i>Spiroplasma</i> or <i>Wolbachia</i> endosymbionts involves deubiquitylases as well. Interference with the host ubiquitin system may therefore be a common theme among endosymbiont-mediated reproductive alterations.</p>","PeriodicalId":7946,"journal":{"name":"Annual review of microbiology","volume":"77 ","pages":"299-316"},"PeriodicalIF":8.5000,"publicationDate":"2023-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual review of microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1146/annurev-micro-041020-024616","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/6/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 2

Abstract

Among endosymbiotic bacteria living within eukaryotic cells, Wolbachia is exceptionally widespread, particularly in arthropods. Inherited through the female germline, it has evolved ways to increase the fraction of bacterially infected offspring by inducing parthenogenesis, feminization, male killing, or, most commonly, cytoplasmic incompatibility (CI). In CI, Wolbachia infection of males causes embryonic lethality unless they mate with similarly infected females, creating a relative reproductive advantage for infected females. A set of related Wolbachia bicistronic operons encodes the CI-inducing factors. The downstream gene encodes a deubiquitylase or nuclease and is responsible for CI induction by males, while the upstream product when expressed in females binds its sperm-introduced cognate partner and rescues viability. Both toxin-antidote and host-modification mechanisms have been proposed to explain CI. Interestingly, male killing by either Spiroplasma or Wolbachia endosymbionts involves deubiquitylases as well. Interference with the host ubiquitin system may therefore be a common theme among endosymbiont-mediated reproductive alterations.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
沃尔巴克氏体内共生体引起细胞质不亲和性的分子生物学。
在生活在真核细胞内的内共生细菌中,沃尔巴克氏体异常广泛,尤其是在节肢动物中。通过雌性种系遗传,它进化出了通过诱导孤雌生殖、雌性化、雄性杀伤或最常见的细胞质不相容性(CI)来增加细菌感染后代比例的方法。在CI中,雄性沃尔巴克氏体感染会导致胚胎死亡,除非它们与同样感染的雌性交配,从而为感染的雌性创造相对的繁殖优势。一组相关的沃尔巴克氏体双顺反子操纵子编码CI诱导因子。下游基因编码去泛素酶或核酸酶,负责雄性的CI诱导,而在雌性中表达的上游产物结合其精子引入的同源伴侣并挽救生存能力。毒素解毒剂和宿主修饰机制都被提出来解释CI。有趣的是,螺旋体或沃尔巴克氏体内共生体杀死雄性也涉及去泛素酶。因此,对宿主泛素系统的干扰可能是内共生体介导的生殖改变的共同主题。
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 去求助
来源期刊
Annual review of microbiology
Annual review of microbiology 生物-微生物学
CiteScore
18.10
自引率
0.00%
发文量
37
期刊介绍: Annual Review of Microbiology is a Medical and Microbiology Journal and published by Annual Reviews Inc. The Annual Review of Microbiology, in publication since 1947, covers significant developments in the field of microbiology, encompassing bacteria, archaea, viruses, and unicellular eukaryotes. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license. The Impact Factor of Annual Review of Microbiology is 10.242 (2024) Impact factor. The Annual Review of Microbiology Journal is Indexed with Pubmed, Scopus, UGC (University Grants Commission).
期刊最新文献
Understanding the Diversity, Evolution, Ecology, and Applications of Mycoviruses. Mechanisms Underlying Ophiocordyceps Infection and Behavioral Manipulation of Ants: Unique or Ubiquitous? Cyclic Diguanylate in the Wild: Roles During Plant and Animal Colonization How Bacteria Establish and Maintain Outer Membrane Lipid Asymmetry Dimethylsulfoniopropionate (DMSP): From Biochemistry to Global Ecological Significance.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1