Suppr超能文献

双氧化酶通过介导呼吸网络的形成来促进昆虫肠道共生。

Dual oxidase enables insect gut symbiosis by mediating respiratory network formation.

机构信息

Graduate School of Agriculture, Hokkaido University, 060-8589 Sapporo, Japan.

Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 062-8517 Sapporo, Japan.

出版信息

Proc Natl Acad Sci U S A. 2021 Mar 9;118(10). doi: 10.1073/pnas.2020922118.

Abstract

Most animals harbor a gut microbiota that consists of potentially pathogenic, commensal, and mutualistic microorganisms. Dual oxidase (Duox) is a well described enzyme involved in gut mucosal immunity by the production of reactive oxygen species (ROS) that antagonizes pathogenic bacteria and maintains gut homeostasis in insects. However, despite its nonspecific harmful activity on microorganisms, little is known about the role of Duox in the maintenance of mutualistic gut symbionts. Here we show that, in the bean bug , Duox-dependent ROS did not directly contribute to epithelial immunity in the midgut in response to its mutualistic gut symbiont, Instead, we found that the expression of Duox is tracheae-specific and its down-regulation by RNAi results in the loss of dityrosine cross-links in the tracheal protein matrix and a collapse of the respiratory system. We further demonstrated that the establishment of symbiosis is a strong oxygen sink triggering the formation of an extensive network of tracheae enveloping the midgut symbiotic organ as well as other organs, and that tracheal breakdown by Duox RNAi provokes a disruption of the gut symbiosis. Down-regulation of the hypoxia-responsive transcription factor Sima or the regulators of tracheae formation Trachealess and Branchless produces similar phenotypes. Thus, in addition to known roles in immunity and in the formation of dityrosine networks in diverse extracellular matrices, Duox is also a crucial enzyme for tracheal integrity, which is crucial to sustain mutualistic symbionts and gut homeostasis. We expect that this is a conserved function in insects.

摘要

大多数动物都携带有肠道微生物群,其中包括潜在的致病、共生和互利共生微生物。双氧化酶(Duox)是一种众所周知的酶,通过产生活性氧物质(ROS)参与肠道黏膜免疫,对抗致病菌并维持昆虫肠道内的稳态。然而,尽管 Duox 对微生物具有非特异性的有害活性,但人们对其在维持互利共生肠道共生体中的作用知之甚少。在这里,我们发现在豆芫菁中,Duox 依赖性 ROS 并没有直接有助于中肠对其共生肠道共生体的上皮免疫。相反,我们发现 Duox 的表达是气管特异性的,其 RNAi 下调导致气管蛋白基质中二酪氨酸交联的丢失和呼吸系统的崩溃。我们进一步证明,共生的建立是一个强烈的耗氧源,触发了一个广泛的气管网络的形成,这些气管网络包裹着中肠共生器官以及其他器官,而 Duox RNAi 引起的气管破裂会破坏肠道共生关系。缺氧反应转录因子 Sima 或气管形成调节剂 Trachealess 和 Branchless 的下调会产生类似的表型。因此,除了在免疫和在各种细胞外基质中二酪氨酸网络的形成中已知的作用外,Duox 也是气管完整性的关键酶,这对于维持互利共生的共生体和肠道内稳态至关重要。我们预计这是昆虫中保守的功能。

相似文献

引用本文的文献

9
Hundreds of antimicrobial peptides create a selective barrier for insect gut symbionts.数百种抗菌肽为昆虫肠道共生体形成选择性屏障。
Proc Natl Acad Sci U S A. 2024 Jun 18;121(25):e2401802121. doi: 10.1073/pnas.2401802121. Epub 2024 Jun 12.

本文引用的文献

1
Evolutionary and ecological consequences of gut microbial communities.肠道微生物群落的进化和生态后果。
Annu Rev Ecol Evol Syst. 2019 Nov;50(1):451-475. doi: 10.1146/annurev-ecolsys-110617-062453. Epub 2019 Aug 29.
2
Impact of the insect gut microbiota on ecology, evolution, and industry.昆虫肠道微生物群对生态、进化和工业的影响。
Curr Opin Insect Sci. 2020 Oct;41:33-39. doi: 10.1016/j.cois.2020.06.004. Epub 2020 Jun 21.
5
Versatile and Dynamic Symbioses Between Insects and Bacteria.昆虫与细菌之间的多样且动态的共生关系。
Annu Rev Entomol. 2020 Jan 7;65:145-170. doi: 10.1146/annurev-ento-011019-025025. Epub 2019 Oct 8.
8
Development and Function of the Tracheal System.气管系统的发生和功能。
Genetics. 2018 Jun;209(2):367-380. doi: 10.1534/genetics.117.300167.
10
Multiple origins of interdependent endosymbiotic complexes in a genus of cicadas.多种相互依存的内共生复合体起源于一个蝉属。
Proc Natl Acad Sci U S A. 2018 Jan 9;115(2):E226-E235. doi: 10.1073/pnas.1712321115. Epub 2017 Dec 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验