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顶复门中一种α-变形菌内共生体的代谢贡献

Metabolic Contributions of an Alphaproteobacterial Endosymbiont in the Apicomplexan .

作者信息

Hunter Elizabeth Sage, Paight Christopher, Lane Christopher E

机构信息

Department of Biological Sciences, University of Rhode Island, Kingston, RI, United States.

Department of Ecology, Evolution & Marine Biology, University of California, Santa Barbara, Santa Barbara, CA, United States.

出版信息

Front Microbiol. 2020 Dec 1;11:580719. doi: 10.3389/fmicb.2020.580719. eCollection 2020.

Abstract

Apicomplexa is a diverse protistan phylum composed almost exclusively of metazoan-infecting parasites, including the causative agents of malaria, cryptosporidiosis, and toxoplasmosis. A single apicomplexan genus, , was described in 2010 as a mutualist partner to its tunicate host. Here we present genomic and transcriptomic data from the parasitic sister species to this mutualist, , and its associated bacterial endosymbiont. and both infect tunicate hosts, localize to similar organs within these hosts, and maintain bacterial endosymbionts. Though many other protists are known to harbor bacterial endosymbionts, these associations are completely unknown in Apicomplexa outside of the Nephromycidae clade. Our data indicate that a vertically transmitted α-proteobacteria has been retained in each lineage since and diverged. This α-proteobacterial endosymbiont has highly reduced metabolic capabilities, but contributes the essential amino acid lysine, and essential cofactor lipoic acid to . This partnership likely reduces resource competition with the tunicate host. However, our data indicate that the contribution of the single α-proteobacterial endosymbiont in is minimal compared to the three taxa of endosymbionts present in the system, and is a potential explanation for the virulence disparity between these lineages.

摘要

顶复门是一个多样的原生动物门,几乎完全由感染后生动物的寄生虫组成,包括疟疾、隐孢子虫病和弓形虫病的病原体。2010年描述了一个单一的顶复门属,它是其被囊动物宿主的共生伙伴。在这里,我们展示了与其共生体的寄生姐妹物种及其相关细菌内共生体的基因组和转录组数据。 和 都感染被囊动物宿主,定位于这些宿主体内的相似器官,并维持细菌内共生体。虽然已知许多其他原生生物含有细菌内共生体,但在肾孢菌科进化枝之外的顶复门中,这些共生关系完全未知。我们的数据表明,自 和 分化以来,垂直传播的α-变形菌在每个谱系中都得以保留。这种α-变形菌内共生体的代谢能力大幅降低,但为 提供必需氨基酸赖氨酸和必需辅因子硫辛酸。这种共生关系可能减少了与被囊动物宿主的资源竞争。然而,我们的数据表明,与 系统中存在的三种内共生体分类群相比, 中单一α-变形菌内共生体的贡献最小,这是这些谱系之间毒力差异的一个潜在解释。

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