Adaptation to space conditions of novel bacterial species isolated from the International Space Station revealed by functional gene annotations and comparative genome analysis.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Lukasz M Szydlowski, Alper A Bulbul, Anna C Simpson, Deniz E Kaya, Nitin K Singh, Ugur O Sezerman, Paweł P Łabaj, Tomasz Kosciolek, Kasthuri Venkateswaran
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引用次数: 0

Abstract

Background: The extreme environment of the International Space Station (ISS) puts selective pressure on microorganisms unintentionally introduced during its 20+ years of service as a low-orbit science platform and human habitat. Such pressure leads to the development of new features not found in the Earth-bound relatives, which enable them to adapt to unfavorable conditions.

Results: In this study, we generated the functional annotation of the genomes of five newly identified species of Gram-positive bacteria, four of which are non-spore-forming and one spore-forming, all isolated from the ISS. Using a deep-learning based tool-deepFRI-we were able to functionally annotate close to 100% of protein-coding genes in all studied species, overcoming other annotation tools. Our comparative genomic analysis highlights common characteristics across all five species and specific genetic traits that appear unique to these ISS microorganisms. Proteome analysis mirrored these genomic patterns, revealing similar traits. The collective annotations suggest adaptations to life in space, including the management of hypoosmotic stress related to microgravity via mechanosensitive channel proteins, increased DNA repair activity to counteract heightened radiation exposure, and the presence of mobile genetic elements enhancing metabolism. In addition, our findings suggest the evolution of certain genetic traits indicative of potential pathogenic capabilities, such as small molecule and peptide synthesis and ATP-dependent transporters. These traits, exclusive to the ISS microorganisms, further substantiate previous reports explaining why microbes exposed to space conditions demonstrate enhanced antibiotic resistance and pathogenicity.

Conclusion: Our findings indicate that the microorganisms isolated from ISS we studied have adapted to life in space. Evidence such as mechanosensitive channel proteins, increased DNA repair activity, as well as metallopeptidases and novel S-layer oxidoreductases suggest a convergent adaptation among these diverse microorganisms, potentially complementing one another within the context of the microbiome. The common genes that facilitate adaptation to the ISS environment may enable bioproduction of essential biomolecules need during future space missions, or serve as potential drug targets, if these microorganisms pose health risks. Video Abstract.

通过功能基因注释和比较基因组分析揭示从国际空间站分离的新型细菌物种对空间条件的适应性。
背景:国际空间站(ISS)的极端环境对微生物造成了选择性压力,这些微生物是在国际空间站作为低轨道科学平台和人类栖息地的 20 多年服务期间无意引入的。这种压力导致微生物发展出地球上的近亲所没有的新特征,使它们能够适应不利的条件:在这项研究中,我们对从国际空间站分离出的五种新发现的革兰氏阳性细菌的基因组进行了功能注释,其中四种是无芽孢细菌,一种是有芽孢细菌。利用基于深度学习的工具--deepFRI,我们能够对所有研究物种中接近100%的蛋白质编码基因进行功能注释,超越了其他注释工具。我们的比较基因组分析突出了所有五个物种的共同特征,以及这些 ISS 微生物特有的特定遗传特征。蛋白质组分析反映了这些基因组模式,揭示了类似的特征。集体注释表明,这些微生物适应了太空生活,包括通过机械敏感通道蛋白管理与微重力有关的低渗透压力,增加 DNA 修复活动以抵御更强的辐射照射,以及存在增强新陈代谢的移动遗传因子。此外,我们的研究结果表明,某些遗传特征的进化表明了潜在的致病能力,如小分子和多肽合成以及依赖 ATP 的转运体。这些特征是国际空间站微生物独有的,进一步证实了之前的报道,解释了为什么暴露在太空条件下的微生物表现出更强的抗生素耐药性和致病性:我们的研究结果表明,我们所研究的从国际空间站分离出来的微生物已经适应了太空生活。机械敏感通道蛋白、DNA 修复活性增强以及金属肽酶和新型 S 层氧化还原酶等证据表明,这些不同微生物之间存在趋同的适应性,有可能在微生物组的背景下相互补充。有助于适应国际空间站环境的共同基因可能有助于生物生产未来太空任务中所需的基本生物分子,如果这些微生物对健康造成危害,还可能成为潜在的药物靶标。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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