Identifying potential nutrient acquisition mechanisms for long-term survival: adaptive evolution of Halomonas isolated from subseafloor crustal fluids.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-03-21 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1511421
Hans Sebastian, Alberto Robador, Dawson Ray, Angus Angermeyer, Steven D'Hondt, Julie A Huber, Steven E Finkel
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引用次数: 0

Abstract

In nature, microbes must often survive for long periods of time under conditions of nutrient and carbon limitation while also facing extremes in temperature, pressure, and competition with other microbes. One low-carbon, cold, and high pressure environment is the subseafloor crustal aquifer, where fluids circulate through old ocean crust. While microbial communities are known to be present in these fluids and contribute to biogeochemical cycling, the survival strategies of microbes in these communities is poorly constrained. In this study, multiple Halomonas strains were isolated from subseafloor crustal fluids of North Pond, a site located on the western flank of the Mid-Atlantic Ridge. These organisms are able to grow under laboratory conditions in minimal medium without the addition of carbon sources, as well as in rich nutrient conditions. We found that these Halomonas strains are highly related to each other in genomic content, but each strain has acquired unique mutations and/or undergone genomic rearrangements, suggesting that the strains were all derived from a single ancestral Halomonas progenitor. After serial passage of isolates from this Halomonas population under rich nutrient conditions in the laboratory, we identified mutants that can no longer scavenge scarce nutrients in minimal medium with no added carbon. Genomic analysis identified several genes that appear to be essential for survival under extremely low-nutrient condition, including several hypothetical proteins predicted to function as lipases, peptidases, or nutrient transporters. One of these genes was mutated in six out of the eight lineages studied, indicating that this hypothetical lipase protein is selected against during growth in rich medium, but may be required for growth under low-nutrient conditions. The application of an adaptive evolution platform selecting for survival and growth under one environmental condition that simultaneously selects against survival in different environments may prove to be a very useful tool for identifying genes and metabolic pathways in a wide variety of complex environments.

确定长期生存的潜在营养获取机制:从海底地壳流体中分离的盐单胞菌的适应性进化。
在自然界中,微生物通常必须在营养和碳限制条件下长期生存,同时还要面对极端的温度、压力以及与其他微生物的竞争。地壳下含水层就是一个低碳、寒冷和高压的环境,液体在古老的海洋地壳中循环。虽然已知这些流体中存在微生物群落,并有助于生物地球化学循环,但对这些群落中微生物的生存策略却知之甚少。在这项研究中,从位于大西洋中脊西侧的北塘海底地壳流体中分离出了多种卤单胞菌菌株。在实验室条件下,这些生物既能在不添加碳源的最小培养基中生长,也能在富营养条件下生长。我们发现,这些卤单胞菌株在基因组内容上彼此高度相关,但每个菌株都获得了独特的突变和/或经历了基因组重排,这表明这些菌株都来自一个单一的卤单胞菌祖先。在实验室富营养条件下对来自该哈洛单胞菌群体的分离株进行连续培养后,我们发现了一些突变株,它们无法再在不添加碳的最小培养基中清除稀缺的营养物质。基因组分析发现了几个在极低营养条件下生存所必需的基因,包括几个被预测为脂肪酶、肽酶或营养转运体的假定蛋白。在所研究的 8 个品系中,有 6 个品系的其中一个基因发生了突变,这表明这种假定的脂肪酶蛋白在富营养化培养基中生长时会被选择性抑制,但在低营养条件下生长可能是必需的。在一种环境条件下选择生存和生长的适应性进化平台,同时在不同环境下选择不生存的适应性进化平台,可能被证明是在各种复杂环境中鉴定基因和代谢途径的非常有用的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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