Tamre Erik, Fournier Gregory
Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Department of Earth Sciences, Dartmouth College, Hanover, New Hampshire, USA.
Appl Environ Microbiol. 2025 Aug 12:e0166224. doi: 10.1128/aem.01662-24.
Reduced iron was abundant in Earth's surface environments before their oxygenation, so iron oxidation could have been a common metabolism on the early Earth. Consequently, modern microbial iron oxidation is sometimes seen as a holdover from an earlier biosphere, but the continuity of involved lineages or the metabolic process itself has not been verified. Modern neutrophilic iron oxidizers use cytochrome-porin Cyc2 as the initial electron acceptor in iron oxidation. With the protein as a proxy for the metabolism, we performed a phylogenetic analysis of Cyc2 to understand the evolutionary history of this microbial iron oxidation pathway. In addition to known iron oxidizers, we identified Cyc2 orthologs in gammaproteobacterial endosymbionts of lucinid bivalves. These bivalves have a robust fossil record and rely on seagrass meadows that only appear in the Cretaceous, providing a valuable time calibration in the evolutionary history of Cyc2. Our molecular clock analysis shows that extant sampled Cyc2 diversity has surprisingly recent common ancestry, and iron oxidation metabolisms in Gallionellaceae, Zetaproteobacteria, and photoferrotrophic Chlorobi likely originated in the Neoproterozoic or the Phanerozoic via multiple transfer events. The groups responsible for microbial iron oxidation have thus changed over Earth history, possibly reflecting the instability of niches with sufficient reduced iron. We note that frequent transfer and changing taxonomic distribution may be a general pattern for traits which are selected sporadically across space and time. Based on iron metabolism and other processes, we explore this concept of a trait's "clade fidelity" (or lack thereof) and establish its evolutionary importance.IMPORTANCEBacteria can oxidize iron to produce energy. As there was plenty of reduced iron available on the early Earth and there is only a little today, it was sometimes thought that bacteria that oxidize iron today are a small remnant of a larger group that used to do it. We studied the evolutionary history of the iron oxidation pathway that modern bacteria use, and we found that they developed that pathway relatively recently: whatever did it in the past is no longer around today. It would probably be hard for any group of organisms to keep doing iron oxidation over billions of years since iron availability is so variable: they are likely to go extinct or lose this ability at some point. We suggest this as a general trend in evolution that traits which are only sporadically useful are commonly lost-and then re-invented or re-distributed-or the trait will go extinct.
在地球表面环境氧化之前,还原态铁大量存在,因此铁氧化可能是早期地球上一种常见的代谢方式。所以,现代微生物铁氧化有时被视为早期生物圈遗留下来的现象,但相关谱系或代谢过程本身的连续性尚未得到证实。现代嗜中性铁氧化菌在铁氧化过程中使用细胞色素孔蛋白Cyc2作为初始电子受体。以该蛋白质作为这种代谢方式的代表,我们对Cyc2进行了系统发育分析,以了解这种微生物铁氧化途径的进化历史。除了已知的铁氧化菌,我们还在亮蛤双壳类动物的γ-变形菌内共生体中鉴定出了Cyc2直系同源物。这些双壳类动物有丰富的化石记录,并且依赖仅在白垩纪出现的海草草甸,这为Cyc2的进化历史提供了有价值的时间校准。我们的分子钟分析表明,现存采样的Cyc2多样性有着惊人的近代共同祖先,Gallionellaceae、Zetaproteobacteria和光合铁营养绿菌门中的铁氧化代谢可能通过多次转移事件起源于新元古代或显生宙。因此,在地球历史上,负责微生物铁氧化的类群发生了变化,这可能反映了具有充足还原态铁的生态位的不稳定性。我们注意到,频繁的转移和不断变化的分类分布可能是在空间和时间上偶尔被选择的性状的普遍模式。基于铁代谢和其他过程,我们探讨了性状“进化枝保真度”(或缺乏进化枝保真度)的概念,并确立了其进化重要性。
重要性
细菌可以氧化铁来产生能量。由于早期地球上有大量的还原态铁,而如今只有少量,所以有时人们认为如今氧化铁的细菌是过去进行这种代谢的更大群体的一小部分残留。我们研究了现代细菌所使用的铁氧化途径的进化历史,发现它们相对较晚才发展出该途径:过去进行铁氧化的生物如今已不复存在。由于铁的可利用性变化很大,任何生物群体要在数十亿年里持续进行铁氧化可能都很困难:它们很可能在某个时候灭绝或失去这种能力。我们认为这是进化中的一个普遍趋势,即那些只是偶尔有用的性状通常会丢失,然后被重新发明或重新分布,否则该性状就会灭绝。