Lan Liu, Zheng-Han Lian, Ai-Ping Lv, Nimaichand Salam, Jian-Chao Zhang, Meng-Meng Li, Wei-Min Sun, Sha Tan, Zhen-Hao Luo, Lei Gao, Yang Yuan, Yu-Zhen Ming, Yu-Ting OuYang, Yu-Xian Li, Ze-Tao Liu, Chao-Jian Hu, Ying Chen, Zheng-Shuang Hua, Wen-Sheng Shu, Brian P Hedlund, Wen-Jun Li, Jian-Yu Jiao
{"title":"一种流行的细菌门CSP1-3的化学自养特性的见解,这里是Sysuimicrobiota。","authors":"Lan Liu, Zheng-Han Lian, Ai-Ping Lv, Nimaichand Salam, Jian-Chao Zhang, Meng-Meng Li, Wei-Min Sun, Sha Tan, Zhen-Hao Luo, Lei Gao, Yang Yuan, Yu-Zhen Ming, Yu-Ting OuYang, Yu-Xian Li, Ze-Tao Liu, Chao-Jian Hu, Ying Chen, Zheng-Shuang Hua, Wen-Sheng Shu, Brian P Hedlund, Wen-Jun Li, Jian-Yu Jiao","doi":"10.1093/nsr/nwae378","DOIUrl":null,"url":null,"abstract":"<p><p>Candidate bacterial phylum CSP1-3 has not been cultivated and is poorly understood. Here, we analyzed 112 CSP1-3 metagenome-assembled genomes and showed they are likely facultative anaerobes, with 3 of 5 families encoding autotrophy through the reductive glycine pathway (RGP), Wood-Ljungdahl pathway (WLP) or Calvin-Benson-Bassham (CBB), with hydrogen or sulfide as electron donors. Chemoautotrophic enrichments from hot spring sediments and fluorescence <i>in situ</i> hybridization revealed enrichment of six CSP1-3 genera, and both transcribed genes and DNA-stable isotope probing were consistent with proposed chemoautotrophic metabolisms. Ancestral state reconstructions showed that the ancestors of phylum CSP1-3 may have been acetogens that were autotrophic via the RGP, whereas the WLP and CBB were acquired by horizontal gene transfer. Our results reveal that CSP1-3 is a widely distributed phylum with the potential to contribute to the cycling of carbon, sulfur and nitrogen. The name <i>Sysuimicrobiota</i> phy. nov. is proposed.</p>","PeriodicalId":18842,"journal":{"name":"National Science Review","volume":"11 11","pages":"nwae378"},"PeriodicalIF":16.3000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11604079/pdf/","citationCount":"0","resultStr":"{\"title\":\"Insights into chemoautotrophic traits of a prevalent bacterial phylum CSP1-3, herein <i>Sysuimicrobiota</i>.\",\"authors\":\"Lan Liu, Zheng-Han Lian, Ai-Ping Lv, Nimaichand Salam, Jian-Chao Zhang, Meng-Meng Li, Wei-Min Sun, Sha Tan, Zhen-Hao Luo, Lei Gao, Yang Yuan, Yu-Zhen Ming, Yu-Ting OuYang, Yu-Xian Li, Ze-Tao Liu, Chao-Jian Hu, Ying Chen, Zheng-Shuang Hua, Wen-Sheng Shu, Brian P Hedlund, Wen-Jun Li, Jian-Yu Jiao\",\"doi\":\"10.1093/nsr/nwae378\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Candidate bacterial phylum CSP1-3 has not been cultivated and is poorly understood. Here, we analyzed 112 CSP1-3 metagenome-assembled genomes and showed they are likely facultative anaerobes, with 3 of 5 families encoding autotrophy through the reductive glycine pathway (RGP), Wood-Ljungdahl pathway (WLP) or Calvin-Benson-Bassham (CBB), with hydrogen or sulfide as electron donors. Chemoautotrophic enrichments from hot spring sediments and fluorescence <i>in situ</i> hybridization revealed enrichment of six CSP1-3 genera, and both transcribed genes and DNA-stable isotope probing were consistent with proposed chemoautotrophic metabolisms. Ancestral state reconstructions showed that the ancestors of phylum CSP1-3 may have been acetogens that were autotrophic via the RGP, whereas the WLP and CBB were acquired by horizontal gene transfer. Our results reveal that CSP1-3 is a widely distributed phylum with the potential to contribute to the cycling of carbon, sulfur and nitrogen. The name <i>Sysuimicrobiota</i> phy. nov. is proposed.</p>\",\"PeriodicalId\":18842,\"journal\":{\"name\":\"National Science Review\",\"volume\":\"11 11\",\"pages\":\"nwae378\"},\"PeriodicalIF\":16.3000,\"publicationDate\":\"2024-10-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11604079/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"National Science Review\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1093/nsr/nwae378\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"National Science Review","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1093/nsr/nwae378","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Insights into chemoautotrophic traits of a prevalent bacterial phylum CSP1-3, herein Sysuimicrobiota.
Candidate bacterial phylum CSP1-3 has not been cultivated and is poorly understood. Here, we analyzed 112 CSP1-3 metagenome-assembled genomes and showed they are likely facultative anaerobes, with 3 of 5 families encoding autotrophy through the reductive glycine pathway (RGP), Wood-Ljungdahl pathway (WLP) or Calvin-Benson-Bassham (CBB), with hydrogen or sulfide as electron donors. Chemoautotrophic enrichments from hot spring sediments and fluorescence in situ hybridization revealed enrichment of six CSP1-3 genera, and both transcribed genes and DNA-stable isotope probing were consistent with proposed chemoautotrophic metabolisms. Ancestral state reconstructions showed that the ancestors of phylum CSP1-3 may have been acetogens that were autotrophic via the RGP, whereas the WLP and CBB were acquired by horizontal gene transfer. Our results reveal that CSP1-3 is a widely distributed phylum with the potential to contribute to the cycling of carbon, sulfur and nitrogen. The name Sysuimicrobiota phy. nov. is proposed.
期刊介绍:
National Science Review (NSR; ISSN abbreviation: Natl. Sci. Rev.) is an English-language peer-reviewed multidisciplinary open-access scientific journal published by Oxford University Press under the auspices of the Chinese Academy of Sciences.According to Journal Citation Reports, its 2021 impact factor was 23.178.
National Science Review publishes both review articles and perspectives as well as original research in the form of brief communications and research articles.