Viral communities in a pH>10 serpentinite-like environment: insight into diversity and potential roles in modulating the microbiomes by bioactive vitamin B 9 synthesis

Author:

He Yu1ORCID,Zhuo Shiyan1,Gao Donghao12,Pan Yue3,Li Meng45ORCID,Pan Jie45,Jiang Yongguang1,Hu Yidan1,Guo Jinzhi1,Lin Qin6,Sanford Robert A.7ORCID,Sun Weimin8,Shang Jianying39,Wei Na10,Peng Shuming11,Jiang Zhou1,Li Shuyi1,Li Yongzhe1,Dong Yiran1121314ORCID,Shi Liang11213ORCID

Affiliation:

1. School of Environmental Studies, China University of Geosciences, Wuhan, China

2. College of Life Sciences, Wuhan University, Wuhan, China

3. College of Land Science and Technology, China Agricultural University, Beijing, China

4. Archaeal Biology Center, Institute for Advanced Studies, Shenzhen University, Shenzhen, China

5. Shenzhen Key Laboratory of Marine Microbiome Engineering, Institute for Advanced Study, Shenzhen University, Shenzhen, China

6. Shanghai Biozeron Biological Technology Co. Ltd, China, Shanghai, China

7. Department of Earth Science & Environmental Change, University of Illinois Urbana-Champaign, Urbana, llinois, USA

8. Guangdong Institute of Eco-environmental and Soil Science, Guangdong, China

9. Key Laboratory of Arable Land Conservation in North China, Ministry of Agriculture and Rural Affairs, Beijing, China

10. Department of Civil and Environmental Engineering, University of Illinois Urbana-Champaign, Urbana, Illinois, USA

11. Institute of Ecological Environment, Chengdu University of Technology, Chengdu, China

12. State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), Wuhan, China

13. State Environmental Protection Key Laboratory of Source Apportionment and Control of Aquatic Pollution, Ministry of Ecology and Environment, Beijing, China

14. Hubei Key Laboratory of Yangtze Catchment Environmental Aquatic Science, Wuhan, China

Abstract

ABSTRACT Viral communities exist in a variety of ecosystems and play significant roles in mediating biogeochemical processes, whereas viruses inhabiting strongly alkaline geochemical systems remain underexplored. In this study, the viral diversity, potential functionalities, and virus–host interactions in a strongly alkaline environment (pH = 10.4–12.4) exposed to the leachates derived from the serpentinization-like reactions of smelting slags were investigated. The viral populations (e.g., Herelleviridae, Queuovirinae, and Inoviridae) were closely associated with the dominating prokaryotic hosts (e.g., Meiothermus , Trueperaceae, and Serpentinomonas ) in this ultrabasic environment. Auxiliary metabolic genes (AMGs) suggested that viruses may enhance hosts’ fitness by facilitating cofactor biosynthesis, hydrogen metabolism, and carbon cycling. To evaluate the activity of synthesis of essential cofactor vitamin B 9 by the viruses, a viral folA (v folA ) gene encoding dihydrofolate reductase (DHFR) was introduced into a thymidine-auxotrophic strain Escherichia coli MG1655 Δ folA mutant, which restored the growth of the latter in the absence of thymidine. Notably, the homologs of the validated vDHFR were globally distributed in the viromes across various ecosystems. The present study sheds new light on the unique viral communities in hyperalkaline ecosystems and their potential beneficial impacts on the coexisting microbial consortia by supplying essential cofactors. IMPORTANCE This study presents a comprehensive investigation into the diversity, potential functionalities, and virus–microbe interactions in an artificially induced strongly alkaline environment. Functional validation of the detected viral folA genes encoding dihydrofolate reductase substantiated the synthesis of essential cofactors by viruses, which may be ubiquitous, considering the broad distribution of the viral genes associated with folate cycling.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Chinese Central Government via China University of Gecsciences

Publisher

American Society for Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3