Validating the Cyc2 Neutrophilic Iron Oxidation Pathway Using Meta-omics of Zetaproteobacteria Iron Mats at Marine Hydrothermal Vents

被引:54
作者
Mcallister, Sean M. [1 ]
Polson, Shawn W. [2 ]
Butterfield, David A. [3 ,4 ]
Glazer, Brian T. [5 ]
Sylvan, Jason B. [6 ]
Chan, Clara S. [1 ,7 ]
机构
[1] Univ Delaware, Sch Marine Sci & Policy, Newark, DE 19716 USA
[2] Univ Delaware, Ctr Bioinformat & Computat Biol, Newark, DE USA
[3] Univ Washington, Joint Inst Study Atmosphere & Ocean, Seattle, WA 98195 USA
[4] NOAA, Pacific Marine Environm Lab, 7600 Sand Point Way Ne, Seattle, WA 98115 USA
[5] Univ Hawaii, Dept Oceanog, Honolulu, HI 96822 USA
[6] Texas A&M Univ, Dept Oceanog, College Stn, TX 77843 USA
[7] Univ Delaware, Dept Earth Sci, Newark, DE 19716 USA
关键词
Cyc2 Fe oxidation pathway; biogeochemistry; environmental microbiology; hydrothermal vent; iron cycling; iron oxidizers; metagenomics; metatranscriptomics; microbial ecology; Zetaproteobacteria; ACIDITHIOBACILLUS-FERROOXIDANS; GENE-EXPRESSION; MICROBIAL MATS; GENOME; COMMUNITY; DIVERSITY; INSIGHTS; COVERAGE; OXIDASE; PROTEIN;
D O I
10.1128/mSystems.00553-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Zetaproteobacteria create extensive iron (Fe) oxide mats at marine hydrothermal vents, making them an ideal model for microbial Fe oxidation at circumneutral pH. Comparison of neutrophilic Fe oxidizer isolate genomes has revealed a hypothetical Fe oxidation pathway, featuring a homolog of the Fe oxidase Cyc2 from Acidithiobacillus ferrooxidans. However, Cyc2 function is not well verified in neutrophilic Fe oxidizers, particularly in Fe-oxidizing environments. Toward this, we analyzed genomes and metatranscriptomes of Zetaproteobacteria, using 53 new high-quality metagenome-assembled genomes reconstructed from Fe mats at MidAtlantic Ridge, Mariana Backarc, and Loihi Seamount (Hawaii) hydrothermal vents. Phylogenetic analysis demonstrated conservation of Cyc2 sequences among most neutrophilic Fe oxidizers, suggesting a common function. We confirmed the widespread distribution of cyc2 and other model Fe oxidation pathway genes across all represented Zetaproteobacteria lineages. High expression of these genes was observed in diverse Zetaproteobacteria under multiple environmental conditions and in incubations. The putative Fe oxidase gene cyc2 was highly expressed in situ, often as the top expressed gene. The cyc2 gene showed increased expression in Fe(II)amended incubations, with corresponding increases in carbon fixation and central metabolism gene expression. These results substantiate the Cyc2-based Fe oxidation pathway in neutrophiles and demonstrate its significance in marine Fe-mineralizing environments. IMPORTANCE Iron oxides are important components of our soil, water supplies, and ecosystems, as they sequester nutrients, carbon, and metals. Microorganisms can form iron oxides, but it is unclear whether this is a significant mechanism in the environment. Unlike other major microbial energy metabolisms, there is no marker gene for iron oxidation, hindering our ability to track these microbes. Here, we investigate a promising possible iron oxidation gene, cyc2, in iron-rich hydrothermal vents, where iron-oxidizing microbes dominate. We pieced together diverse Zetaproteobacteria genomes, compared these genomes, and analyzed expression of cyc2 and other hypothetical iron oxidation genes. We show that cyc2 is widespread among iron oxidizers and is highly expressed and potentially regulated, making it a good marker for the capacity for iron oxidation and potentially a marker for activity. These findings will help us understand and potentially quantify the impacts of neutrophilic iron oxidizers in a wide variety of marine and terrestrial environments.
引用
收藏
页数:17
相关论文
共 75 条
  • [1] Alneberg J, 2014, NAT METHODS, V11, P1144, DOI [10.1038/NMETH.3103, 10.1038/nmeth.3103]
  • [2] [Anonymous], VALIDATING CYC2 NEUT
  • [3] [Anonymous], THESIS
  • [4] [Anonymous], SUBSEAFLOOR BIOSPHER
  • [5] In-situ incubation of iron-sulfur mineral reveals a diverse chemolithoautotrophic community and a new biogeochemical role for Thiomicrospira
    Barco, Roman A.
    Hoffman, Colleen L.
    Ramirez, Gustavo A.
    Toner, Brandy M.
    Edwards, Katrina J.
    Sylvan, Jason B.
    [J]. ENVIRONMENTAL MICROBIOLOGY, 2017, 19 (03) : 1322 - 1337
  • [6] New Insight into Microbial Iron Oxidation as Revealed by the Proteomic Profile of an Obligate Iron-Oxidizing Chemolithoautotroph
    Barco, Roman A.
    Emerson, David
    Sylvan, Jason B.
    Orcutt, Beth N.
    Meyers, Myrna E. Jacobson
    Ramirez, Gustavo A.
    Zhong, John D.
    Edwards, Katrina J.
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2015, 81 (17) : 5927 - 5937
  • [7] Benson DA, 2013, NUCLEIC ACIDS RES, V41, pD36, DOI [10.1093/nar/gks1195, 10.1093/nar/gkp1024, 10.1093/nar/gkr1202, 10.1093/nar/gkq1079, 10.1093/nar/gkn723, 10.1093/nar/gkl986, 10.1093/nar/gkw1070, 10.1093/nar/gkg057, 10.1093/nar/gkx1094]
  • [8] Trimmomatic: a flexible trimmer for Illumina sequence data
    Bolger, Anthony M.
    Lohse, Marc
    Usadel, Bjoern
    [J]. BIOINFORMATICS, 2014, 30 (15) : 2114 - 2120
  • [9] A precision multi-sampler for deep-sea hydrothermal microbial mat studies
    Breier, J. A.
    Gomez-Ibanez, D.
    Reddington, E.
    Huber, J. A.
    Emerson, D.
    [J]. DEEP-SEA RESEARCH PART I-OCEANOGRAPHIC RESEARCH PAPERS, 2012, 70 : 83 - 90
  • [10] BLAST plus : architecture and applications
    Camacho, Christiam
    Coulouris, George
    Avagyan, Vahram
    Ma, Ning
    Papadopoulos, Jason
    Bealer, Kevin
    Madden, Thomas L.
    [J]. BMC BIOINFORMATICS, 2009, 10