期刊论文详细信息
Annals of Occupational and Environmental Medicine
Merging metagenomics and geochemistry reveals environmental controls on biological diversity and evolution
Jason Raymond1  Eric S Boyd2  Eric B Alsop1 
[1]School of Earth and Space Exploration, Arizona State University, ISTB4, Room 795, 781 E. Terrace Rd, Tempe, AZ 85287, USA
[2]Wisconsin Astrobiology Research Consortium, University of Wisconsin, Weeks Hall, Madison, WI 53706, USA
关键词: Markov clustering;    Geochemistry;    Hydrothermal ecosystems;    Microbial ecology;    Metagenomics;   
Others  :  834671
DOI  :  10.1186/1472-6785-14-16
 received in 2014-01-29, accepted in 2014-05-16,  发布年份 2014
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【 摘 要 】

Background

The metabolic strategies employed by microbes inhabiting natural systems are, in large part, dictated by the physical and geochemical properties of the environment. This study sheds light onto the complex relationship between biology and environmental geochemistry using forty-three metagenomes collected from geochemically diverse and globally distributed natural systems. It is widely hypothesized that many uncommonly measured geochemical parameters affect community dynamics and this study leverages the development and application of multidimensional biogeochemical metrics to study correlations between geochemistry and microbial ecology. Analysis techniques such as a Markov cluster-based measure of the evolutionary distance between whole communities and a principal component analysis (PCA) of the geochemical gradients between environments allows for the determination of correlations between microbial community dynamics and environmental geochemistry and provides insight into which geochemical parameters most strongly influence microbial biodiversity.

Results

By progressively building from samples taken along well defined geochemical gradients to samples widely dispersed in geochemical space this study reveals strong links between the extent of taxonomic and functional diversification of resident communities and environmental geochemistry and reveals temperature and pH as the primary factors that have shaped the evolution of these communities. Moreover, the inclusion of extensive geochemical data into analyses reveals new links between geochemical parameters (e.g. oxygen and trace element availability) and the distribution and taxonomic diversification of communities at the functional level. Further, an overall geochemical gradient (from multivariate analyses) between natural systems provides one of the most complete predictions of microbial taxonomic and functional composition.

Conclusions

Clustering based on the frequency in which orthologous proteins occur among metagenomes facilitated accurate prediction of the ordering of community functional composition along geochemical gradients, despite a lack of geochemical input. The consistency in the results obtained from the application of Markov clustering and multivariate methods to distinct natural systems underscore their utility in predicting the functional potential of microbial communities within a natural system based on system geochemistry alone, allowing geochemical measurements to be used to predict purely biological metrics such as microbial community composition and metabolism.

【 授权许可】

   
2014 Alsop et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Allen EE, Banfield JF: Community genomics in microbial ecology and evolution. Nat Rev Microbiol 2005, 3:489-498.
  • [2]DeLong EF, Preston CM, Mincer T, Rich V, Hallam SJ, Frigaard N-U, Martinez A, Sullivan MB, Edwards R, Brito BR, Chisholm SW, Karl DM: Community genomics among stratified microbial assemblages in the ocean’s interior. Science 2006, 311:496-503.
  • [3]Kunin V, Raes J, Harris JK, Spear JR, Walker JJ, Ivanova N, von Mering C, Bebout BM, Pace NR, Bork P, Hugenholtz P: Millimeter-scale genetic gradients and community-level molecular convergence in a hypersaline microbial mat. Mol Syst Biol 2008, 4:198.
  • [4]Little AEF, Robinson CJ, Peterson SB, Raffa KF, Handelsman J: Rules of engagement: interspecies interactions that regulate microbial communities. Annu Rev Microbiol 2008, 62:375-401.
  • [5]Hamilton TL, Koonce E, Howells A, Havig JR, Jewell T, De La Torre JR, Peters JW, Boyd ES: Competition for Ammonia Influences the Structure of Chemotrophic Communities in Geothermal Springs. Appl Environ Microbiol 2013, 80:653-661. No. 2
  • [6]Dinsdale EA, Edwards RA, Hall D, Angly F, Breitbart M, Brulc JM, Furlan M, Desnues C, Haynes M, Li L, McDaniel L, Moran MA, Nelson KE, Nilsson C, Olson R, Paul J, Brito BR, Ruan Y, Swan BK, Stevens R, Valentine DL, Thurber RV, Wegley L, White BA, Rohwer F: Functional metagenomic profiling of nine biomes. Nature 2008, 452:629-632.
  • [7]Gianoulis TA, Raes J, Patel PV, Bjornson R, Korbel JO, Letunic I, Yamada T, Paccanaro A, Jensen LJ, Snyder M, Bork P, Gerstein MB: Quantifying environmental adaptation of metabolic pathways in metagenomics. PNAS 2009, 106:1374-1379. No. 2
  • [8]Brock TD: Micro-organisms adapted to High Temperatures. Published online 1967, 214:882-885. doi:101038/214882a0
  • [9]Boyd ES, Hamilton TL, Spear JR, Lavin M, Peters JW: [FeFe]-hydrogenase in Yellowstone National Park: evidence for dispersal limitation and phylogenetic niche conservatism. ISME J 2010, 4:1485-1495.
  • [10]Hamilton TL, Lange RK, Boyd ES, Peters JW: Biological nitrogen fixation in acidic high-temperature geothermal springs in Yellowstone National Park, Wyoming. Environ Microbiol 2011, 13:2204-2215.
  • [11]Cox A, Shock EL, Havig JR: The transition to microbial photosynthesis in hot spring ecosystems. Chem Geol 2011, 280:344-351.
  • [12]Boyd ES, Fecteau KM, Havig JR, Shock EL, Peters JW: Modeling the Habitat Range of Phototrophs in Yellowstone National Park: Toward the Development of a Comprehensive Fitness Landscape. Front Microbiol 2012, 3:221.
  • [13]Tyson GW, Chapman J, Hugenholtz P, Allen EE, Ram RJ, Richardson PM, Solovyev VV, Rubin EM, Rokhsar DS, Banfield JF: Community structure and metabolism through reconstruction of microbial genomes from the environment. Nature 2004, 428:37-43.
  • [14]Venter JC, Remington K, Heidelberg JF, Halpern AL, Rusch D, Eisen JA, Wu D, Paulsen I, Nelson KE, Nelson W, Fouts DE, Levy S, Knap AH, Lomas MW, Nealson K, White O, Peterson J, Hoffman J, Parsons R, Baden-Tillson H, Pfannkoch C, Rogers Y-H, Smith HO: Environmental Genome Shotgun Sequencing of the Sargasso Sea. Science 2004, 304:66-74.
  • [15]Van Dongen SM: Graph clustering by flow simulation. 2000.
  • [16]Enright AJ, Van Dongen S, Ouzounis CA: An efficient algorithm for large-scale detection of protein families. Nucleic Acids Res 2002, 30:1575-1584.
  • [17]Swingley WD, Blankenship RE, Raymond J: Integrating Markov Clustering and Molecular Phylogenetics to Reconstruct the Cyanobacterial Species Tree from Conserved Protein Families. Mol Biol Evol 2008, 25:643-654.
  • [18]Shih Y-K, Parthasarathy S: Identifying functional modules in interaction networks through overlapping Markov clustering. Bioinformatics 2012, 28:i473-i479.
  • [19]Tanaseichuk O, Borneman J, Jiang T: Separating metagenomic short reads into genomes via clustering. Algorithms Mol Biol 2012, 7:27. BioMed Central Full Text
  • [20]Klatt CG, Wood JM, Rusch DB, Bateson MM, Hamamura N, Heidelberg JF, Grossman AR, Bhaya D, Cohan FM, Kühl M, Bryant DA, Ward DM: Community ecology of hot spring cyanobacterial mats: predominant populations and their functional potential. ISME J 2011, 5:1262-1278.
  • [21]Yamada T, Waller AS, Raes J, Zelezniak A, Perchat N, Perret A, Salanoubat M, Patil KR, Weissenbach J, Bork P: Prediction and identification of sequences coding for orphan enzymes using genomic and metagenomic neighbours. Mol Syst Biol 2012, 8:581.
  • [22]Fukami-Kobayashi K, Tomoda S, Gō M: Evolutionary clustering and functional similarity of RNA-binding proteins. FEBS Lett 1993, 335:289-293.
  • [23]Tatusov RL, Koonin EV, Lipman DJ: A Genomic Perspective on Protein Families. Science 1997, 278:631-637.
  • [24]Swingley WD, Meyer-Dombard DR, Shock EL, Alsop EB, Falenski HD, Havig JR, Raymond J: Coordinating Environmental Genomics and Geochemistry Reveals Metabolic Transitions in a Hot Spring Ecosystem. PLoS One 2012, 7:e38108.
  • [25]Inskeep WP: The YNP Metagenome Project: Environmental Parameters Responsible for Microbial Distribution in the Yellowstone Geothermal Ecosystem. Front Microbiol 2013, 4:67.
  • [26]Grigoriev IV, Nordberg H, Shabalov I, Aerts A, Cantor M, Goodstein D, Kuo A, Minovitsky S, Nikitin R, Ohm RA, Otillar R, Poliakov A, Ratnere I, Riley R, Smirnova T, Rokhsar D, Dubchak I: The Genome Portal of the Department of Energy Joint Genome Institute. Nucl Acids Res 2011, 40:D25-32.
  • [27]Inskeep WP, Klatt CG: Community Structure and Function of High-temperature Chlorophototrophic Microbial Mats Inhabiting Diverse Geothermal Environments. Front Microbiol 2013, 4:106.
  • [28]Inskeep WP: Phylogenetic and functional analysis of metagenome sequence from high-temperature archaeal habitats demonstrate linkages between metabolic potential and geochemistry. Front Microbiol 2013, 4:95.
  • [29]Inskeep WP, Takacs Vesbach C: Metagenome Sequence Analysis of Filamentous Microbial Communities Obtained from Geochemically Distinct Geothermal Channels Reveals Specialization of Three Aquificales Lineages. Front Microbiol 2013, 4:84.
  • [30]Boyd ES, Wang J, He L: The role of tetraether lipid composition in the adaptation of thermophilic archaea to acidity. Front Microbiol 2013, 4:62.
  • [31]Pearson A, Pi Y, Zhao W, Li W, Li Y, Inskeep W, Perevalova A, Romanek C, Li S, Zhang CL: Factors Controlling the Distribution of Archaeal Tetraethers in Terrestrial Hot Springs. Appl Environ Microbiol 2008, 74:3523-3532.
  • [32]Shock EL, Holland M, Meyer-Dombard D, Amend JP, Osburn GR, Fischer TP: Quantifying inorganic sources of geochemical energy in hydrothermal ecosystems, Yellowstone National Park, USA. Geochim Cosmochim Acta 2010, 74:4005-4043.
  • [33]Mantel N, Haenszel W: Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959, 22:719-748.
  • [34]Turnbaugh PJ, Hamady M, Yatsunenko T, Cantarel BL, Duncan A, Ley RE, Sogin ML, Jones WJ, Roe BA, Affourtit JP, Egholm M, Henrissat B, Heath AC, Knight R, Gordon JI: A core gut microbiome in obese and lean twins. Nature 2009, 457:480-484.
  • [35]Toulza E, Tagliabue A, Blain S, Piganeau G: Analysis of the Global Ocean Sampling (GOS) Project for Trends in Iron Uptake by Surface Ocean Microbes. PLoS One 2012, 7(2):e30931.
  • [36]Sharpton TJ, Riesenfeld SJ, Kembel SW, Ladau J, O’Dwyer JP, Green JL, Eisen JA, Pollard KS: PhylOTU: A High-Throughput Procedure Quantifies Microbial Community Diversity and Resolves Novel Taxa from Metagenomic Data. PLoS Comput Biol 2011, 7:e1001061.
  • [37]Zak JC, Willig MR, Moorhead DL, Wildman HG: Functional diversity of microbial communities: A quantitative approach. Soil Biol Biochem 1994, 26:1101-1108.
  • [38]Brown JH, Gillooly JF, Allen AP, Savage VM, West GB: TOWARD A METABOLIC THEORY OF ECOLOGY. Ecology 2004, 85:1771-1789.
  • [39]Lozupone C, Knight R: UniFrac: a New Phylogenetic Method for Comparing Microbial Communities. Appl Environ Microbiol 2005, 71:8228-8235.
  • [40]Valentine DL: Adaptations to energy stress dictate the ecology and evolution of the Archaea. Nat Rev Micro 2007, 5:316-323.
  • [41]Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. J Mol Biol 1990, 215:403-410.
  • [42]Felsenstein J: PHYLIP - Phylogeny Inference Package (Version 3.2). Cladistics 1989, 5:164-166.
  • [43]Stajich JE, Block D, Boulez K, Brenner SE, Chervitz SA, Dagdigian C, Fuellen G, Gilbert JGR, Korf I, Lapp H, Lehväslaiho H, Matsalla C, Mungall CJ, Osborne BI, Pocock MR, Schattner P, Senger M, Stein LD, Stupka E, Wilkinson MD, Birney E: The Bioperl Toolkit: Perl Modules for the Life Sciences. Genome Res 2002, 12:1611-1618.
  • [44]Development Core Team: R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing; 2005.
  • [45]Dixon P: VEGAN, a package of R functions for community ecology. J Veg Sci 2003, 14:927-930.
  • [46]Kanehisa M, Goto S: KEGG: Kyoto Encyclopedia of Genes and Genomes. Nucl Acids Res 2000, 28:27-30.
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