Analysis of rumen microbial community in cattle through the integration of metagenomic and network-based approaches

A better understanding of the composition of rumen microbial communities and the association between host genetic and microbial activities has important applications and implication in bioscience. Being capable of revealing the full extent of microbial gene diversity, metagenomics-based approaches hold great promises in this endeavor. This study investigates the rumen microbial community in cattle through the integration of metagenomic and network-based approaches. Based on the relative abundance of 1570 microbial genes identified in a metagenomics analysis, the co-abundance network was constructed and functional modules of microbial genes were identified. One of the main contributions of this study is to develop a random matrix theory-based approach to automatically determine the correlation threshold used to construct the co-abundance network. It has been shown that the network exhibits a highly modular structure with each of the three main modules well separated. The involvement of KEGG pathways in each module was analysed. A close look at the abundance profiles highlights that Module B is strongly associated with methane emissions while Module C is highly enriched with microbial genes associated with feed conversion efficiency.

[1]  Fidel Ramírez,et al.  Computing topological parameters of biological networks , 2008, Bioinform..

[2]  Pradip K. Srimani,et al.  Application of Random Matrix Theory to Analyze Biological Data , 2011 .

[3]  Mick Watson,et al.  Bovine Host Genetic Variation Influences Rumen Microbial Methane Production with Best Selection Criterion for Low Methane Emitting and Efficiently Feed Converting Hosts Based on Metagenomic Gene Abundance , 2016, PLoS genetics.

[4]  Cynthia M. Lakon,et al.  How Correlated Are Network Centrality Measures? , 2008, Connections.

[5]  Peter H. Janssen,et al.  Structure of the Archaeal Community of the Rumen , 2008, Applied and Environmental Microbiology.

[6]  B. Eynard,et al.  Random matrices. , 2015, 1510.04430.

[7]  A. Gessner,et al.  Analyses of Intestinal Microbiota: Culture versus Sequencing. , 2015, ILAR journal.

[8]  Feng Luo,et al.  Constructing gene co-expression networks and predicting functions of unknown genes by random matrix theory , 2007, BMC Bioinformatics.

[9]  M. P. Bryant,et al.  Bacterial species of the rumen. , 1959, Bacteriological reviews.

[10]  Giovanni Scardoni,et al.  Analyzing biological network parameters with CentiScaPe , 2009, Bioinform..

[11]  Feng Luo,et al.  Molecular ecological network analyses , 2012, BMC Bioinformatics.

[12]  J. Handelsman Metagenomics: Application of Genomics to Uncultured Microorganisms , 2004, Microbiology and Molecular Biology Reviews.

[13]  A. Barabasi,et al.  Network biology: understanding the cell's functional organization , 2004, Nature Reviews Genetics.

[14]  Mick Watson,et al.  The rumen microbial metagenome associated with high methane production in cattle , 2015, BMC Genomics.

[15]  Eugene L. Madsen,et al.  Comparative Survey of Rumen Microbial Communities and Metabolites across One Caprine and Three Bovine Groups, Using Bar-Coded Pyrosequencing and 1H Nuclear Magnetic Resonance Spectroscopy , 2012, Applied and Environmental Microbiology.

[16]  Yannick Malevergne,et al.  Collective origin of the coexistence of apparent random matrix theory noise and of factors in large sample correlation matrices , 2002, cond-mat/0210115.

[17]  S. Tringe,et al.  Metagenomic Discovery of Biomass-Degrading Genes and Genomes from Cow Rumen , 2011, Science.

[18]  Julien Boccard,et al.  Rumen microbial communities influence metabolic phenotypes in lambs , 2015, Front. Microbiol..

[19]  Min Wang,et al.  Erratum: Rumen microbial community composition varies with diet and host, but a core microbiome is found across a wide geographical range , 2016, Scientific Reports.

[20]  E. Wigner On the Distribution of the Roots of Certain Symmetric Matrices , 1958 .

[21]  Jukka-Pekka Onnela,et al.  Community Structure in Time-Dependent, Multiscale, and Multiplex Networks , 2009, Science.

[22]  Jens Möhring,et al.  Changes in Rumen Microbial Community Composition during Adaption to an In Vitro System and the Impact of Different Forages , 2016, PloS one.

[23]  Gemma Henderson,et al.  Determining the culturability of the rumen bacterial microbiome , 2014, Microbial biotechnology.

[24]  P. Shannon,et al.  Cytoscape: a software environment for integrated models of biomolecular interaction networks. , 2003, Genome research.

[25]  Huiru Zheng,et al.  Integrating Omic Data with a Multiplex Network-based Approach for the Identification of Cancer Subtypes. , 2016, IEEE transactions on nanobioscience.

[26]  S. Denman,et al.  Recent developments in nucleic acid based techniques for use in rumen manipulation , 2009 .

[27]  Georgios A. Pavlopoulos,et al.  Metagenomics: Tools and Insights for Analyzing Next-Generation Sequencing Data Derived from Biodiversity Studies , 2015, Bioinformatics and biology insights.