Species-level functional profiling of metagenomes and metatranscriptomes

被引:1065
作者
Franzosa, Eric A. [1 ,2 ]
McIver, Lauren J. [1 ,2 ]
Rahnavard, Gholamali [1 ,2 ]
Thompson, Luke R. [3 ]
Schirmer, Melanie [1 ,2 ]
Weingart, George [1 ]
Lipson, Karen Schwarzberg [4 ]
Knight, Rob [3 ,5 ]
Caporaso, J. Gregory [4 ]
Segata, Nicola [6 ]
Huttenhower, Curtis [1 ,2 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[2] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[3] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[4] No Arizona Univ, Pathogen & Microbiome Inst, Flagstaff, AZ 86011 USA
[5] Univ Calif San Diego, Dept Comp Sci & Engn, San Diego, CA 92103 USA
[6] Univ Trento, Ctr Integrat Biol, Trento, Italy
关键词
MICROBIOME; DATABASE; DIVERSITY; ALIGNMENT; STRAINS; SEARCH; OMICS; GENE; TOOL;
D O I
10.1038/s41592-018-0176-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Functional profiles of microbial communities are typically generated using comprehensive metagenomic or metatranscriptomic sequence read searches, which are time-consuming, prone to spurious mapping, and often limited to community-level quantification. We developed HUMAnN2, a tiered search strategy that enables fast, accurate, and species-resolved functional profiling of host-associated and environmental communities. HUMAnN2 identifies a community's known species, aligns reads to their pangenomes, performs translated search on unclassified reads, and finally quantifies gene families and pathways. Relative to pure translated search, HUMAnN2 is faster and produces more accurate gene family profiles. We applied HUMAnN2 to study clinal variation in marine metabolism, ecological contribution patterns among human microbiome pathways, variation in species' genomic versus transcriptional contributions, and strain profiling. Further, we introduce 'contributional diversity' to explain patterns of ecological assembly across different microbial community types.
引用
收藏
页码:962 / +
页数:10
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