4.8 Article

Functional sequencing read annotation for high precision microbiome analysis

Journal

NUCLEIC ACIDS RESEARCH
Volume 46, Issue 4, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkx1209

Keywords

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Funding

  1. NSF CAREER [1553289]
  2. TU Munchen - Institute for advanced study Hans Fischer fellowship
  3. German Excellence Initiative
  4. EU Seventh Framework Programme [291763]
  5. NIH/NIGMS [U01 GM115486]
  6. biobank popgen (German Ministry for Education and Research) [01EY1103]
  7. German Research Foundation (DFG) Excellence Cluster [306/2]
  8. German Federal Ministry of Education and Research (BMBF) project 'SysINFLAME' [01ZX1306A]
  9. German Research Foundation (DFG)
  10. Technical University of Munich
  11. Div Of Biological Infrastructure
  12. Direct For Biological Sciences [1553289] Funding Source: National Science Foundation

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The vast majority of microorganisms on Earth reside in often-inseparable environment-specific communities-microbiomes. Meta-genomic/transcriptomic sequencing could reveal the otherwise inaccessible functionality of micro-biomes. However, existing analytical approaches focus on attributing sequencing reads to known genes/genomes, often failing to make maximal use of available data. We created faser (functional annotation of sequencing reads), an algorithm that is optimized to map reads to molecular functions encoded by the read-correspondent genes. The mi-faser microbiome analysis pipeline, combining faser with our manually curated reference database of protein functions, accurately annotates microbiome molecular functionality. mi-faser's minutes-permicrobiome processing speed is significantly faster than that of other methods, allowing for large scale comparisons. Microbiome function vectors can be compared between different conditions to highlight environment-specific and/or time-dependent changes in functionality. Here, we identified previously unseen oil degradation-specific functions in BP oil-spill data, as well as functional signatures of individual-specific gut microbiome responses to a dietary intervention in children with Prader-Willi syndrome. Our method also revealed variability in Crohn's Disease patient microbiomes and clearly distinguished them from those of related healthy individuals. Our analysis highlighted themicrobiome role in CD pathogenicity, demonstrating enrichment of patient microbiomes in functions that promote inflammation and that help bacteria survive it.

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