A complementary metaproteomic approach to interrogate microbiome cultivated from clinical colon biopsies

Author:

Duong Van‐An1ORCID,Enkhbayar Altai2,Bhasin Nobel3,Senavirathna Lakmini1,Preisner Eva C.4,Hoffman Kristi L.4,Shukla Richa3,Jenq Robert R.25,Cheng Kai6,Bronner Mary P.7,Figeys Daniel6ORCID,Britton Robert A.4,Pan Sheng12,Chen Ru3

Affiliation:

1. The Brown Foundation Institute of Molecular Medicine McGovern Medical School, The University of Texas Health Science Center at Houston Houston Texas USA

2. The University of Texas MD Anderson Cancer Center UTHealth Houston Graduate School of Biomedical Sciences Houston Texas USA

3. Department of Medicine Baylor College of Medicine Houston Texas USA

4. Department of Molecular Virology and Microbiology Baylor College of Medicine Houston Texas USA

5. Department of Genomic Medicine, Division of Cancer Medicine The University of Texas MD Anderson Cancer Center Houston Texas USA

6. School of Pharmaceutical Sciences, Faculty of Medicine University of Ottawa Ottawa Ontario Canada

7. Department of Pathology University of Utah Salt Lake City USA

Abstract

AbstractThe human gut microbiome plays a vital role in preserving individual health and is intricately involved in essential functions. Imbalances or dysbiosis within the microbiome can significantly impact human health and are associated with many diseases. Several metaproteomics platforms are currently available to study microbial proteins within complex microbial communities. In this study, we attempted to develop an integrated pipeline to provide deeper insights into both the taxonomic and functional aspects of the cultivated human gut microbiomes derived from clinical colon biopsies. We combined a rapid peptide search by MSFragger against the Unified Human Gastrointestinal Protein database and the taxonomic and functional analyses with Unipept Desktop and MetaLab‐MAG. Across seven samples, we identified and matched nearly 36,000 unique peptides to approximately 300 species and 11 phyla. Unipept Desktop provided gene ontology, InterPro entries, and enzyme commission number annotations, facilitating the identification of relevant metabolic pathways. MetaLab‐MAG contributed functional annotations through Clusters of Orthologous Genes and Non‐supervised Orthologous Groups categories. These results unveiled functional similarities and differences among the samples. This integrated pipeline holds the potential to provide deeper insights into the taxonomy and functions of the human gut microbiome for interrogating the intricate connections between microbiome balance and diseases.

Funder

National Institutes of Health

Publisher

Wiley

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