Performance of a Shotgun Prediction Model for Colorectal Cancer When Using 16S rRNA Sequencing Data

Author:

Ramon Elies12,Obón-Santacana Mireia123,Khannous-Lleiffe Olfat45,Saus Ester45ORCID,Gabaldón Toni4567ORCID,Guinó Elisabet123,Bars-Cortina David12,Ibáñez-Sanz Gemma128ORCID,Rodríguez-Alonso Lorena8,Mata Alfredo9,García-Rodríguez Ana10ORCID,Moreno Victor12311ORCID

Affiliation:

1. Colorectal Cancer Group, ONCOBELL Program, Institut de Recerca Biomedica de Bellvitge (IDIBELL), L’Hospitalet de Llobregat, 08908 Barcelona, Spain

2. Unit of Biomarkers and Suceptibility (UBS), Oncology Data Analytics Program (ODAP), Catalan Institute of Oncology (ICO), L’Hospitalet del Llobregat, 08908 Barcelona, Spain

3. Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), 28029 Madrid, Spain

4. Barcelona Supercomputing Centre (BSC-CNS), 08034 Barcelona, Spain

5. Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain

6. Catalan Institution for Research and Advanced Studies (ICREA), 08010 Barcelona, Spain

7. Centro de Investigación Biomédica En Red de Enfermedades Infecciosas (CIBERINFEC), 08028 Barcelona, Spain

8. Gastroenterology Department, Bellvitge University Hospital, L’Hospitalet de Llobregat, 08907 Barcelona, Spain

9. Digestive System Service, Moisés Broggi Hospital, 08970 Sant Joan Despí, Spain

10. Endoscopy Unit, Digestive System Service, Viladecans Hospital-IDIBELL, 08840 Viladecans, Spain

11. Department of Clinical Sciences, Faculty of Medicine and Health Sciences, Universitat de Barcelona Institute of Complex Systems (UBICS), University of Barcelona (UB), L’Hospitalet de Llobregat, 08908 Barcelona, Spain

Abstract

Colorectal cancer (CRC), the third most common cancer globally, has shown links to disturbed gut microbiota. While significant efforts have been made to establish a microbial signature indicative of CRC using shotgun metagenomic sequencing, the challenge lies in validating this signature with 16S ribosomal RNA (16S) gene sequencing. The primary obstacle is reconciling the differing outputs of these two methodologies, which often lead to divergent statistical models and conclusions. In this study, we introduce an algorithm designed to bridge this gap by mapping shotgun-derived taxa to their 16S counterparts. This mapping enables us to assess the predictive performance of a shotgun-based microbiome signature using 16S data. Our results demonstrate a reduction in performance when applying the 16S-mapped taxa in the shotgun prediction model, though it retains statistical significance. This suggests that while an exact match between shotgun and 16S data may not yet be feasible, our approach provides a viable method for comparative analysis and validation in the context of CRC-associated microbiome research.

Funder

Instituto de Salud Carlos III

Spanish Association Against Cancer (AECC) Scientific Foundation

Fundació Marató TV3

Instituto de Salud Carlos III Sara Borrell

Spanish Ministerio de Universidades

Spanish Ministry of Science and Innovation

Catalan Research Agency

European Union’s Horizon 2020 research and innovation programme

Gordon and Betty Moore Foundation

“La Caixa” foundation

Plataforma Biobancos

Catalan Institute of Oncology

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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