Parvimonas micra can translocate from the subgingival sulcus of the human oral cavity to colorectal adenocarcinoma

Author:

Conde‐Pérez Kelly1ORCID,Buetas Elena2ORCID,Aja‐Macaya Pablo1,Martin‐De Arribas Elsa3,Iglesias‐Corrás Iago3,Trigo‐Tasende Noelia1,Nasser‐Ali Mohammed1,Estévez Lara S.4,Rumbo‐Feal Soraya1,Otero‐Alén Begoña4,Noguera Jose F.5,Concha Ángel4,Pardiñas‐López Simón6,Carda‐Diéguez Miguel2,Gómez‐Randulfe Igor7,Martínez‐Lago Nieves7,Ladra Susana3,Aparicio Luis A.7,Bou Germán1,Mira Alex2ORCID,Vallejo Juan A.1ORCID,Poza Margarita18ORCID

Affiliation:

1. meiGAbiome, Microbiology Research Group, Servicio de Microbiología Center for Advanced Scientific Research (CICA), Institute of Biomedical Research (INIBIC), University Hospital of A Coruña (HUAC), University of A Coruña (UDC), CIBER of Infectious Diseases (CIBERINFEC‐ISCIII), Hospital Universitario Spain

2. Genomic and Health Department FISABIO Foundation, Center for Advanced Research in Public Health Valencia Spain

3. Database Laboratory Research Center for Information and Communication Technologies (CITIC), University of A Coruña (UDC), Campus de Elviña Spain

4. Pathological Anatomy Service and Biobank University Hospital of A Coruña (HUAC), Institute of Biomedical Research (INIBIC), Hospital Universitario Spain

5. General and Digestive Surgery Service University Hospital of A Coruña (HUAC), Hospital Universitario Spain

6. Periodontology and Oral Surgery Pardiñas Medical Dental Clinic, Cell Therapy and Regenerative Medicine Group, Institute of Biomedical Research (INIBIC) A Coruña Spain

7. Medical Oncology Department University Hospital of A Coruña (HUAC), Maternal and Child Hospital Spain

8. Microbiome and Health Group, Faculty of Sciences University of A Coruña (UDC), Campus da Zapateira Spain

Abstract

Oral and intestinal samples from a cohort of 93 colorectal cancer (CRC) patients and 30 healthy controls (non‐CRC) were collected for microbiome analysis. Saliva (28 non‐CRC and 94 CRC), feces (30 non‐CRC and 97 CRC), subgingival fluid (20 CRC), and tumor tissue samples (20 CRC) were used for 16S metabarcoding and/or RNA sequencing (RNAseq) approaches. A differential analysis of the abundance, performed with the ANCOM‐BC package, adjusting the P‐values by the Holm‐Bonferroni method, revealed that Parvimonas was significantly over‐represented in feces from CRC patients (P‐value < 0.001) compared to healthy controls. A total of 11 Parvimonas micra isolates were obtained from the oral cavity and adenocarcinoma of CRC patients. Genome analysis identified a pair of isolates from the same patient that shared 99.2% identity, demonstrating that P. micra can translocate from the subgingival cavity to the gut. The data suggest that P. micra could migrate in a synergistic consortium with other periodontal bacteria. Metatranscriptomics confirmed that oral bacteria were more active in tumor than in non‐neoplastic tissues. We suggest that P. micra could be considered as a CRC biomarker detected in non‐invasive samples such as feces.

Funder

Fundación Científica Asociación Española Contra el Cáncer

Instituto de Salud Carlos III

Ministerio de Ciencia e Innovación

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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