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Differences in the bacteriome of swab, saliva, and tissue biopsies in oral cancer

  • Divya Gopinath
  • , Rohit Kunnath Menon
  • , Chong Chun Wie
  • , Moinak Banerjee
  • , Swagatika Panda
  • , Deviprasad Mandal
  • , Paresh Kumar Behera
  • , Susanta Roychoudhury
  • , Supriya Kheur
  • , Michael George Botelho
  • , Newell W. Johnson
  • Prince Philip Dental Hospital
  • International Medical University
  • Monash University Malaysia
  • Rajiv Gandhi Centre for Biotechnology
  • Siksha ‘O’ Anusandhan University
  • Head and Neck Oncology
  • Saroj Gupta Cancer Centre and Research Institute
  • Dr. D. Y. Patil Vidyapeeth, Pune
  • Griffith University Queensland
  • King's College London

Research output: Contribution to journalArticlepeer-review

56 Scopus citations

Abstract

Microbial dysbiosis has been implicated in the pathogenesis of oral cancer. We analyzed the compositional and metabolic profile of the bacteriome in three specific niches in oral cancer patients along with controls using 16SrRNA sequencing (Illumina Miseq) and DADA2 software. We found major differences between patients and control subjects. Bacterial communities associated with the tumor surface and deep paired tumor tissue differed significantly. Tumor surfaces carried elevated abundances of taxa belonging to genera Porphyromonas, Enterobacteriae, Neisseria, Streptococcus and Fusobacteria, whereas Prevotella, Treponema, Sphingomonas, Meiothermus and Mycoplasma genera were significantly more abundant in deep tissue. The most abundant microbial metabolic pathways were those related to fatty-acid biosynthesis, carbon metabolism and amino-acid metabolism on the tumor surface: carbohydrate metabolism and organic polymer degradation were elevated in tumor tissues. The bacteriome of saliva from patients with oral cancer differed significantly from paired tumor tissue in terms of community structure, however remained similar at taxonomic and metabolic levels except for elevated abundances of Streptococcus, Lactobacillus and Bacteroides, and acetoin-biosynthesis, respectively. These shifts to a pro-inflammatory profile are consistent with other studies suggesting oncogenic properties. Importantly, selection of the principal source of microbial DNA is key to ensure reliable, reproducible and comparable results in microbiome studies.

Original languageEnglish
Article number1181
JournalScientific Reports
Volume11
Issue number1
DOIs
StatePublished - Dec 2021
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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