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The gut microbe pair of Oribacterium sp. GMB0313 and Ruminococcus sp. GMB0270 confers complete protection against SARS-CoV-2 infection by activating CD8+ T cell-mediated immunity

  • Mingda Wang
  • , Enkhchimeg Lkhagva
  • , Sura Kim
  • , Chongkai Zhai
  • , Md Minarul Islam
  • , Hyeon J. Kim*
  • , Seong Tshool Hong*
  • *Corresponding author for this work
  • Jeonbuk National University
  • Shandong First Medical University & Shandong Academy of Medical Sciences
  • Luoyang Polytechnic
  • The Lundquist Institute

Research output: Contribution to journalJournal articlepeer-review

Abstract

Despite the potential protective role of the gut microbiome against COVID-19, specific microbes conferring resistance to COVID-19 have not yet been identified. In this work, we aimed to identify and validate gut microbes at the species level that provide protection against SARS-CoV-2 infection. To identify gut microbes conferring protection against COVID-19, we conducted a fecal microbiota transplantation (FMT) from an individual with no history of COVID-19 infection or immunization into a lethal COVID-19 hamster model. FMT from this COVID-19-resistant donor resulted in significant phenotypic changes related to COVID-19 sensitivity in the hamsters. Metagenomic analysis revealed distinct differences in the gut microbiome composition among the hamster groups, leading to the identification of two previously unknown bacterial species: Oribacterium sp. GMB0313 and Ruminococcus sp. GMB0270, both associated with COVID-19 resistance. Subsequently, we conducted a proof-of-concept confirmation animal experiment adhering to Koch’s postulates. Oral administration of this gut microbe pair, Oribacterium sp. GMB0313 and Ruminococcus sp. GMB0270, to the hamsters provided complete protection against SARS-CoV-2 infection through the activation of CD8+ T cell mediated immunity. The prophylactic efficacy of the gut microbe pair against SARS-CoV-2 infection was comparable to, or even superior to, current mRNA vaccines. This strong prophylactic efficacy suggests that the gut microbe pair could be developed as a host-directed universal vaccine for all betacoronaviruses, including potential future emerging viruses.

Original languageEnglish
Article number2342497
JournalGut Microbes
Volume16
Issue number1
DOIs
StatePublished - 2024

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

Keywords

  • betacoronavirus
  • CD8+ T cell
  • COVID-19
  • gut microbiome
  • host-directed vaccine
  • SARS-CoV-2
  • universal vaccine

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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