Evidence map›Paper›PMID 35325013›Full record

ArticlePLoS pathogens2022

Mice infected with Mycobacterium tuberculosis are resistant to acute disease caused by secondary infection with SARS-CoV-2.

Oscar Rosas Mejia, Erin S Gloag, Jianying Li, Marisa Ruane-Foster, Tiffany A Claeys, Daniela Farkas, Shu-Hua Wang, Laszlo Farkas, Gang Xin, Richard T Robinson

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Crosstalk betweenFrontiers in immunology · 2026
    Article
  6. Review
  7. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Protective interplay:Frontiers in immunology · 2024
    Article
  18. Diverse interactions ofFrontiers in tuberculosis · 2024
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Oscar Rosas MejiaDepartment of Microbial Infection and Immunity.
Erin S GloagDepartment of Microbial Infection and Immunity.
Jianying LiPelotonia Institute for Immuno-Oncology.
Marisa Ruane-FosterDepartment of Microbial Infection and Immunity.
Tiffany A ClaeysDepartment of Microbial Infection and Immunity.
Daniela FarkasDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Davis Heart and Lung Research Institute.
Shu-Hua WangDepartment of Infectious Disease, The Ohio State University, Columbus, Ohio, United States of America.
Laszlo FarkasDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Davis Heart and Lung Research Institute.
Gang XinDepartment of Microbial Infection and Immunity.
Richard T RobinsonDepartment of Microbial Infection and Immunity.ORCID 0000-0002-4699-515X
Sutter Davis Hospital · USThe Ohio State University · US

Funding

Regulation of human IL12/IL23 responsiveness by IL12RB1R01AI121212 · NIAID · OHIO STATE UNIVERSITY · PI ROBINSON, RICHARD · 2016 to 2020
$1.9M
American Heart Association-American Stroke AssociationNIAID NIH HHS R01 AI121212
6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb) and SARS-CoV-2 (CoV2) are the leading causes of death due to infectious disease. Although Mtb and CoV2 both cause serious and sometimes fatal respiratory infections, the effect of Mtb infection and its associated immune response on secondary infection with CoV2 is unknown. To address this question we applied two mouse models of COVID19, using mice which were chronically infected with Mtb. In both model systems, Mtb-infected mice were resistant to the pathological consequences of secondary CoV2 infection, and CoV2 infection did not affect Mtb burdens. Single cell RNA sequencing of coinfected and monoinfected lungs demonstrated the resistance of Mtb-infected mice is associated with expansion of T and B cell subsets upon viral challenge. Collectively, these data demonstrate that Mtb infection conditions the lung environment in a manner that is not conducive to CoV2 survival.

Indexed as

CoinfectionCOVID-19Mycobacterium tuberculosisAcute DiseaseAnimalsMiceMice, Inbred C57BLSARS-CoV-2

Identifiers

PMID35325013
PMCPMC8946739
OpenAlexW4220966209

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.