Evidence map›Paper›PMID 34292313›Full record

ArticleThe Journal of experimental medicine2021

Single cell analysis of M. tuberculosis phenotype and macrophage lineages in the infected lung.

Davide Pisu, Lu Huang, Vipin Narang, Monique Theriault, Gabrielle Lê-Bury, Bernett Lee, Agnes E Lakudzala, David T Mzinza, David V Mhango, Steven C Mitini-Nkhoma and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 136 papers.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

136 citing papers in PubMed, 185 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. A specialized CD107aiScience · 2026
    Article
  5. Review
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  7. MakingCell insight · 2026
    Review
  8. Microbiology spectrum · 2026
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  9. mBio · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Diverse infection models demonstrate robust resistance ofbioRxiv : the preprint server for biology · 2026
    Article
  18. Article
  19. Review
  20. Modulation of Ferroptosis During EarlybioRxiv : the preprint server for biology · 2026
    Article

76 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 4 countries.

Davide PisuMicrobiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY.ORCID 0000-0001-5641-8877
Lu HuangMicrobiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY.ORCID 0000-0002-7820-2177
Vipin NarangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore.ORCID 0000-0001-8669-9964
Monique TheriaultMicrobiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY.ORCID 0000-0002-9502-3402
Gabrielle Lê-BuryMicrobiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY.ORCID 0000-0002-4650-5990
Bernett LeeSingapore Immunology Network, Agency for Science, Technology and Research, Singapore.ORCID 0000-0002-2709-1972
Agnes E LakudzalaMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0002-3013-9586
David T MzinzaMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0002-5999-8616
David V MhangoMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0001-7464-4261
Steven C Mitini-NkhomaMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0002-3276-6890
Kondwani C JamboMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0002-3195-2210
Amit SinghalSingapore Immunology Network, Agency for Science, Technology and Research, Singapore.ORCID 0000-0003-3913-8798
Henry C MwandumbaMalawi Liverpool Wellcome Trust Clinical Research Program, University of Malawi College of Medicine, Blantyre, Malawi.ORCID 0000-0003-4470-3608
David G RussellMicrobiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY.ORCID 0000-0002-9748-750X
University of Liverpool · GBCornell University · USAgency for Science, Technology and Research · SG

Funding

A mechanistic understanding of tuberculosis progression through bacterial reporter strainsR01AI134183 · NIAID · CORNELL UNIVERSITY · PI RUSSELL, DAVID G · 2017 to 2021
$3.5M
Lung immune function in human TB infection and its perturbation by HIV-1.R01AI155319 · NIAID · CORNELL UNIVERSITY · PI MWANDUMBA, HENRY CHARLES, RUSSELL, DAVID G · 2020 to 2024
$3.3M
Lung-Protective Mechanisms of Metformin in TBR01HL152078 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KORNFELD, HARDY, SINGHAL, AMIT · 2021 to 2024
$2.5M
Are HIV-1-Infected Alveolar Macrophages Productive Sites of Viral Persistence?R33AI136097 · NIAID · CORNELL UNIVERSITY · PI RUSSELL, DAVID G · 2020 to 2022
$1.2M
Are HIV-1-Infected Alveolar Macrophages Productive Sites of Viral Persistence?R21AI136097 · NIAID · CORNELL UNIVERSITY · PI RUSSELL, DAVID G · 2018 to 2019
$426k
Gates Foundation OPP1108452Medical Research Council MR/P020526/1Medical Research Council MR/T008822/1NHLBI NIH HHS R01 HL152078NIAID NIH HHS R01 AI134183NIAID NIH HHS R01 AI155319NIAID NIH HHS R21 AI136097NIAID NIH HHS R33 AI136097NIH HHS AI134183NIH HHS R01HL152078
6 · The paper itself

Abstract

In this study, we detail a novel approach that combines bacterial fitness fluorescent reporter strains with scRNA-seq to simultaneously acquire the host transcriptome, surface marker expression, and bacterial phenotype for each infected cell. This approach facilitates the dissection of the functional heterogeneity of M. tuberculosis-infected alveolar (AMs) and interstitial macrophages (IMs) in vivo. We identify clusters of pro-inflammatory AMs associated with stressed bacteria, in addition to three different populations of IMs with heterogeneous bacterial phenotypes. Finally, we show that the main macrophage populations in the lung are epigenetically constrained in their response to infection, while inter-species comparison reveals that most AMs subsets are conserved between mice and humans. This conceptual approach is readily transferable to other infectious disease agents with the potential for an increased understanding of the roles that different host cell populations play during the course of an infection.

Indexed as

AnimalsAntitubercular AgentsBronchoalveolar Lavage FluidCD11 AntigensEpigenesis, GeneticGene Expression Regulation, BacterialHemeHost-Pathogen InteractionsHumansLungMacrophages, AlveolarMiceMice, Inbred C57BLMicroorganisms, Genetically-ModifiedMycobacterium tuberculosisSequence Analysis, RNAAntitubercular AgentsCD11 AntigensHemeItgax protein, mouse

Identifiers

PMID34292313
PMCPMC8302446
OpenAlexW3185416158

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.