Evidence map›Paper›PMID 39472555›Full record

ArticleNature communications2024

Microbial dynamics and pulmonary immune responses in COVID-19 secondary bacterial pneumonia.

Natasha Spottiswoode, Alexandra Tsitsiklis, Victoria T Chu, Hoang Van Phan, Catherine DeVoe, Christina Love, Rajani Ghale, Joshua Bloomstein, Beth Shoshana Zha, Cole P Maguire and 17 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Host-Microbe Multiomic Profiling Predicts Mortality in Sepsis.American journal of respiratory and critical care medicine · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. PFKFB2-Driven Glycolysis Promotes Dendritic Cell Maturation and Exacerbates Acute Lung Injury.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. Article
  13. Review
  14. Review
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

27 authors.

Natasha Spottiswoode *Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0001-6157-3716
Alexandra Tsitsiklis *Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Victoria T ChuDepartment of Pediatrics, University of California, San Francisco, CA, USA.ORCID 0000-0002-7480-965X
Hoang Van PhanDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Catherine DeVoeDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-7861-274X
Christina LoveDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Rajani GhaleDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA.
Joshua BloomsteinDepartment of Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-7395-1910
Beth Shoshana ZhaDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-4190-2823
Cole P MaguireUniversity of Texas, Austin, TX, USA.ORCID 0000-0001-8986-9762
Abigail GlascockChan Zuckerberg Biohub San Francisco, San Francisco, CA, USA.
Aartik SarmaDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-7508-7345
Peter M MouraniDepartment of Pediatrics, Arkansas Children's, Little Rock, AR, USA.ORCID 0000-0002-1829-3775
Katrina L KalantarChan Zuckerberg Initiative, Redwood City, CA, USA.
Angela DetweilerChan Zuckerberg Biohub San Francisco, San Francisco, CA, USA.ORCID 0000-0001-7026-5467
Norma NeffChan Zuckerberg Biohub San Francisco, San Francisco, CA, USA.ORCID 0000-0001-7141-5420
Sidney C HallerDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.
COMET Consortium
Joseph L DeRisiChan Zuckerberg Biohub San Francisco, San Francisco, CA, USA.
David J ErleDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-2171-0648
Carolyn M HendricksonDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0003-4662-2385
Kirsten N KangelarisDepartment of Medicine, University of California, San Francisco, CA, USA.
Matthew F KrummelDepartment of Pathology, University of California, San Francisco, CA, USA.ORCID 0000-0001-7915-3533
Michael A MatthayDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0003-3039-8155
Prescott G WoodruffDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.
Carolyn S CalfeeDivision of Pulmonary, Department of Medicine, Critical Care, Allergy and Sleep Medicine, University of California, San Francisco, CA, USA.
Charles R LangelierDivision of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA, USA. chaz.langelier@ucsf.edu.ORCID 0000-0002-6708-4646

Funding

Understanding Asthma EndotypesU19AI077439 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PRESCOTT G WOODRUFF · 2008 to 2026
$41.1M
BIOLOGY OF INFECTIOUS DISEASES TRAINING PROGRAMT32AI007641 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHEW G DORSEY · 2000 to 2026
$6.9M
Precision Medicine in the Acute Respiratory Distress SyndromeR35HL140026 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2018 to 2024
$6.8M
Integrated Host/Microbe Metagenomics to Improve Lower Respiratory Tract Infection Diagnosis in Critically Ill ChildrenR01HL155418 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LANGELIER, CHARLES · 2021 to 2024
$1.6M
Evolution and resolution of ARDS molecular phenotypesK23HL163491 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Aartik Sarma · 2023 to 2026
$750k
Metagenomic surveillance of pathogen and antimicrobial resistance gene transmission in hospitalized neonatesK23AI185326 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHU, VICTORIA TIEN-YU · 2024 to 2025
$395k
Transcriptomic signatures of airway inflammation in acute respiratory diseasesF32HL151117 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SARMA, AARTIK · 2020 to 2022
$206k
NHLBI NIH HHS F32 HL151117NHLBI NIH HHS K23 HL163491NHLBI NIH HHS R01 HL155418NHLBI NIH HHS R35 HL140026NIAID NIH HHS K23 AI185326NIAID NIH HHS T32 AI007641NIAID NIH HHS U19 AI077439
6 · The paper itself

Abstract

Secondary bacterial pneumonia (2°BP) is associated with significant morbidity following respiratory viral infection, yet remains incompletely understood. In a prospective cohort of 112 critically ill adults intubated for COVID-19, we comparatively assess longitudinal airway microbiome dynamics and the pulmonary transcriptome of patients who developed 2°BP versus controls who did not. We find that 2°BP is significantly associated with both mortality and corticosteroid treatment. The pulmonary microbiome in 2°BP is characterized by increased bacterial RNA mass and dominance of culture-confirmed pathogens, detectable days prior to 2°BP clinical diagnosis, and frequently also present in nasal swabs. Assessment of the pulmonary transcriptome reveals suppressed TNFα signaling in patients with 2°BP, and sensitivity analyses suggest this finding is mediated by corticosteroid treatment. Further, we find that increased bacterial RNA mass correlates with reduced expression of innate and adaptive immunity genes in both 2°BP patients and controls. Taken together, our findings provide fresh insights into the microbial dynamics and host immune features of COVID-19-associated 2°BP, and suggest that suppressed immune signaling, potentially mediated by corticosteroid treatment, permits expansion of opportunistic bacterial pathogens.

Indexed as

COVID-19LungMicrobiotaPneumonia, BacterialSARS-CoV-2Adaptive ImmunityAdrenal Cortex HormonesAdultAgedFemaleHumansImmunity, InnateMaleMiddle AgedProspective StudiesRNA, BacterialAdrenal Cortex HormonesRNA, BacterialTumor Necrosis Factor-alpha

Identifiers

PMID39472555
PMCPMC11522429

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.