Evidence map›Paper›PMID 35262080›Full record

ArticlebioRxiv : the preprint server for biology2022

Gut microbiome dysbiosis during COVID-19 is associated with increased risk for bacteremia and microbial translocation.

Mericien Venzon, Lucie Bernard-Raichon, Jon Klein, Jordan E Axelrad, Chenzhen Zhang, Grant A Hussey, Alexis P Sullivan, Arnau Casanovas-Massana, Maria G Noval, Ana M Valero-Jimenez and 15 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 15 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 3 institutions in 1 country.

Mericien VenzonVilcek Institute of Graduate Biomedical Sciences, New York University Grossman School of Medicine, New York, NY, USA.
Lucie Bernard-RaichonKimmel Center for Biology and Medicine at the Skirball Institute, New York University Grossman School of Medicine, New York, NY, USA.
Jon KleinDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
Jordan E AxelradDivision of Gastroenterology, Department of Medicine, New York University Grossman School of Medicine, New York, NY, USA.
Chenzhen ZhangInstitute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA.
Grant A HusseyInstitute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA.
Alexis P SullivanInstitute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA.
Arnau Casanovas-MassanaDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
Maria G NovalDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Ana M Valero-JimenezDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Juan GagoVilcek Institute of Graduate Biomedical Sciences, New York University Grossman School of Medicine, New York, NY, USA.
Gregory PutzelDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Alejandro PirontiDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Evan WilderDivision of Gastroenterology, Department of Medicine, New York University Grossman School of Medicine, New York, NY, USA.
Yale IMPACT Research Team
Lorna E ThorpeDepartment of Population Health, New York University Grossman School of Medicine, New York, NY, USA.
Dan R LittmanKimmel Center for Biology and Medicine at the Skirball Institute, New York University Grossman School of Medicine, New York, NY, USA.
Meike DittmannDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Kenneth A StaplefordDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Bo ShopsinDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Victor J TorresDepartment of Microbiology, New York University Grossman School of Medicine, New York, NY, USA.
Albert I KoDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
Akiko IwasakiDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
Ken CadwellKimmel Center for Biology and Medicine at the Skirball Institute, New York University Grossman School of Medicine, New York, NY, USA.
Jonas SchluterInstitute for Systems Genetics, New York University Grossman School of Medicine, New York, NY, USA.
New York University · USYale University · USHoward Hughes Medical Institute · US

Funding

OTA-21-015A Post-Acute Sequelae of SARS-CoV-2 Infection Initiative: NYU Langone Health Clinical Science Core, Data Resource Core, and PASC Biorepository CoreOT2HL161847 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI GROSS, RACHEL SHARON, HORWITZ, LEORA · 2021 to 2025
$651.0M
Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Lewis Possemato · 1985 to 2026
$83.1M
Diabetes, Digestive, and Kidney Diseases Extramural ResearchR01DK093668 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 2011 to 2026
$7.3M
Redefining the role of autophagy in bacterial diseaseR01AI121244 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 2017 to 2026
$5.6M
The role of autophagy gene Atg16L1 in allogeneic hematopoietic stem cell transplantation - Resubmission - 1R01HL123340 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA, VAN DEN BRINK, MARCEL R M · 2015 to 2022
$5.2M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Mechanisms of MRSA intestinal colonizationR01AI140754 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SHOPSIN, BO · 2020 to 2024
$3.5M
Interactions between helminth colonization and the gut microbiotaR01AI130945 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA · 2018 to 2022
$3.3M
The unleashed microbiome of cancer patients as a discovery platform for rational microbiome engineeringDP2AI164318 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SCHLUTER, JONAS · 2021 to 2025
$2.5M
ELF1 - Molecular mechanisms of a novel transcription factor with broad antiviral activityR01AI143639 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WEISER, JEFFREY NEAL · 2019 to 2023
$2.5M
Mechanisms of fungal involvement during intestinal diseaseR01DK124336 · NIDDK · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2020 to 2023
$1.8M
NCATS NIH HHS UL1 TR001863NCI NIH HHS P30 CA016087NHLBI NIH HHS OT2 HL161847NHLBI NIH HHS R01 HL123340NIAID NIH HHS DP2 AI164318NIAID NIH HHS R01 AI121244NIAID NIH HHS R01 AI130945NIAID NIH HHS R01 AI140754NIAID NIH HHS R01 AI143639NIAID NIH HHS R21 AI139374NIAID NIH HHS T32 AI100853NIDDK NIH HHS R01 DK093668NIDDK NIH HHS R01 DK124336NIH HHS S10 OD021747
6 · The paper itself

Abstract

The microbial populations in the gut microbiome have recently been associated with COVID-19 disease severity. However, a causal impact of the gut microbiome on COVID-19 patient health has not been established. Here we provide evidence that gut microbiome dysbiosis is associated with translocation of bacteria into the blood during COVID-19, causing life-threatening secondary infections. Antibiotics and other treatments during COVID-19 can potentially confound microbiome associations. We therefore first demonstrate in a mouse model that SARS-CoV-2 infection can induce gut microbiome dysbiosis, which correlated with alterations to Paneth cells and goblet cells, and markers of barrier permeability. Comparison with stool samples collected from 96 COVID-19 patients at two different clinical sites also revealed substantial gut microbiome dysbiosis, paralleling our observations in the animal model. Specifically, we observed blooms of opportunistic pathogenic bacterial genera known to include antimicrobial-resistant species in hospitalized COVID-19 patients. Analysis of blood culture results testing for secondary microbial bloodstream infections with paired microbiome data obtained from these patients indicates that bacteria may translocate from the gut into the systemic circulation of COVID-19 patients. These results are consistent with a direct role for gut microbiome dysbiosis in enabling dangerous secondary infections during COVID-19.

Identifiers

PMID35262080
PMCPMC8902880
OpenAlexW3177555480

What OpenQuestion holds

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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.