Evidence map›Paper›PMID 33727397›Full record

ArticlemSystems2021

Integrative Transkingdom Analysis of the Gut Microbiome in Antibiotic Perturbation and Critical Illness.

Bastiaan W Haak, Ricard Argelaguet, Cormac M Kinsella, Robert F J Kullberg, Jacqueline M Lankelma, Martin Deijs, Michelle Klein, Maarten F Jebbink, Floor Hugenholtz, Sarantos Kostidis and 9 more

Open access · goldAbstract read
In one paragraph

Article in mSystems, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.8field-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

47 citing papers in PubMed, 73 citations in OpenAlex.

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  10. The gastrointestinal microbiome in critical illness: A Clinician's guide to mechanisms, emerging tools, and therapeutic questions.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2025
    Review
  11. Butyrate-producing gut bacteriumThe European respiratory journal · 2025
    Article
  12. Article
  13. Anti-Anaerobic Antibiotics, Gut Microbiota, and Sepsis-associated Acute Kidney Injury.American journal of respiratory and critical care medicine · 2025
    Article
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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

19 authors at 4 institutions in 3 countries.

Bastiaan W Haak *Center for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands b.w.haak@amsterdamumc.nl.ORCID https://orcid.org/0000-0002-3903-5441
Ricard Argelaguet *European Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0003-3199-3722
Cormac M KinsellaLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Robert F J KullbergCenter for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.
Jacqueline M LankelmaCenter for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.
Martin DeijsLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Michelle KleinLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Maarten F JebbinkLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Floor HugenholtzCenter for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.
Sarantos KostidisCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, The Netherlands.
Martin GieraCenter for Proteomics and Metabolomics, Leiden University Medical Center, Leiden, The Netherlands.
Theodorus B M HakvoortTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Wouter J de JongeTytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Marcus J SchultzDepartment of Intensive Care, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Tom van GoolDepartment of Parasitology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
Tom van der PollCenter for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.
Willem M de VosLaboratory of Microbiology, Wageningen University, Wageningen, The Netherlands.
Lia M van der HoekLaboratory of Experimental Virology, Department of Medical Microbiology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.
W Joost WiersingaCenter for Experimental and Molecular Medicine, Amsterdam UMC, Location AMC, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.
Amsterdam University Medical Centers · NLLeiden University Medical Center · NLEuropean Bioinformatics Institute · GBUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial microbiota play a critical role in mediating local and systemic immunity, and shifts in these microbial communities have been linked to impaired outcomes in critical illness. Emerging data indicate that other intestinal organisms, including bacteriophages, viruses of eukaryotes, fungi, and protozoa, are closely interlinked with the bacterial microbiota and their host, yet their collective role during antibiotic perturbation and critical illness remains to be elucidated. We employed multi-omics factor analysis (MOFA) to systematically integrate the bacterial (16S rRNA), fungal (intergenic transcribed spacer 1 rRNA), and viral (virus discovery next-generation sequencing) components of the intestinal microbiota of 33 critically ill patients with and without sepsis and 13 healthy volunteers. In addition, we quantified the absolute abundances of bacteria and fungi using 16S and 18S rRNA PCRs and characterized the short-chain fatty acids (SCFAs) butyrate, acetate, and propionate using nuclear magnetic resonance spectroscopy. We observe that a loss of the anaerobic intestinal environment is directly correlated with an overgrowth of aerobic pathobionts and their corresponding bacteriophages as well as an absolute enrichment of opportunistic yeasts capable of causing invasive disease. We also observed a strong depletion of SCFAs in both disease states, which was associated with an increased absolute abundance of fungi with respect to bacteria. Therefore, these findings illustrate the complexity of transkingdom changes following disruption of the intestinal bacterial microbiome.

Indexed as

bacteriabacteriophagesdata integrationfungimicrobiomemulti-omics

Identifiers

PMID33727397
PMCPMC8546997
OpenAlexW3138763339

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.