Evidence map›Paper›PMID 38496464›Full record

ArticleResearch square2024

Major alteration of Lung Microbiome and the Host Reaction in critically ill COVID-19 Patients with high viral load.

Ingrid G Bustos, Rosana Wiscovitch-Russo, Harinder Singh, Benjamín L Sievers, Michele Matsuoka, Marcelo Freire, Gene S Tan, Mónica P Cala, Jose L Guerrero, Ignacio Martin-Loeches and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2024. 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 4 countries.

Ingrid G BustosUniversidad de la Sabana.
Rosana Wiscovitch-RussoJ Craig Venter Institute.
Harinder SinghJ Craig Venter Institute.
Benjamín L SieversJ Craig Venter Institute.
Michele MatsuokaJ Craig Venter Institute.
Marcelo FreireJ Craig Venter Institute.
Gene S TanJ Craig Venter Institute.
Mónica P CalaMetCore- Metabolomics Core Facility, Universidad de Los Andes.
Jose L GuerreroMetCore- Metabolomics Core Facility, Universidad de Los Andes.
Ignacio Martin-LoechesSt James's Hospital.
Norberto Gonzalez-JuarbeJ Craig Venter Institute.
Luis Felipe ReyesUniversidad de la Sabana.
J. Craig Venter Institute · USUniversidad de La Sabana · CO

Funding

Endolysins as tools to eradicate pneumococcal biofilms and development ofprotective immunityR01AI168313 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI Norberto Gonzalez-Juarbe · 2023 to 2026
$3.5M
Microbiome in Asthma Induced by Environmental Particle ExposureR01ES030227 · NIEHS · J. CRAIG VENTER INSTITUTE, INC. · PI FEDULOV, ALEXEY V, GONZALEZ-JUARBE, NORBERTO · 2019 to 2023
$3.4M
Development of novel protein-based vaccine formulations to prevent pneumococcal colonization and diseaseR21AI148722 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI GONZALEZ-JUARBE, NORBERTO · 2020 to 2021
$542k
NIAID NIH HHS R01 AI168313NIAID NIH HHS R21 AI148722NIEHS NIH HHS R01 ES030227
6 · The paper itself

Abstract

Background: Patients with COVID-19 under invasive mechanical ventilation are at higher risk of developing ventilator-associated pneumonia (VAP), associated with increased healthcare costs, and unfavorable prognosis. The underlying mechanisms of this phenomenon have not been thoroughly dissected. Therefore, this study attempted to bridge this gap by performing a lung microbiota analysis and evaluating the host immune responses that could drive the development of VAP. Materials and methods: In this prospective cohort study, mechanically ventilated patients with confirmed SARS-CoV-2 infection were enrolled. Nasal swabs (NS), endotracheal aspirates (ETA), and blood samples were collected initially within 12 hours of intubation and again at 72 hours post-intubation. Plasma samples underwent cytokine and metabolomic analyses, while NS and ETA samples were sequenced for lung microbiome examination. The cohort was categorized based on the development of VAP. Data analysis was conducted using RStudio version 4.3.1. Results: In a study of 36 COVID-19 patients on mechanical ventilation, significant differences were found in the nasal and pulmonary microbiome, notably in Conclusions: This study reveals a critical link between respiratory microbiome alterations and ventilator-associated pneumonia in COVID-19 patients, with elevated SARS-CoV-2 levels and metabolic changes, providing novel insights into the underlying mechanisms of VAP with potential management and prevention implications.

Indexed as

COVID-19CytokinesMechanical VentilationMetabolomeMicrobiotamicrobiota-virus-disease interactions

Identifiers

PMID38496464
PMCPMC10942552
OpenAlexW4392598305

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.