Evidence map›Paper›PMID 39915668›Full record

ArticleScientific reports2025

Pathogenic and periodontal bacteria may contribute to the fatal outcome of critically ill elderly COVID-19 patients.

L Johana Madroñero, Eliana P Calvo, Carolina Coronel-Ruiz, Myriam L Velandia-Romero, María Angélica Calderón-Peláez, Jhann A Arturo, Adriana P Franco-Rodríguez, Ricardo Gutiérrez-Pérez, Lady S López, Félix G Delgado and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

14 authors.

L Johana MadroñeroGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Eliana P CalvoGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia. calvoeliana@unbosque.edu.co.ORCID 0000-0002-9135-0748
Carolina Coronel-RuizGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Myriam L Velandia-RomeroGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
María Angélica Calderón-PeláezGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Jhann A ArturoGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Adriana P Franco-RodríguezClínica Meta, Villavicencio, Colombia.
Ricardo Gutiérrez-PérezClínica Meta, Villavicencio, Colombia.
Lady S LópezGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Félix G DelgadoGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Sigrid J Camacho-OrtegaGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Lilia J Bernal-CepedaGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Sonia P BohórquezGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.
Jaime E CastellanosGrupo de Virología, Vicerrectoría de Investigaciones, Universidad El Bosque, Bogotá, Colombia.

Funding

Colombian Ministry of Sciences and Technology Contract 377-2020; Grant 1308101577416
6 · The paper itself

Abstract

Some studies suggest that the respiratory microbiome of COVID-19 patients differs from that of healthy individuals, infected patients may have reduced diversity and increased levels of opportunistic bacteria, however, the role of the microbiome in fatal SARS-CoV-2 infection remains poorly understood. Our study aimed to determine whether there are differences in the respiratory microbiome between patients who recovered from COVID-19 and those who died, by characterizing the bacterial communities of both groups. A total of 24 patients who recovered from COVID-19 and 24 who died were included in the study, patient data were analyzed for signs, symptoms and clinical variables. Airway samples were collected and the 16 S rRNA variable regions V3-V4 were amplified and sequenced using the Illumina MiSeq platform. Elevated levels of blood urea nitrogen, creatinine and lactate dehydrogenase, and higher frequencies of cardiovascular disease, diabetes mellitus and renal disease were observed in patients with a fatal outcome. Compared to patients who recovered from COVID-19, patients who died exhibited a microbiome enriched in periodontal and pathogenic bacteria such as Klebsiella pneumoniae. Our results highlighted a dual relationship between SARS CoV-2 infection and an exacerbated periodontopathogen-induced immune response.

Indexed as

BacteriaCOVID-19MicrobiotaAgedAged, 80 and overCritical IllnessFemaleHumansMaleMiddle AgedSARS-CoV-216S rRNA sequencingCOVID-19Fatal outcomeMicrobiomeSARS CoV-2Severe disease

Identifiers

PMID39915668
PMCPMC11802917

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.