Evidence map›Paper›PMID 38206940›Full record

ArticlePloS one2024

The salivary microbiota of patients with acute lower respiratory tract infection-A multicenter cohort study.

Matthew B Rogers, Ashley Harner, Megan Buhay, Brian Firek, Barbara Methé, Alison Morris, Octavia M Peck Palmer, Susan B Promes, Robert L Sherwin, Lauren Southerland and 4 more

Erratum issuedOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Matthew B RogersUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0002-4958-8971
Ashley HarnerUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Megan BuhayUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Brian FirekUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Barbara MethéUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Alison MorrisUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Octavia M Peck PalmerUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0002-0169-6623
Susan B PromesPennsylvania State University, State College, Pennsylvania, United States of America.
Robert L SherwinWayne State University, Detroit, Michigan, United States of America.
Lauren SoutherlandThe Ohio State University Wexner Medical Center, Columbus, Ohio, United States of America.
Alexandre R VieiraUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0003-3392-6881
Sachin YendeUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Michael J MorowitzUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
David T HuangUniversity of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID 0000-0001-7649-1633
University of Pittsburgh · USPennsylvania State University · USThe Ohio State University Wexner Medical Center · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human microbiome contributes to health and disease, but the oral microbiota is understudied relative to the gut microbiota. The salivary microbiota is easily accessible, underexplored, and may provide insight into response to infections. We sought to determine the composition, association with clinical features, and heterogeneity of the salivary microbiota in patients with acute lower respiratory tract infection (LRTI). We conducted a multicenter prospective cohort study of 147 adults with acute LRTI presenting to the emergency department of seven hospitals in three states (Pennsylvania, Michigan, and Ohio) between May 2017 and November 2018. Salivary samples were collected in the emergency department, at days 2-5 if hospitalized, and at day 30, as well as fecal samples if patients were willing. We compared salivary microbiota profiles from patients to those of healthy adult volunteers by sequencing and analyzing bacterial 16-rRNA. Compared to healthy volunteers, the salivary microbiota of patients with LRTI was highly distinct and strongly enriched with intestinal anaerobes such as Bacteroidaceae, Ruminococcaceae, and Lachnospiraceae (e.g., mean 10% relative abundance of Bacteroides vs < 1% in healthy volunteers). Within the LRTI population, COPD exacerbation was associated with altered salivary microbiota composition compared to other LRTI conditions. The largest determinant of microbiota variation within the LRTI population was geography (city in which the hospital was located).

Indexed as

Gastrointestinal MicrobiomeMicrobiotaRespiratory Tract InfectionsAdultFecesHumansProspective StudiesRNA, Ribosomal, 16SRNA, Ribosomal, 16S

Identifiers

PMID38206940
PMCPMC10783762
OpenAlexW4390738502

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.