Evidence map›Paper›PMID 35035953›Full record

ReviewTherapeutic advances in infectious disease

Lung microbiota dysbiosis and the implications of SARS-CoV-2 infection in pregnancy.

Henry C Ezechukwu, Cornelius A Diya, Ifunanya J Egoh, Mayowa J Abiodun, John-Ugwuanya A Grace, God'spower R Okoh, Kayode T Adu, Oyelola A Adegboye

Open access · goldAbstract readReview
In one paragraph

Review in Therapeutic advances in infectious disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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

8 authors at 4 institutions in 2 countries.

Henry C EzechukwuDepartment of Medical Biochemistry, Eko University of Medicine and Health Sciences, Ijanikin, Lagos, Nigeria.
Cornelius A DiyaDepartment of Medical Biochemistry, Eko University of Medicine and Health Sciences, Ijanikin, Lagos State, Nigeria.
Ifunanya J EgohDepartment of Virology, University of Ibadan, Ibadan, Nigeria.
Mayowa J AbiodunDepartment of Cell Biology, University of Lagos, Akoka, Lagos State, Nigeria.
John-Ugwuanya A GraceMedbury Medical Service, Ikeja, Lagos State, Nigeria.
God'spower R OkohCollege of Public Health, Medical and Veterinary Sciences, Division of Tropical Health and Medicine, James Cook University, Townsville, QLD, Australia.
Kayode T AduProbioWorld Consulting Group, James Cook University, Townsville, QLD, Australia.
Oyelola A AdegboyeAustralian Institute of Tropical Health and Medicine, James Cook University, Townsville, QLD 4811, Australia.ORCID https://orcid.org/0000-0002-9793-8024
Australian Institute of Tropical Health and Medicine · AUUniversity of Ibadan · NGUniversity of Lagos · NGWalter and Eliza Hall Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are a great number of beneficial commensal microorganisms constitutively colonizing the mucosal lining of the lungs. Alterations in the microbiota profile have been associated with several respiratory diseases such as pneumonia and allergies. Lung microbiota dysbiosis might play an important role in the pathogenic mechanisms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) as well as elicit other opportunistic infections associated with coronavirus disease 2019 (COVID-19). With its increasing prevalence and morbidity, SARS-CoV-2 infection in pregnant mothers is inevitable. Recent evidence shows that angiotensin-converting enzyme 2 (ACE2) and transmembrane protease serine 2 (TMPRSS2) act as an entry receptor and viral spike priming protein, respectively, for SARS-CoV-2 infection. These receptor proteins are highly expressed in the maternal-fetal interface, including the placental trophoblast, suggesting the possibility of maternal-fetal transmission. In this review, we discuss the role of lung microbiota dysbiosis in respiratory diseases, with an emphasis on COVID-19 and the possible implications of SARS-CoV-2 infection on pregnancy outcome and neonatal health.

Indexed as

COVID-19microbiomemicrobiota dysbiosispregnancy outcomeSARS-CoV-2

Identifiers

PMID35035953
PMCPMC8753069
OpenAlexW3184025682

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.