Evidence map›Paper›PMID 34122366›Full record

ArticleFrontiers in microbiology2021

Respiratory Co-Infections: Modulators of SARS-CoV-2 Patients' Clinical Sub-Phenotype.

Priyanka Mehta, Shweta Sahni, Samreen Siddiqui, Neha Mishra, Pooja Sharma, Sachin Sharma, Akansha Tyagi, Partha Chattopadhyay, A Vivekanand, Priti Devi and 17 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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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

27 authors at 4 institutions in 1 country.

Priyanka MehtaGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Shweta SahniGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Samreen SiddiquiMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Neha MishraGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Pooja SharmaGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Sachin SharmaGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Akansha TyagiMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Partha ChattopadhyayGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
A VivekanandGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Priti DeviGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Azka KhanGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Swati WaghdhareMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Sandeep BudhirajaMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Bharathram UppiliGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Ranjeet MauryaGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Vivek NangiaMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Uzma ShamimGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Pranjal P HazarikaMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Saruchi WadhwaGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Nishu TyagiGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Arun DewanMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Bansidhar TaraiMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Poonam DasMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Mohammed FaruqGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Anurag AgrawalGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Sujeet JhaMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, New Delhi, India.
Rajesh PandeyGenomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India.
Institute of Genomics and Integrative Biology · INMax Super Speciality Hospital · INAcademy of Scientific and Innovative Research · INMax Healthcare · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-infection with ancillary pathogens is a significant modulator of morbidity and mortality in infectious diseases. There have been limited reports of co-infections accompanying SARS-CoV-2 infections, albeit lacking India specific study. The present study has made an effort toward elucidating the prevalence, diversity and characterization of co-infecting respiratory pathogens in the nasopharyngeal tract of SARS-CoV-2 positive patients. Two complementary metagenomics based sequencing approaches, Respiratory Virus Oligo Panel (RVOP) and Holo-seq, were utilized for unbiased detection of co-infecting viruses and bacteria. The limited SARS-CoV-2 clade diversity along with differential clinical phenotype seems to be partially explained by the observed spectrum of co-infections. We found a total of 43 bacteria and 29 viruses amongst the patients, with 18 viruses commonly captured by both the approaches. In addition to SARS-CoV-2, Human Mastadenovirus, known to cause respiratory distress, was present in a majority of the samples. We also found significant differences of bacterial reads based on clinical phenotype. Of all the bacterial species identified, ∼60% have been known to be involved in respiratory distress. Among the co-pathogens present in our sample cohort, anaerobic bacteria accounted for a preponderance of bacterial diversity with possible role in respiratory distress.

Indexed as

anaerobic bacteriaco-infectionCOVID-19holotranscriptomemetagenomicsrespiratory virusesRVOP

Identifiers

PMID34122366
PMCPMC8193731
OpenAlexW3169938151

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.