Evidence map›Paper›PMID 34811761›Full record

ReviewJournal of medical virology2022

Emerging SARS-CoV-2 variants can potentially break set epidemiological barriers in COVID-19.

Ashutosh Kumar, Rakesh Parashar, Sujeet Kumar, Muneeb A Faiq, Chiman Kumari, Maheswari Kulandhasamy, Ravi K Narayan, Rakesh K Jha, Himanshu N Singh, Pranav Prasoon and 2 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of medical virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 60 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

12 authors at 4 institutions in 3 countries.

Ashutosh KumarEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID http://orcid.org/0000-0003-1589-9568
Rakesh ParasharEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-2428-8622
Sujeet KumarEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0001-5427-8735
Muneeb A FaiqEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-1430-3139
Chiman KumariEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-9116-8380
Maheswari KulandhasamyEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-6769-2596
Ravi K NarayanEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0003-2510-6744
Rakesh K JhaEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0003-1292-5927
Himanshu N SinghEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0003-4111-5165
Pranav PrasoonEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-5035-3619
Sada N PandeyEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0003-3201-2287
Kamla KantEtiologically Elusive Disorders Research Network (EEDRN), New Delhi, India.ORCID https://orcid.org/0000-0002-8966-6268
Education and Research Network · INColumbia University Irving Medical Center · USOxford Policy Management · GBUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Young age, female sex, absence of comorbidities, and prior infection or vaccination are known epidemiological barriers for contracting the new infection and/or increased disease severity. Demographic trends from the recent coronavirus disease 2019 waves, which are believed to be driven by newer severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, indicate that the aforementioned epidemiological barriers are being breached and a larger number of younger and healthy individuals are developing severe disease. The new SARS-CoV-2 variants have key mutations that can induce significant changes in the virus-host interactions. Recent studies report that, some of these mutations, singly or in a group, enhance key mechanisms, such as binding of the receptor-binding domain (RBD) of the viral spike protein with the angiotensin-converting enzyme 2 (ACE2) receptor in the host-cells, increase the glycosylation of spike protein at the antigenic sites, and enhance the proteolytic cleavage of the spike protein, thus leading to improved host-cell entry and the replication of the virus. The putative changes in the virus-host interactions imparted by the mutations in the RBD sequence can potentially be the reason behind the breach of the observed epidemiological barriers. Susceptibility for contracting SARS-CoV-2 infection and the disease outcomes are known to be influenced by host-cell expressions of ACE2 and other proteases. The new variants can act more efficiently, and even with the lesser availability of the viral entry-receptor and the associated proteases, can have more efficient host-cell entry and greater replication resulting in high viral loads and prolonged viral shedding, widespread tissue-injury, and severe inflammation leading to increased transmissibility and lethality. Furthermore, the accumulating evidence shows that multiple new variants have reduced neutralization by both, natural and vaccine-acquired antibodies, indicating that repeated and vaccine breakthrough infections may arise as serious health concerns in the ongoing pandemic.

Indexed as

COVID-19Disease SusceptibilityHost-Pathogen InteractionsHumansImmune EvasionMutationSARS-CoV-2Spike Glycoprotein, CoronavirusVirus InternalizationVirus ReplicationSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19epidemiologymutationpandemicSARS-CoV-2 variantswaves

Identifiers

PMID34811761
PMCPMC9011477
OpenAlexW3216036304

What OpenQuestion holds

Textmetadata
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.