Evidence map›Paper›PMID 38090396›Full record

ArticleCureus2023

Genomic Characterization of an Emerging SARS-CoV-2 Variant During the Early Second Wave of the SARS-CoV-2 Pandemic in Maharashtra, India.

Rajesh P Karyakarte, Rashmita Das, Suvarna Joshi, Athira Jayaram, Sushma Yanamandra, Smriti Shende, Nyabom Taji, Srushti Rane, Reshma Bawale, Geetanjali P Chaudhari and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Cureus, 2023. 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
0.2field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Observational
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 at 1 institution in 1 country.

Rajesh P KaryakarteMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Rashmita DasMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Suvarna JoshiMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Athira JayaramMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Sushma YanamandraMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Smriti ShendeMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Nyabom TajiMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Srushti RaneMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Reshma BawaleMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Geetanjali P ChaudhariMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Bhagyashree KarekarMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Shivani R SakalkarMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Rahul G TiwariMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
Madhuri G JadhavMicrobiology, B. J. Government Medical College & Sassoon General Hospitals, Pune, IND.
B. J. Medical College & Sassoon Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has led to a global health crisis, with various variants emerging over time. In India, particularly in Maharashtra, a resurgence of cases and distinct transmission patterns have been observed. This study aimed to identify and characterize the circulating SARS-CoV-2 variants during the early second wave in Maharashtra, India. Materials and methods Nasopharyngeal swabs were collected from 24 RT-PCR-positive coronavirus disease of 2019 (COVID-19) cases across four districts of Maharashtra. Whole genome sequencing (WGS) was performed using the ARTIC amplicon sequencing protocol, and the data were analyzed. Results A total of 189 amino-acid mutations were identified across the 24 samples. Compared to the Indian genomes, 44 amino-acid mutations were unique to 24 genomes. Clade 20A was the most prevalent (66.66%), followed by 20B and 21B. The lineage B.1.36 (45.83%) was the most common, followed by B.1.617.1 (16.67%). The D614G mutation was the most frequent spike mutation (95.83%). Four samples from the Amravati district clustered distinctly under Clade 21B with spike mutations E154K in the N-terminal domain (NTD), L452R and E484Q in the receptor-binding domain (RBD) and P681R in proximity to the furin cleavage site. The temporal distribution of samples revealed the presence of Clade 21B in Maharashtra since the 31st of January 2021. Conclusion The study provides valuable insights into the circulating SARS-CoV-2 variants during the early second wave in Maharashtra, highlighting specific clades and mutations. The unique clustering patterns and the high prevalence of immune-escape mutations emphasize the need for continuous monitoring and genomic surveillance.

Indexed as

b.1.617.1clade 21bcovid-19e484qkappa variantl452rn440kp681rsars-cov-2 (severe acute respiratory syndrome coronavirus-2)sars-cov-2 whole-genome sequencing

Identifiers

PMID38090396
PMCPMC10711336
OpenAlexW4388568638

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.