Evidence map›Paper›PMID 40006937›Full record

ArticleViruses2025

Evaluation of Genomic Surveillance of SARS-CoV-2 Virus Isolates and Comparison of Mutational Spectrum of Variants in Bangladesh.

Abeda Sultana, Laila Anjuman Banu, Mahmud Hossain, Nahid Azmin, Nurun Nahar Nila, Sharadindu Kanti Sinha, Zahid Hassan

Abstract read
In one paragraph

Article in Viruses, 2025. 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
–field-weighted citation impact
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. 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

7 authors.

Abeda SultanaDepartment of Anatomy, Dhaka Medical College, Dhaka 1000, Bangladesh.
Laila Anjuman BanuDepartment of Anatomy, Dhaka Medical College, Dhaka 1000, Bangladesh.ORCID 0000-0003-4409-9009
Mahmud HossainLaboratory of Neuroscience and Neurogenetics, Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka 1000, Bangladesh.ORCID 0000-0003-2342-3404
Nahid AzminDepartment of Anatomy, Shahabuddin Medical College, Dhaka 1212, Bangladesh.
Nurun Nahar NilaLaboratory of Neuroscience and Neurogenetics, Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka 1000, Bangladesh.
Sharadindu Kanti SinhaDepartment of Pharmacology, Bangabandhu Sheikh Mujib Medical University, Dhaka 1000, Bangladesh.
Zahid HassanDepartment of Physiology and Molecular Biology, Bangladesh University of Health Sciences, Dhaka 1216, Bangladesh.

Funding

Integrated Health Science Research and Development Fund, The Ministry of Health, Government of Bangladesh; September, 2022
6 · The paper itself

Abstract

The SARS-CoV-2-induced disease, COVID-19, remains a worldwide public health concern due to its high rate of transmission, even in vaccinated and previously infected people. In the endemic state, it continues to cause significant pathology. To elu- cidate the viral mutational changes and screen the emergence of new variants of concern, we conducted this study in Bangladesh. The viral RNA genomes extracted from 25 ran- domly collected samples of COVID-19-positive patients from March 2021 to February 2022 were sequenced using Illumina COVID Seq protocol and genomic data processing, as well as evaluations performed in DRAGEN COVID Lineage software. In this study, the percentage of Delta, Omicron, and Mauritius variants identified were 88%, 8%, and 4%, respectively. All of the 25 samples had 23,403 A>G (D614G, S gene), 3037 C>T (nsp3), and 14,408 C>T (nsp12) mutations, where 23,403 A>G was responsible for increased transmis- sion. Omicron had the highest number of unique mutations in the spike protein (i.e., sub- stitutions, deletions, and insertions), which may explain its higher transmissibility and immune-evading ability than Delta. A total of 779 mutations were identified, where 691 substitutions, 85 deletions, and 3 insertion mutations were observed. To sum up, our study will enrich the genomic database of SARS-CoV-2, aiding in treatment strategies along with understanding the virus's preferences in both mutation type and mutation site for predicting newly emerged viruses' survival strategies and thus for preparing to coun- teract them.

Indexed as

COVID-19Genome, ViralMutationSARS-CoV-2BangladeshGenomicsHumansPhylogenyRNA, ViralSpike Glycoprotein, CoronavirusRNA, ViralSpike Glycoprotein, CoronavirusBangladeshCOVID-19DeltaMauritiusmutationOmicronSARS-CoV-2

Identifiers

PMID40006937
PMCPMC11860708

What OpenQuestion holds

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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.