Evidence map›Paper›PMID 36679850›Full record

ArticleVaccines2022

Genomic Tracking of SARS-CoV-2 Variants in Myanmar.

Khine Zaw Oo, Zaw Win Htun, Nay Myo Aung, Ko Ko Win, Kyaw Zawl Linn, Sett Paing Htoo, Phyo Kyaw Aung, Thet Wai Oo, Myo Thiha Zaw, Linn Yuzana Ko and 3 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2022. 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
0.1field-weighted citation impact, top 53% 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. 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

13 authors at 1 institution in 1 country.

Khine Zaw OoDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.ORCID 0000-0003-0383-7730
Zaw Win HtunDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Nay Myo AungDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Ko Ko WinDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Kyaw Zawl LinnDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Sett Paing HtooDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.ORCID 0000-0003-1908-565X
Phyo Kyaw AungDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Thet Wai OoDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Myo Thiha ZawDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Linn Yuzana KoDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Kyaw Myo TunDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Kyee MyintDefence Services Medical Research Centre, Biological Toxin Research Department, Nay Pyi Taw 15021, Myanmar.
Ko Ko LwinDirectorate of Medical Services, Nay Pyi Taw 15013, Myanmar.
Myanmar Oxford Clinical Research Unit · MM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In December 2019, the COVID-19 disease started in Wuhan, China. The WHO declared a pandemic on 12 March 2020, and the disease started in Myanmar on 23 March 2020. In December 2020, different variants were brought worldwide, threatening global health. To counter those threats, Myanmar started the COVID-19 variant surveillance program in late 2020. Whole genome sequencing was done six times between January 2021 and March 2022. Among them, 83 samples with a PCR threshold cycle of less than 25 were chosen. Then, we used MiSeq FGx for sequencing and Illumina DRAGEN COVIDSeq pipeline, command line interface, GISAID, and MEGA version 7 for data analysis. In January 2021, no variant was detected. The second run, during the rise of cases in June 2021, showed Alpha, Delta, and Kappa variants. The third and the fourth runs in August and December showed only a Delta variant. Omicron and Delta variants were detected during the fifth run in January 2022. The sixth run in March 2022 showed only Omicron BA.2. Amino acid mutation at the receptor binding domain of Spike glycoprotein started since the second run coupling with high transmission, recurrence, and vaccine escape. We also found the mutation at the primer targets used in current RT-PCR platforms, but there was no mutation at the existing antiviral drug targets. The occurrence of multiple variants and mutations claimed vigilance at ports of entry and preparedness for effective control measures. Genomic surveillance with the observation of evolutionary data is required to predict imminent threats of the current disease and diagnose emerging infectious diseases.

Indexed as

COVID-19MyanmarSARS-CoV-2sequencingvariant

Identifiers

PMID36679850
PMCPMC9862072
OpenAlexW4313502933

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.