Evidence map›Paper›PMID 35749403›Full record

ArticlePloS one2022

Evaluation of a commercial SARS-CoV-2 multiplex PCR genotyping assay for variant identification in resource-scarce settings.

Chijioke N Umunnakwe, Zinhle N Makatini, Mathapelo Maphanga, Anele Mdunyelwa, Khamusi M Mlambo, Puseletso Manyaka, Monique Nijhuis, Annemarie Wensing, Hugo A Tempelman

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

9 authors.

Chijioke N UmunnakweNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.ORCID 0000-0001-5879-8658
Zinhle N MakatiniNdlovu Research Consortium, Dennilton, Limpopo Province, South Africa.
Mathapelo MaphangaNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.
Anele MdunyelwaNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.
Khamusi M MlamboNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.
Puseletso ManyakaNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.
Monique NijhuisNdlovu Research Consortium, Dennilton, Limpopo Province, South Africa.
Annemarie WensingNdlovu Research Consortium, Dennilton, Limpopo Province, South Africa.
Hugo A TempelmanNdlovu Research Centre and Laboratories, Dennilton, Limpopo Province, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapid emergence and spread of numerous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants across the globe underscores the crucial need for continuous SARS-CoV-2 surveillance to ensure that potentially more pathogenic variants are detected early and contained. Whole genome sequencing (WGS) is currently the gold standard for COVID-19 surveillance; however, it remains cost-prohibitive and requires specialized technical skills. To increase surveillance capacity, especially in resource-scarce settings, supplementary methods that are cost- and time-effective are needed. Real-time multiplex PCR genotyping assays offer an economical and fast solution for screening circulating and emerging variants while simultaneously complementing existing WGS approaches. In this study we evaluated the AllplexTM SARS-CoV-2 Variants II multiplex real-time PCR genotyping assay, Seegene (South Korea), and implemented it in retrospectively characterizing circulating SARS-CoV-2 variants in a rural South African setting between April and October 2021, prior to the emergence of the Omicron variant in South Africa. The AllplexTM SARS-CoV-2 Variants II real-time PCR assay demonstrated perfect concordance with whole-genome sequencing in detecting Beta and Delta variants and exhibited high specificity, sensitivity and reproducibility. Implementation of the assay in characterization of SARS-CoV-2 variants between April and October 2021 in a rural South African setting revealed a rapid shift from the Beta to the Delta variant between April and June. All specimens successfully genotyped in April were Beta variants and the Delta variant was not detected until May. By June, 78% of samples genotyped were Delta variants and in July >95% of all genotyped samples were Delta variants. The Delta variant continued to predominate through to the end of our analysis in October 2021. Taken together, a commercial SARS-CoV-2 variant genotyping assay detected the rapid rate at which the Delta variant displaced the Beta variant in Limpopo, an under-monitored province in South Africa. Such assays provide a quick and cost-effective method of monitoring circulating variants and should be used to complement genomic sequencing for COVID-19 surveillance especially in resource-scarce settings.

Indexed as

COVID-19SARS-CoV-2GenotypeHumansMultiplex Polymerase Chain ReactionReproducibility of ResultsRetrospective Studies

Identifiers

PMID35749403
PMCPMC9231807

What OpenQuestion holds

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Registered trials

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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.