Evidence map›Paper›PMID 35598737›Full record

ArticleInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2022

Whole-genome sequencing of SARS-CoV-2 reveals diverse mutations in circulating Alpha and Delta variants during the first, second, and third waves of COVID-19 in South Kivu, east of the Democratic Republic of the Congo.

Patrick Bisimwa Ntagereka, Samuel O Oyola, Simon Patrick Baenyi, Gilbert Kibet Rono, Ahadi Bwihangane Birindwa, Dieudonné Wasso Shukuru, Tshass Chasinga Baharanyi, Théophile Mitima Kashosi, Jean-Paul Cikwanine Buhendwa, Parvine Basimane Bisimwa and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

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  16. Safety and immunogenicity of inactivated SARS-CoV-2 vaccines in people with gastrointestinal cancer.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
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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

13 authors at 3 institutions in 2 countries.

Patrick Bisimwa NtagerekaUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo. Electronic address: patrick.ntagereka@gmail.com.
Samuel O OyolaInternational Livestock Research Institute (ILRI), Nairobi, Kenya.
Simon Patrick BaenyiUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo.
Gilbert Kibet RonoInternational Livestock Research Institute (ILRI), Nairobi, Kenya.
Ahadi Bwihangane BirindwaUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo.
Dieudonné Wasso ShukuruUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo.
Tshass Chasinga BaharanyiUniversité Evangélique en Afrique, Faculty of Medicine, Bukavu, Democratic Republic of the Congo.
Théophile Mitima KashosiUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo.
Jean-Paul Cikwanine BuhendwaUniversité Evangélique en Afrique, Faculty of Medicine, Bukavu, Democratic Republic of the Congo.
Parvine Basimane BisimwaUniversité Evangélique en Afrique, Faculty of Medicine, Bukavu, Democratic Republic of the Congo.
Aline Byabene KusinzaUniversité Evangélique en Afrique, Faculty of Medicine, Bukavu, Democratic Republic of the Congo.
Rodrigue Ayagirwe BasengereUniversité Evangélique en Afrique, Molecular Biology Laboratory, Bukavu, Democratic Republic of the Congo.
Denis MukwegeUniversité Evangélique en Afrique, Faculty of Medicine, Bukavu, Democratic Republic of the Congo; Panzi General Referral Hospital, Gynecology and General Surgery, Bukavu, Democratic Republic of the Congo.
Université Evangélique en Afrique · CDInternational Livestock Research Institute · KEKinshasa General Hospital · CD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe used whole-genome sequencing of SARS-CoV-2 to identify variants circulating in the Democratic Republic of the Congo and obtain molecular information useful for diagnosis, improving treatment, and general pandemic control strategies.

methodsA total of 74 SARS-CoV-2 isolates were sequenced using Oxford Nanopore platforms. Generated reads were processed to obtain consensus genome sequences. Sequences with more than 80% genome coverage were used for variant calling, phylogenetic analysis, and classification using Pangolin lineage annotation nomenclature.

resultsPhylogenetic analysis based on Pangolin classification clustered South Kivu sequences into seven lineages (A.23.1, B.1.1.6, B.1.214, B.1.617.2, B.1.351, C.16, and P.1). The Delta (B.1.617.2) variant was the most dominant and responsible for outbreaks during the third wave. Based on the Wuhan reference genome, 289 distinct mutations were detected, including 141 missenses, 123 synonymous, and 25 insertions/deletions when our isolates were mapped to the Wuhan reference strain. Most of these point mutations were located within the coding sequences of the SARS-CoV-2 genome that includes spike, ORF1ab, ORF3, and nucleocapsid protein genes. The most common mutation was D614G (1841A>G) observed in 61 sequences, followed by L4715L (14143 C>T) found in 60 sequences.

conclusionOur findings highlight multiple introductions of SARS-CoV-2 into South Kivu through different sources and subsequent circulation of variants in the province. These results emphasize the importance of timely monitoring of genetic variation and its effect on disease severity. This work set a foundation for the use of genomic surveillance as a tool for future global pandemic management and control.

Indexed as

COVID-19SARS-CoV-2AnimalsDemocratic Republic of the CongoGenome, ViralHumansMutationPangolinsPhylogenyCOVID-19Genetic evolutionPandemicSARS-CoV-2South KivuVariants

Identifiers

PMID35598737
PMCPMC9119719
OpenAlexW4280648022

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.