Evidence map›Paper›PMID 34695371›Full record

ArticleThe Lancet. Global health2021

Genomic epidemiology and the role of international and regional travel in the SARS-CoV-2 epidemic in Zimbabwe: a retrospective study of routinely collected surveillance data.

Tapfumanei Mashe, Faustinos Tatenda Takawira, Leonardo de Oliveira Martins, Muchaneta Gudza-Mugabe, Joconiah Chirenda, Manes Munyanyi, Blessmore V Chaibva, Andrew Tarupiwa, Hlanai Gumbo, Agnes Juru and 27 more

Abstract read
In one paragraph

Article in The Lancet. Global health, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors.

Tapfumanei MasheNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe. Electronic address: mashet2006@yahoo.co.uk.
Faustinos Tatenda TakawiraNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Leonardo de Oliveira MartinsQuadram Institute Bioscience, Norwich, UK.
Muchaneta Gudza-MugabeWHO, Harare, Zimbabwe.
Joconiah ChirendaDepartment of Surgical Sciences, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Manes MunyanyiDepartment of Health Information and Surveilance, Ministry of Health and Child Care, Harare, Zimbabwe.
Blessmore V ChaibvaDepartment of Pharmacy Services, Ministry of Health and Child Care, Harare, Zimbabwe.
Andrew TarupiwaNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Hlanai GumboNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Agnes JuruNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Charles NyagupeNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Vurayai RuhanyaDepartment of Surgical Sciences, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Isaac PhiriDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Portia ManangaziraDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Alexander GoredemaDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Sydney DandaDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Israel ChabataDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Janet JongaDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Rutendo MunhariraDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Kudzai MasundaHarare City Health Department, Beatrice Road Infectious Diseases Hospital, Harare, Zimbabwe.
Innocent MukeredziHarare City Health Department, Beatrice Road Infectious Diseases Hospital, Harare, Zimbabwe.
Douglas MangwanyaDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
Alex TrotterQuadram Institute Bioscience, Norwich, UK.
Thanh Le VietQuadram Institute Bioscience, Norwich, UK.
Steven RudderQuadram Institute Bioscience, Norwich, UK.
Gemma KayQuadram Institute Bioscience, Norwich, UK.
David BakerQuadram Institute Bioscience, Norwich, UK.
Gaetan ThilliezQuadram Institute Bioscience, Norwich, UK.
Ana Victoria GutierrezQuadram Institute Bioscience, Norwich, UK.
Justin O'GradyQuadram Institute Bioscience, Norwich, UK.
Maxwell HoveDepartment of Curative Services, Ministry of Health and Child Care, Harare, Zimbabwe.
Sekesai Mutapuri-ZinyoweraNational Microbiology Reference Laboratory, Ministry of Health and Child Care, Harare, Zimbabwe.
Andrew J PageQuadram Institute Bioscience, Norwich, UK.
Robert A KingsleyQuadram Institute Bioscience, Norwich, UK; School of Biological Sciences, University of East Anglia, Norwich, UK. Electronic address: rob.kingsley@quadram.ac.uk.
Gibson MhlangaDepartment of Epidemiology and Disease Control, Ministry of Health and Child Care, Harare, Zimbabwe.
COVID-19 Genomics UK Consortium
SARS-CoV-2 Research Group

Funding

Medical Research Council MC_PC_19027Wellcome Trust
6 · The paper itself

Abstract

backgroundAdvances in SARS-CoV-2 sequencing have enabled identification of new variants, tracking of its evolution, and monitoring of its spread. We aimed to use whole genome sequencing to describe the molecular epidemiology of the SARS-CoV-2 outbreak and to inform the implementation of effective public health interventions for control in Zimbabwe.

methodsWe performed a retrospective study of nasopharyngeal samples collected from nine laboratories in Zimbabwe between March 20 and Oct 16, 2020. Samples were taken as a result of quarantine procedures for international arrivals or to test for infection in people who were symptomatic or close contacts of positive cases. Samples that had a cycle threshold of less than 30 in the diagnostic PCR test were processed for sequencing. We began our analysis in July, 2020 (120 days since the first case), with a follow-up in October, 2020 (at 210 days since the first case). The phylogenetic relationship of the genome sequences within Zimbabwe and global samples was established using maximum likelihood and Bayesian methods.

findingsOf 92 299 nasopharyngeal samples collected during the study period, 8099 were PCR-positive and 328 were available for sequencing, with 156 passing sequence quality control. 83 (53%) of 156 were from female participants. At least 26 independent introductions of SARS-CoV-2 into Zimbabwe in the first 210 days were associated with 12 global lineages. 151 (97%) of 156 had the Asp614Gly mutation in the spike protein. Most cases, 93 (60%), were imported from outside Zimbabwe. Community transmission was reported 6 days after the onset of the outbreak.

interpretationInitial public health interventions delayed onset of SARS-CoV-2 community transmission after the introduction of the virus from international and regional migration in Zimbabwe. Global whole genome sequence data are essential to reveal major routes of spread and guide intervention strategies.

fundingWHO, Africa CDC, Biotechnology and Biological Sciences Research Council, Medical Research Council, National Institute for Health Research, and Genome Research Limited.

Indexed as

EpidemicsGenome, ViralPublic Health SurveillanceTravel-Related IllnessAdolescentAdultChildChild, PreschoolCOVID-19FemaleHumansInfantMaleMiddle AgedMolecular EpidemiologyRetrospective Studies

Identifiers

PMID34695371
PMCPMC8536247

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