Community SARS-CoV-2 seroprevalence before and after the second wave of SARS-CoV-2 infection in Harare, Zimbabwe.

SARS-CoV-2 seroprevalence Zimbabwe

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 04 08 2021
revised: 05 10 2021
accepted: 06 10 2021
entrez: 1 11 2021
pubmed: 2 11 2021
medline: 2 11 2021
Statut: ppublish

Résumé

By the end of July 2021 Zimbabwe, has reported over 100,000 SARS-CoV-2 infections. The true number of SARS-CoV-2 infections is likely to be much higher. We conducted a seroprevalence survey to estimate the prevalence of past SARS-CoV-2 in three high-density communities in Harare, Zimbabwe before and after the second wave of SARS-CoV-2. Between November 2020 and April 2021 we conducted a cross-sectional study of randomly selected households in three high-density communities (Budiriro, Highfield and Mbare) in Harare. Consenting participants answered a questionnaire and a dried blood spot sample was taken. Samples were tested for anti-SARS-CoV-2 nucleocapsid antibodies using the Roche e801 platform. A total of 2340 individuals participated in the study. SARS-CoV-2 antibody results were available for 70·1% (620/885) and 73·1% (1530/2093) of eligible participants in 2020 and 2021. The median age was 22 (IQR 10-37) years and 978 (45·5%) were men. SARS-CoV-2 seroprevalence was 19·0% (95% CI 15·1-23·5%) in 2020 and 53·0% (95% CI 49·6-56·4) in 2021. The prevalence ratio was 2·47 (95% CI 1·94-3·15) comparing 2020 with 2021 after adjusting for age, sex, and community. Almost half of all participants who tested positive reported no symptoms in the preceding six months. Following the second wave, one in two people had been infected with SARS-CoV-2 suggesting high levels of community transmission. Our results suggest that 184,800 (172,900-196,700) SARS-CoV-2 infections occurred in these three communities alone, greatly exceeding the reported number of cases for the whole city. Further seroprevalence surveys are needed to understand transmission during the current third wave despite high prevalence of past infections. GCRF, Government of Canada, Wellcome Trust, Bavarian State Ministry of Sciences, Research, and the Arts.

Sections du résumé

BACKGROUND BACKGROUND
By the end of July 2021 Zimbabwe, has reported over 100,000 SARS-CoV-2 infections. The true number of SARS-CoV-2 infections is likely to be much higher. We conducted a seroprevalence survey to estimate the prevalence of past SARS-CoV-2 in three high-density communities in Harare, Zimbabwe before and after the second wave of SARS-CoV-2.
METHODS METHODS
Between November 2020 and April 2021 we conducted a cross-sectional study of randomly selected households in three high-density communities (Budiriro, Highfield and Mbare) in Harare. Consenting participants answered a questionnaire and a dried blood spot sample was taken. Samples were tested for anti-SARS-CoV-2 nucleocapsid antibodies using the Roche e801 platform.
FINDINGS RESULTS
A total of 2340 individuals participated in the study. SARS-CoV-2 antibody results were available for 70·1% (620/885) and 73·1% (1530/2093) of eligible participants in 2020 and 2021. The median age was 22 (IQR 10-37) years and 978 (45·5%) were men. SARS-CoV-2 seroprevalence was 19·0% (95% CI 15·1-23·5%) in 2020 and 53·0% (95% CI 49·6-56·4) in 2021. The prevalence ratio was 2·47 (95% CI 1·94-3·15) comparing 2020 with 2021 after adjusting for age, sex, and community. Almost half of all participants who tested positive reported no symptoms in the preceding six months.
INTERPRETATION CONCLUSIONS
Following the second wave, one in two people had been infected with SARS-CoV-2 suggesting high levels of community transmission. Our results suggest that 184,800 (172,900-196,700) SARS-CoV-2 infections occurred in these three communities alone, greatly exceeding the reported number of cases for the whole city. Further seroprevalence surveys are needed to understand transmission during the current third wave despite high prevalence of past infections.
FUNDING BACKGROUND
GCRF, Government of Canada, Wellcome Trust, Bavarian State Ministry of Sciences, Research, and the Arts.

Identifiants

pubmed: 34723165
doi: 10.1016/j.eclinm.2021.101172
pii: S2589-5370(21)00452-1
pmc: PMC8542175
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101172

Subventions

Organisme : Wellcome Trust
ID : 206316/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/R010161/1
Pays : United Kingdom

Informations de copyright

© 2021 The Author(s).

Déclaration de conflit d'intérêts

AW declared that Roche provided reagents and machine for discounted rates for all projects involving SARS-CoV-2 serology. AW holds part of a patent application with the German Patent and Trade Mark Office relating to safe transport of DBS for analytical purpose; this application was not used in the current study. RAF received funding from the Wellcome Trust since 2017, is a member of the Zimbabwe national COVID19 Advisory Panel and a member of the CDC Africa Strategic Advisory Group of Experts for COVID19. All the other authors report no conflicts.

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Auteurs

Arun Fryatt (A)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Victoria Simms (V)

Biomedical Research and Training Institute, Harare, Zimbabwe.
MRC International Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.

Tsitsi Bandason (T)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Nicol Redzo (N)

Biomedical Research and Training Institute, Harare, Zimbabwe.

Ioana D Olaru (ID)

Biomedical Research and Training Institute, Harare, Zimbabwe.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.

Chiratidzo E Ndhlovu (CE)

Internal Medicine Unit, University of Zimbabwe Faculty of Medicine and Health Sciences, Harare, Zimbabwe.

Hilda Mujuru (H)

Department of Paediatrics and Child Health, University of Zimbabwe Faculty of Medicine and Health Sciences, Harare, Zimbabwe.

Simbarashe Rusakaniko (S)

Department of Community Medicine, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.

Michael Hoelscher (M)

Division of Infectious Diseases and Tropical Medicine, Medical Center of the University of Munich, Munich, Germany.
German Center for Infection Research (DZIF), Partner Site Munich, Munich, Germany.

Raquel Rubio-Acero (R)

Division of Infectious Diseases and Tropical Medicine, Medical Center of the University of Munich, Munich, Germany.

Ivana Paunovic (I)

Division of Infectious Diseases and Tropical Medicine, Medical Center of the University of Munich, Munich, Germany.

Andreas Wieser (A)

Division of Infectious Diseases and Tropical Medicine, Medical Center of the University of Munich, Munich, Germany.
German Center for Infection Research (DZIF), Partner Site Munich, Munich, Germany.

Prosper Chonzi (P)

Harare City Health, Harare, Zimbabwe.

Kudzai Masunda (K)

Harare City Health, Harare, Zimbabwe.

Rashida A Ferrand (RA)

Biomedical Research and Training Institute, Harare, Zimbabwe.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.

Katharina Kranzer (K)

Biomedical Research and Training Institute, Harare, Zimbabwe.
Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Division of Infectious Diseases and Tropical Medicine, Medical Center of the University of Munich, Munich, Germany.

Classifications MeSH