Abstract

In a context where SARS-CoV-2 population-wide testing is implemented, clinical features and antibody response in those infected have never been documented in Africa. Yet, the information provided by analyzing data from population-wide testing is critical to understand the infection dynamics and devise control strategies. We described clinical features and assessed antibody response in people screened for SARS-CoV-2 infection. We analyzed data from a cohort of 3464 people that we molecularly screened for SARS-CoV-2 infection in our routine activity. We recorded people SARS-CoV-2 diagnosis, age, gender, blood types, white blood cells (WBC), symptoms, chronic disease status and time to SARS-CoV-2 RT-PCR conversion from positive to negative. We calculated the age-based distribution of SARS-CoV-2 infection, analyzed the proportion and the spectrum of COVID-19 severity. Furthermore, in a nested sub-study, we screened 83 COVID-19 patients and 319 contact-cases for anti-SARS-CoV-2 antibodies. Males and females accounted for respectively 51% and 49% of people screened. The studied population median and mean age were both 39 years. 592 out of 3464 people (17.2%) were diagnosed with SARS-CoV-2 infection with males and females representing, respectively, 53% and 47%. The median and mean ages of SARS-CoV-2 infected subjects were 37 and 38 years respectively. The lowest rate of infection (8%) was observed in the elderly (aged > 60). The rate of SARS-Cov-2 infection in both young (18–35 years old) and middle-aged adults (36–60 years old) was around 20%. The analysis of SARS-CoV-2 infection age distribution showed that middle-aged adults accounted for 54.7% of SARS-CoV-2 positive persons, followed respectively by young adults (33.7%), children (7.7%) and elderly (3.8%). 68% (N = 402) of SARS-CoV-2 infected persons were asymptomatic, 26.3% (N = 156) had influenza-like symptoms, 2.7% (N = 16) had influenza-like symptoms associated with anosmia and ageusia, 2% (N = 11) had dyspnea and 1% (N = 7) had respiratory failure, which resulted in death. Data also showed that 12% of SARS-CoV-2 infected subjects, had chronic diseases. Hypertension, diabetes, and asthma were the top concurrent chronic diseases representing respectively 58%, 25% and 12% of recorded chronic diseases. Half of SARS-CoV-2 RT-PCR positive patients were cured within 14 days following the initiation of the anti-COVID-19 treatment protocol. 78.3% of COVID-19 patients and 55% of SARS-CoV-2 RT-PCR confirmed negative contact-cases were positive for anti-SARS-CoV-2 antibodies. Patients with severe-to-critical illness have higher leukocytes, higher neutrophils and lower lymphocyte counts contrarily to asymptomatic patients and patients with mild-to-moderate illness. Neutrophilic leukopenia was more prevalent in asymptomatic patients and patients with mild-to-moderate disease for 4 weeks after diagnosis (27.1–42.1%). In Patients with severe-to-critical illness, neutrophilic leukocytosis or neutrophilia (35.6–50%) and lymphocytopenia (20–40%) were more frequent. More than 60% of participants were blood type O. It is also important to note that infection rate was slightly higher among A and B blood types compared with type O. In this African setting, young and middle-aged adults are most likely driving community transmission of COVID-19. The rate of critical disease is relatively low. The high rate of anti-SARS-CoV-2 antibodies observed in SARS-CoV-2 RT-PCR negative contact cases suggests that subclinical infection may have been overlooked in our setting.

Details

Title
Dynamic and features of SARS-CoV-2 infection in Gabon
Author
Amandine, Mveang Nzoghe 1 ; Guy-Stephan, Padzys 2 ; Maloupazoa Siawaya Anicet Christel 3 ; Marisca, Kandet Yattara 4 ; Leboueny Marielle 3 ; Avome Houechenou Rotimi Myrabelle 3 ; Cyrien, Bongho Eliode 3 ; Mba-Mezeme Cedrick 2 ; Ofilia, Mvoundza Ndjindji 3 ; Claude, Biteghe-Bi-Essone Jean 3 ; Boulende Alain 3 ; Essone, Paulin N 5 ; Ndong Sima Carene Anne Alene 6 ; Ulysse, Minkobame 7 ; Zang Eyi Carinne 8 ; Ndeboko Bénédicte 9 ; Voloc Alexandru 10 ; Meye Jean-François 11 ; Ategbo Simon 10 ; Djoba Siawaya Joel Fleury 12 

 CHU-Mère-EnfantFondation Jeanne EBORI, Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, Libreville, Gabon 
 Université Des Sciences Et Techniques de Masuku, Département de Biologie Cellulaire et Physiologie, Faculté Des Sciences, Franceville, Gabon (GRID:grid.430699.1) (ISNI:0000 0004 0452 416X) 
 CHU-Mère-EnfantFondation Jeanne EBORI, Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, Libreville, Gabon (GRID:grid.430699.1) 
 Hôpital Des Instruction des Armes D’Akanda, Libreville-Nord, Gabon (GRID:grid.430699.1) 
 Laboratoire National de Santé Publique, Libreville, Gabon (GRID:grid.430699.1); Centre de Recherches Médicales de Lambaréné, Lambaréné, Gabon (GRID:grid.452268.f) 
 CHU-Mère-EnfantFondation Jeanne EBORI, Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, Libreville, Gabon (GRID:grid.452268.f); Stellenbosch University, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch, South Africa (GRID:grid.11956.3a) (ISNI:0000 0001 2214 904X) 
 Pôle mère, CHU- Mère-Enfant Fondation Jeanne EBORI, Libreville, Gabon (GRID:grid.11956.3a) 
 Pôle enfant, CHU- Mère-Enfant Fondation Jeanne EBORI, Libreville, Gabon (GRID:grid.11956.3a) 
 CHU-Mère-EnfantFondation Jeanne EBORI, Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, Libreville, Gabon (GRID:grid.11956.3a); Université Des Sciences de La Santé, Département de Biologie Cellulaire and Moléculaire-Génétique, Faculté de Médecine, Libreville, Gabon (GRID:grid.502965.d) 
10  Pôle enfant, CHU- Mère-Enfant Fondation Jeanne EBORI, Libreville, Gabon (GRID:grid.502965.d) 
11  Pôle mère, CHU- Mère-Enfant Fondation Jeanne EBORI, Libreville, Gabon (GRID:grid.502965.d) 
12  CHU-Mère-EnfantFondation Jeanne EBORI, Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, Libreville, Gabon (GRID:grid.502965.d) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2522497578
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.