Dynamic and features of SARS-CoV-2 infection in Gabon
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...
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Nature Publishing Group
2021-05-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-021-87043-y |
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language |
English |
format |
Article |
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DOAJ |
author |
Amandine Mveang Nzoghe Guy-Stephan Padzys Anicet Christel Maloupazoa Siawaya Marisca Kandet Yattara Marielle Leboueny Rotimi Myrabelle Avome Houechenou Eliode Cyrien Bongho Cedrick Mba-Mezeme Ofilia Mvoundza Ndjindji Jean Claude Biteghe-Bi-Essone Alain Boulende Paulin N. Essone Carene Anne Alene Ndong Sima Ulysse Minkobame Carinne Zang Eyi Bénédicte Ndeboko Alexandru Voloc Jean-François Meye Simon Ategbo Joel Fleury Djoba Siawaya |
spellingShingle |
Amandine Mveang Nzoghe Guy-Stephan Padzys Anicet Christel Maloupazoa Siawaya Marisca Kandet Yattara Marielle Leboueny Rotimi Myrabelle Avome Houechenou Eliode Cyrien Bongho Cedrick Mba-Mezeme Ofilia Mvoundza Ndjindji Jean Claude Biteghe-Bi-Essone Alain Boulende Paulin N. Essone Carene Anne Alene Ndong Sima Ulysse Minkobame Carinne Zang Eyi Bénédicte Ndeboko Alexandru Voloc Jean-François Meye Simon Ategbo Joel Fleury Djoba Siawaya Dynamic and features of SARS-CoV-2 infection in Gabon Scientific Reports |
author_facet |
Amandine Mveang Nzoghe Guy-Stephan Padzys Anicet Christel Maloupazoa Siawaya Marisca Kandet Yattara Marielle Leboueny Rotimi Myrabelle Avome Houechenou Eliode Cyrien Bongho Cedrick Mba-Mezeme Ofilia Mvoundza Ndjindji Jean Claude Biteghe-Bi-Essone Alain Boulende Paulin N. Essone Carene Anne Alene Ndong Sima Ulysse Minkobame Carinne Zang Eyi Bénédicte Ndeboko Alexandru Voloc Jean-François Meye Simon Ategbo Joel Fleury Djoba Siawaya |
author_sort |
Amandine Mveang Nzoghe |
title |
Dynamic and features of SARS-CoV-2 infection in Gabon |
title_short |
Dynamic and features of SARS-CoV-2 infection in Gabon |
title_full |
Dynamic and features of SARS-CoV-2 infection in Gabon |
title_fullStr |
Dynamic and features of SARS-CoV-2 infection in Gabon |
title_full_unstemmed |
Dynamic and features of SARS-CoV-2 infection in Gabon |
title_sort |
dynamic and features of sars-cov-2 infection in gabon |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
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. |
url |
https://doi.org/10.1038/s41598-021-87043-y |
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doaj-7c7c5c454d7f47b2bfea2b16be1f75382021-05-09T11:35:15ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111010.1038/s41598-021-87043-yDynamic and features of SARS-CoV-2 infection in GabonAmandine Mveang Nzoghe0Guy-Stephan Padzys1Anicet Christel Maloupazoa Siawaya2Marisca Kandet Yattara3Marielle Leboueny4Rotimi Myrabelle Avome Houechenou5Eliode Cyrien Bongho6Cedrick Mba-Mezeme7Ofilia Mvoundza Ndjindji8Jean Claude Biteghe-Bi-Essone9Alain Boulende10Paulin N. Essone11Carene Anne Alene Ndong Sima12Ulysse Minkobame13Carinne Zang Eyi14Bénédicte Ndeboko15Alexandru Voloc16Jean-François Meye17Simon Ategbo18Joel Fleury Djoba Siawaya19Unité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIDépartement de Biologie Cellulaire et Physiologie, Faculté Des Sciences, Université Des Sciences Et Techniques de MasukuUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIHôpital Des Instruction des Armes D’AkandaUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIDépartement de Biologie Cellulaire et Physiologie, Faculté Des Sciences, Université Des Sciences Et Techniques de MasukuUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORILaboratoire National de Santé PubliqueUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIPôle mère, CHU- Mère-Enfant Fondation Jeanne EBORIPôle enfant, CHU- Mère-Enfant Fondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIPôle enfant, CHU- Mère-Enfant Fondation Jeanne EBORIPôle mère, CHU- Mère-Enfant Fondation Jeanne EBORIPôle enfant, CHU- Mère-Enfant Fondation Jeanne EBORIUnité de Recherche et Diagnostics Spécialisé, Service Laboratoire, CHU-Mère-EnfantFondation Jeanne EBORIAbstract 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.https://doi.org/10.1038/s41598-021-87043-y |