Comparative Performance of Serological (IgM/IgG) and Molecular Testing (RT-PCR) of COVID-19 in Three Private Universities in Cameroon during the Pandemic

Author:

Kamga Wouambo Rodrigue12ORCID,Djuikoué Cecile Ingrid23ORCID,Esemu Livo Forgu45ORCID,Kagoue Simeni Luc Aime26ORCID,Tchitchoua Murielle Chantale3,Djouela Djoulako Paule Dana27ORCID,Fokam Joseph89ORCID,Singwe-Ngandeu Madeleine10,Mpoudi Ngolé Eitel4,Apalata Teke11ORCID

Affiliation:

1. Section of Hepatology, Department of Medicine II, University of Leipzig Medical Centre, 04103 Leipzig, Germany

2. American Society for Microbiology (ASM), ASM Cameroon, Bangangte, Cameroon

3. Faculty of Health Science, Université des Montagnes, Bangangte, Cameroon

4. Laboratory of Fundamental Virology, Centre for Research on Emerging and Reemerging Diseases (CREMER), Yaounde, Cameroon

5. Department of Biomedical Sciences, Faculty of Health Science, University of Buea, Buea, Cameroon

6. Department of Microbiology, Faculty of Health Science, University of Buea, Buea, Cameroon

7. Faculty of Medicine, Sorbonne University, 75013 Paris, France

8. Department of Medical Laboratory Sciences, Faculty of Health Science, University of Buea, Buea, Cameroon

9. Chantal BIYA International Reference Centre for Research on HIV/AIDS Prevention and Management (CIRCB), Yaoundé, Cameroon

10. Faculty of Medicine and Biomedical science, University of Yaounde 1, Yaounde, Cameroon

11. Faculty of Health Sciences & National Health Laboratory Services, Walter Sisulu University, Mthatha 5099, South Africa

Abstract

Background: COVID-19 remains a rapidly evolving and deadly pandemic worldwide. This necessitates the continuous assessment of existing diagnostic tools for a robust, up-to-date, and cost-effective pandemic response strategy. We sought to determine the infection rate (PCR-positivity) and degree of spread (IgM/IgG) of SARS-CoV-2 in three university settings in Cameroon Method: Study volunteers were recruited from November 2020 to July 2021 among COVID-19 non-vaccinated students in three Universities from two regions of Cameroon (West and Centre). Molecular testing was performed by RT-qPCR on nasopharyngeal swabs, and IgM/IgG antibodies in plasma were detected using the Abbott Panbio IgM/IgG rapid diagnostic test (RDT) at the Virology Laboratory of CREMER/IMPM/MINRESI. The molecular and serological profiles were compared, and p < 0.05 was considered statistically significant. Results: Amongst the 291 participants enrolled (mean age 22.59 ± 10.43 years), 19.59% (57/291) were symptomatic and 80.41% (234/291) were asymptomatic. The overall COVID-19 PCR-positivity rate was 21.31% (62/291), distributed as follows: 25.25% from UdM-Bangangte, 27.27% from ISSBA-Yaounde, and 5% from IUEs/INSAM-Yaounde. Women were more affected than men (28.76% [44/153] vs. 13.04% [18/138], p < 0.0007), and had higher seropositivity rates to IgM+/IgG+ (15.69% [24/153] vs. 7.25% [10/138], p < 0.01). Participants from Bangangté, the nomadic, and the “non-contact cases” primarily presented an active infection compared to those from Yaoundé (p= 0.05, p = 0.05, and p = 0.01, respectively). Overall IgG seropositivity (IgM−/IgG+ and IgM+/IgG+) was 24.4% (71/291). A proportion of 26.92% (7/26) presenting COVID-19 IgM+/IgG− had negative PCR vs. 73.08% (19/26) with positive PCR, p < 0.0001. Furthermore, 17.65% (6/34) with COVID-19 IgM+/IgG+ had a negative PCR as compared to 82.35% with a positive PCR (28/34), p < 0.0001. Lastly, 7.22% (14/194) with IgM−/IgG− had a positive PCR. Conclusion: This study calls for a rapid preparedness and response strategy in higher institutes in the case of any future pathogen with pandemic or epidemic potential. The observed disparity between IgG/IgM and the viral profile supports prioritizing assays targeting the virus (nucleic acid or antigen) for diagnosis and antibody screening for sero-surveys.

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference63 articles.

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