Use of Mpox Multiplex Serology in the Identification of Cases and Outbreak Investigations in the Democratic Republic of the Congo (DRC)

Author:

Kinganda-Lusamaki Eddy123ORCID,Baketana Lionel Kinzonzi2,Ndomba-Mukanya Etienne2ORCID,Bouillin Julie1,Thaurignac Guillaume1ORCID,Aziza Adrienne Amuri2,Luakanda-Ndelemo Gradi2,Nuñez Nicolas Fernandez1ORCID,Kalonji-Mukendi Thierry4ORCID,Pukuta Elisabeth Simbu2,Nkuba-Ndaye Antoine123ORCID,Lofiko Emmanuel Lokilo2,Kibungu Emile Malembi4,Lushima Robert Shongo4,Ayouba Ahidjo1ORCID,Mbala-Kingebeni Placide23,Muyembe-Tamfum Jean-Jacques23,Delaporte Eric1,Peeters Martine1,Ahuka-Mundeke Steve23

Affiliation:

1. TransVIHMI, University of Montpellier (UM), French Institute of Health and Medical Research (INSERM), French National Research Institute for Sustainable Development (IRD), 34394 Montpellier, France

2. Institut National de Recherche Biomédicale (INRB), Kinshasa P.O. Box 1197, Democratic Republic of the Congo

3. Service de Microbiologie, Département de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa P.O. Box 127, Democratic Republic of the Congo

4. Programme National de Lutte Contre le Monkeypox et les Fièvres Hémorragiques Virales, Ministère de la Santé (PNLMPX-FHV), Kinshasa P.O. Box 1197, Democratic Republic of the Congo

Abstract

Human Mpox cases are increasingly reported in Africa, with the highest burden in the Democratic Republic of Congo (DRC). While case reporting on a clinical basis can overestimate infection rates, laboratory confirmation by PCR can underestimate them, especially on suboptimal samples like blood, commonly used in DRC. Here we used a Luminex-based assay to evaluate whether antibody testing can be complementary to confirm cases and to identify human transmission chains during outbreak investigations. We used left-over blood samples from 463 patients, collected during 174 outbreaks between 2013 and 2022, with corresponding Mpox and VZV PCR results. In total, 157 (33.9%) samples were orthopox-PCR positive and classified as Mpox+; 124 (26.8%) had antibodies to at least one of the three Mpox peptides. The proportion of antibody positive samples was significantly higher in Mpox positive samples (36.9%) versus negative (21.6%) (p < 0.001). By combining PCR and serology, 66 additional patients were identified, leading to an Mpox infection rate of 48.2% (223/463) versus 33.9% when only PCR positivity is considered. Mpox infections were as such identified in 14 additional health zones and 23 additional outbreaks (111/174 (63.8%) versus 88/174 (50.6%)). Our findings highlight the urgent need of rapid on-site diagnostics to circumvent Mpox spread.

Funder

ANRS-MIE (projet PANAFPOX), Agence Française de Développement through the AFROSCREEN project

BiodivERsA ERA-Net COFUND programme

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

Reference33 articles.

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2. Malik, Y.S., Singh, R.K., and Dhama, K. (2020). Animal-Origin Viral Zoonoses, Livestock Diseases and Management; Springer.

3. WHO (2023, June 06). WHO Recommends New Name for Monkeypox Disease. Available online: https://www.who.int/news/item/28-11-2022-who-recommends-new-name-for-monkeypox-disease.

4. A Human Infection Caused by Monkeypox Virus in Basankusu Territory, Democratic Republic of the Congo;Ladnyj;Bull. World Health Organ.,1972

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