Epidemiology, Genomic Diversity, and Evolutionary Dynamics of Human Metapneumovirus Over 7 Years of Integrated Community‐ and Hospital‐Based Sentinel Surveillance in Senegal, 2018–2024

ABSTRACT Background In late 2024, a major human metapneumovirus (HMPV) outbreak in China caused widespread pneumonia and thousands of hospitalizations, drawing global attention to this virus. In Senegal, a concomitant rise in HMPV detections was observed in both community and hospital settings. This study aimed to describe the epidemiology, genomic diversity, and the evolutionary dynamics of HMPV strains circulating in Senegal over 7 years of integrated community‐ and hospital‐based surveillance (2018–2024). Methods Nasopharyngeal samples were tested using multiplex real‐time reverse transcription polymerase chain reaction. A subset of HMPV isolates underwent sequencing, followed by phylogenetic and Bayesian evolutionary analyses. Results HMPV was detected in 3.3% ( n = 19,204) of tested specimens. The highest positivity rate was observed among infants aged ≤ 11 months (31.2%), with decreasing rates in older age groups. Following COVID‐19 related disruptions, HMPV circulation re‐established a seasonal pattern after 2022, peaking during the rainy season. Genomic analyses revealed sustained cocirculation of sublineages A2b1, A2b2, B1, and B2, with periodic lineage replacement every 1–3 years. Genetic variability was predominantly observed in the G glycoprotein, with evidence of positive selection at codons 102, 153, 167, 169, 179, 181, and 202. Estimated evolutionary rates were 9.30 × 10 −4 substitutions per site per year for HMPV‐A and 9.86 × 10 −4 substitutions per site per year for HMPV‐B. Phylogeographic analyses indicate that HMPV epidemics in Senegal are driven by repeated introductions and ongoing exchange with other regions. Conclusions Our findings indicate sustained circulation and dynamic turnover of pre‐existing sublineages rather than the emergence of a novel variant within the population, especially in infants aged ≤ 11 months.

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Journal
Influenza and Other Respiratory Viruses
Published
2026-06-30
DOI
https://doi.org/10.1111/irv.70290
Primary Topic
Respiratory viral infections research
Type
article
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article

Epidemiology, Genomic Diversity, and Evolutionary Dynamics of Human Metapneumovirus Over 7 Years of Integrated Community‐ and Hospital‐Based Sentinel Surveillance in Senegal, 2018–2024

Safiétou Sankhe, A Diallo Sall, Moussa Moïse Diagne, Ndiendé Koba Ndiaye et al.
Influenza and Other Respiratory Viruses
Respiratory viral infections research
article

Epidemiology, Genomic Diversity, and Evolutionary Dynamics of Human Metapneumovirus Over 7 Years of Integrated Community‐ and Hospital‐Based Sentinel Surveillance in Senegal, 2018–2024

Safiétou Sankhe, A Diallo Sall, Moussa Moïse Diagne, Ndiendé Koba Ndiaye, Mamadou Malado Jallow, Ndongo Dia, Cheikh Loucoubar, Seynabou Mbaye Ba Souna Diop, Mamadou Aliou Barry, Ndeye Awa Ndiaye, Mareme Seye Thiam, Deborah Goudiaby, Ndaraw Diack, Marie Pedepa Mendy, Samba Niang Sagne
article en

Abstract

ABSTRACT Background In late 2024, a major human metapneumovirus (HMPV) outbreak in China caused widespread pneumonia and thousands of hospitalizations, drawing global attention to this virus. In Senegal, a concomitant rise in HMPV detections was observed in both community and hospital settings. This study aimed to describe the epidemiology, genomic diversity, and the evolutionary dynamics of HMPV strains circulating in Senegal over 7 years of integrated community‐ and hospital‐based surveillance (2018–2024). Methods Nasopharyngeal samples were tested using multiplex real‐time reverse transcription polymerase chain reaction. A subset of HMPV isolates underwent sequencing, followed by phylogenetic and Bayesian evolutionary analyses. Results HMPV was detected in 3.3% ( n = 19,204) of tested specimens. The highest positivity rate was observed among infants aged ≤ 11 months (31.2%), with decreasing rates in older age groups. Following COVID‐19 related disruptions, HMPV circulation re‐established a seasonal pattern after 2022, peaking during the rainy season. Genomic analyses revealed sustained cocirculation of sublineages A2b1, A2b2, B1, and B2, with periodic lineage replacement every 1–3 years. Genetic variability was predominantly observed in the G glycoprotein, with evidence of positive selection at codons 102, 153, 167, 169, 179, 181, and 202. Estimated evolutionary rates were 9.30 × 10 −4 substitutions per site per year for HMPV‐A and 9.86 × 10 −4 substitutions per site per year for HMPV‐B. Phylogeographic analyses indicate that HMPV epidemics in Senegal are driven by repeated introductions and ongoing exchange with other regions. Conclusions Our findings indicate sustained circulation and dynamic turnover of pre‐existing sublineages rather than the emergence of a novel variant within the population, especially in infants aged ≤ 11 months.

Influenza and Other Respiratory VirusesVol. 20(7)
Institut Pasteur de Dakar (SN)
Good health and well-being
Openalex Percentile: Top 8%
Respiratory viral infections research
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