Surface sampling for mpox virus in multiple healthcare settings in Sierra Leone, June 2025
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Background
As mpox virus (MPXV) has continued to expand geographically, critical knowledge gaps in environmental persistence in resource-limited healthcare settings remain. Despite evidence of fomite-mediated transmission, no empirical data exist on surface contamination in West African hospitals during active mpox outbreaks.
Methods
In this cross-sectional study, we conducted a systematic environmental surveillance study at two major hospitals in Sierra Leone (Connaught Hospital, Freetown; Bo Government Hospital, Bo) during peak transmission (June 2025). A total of 89 high-contact surfaces were sampled across clinical and non-clinical zones using standardized protocols. MPXV DNA was extracted via robotic MagMax protocols and detected through quantitative real-time PCR targeting the B6R gene.
Results
Overall, 13.5% (12/89) of surfaces tested positive by PCR for MPXV, with geographic variation: Freetown (14.0%, 7/50) vs. Bo (12.8%, 5/39). Cycle threshold values (32.34–39.86) indicated low-to-moderate viral genomes. Critical contamination hotspots were identified, with doors representing 42% (5/12) of positive samples; predominantly ward entrances, staff offices, and bathrooms. Patient beds and clinical instruments constituted secondary risk zones (8.3% each).
Conclusions
This first-in-region study demonstrates quantifiable MPXV genomes from surfaces in Sierra Leonean healthcare facilities, providing support for patients with mpox, highlighting areas for infection prevention and control (IPC) considerations. The predominance of doors as high-risk fomites underscores the need for targeted disinfection protocols. Our findings establish environmental surveillance as a vital component of mpox control in clinical settings and provide evidence for IPC resource prioritization, including enhanced disinfection of high-touch surfaces and integration of IPC monitoring into national outbreak response frameworks.
