Evidence map›Paper›PMID 42764366›Full record

ArticleInternational journal of health geographics2026

Influence of spatial connectivity on the spread of Mpox in Maï-Ndombe province, Democratic Republic of the Congo, 2025.

Christian M Ibolobolo, Harry César Kayembe, Didier Bompangue, Dav M Ebengo

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Article in International journal of health geographics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Christian M IboloboloInstitut One Health pour l'Afrique (INOHA), University of Kinshasa, Kinshasa, Democratic Republic of the Congo. christianibolobolomobali@gmail.com.
Harry César KayembeInstitut One Health pour l'Afrique (INOHA), University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Didier BompangueInstitut One Health pour l'Afrique (INOHA), University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Dav M EbengoInstitut One Health pour l'Afrique (INOHA), University of Kinshasa, Kinshasa, Democratic Republic of the Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman mobility is a major determinant of the spatial spread of emerging infectious diseases. In Maï-Ndombe province, Democratic Republic of the Congo, dependence on waterways as the primary transport network, combined with a degraded road infrastructure and marked environmental constraints, creates profound heterogeneity in spatial connectivity between health zones. In this context, the spread of Mpox shows an irregular spatial distribution whose structural mechanisms remain poorly understood, partly due to the scarcity of mobility data and the fragility of surveillance systems.

objectiveTo quantify the intra-provincial spatial connectivity of Maï-Ndombe by simultaneously integrating road and river networks, and to assess its influence on the spread of Mpox between 2022 and 2025.

methodsA spatial connectivity analysis based on an enhanced gravity model integrating demographic attractiveness and a distance-cost factor accounting for slope and land use via the Fuzzy-AHP method was combined with a spatialized metapopulation SEIR model. Inter-zone flows, centrality, and accessibility were quantified. The performance of SEIR models with and without connectivity was compared using RMSE, MAE, and precision gain per zone.

resultsFlows are strongly concentrated around pivotal zones (Bokoro, Nioki, Mushie), while peripheral areas (Mimia, Oshwe, Kiri) remain structurally isolated, with accessibility provided primarily by river corridors (Gini index = 0.65; CV = 1.52). The integration of connectivity degrades the overall model fit (ΔRMSE = -0.468), reflecting the predominance of local transmission at the provincial scale. However, this aggregate degradation conceals marked spatial heterogeneity: connectivity significantly improves predictions in highly connected zones (Bokoro: +59.8%; Mushie: +33.3%; Nioki: +17.3%), while degrading them in poorly connected zones (Kiri: -46.1%; Mimia: -27.4%; Oshwe: -22.4%).

conclusionSpatial connectivity does not strengthen the overall prediction of incidence, but structures the spatial redistribution of epidemic risk. The aggregate model degradation reflects both the limitations of the surveillance system and structural constraints of the gravity model, particularly the use of static populations as denominators and the absence of temporal exposure duration at destination zones. These results highlight the importance of targeting surveillance interventions in high-centrality areas, while developing metapopulation approaches that integrate the temporal dimension of mobility to improve preparedness for future Mpox outbreaks in tropical forest environments.

Indexed as

Mpox, MonkeypoxSpatial AnalysisDemocratic Republic of the CongoHumansRiversHuman mobilityInfectious disease transmissionMaï-Ndombe provinceMpoxSpatial connectivity

Identifiers

PMID42764366
PMCPMC13591832

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.