Risk estimation for air travel-induced malaria transmission in central Europe - A mathematical modelling study
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Risk estimation for air travel-induced malaria transmission in central Europe - A mathematical modelling study. / Pondorfer, Susanne G; Jaeger, Veronika K; Scholz-Kreisel, Peter; Horn, Johannes; Krumkamp, Ralf; Kreuels, Benno; Mikolajczyk, Rafael T; Karch, André.
In: TRAVEL MED INFECT DI, Vol. 36, 01.02.2020, p. 101564.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Risk estimation for air travel-induced malaria transmission in central Europe - A mathematical modelling study
AU - Pondorfer, Susanne G
AU - Jaeger, Veronika K
AU - Scholz-Kreisel, Peter
AU - Horn, Johannes
AU - Krumkamp, Ralf
AU - Kreuels, Benno
AU - Mikolajczyk, Rafael T
AU - Karch, André
N1 - Copyright © 2020 Elsevier Ltd. All rights reserved.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - BACKGROUND: Aim of our study was to identify conditions under which malaria transmission caused by imported infectious mosquitoes or travellers could occur at large central European airports, and if such transmission could be sustained by indigenous mosquitoes.METHODS: We developed a deterministic and a stochastic compartmental Susceptible-Exposed-Infectious-Recovered-Susceptible (humans)/Susceptible-Exposed-Infectious (mosquitoes) model with two mosquito (imported Anopheles gambiae, indigenous A. plumbeus) and three human (travellers, airport personnel exposed/not exposed to imported A. gambiae) populations. We assessed various scenarios to identify combinations of model parameters leading to ongoing malaria transmission at the airport.RESULTS: The number of infected airport personnel was low (five infected employees/six months) under assumptions reflecting possible future climatic conditions, current passenger mobility and no desinsection of airports/aircraft. Almost all infections among airport personnel were directly due to bites by imported A. gambiae. Indigenous mosquitoes would need to have comparable transmission parameters to A. gambiae to sustain disease transmission. Incoming infectious passengers play only a minor role in malaria transmission. Use of aircraft/airport desinsection led to no transmission events in the model.CONCLUSION: Our study shows that sustainable air travel-induced malaria transmission in central Europe is unlikely under current conditions or conditions which might become realistic in the next century.
AB - BACKGROUND: Aim of our study was to identify conditions under which malaria transmission caused by imported infectious mosquitoes or travellers could occur at large central European airports, and if such transmission could be sustained by indigenous mosquitoes.METHODS: We developed a deterministic and a stochastic compartmental Susceptible-Exposed-Infectious-Recovered-Susceptible (humans)/Susceptible-Exposed-Infectious (mosquitoes) model with two mosquito (imported Anopheles gambiae, indigenous A. plumbeus) and three human (travellers, airport personnel exposed/not exposed to imported A. gambiae) populations. We assessed various scenarios to identify combinations of model parameters leading to ongoing malaria transmission at the airport.RESULTS: The number of infected airport personnel was low (five infected employees/six months) under assumptions reflecting possible future climatic conditions, current passenger mobility and no desinsection of airports/aircraft. Almost all infections among airport personnel were directly due to bites by imported A. gambiae. Indigenous mosquitoes would need to have comparable transmission parameters to A. gambiae to sustain disease transmission. Incoming infectious passengers play only a minor role in malaria transmission. Use of aircraft/airport desinsection led to no transmission events in the model.CONCLUSION: Our study shows that sustainable air travel-induced malaria transmission in central Europe is unlikely under current conditions or conditions which might become realistic in the next century.
U2 - 10.1016/j.tmaid.2020.101564
DO - 10.1016/j.tmaid.2020.101564
M3 - SCORING: Journal article
C2 - 32004733
VL - 36
SP - 101564
JO - TRAVEL MED INFECT DI
JF - TRAVEL MED INFECT DI
SN - 1477-8939
ER -