Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/43160
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dc.contributor.authorBORREMANS, Benny-
dc.contributor.authorMummah, RO-
dc.contributor.authorGuglielmino, AH-
dc.contributor.authorGalloway, RL-
dc.contributor.authorHENS, Niel-
dc.contributor.authorPrager, KC-
dc.contributor.authorLloyd-Smith, JO-
dc.date.accessioned2024-06-14T12:44:55Z-
dc.date.available2024-06-14T12:44:55Z-
dc.date.issued2023-
dc.date.submitted2024-06-14T12:40:42Z-
dc.identifier.citationMethods in Ecology and Evolution, 14 (10) , p. 2654 -2667-
dc.identifier.urihttp://hdl.handle.net/1942/43160-
dc.description.abstract1. Studies of infectious disease ecology would benefit greatly from knowing when individuals were infected, but estimating this time of infection can be challenging, especially in wildlife. Time of infection can be estimated from various types of data, with antibody-level data being one of the most promising sources of information. The use of antibody levels to back-calculate infection time requires the development of a host-pathogen system-specific model of antibody dynamics, and a leading challenge in such quantitative serology approaches is how to model antibody dynamics in the absence of experimental infection data. 2. We present a way to model antibody dynamics in a Bayesian framework that facilitates the incorporation of all available information about potential infection times and apply the model to estimate infection times of Channel Island foxes infected with Leptospira interrogans. 3. Using simulated data, we show that the approach works well across a broad range of parameter settings and can lead to major improvements in infection time estimates that depend on system characteristics such as antibody decay rate and variation in peak antibody levels after exposure. When applied to field data we saw reductions up to 83% in the window of possible infection times. 4. The method substantially simplifies the challenge of modelling antibody dynamics in the absence of individuals with known infection times, opens up new opportunities in wildlife disease ecology and can even be applied to cross-sectional data once the model is trained. K E Y W O R D S antibody decay, bayesian dynamic model, disease ecology, incidence, quantitative serology, time of infection, transmission dynamics, wildlife disease This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.-
dc.description.sponsorshipBenny Borremans was supported by the European Commission Horizon 2020 Marie Sklodowska-Curie Actions (grant no. 707840). James Lloyd-Smith was supported by the Defence Advanced Research Projects Agency DARPA PREEMPT #D18AC00031 and the UCLA AIDS Institute and Charity Treks. James Lloyd-Smith and K. C. Prager were supported by the U.S. National Science Foundation (DEB-1557022, OCE-1335657 and DEB-2245631), the Strategic Environmental Research and Development Program (SERDP, RC-2635) of the U.S. Department of Defence, and the Cooperative Ecosystem Studies Unit Cooperative Agreement #W9132T1920006. The authors would like to express their gratitude and respect for the tremendous work performed by all personnel involved in the field work. The findings and conclusions in this report are those of the author(s) and do not necessarily represent the official position of the Centers for Disease Control and Prevention.-
dc.language.isoen-
dc.publisherWILEY-
dc.rights2023 The Authors. Methods in Ecology and Evolution published by John Wiley & Sons Ltd on behalf of British Ecological Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes-
dc.subject.otherantibody decay-
dc.subject.otherbayesian dynamic model-
dc.subject.otherdisease ecology-
dc.subject.otherincidence-
dc.subject.otherquantitative serology-
dc.subject.othertime of infection-
dc.subject.othertransmission dynamics-
dc.subject.otherwildlife disease-
dc.titleInferring time of infection from field data using dynamic models of antibody decay-
dc.typeJournal Contribution-
dc.identifier.epage2667-
dc.identifier.issue10-
dc.identifier.spage2654-
dc.identifier.volume14-
local.bibliographicCitation.jcatA1-
local.publisher.place111 RIVER ST, HOBOKEN 07030-5774, NJ-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.type.programmeH2020-
local.relation.h2020707840-
dc.identifier.doi10.1111/2041-210X.14165-
dc.identifier.isi001051698200001-
local.provider.typeWeb of Science-
local.uhasselt.internationalyes-
item.fullcitationBORREMANS, Benny; Mummah, RO; Guglielmino, AH; Galloway, RL; HENS, Niel; Prager, KC & Lloyd-Smith, JO (2023) Inferring time of infection from field data using dynamic models of antibody decay. In: Methods in Ecology and Evolution, 14 (10) , p. 2654 -2667.-
item.fulltextWith Fulltext-
item.contributorBORREMANS, Benny-
item.contributorMummah, RO-
item.contributorGuglielmino, AH-
item.contributorGalloway, RL-
item.contributorHENS, Niel-
item.contributorPrager, KC-
item.contributorLloyd-Smith, JO-
item.accessRightsOpen Access-
crisitem.journal.issn2041-210X-
crisitem.journal.eissn2041-2096-
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