Title
Fluorescent biomarkers demonstrate prospects for spreadable vaccines to control disease transmission in wild bats
Date Issued
01 December 2019
Access level
open access
Resource Type
journal article
Author(s)
Bakker K.M.
Rocke T.E.
Osorio J.E.
Abbott R.C.
Carrera J.E.
Streicker D.G.
Publisher(s)
Nature Research
Abstract
Vaccines that autonomously transfer among individuals have been proposed as a strategy to control infectious diseases within inaccessible wildlife populations. However, rates of vaccine spread and epidemiological efficacy in real-world systems remain elusive. Here, we investigate whether topical vaccines that transfer among individuals through social contacts can control vampire bat rabies—a medically and economically important zoonosis in Latin America. Field experiments in three Peruvian bat colonies, which used fluorescent biomarkers as a proxy for the bat-to-bat transfer and ingestion of an oral vaccine, revealed that vaccine transfer would increase population-level immunity up to 2.6 times beyond the same effort using conventional, non-spreadable vaccines. Mathematical models showed that observed levels of vaccine transfer would reduce the probability, size and duration of rabies outbreaks, even at low but realistically achievable levels of vaccine application. Models further predicted that existing vaccines provide substantial advantages over culling bats—the policy currently implemented in North, Central and South America. Linking field studies with biomarkers to mathematical models can inform how spreadable vaccines may combat pathogens of health and conservation concern before costly investments in vaccine design and testing.
Start page
1697
End page
1704
Volume
3
Issue
12
Language
English
OCDE Knowledge area
Ciencia veterinaria
Scopus EID
2-s2.0-85075382479
PubMed ID
Source
Nature Ecology and Evolution
ISSN of the container
2397-334X
Sponsor(s)
K.M.B. was supported by NIH award F32AI134016, and computational resources were provided by NIH award U01GM110712. D.G.S. was supported by a Sir Henry Dale Fellowship that was jointly funded by the Wellcome Trust and Royal Society (102507/Z/13/Z). Additional funding was provided via a Challenge Grant from the Royal Society to D.G.S., T.E.R., J.E.O., C.S. and N.F. (CH160097). The authors are grateful to D. Walsh, M. Viana and the Streicker Group for comments on earlier versions of this manuscript. Any use of trade, product or firm names does not imply endorsement by the US Government.
Sources of information:
Directorio de Producción Científica
Scopus