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Genomic and epidemiological monitoring of yellow fever virus transmission potential

Genomic and epidemiological monitoring of yellow fever virus transmission potential
Genomic and epidemiological monitoring of yellow fever virus transmission potential
Despite the existence of an effective vaccine for yellow fever, there are still almost 80,000 fatalities from this infection each year. Since 2016, there has been a resurgence of cases in Africa and South America—and this at a time when the vaccine is in short supply. The worry is that yellow fever will spread from the forests to the cities, because its vector, Aedes spp. mosquitoes, are globally ubiquitous. Faria et al. integrate genomic, epidemiological, and case distribution data from Brazil to estimate patterns of geographic spread, the risks of virus exposure, and the contributions of rural versus urban transmission (see the Perspective by Barrett). Currently, the yellow fever epidemic in Brazil seems to be driven by infections acquired while visiting forested areas and indicates spillover from susceptible wild primates.Science, this issue p. 894; see also p. 847The yellow fever virus (YFV) epidemic in Brazil is the largest in decades. The recent discovery of YFV in Brazilian Aedes species mosquitos highlights a need to monitor the risk of reestablishment of urban YFV transmission in the Americas. We use a suite of epidemiological, spatial, and genomic approaches to characterize YFV transmission. We show that the age and sex distribution of human cases is characteristic of sylvatic transmission. Analysis of YFV cases combined with genomes generated locally reveals an early phase of sylvatic YFV transmission and spatial expansion toward previously YFV-free areas, followed by a rise in viral spillover to humans in late 2016. Our results establish a framework for monitoring YFV transmission in real time that will contribute to a global strategy to eliminate future YFV epidemics.
0036-8075
894-899
Faria, N. R.
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Kraemer, M. U. G.
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Hill, S. C.
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Goes de Jesus, J.
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Aguiar, R. S.
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Iani, F. C. M.
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Xavier, J.
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Quick, J.
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du Plessis, L.
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Dellicour, S.
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Thézé, J.
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Carvalho, R. D. O.
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Baele, G.
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Wu, C.-H.
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Lourenço, J.
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Obolski, U.
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Abade, L.
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Vasylyeva, T. I.
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Giovanetti, M.
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Yi, D.
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Weiss, D. J.
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Pullan, S. T.
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Carroll, M.
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de Oliveira, T.
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Lemey, P.
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Trindade, G. S.
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Cauchemez, S.
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Alcantara, L. C. J.
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Pybus, O. G.
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Faria, N. R.
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Kraemer, M. U. G.
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Hill, S. C.
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Goes de Jesus, J.
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Iani, F. C. M.
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Xavier, J.
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Quick, J.
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du Plessis, L.
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Dellicour, S.
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Thézé, J.
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Lourenço, J.
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Obolski, U.
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Vasylyeva, T. I.
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Giovanetti, M.
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Weiss, D. J.
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Fonseca, V.
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Adelino, T. E. R.
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Oliveira, M. A. A.
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dos Santos, F. C. P.
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Azevedo, V.
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Araujo, E. S. M.
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Mendonça, M. C. L.
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dos Santos, C. D.
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dos Santos, C. D.
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Okumoto, O.
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Pybus, O. G.
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Faria, N. R., Kraemer, M. U. G., Hill, S. C., Goes de Jesus, J., Aguiar, R. S., Iani, F. C. M., Xavier, J., Quick, J., du Plessis, L., Dellicour, S., Thézé, J., Carvalho, R. D. O., Baele, G., Wu, C.-H., Silveira, P. P., Arruda, M. B., Pereira, M. A., Pereira, G. C., Lourenço, J., Obolski, U., Abade, L., Vasylyeva, T. I., Giovanetti, M., Yi, D., Weiss, D. J., Wint, G. R. W., Shearer, F. M., Funk, S., Nikolay, B., Fonseca, V., Adelino, T. E. R., Oliveira, M. A. A., Silva, M. V. F., Sacchetto, L., Figueiredo, P. O., Rezende, I. M., Mello, E. M., Said, R. F. C., Santos, D. A., Ferraz, M. L., Brito, M. G., Santana, L. F., Menezes, M. T., Brindeiro, R. M., Tanuri, A., dos Santos, F. C. P., Cunha, M. S., Nogueira, J. S., Rocco, I. M., da Costa, A. C., Komninakis, S. C. V., Azevedo, V., Chieppe, A. O., Araujo, E. S. M., Mendonça, M. C. L., dos Santos, C. D., dos Santos, C. D., Mares-Guia, A. M., Nogueira, R. M. R., Sequeira, P. C., Abreu, R. G., Garcia, M. H. O., Abreu, A. L., Okumoto, O., Kroon, E. G., de Albuquerque, C. F. C., Lewandowski, K., Pullan, S. T., Carroll, M., de Oliveira, T., Sabino, E. C., Souza, R. P., Suchard, M. A., Lemey, P., Trindade, G. S., Drumond, B. P., Filippis, A. M. B., Loman, N. J., Cauchemez, S., Alcantara, L. C. J. and Pybus, O. G. (2018) Genomic and epidemiological monitoring of yellow fever virus transmission potential. Science, 361 (6405), 894-899. (doi:10.1126/science.aat7115).

Record type: Article

Abstract

Despite the existence of an effective vaccine for yellow fever, there are still almost 80,000 fatalities from this infection each year. Since 2016, there has been a resurgence of cases in Africa and South America—and this at a time when the vaccine is in short supply. The worry is that yellow fever will spread from the forests to the cities, because its vector, Aedes spp. mosquitoes, are globally ubiquitous. Faria et al. integrate genomic, epidemiological, and case distribution data from Brazil to estimate patterns of geographic spread, the risks of virus exposure, and the contributions of rural versus urban transmission (see the Perspective by Barrett). Currently, the yellow fever epidemic in Brazil seems to be driven by infections acquired while visiting forested areas and indicates spillover from susceptible wild primates.Science, this issue p. 894; see also p. 847The yellow fever virus (YFV) epidemic in Brazil is the largest in decades. The recent discovery of YFV in Brazilian Aedes species mosquitos highlights a need to monitor the risk of reestablishment of urban YFV transmission in the Americas. We use a suite of epidemiological, spatial, and genomic approaches to characterize YFV transmission. We show that the age and sex distribution of human cases is characteristic of sylvatic transmission. Analysis of YFV cases combined with genomes generated locally reveals an early phase of sylvatic YFV transmission and spatial expansion toward previously YFV-free areas, followed by a rise in viral spillover to humans in late 2016. Our results establish a framework for monitoring YFV transmission in real time that will contribute to a global strategy to eliminate future YFV epidemics.

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More information

Accepted/In Press date: 20 July 2018
Published date: 31 August 2018

Identifiers

Local EPrints ID: 438679
URI: http://eprints.soton.ac.uk/id/eprint/438679
ISSN: 0036-8075
PURE UUID: 64953a12-a168-4d97-8f49-4026e078effa
ORCID for C.-H. Wu: ORCID iD orcid.org/0000-0001-9386-725X

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Date deposited: 20 Mar 2020 17:33
Last modified: 17 Mar 2024 04:00

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Contributors

Author: N. R. Faria
Author: M. U. G. Kraemer
Author: S. C. Hill
Author: J. Goes de Jesus
Author: R. S. Aguiar
Author: F. C. M. Iani
Author: J. Xavier
Author: J. Quick
Author: L. du Plessis
Author: S. Dellicour
Author: J. Thézé
Author: R. D. O. Carvalho
Author: G. Baele
Author: C.-H. Wu ORCID iD
Author: P. P. Silveira
Author: M. B. Arruda
Author: M. A. Pereira
Author: G. C. Pereira
Author: J. Lourenço
Author: U. Obolski
Author: L. Abade
Author: T. I. Vasylyeva
Author: M. Giovanetti
Author: D. Yi
Author: D. J. Weiss
Author: G. R. W. Wint
Author: F. M. Shearer
Author: S. Funk
Author: B. Nikolay
Author: V. Fonseca
Author: T. E. R. Adelino
Author: M. A. A. Oliveira
Author: M. V. F. Silva
Author: L. Sacchetto
Author: P. O. Figueiredo
Author: I. M. Rezende
Author: E. M. Mello
Author: R. F. C. Said
Author: D. A. Santos
Author: M. L. Ferraz
Author: M. G. Brito
Author: L. F. Santana
Author: M. T. Menezes
Author: R. M. Brindeiro
Author: A. Tanuri
Author: F. C. P. dos Santos
Author: M. S. Cunha
Author: J. S. Nogueira
Author: I. M. Rocco
Author: A. C. da Costa
Author: S. C. V. Komninakis
Author: V. Azevedo
Author: A. O. Chieppe
Author: E. S. M. Araujo
Author: M. C. L. Mendonça
Author: C. D. dos Santos
Author: C. D. dos Santos
Author: A. M. Mares-Guia
Author: R. M. R. Nogueira
Author: P. C. Sequeira
Author: R. G. Abreu
Author: M. H. O. Garcia
Author: A. L. Abreu
Author: O. Okumoto
Author: E. G. Kroon
Author: C. F. C. de Albuquerque
Author: K. Lewandowski
Author: S. T. Pullan
Author: M. Carroll
Author: T. de Oliveira
Author: E. C. Sabino
Author: R. P. Souza
Author: M. A. Suchard
Author: P. Lemey
Author: G. S. Trindade
Author: B. P. Drumond
Author: A. M. B. Filippis
Author: N. J. Loman
Author: S. Cauchemez
Author: L. C. J. Alcantara
Author: O. G. Pybus

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