Genomic and structural features of the yellow fever virus from the 2016–2017 Brazilian outbreak

Mariela Martínez Gómez(Fundação Oswaldo Cruz), Filipe Vieira Santos de Abreu(Instituto Federal de Educação Ciência e Tecnologia do Norte de Minas Gerais), Alexandre Araújo Cunha dos Santos(Fundação Oswaldo Cruz), Iasmim Silva de Mello(Fundação Oswaldo Cruz), Marta Pereira Santos(Fundação Oswaldo Cruz), Ieda Pereira Ribeiro(Fundação Oswaldo Cruz), Anielly Ferreira-de-Brito(Fundação Oswaldo Cruz), Rafaella Moraes de Miranda(Fundação Oswaldo Cruz), María G. Castro(Fundação Oswaldo Cruz), Mário Sérgio Ribeiro(Secretaria da Saúde), Roberto da Costa Laterrière(Secretaria da Saúde), Shirlei Ferreira de Aguiar, Guilherme Louzada Silva Meira, Deborah Antunes(Fundação Oswaldo Cruz), Pedro Henrique Monteiro Torres(Fundação Oswaldo Cruz), Daiana Mir(Fundação Oswaldo Cruz), Ana Carolina Paulo Vicente(Fundação Oswaldo Cruz), Ana Carolina Ramos Guimarães(Fundação Oswaldo Cruz), Ernesto R. Caffarena(Fundação Oswaldo Cruz), Gonzalo Bello(Fundação Oswaldo Cruz), Ricardo Lourenço‐de‐Oliveira(Fundação Oswaldo Cruz), Myrna C. Bonaldo(Fundação Oswaldo Cruz)
Journal of General Virology
February 22, 2018
Cited by 56Open Access
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Abstract

Southeastern Brazil has been suffering a rapid expansion of a severe sylvatic yellow fever virus (YFV) outbreak since late 2016, which has reached one of the most populated zones in Brazil and South America, heretofore a yellow fever-free zone for more than 70 years. In the current study, we describe the complete genome of 12 YFV samples from mosquitoes, humans and non-human primates from the Brazilian 2017 epidemic. All of the YFV sequences belong to the modern lineage (sub-lineage 1E) of South American genotype I, having been circulating for several months prior to the December 2016 detection. Our data confirm that viral strains associated with the most severe YF epidemic in South America in the last 70 years display unique amino acid substitutions that are mainly located in highly conserved positions in non-structural proteins. Our data also corroborate that YFV has spread southward into Rio de Janeiro state following two main sylvatic dispersion routes that converged at the border of the great metropolitan area comprising nearly 12 million unvaccinated inhabitants. Our original results can help public health authorities to guide the surveillance, prophylaxis and control measures required to face such a severe epidemiological problem. Finally, it will also inspire other workers to further investigate the epidemiological and biological significance of the amino acid polymorphisms detected in the Brazilian 2017 YFV strains.


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