2019
DOI: 10.1590/s1678-9946201961057
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Circulation of Chikungunya virus East-Central-South Africa genotype during an outbreak in 2016-17 in Piaui State, Northeast Brazil

Abstract: This is an open-access article distributed under the terms of the Creative Commons Attribution License.

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Cited by 12 publications
(7 citation statements)
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References 33 publications
(40 reference statements)
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“…The CHIKV ECSA genotype was first reported in Brazil in 2014, in Feira de Santana, Bahia, in the Northeast region and, in the following years, spread to other states, being identified in Bahia (2014–2017) [ 9 , 48 , 49 ], Alagoas (2016) [ 46 , 50 ], Piauí (2016–2017) [ 51 ], Sergipe (2016) [ 38 ], and Maranhão (2017) [ 40 ]. It was also identified in the Southeast region, in Rio de Janeiro (2016–2018) [ 52 , 53 ] and Minas Gerais (2017) [ 54 ].…”
Section: Discussionmentioning
confidence: 99%
“…The CHIKV ECSA genotype was first reported in Brazil in 2014, in Feira de Santana, Bahia, in the Northeast region and, in the following years, spread to other states, being identified in Bahia (2014–2017) [ 9 , 48 , 49 ], Alagoas (2016) [ 46 , 50 ], Piauí (2016–2017) [ 51 ], Sergipe (2016) [ 38 ], and Maranhão (2017) [ 40 ]. It was also identified in the Southeast region, in Rio de Janeiro (2016–2018) [ 52 , 53 ] and Minas Gerais (2017) [ 54 ].…”
Section: Discussionmentioning
confidence: 99%
“…A year later, in 2014, in Brazil, the co-circulation of the Asian and ECSA genotypes were reported in Northern and Northeastern, respectively [8,9]. Since then, the ECSA genotype has been detected in several other Brazilian states in the northeastern, southeastern, and northern regions, exerting a serious threat to public health [10][11][12][13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%
“…In the present study, variations in the structural and non-structural genes ranged up to 39, with more mutations observed in the non-structural genes. In the case of the envelope proteins, substitutions such as E1-K211E, E2-G55R, E2-H73Y, E2-V264A, E3-V42I, and E3-P59S have implications for neurovirulence during pathogenesis ( Barr and Vaidhyanathan 2019 ; Cardoso et al. 2019 ).…”
Section: Discussionmentioning
confidence: 99%