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Advisor(s)
Abstract(s)
A tecnologia de sequenciação de nova geração (NGS) permite uma análise
genética do vírus da gripe muito mais profunda, quando comparada com
a sequenciação pelo método de Sanger, pois permite a análise do genoma
viral completo (e não apenas do gene da hemaglutinina). O presente estudo
teve como objectivo realizar a análise filogenética e mutacional do vírus
da gripe A(H3) de forma a pesquisar possíveis marcadores genéticos e padrões
de recombinação que estejam relacionados com a efectividade vacinal.
Foram obtidas sequências do genoma completo para 179 vírus A(H3),
detectados em casos de síndroma gripal no âmbito do projecto EuroEVA/IMOVE+
durante duas épocas de gripe: 2016/2017 e 2017/2018. Dos vírus
sequenciados, 28 pertenciam a vírus de casos vacinados (15,6%). Destes,
apenas 16 apresentaram mutações não encontradas em casos não vacinados,
no entanto, todas elas emergiram de forma esporádica. Foi revelada
a existência de recombinação genómica intrasubtípica, e identificados 4
perfis distintos de recombinação. O grupo em que todos os segmentos genómicos
são semelhantes a A/Singapore/INFIMH-16-0019/2016 foi o que
registou uma maior percentagem de falhas da vacina (20,3%).
Nex t-generation sequencing technology allow a much deeper genetic analysis of influenza virus comparing to Sanger sequencing, since allows a whole genome analysis instead of a HA-based one. The present study aimed to per form phylogenetic and mutational analysis of influenza A(H3) viruses in order to search for putative genetic markers, as well as reassor tment patterns related with vaccine ef fectiveness. Were obtained whole genome sequences for 179 influenza A(H3) viruses, detected in ILI cases in the scope of EuroEVA/I-MOVE+ project during 2 winter seasons: 2016/2017 and 2017/2018. From sequenced viruses, 28 were from vaccinated cases (15.6%). From these, 16 presented mutations, not found in viruses from non-vaccinated cases, however, these mutations have emerged sporadically. Were identified four dif ferent patterns of intrasubtype reassor tment. The group with an A/Singapore/INFIMH-16-0019/2016-like profile included a higher percentage of vaccine failures (20.3%).
Nex t-generation sequencing technology allow a much deeper genetic analysis of influenza virus comparing to Sanger sequencing, since allows a whole genome analysis instead of a HA-based one. The present study aimed to per form phylogenetic and mutational analysis of influenza A(H3) viruses in order to search for putative genetic markers, as well as reassor tment patterns related with vaccine ef fectiveness. Were obtained whole genome sequences for 179 influenza A(H3) viruses, detected in ILI cases in the scope of EuroEVA/I-MOVE+ project during 2 winter seasons: 2016/2017 and 2017/2018. From sequenced viruses, 28 were from vaccinated cases (15.6%). From these, 16 presented mutations, not found in viruses from non-vaccinated cases, however, these mutations have emerged sporadically. Were identified four dif ferent patterns of intrasubtype reassor tment. The group with an A/Singapore/INFIMH-16-0019/2016-like profile included a higher percentage of vaccine failures (20.3%).
Description
Keywords
Vírus da Gripe Influenza Vírus da Gripe A(H3) Vacina Antigripal Efetividade da Vacina Época 2016/2017 Época 2017/2018 Infecções Respiratórias Doenças Infecciosas Sequenciação de Nova Geração Sequenciação do Genoma Completo Vigilância Laboratorial Saúde Pública Portugal
Pedagogical Context
Citation
Boletim Epidemiológico Observações. 2018;7(Supl 10):22-28
Publisher
Instituto Nacional de Saúde Doutor Ricardo Jorge, IP
