Low prevalence of influenza A strains with resistance markers in Brazil during 2017–2019 seasons

神经氨酸酶 奥司他韦 病毒学 抗药性 病毒 抗性突变 甲型流感病毒 神经氨酸酶抑制剂 大流行 氨基酸取代 生物 突变 微生物学 医学 聚合酶链反应 基因 遗传学 2019年冠状病毒病(COVID-19) 逆转录酶 传染病(医学专业) 疾病 病理
作者
Thiago das Chagas Sousa,Jessica Santa Cruz Carvalho Martins,Milene Dias Miranda,Cristiana C. Garcia,Paola Cristina Resende,Cliomar Alves do Santos,Maria do Carmo Debur,Rodrigo Ribeiro Rodrigues,Andréa Cony Cavalcanti,Tatiana Schäffer Gregianini,Felipe Campos de Melo Iani,Felicidade Mota Pereira,Sandra Bianchini Fernandes,Jessylene de Almeida Ferreira,Katia Corrêa de Oliveira Santos,Fernando Couto Motta,David W. Brown,Walquíria Aparecida Ferreira de Almeida,Marilda Mendonça Siqueira,Aline da Rocha Matos
出处
期刊:Frontiers in Public Health [Frontiers Media]
卷期号:10 被引量:1
标识
DOI:10.3389/fpubh.2022.944277
摘要

The influenza A virus (IAV) is of a major public health concern as it causes annual epidemics and has the potential to cause pandemics. At present, the neuraminidase inhibitors (NAIs) are the most widely used anti-influenza drugs, but, more recently, the drug baloxavir marboxil (BXM), a polymerase inhibitor, has also been licensed in some countries. Mutations in the viral genes that encode the antiviral targets can lead to treatment resistance. Worldwide, a low prevalence of antiviral resistant strains has been reported. Despite that, this situation can change rapidly, and resistant strain surveillance is a priority. Thus, the aim of this was to evaluate Brazilian IAVs antiviral resistance from 2017 to 2019 through the identification of viral mutations associated with reduced inhibition of the drugs and by testing the susceptibility of IAV isolates to oseltamivir (OST), the most widely used NAI drug in the country. Initially, we analyzed 282 influenza A(H1N1)pdm09 and 455 A(H3N2) genetic sequences available on GISAID. The amino acid substitution (AAS) NA:S247N was detected in one A(H1N1)pdm09 strain. We also identified NA:I222V ( n = 6) and NA:N329K ( n = 1) in A(H3N2) strains. In addition, we performed a molecular screening for NA:H275Y in 437 A(H1N1)pdm09 samples, by pyrosequencing, which revealed a single virus harboring this mutation. Furthermore, the determination of OST IC 50 values for 222 A(H1N1)pdm09 and 83 A(H3N2) isolates revealed that all isolates presented a normal susceptibility profile to the drug. Interestingly, we detected one A(H3N2) virus presenting with PA:E119D AAS. Moreover, the majority of the IAV sequences had the M2:S31N adamantanes resistant marker. In conclusion, we show a low prevalence of Brazilian IAV strains with NAI resistance markers, in accordance with what is reported worldwide, indicating that NAIs still remain an option for the treatment of influenza infections in Brazil. However, surveillance of influenza resistance should be strengthened in the country for improving the representativeness of investigated viruses and the robustness of the analysis.

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