Resurgence of influenza with increased genetic diversity of circulating viruses during the 2022-2023 season.

Neli Korsun, Ivelina Trifonova, Iveta Madzharova, Iva Christova
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Abstract

Introduction. After two seasons of absence and low circulation, influenza activity increased significantly in the winter of 2022-2023. This study aims to characterize virological and epidemiological aspects of influenza infection in Bulgaria during the 2022-2023 season and perform a phylogenetic/molecular analysis of the hemagglutinin (HA) and neuraminidase (NA) sequences of representative influenza strains.Hypothesis/Gap Statement. Influenza A and B viruses generate new genetic groups/clades each season, replacing previously circulating variants. This results in increased antigenic distances from current vaccine strains. Strengthening existing influenza surveillance is essential to meet the challenges posed by the co-circulation of influenza and SARS-CoV-2.Methodology. We tested 2713 clinical samples from patients with acute respiratory illnesses using a multiplex real-time RT-PCR kit (FluSC2) to detect influenza A/B and Severe acute respiratory syndrome coronavirus-2(SARS-CoV-2) simultaneously. Representative Bulgarian influenza strains were sequenced at the WHO Collaborating Centres in London, UK, and Atlanta, USA.Results. Influenza virus was detected in 694 (25.6 %) patients. Of these, 364 (52.4 %), 213 (30.7 %) and 117 (16.9 %) were positive for influenza A(H1N1)pdm09, A(H3N2) and B/Victoria lineage virus, respectively. HA genes of the 47 influenza A(H1N1)pdm09 viruses fell into clades 5a.2. and 5a.2a.1 within the 6B.5A.1A.5a.2 group. Twenty-seven A(H3N2) viruses belonging to subclades 2b, 2a.1, 2a.1b and 2a.3a.1 within the 3C.2a1b.2a.2 group were analysed. All 23 sequenced B/Victoria lineage viruses were classified into the V1A.3a.2 group. We identified amino acid substitutions in HA and NA compared with the vaccine strains, including several substitutions in the HA antigenic sites.Conclusion. The study's findings showed genetic diversity among the influenza A viruses and, to a lesser extent, among B viruses, circulating in the first season after the lifting of anti-COVID-19 measures.

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2022-2023 年流感季节期间,随着流行病毒基因多样性的增加,流感再次爆发。
前言在经历了两个季节的缺席和低流行之后,2022-2023 年冬季的流感活动显著增加。本研究旨在描述 2022-2023 年流感季节保加利亚流感感染的病毒学和流行病学特征,并对代表性流感病毒株的血凝素(HA)和神经氨酸酶(NA)序列进行系统发育/分子分析。甲型和乙型流感病毒每个季节都会产生新的基因组/支系,取代以前流行的变种。这导致与当前疫苗毒株的抗原性距离增大。为了应对流感和 SARS-CoV-2 病毒共同流行所带来的挑战,加强现有的流感监测工作至关重要。我们使用多重实时 RT-PCR 试剂盒(FluSC2)检测了 2713 份急性呼吸道疾病患者的临床样本,以同时检测甲型/乙型流感和严重急性呼吸系统综合征冠状病毒-2(SARS-CoV-2)。位于英国伦敦和美国亚特兰大的世界卫生组织合作中心对具有代表性的保加利亚流感病毒株进行了测序。在 694 名(25.6%)患者中检测到流感病毒。其中,364 人(52.4%)、213 人(30.7%)和 117 人(16.9%)分别对甲型 H1N1、甲型 H3N2 和乙型/维多利亚系流感病毒呈阳性反应。47 个甲型 H1N1 pdm09 流感病毒的 HA 基因属于 6B.5A.1A.5a.2 组中的 5a.2 支系和 5a.2a.1 支系。分析了属于 3C.2a1b.2a.2 组中 2b、2a.1、2a.1b 和 2a.3a.1 亚支系的 27 种 A(H3N2) 病毒。所有 23 个测序的 B/Victoria 系病毒都被归入 V1A.3a.2 组。与疫苗株相比,我们发现了 HA 和 NA 的氨基酸替换,包括 HA 抗原位点的几个替换。研究结果显示了甲型流感病毒之间的遗传多样性,其次是乙型流感病毒之间的遗传多样性。
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