Detection of reassortant influenza B strains from 2004 to 2015 seasons in Barcelona (Catalonia, Spain) by whole genome sequencing

•This work includes a ten-year FLUBV surveillance based on WGS.•Both FLUBV lineages were detected during the study period.•Phylogenetic analyses revealed that strains belonged to different genetic groups.•Intra-lineage reassortments in PB1, PB2, NA, and NS segments were detected.•An inter-lineage re...

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Veröffentlicht in:Virus research 2023-06, Vol.330, p.199089-199089, Article 199089
Hauptverfasser: Andrés, Cristina, del Cuerpo, Margarita, Rabella, Núria, Piñana, Maria, Iglesias-Cabezas, Manuel Jesús, González-Sánchez, Alejandra, Esperalba, Juliana, Rando, Ariadna, Martín, Maria Carmen, Fuentes, Francisco, Rubio, Susana, Saubi, Narcís, Pumarola, Tomàs, Antón, Andrés
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Sprache:eng
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Zusammenfassung:•This work includes a ten-year FLUBV surveillance based on WGS.•Both FLUBV lineages were detected during the study period.•Phylogenetic analyses revealed that strains belonged to different genetic groups.•Intra-lineage reassortments in PB1, PB2, NA, and NS segments were detected.•An inter-lineage reassortment in NP was observed amongst B/Vic viruses from different seasons. Influenza B viruses (FLUBV) have segmented genomes which enables the virus to evolve by segment reassortment. Since the divergence of both FLUBV lineages, B/Victoria/2/87 (FLUBV/VIC) and B/Yamagata/16/88 (FLUBV/YAM), PB2, PB1 and HA have kept the same ancestor, while some reassortment events in the other segments have been reported worldwide. The aim of the present study was to find out reassortment episodes in FLUBV strains detected in cases attended at Hospital Universitari Vall d'Hebron and Hospital de la Santa Creu i Sant Pau (Barcelona, Spain) from 2004 to 2015 seasons. From October 2004 to May 2015, respiratory specimens were received from patients with respiratory tract infection suspicion. Influenza detection was carried out by either cell culture isolation, immunofluorescence or PCR-based assays. A RT-PCR was performed to distinguish both lineages by agarose gel electrophoresis. Whole genome amplification was performed using the universal primer set by Zhou et al. in 2012, and subsequently sequenced using Roche 454 GS Junior platform. Bioinformatic analysis was performed to characterise the sequences with B/Malaysia/2506/2007 and B/Florida/4/2006 corresponding sequences as reference of (B/VIC) and (B/YAM), respectively. A total of 118 FLUBV (75 FLUBV/VIC and 43 FLUBV/YAM), from 2004 to 2006, 2008–2011 and 2012–2015 seasons, were studied. The whole genome of 58 FLUBV/VIC and 42 FLUBV/YAM viruses was successfully amplified. Based on HA sequences, most FLUBV/VIC viruses (37; 64%) belonged to clade 1A (B/Brisbane/60/2008) except to 11 (19%), which fell within clade 1B (B/HongKong/514/2009) and 10 (17%) to B/Malaysia/2506/2004. Nine (20%) FLUBV/YAM viruses belonged to clade 2 (B/Massachusetts/02/2012), 18 (42%) to clade 3 (B/Phuket/3073/2013) and 15 (38%) fell within Florida/4/2006. Numerous intra-lineage reassortments in PB2, PB1, NA and NS were found in 2 2010–2011 viruses. An important inter-lineage reassortment event from 2008 to 2009 (11), 2010–2011 (26) and 2012–2013 (3) FLUBV/VIC (clade 1) strains to FLUBV/YAM (clade 3) was found, in addition to 1 reassortant NS in 2010–2011 B
ISSN:0168-1702
1872-7492
DOI:10.1016/j.virusres.2023.199089