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PLoS One . Molecular characterization of haemagglutinin genes of influenza B viruses circulating in Ghana during 2016 and 2017

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  • PLoS One . Molecular characterization of haemagglutinin genes of influenza B viruses circulating in Ghana during 2016 and 2017


    PLoS One


    . 2022 Sep 23;17(9):e0271321.
    doi: 10.1371/journal.pone.0271321. eCollection 2022.
    Molecular characterization of haemagglutinin genes of influenza B viruses circulating in Ghana during 2016 and 2017


    Alhassan Mohammed Yakubu 1 2 , Nii Ayite Aryee 1 , Evelyn Yayra Bonney 3 , Erasmus Nikoi Kotey 3 4 5 , Joseph Humphrey Kofi Bonney 3 5 , Michael R Wiley 6 , Catherine B Pratt 6 , Grace Korkor Ababio 1 , Shieley Nimo-Paintsil 5 , Naiki Puplampu 5 , Seth Attoh 7 , Raymond D Fatchu 7 , Edward Owusu Nyarko 2 , Anne Fox 5 , Chaselynn M Watters 5 , Terrel Sanders 5 , Andrew G Letizia 8 , William Kwabena Ampofo 3



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    Abstract

    Recent reports of haemagglutinin antigen (HA) mismatch between vaccine composition strains and circulating strains, have led to renewed interest in influenza B viruses. Additionally, there are concerns about resistance to neuraminidase inhibitors in new influenza B isolates. To assess the potential impact in Ghana, we characterized the lineages of influenza B viruses that circulated in Ghana between 2016 and 2017 from different regions of the country: Southern, Northern and Central Ghana. Eight representative specimens from the three regions that were positive for influenza B virus by real-time RT-PCR were sequenced and compared to reference genomes from each lineage. A total of eleven amino acids substitutions were detected in the B/Victoria lineage and six in the B/Yamagata lineage. The strains of influenza B viruses were closely related to influenza B/Brisbane/60/2008 and influenza B/Phuket/3073/2013 for the Victoria and Yamagata lineages, respectively. Three main amino acid substitutions (P31S, I117V and R151K) were found in B/Victoria lineages circulating between 2016 and 2017, while one strain of B/Victoria possessed a unique glycosylation site at amino acid position 51 in the HA2 subunit. Two main substitutions (L172Q and M251V) were detected in the HA gene of the B/Yamagata lineage. The U.S. CDC recently reported a deletion sub-group in influenza B virus, but this was not identified among the Ghanaian specimens. Close monitoring of the patterns of influenza B evolution is necessary for the efficient selection of representative viruses for the design and formulation of effective influenza vaccines.


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