tetano
Editor, Senior Moderator
Avian Pathol
. 2024 Oct 9:1-14.
doi: 10.1080/03079457.2024.2403427. Online ahead of print. Continuing evolution of H5N1 highly pathogenic avian influenza viruses of clade 2.3.2.1a G2 genotype in domestic poultry of Bangladesh during 2018-2021
Mohammed Nooruzzaman[SUP] 1 2 [/SUP], Tanjin Tamanna Mumu[SUP] 1 [/SUP], Ismail Hossain[SUP] 1 [/SUP], Congriev Kumar Kabiraj[SUP] 1 [/SUP], Jahan Ara Begum[SUP] 1 [/SUP], Mohammad Mijanur Rahman[SUP] 1 [/SUP], Md Zulfekar Ali[SUP] 3 [/SUP], Mohammed Giasuddin[SUP] 3 [/SUP], Jacqueline King[SUP] 4 [/SUP], Diego G Diel[SUP] 2 [/SUP], Emdadul Haque Chowdhury[SUP] 1 [/SUP], Timm Harder[SUP] 4 [/SUP], Mohammad Rafiqul Islam[SUP] 1 [/SUP], Rokshana Parvin[SUP] 1 [/SUP]
Affiliations
We characterized 15 H5N1 HPAI viruses from different small- and medium-scale poultry flocks across Bangladesh during 2018-2021 based on their complete genome sequences. The antigenic relatedness of H5N1 HPAI viruses from different timepoints was analysed. During 2020-2021, 42.11% of the flocks tested positive for at least one of the respiratory infections, with 15.79% showing influenza A virus, of which 8.77% tested positive for HPAIV H5N1. Co-infections with two to four pathogens were detected in 15.8% of flocks. Phylogeny and gene constellation analyses based on complete genome sequences of 15 HPAI viruses revealed the continuing circulation of H5 clade 2.3.2.1a genotype G2 viruses. In the HA protein of the study isolates, functionally meaningful mutations caused the loss of an N-linked glycosylation site (T156A), a modified antigenic site A (S141P), and a mutation in the receptor binding pocket (E193R/K). Consequently, antigenic analysis revealed a significant loss of cross-reactivity between viruses from different host species and periods. Most viruses displayed oseltamivir resistance markers at positions V96, I97, S227, and N275 (N1 numbering) of the NA protein. In addition, for the PB2, M1, and NS1 proteins, significant mutations were noticed that have been associated with polymerase activity and increased virulence for mammals in all study isolates. These results highlight the need for intensified genomic surveillance of HPAI circulating in poultry in Bangladesh and for establishing appropriate control measures to decrease the circulation of these viruses in poultry in the country.
Keywords: Avian influenza; Bangladesh; HPAI H5N1; antigenic cartography; clade 2.3.2.1a; poultry.
. 2024 Oct 9:1-14.
doi: 10.1080/03079457.2024.2403427. Online ahead of print. Continuing evolution of H5N1 highly pathogenic avian influenza viruses of clade 2.3.2.1a G2 genotype in domestic poultry of Bangladesh during 2018-2021
Mohammed Nooruzzaman[SUP] 1 2 [/SUP], Tanjin Tamanna Mumu[SUP] 1 [/SUP], Ismail Hossain[SUP] 1 [/SUP], Congriev Kumar Kabiraj[SUP] 1 [/SUP], Jahan Ara Begum[SUP] 1 [/SUP], Mohammad Mijanur Rahman[SUP] 1 [/SUP], Md Zulfekar Ali[SUP] 3 [/SUP], Mohammed Giasuddin[SUP] 3 [/SUP], Jacqueline King[SUP] 4 [/SUP], Diego G Diel[SUP] 2 [/SUP], Emdadul Haque Chowdhury[SUP] 1 [/SUP], Timm Harder[SUP] 4 [/SUP], Mohammad Rafiqul Islam[SUP] 1 [/SUP], Rokshana Parvin[SUP] 1 [/SUP]
Affiliations
- PMID: 39382006
- DOI: 10.1080/03079457.2024.2403427
We characterized 15 H5N1 HPAI viruses from different small- and medium-scale poultry flocks across Bangladesh during 2018-2021 based on their complete genome sequences. The antigenic relatedness of H5N1 HPAI viruses from different timepoints was analysed. During 2020-2021, 42.11% of the flocks tested positive for at least one of the respiratory infections, with 15.79% showing influenza A virus, of which 8.77% tested positive for HPAIV H5N1. Co-infections with two to four pathogens were detected in 15.8% of flocks. Phylogeny and gene constellation analyses based on complete genome sequences of 15 HPAI viruses revealed the continuing circulation of H5 clade 2.3.2.1a genotype G2 viruses. In the HA protein of the study isolates, functionally meaningful mutations caused the loss of an N-linked glycosylation site (T156A), a modified antigenic site A (S141P), and a mutation in the receptor binding pocket (E193R/K). Consequently, antigenic analysis revealed a significant loss of cross-reactivity between viruses from different host species and periods. Most viruses displayed oseltamivir resistance markers at positions V96, I97, S227, and N275 (N1 numbering) of the NA protein. In addition, for the PB2, M1, and NS1 proteins, significant mutations were noticed that have been associated with polymerase activity and increased virulence for mammals in all study isolates. These results highlight the need for intensified genomic surveillance of HPAI circulating in poultry in Bangladesh and for establishing appropriate control measures to decrease the circulation of these viruses in poultry in the country.
Keywords: Avian influenza; Bangladesh; HPAI H5N1; antigenic cartography; clade 2.3.2.1a; poultry.