tetano
Editor, Senior Moderator
Emerg Microbes Infect
. 2024 May 7:2353292.
doi: 10.1080/22221751.2024.2353292. Online ahead of print. Pigs are highly susceptible to but do not transmit mink-derived highly pathogenic avian influenza virus H5N1 clade 2.3.4.4b
Taeyong Kwon[SUP] 1 [/SUP], Jessie D Trujillo[SUP] 1 [/SUP], Mariano Carossino[SUP] 2 [/SUP], Eu Lim Lyoo[SUP] 1 [/SUP], Chester D McDowell[SUP] 1 [/SUP], Konner Cool[SUP] 1 [/SUP], Franco S Matias-Ferreyra[SUP] 1 [/SUP], Trushar Jeevan[SUP] 3 [/SUP], Igor Morozov[SUP] 1 [/SUP], Natasha N Gaudreault[SUP] 1 [/SUP], Udeni B R Balasuriya[SUP] 2 [/SUP], Richard J Webby[SUP] 3 [/SUP], Nikolaus Osterrieder[SUP] 1 4 [/SUP], Juergen A Richt[SUP] 1 [/SUP]
Affiliations
Rapid evolution of highly pathogenic avian influenza viruses (HPAIVs) is driven by antigenic drift but also by reassortment, which might result in robust replication in and transmission to mammals. Recently, spillover of clade 2.3.4.4b HPAIV to mammals including humans, and their transmission between mammal species has been reported. This study aimed to evaluate the pathogenicity and transmissibility of a mink-derived clade 2.3.4.4b H5N1 HPAIV isolate from Spain in pigs. Experimental infection caused interstitial pneumonia with necrotizing bronchiolitis with high titers of virus present in the lower respiratory tract and 100% seroconversion. Infected pigs shed limited amount of virus, and importantly, there was no transmission to contact pigs. Notably, critical mammalian-like mutations such as PB2-E627K and HA-Q222L emerged at low frequencies in principal-infected pigs. It is concluded that pigs are highly susceptible to infection with the mink-derived clade 2.3.4.4b H5N1 HPAIV and provide a favorable environment for HPAIV to acquire mammalian-like adaptations.
Keywords: H5N1 clade 2.3.4.4b; Pigs; highly pathogenic avian influenza virus; mammalian-like mutations.
. 2024 May 7:2353292.
doi: 10.1080/22221751.2024.2353292. Online ahead of print. Pigs are highly susceptible to but do not transmit mink-derived highly pathogenic avian influenza virus H5N1 clade 2.3.4.4b
Taeyong Kwon[SUP] 1 [/SUP], Jessie D Trujillo[SUP] 1 [/SUP], Mariano Carossino[SUP] 2 [/SUP], Eu Lim Lyoo[SUP] 1 [/SUP], Chester D McDowell[SUP] 1 [/SUP], Konner Cool[SUP] 1 [/SUP], Franco S Matias-Ferreyra[SUP] 1 [/SUP], Trushar Jeevan[SUP] 3 [/SUP], Igor Morozov[SUP] 1 [/SUP], Natasha N Gaudreault[SUP] 1 [/SUP], Udeni B R Balasuriya[SUP] 2 [/SUP], Richard J Webby[SUP] 3 [/SUP], Nikolaus Osterrieder[SUP] 1 4 [/SUP], Juergen A Richt[SUP] 1 [/SUP]
Affiliations
- PMID: 38712345
- DOI: 10.1080/22221751.2024.2353292
Rapid evolution of highly pathogenic avian influenza viruses (HPAIVs) is driven by antigenic drift but also by reassortment, which might result in robust replication in and transmission to mammals. Recently, spillover of clade 2.3.4.4b HPAIV to mammals including humans, and their transmission between mammal species has been reported. This study aimed to evaluate the pathogenicity and transmissibility of a mink-derived clade 2.3.4.4b H5N1 HPAIV isolate from Spain in pigs. Experimental infection caused interstitial pneumonia with necrotizing bronchiolitis with high titers of virus present in the lower respiratory tract and 100% seroconversion. Infected pigs shed limited amount of virus, and importantly, there was no transmission to contact pigs. Notably, critical mammalian-like mutations such as PB2-E627K and HA-Q222L emerged at low frequencies in principal-infected pigs. It is concluded that pigs are highly susceptible to infection with the mink-derived clade 2.3.4.4b H5N1 HPAIV and provide a favorable environment for HPAIV to acquire mammalian-like adaptations.
Keywords: H5N1 clade 2.3.4.4b; Pigs; highly pathogenic avian influenza virus; mammalian-like mutations.