Indeed, following its first appearance over 25 years ago among domestic birds (ducks and chickens) in South-Eastern Asia, alongside a number of fatal and non-lethal cases of infection in people as well as in domestic and wild mammalian species, thousands of additional episodes have recently occurred across the globe in poultry farms as well as in wild terrestrial and marine birds (e.g. seagulls, pelicans and cormorants) and, most notably, among aquatic mammals including sea lions, seals, porpoises and bottlenose dolphins. Within this framework, the mass involvement of seabirds, sea lions and, to a lesser extent, of bottlenose dolphins along the coast of Peru (as well as of other South American Countries) is a matter of concern, in view of the "clade 184.108.40.206b" as the "common denominator" behind all these cases of HPAI A(H5N1) infection, often leading to a fatal outcome due to the marked neurotropism and neuropathogenicity displayed by the virus in pinnipeds and in cetaceans (Leguia et al., 2023).
Still noteworthy, an outbreak of HPAI A(H5N1) virus infection has been recently detected in intensively farmed minks from the Galicia region of Spain (Montserrat et al., 2023). As previously reported in intensive mink herds from The Netherlands and Denmark, where the "cluster 5" variant of concern (VOC) developed following SARS-CoV-2 acquirement from infected people (viral spillover), with subsequent transmission of the mutated virus to humans (viral spillback) (Di Guardo, 2023), also in this case the viral pathogen - which could have been transferred by infected seagulls - underwent a number of mutational events in mink, followed by sustained intraspecies transmission of the mutated virus (Montserrat et al., 2023). In this respect, although the high susceptibility of mink to circulating human and avian influenza viruses is not new to the scientific community (Sun et al., 2021), it should be additionally emphasized that the alanine (A) mutation found at position 271 of PB2 (T271A) from all mink viruses is a well-known pathogenicity determinant increasing the polymerase enzyme activity of influenza A viruses in mammalian host cells and mice (Bussey et al., 2010).
Notwithstanding the above, very few cases of human infection associated with the newly emerged A(H5N1) 220.127.116.11b clade have been hitherto identified, with a lethal disease case having been recently diagnosed in an 11 years-old girl from Cambodia, in whom this fatality was caused by the HPAI A(H5N1) 18.104.22.168c clade, widely circulating in poultry farms from that geographic area (Mallapaty, 2023). From 2003 until the end of 2022, almost 900 cases of human infection caused by the HPAI A(H5N1) virus have been officially reported, with more than the half of them having been characterized by a fatal outcome. Of course, the "human exposure risk" does not equally involve all of us, provided that some professional categories - i.e. people working in poultry farms as well as in avian slaughterhouses, alongside veterinarians working in the aforementioned facilities and/or performing necropsies on domestic and wild birds - tend to be more exposed than others. Within such a context, although this zoonotic, multi-segmented RNA viral pathogen has hitherto shown a low human-to-human transmission efficiency, its high propensity to undergo genetic recombination and reassortment events undoubtedly represents a great concern issue.
Besides, the recent finding of a mutated A(H5N1) strain in intensely reared mink from the Galicia region of Spain, among which the virus spread rapidly and diffusely (Montserrat et al., 2023), raises further concern in this direction. Once again, as the SARS-CoV-2 pandemic has clearly taught us, the One Health principle should be the "polar star" around which the eco-epidemiological surveillance of HPAI A(H5N1) and, more in general, of all animal and human influenza viruses should be put in place worldwide, within a global multidisciplinary and intersectorial collaboration effort, a key element of which resides in the continuous uploading into public repositories as well as in the mutual exchange of viral genomic sequences among all laboratories involved in the aforementioned surveillance activities.
Bussey KA, Bousse TL, Desmet EA, Kim B, Takimoto T. PB2 residue 271 plays a key role in enhanced polymerase activity of influenza A viruses in mammalian host cells. J. Virol. 2010; 84: 4395-4406. https://doi.org/10.1128/JVI.02642-09.
Di Guardo G. The SARS-CoV-2 pandemic at the wildlife-domestic animal-human interface. Pathogens 2023; 12(2): 222. doi: 10.3390/pathogens12020222.
Leguia M, et al. Highly pathogenic avian influenza A (H5N1) in marine mammals and seabirds in Peru. https://doi.org/10.1101/2023.03.03.531008doi: bioRxiv preprint. March 03, 2023.
Mallapaty S. Girl who died of bird flu did not have widely-circulating variant. Nature 2023. doi: https://doi.org/10.1038/d41586-023-00585-1.
Montserrat A, et al. Highly pathogenic avian influenza A(H5N1) virus infection in farmed minks, Spain, October 2022. Euro Surveill. 2023; 28(3): pii=2302300001. https://doi.org/10.2807/1560-7917.ES.2023.28.3.2300001.
Sun H, et al. Mink is a highly susceptible host species to circulating human and avian influenza viruses. Emerg. Microbes Infect. 2021; 10: 472-480. https://doi.org/10.1080/22221751.2021.1899058 PMID: 33657971.
Giovanni Di Guardo, DVM, Dipl. ECVP, Editorial Board Member, Pathogens, Retired Professor of General Pathology and Veterinary Pathophysiology at the Veterinary Medical Faculty of the University of Teramo, 64100 Teramo, Italy Private address: Viale Pasteur, 77 00144 - EUR - Rome, Italy (E-mail address: email@example.com)