28 May 2026, 08:30 hours; Rome
This update covers avian influenza viruses (AIV) with zoonotic potential occurring worldwide, i.e. H5Nx, H7Nx high pathogenicity avian influenza (HPAI) viruses and H3N8, H5Nx, H6N1, H7Nx, H9N2, H10Nx and H11 low pathogenicity avian influenza (LPAI).
Specific information is available for Avian Influenza A(H7N9) virus viruses and Sub-Saharan Africa HPAI in related FAO Avian Influenza situation updates.
HPAI outbreaks in animals officially reported since last update (23 April 2026): in total, 763 outbreaks / events have been reported in 31 countries/territories caused by H5Nx (95), H5N1 (659), H5N5 (3), H5N9 (3) and H7N3 (3) (see Table 1 for details).
LPAI events in animals officially reported since the last update: 0 new events were reported.
Number of human cases officially reported since the last update: 5 new events were reported. [ref1, ref2, ref3, ref4, ref5].
Map 1. Global distribution of AIV with zoonotic potential observed since 1 October 2025 (i.e. current wave)

Symbols may overlap for events in similar geographic locations.
Notes: Refer to the disclaimer available on this webpage for the names and boundaries in this map. The final boundary between the Sudan and South Sudan has not yet been determined. The final status of the Abyei area is not yet determined. The dotted line represents approximately the Line of Control in Jammu and Kashmir agreed upon by India and Pakistan. The final status of Jammu and Kashmir has not yet been agreed upon by the parties.
Source: United Nations Geospatial. 2020. Map of the World. [Cited June 2026]. Modified with GLW 4 data and Emergency Prevention System Global Animal Disease Information System (EMPRES-i), WOAH and National Authorities data, 2025.
Map 2. Global distribution of AIV with zoonotic potential* observed in the period 1 October 2024 to 30 September 2025 (i.e. previous wave)
Symbols may overlap for events in similar geographic locations.
Notes: Refer to the disclaimer available on this webpage for the names and boundaries in this map. Final boundary between the Sudan and South Sudan has not yet been determined. Final status of the Abyei area is not yet determined.
Dotted line represents approximately the Line of Control in Jammu and Kashmir agreed upon by India and Pakistan. The final status of Jammu and Kashmir has not yet been agreed upon by the parties.
Source: United Nations Geospatial. 2020. Map of the World. [Cited October 2025]. Modified with GLW 4 data and Emergency Prevention System Global Animal Disease Information System (EMPRES-i), WOAH and National Authorities data, 2024.
October – December 2024

January – March 2025

April – June 2025

July – September 2025

Symbols may overlap for events in similar geographic locations.
Notes: Refer to the disclaimer available on this webpage for the names and boundaries in this map. Final boundary between the Sudan and South Sudan has not yet been determined. Final status of the Abyei area is not yet determined. Dotted line represents approximately the Line of Control in Jammu and Kashmir agreed upon by India and Pakistan. The final status of Jammu and Kashmir has not yet been agreed upon by the parties.
Source: United Nations Geospatial. 2020. Map of the World. [Cited October 2025]. Modified with GLW 4 data and Emergency Prevention System Global Animal Disease Information System (EMPRES-i), WOAH and National Authorities data, 2024.
Table 1. High pathogenicity avian influenza viruses with zoonotic potential reported since the last update
| Virus | Country/Area | Last observed outbreak | # events reported since the last update | Total # events reported since 1 Oct. 2025 | Species affected since the last update |
|---|---|---|---|---|---|
H5 |
Japan |
22/05/2026 |
9 |
31 |
Large-billed crow; Fox |
Peru |
28/04/2026 |
19 |
26 |
Chicken, Duck, Goose, Turkey, Non-poultry birds |
|
United States of America7 |
18/05/2026 |
67 |
1 761 |
American white pelican, Bald eagle, Black vulture, Cackling goose, Canada goose, Eared grebe, Great horned owl, Greater white-fronted goose, Green-winged teal, Little blue heron, Mallard, Peregrine falcon, Red-tailed hawk, Ross's goose, Snow goose, Swan, Turkey vulture, Vulture, Wood duck; California sea lion |
|
H5N1 |
Argentina |
05/05/2026 |
1 |
24 |
Chicken, Duck, Turkey |
Austria |
20/05/2026 |
9 |
99 |
Mute Swan, Saker Falcon |
|
Belgium |
10/04/2026 |
2 |
356 |
Herring Gull, Snow Goose |
|
Cambodia |
22/04/2026 |
1 |
7 |
Chicken |
|
Canada3 |
16/05/2026 |
8 |
122 |
Poultry; Cat |
|
Chile12 |
04/05/2026 |
23 |
36 |
Non-poultry birds; Black-necked swan, Cape Barren Goose, Coscoroba swan, Little Egret |
|
China |
30/04/2026 |
1 |
37 |
Quail |
|
Czech Republic |
04/05/2026 |
2 |
100 |
Chicken |
|
Denmark |
21/04/2026 |
6 |
255 |
Eurasian buzzard, Northern Goshawk, Rook, Western Marsh-harrier |
|
Estonia |
12/05/2026 |
2 |
34 |
Non-poultry birds; Barnacle Goose |
|
Finland |
07/05/2026 |
2(in W) |
32 |
Barnacle Goose, Eurasian Eagle-Owl |
|
France |
18/05/2026 |
23 |
474 |
Chicken, Duck, Non-poultry birds; Anatidae, Black-legged Kittiwake, Canada Goose, Common Crane, Common Moorhen, Common Teal, Grey Heron, Greylag Goose, Herring Gull, Mute Swan, Sanderling |
|
Germany |
17/04/2026 |
403 |
3 973 |
Chicken, Duck; Accipitridae, Anatidae, Anserinae, Ardeidae, Barnacle Goose, Black-headed Gull, Black-necked swan, Bufflehead, California Quail, Canada Goose, Carrion Crow, Caspian Gull, Chicken, Ciconiidae, Common Coot, Common Eider, Common Kestrel, Common Scoter, Common Shelduck, Cygnus, Egyptian Goose, Eurasian Buzzard, Eurasian Eagle-Owl, Eurasian oystercatcher, Falconidae, Goosander, Great black-backed Gull, Great Crested Grebe, Great Cormorant, Greater white-fronted Goose, Grey Heron, Grey Partridge, Greylag Goose, Gruidae, Herring Gull, Hooded Merganser, Laridae, Lesser Black-backed Gull, Lesser Scaup, Mallard, Mew Gull, Muscovy Duck, Mute Swan, Northern Gannet, Northern Pintail, Peregrine Falcon, Phalacrocoracidae, Phasianidae, Rallidae, Red Kite, Red-breasted Goose, Scaly-sided merganser, Scarlet Ibis, Smew, Strigidae, Swan Goose, Taiga Bean Goose, Tawny owl, Tufted Duck, Turkey, Tytonidae, White Stork, Whooper swan |
|
Iceland |
06/02/2026 |
2 |
4 |
Greylag Goose |
|
Italy |
05/04/2026 |
1 |
164 |
Mute Swan |
|
Japan |
23/04/2026 |
2 |
160 |
Chicken; Large-billed crow |
|
Republic of Korea |
09/04/2026 |
14 |
115 |
Bean Goose, Cinereous Vulture, Great White Egret, Greater White-fronted Goose, Grey Heron, Whooper Swan |
|
Mexico |
02/03/2026 |
1 |
7 |
American Black Vulture |
|
Moldova |
25/03/2026 |
2 |
7 |
Mute Swan, Phalacrocoracidae |
|
Montenegro |
10/03/2026 |
2 |
5 |
Poultry |
|
Nepal |
14/04/2026 |
7 |
40 |
Chicken (mostly Layers, but also broilers, backyards) |
|
Netherlands (Kingdom of the) |
22/05/2026 |
7 |
426 |
Chicken;Eurasian Curlew, Greylag Goose, Herring Gull, Mallard, Peregrin falcon |
|
Norway |
19/05/2026 |
8 |
64 |
Anserinae, Greylag Goose, Northern Gannet, Pink-footed Goose |
|
The Philippines |
08/05/2026 |
1 |
17 |
Duck |
|
Poland |
21/05/2026 |
60 |
461 |
Chicken, Duck, Goose, Turkey, Non-poultry birds; Eurasian Jackdaw, Grey Heron, Greylag Goose, Red Kite, Mute Swan, White Stork |
|
Sweden |
26/03/2026 |
2 |
125 |
Great Cormorant, Peregrin falcon |
|
Ukraine |
21/04/2026 |
1 |
4 |
Non-poultry birds |
|
United Kingdom of Great Britain and Northern Ireland6 |
14/05/2026 |
14 |
864 |
Buzzard, Eurasian Buzzard, Goshawk, Mute Swan, Pink Footed Goose |
|
United States of America7 |
26/05/2026 |
45 |
2 981 |
Chicken, Duck, Turkey, WOAH Poultry, WOAH Non-Poultry; Canada goose, Common murre, Herring gull, Mallard, Snow goose; California sea lion, Cattle, Northern elephant seal, Red fox, Sea otter |
|
Viet Nam |
18/05/2026 |
7 |
48 |
Chicken, Duck, Poultry |
|
H5N5 |
Iceland |
10/03/2026 |
2 |
6 |
Black-legged Kittiwake, Common Raven |
Norway |
14/05/2026 |
1 |
2 |
Walrus, Polar Bear |
|
H5N9 |
Republic of Korea |
09/03/2026 |
3 |
15 |
Wild birds (unspecified) |
H7N3 |
Mexico |
07/04/2026 |
3 |
4 |
Poultry |
Data was retrieved from WOAH WAHIS portal and Sharing other important animal health information with WOAH page [link], government websites. Data cutoff time: reported on 26 March 2026, 8:30 CET. $:estimate. ‡: date of confirmation, R: reported date, §: counting Izumi Wintering Habitat of Cranes (Ramsar) as 1 event. Notes: Only those reporting events in animals since the last update are listed in the table. Codes: D:domestic, C:captivity, W:Wild birds, DF: Dairy farm, E:Environment, M: mammalian species other than humans. For more information, consult dedicated webpage of the: 1: British Antarctic Survey (BAS) [link], 2: Australian Government [link], 3: Canada Food and Inspection Agency dashboard [link], 4: TierSeuchenInformationsSystem - Friedrich-Loeffler-Institut [link], 5: Ministry of the Environment [link] 6: Animal and Plant Health Agency (APHA) [link], 7: USDA Animal and Plant Health Inspection Service (USDA/APHIS) [link], 8: Scientific Committee on Antarctic Research (SCAR) [link], 9: The Philippines: Bureau of Animal Industry [link], 10: Brazil: Ministério da Agricultura e Pecuária [link], 11: Indonesia: Laporan Perkembangan Avian Influenza – HPAI [link]. 12: Chile SAG dashboard [linkA and linkB]. 13: Argentina Senasa [link]. Bold: the first report of infection in the species. The full list of bird and mammalian species affected by H5Nx HPAI are here.
OVERVIEW
Giacinti, J.A., Signore, A., Torchetti, M., Enrique Valdez-Gómez, H., Javier Alcazar-Ramiro, C., Berhane, Y., Bevins S, et al. 2026. North American perspective on the highly pathogenic avian influenza H5Nx clade 2.3.4.4b outbreak (November 2021 - March 2025). Can J Microbiol, 2026 May 11. [reference]
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Mohammad, I., Hajelbashir, M.I., El-Bidawy, M.H., Abuderman, A., Satea, M., Arafah, A.M.R., Ansari, M.R., et al. 2026. Deciphering HPAI Influenza A Virus (H5N1): Molecular Basis of Pathogenicity, Zoonotic Potential, and Advances in Vaccination Strategies. Viruses, 18(4):410. [reference]
DOMESTIC
Meseko, C., Zecchin, B., Go-Maro, E.W., Dianati, M., Mkpuma, N., Inuwa, B., Bakam, J., et al. 2026. Emergence and Rapid Spread of a New Reassortant High Pathogenicity H5N1 Clade 2.3.4.4b Avian Influenza Virus in Nigeria. Influenza Other Respir Viruses, 20(5): e70260. [reference]
Oremush, R., Aubry, P., Parmley, E.J., Poljak, Z. & Greer, A. 2026. Determining the Environmental and Ecological Factors Associated With Poultry Farm Spillover of Highly Pathogenic Avian Influenza (H5N1) in British Columbia, Canada. Zoonoses Public Health, 2026 May 15. [reference]
Crespo-Bellido, A., Trovão, N.S., Puryear, W., Maksiaev, A., Pekar, J.E., Baele, G., Dellicour, S. & Nelson MI. 2026. Emergence of D1.1 reassortant H5N1 avian influenza viruses in North America. bioRxiv, 2026 Apr 20:2025.12.19.695329. [reference] Preprint
Chang, T., Lee, S., Kim, J.I. & Min, K.-D. 2026. Spatiotemporal Dynamics of Highly Pathogenic Avian Influenza H5 Virus Introductions and Regional Spread in the Republic of Korea. BioRxiv, 2026.05.21.726857 [reference] Preprint
Chen, L.H., Lin, Y.J., Liu, Y.P., Li, W.C., Tu, Y.C., Hu, S.C., Hsu, W.C., et al. 2026. Distinct infectivity, pathogenicity, and adaptive evolution of clade 2.3.4.4 H5N2 avian influenza viruses in chickens in Taiwan. Poult Sci, 105(7):106913. [reference]
Goujgoulova, G., Stoimenov, G. & Koev, K. 2026. Molecular Characterization of Highly Pathogenic Avian Influenza H5N1 Viruses Circulating in Bulgaria During 2024-2025: Evidence for Hidden Circulation and Zoonotic Risk Markers. Int J Mol Sci, 27(4):1711. [reference]
Höller, P., Asp, E., Pärssinen, J., Phouthana, V., Soulinthone, N., Keopaseuth, S., Chanda, K., Ling, J., Lindahl, J.F. & Naguib, M.M. 2026. Avian influenza and coronaviruses in live animal and wet markets in Laos: prevalence and public health considerations. Front Cell Infect Microbiol, 16:1786183. [reference]
Hartady, T., Sugandi, S.D. & Viqih, M. 2026. A Case of Avian Influenza Co-Infection and Multifactorial Diseases in a Broiler Chicken Farm in Majalengka, West Java, Indonesia. Vet Sci, 13(4):364. [reference]
Briand, F.X., Martenot, C., Massin, P., Cherbonnel, M., Orosco, A., Souchaud, F., Louboutin, K., et al. 2026. Re-emergence of a highly pathogenic avian influenza H5N1 virus of clade 2.3.4.4b in poultry in France. Infect Genet Evol, 142:105958. [reference]
Chen, Y., Xiong, J., Wang, Y., Huang, S., Fan, M., Yang, H., Hu, Z., et al. 2026. Host Factors Potentially Contributing to Increased Susceptibility in Certain Layer Chicken Lines. Curr Issues Mol Biol, 48(4):359. [reference]
EFSA Panel on Biological Hazards (BIOHAZ). 2026. Risk to public and/or animal health of the treatment of dead-in-shell chicks (Category 2 material) to be used as raw material for the production of biogas or compost with Category 3 approved method. EFSA J, 13(11):4306. [reference]
WILD
Günther, A., Herrmann, C., Sehl-Ewert, J., Piro, S., Ahrens, A.K., Calvelage, S., Pohlmann, A., Beer, M. & Harder, T. 2026. Highly Pathogenic Avian Influenza A(H5N1) Clade 2.3.4.4b Virus and Mass Mortality in Eurasian Cranes, Germany, 2025. Emerg Infect Dis, 32(5): 779-783. [reference]
Benedetti, E., Artuso, M.C., Byrne, A., Garibotto, M.B., Avaro, M., Piccini, L., Chamorro, A., et al. 2026. Emergence and Evolution of Triple Reassortant Highly Pathogenic Avian Influenza A(H5N1) Virus, Argentina, 2025. Viruses, 18(5):525. [reference]
Marandino, A., Tomás, G., Panzera, Y., Uriarte, V., Russi, V., Pérez, R., et al. 2026. Reassortant High Pathogenicity Avian Influenza A(H5N1) Viruses During the Reemergence in Uruguay Suggest Increasing Genetic Diversity in South America. Viruses, 18(5):558. [reference]
Clessin, A., Brusselmans, M., Hong, S.L., Tornos, J., Lejeune, M., Shao, Y., Briand, F.X., et al. 2026. Dispersal, adaptation and persistence of H5N1 in the sub-Antarctic and Antarctica. bioRxiv, 2026 Mar 31:2026.03.20.713283. [reference] Preprint
Vanstreels, R.E.T., Serafini, P.P., Giacinti, J., Younger, J., Huyvaert, K.P., Wille, M., Roberts, L., Gamble, A. & Uhart, M.M. 2026. A public database to monitor the spread and impacts of high pathogenicity avian influenza viruses on albatrosses and petrels. Biodivers Data J, 2026 May 15;14:e186836. [reference & reference]
Provencher, J.F., Morrill, A., Hennin, H.L., Giacinti, J.A., Berhane, Y., Zhmendak, D., Xu, W., Love, O.P., Forbes, M.R. & Gilchrist, H.G. 2026. Interannual differences in common eider duck exposure to avian influenza viruses at an Arctic colony. Conserv Physiol, 14(1): coag033. [reference]
Knief, U., Bouwhuis, S., Globig, A., Günther, A. & Courtens W. 2026. Counting cases, conserving species: addressing highly pathogenic avian influenza in wildlife. Biol Rev Camb Philos Soc, 2026 May 8. [reference]
Wang, X., Ling, Z., Chen, X., Mishra, S. & Dong, L. Host-Pathogen Network and Eco-Evolutionary Drivers of Avian Influenza Transmission in Wild Birds. Ecol Lett, 29(6):e70391. [reference]
MAMMAL
Günther, A., Wassermann, J., Heck, J., Bussi, M., Aebischer, A., Staubach, C., Bergmann, H., et al. 2026. Serologic Surveillance of Highly Pathogenic Avian Influenza Virus Subtype H5 in Wildlife, Northeast Germany, 2023-2025. Emerg Infect Dis, 32(5). [reference]
Dressler, A., Wagner-Wiening, C., Tegtmeyer, B., Haag-Milz, S., Demattio, B., Dürrwald, R., Harder, T., Salditt, A.& Köster, J. 2026. Highly pathogenic avian influenza A(H5N1) in poultry and domestic cats and occupational exposure among veterinary and other first responders, Germany, February 2026. Euro Surveill, 31(17). [reference]
Quirk, G.E., Vu, M.N., Le Sage, V., Bushfield-Thomason, K., Nguyen, H.D.& Lakdawala, S.S. 2026. Variable transmission efficiency of mammalian origin HPAI D1.1 H5N1 strains in ferrets. bioRxiv, 2026.05.07.722809. [reference] Preprint
Wong, F.Y., Cronin, P., Zhang, R., Hidano, A., Siegers, J.Y., Low, D.H.W., Holt, H., et al. 2026. Multiplex serological profiling reveals diverse avian and mammalian influenza A virus exposure in swine. iScience, 29(5):115743. [reference]
DAIRY
Lee, C., Tarbuck, N.N., Cochran, H.J., Foreman, B.M., Boley, P., Khatiwada, S., Dhakal, A., et al. 2026. Dairy cows infected with influenza A(H5N1) reveals low infectious dose and transmission barriers. Nat Commun, 2026 May 24. [reference]
Puchades-Colera, P., Girón-Guzmán, I., Moragas, G.S., Pérez-Cataluña, A. 2026. Methods for detecting highly pathogenic avian influenza H5N1 virus in dairy processing environments. Front Microbiol Sec. Food Microbiology [reference]
Malladi, S., Carestia, A., Seys, S.A., Ssematimba, A., Leone, W., Remmenga, M., Stenkamp-Strahm, C., Lombard, J.E. 2026. Estimating the Within-herd Transmission Rate of Highly Pathogenic Avian Influenza H5N1 Virus in a Dairy Herd using an Approximate Bayesian Computation Approach. J Dairy Sci, 2026 May 18:S0022-0302(26)02842-0. [reference]
Ding, K. & Ding, Y. 2026. H5N1 avian influenza in dairy cattle: Molecular adaptation, transmission mechanisms, and control strategies. Virology, 621:110927. [reference]
Wiggins, J., Madapong, A. & Weaver, E.A. 2026. Dual-route H5N1 vaccination induces systemic and mucosal immunity in murine and bovine models. NPJ Vaccines, 2026 Apr 21. [reference]
Stenkamp-Strahm, C., Melody, B., Brinson, P., McCluskey, B. & Lombard, J. 2026. A longitudinal study of influenza A viral detection in bulk tank and pen-level milk collected from dairy farms in California affected by Highly Pathogenic Avian Influenza H5N1. J Dairy Sci, 2026 May 4:S0022-0302(26)01737-6. [reference]
Schafers, J., Warren, C.J., Yang, J., Zhang, J., Cole, S.J., Cooper, J., Drewek, K., et al. 2026. Stability of influenza viruses in the milk of cows and sheep. J Gen Virol, 107(5):002257. [reference]
Miller, M.R., Frost, K., Smith, E.L., Jin, Y., Ulaszek, J., Kmet, M., Hettwer, K., et al. 2026. Evaluation of PCR-Based H5N1 Influenza Detection Methods in Milk from an Inter-laboratory Comparison Study Demonstrating Method-Dependent Sensitivity Variability. J Food Prot, 2026 May 6:100798. [reference]
HUMAN
Nguyen, P.N.T., Hung, N.T., Minh, N.N.Q., Hong, N.T.T., Huong, N.T.T., Hiep, C.M., Nhan, L.N.T., et al. 2026. Central Nervous System Involvement by Novel Clade 2.3.2.1e H5N1 Avian Influenza Virus in a Paediatric Patient. Open Forum Infectious Diseases, ofag283. [reference]
Kibiger, L., Oltean, H.N., Leitz, L., Krause, E., Barrett, D., Halloran, A., Yomogida, K., et al. 2026. Fatal Human Case of Highly Pathogenic Avian Influenza A(H5N5) in a Backyard Flock Owner - Washington, November 2025. MMWR Morb Mortal Wkly Rep, 75(17):221-225. [reference]
Vaughan, A., Joyce, A., Traub, E., Jae, M., Beeler, E., Paiva, E., Ananian, K., et al. 2026. Serologic Evidence of Highly Pathogenic Avian Influenza A(H5N1) Virus Infection in a Veterinary Professional Exposed to an Infected Domestic Cat - Los Angeles County, California, December 2024-January 2025. MMWR Morb Mortal Wkly Rep, 75(17):215-220. [reference]
Cordero-Ortiz, M., Solís-Hernández, M., Cayetano-Mondragón, M., Guzmán, N.C., Valenzuela, O., Mata-Haro, V., Giménez-Lirola, L.G. & Hernández, J. 2026. Antibody Recognition of Highly and Low-Pathogenic A/H5Nx Influenza Viruses in Sera of Mexican Donors. Pathogens, 15(4):352. [reference]
Lite, T.L., Goya, S., Davis, M.L., Morris, A.E., Bryson-Cahn, C., Vengerovsky, A., Corpuz, C.G., et al. 2026. Human Infection with Highly Pathogenic Avian Influenza A(H5N5) Virus. N Engl J Med, 2026 May 7. [reference]
Vargas-Maldonado, N., Shetty, N., Ferreri, L.M., Pauly, M.D., Patatanian, K., Danzy, S., Shephard, M.J., et al. 2026. Controlled human influenza infection reveals heterogeneous expulsion of infectious virus into air. Cell, 189(10):2834-2844.e23. [reference]
Budt, M., Barac, I., Kohs, J., Krischuns, T., Naffakh, N. & Wolff, T. 2026. Historical Pandemic and Contemporary Influenza A Viruses Reveal PB2 M631L as a Convergent Adaptation to Human ANP32. Microorganisms, 14(4):859. [reference]
Gill, D. & Oxford, J. 2026. The 'Spanish' influenza pandemic: new evidence for influenza outbreaks in England and France prior to 1918. Med Hist, 2026 Apr 22:1-20. [reference]
Wang, W., Xing, J., Jiang, H., Lu, F., Huang, H., Zhang, Y., Sun, A., et al. 2026. Human infections with avian influenza A(H5) viruses with potential pandemic risk: 1997-2025. Natl Sci Rev, 13(7):nwaf471. [reference]
VIRUS
Oh, H. 2026. Fever as thermal barrier: avian‑origin PB1 enables influenza A viruses to overcome mammalian febrile defense. Signal Transduct Target Ther, 11(1):187. [reference]
Steiner, J., Mwanga, M., Oberholster, L., Licheri, M., Licheri, M.F., Nathues, H., Dijkman, R. & Kelly, J.N. 2026. Concurrent Detection of Swine-Origin Influenza A(H1N1) Virus in Pigs and Farmer, Switzerland. Emerg Infect Dis, 32(6). [reference]
Zhao, Y., Liu, C., Xia, C., Li, Y., Wang, Y., Hou, B., Gao, H., et al. 2026. Genetic characterization of a novel triple-reassortant influenza A (H1N2) virus from pigs, China, 2021. Front Microbiol, 17:1779293. [reference]
Daines, R., Sadeyen, J.-R., Chang, P. & Iqbal, M. 2026. Mapping hemagglutinin residues driving antigenic diversity in H5Nx avian influenza viruses. J Virol, 2026 Apr 30:e0009526. [reference]
Miao, X., Zhao, X., Zhang, N., Yin, Y., Xu, X., Wang, J., Chen, S., Wu, H., Peng, D., Qin, T. & Liu, X. 2026. Surveillance and biological characterization of H3 subtype avian influenza viruses in Eastern China. Virulence, 17(1):2673657. [reference]
Yehia, N., Ibrahim, M., Shady, R.M., Mohamed, A.A.E., Said, D., Taha, M.E., Arafa, A., et al. 2026. Concurrent circulation of avian influenza viruses H5N1 and H9N2 enhances the genetic evolution of reassortant viruses in Egyptian poultry populations. PLoS One, 21(5):e0348609. [reference]
Deng, L., Shah, T., Wang, Y., Cheng, P., Kui, Y., Wang, B. & Xia, X. 2026. Characterization and Genetic Evolution of H6N2 Subtype AIV Isolates from Aquatic Birds. Microorganisms, 14(4):895. [reference]
Shen, J., Liu, L., Zhang, N., Guan, M., Zhang, Y., Cui, P., Lin, W., et al. 2026. Genesis and biological features of H7 avian influenza viruses in migratory birds and implications for cross-species infection. Journal of Integrative Agriculture, 2026. [reference]
Qu, R., Yang, L., Li, S., Chen, C., Zhang, H., Cao, K., Zhou, W., et al. 2026. Disentangling the drivers and host-mediated global spread of H7 influenza A virus. Nat Commun, 2026 May 6. [reference]
Chen, X., Liu, H., Jiang, L., Hong, X., Kong, M., Wang, X., Hu, Z., et al. 2026. PA-X I94V mutation modulates the pathogenicity of the highly pathogenic H7N9 influenza A virus in mice and chickens. Vet Microbiol, 319:111044. [reference]
Zhao, Y., Liu, C., Li, Y., Wang, Y., Hou, B., Gao, H., Liu, Z., et al. 2026. Genetic and biological characterization of H9N2 avian influenza viruses isolated from swine in China. BMC Vet Res, 2026 May 8. [reference]
Garcia-Glaessner, A., Crespo-Bellido, A., Muñoz-Saavedra, B., Juarez, D., Barrera, P., Salmon-Mulanovich, G. & Checahuari-Jarata, S.E. 2026. Outbreak of H9N2 avian influenza viruses in lesser rhea in Peru, June-July 2025. BioRxiv, 2026.05.08.723762 [reference] Preprint
Mu, Y., Wang, X., Xu, J., Yang, Y., Wang, J., Liu, J. & Chen, L. 2026. Pathogen identification and analysis of broiler bronchial obstruction syndrome using high-throughput sequencing technology. Poult Sci, 105(8):107032. [reference]
Pariani, E., Puzelli, S., Del Castillo, G., Romano, G., Mezzadri, L., Galli, C., Sciabica, I.M., et al. 2026. Collaborating Centres’ Study Group on Influenza. Imported case of avian influenza A(H9N2) virus infection in a patient with miliary tuberculosis, Italy, March 2026. Euro Surveill, 31(15):2600285. [reference]
Bhat, S., Sadeyen, J.R., Yang, J., Chrzastek, K., Karunarathna, T.K., Schlachter, A.L., Qureshi, M., et al. 2026. A G57 (BJ/94-like) H9N2 avian influenza virus exhibits enhanced replication and tissue dissemination in chickens compared with a G1-B virus. J Gen Virol, 107(5). [reference]
Liu, Z., Fan, M., Zheng, Y., Zeng, Y., Hou, C. & Ping, J. 2026. Gga-miR-449c suppresses H9N2 influenza virus replication via targeting the viral genome and suppressor of cytokine signaling 3. Int J Biol Macromol, 2026 May 12:152524. [reference]
Singh, G., Bhavsar, D., Ferreri, L.M., Nardulli, J.R., Gleason, C., Lyttle, N., Chen, Y., Lowen, A.C., Simon, V. & Krammer, F. 2026. Cross-reactive human antibody responses to H9N2 influenza virus, New York, United States, 2025. Euro Surveill, 31(20). [reference]
Wang, W., Yang, F., Liu, K., Cai, M., Guo, Y., Duan, X., Fang, Z., Olovo, C.V., Shi, W., Liu, S., Zhou, J., Wang, X. & Zhang, P. 2026. A mouse model of human-derived H10N3 influenza enables preclinical evaluation of antiviral efficacy. Antiviral Res, 2026 May 18:106436. [reference]
Zhu, M., Wang, R., Li, X., Zhou, H. & Chen, Y. 2026. Canine influenza virus at the human-animal interface: origins, adaptive evolution, and implications for public health. Virology, 621:110943. [reference]
ASSAY
Frederick, J.C., Lacek, K.A., Wersebe, M.J., Shu, B., Keong, L.M., DaSilva, J., Wilson, M.M., et al. 2026. Next-Generation Sequencing Strategies During the 2024-2025 Avian Influenza A(H5N1) Emergency Response in the U.S. Viruses, 18(4):482. [reference]
Shao, Y., Suchard, M.A., Rambaut, A., Ji, X., Lemey, P., Vasylyeva, T.I.& Baele, G. 2026. Parallel algorithms for phylogenetic inference under a structured coalescent approximation. Proc Natl Acad Sci U S A, 123(18):e2602412123. [reference]
Perlas, A., Reska, T., Sánchez-Cano, A., Mejías-Molina, C., Gygax, D., Martínez-Puchol, S., Rusiñol, M., et al. 2026. Real-time genomic pathogen, resistance, and host range characterization from passive water sampling of wetland ecosystems. Appl Environ Microbiol, 2026 Apr 24:e0254325. [reference]
ASSESSMENT/MODELLING
Rolfes, M.A., Bauck, L., Lipton, B.A., Margrey, S.F., Campagna, R.A., Harker, E., Basler, C.A., et al. 2026. Knowledge, Attitudes, and Practices Regarding Avian Influenza Among Owners of Backyard Flocks - United States, July-December 2025. MMWR Morb Mortal Wkly Rep, 75(18):234-239. [reference]
Chanchaidechachai, T., Stegeman, A., Velkers, F.C., Gonzales, J.L. & Fischer, E.A.J. 2026. Assessing the impact of outdoor farming, farm size, and farm density on highly pathogenic avian influenza epidemics: A modelling study in the Netherlands. One Health, 22:101424. [reference]
Fathelrahman, E., Mohamed Ali, M, Challa, T.G., Osman, R., Elawad, A.I., Al Nuaimat, M.H., Saeed, M.M., et al. 2026. Modeling and assessing Highly Pathogenic Avian Influenza (HPAI) spread, epidemiological control measures, and cost. PLoS One, 21(4):e0340004. [reference]
Wang, M., Laison, E.K.E., Philippsen, T., Ghaemi, S., Liu, J., Moyles, I., Signore, A., Ma, J. & Nasri, B. 2026. Mechanistic modelling of highly pathogenic avian influenza: A scoping review revealing critical gaps in cross-species transmission models. PLoS One, 21(4):e0347929. [reference]
Jindal, M., Lim, S. & MacIntyre, C.R. 2026. Machine Learning-Based Geospatial Risk Modeling of Global Avian Influenza Outbreaks. Transbound Emerg Dis, 2026:6615342. [reference]
Guirales-Medrano, S., Ocaña, K., Obeid, K., Alexander, R., Ford, C.T. & Janies, D. 2026. Computational Structural Analysis Predicts Host-Range Promiscuity and Antiviral Resistance in North American H5N1 Lineages. Comput Struct Biotechnol J, 35(1):0066. [reference]
America
Asia
North Africa and Middle East
Sub-Saharan Africa
Figure 1. Number of countries reported HPAI since 1 October 2025 by subtype (left) and by region (right) as of 21 May 2026

Source: WOAH WAHIS portal, government and publications.
Table 2. Epidemiological overview for avian influenza viruses viruses known to have caused zoonotic infections in the past 20 years
Subtype | Epidemiological situation overview |
|---|---|
H5Nx Gs/GD HPAI (1996) | High pathogenicity avian influenza viruses (HPAIVs) of the H5N1 subtype were detected in geese in Guangdong Province, China in 1996. Viruses related to but not directly descended from A/Goose/Guangdong/1/96 (Gs/GD), the virus identified in China at the time have persisted, as high pathogenicity viruses Gs/GD-related HPAIVs have caused outbreaks in poultry across all regions globally other than Oceania. The initial viruses in this lineage were of the A(H5N1) subtype but other subtypes (including H5N2, H5N3 H5N5, H5N6, H5N8) have emerged, mainly in the past 10 years, as a result of reassortment with other avian influenza viruses. The common feature of these viruses is an HA gene related back to the original Gs/GD/96 virus. The HA gene of these viruses has evolved over the past 28 years, initially into 10 clades (clade 0 to 9) of which descendents of clade 2 viruses are the only ones that continue to circulate. Multiple 5th order clades persist such as the one that is currently dominant globally – clade 2.3.4.4b - whereas others have emerged and disappeared. Multiple genotypes carrying different combinations of the eight influenza A segmented genes have emerged in Gs/GD-related viruses, as a result of co-infection of birds with different avian influenza viruses that facilitated reassortment. Of considerable significance in the past has been reassortment with enzootic A(H9N2) viruses. Eurasian lineage clade 2.3.4.4b viruses formed multiple genotypes and those that crossed to North America have reassorted with North American wild bird avian influenza viruses to produced additional genotypes. Two separate systems for naming genotypes of clade 2.3.4.4b have been developed for Eurasian and North American viruses (Fusaro, et al., 2024, Youk, et al., 2023). The clade 2.3.4.4b A(H5N1) viruses detected in dairy cattle in North America in 2024 fell initially within genotype B3.13 [link] and more recently genotype D1.1 [link] using the North American naming system. Some Gs/GD-related viruses have produced severe zoonotic infections in humans, first identified in 1997 when an A(H5N1) clade 0 virus in Hong Kong SAR, China caused disease outbreaks in poultry in farms and markets as well as severe disease in humans. In several cases there was some evidence of limited onward transmission in humans and this event raised concerns that it might be the beginning of a human influenza pandemic. Despite the successful efforts to eradicate this particular strain, other Gs/GD-related viruses persisted and evolved in China, becoming more adept at infecting domestic ducks. By 2003 spread of these viruses via wild birds and live bird trade occurred across East and Southeast Asia, resulting in additional zoonotic infection in humans [link]. The important role of wild birds in the transmission of these viruses over long distances became apparent in 2005 when Gs/GD-related HPAIVs (clade 2.2) spread, primarily via wild birds, across Eurasia, and parts of Africa from western China. Most high-income countries eliminated this virus from poultry, but it persisted in several low and middle- income countries. Gs/GD-related viruses continued to evolve and spread. Additional intercontinental waves of transmission have occurred with the two most significant being those in 2014 (clade 2.3.4.4c) and from 2016 onwards (clade 2.3.4.4b). The clade 2.3.4.4b wave commenced in Asia and spread to Europe and Africa. In 2020, that also resulted in spread of these viruses to North America (2014-15 and 2021-22), with the latest outbreak extending through central and South America and to sub-Antarctic islands. In 2022/2023, H5N1 2.3.4.4b caused extensive infection in coastal seabirds and mass die-offs of numerous ecologically important wild bird species. Since 2024, H5N1 2.3.4.4b caused infection in goats (1 farm), alpaca (1 backyard farm), swine (1 farm) and dairy cattle (1 107 farms as of 27 May 2026) in the United States of America, see HERE.
In 2025, H5N1 2.3.4.4b caused infection in sheep in the United Kingdom, see HERE; and H5 antibodies were also found in sheep in Norway. [link1, link2] Clade 2.3.4.4b A (H5N1) viruses have caused few human cases but have resulted in multiple mammalian cases including aquatic mammals. For an updated list of bird and mammalian species affected with A(H5Nx) see HERE. Among the other Gs/GD-related virus clades that remain endemic in specific areas are clade 2.3.2.1a H5N1 viruses that have persisted in South Asia since 2010 and rarely associated with disease in humans. Clade 2.3.2.1g viruses have been present in Indonesia since 2012 and clade 2.3.2.1c/e viruses are still circulating in Cambodia, Viet Nam and Lao People’s Democratic Republic. A novel reassortant influenza A(H5N1) virus has been detected in poultry in Cambodia (since 2023), Lao People's Democratic Republic and Viet Nam (since 2022) and was also detected in the human cases reported from Cambodia since late 2023 and Viet Nam in 2024. This virus contains the surface proteins from clade 2.3.2.1c that has circulated locally, but internal genes from a more recent clade 2.3.4.4b virus. [link] For an updated list of confirmed human cases with A(H5N1) see HERE and HERE. In addition, since the first human case of A(H5N6) was reported in Sichuan, China in 2014, 94 human cases have been associated with clade 2.3.4.4b and 2.3.4.4h A(H5N6) viruses with most of these occurring in 2021 and 2022 [link]. The first human cases (asymptomatic) of A(H5N8) were reported in Astrakhan Oblast, Russian Federation [link] in adults who engaged in depopulation on a layer farm due to H5N8 HPAI in December 2020 [link]. The influenza A(H5N8) viruses isolated from this poultry outbreak in Astrakhan belonged to clade 2.3.4.4b [GISAID EPI_ISL_1038924]; the first human case (fatal) of A(H5N5) was reported in November 2025 in the United States of America with reported exposure to poultry. [link] |
| Avian origin H3N8 LPAI | An Influenza A(H3N8) virus lineage emerged in live bird markets in southern China in mid-2021. Since then, three human cases of Influenza A(H3N8) have been reported: In April 2022, the first human clinical case associated with this lineage was reported in Henan Province, China and was associated with severe disease [link]. In May 2022, a 5-year-old boy was diagnosed with a mild influenza A(H3N8) infection in Changsha City, Hunan Province, China. On 27 March 2023, a third human case was reported from Guangdong Province, China in a 56-year-old female with underlying illness who subsequently died. One of the A(H3N8) viruses isolated from a human was found to be transmissible by air in ferrets [link] but no evidence of sustained human transmission has been reported. |
H5N5 HPAI (2025) | One human case in China with reported exposure to poultry. [link] |
H7N4 LPAI (2017) | The first human case (fatal) was reported in November 2025 in the United States of America with reported exposure to poultry. [link] |
H7N7 LPAI | One human case of H7N7 was reported in a duck farmer in Taiwan Province of China. More than 90 cases have been reported since 1959, mostly mild with one fatal case. [link] |
H7N9 LPAI (2013) & HPAI (2017) | Reported only in China with over 1 000 human cases between 2013 and 2017 with a marked increase in 2017 compared to previous waves. Most human cases exposed in live bird markets. Nation-wide vaccination campaign in poultry since Sep 2017: Last reported human case in 2019 [link]. See FAO H7N9 situation update Figure 5. |
| H9N2 LPAI | First human case reported in 1998. To date, more than 140 influenza A(H9N2) human cases diagnosed worldwide, many of them were reported from China since December 2015. Most cases mild and involving children. Only two fatal cases reported. [link] Endemic in multiple countries in Africa and Asia, a cause of significant production losses and mortalities in poultry production systems. Three major lineages and multiple genotypes. |
| H10Nx LPAI | To date, seven influenza A(H10N3) human infections have been reported globally [link]. In May 2021, the first case in Jiangsu Province, China [link], then in Zhejiang (2022), Yunnan and Guangxi (2024) and Shaanxi and Guangdong (2025) provinces in China. The first influenza A(H10N5) human infection was reported in Zhejiang Province, China [link]. Since 2013, three influenza A(H10N8) human infections have been reported in Jiangxi Province, China. [link] |
For high-level, the recommendations from the FAO Global Dialogue - Tackling high pathogenicity avian influenza together provide a clear framework for coordinated science-based actions on Early detection, Rapid response, Biosecurity, Vaccination, Business and trade dimensions, One Health and systems-based approaches, Public-private partnerships.
For grass root level. the practical recommendations for day-to-day activities are suggested below to mitigate risk and reduce impact of HPAI.
General recommendations
It is important to report sick or dead birds – both wild birds and poultry - or wild mammals to local authorities (veterinary services, public health officials, community leaders etc.). These should be tested for avian
influenza viruses.
Recommendations to poultry producers
Farmers and poultry producers should step up their biosecurity measures in order to prevent potential virus introduction from wild birds or their faeces.
Recommendations to hunters
Hunting associations and wildlife authorities should be aware that avian influenza viruses might be present in waterfowl and some other species hunted and that hunting, handling and dressing of shot game carries the risk
of spreading avian influenza viruses to susceptible poultry.
Recommendations to national authorities
Increase surveillance efforts for the early detection of influenza viruses in poultry and dead wild species including certain mammals.
For full recommendations including non-avian species please see [link].
Note: many publication links have been moved into ‘More important links’ below.
Next issue: 25 June 2026
Information provided herein is current as of the date of issue. Information added or changed since the last Global AIV with Zoonotic Potential situation update appears in orange. Human cases are depicted in the geographic location of their report. For some cases, exposure may have occurred in one geographic location but reported in another. For cases with unknown onset date, reporting date was used instead. FAO compiles information drawn from multiple national (Ministries of Agriculture or Livestock, Ministries of Health, Provincial Government websites; Centers for Disease Prevention and Control [CDC]) and international sources (World Health Organization [WHO], World Organisation for Animal Health [WOAH]), as well as peer reviewed scientific articles. FAO makes every effort to ensure, but does not guarantee, accuracy, completeness or authenticity of the information. The boundaries and names shown and the designations used on these map(s) do not imply the expression of any opinion whatsoever on the part of FAO concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers and boundaries. Dashed lines on maps represent approximate border lines for which there may not yet be full agreement.
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