22 January 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 December 2025): in total, 1 391 outbreaks/events have been reported in 39 countries/territories caused by H5Nx (524), H5N1 (857), H5N5 (2), H5N8 (2), H5N9 (3) and HxNx (3) (see Table 1 for details).
LPAI events in animals officially reported since the last update: 3 new events were reported. [ref1, ref2]
Number of human cases officially reported since the last update: 6 new events were reported. [ref1, ref2]
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 January 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 | # events reported since 1 Oct. 2025 | Species affected since the last update |
|---|---|---|---|---|---|
H5 |
Belgium |
17/12/2025 |
2 |
23 |
Eurasian Woodcock, Great Cormorant |
Finland |
14/11/2025 |
1 |
1 |
Whooper swan |
|
Italy |
29/12/2025 |
6 |
6 |
Common Teal, Eurasian Wigeon, Mute Swan |
|
Japan |
07/01/2026 |
2 |
6 |
Large-billed crow, Mallard |
|
The Philippines |
09/01/2026R |
1 |
5 |
Chicken, Quail |
|
Spain |
14/11/2025 |
1 |
1 |
Griffon Vulture |
|
United States of America7 |
16/01/2026R |
511$ |
1 423$ |
Duck, backyard WOAH-poultry; American crow, American white pelican, American wigeon, Bald eagle, Barred owl, Black skimmer, Black vulture, Black-billed magpie, Black-necked stilt, Blue-winged teal, Bufflehead, Cackling goose, Canada goose, Common goldeneye, Common grackle, Cooper's hawk, Crow, Duck, Fish crow, Gadwall, Glaucous-winged gull, Goose, Great horned owl, Greater white-fronted goose, Green-winged teal, Gull, Hawk, Hooded merganser, Laughing gull, Lesser scaup, Mallard, Mottled duck, Muscovy duck, Mute swan, Northern pintail, Northern shoveler, Pied-billed grebe, Redhead duck, Red-tailed hawk, Ring-necked duck, Ross's goose, Sanderling, Snow goose, Trumpeter swan, Turkey vulture, Western gull, Willet, Wood duck; Red fox, Striped skunk |
|
H5N1 |
Austria |
19/01/2026 |
4 |
52 |
Eurasian Sparrowhawk, Common Buzzard, Grey Heron, Sylviidae |
Belgium |
20/01/2026 |
10 |
174 |
Chicken, Mule duck, Turkey, Poultry, Non-poultry birds |
|
Brazil |
13/01/2026 |
2 |
2 |
Non-poultry birds (multi-species backyard) |
|
Bulgaria |
05/01/2026 |
2 |
9 |
Chicken, Mallard duck, Poultry |
|
Canada |
26/12/2026 |
14 |
103 |
Chicken, Duck, Turkey, Poultry, non-commercial poultry backyard |
|
China |
15/01/2026 |
8 |
18 |
Chicken; Greylag Goose, Phalacrocoracidae, Ruddy Shelduck |
|
Colombia |
23/12/2025 |
3 |
7 |
Duck, Non-poultry birds |
|
Czech Republic |
16/01/2026 |
11 |
42 |
mix hobby flock; Grey Heron, Mallard, Mute Swan |
|
Denmark |
08/01/2026 |
28 |
123 |
Chicken, Duck, Pheasant, Pigeon, Turkey; Barnacle Goose, Canada Goose, Common Buzzard, Eurasian Sparrowhawk, Greylag Goose, Mute Swan, Peregrine Falcon, Pink-footed Goose, Whooper swan |
|
Estonia |
09/01/2026 |
2 |
7 |
Chicken, Pheasant; Laridae |
|
France |
14/01/2026 |
10 |
297 |
Chicken, Duck, Guinea fowl, Turkey, Poultry |
|
Germany |
14/01/2026 |
254 |
2 401 |
Chicken, Duck, Goose, Turkey, Non-poultry birds; Accipitridae, Anatidae, Grey Heron, Gruidae, Laridae, Mallard, Phalacrocoracidae, Strigidae, Sulidae |
|
Hungary |
12/01/2026 |
5 |
20 |
Chicken, Goose, Turkey |
|
India |
16/12/2025 |
11 |
21 |
Duck, Quail, Poultry |
|
Iraq |
09/01/2026 |
1 |
3 |
Chicken |
|
Israel |
15/01/2026 |
7 |
8 |
Duck; Black-headed Gull, Common Kestrel, Great Cormorant |
|
Italy |
02/01/2026 |
10 |
120 |
Chicken, Duck, Goose, Turkey |
|
Japan |
13/01/2026 |
15 |
83 |
Chicken; Eastern buzzard, Large-billed crow, Mallard; environmental sample (water) |
|
Republic of Korea |
19/01/2026 |
18 |
53 |
Chicken, Duck, Quail |
|
Latvia |
29/12/2025 |
2 |
28 |
Chicken; Whooper Swan |
|
Lithuania |
31/12/2025 |
1 |
20 |
Mute Swan |
|
Moldova |
14/01/2026 |
2 |
2 |
Mute Swan |
|
Netherlands (Kingdom of the) |
14/01/2026 |
36 |
275 |
Chicken, Turkey; Caspian Gull, Common Buzzard, Common Kestrel, Common Starling, Common Teal, Eurasian Curlew, Greater white-fronted Goose, Greylag Goose, Herring Gull, Mallard, Mute Swan, Pink-footed Goose |
|
Nigeria |
05/01/2026 |
2 |
20 |
Poultry |
|
Norway |
12/01/2026 |
6 |
17 |
Canada Goose, Mute Swan |
|
The Philippines |
January 2026 |
1 |
5 |
Poultry |
|
Poland |
17/01/2026 |
62 |
109 |
Chicken, Duck, Goose. Non-poultry bird; Black-headed Gull, Common Buzzard, Great Cormorant, Greater white-fronted Goose, Greylag Goose, Mallard, Mute Swan, Passeriformes, Rook, Taiga Bean Goose |
|
Portugal |
26/12/2025 |
2 |
26 |
Chicken; Yellow-legged Gull |
|
Slovenia |
08/01/2026 |
6 |
15 |
Anatidae, Mute Swan |
|
South Africa |
06/12/2025 |
2 |
30 |
Poultry |
|
Spain |
08/01/2026 |
2 |
127 |
Chicken; White Stork |
|
Sweden |
01/01/2026 |
8 |
55 |
Chicken; Barnacle Goose, Canada Goose, Herring Gull, Mallard |
|
Switzerland |
08/01/2026 |
8 |
16 |
Black-headed Gull, Common Goldeneye, Grey Heron, Greylag Goose, Little Egret, Mute Swan |
|
Ukraine |
15/01/2026 |
1 |
2 |
Mute Swan |
|
United Kingdom of Great Britain and Northern Ireland6 |
19/01/2026 |
124 |
548 |
Chicken, Duck, Turkey, Poultry; Anserinae, Barnacle Goose, Black-headed Gull, Canada Goose, Common Buzzard, Cygnus, Eurasian buzzard, Eurasian Curlew, Eurasian Sparrowhawk, Great Cormorant, Greylag Goose, Herring Gull, Mew Gull, Mute Swan, Peregrine Falcon, Pink-footed Goose, Whooper swan |
|
United States of America7 |
16/01/2026 |
174 |
1 409 |
Chicken, Duck, Turkey, Upland Game Bird, WOAH Poultry, WOAH Non-Poultry, Live Bird Market; African grey parrot, American crow, American white pelican, Bald eagle, Barn owl, Black turnstone, Black vulture, Black-necked stilt, Bonaparte's gull, Cackling goose, Canada goose, Common grackle, Common raven, Crow, Glaucous gull, Great horned owl, Green-winged teal, Gull, Herring gull, Hooded merganser, Mallard, Mottled duck, Northern harrier, Northern pintail, Northern shoveler, Peregrine falcon, Red-tailed hawk, Ross's goose, Sanderling, Snow goose, Snowy owl, Swan, Trumpeter swan, Turkey vulture, Western gull; Fox |
|
Viet Nam |
22/12/2025 |
3 |
32 |
Chicken, Poultry |
|
H5N2 |
Latvia |
12/01/2026 |
1 |
1 |
Mallard |
Sweden |
14/01/2026 |
1 |
1 |
Barnacle Goose |
|
H5N8 |
The Philippines |
30/09/2025 |
2 |
2 |
Duck |
H5N9 |
Republic of Korea |
21/01/2026 |
3 |
6 |
Duck |
HxNx |
Indonesia |
December 2025 |
2 |
2 |
Chicken, Muscovy duck |
Japan |
21/01/2026 |
1 |
1 |
Chicken |
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 23 December 2025, 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]. Bold: the first report of infection in the species. The full list of bird and mammalian species affected by H5Nx HPAI are here.
Table 2. Low pathogenicity avian influenza viruses with zoonotic potential reported since the last update
| Virus | Country/Area | Last observed outbreak | # events reported since the last update | # events reported since the last update | Species affected during the reporting preiod |
|---|---|---|---|---|---|
H5N1 | United Kingdom | 15/01/2026 | 1 | 1 | Poultry |
H7N7 |
China |
15/12/2026 |
2 |
2 |
Black-faced spoonbill; Environmental sample (Anatidae faeces) |
Wild
Crespo-Bellido, A. Trovão, N.S., Maksiaev, A., Baele, G., Dellicour, S. & Nelson, M.I. 2025. Emergence of D1.1 reassortant H5N1 avian influenza viruses in North America. BioRxiv, [reference] Preprint
Zhang, P. & MacIntyre, C.R. 2025. An overview of HPAI H5N1 clade 2.3.4.4b and its emerging threat in mainland Australia: Identified knowledge gaps. One Health, 22:101292. [reference]
Ross, T.A., Ryding, S., Lisovski, S., Driessen, J., Mowat, E., Todd, S., Purnell, C., Spence, A., Vitali, S., Yu, H. & Klaassen. M. 2026. AviFluMap: An interactive tool to assess H5N1 avian influenza incursion risk in Australia via migratory birds. Ecological Informatics, 103603. [reference - reference]
Mursel, S., Davison, B.D., McAndrew, T., Khan, B. & Bocchini, P. 2025. Spatiotemporal Dynamics of Avian Influenza: Understanding Avian Influenza Transmission via Mallard Migration Data. Interdiscip Perspect Infect Dis, 2025:5555858. [reference]
Si, Y.-J., Lee, S-H., Lee, H.-E., Kim, D.-J., Jeong, H., Lee, S. & Lee, D.-H. 2026. Early Detection and Genetic Characterization of Clade 2.3.4.4b H5N1 and H5N9 Highly Pathogenic Avian Influenza Viruses at the Onset of Fall Migration in Wild Birds during October 2025 in South Korea. Front Cell Infect Microbiol, [reference]
Veldhuis Kroeze, E.J.B., Bellido Martin, B., Mols, V.C., Begeman, L., Fouchier, R.A.M. & Kuiken, T. 2025. Pathology and virology of natural high pathogenicity avian influenza A(H5N1) Gs/GD genotype BB virus infection in wild black-headed gulls (Chroicocephalus ridibundus). Vet Res, 56(1):234. [reference]
Hjulsager, C.K., Liang, Y., Thorup, C., Larsen, L.E., Jensen, T.K., Breum, S. & Bregnballe, T. 2025. Mass mortalities caused by different genotypes of HPAIV H5N1 clade 2.3.4.4b in colony breeding Black-headed Gulls and Sandwich Terns in Denmark 2022 and 2023. Can J Microbiol, 2026 Jan 10. [reference]
Rahman, I., Wight, J., Cunningham, J.T., Ochoa, P.S., Wallace, H.L., Ward, C.R., Hedd, A., et al. 2026. Surveillance of live birds for active and past infections reveals the impact of highly pathogenic H5N1 on seabird populations in Atlantic Canada. Can J Microbiol, 2026 Jan 16. [reference]
Rimondi, A., Vanstreets, R., Nelson, M., Olivera, V., Gallo, L., Durant, A., Quintana, F., et al. 2025. Persistence and spillback of mammal-adapted H5N1 genotype B3.2 viruses among South American seabirds and marine mammals. Res Sq, 2025 Nov 4:rs.3.rs-7960151. [reference] Preprint
Couty, M., Guinat, C., Fornasiero, D., Briand, F.X., Henry, P.Y., Grasland, B., Palumbo, L. & Le Loc'h, G. 2026. The role of wild birds in the global highly pathogenic avian influenza H5 panzootic, 2020-2023. NPJ Biodivers, 5(1):1. [reference]
Iervolino, M., Günther, A., Begeman, L., Aguado, B., Bestebroer, T.M., Bellido-Martin, B., Coerper, A., et al. 2026. The expanding H5N1 avian influenza panzootic causes high mortality of skuas in Antarctica. Sci Rep, 2026 Jan 14. [reference]
Domestic
Freier, L., Breithaupt, A., Kuryshko, M., Palme, D.I., Weigend, S., Abdelwhab, E.M. & Blohm, U. 2026. Host genetics, lung T-cell immunity, and laying activity determine the disease outcome in avian influenza virus-infected chickens. Vet Res, 2026 Jan 2. [reference]
Wu, S.X., Davis, C.N., Arnold, M. & Tildesley, M.J. 2026. The role of ducks in detecting Highly Pathogenic Avian Influenza in small-scale backyard poultry farms. PLoS Comput Biol, 2026 Jan 9;22(1):e1013357. [reference]
Nyarko, S.O., Asante, I.A., Sarpong, G.M., Boatemaa, L., Kwasah, L., Awuku-Larbi, Y., Magnusen, V., et al. 2026. Evidence of High Pathogenic Avian Influenza H5N1 Clade 2.3.4.4b Among Poultry in Ghana From 2021 to 2022. Vet Med Sci, 12(1):e70744. [reference]
Leonard, M., Bonney, P., Cardona, C., Ssematimba, A., St Charles, K.M., Martin, S.W., Alexander, C. & Marusak, R. 2025. Movements of poultry product off HPAI-infected premises: using science-based standards for achieving confidence in risk. Can J Microbiol, 2025 Dec 23. [reference]
Niel, K.R., St Charles, K.M., Elissa, J.Y., Lighty, M.E., Ssematimba, A., Culhane, M., Crespo-Bellido, A., Trovão, N.S., Nelson, M.I. & Cardona, C. 2025. Highly Pathogenic Avian Influenza (HPAI H5N1, Clade 2.3.4.4b, genotype C2.1) in Commercial Ring-Necked Pheasants During the 2022 Outbreak in the United States. Can J Microbiol, 2025 Dec 22. [reference]
St Charles, K.M., Ssematimba, A., Bonney, P. & Cardona, C. 2025. Evaluation of transmission metrics in a slow-spreading highly pathogenic avian influenza (HPAI) outbreak in a commercial upland game bird system. Can J Microbiol, 2025 Dec 22. [reference]
Ibrahim, M., Said, A., Wahba, M.A. & Yehia, N. 2025. Genetic and antigenic analysis of the highly pathogenic avian influenza H5N8 virus clade 2.3.4.4b isolated from waterfowl in Egypt during 2022; evidence of brain-specific HA mutations. Br Poult Sci, 2026 Jan 7:1-10. [reference]
Adachi, K., Handharyani, E., Ueno, S. & Tsukamoto, Y. 2026. Comparative Hemagglutination of Avian Influenza A/H5N1 Viruses by Erythrocytes from Ostrich, Emu, Japanese Quail, Chicken and Horse. Open Journal of Veterinary Medicine, 16:1-15. [reference]
Ahn, J.J., Yu, T.C., Dadonaite, B., Radford, C.E. & Bloom, J.D. 2026. Influenza hemagglutinin subtypes have different sequence constraints despite sharing extremely similar structures. BioRxiv, [reference] Preprint
Mammals
Larsen, S.V., Israelson, R., Torp, C., Larsen, L.E., Jensen, H.E. & Kristensen, C. 2025. Transmission, Pathological and Clinical Manifestations of Highly Pathogenic Avian Influenza A Virus in Mammals with Emphasis on H5N1 Clade 2.3.4.4b. Viruses, 17(12):1548. [reference]
Panova, A.S., Gudymo, A.S., Kolosova, N.P., Danilenko, A.V., Shadrinova, K.N., Danilchenko, N.V., Perfilieva, O.N., et al. 2025. Genotype A3 influenza A(H5N1) isolated from fur seals shows high virulence in mammals, but not airborne transmission. Sci Rep, 15(1):44463. [reference]
Pérez-Sánchez, T., Báez, J.C. & Johnstone, C. 2025. Concern for Highly Pathogenic Avian Influenza Spillover into Cetaceans. Viruses, 17(12):1536. [reference]
Gwon, S.-H., Park, S.-I., Jeong, H., Kim, D., Son, Y., Lee, M.-a., Lee, K., et al. 2026. Fatal H5N1 Highly Pathogenic Avian Influenza with Retrograde Neuroinvasion in a Free-Ranging Leopard Cat (Prionailurus bengalensis) During a Wild Bird Outbreak in South Korea. Animals, 16(2):200. [reference]
Butt, S.L., de Oliveira, P.S.B., Rani, R., Nooruzzaman, M., Diaz, A.N., Glover, S., Young, A.J., Sharma, B. & Diel, D.G. 2026. Novel recombinant H5-based vaccine provides effective protection against H5N1 influenza virus in cats. NPJ Vaccines, 2026 Jan 12. [reference]
Dairy
Tarbuck, N.N., Cochran, H.J., Martin, E.A., Liu, M., Kulchytsky, K.S., Leone, W.M., Webby, R.J., Warren, C.J., Bowman, A.S. 2026. Natural H5N1 immunity in dairy cows is durable and cross-protective but non-sterilizing. BioRxiv, [reference] Preprint
Dholakia, V., Quantrill, J.L., Richardson, S.A.S., Pankaew, N., Brown, M.D., Yang, J., Capelastegui, F., et al. 2026. Polymerase mutations underlie early adaptation of H5N1 influenza virus to dairy cattle and other mammals. Nat Commun, 2026 Jan 16. [reference]
Eales, O., McCaw, J.M. & Shearer, F.M. 2025. Modeling of H5N1 influenza virus kinetics during dairy cattle infection suggests the timing of infectiousness. PLoS Biol, 24(1):e3003586. [reference]
Olthof, L., Krogstad, K.C. & Bradford, B.J. 2025. Cow-level factors associated with risk of clinical highly pathogenic avian influenza H5N1 infection and impacts on health and productivity in lactating dairy cattle. J Dairy Sci, 2025 Dec 31:S0022-0302(25)01054-9. [reference]
EFSA Panel on Animal Health and Welfare (AHAW); Alvarez, J., Boklund, A.E., Dippel, S., Dórea, F., Figuerola, J., Herskin, M.S., et al. 2025. Risk of infection of dairy cattle in the EU with highly pathogenic avian influenza virus affecting dairy cows in the United States of America (H5N1, Eurasian lineage goose/Guangdong clade 2.3.4.4b. genotype B3.13). EFSA J, 23(12):e9801. [reference]
Virus
Bi, Z. 2026. Adaptation differences and mechanisms of influenza viruses to ANP32 proteins across species. J Virol, 2026 Jan 5:e0190025. [reference]
Zhu, W., Xu, Z., Wang, X., Li, X., Li, Z., Dong, G., Yang, L., et al. 2025. Low-replication influenza virus mediates high pathogenicity through an inflammation-driven lung-heart-brain axis in mice. Emerg Microbes Infect. 2026 Dec;15(1):2608406. [reference]
Mei, M., Zhang, X., Wu, Q., Xu, M. & Zhao, Y. 2026. Virulence and transmission characteristic of H3N8 avian influenza virus circulating in chickens in China. Virulence, 2026 Jan 7:2613516. [reference]
Jin, Y., Cui, H., Jiang, L., Li, L., Zheng, J., Zhang, Y., Wang, H., et al. 2025. From Surfaces to Spillover: Environmental Persistence and Indirect Transmission of Influenza A(H3N8) Virus. Microorganisms, 2025 Dec 6;13(12):2782. [reference]
Silaban, J., Ogada, S., Naseem, M.N., Baek, Y.H., Song, M.S. & Ommeh, S.C. 2025. Phylogenetic Analysis of Highly Pathogenic Avian Influenza H7 Viruses in Australia and New Zealand Suggests Local Viral Evolution. Vet Sci, 2025 Dec 17;12(12):1208. [reference]
Luo, Y., Dong, M., Shen, Y., Xiang, X., Lv, J., Sun, Y., Li, Y., et al. 2025. Impact of viral ribonucleoprotein complex genetic stability on pathogenicity in H9N2 and H6N2 avian influenza viruses. Dev Comp Immunol, 2025 Dec 27;175:105544. [reference]
Han, J., Chang, W., Jing, Z., Xiao, D., Ji, T., Fang, J., Song, M., Li, W., Wang, J. & Deng, W. 2025. Synergistic virulence of H9N2 AIV and APEC co-infection in laying hens involves a critical role for macrophage-mediated hyper-inflammation via the MAPK/NF-κB axis. Vet Microbiol, 2025 Dec 24;313:110846. [reference]
Bhavsar, D., León, A.N., Hsu, W.L., Puente-Massaguer, E., Ferguson, J.A., Han, J., Wilson, P., Ward, A.B. & Krammer, F. 2026. Structural and functional characterization of the antigenicity of influenza A virus hemagglutinin subtype H15. Cell Rep, 2026 Jan 2;45(1):116773. [reference]
Falsini, A., Fiori, A., Montomoli, E., Muzyka, N., Muzyka, D. & Trombetta, C.M. 2026. Circulation of influenza D virus in Ukraine: A multi-species serological study. Acta Trop, 2026 Jan 13;274:107980. [reference]
Trombetta, C.M., Fiori, A., Falsini,A., Pellegrini, F., Le Poder, S., Eichenbaum, A., Cardona, V., et al. 2026. Serological investigation of influenza D virus in cats and dogs in Europe. 2026. BioRxiv, Preprint [reference]
Li, H., Yan, W., Liu, X., Gao, B., Peng, J., Jiang, F., Cui, Q., et al. 2026. Emergence and Phylodynamics of Influenza D Virus in Northeast China Reveal Sporadic Detection and Predominance of the D/Yamagata/2019 Lineage in Cattle. Viruses, 18(1), 93. [reference]
Xue, L., Guo, T., Feng, Y., San, Z., Wang, D. & Guo, L. 2026. An influenza D virus in D/Yama2019 lineage from stillbirth fetus of cattle in China. J Vet Med Sci, 2026 Jan 14. [reference]
Shen, M., Yu, J., Fu, B., Yu, C., Cui, C., Chen, S., Liu, C., Wang, K. & Wang, Z. 2025. Influenza D Virus in Black Donkeys, Northern China. Emerg Infect Dis, 31(12):2339-2340. [reference]
Assessment/Modelling
Guo, D. & Pu, H. 2025. Factors Influencing the Willingness of Layer Specialized Households to Participate in Cooperative Avian Influenza Prevention and Control: Evidence from China. Vet Sci, 12(12):1194. [reference]
Whitlow, H., Gokool, S., Clapp, G., Bueno, I., Logunleko, M., Moore, P., Masterton, S, et al. 2026. Biosecurity Uptake and Perceived Risk of Avian Influenza Among People in Contact With Birds. Zoonoses Public Health, 2026 Jan 6. [reference]
Davis, C.N., Hill, E.M., Jewell, C.P., Rysava, K., Thompson, R.N. & Tildesley, M.J. 2026. A modelling assessment of the impact of control measures on highly pathogenic avian influenza transmission in poultry in Great Britain. PLoS Comput Biol, 2026 Jan 5;22(1):e1013874. [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 January 2026 (territory/area or sub/Antarctic zone)

Source: WOAH WAHIS portal, government and publications.
Table 3. 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 (1 084 farms as of 21 January 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, 91 human cases have been associated with clade 2.3.4.4b A(H5Nx/y) and 2.3.4.4h A(H5N6) viruses with most of these occurring in 2021 and 2022. |
| 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] |
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, three 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 (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] |
FAO recommends intensified surveillance and awareness raising by national authorities.
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: 26 Feb 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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