
27 March 2025, 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). Read the HPAI Lunar New Year alert.
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 (27 February 2025): in total, 677 outbreaks/events have been reported in five geographic regions caused by H5Nx (157), H5N1 (512) and H5N5 (4), H7N6 (1), H7N8 (2) and H7N9 (1) (see Table 1 for details).
LPAI events in animals officially reported since the last update (27 February 2025): 0 new events were reported.
Number of human cases officially reported since last update (27 December 2024): 1 new event was reported.1
Map 1. Global distribution of AIV with zoonotic potential* observed since 1 October 2024 (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. 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 March 2025]. 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 2023 to 30 September 2024 (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 January 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 October2024 | Species affected during the reporting preiod |
---|---|---|---|---|---|
H5 |
Bangladesh |
11/03/2025 |
1 |
1 |
Poultry |
Belgium |
27/02/2025 |
2 |
2 |
European Wildcat, Red Fox |
|
Japan |
19/03/2025 |
9 |
13 |
Large-billed crow |
|
Peru |
25/02/2025 |
1 |
32 |
Quail, Turkey |
|
Republic of Korea |
25/03/2025 |
3* |
3* |
Chicken; Leopard cat. |
|
Togo |
20/02/2025 |
1 |
1 |
Poultry |
|
United States of America7 |
21/03/2025 |
140 |
1 470 |
American black duck, Black vulture, Cackling goose, Canada goose, Mallard, Mallard/Black duck hybrid, Peregrine falcon, Red-breasted merganser, Red-tailed hawk; Black bear, Bobcat, Bottlenose dolphin, Domestic cat, House mouse, Red fox, Striped skunk |
|
H5N1
|
Albania |
02/03/2025 |
1 |
5 |
Poultry |
Antarctica/zone8 |
18/02/2025 |
? |
40 |
|
|
Belgium |
05/03/2025 |
17 |
31 |
Gallus gallus; Black-headed Gull, Canada Goose, Common Buzzard, Common Moorhen, Great Cested Grebe, Grey Heron, Greylag Goose, Herring Gull, Mew Gull |
|
Bulgaria |
18/03/2025 |
1 |
7 |
Poultry |
|
Cambodia |
07/03/2025 |
5 |
7 |
Chicken, Poultry, unspecified wild bird |
|
Canada |
12/03/2025 |
4 |
105 |
Chicken, Duck, Tirkey, Non-poultry (goose, peacock) |
|
China |
14/03/2025 |
4 |
42 |
Chicken; Black-faced spoonbill |
|
Czech Republic |
19/02/2025 |
6 |
38 |
Non-poultry (chicken, duck, Indian Runner duck, Emu, etc); mute swan |
|
Denmark |
09/03/2025 |
6 |
14 |
Common Buzzard, Greylag Goose, Mute Swan, Red Kite, White-tailed Sea-eagle |
|
Finland |
09/03/2025 |
2 |
4 |
Canada Goose, Northern Goshawk |
|
France |
10/03/2025 |
8 |
34 |
Black-headed Gull, Herring Gull, Mute Swan, White Stork |
|
Germany |
13/03/2025 |
50 |
209 |
Laying hens, Non-poultry birds; Accipitridae, Anatidae, Cygnus, Laridae |
|
Greece |
27/02/2025 |
1 |
3 |
Dalmatian Pelican |
|
Hungary |
23/03/2025 |
46 |
292 |
Chicken, duck, goose; Common Buzzard, Mute Swan |
|
India |
14/02/2025 |
1 |
50 |
Poultry |
|
Ireland |
14/03/2025 |
5 |
10 |
Common Buzzard, Common Starling, Mute Swan, Whooper swan |
|
Japan |
18/03/2025 |
15 |
126 |
Carrion crow, Eastern buzzard, Large-billed crow, Northern Goshawk, Whooper swan |
|
Mexico |
08/02/2025 |
1 |
13 |
Snow Goose |
|
Moldova |
03/03/2025 |
1 |
37 |
Non-poultry birds |
|
Netherlands (Kingdom of the) |
18/03/2025 |
29 |
185 |
Poultry; Barnacle Goose, Black-headed Gull, Canada Goose, Caspian Gull, Common Buzzard, Great black-backed Gull, Herring Gull, Mallard, Mew Gull, Mute Swan, Peregrine Falcon, Ruddy Turnstone, Spot-tailed Goshawk; Phasianidae |
|
Nigeria |
16/03/2025 |
1 |
15 |
Poultry |
|
Norway |
03/03/2025 |
1 |
2 |
Peregrine Falcon |
|
Poland |
24/03/2025 |
39 |
158 |
Poultry, Non-poultry; Greylag Goose, Mute Swan, Tawny owl |
|
Republic of Korea |
21/03/2025 |
8 |
83 |
Chicken, Duck; unspecified wild bird |
|
Romania |
11/03/2025 |
4 |
10 |
Non-poultry birds; Caspian Gull, Mallard |
|
Russian Federation |
19/02/2025 |
3 |
3 |
Carrion Crow |
|
Spain |
05/02/2025 |
1 |
17 |
Peregrine Falcon |
|
St. Helena |
12/09/2024 |
1 |
1 |
Brown skua |
|
Sweden |
18/03/2025 |
8 |
8 |
Pheasant; Barnacle Goose, Greylag Goose, Herring Gull, Mute Swan, Northern Lapwing, Peregrin falcon, Whooper swan |
|
Togo |
19/03/2025 |
3 |
3 |
Chicken |
|
Ukraine |
17/03/2025 |
2 |
8 |
Chicken, Duck, Goose, Guinea fowl, Pheasant, Pigeon, Swan, Jay, Falcon |
|
United Kingdom of Great Britain and Northern Ireland |
17/03/2025 |
131 |
254 |
Chicken, Goose, Turkey; Accipitridae, Anatidae, Anserinae, Ardeidae, Black-headed Gull, Canada Goose, Common Buzzard, Common Eider, Common Kestrel, Common Pheasant, Common Starling, Eurasian Sparrowhawk, Great black-backed Gull, Great Cormorant, Grey Heron, Greylag Goose, Herring Gull, Laridae, Long Eared Owl, Mew Gull, Mute Swan, Peregrine Falcon, Pink-footed Goose, Razorbill, Red Kite, Tawny owl, Tundra swan, White-tailed Sea-eagle, Whooper swan; grey seal, sheep |
|
United States of America7 |
25/03/2025 |
105 |
2 249 |
WOAH Poultry, WOAH Non-Poultry, Chicken, Duck, Turkey, Live bird market; American coot, American white pelican, Black vulture, Cackling goose, Canada goose, Cooper's hawk, Grackle, Great horned owl, Green-winged teal, Peregrine falcon, Sandhill crane, Turkey vulture; Cat, Cattle, Harbor seal, House mouse, Striped skunk |
|
Viet Nam |
February 2025 |
1 |
18 |
Poultry |
|
H5N5 |
Iceland |
03/02/2025 |
1 |
36 |
Cat |
United Kingdom6 |
17/02/2025 |
3 |
37 |
Common Barn-Owl, Herring Gull, Grey seal |
|
H7N8 |
Australia |
22/02/2025 |
2 |
4 |
Commercial free-range egg farms |
H7N9 |
United States of America7 |
08/03/2025 |
1 |
1 |
Chicken |
Data was retrieved from WOAH WAHIS portal, government websites. Data cutoff time: reported on 27 February 2025, 8:30 CEST. $:estimate. ‡: date of confirmation, §: 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, those reporting for the first time since 1 October 2024 in red. 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]. The full list of bird and mammalian species affected by H5Nx HPAI are available HERE.
Domestic
Zikibayeva, K.B., Svanbayev, A.A., Akhmetsadykov, N.N., Kudaibergenova, K.N., Akhmetsadykova, S.N., Nurolda, E.N. & Kydyrmanov, A.I. 2025. Epidemiological investigation of poultry infectious in Kazakhstan (2021-2024). Front Vet Sci, 2025 Feb 11;11:1520606. [reference]
Pawar, S.D., Keng, S.S., Tare, D.S., Balakrishnan, A.S.S, Koshy, J., Potdar, V. & Vipat, V, et al. 2025. Evidence of novel reassortment in clade 2.3.4.4b avian influenza H5N1 viruses, India, 2024. Virology, 606:110482. [reference]
Wild bird
Moutinho, S. 2025. H5N1 avian flu is spreading rapidly in Antarctica. Science, 387(6739):1130-1131. [reference]
Indykiewicz, P., Przymencki, M., Minias, P., Jakubas, D., Litwiniak, K., Zieliński, P., Janiszewski, T, et al. 2025. Impact of highly pathogenic avian influenza virus (HPAIV) on Black-headed Gulls Chroicocephalus ridibundus population in Poland in 2023. Avian Pathol, 2025 Mar 5:1-14. [reference]
McLaughlin, A., Giacinti, J., Sarma, S.N., Brown, M.G.C., Ronconi, R.A., Lavoie, R.A. Eng M.L., et al. 2025. Examining avian influenza virus exposure in seabirds of the northwest Atlantic in 2022 and 2023 via antibodies in eggs. Conserv Physiol, 13(1):coaf010. [reference]
Rayment, K.M., Franzen-Klein, D., Kurimo-Beechuk, E., Poulson, R.L., Brown, J., Mendoza, K., Etterson, M, et al. 2025. Exposure and survival of wild raptors during the 2022-2023 highly pathogenic influenza a virus outbreak. Sci Rep, 15(1):6574. [reference]
Mammal
Kwon, T., Trujillo, J.D., Carossino, M., Machkovech, H.M., Cool, K., Lyoo, E.L., Singh, G, et al. 2025. Pathogenicity and transmissibility of bovine-derived HPAI H5N1 B3.13 virus in pigs. bioRxiv, 2025 Mar 7:2025.03.04.641414. Preprint [reference]
Ramey, A.M., Beckmen, K.B., Saalfeld, D.T., Nicholson, K.L., Mangipane, B.A., Scott, L.C., Stallknecht, D.E. & Poulson, R.L. 2025. Exposure of Wild Mammals to Influenza A(H5N1) Virus, Alaska, USA, 2020-2023. Emerg Infect Dis, 31(4):804-808. [reference]
Turner, H.M., Fuller, A.K., Twining, J.P., Hitchener, G.R., Fadden, M.A., Stallknecht, D.E., Poulson, R.L, et al. 2025. Highly Pathogenic Avian Influenza Virus Exposure and Infection in Free-Ranging Bobcats (Lynx rufus) in New York, USA. J Wildl Dis, 2025 Mar 19. [reference]
Pardo-Roa, C., Nelson, M.I., Ariyama, N., Aguayo, C., Almonacid, L.I., Gonzalez-Reiche, A.S., Muñoz, G, et al. 2025. Cross-species and mammal-to-mammal transmission of clade 2.3.4.4b highly pathogenic avian influenza A/H5N1 with PB2 adaptations. Nat Commun, 2025 Mar 6;16(1):2232. [reference]
Le Sage, V., Werner, B.D., Merrbach, G.A., Petnuch, S.E., O'Connell, A.K., Simmons, H.C., McCarthy, K.R, et al. 2025. Influenza A(H5N1) Immune Response among Ferrets with Influenza A(H1N1) pdm09 Immunity. Emerg Infect Dis, 31(3):477-487. [reference]
Mahmoud, S.H., Khattab, M.S., Yehia, N., Zanaty, A., Arafa, A.E.S. & Khalil, A.A. 2025. Pathogenicity of Highly Pathogenic Avian Influenza A/H5Nx Viruses in Avian and Murine Models. Pathogens, 2025 Feb 4;14(2):149. [reference]
Dairy
Octaviani, C.P., Huang, P., Bi-Hung, P., Gray, G.C. & Tseng, C.K. 2025. Superior replication, pathogenicity, and immune evasion of a Texas dairy cattle H5N1 virus compared to a historical avian isolate. Sci Rep, 15(1):8797. [reference]
Lang, Y., Shi, L., Roy, S., Gupta, D., Dai, C., Khalid, M.A., Zhang, M.Z, et al. 2025.Detection of antibodies against influenza A viruses in cattle. J Virol, 2025 Mar 25:e0213824. [reference]
Levine, M.Z., Liu, F., Bagdasarian, N., Holiday, C., Jefferson, S., Li, Z.N., Pappas, C, et al. 2025. Neutralizing Antibody Response to Influenza A(H5N1) Virus in Dairy Farm Workers, Michigan, USA. Emerg Infect Dis, 31(4):876-878. [reference]
Paravinja, N., Herrmann, L., Dzijan, I., Rinder, M. & Neubauer-Juric, A. 2025. Highly Pathogenic Avian Influenza Virus in Mammals: Lack of Detection in Cattle With Respiratory Tract Infections and Genetic Analysis of Sporadic Spillover Infections in Wild Mammals in Bavaria, Southern Germany, 2022-2023. Zoonoses Public Health, Mar 11. [reference]
Zhu, S., Harriman, K., Liu, C., Kraushaar, V., Hoover, C., Shim, K., Brummitt, S.I, et al. 2025. Human Cases of Highly Pathogenic Avian Influenza A(H5N1) - California, September-December 2024. MMWR Morb Mortal Wkly Rep, 74(8):127-133. [reference]
Kaiser, F., Cardenas, S., Yinda, K.C., Mukesh, R.K., Ochwoto, M., Gallogly, S., Wickenhagen, A, et al. 2025. Highly Pathogenic Avian Influenza A(H5N1) Virus Stability in Irradiated Raw Milk and Wastewater and on Surfaces, United States. Emerg Infect Dis, 31(4):833-837. [reference]
Viruses
Ort, J.T., Zolnoski, S.A., Lam, T.T., Neher, R. & Moncla, L.H. 2025. Development of avian influenza A(H5) virus datasets for Nextclade enables rapid and accurate clade assignment. bioRxiv, 2025 Feb 3:2025.01.07.631789. Preprint. [reference]
Yan, M., Ma, T., Shi, X., Chen, Q., Li, L., Xu, B., Pan, X, et al. 2025. Isolation and Characterization of H1 Subtype Swine Influenza Viruses Recently Circulating in China. Viruses, 17(2):185. [reference]
He, F., Yu, H., Liu, L., Li, X., Xing, Y., Yang, L., Yang, P., Zhu, L. & Li, Z. 2025. Antigenicity and genetic properties of an Eurasian avian-like H1N1 swine influenza virus in Jiangsu Province, China. Biosaf Health, 6(6):319-326. [reference]
Wasik, B.R., Damodaran, L., Maltepes, M.A., Voorhees, I.E.H., Leutenegger, C.M., Newbury, S., Moncla, L.H., Dalziel, B.D., Goodman, L.B. & Parrish CR. 2025. The evolution and epidemiology of H3N2 canine influenza virus after 20 years in dogs. Epidemiol Infect, 153:e47. [reference]
Zhang, C., Zhao, C., Huang, J., Wang, Y., Jiang, B., Zheng, H., Zhuang, M, et al. 2025. Emergence of a novel reassortant H3N3 avian influenza virus with enhanced pathogenicity and transmissibility in chickens in China. Vet Res, 56(1):56. [reference]
Hermann, E. & Krammer, F. 2025. Clade 2.3.4.4b H5N1 neuraminidase has a long stalk, which is in contrast to most highly pathogenic H5N1 viruses circulating between 2002 and 2020. mBio. 2025 Feb 26:e0398924. [reference]
Vázquez-Pérez, J.A., Wong-Arámbula, C., Solís-Hernández, M., Becerril-Vargas, E., Barrera-Badillo, G., Ahumada-Topete, V.H., Avila-Rios, S. 2025, et al. Mexico's Laboratory-Confirmed Human Case of Infection with the Influenza A(H5N2) Virus. Viruses, 17(2):205. [reference]
Wang, X., Wang, X., Hao, X., Gao, R., Lu, X., Yang, W., Chen, Y, et al. 2025. The Novel H10N3 Avian Influenza Virus Triggers Lethal Cytokine Storm by Activating Multiple Forms of Programmed Cell Death in Mammalian Lungs. Int J Mol Sci, 26(5):1977. [reference]
Yang, J., Zheng, S., Sun, J., Wu, H., Zhang, D., Wang, Y., Tian, T, et al. 2025. A human-infecting H10N5 avian influenza virus: Clinical features, virus reassortment, receptor-binding affinity, and possible transmission routes. J Infect, 90(4):106456. [reference]
Li, X., Li, A., Qu, F., Li, Y., Chen, F., Lv, X., An, Q, et al. 2025. Evaluation of Global Distribution, Genetic Evolution, and Mammalian Infectivity and Pathogenicity of H13 and H16 Avian Influenza Viruses. Emerg Microbes Infect, 2025 Mar 25:2482695. [reference]
Review
Jindal, M., Stone, H., Lim, S. & MacIntyre, C.R. 2025. A Geospatial Perspective Toward the Role of Wild Bird Migrations and Global Poultry Trade in the Spread of Highly Pathogenic Avian Influenza H5N1. Geohealth. 9(3):e2024GH001296. [reference]
Galli, M., Giacomelli, A., Lai, A. & Zehender, G. 2025. H5N1 influenza A virus: lessons from past outbreaks and emerging threats. Infez Med, 33(1):76-89. [reference]
The Lancet. 2025. H5N1 avian influenza: technical solutions, political challenges. Lancet, 405(10480):671. [reference]
Epidemiological surveillance / Risk assessment / Tools
Arınık, N., Interdonato, R., Roche, M. & Teisseire, M.2025. Linked avian influenza epidemiological and genomic data in EMPRES-i for epidemic intelligence (2012-2021). Data Brief, 59:111410. [reference]
Branda, F., Mohapatra, R.K., Tuglo, L.S., Ciccozzi, M. & Scarpa, F. 2025. Real-time epidemiological surveillance data: tracking the occurrences of avian influenza outbreaks around the world. BMC Res Notes, 18(1):95. [reference]
Goujgoulova, G. & Koev, K. 2025. Risk Assessment of Spread of the Influenza A Virus in Cows in South Bulgaria. Viruses, 17(2):246. [reference]
Hoyos-Cerón, T., Albarrán-Tamayo, F., Bañuelos-Hernández, B. & Londoño-Avendaño, M.A. 2025. Disparities in Influenza Control and Surveillance in Latin America and the Caribbean. Viruses, 17(2):225. [reference]
Hosseini, P., Syndicus, I., Houghton, E., Alarcon, P., Fournie, G., Guitian, J., Paterson, A., et al. Qualitative studies on farm managers perception of risk from HPAIV and implementation of biosecurity measures on UK poultry farms. Prev Vet Med, 2025 Feb 15;239:106445. [reference]
Giussani, E., Sartori, A., Salomoni, A., Cavicchio, L., de Battisti, C., Pastori, A., Varotto, M., et al. 2025. FluMut: a tool for mutation surveillance in highly pathogenic H5N1 genomes. Virus Evol, 11(1):veaf011. [reference]
Robertson, H., Han, B.A., Castellanos, A.A., Rosado, D., Stott, G., Zimmerman, R., Drake, J.M. & Graeden, E. 2025. Understanding ecological systems using knowledge graphs: an application to highly pathogenic avian influenza. Bioinform Adv, 5(1):vbaf016. [reference]
Modelling
Ford, C.T., Yasa, S., Obeid, K., Jaimes, R. 3rd, Tomezsko, P.J., Guirales-Medrano, S., White, R.A. 3rd & Janies, D. 2025. Large-scale computational modelling of H5 influenza variants against HA1-neutralising antibodies. EBioMedicine, 114:105632. [reference]
Takekawa, J.Y., Choi, C.Y., Prosser, D.J., Sullivan, J.D., Batbayar, N. & Xiao, X. 2025. Perpetuation of Avian Influenza from Molt to Fall Migration in Wild Swan Geese (Anser cygnoides): An Agent-Based Modeling Approach. Viruses, 17(2):196. [reference]
Kjær, L.J., Kirkeby, C.T., Boklund, A.E., Hjulsager, C.K., Fox, A.D. & Ward, M.P. 2025. Prediction models show differences in highly pathogenic avian influenza outbreaks in Japan and South Korea compared to Europe. Sci Rep, 15(1):6783. [reference]
America
Asia
North Africa and Middle East
Sub-Saharan Africa
Figure 1. Number of countries reported HPAI since 1 October 2024 by subtype (left) and by region (right) as of 21 March 2025 (territory/area or sub/Antarctic zone)
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 within the Goose/Guangdong/1/96- lineage (Gs/GD) were first detected in geese in Guangdong Province, China in 1996. They have persisted, as high pathogenicity viruses, since then and 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, 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) virus detected in dairy cattle in North America in 2024 falls within genotype 3.13 using the North American naming system. [link] Some Gs/GD viruses have produced severe zoonotic infections in humans, first identified in 1997 when an A(H5N1) clade 0 virus in the Gs/GD lineage 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 viruses within this lineage 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 a Gs/GD virus (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. Viruses within the Gs/GD lineage 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) 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. These waves involved multiple N subtypes. 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. For an updated list of bird species affected with A(H5Nx) see HERE In 2024, H5N1 2.3.4.4b caused infection in goats (1 farm) and dairy cattle (993 farms, as of 26 March 2025) in the United States of America. See HERE. USDA shared the Whole Genome Sequences, see HERE. In 2025, H5N1 2.3.4.4b caused infection in sheep in the United Kingdom, see HERE. Among the other Gs/GD 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 2.3.2.1c/e viruses have been present in Indonesia since 2012 and related 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]. Of the 15 recent human cases, seven of which were fatal, recorded in Cambodia (6) and Viet Nam (1). For an updated list of confirmed human cases with A(H5N1) see 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. 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 mammalian species affected with A(H5Nx) see HERE |
Avian origin H3N8 LPAI |
An Influenza A(H3N8) virus lineage emerged in live bird markets in southern China in mid 2021 [link]. 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. 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 illneses 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. |
H7N4 LPAI (2017) |
One human case in China with reported exposure to poultry. |
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 |
H9N2 LPAI |
First human case reported in 1998. To date, about 100 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], in September 2022, a second case in Zhejiang Province, China [link], in February 2024, the third case in Yunnan Province, China [link]. The first influenza A(H10N5) human infection was reported in Zhejiang 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].
Updates on avian influenza infection in dairy cattle have been shared by USDA, US CDC and US FDA through the following sites:
Next issue: 24 April 2025
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.
If interested in a previous issue please send an email to EMPRES-Animal Health specifying the intended use of the document.