23 July 2026, 17:00 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 (29 June 2026): in total, 209 outbreaks / events have been reported in 25 countries/territories caused by H5Nx (1), H5N1 (201), H5N5 (3), H7N3 (1) and HxNx (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: 3 new events were reported. [ref1, ref2, ref3]
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 July 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 |
United States of America7 |
14/07/2026R |
1 |
1703 |
American crow, Herring gull |
H5N1 |
Australia |
23/07/2026 |
17 |
17 |
Southern Giant Petrel, Swift tern |
Austria |
7/13/2026 |
1 |
100 |
Common Barn-Owl |
|
Belgium |
17/06/2026 |
1 |
361 |
Canada Goose |
|
Canada3 |
04/05/2026 |
1 |
125 |
Short-eared Owl |
|
Chile |
04/05/2026 |
2 |
37 |
Non-poultry birds |
|
Colombia |
12/06/2026 |
1 |
9 |
Non-poultry birds |
|
Denmark |
08/07/2026 |
3 |
261 |
Barnacle Goose, Canada Goose, Eurasian oystercatcher |
|
Germany |
29/06/2026 |
59 |
4106 |
Chicken, duck; Ardeidae, Barnacle Goose, Brent Goose, Ciconiidae, Common Buzzard, Common Shelduck, Cygnus, Greylag Goose, Rallidae |
|
Indonesia |
5/17/2026 |
11 |
36 |
Poultry |
|
Namibia |
03/02/2026 |
1 |
2 |
Swift tern |
|
Nepal |
05/07/2026 |
26 |
93 |
Chicken, duck; Black-faced Ibis, Indian Pond-Heron; Kalij pheasant |
|
Netherlands (Kingdom of the) |
16/07/2026 |
13 |
466 |
Non-poultry birds; Black-headed Gull, Eurasian Spoonbill, Greylag Goose, Mallard, Mute Swan |
|
New Zealand |
15/07/2026R |
2 |
2 |
Brown skua, Swamp harrier hawk |
|
Nigeria |
22/06/2026 |
2 |
31 |
Poultry |
|
Norway |
05/06/2026 |
1 |
71 |
Common Eider |
|
Peru |
07/072026 |
2 |
49 |
Backyard poultry, duck, fighting cock |
|
The Philippines |
10/07/2026 |
3 |
21 |
Chicken, Duck. Note: in addition to ongoing outbreaks in three cities, outbreaks in four other cities in March-May were posted on WAHIS. |
|
Poland |
15/07/2026 |
2 |
466 |
Chicken, duck, poultry; White Stork |
|
Portugal |
08/06/2026 |
8 |
33 |
Non-poultry birds; Anatidae, Andean Teal, Ciconiidae, Eurasian Spoonbill, Great White Pelican, Gruidae, Herring Gull, Laridae, Lesser Black-backed Gull, Mandarin Duck, Northern Bald Ibis, Northern Gannet, Peacock, Pelecanidae, Purple Swamphen, Rheidae, Spur-winged Goose, Threskiornithidae, Wood Duck, Yellow-legged Gull |
|
South Africa |
08/06/2026 |
3 |
47 |
Poultry; Hartlaub's Gull, Little Stint |
|
Togo |
09/07/2026 |
5 |
5 |
Chicken |
|
United States of America7 |
17/07/2026R |
15 |
3172 |
Chicken; Common raven; Cattle |
|
Viet Nam |
19/07/2026 |
22 |
86 |
Chicken, Duck, Muscovy duck, Poultry |
|
H5N5 |
Canada |
01/01/2026 |
3 |
7 |
American crow, Canada Goose, Great black-backed Gull, Herring Gull, Ring-billed gull, Turkey Vulture |
H7N3 |
Mexico |
22/06/2026 |
1 |
5 |
Plain chachalaca |
HxNx |
Honduras |
08/07/2026 |
3 |
7 |
Non-poultry birds; Black Vulture |
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 25 June 2026, 8:30 CEST. $: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.
Domestic
Features of the epizootic process and ways to improve measures to combat avian flu. Br Poult Sci, 2026 Jun 29:1-10. [reference]
Biosecurity deficiencies in HPAI-affected poultry farms in Korea, 2020/2021–2024/2025 seasons. Front Vet Sci, 13:1863522. [reference]
Spatiotemporal distribution trends and driving factors of avian influenza in poultry in China. One Health, 23:101483. [reference]
Characterization of practices influencing avian influenza virus transmission risk in live bird markets in Northern Vietnam. Prev Vet Med, 255:106958. [reference]
Review of avian influenza outbreaks in Nigeria 2006-2025. Open Vet J, 15(12):6146-6165. [reference]
Characterization of oseltamivir-resistant A(H5N1) clade 2.3.4.4b, genotype D1.1 variants identified in poultry farms of British Columbia, Canada. Emerg Microbes Infect, 15(1):2686474. [reference]
Facilitated Molting as a Management Strategy During a Low-Pathogenic H1N2 Avian Influenza Outbreak in a Breeder Turkey Flock. Avian Dis, 70(2):224-227. [reference]
Post-vaccination surveillance during the first year of duck vaccination against highly pathogenic avian influenza in France: Adherence to protocols and first outcomes in terms of viral circulation. Prev Vet Med, 255:106956. [reference]
Molecular Characterization of H5N1 Clade 2.3.4.4b Virus in Vaccinated Layer Chickens. Viruses, 18(6):589. [reference]
Early challenge with LPAI-H9N2 followed by vNDV-VII.1.1 in vaccinated and unvaccinated broilers: a comprehensive study. Avian Pathol, 55(4):469-486. [reference]
Virus and host-associated variations in the interaction of low-pathogenic avian influenza viruses with the epithelial target tissue of the chicken reproductive tract. Vet Res, 57(1):116. [reference]
Wild
Between-species contagion drives HPAI transmission and mass mortality in seabirds. J Anim Ecol, 2026 Jul 6. [reference]
Ecological shifts in avian influenza viruses following HPAIV introductions in southwestern Alaska, 2011-2024. Npj Viruses, 2026 Jul 17. [reference]
Rapid Expansion of Highly Pathogenic Avian Influenza A(H5N1) Clade 2.3.4.4b Genotype D1.1 Virus across Flyway Regions, North America, Fall 2024. Emerg Infect Dis, 32(8). [reference]
An outbreak of H5N1 clade 2.3.4.4b highly pathogenic avian influenza in California condors (Gymnogyps californianus). Vet Pathol, 2026 Jul 3:3009858261457964. [reference]
Spatial association of seabirds and aquatic birds with highly pathogenic avian influenza (H5N1) outbreaks in Brazil: A nationwide ecological and statistical modelling approach. PLoS One, 21(7):e0350505. [reference]
Marked Antigenic Divergence and Evolutionary Analysis of H5 AIVs from Wild Birds in East China, 2013-2022. Animals (Basel), 16(13):2109. [reference]
Clade 2.3.4.4b H5N1 HPAIV from Migratory Birds in Beidaihe Wetland, North China. Viruses, 18(6):595. [reference]
High pathogenicity avian influenza A (H5N1) viruses isolated from poultry and wild birds in Japan during the 2024-2025 season. Microbiol Spectr, 2026 Jul 14:e0029326. [reference]
Sero-epidemiological profiling of duck viral hepatitis, avian influenza, and Newcastle disease in transboundary waterfowl populations along the Indonesia-Malaysia border of West Kalimantan. Vet World, 19(5):2160-2171. [reference]
As bird flu threatens, New Zealand vaccinates endangered birds., 393(6807):126-127. [reference]
Ecology of Low Pathogenicity Avian Influenza Virus H7 in Wild Birds in South-Eastern Australia Prior to Emergence of High Pathogenicity Avian Influenza H7 in Poultry. Influenza Other Respir Viruses. 2026 Jul;20(7):e70285. [reference]
Mammal
High Mortality and Reduced Pup Production in Eared Seals Following the 2023 Highly Pathogenic Avian Influenza Outbreak in Patagonia. Biol Bull, 249(1):30-45. [reference]
Mass mortality events in aquatic mammals caused by avian influenza viruses. Curr Opin Virol, 77:101566. [reference]
Effectiveness of baloxavir marboxil in nonhuman primates infected with highly pathogenic avian influenza A(H7N9) virus. EBioMedicine, 129:106350. [reference]
Detection of Highly Pathogenic Avian Influenza A(H5N1) Clade 2.3.4.4b Genotype D1.2 Virus in Swine after Experimental Inoculation. Emerg Infect Dis, 32(8). [reference]
Receptor profiling and growth assessment of influenza A virus in porcine mammary and non-mammary tissues and derived cells. J Virol, 2026 Jul 6:e0061526. [reference]
Single-cell and spatial transcriptomic profiling reveals distinct immune landscapes in murine lungs infected with H1N1 versus H5N1 influenza viruses. J Virol, 2026 Jun 29:e0074626. [reference]
Dairy
Detection of antibodies against avian influenza in European dairy cattle, the Netherlands, January 2026. Euro Surveill, 31(25):2600464. [reference]
Isolation and characterization of a clade 2.3.4.4b genotype D1.1 H5N1 virus from dairy cattle in Wisconsin. J Virol, 2026 Jul 10:e0076126. [reference]
Cellular tropism of highly pathogenic avian influenza (HPAI) A(H5N1) clade 2.3.4.4b viruses in human respiratory and bovine mammary epithelial cells. Microbiol Spectr, 2026 Jul 17:e0137726. [reference]
Isolation of Infectious Highly Pathogenic Avian Influenza A(H5N1) Virus from Fetal Bovine Serum, United States, 2025. Emerg Infect Dis, 32(8). [reference]
Beyond H5N1: Influenza A virus infection in bovine udder organoids. Emerg Microbes Infect, 2026 Jul 2:2698239. [reference]
Bovine-derived H5N1 influenza virus efficiently infects lactating swine via the mammary gland. bioRxiv, 2026.07.18.739312. [reference Preprint]
A bovine H5N1 virus efficiently replicates in differentiated human nasal epithelial cells. Npj Viruses, 2026 Jun 24. [reference]
Investigation of vehicles as potential pathways for between-farm transmission of influenza A virus in US dairy herds. JDS Commun, 7(4):518-522. [reference]
Viruses
The receptor landscape of influenza A viruses. J Virol. 2026 Jul 16:e0144325. [reference]
Lactylation of Influenza Virus Polymerase Acidic Protein Promotes Viral Replication and Pathogenicity. bioRxiv, 2026.07.10.737663. [reference Preprint]
Emergence of Novel Reassortant H3N2 Avian Influenza Viruses in Southern China: Genetic Complexity and Pathogenicity in Chickens and Mice. Animals (Basel), 16(12):1765. [reference]
Comparative study of hemagglutinin adsorption from influenza A H1N1, H3N2, and H5N1 strains on model surfaces using a quartz crystal microbalance. Colloids Surf B Biointerfaces, 267:115964. [reference]
Emerged N193S mutation of PA-X protein disabled the immunity of mucosal dendritic cells for regulating virulence of clade 2.3.4.4b H5 subtype virus. Emerg Microbes Infect, 15(1):2695530. [reference]
Characterization and pathogenicity of a novel triple-reassortant H6N6 avian influenza virus associated with reproductive failure in breeding ducks. Poult Sci, 105(10):107308. [reference]
Characterization of the novel H6N1 avian influenza viruses in a broiler duck farm in Korea from 2023 to 2024. Vet Res Commun, 50(5):420. [reference]
Autoantibodies against type I interferons in patients with zoonotic H7N9 influenza: an observational case-control study. EBioMedicine, 130:106387. [reference]
Deciphering interferon functions in avian influenza using receptor knockout models in the natural host. Elife, 14:RP107855. [reference]
In vitro and in vivo studies of GAPLINC identify it as a critical host factor involved in the regulation of influenza A virus infection. Vet Res, 57(136). [reference]
Research Progress on Avian Influenza Virus and Autophagy: A Review. Pathogens, 15(6):623. [reference]
Complete genome sequence of BLRI-developed inactivated avian influenza A/H9N2 vaccine strain in Bangladesh. Microbiol Resour Announc, 2026 Jun 25:e0030426. [reference]
Epidemiological and Virological Characteristics of H9N2 Avian Influenza Virus in Jiangsu Province, China, 2024. Viruses, 18(6):687. [reference]
HA thermostability mutations S84F, G167N, and D168N potentiate H9N2 virus transmission in a warming environment. Emerg Microbes Infect, 15(1):2695528. [reference]
Severe pneumonia and acute respiratory distress syndrome caused by avian influenza A (H10N3) in a young female: a case report. Infection, 2026 Jul 17. [reference]
Assay
Supporting molecular detection of A(H5N1) through development and characterization of RNA reference materials. Anal Bioanal Chem. 2026 Jul 22. [reference]
Evaluation of serologic assays for detection and quantification of influenza antibodies in milk samples from H5N1 highly pathogenic avian influenza virus infected dairy cows. Front. Vet. Sci. [reference]
Validation of sample pooling for high-throughput RT-qPCR subtyping of avian influenza A(H5). Microbiol Spectr, 2026 Jul 13:e0085026. [reference]
Evaluation of IndiMix JOE with Intype IC-RNA as an Alternative to AgPath-ID for Influenza A Virus Detection in Avian and Bovine Samples. Pathogens, 15(6):600. [reference]
Toward a quality-managed operational architecture for wastewater surveillance of zoonotic and emerging pathogens. Appl Environ Microbiol, 2026 Jul 10:e0095026. [reference]
Analysis & Modelling
From Clustered to Sporadic: Structural Shifts in the Spatiotemporal Dynamics of HPAI Following the 2017 Policy Reinforcement in South Korea (2003-2025). Transbound Emerg Dis, 2026(1):e5747471. [reference]
Modeling and control of highly pathogenic avian influenza in poultry using network disease dynamics. Infect Dis Model, 11(4):1624-1644. [reference]
Avian Influenza at the Wild Bird-Poultry Interface: An Asia-Focused Review with Ecological Risk Scenarios for China. Animals (Basel), 16(13):1937. [reference]
A phylogeny-informed mathematical modeling of HPAI H5N1 transmission dynamics and effectiveness of control measures. One Health, 23:101490. [reference]
A Unified Benchmark and Conditional Sequence Modeling Framework for Future Influenza Evolution Prediction. In: Bioinformatics Research and Applications. ISBRA 2026. Springer, Singapore. [reference]
Overview
Perspective on human diagnostic and national reference laboratory preparedness for zoonotic influenza in Europe. Euro Surveill, 31(27):2500918. [reference]
Avian influenza overview March-May 2026. EFSA J, 24(7):e10196. [reference]
Avian influenza virus H5N1 and H9N2 subtypes in different birds and humans: Findings from an extensive evaluation. Open Vet J, 16(1):1-14. [reference]
Occupational Zoonotic Risk at India's Human-Animal Interface: Statutory Origins and a Regulatory Pathway for the Compensation-Prevention Disconnect. Am J Ind Med, 2026 Jul 14. [reference]
Preparing for the Next Pandemic: Learning From COVID-19 to Build What Comes Next. Open Forum Infect Dis, 13(7):ofag348. [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 20 July 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. . In 2026, H5N1 clade 2.3.4.4b virus reached Australia and New Zealand, with evidence suggesting introduction through migratory wild birds originating from sub‑Antarctic/Antarctic zones. Since 2024, H5N1 2.3.4.4b caused infection in goats (1 farm), alpaca (1 backyard farm), swine (1 farm) and dairy cattle (1 169 farms in 20 states, as of 23 July 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: 27 August 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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