Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link

Disclaimer: Early release articles are not considered as final versions. Any changes will be reflected in the online version in the month the article is officially released.

Volume 32, Number 9—September 2026

Dispatch

Seroprevalence of Influenza A(H5N1) Virus in Domestic Cats at Epicenter of Dairy Cattle Outbreaks, California, USA, 2024–2026

Author affiliation: University of Maryland School of Public Health, College Park, Maryland, USA (I.G. Bemis, E.A. Fadaka, S. Perez, K.K. Coleman); University of Maryland College of Agriculture and Natural Resources, College Park (I.G. Bemis, K.K. Coleman); University of Texas Medical Branch Division of Infectious Diseases, Galveston, Texas, USA (I. Shittu, G.C. Gray); Cross Street Small Animal Veterinary Hospital, Tulare, California, USA (J.F. Gomez)

Suggested citation for this article

Abstract

We conducted a serologic study of domestic cats near the epicenter of the dairy cattle outbreaks of influenza A(H5N1) in California, USA. Three of the 12 cats sampled within 2 km of farms had neutralizing antibodies against H5N1 virus. Proximity to dairy farms was a statistically significant risk factor for seropositivity.

Highly pathogenic avian influenza A(H5N1) clade 2.3.4.4b is emerging in domestic cats (Felis catus), presenting urgent public health and animal welfare implications. Historically, cats have not been widely considered important hosts of influenza viruses. However, sporadic infections and outbreaks of avian influenza viruses in cats have occurred for >20 years (1). The emergence of H5N1 clade 2.3.4.4b virus has resulted in widespread mammalian infections (2,3), including an alarming increase in infections among domestic cats, in which the estimated case-fatality rate is 90% (1). Although most of those infections emerged from direct bird-to-cat transmission, several recent outbreaks among US cats have involved infected dairy farms (46) or links to workers in the dairy industry (7). Contaminated raw dairy milk (5,8) and raw meat–based diets (9) have been identified as sources of infection in cats.

Like swine, cats have α-2,6- and α-2,3-linked sialic acid receptors (10) and can be co-infected with avian and human influenza viruses. Thus, with widespread H5N1 virus infections, a growing potential exists for influenza virus co-infections in domestic cats that could result in viral reassortment and selection for novel human-adapted viruses. Infections resulting from cat-to-human transmission of avian influenza have been documented 3 times in the United States, including in a veterinarian and an animal shelter worker exposed to shelter cats infected with influenza A(H7N2) virus in New York, New York, in 2016 (11,12) and in a veterinary professional exposed to a domestic cat infected with H5N1 virus in Los Angeles, California, in 2024 (13). Suspected human-to-cat transmission of H5N1 virus also occurred in 2024 in Michigan, resulting in the deaths of 2 house cats (7). Ten additional cats died from another H5N1 outbreak in 2024 in South Dakota (14) in which cattle-to-bird-to-cat transmission was suspected.

Although several US dairy industry–related outbreaks of H5N1 among cats have been reported, the resulting seroprevalence of H5N1 virus among domestic cats near affected dairy farms is unknown. Therefore, we performed a serosurvey of domestic cats at the epicenter of the 2024–2025 dairy cattle outbreaks in California’s Central Valley.

The Study

An animal welfare organization in Tulare County, California, provided serum samples collected from cats during routine blood draws. Because serum samples from routine blood draws were provided, an ethics review was not required. We shipped aliquots to the University of Maryland (College Park, MD, USA) and the University of Texas Medical Branch (Galveston, TX, USA) and tested them using ELISA and H5 microneutralization assays (Appendix). We compared approximate age, sex, weight, and distance to nearest dairy farm between seropositive and seronegative cats (Appendix).

Figure 1

Timeline of highly pathogenic avian influenza A(H5N1) dairy cattle outbreaks and domestic cat (Felis catus) serum sample collection, Central Valley, California, USA, 2024–2026. USDA, US Department of Agriculture.

Figure 1. Timeline of highly pathogenic avian influenza A(H5N1) dairy cattle outbreaks and domestic cat (Felis catus) serum sample collection, Central Valley, California, USA, 2024–2026. USDA, US Department of Agriculture. ...

During December 2024–March 2026, we collected 73 serum samples from indoor and outdoor cats (Figure 1) within 9.7 km (6 miles) of >1 dairy farms (mean 4.7 km [2.9 miles]). Among the 73 cats, 3 tested positive for both influenza A virus nucleoprotein antibodies and neutralizing antibodies against H5 clade 2.3.4.4b. One indoor-only and 1 outdoor feral cat had neutralizing antibody titers of 1:160, and 1 indoor-only cat had a titer of 1:640, indicating strong positivity and 100% agreement between the ELISA and microneutralization assay. All negative samples had titers of <1:20.

Figure 2

Grouped distance to the nearest dairy farm for domestic cats (Felis catus) seropositive and seronegative for highly pathogenic avian influenza A(H5N1) clade 2.3.4.4b virus near epicenter of dairy cattle outbreaks, Central Valley, California, USA, 2024–2026.

Figure 2. Grouped distance to the nearest dairy farm for domestic cats (Felis catus) seropositive and seronegative for highly pathogenic avian influenza A(H5N1) clade 2.3.4.4b virus near epicenter of dairy...

Figure 3

Mean distance to the nearest dairy farm for domestic cats (Felis catus) seropositive and seronegative for influenza A(H5N1) clade 2.3.4.4b virus near epicenter of the dairy cattle outbreaks, Central Valley, California, USA, 2024–2026. Error bars represent SEM.

Figure 3. Mean distance to the nearest dairy farm for domestic cats (Felis catus) seropositive and seronegative for influenza A(H5N1) clade 2.3.4.4b virus near epicenter of the dairy cattle outbreaks,...

Three (25%) of the 12 cats sampled within 2 km (1.24 miles) of dairy farms were seropositive for H5N1 virus (Figure 2), yielding an overall seropositivity rate of 4.1% for all surveyed cats. Seropositive cats had a mean distance to the nearest dairy farm of 1.34 km (0.8 miles), compared with 4.83 km (3 miles) for seronegative cats (p = 0.014) (Figure 3). Average age of surveyed cats was ≈1.6 years (range ≈3 months–4.9 years); 60% were female and 40% male. Age and sex were not significantly different for seropositive and seronegative cats. Of the 73 cats surveyed, 68 (93%) were in rural areas and 5 (7%) in urban areas. All seropositive cats were in rural areas. No indoor cats were fed raw meat or dairy.

Conclusions

Avian influenza A(H5N1) clade 2.3.4.4b is an emerging threat to domestic cats and public health. We report a 25% seropositivity rate for the virus among domestic cats within 2 km (1.2 miles) of dairy farms in the epicenter of the H5N1 cattle outbreaks in California during 2024–2026. Proximity to dairy farms in counties experiencing outbreaks may be a risk factor for H5N1 spillover to indoor and outdoor domestic cats. Our research provides insight into potential H5N1 virus sources and transmission routes among domestic cats in the United States, for which data are scarce. Our results may help refine public health guidance on the prevention of avian influenza in cats and set the stage for future studies.

Although only 3 seropositive cats were identified in our study, their closer proximity to dairy farms compared with seronegative cats is an important epidemiologic finding. Although we cannot determine the source (or sources) of H5N1 among the seropositive cats in our study, their close proximity to dairy farms suggests that cats may share a source of infection with infected cattle or that dairy herds are directly infecting nearby cat populations. Infections and deaths also have been reported among cats exposed to H5N1 on affected dairy farms in Texas (4), New Mexico (5), and Minnesota (6) and among domestic cats near dairy farms in South Dakota (14) and in the households of Michigan dairy industry workers (7). Similar to the South Dakota outbreak (14), cattle-to-bird-to-cat transmission is one plausible explanation for the seropositive feral cat identified in our study. The feral cat was found within 0.8 km (0.5 miles) of a farm and could have wandered and been exposed directly to cattle or contaminated milk or other sources. Cat movement onto influenza-infected farms should be studied, in addition to cat exposure to infected rodents and other small mammals. Regarding the seropositive indoor-only cats in our study, both were from a household of a dairy industry worker, similar to the infections in Michigan cats (7). The route of transmission, including human-to-cat transmission, cannot be confirmed in our study. However, we can rule out raw meat or dairy as a potential source.

Because of the high case-fatality rate in cats with H5N1 virus infection (1), the seroprevalence reported in our study probably is an underestimate of the actual prevalence of H5N1 virus infection in cats in this region. In addition, cats infected with H5N1 virus often have onset of acute encephalitis with multifocal necrosis, resulting in paralysis, blindness, ataxia, and other severe long-term sequelae, sometimes requiring ambulatory assistive devices (8). Such complications may preclude working cats from escaping predation or effectively hunting or deterring rodents on farms. To help mitigate that animal welfare and farm maintenance issue, vaccinating dairy cattle should be considered (15) because it could protect cattle and other at-risk animals on or near farms.

Our study highlights a critical gap in companion animal surveillance and might be helpful to health agencies as they seek approaches to mitigating this emerging infectious disease threat. Proximity to dairy farms was a risk factor for H5N1 spillover to cats in our study. However, cattle-to-cat transmission of H5N1 virus is a relatively new phenomenon, and most cat infections reported in the literature over the past 20 years have been from bird-to-cat transmission (1). To assess the in situ risk for human-adapted reassortant influenza viruses emerging in cats, future work is needed to characterize the seroprevalence of human influenza viruses in cats and avian influenza viruses in cats near outbreaks in poultry and wild birds. Cat surveillance studies also could provide insight into nearby H5N1 outbreaks that have yet to be discovered, fully investigated, or contained.

Mr. Bemis is a comparative biomedical sciences PhD student at the University of Maryland Department of Veterinary Medicine in College Park, Maryland, USA. His primary research interests include animal virology, respiratory virus transmission, virulence factors, viral zoonosis, and reverse zoonosis.

Top

Acknowledgments

We thank the Valley Oak Society for the Prevention of Cruelty to Animals and Alexandra van der Hoeven. We also thank the University of Maryland Baltimore Institute for Clinical and Translational Research and the University of Maryland Strategic Partnership, MPowering the State. We thank Richard J. Webby for sharing the recombinant H5N1 virus (rg-A/bald eagle/Florida/W22-134-OP/2022) used in the microneutralization assay.

Raw data are available and may be provided by the authors upon reasonable request.

This study was funded in part by the University of Maryland Baltimore Institute for Clinical and Translational Research and the University of Maryland Strategic Partnership, MPowering the State (awarded to K.K.C.). Discretionary funding from the University of Maryland School of Public Health, Department of Global, Environmental, and Occupational Health was awarded to K.K.C. This project also was supported in part by US Department of Agriculture Agricultural Research Service (agreement 58-3022-4-048, awarded to G.C.G.).

Author contributions: I.G.B. and K.K.C drafted the initial version of the manuscript, and I.G.B, K.K.C, I.S., J.F.G., and G.C.G provided revisions; K.K.C, I.S., and G.C.G. conceptualized the study; J.F.G. helped provide serum samples; I.G.B and I.S. performed the laboratory work and provided the laboratory data, with the help of E.A.F. and S.P.

Top

References

  1. Coleman  KK, Bemis  IG. Avian influenza virus infections in felines: a systematic review of two decades of literature. Open Forum Infect Dis. 2025;12:ofaf261. DOIPubMedGoogle Scholar
  2. Peacock  TP, Moncla  L, Dudas  G, VanInsberghe  D, Sukhova  K, Lloyd-Smith  JO, et al. The global H5N1 influenza panzootic in mammals. Nature. 2025;637:30413. DOIPubMedGoogle Scholar
  3. US Department of Agriculture. Detections of highly pathogenic avian influenza in mammals. 2026 Jun 26 [cited 2026 Apr 24]. https://www.aphis.usda.gov/livestock-poultry-disease/avian/avian-influenza/hpai-detections/mammals
  4. Burrough  ER, Magstadt  DR, Petersen  B, Timmermans  SJ, Gauger  PC, Zhang  J, et al. Highly pathogenic avian influenza A(H5N1) clade 2.3.4.4b virus infection in domestic dairy cattle and cats, United States. Emerg Infect Dis. 2024;30:133543. DOIPubMedGoogle Scholar
  5. Caserta  LC, Frye  EA, Butt  SL, Laverack  M, Nooruzzaman  M, Covaleda  LM, et al. Spillover of highly pathogenic avian influenza H5N1 virus to dairy cattle. Nature. 2024;634:66976. DOIPubMedGoogle Scholar
  6. Mainenti  M, Siepker  C, Magstadt  DR, Gauger  P, Baum  D, Petersen  B, et al. Distribution of lesions and detection of influenza A(H5N1) virus, clade 2.3.4.4b, in ante- and postmortem samples from naturally infected domestic cats on U.S. dairy farms. J Vet Diagn Invest. 2025;37:2735. DOIPubMedGoogle Scholar
  7. Naraharisetti  R, Weinberg  M, Stoddard  B, Stobierski  MG, Dodd  KA, Wineland  N, et al. Highly pathogenic avian influenza A(H5N1) virus infection of indoor domestic cats within dairy industry worker households—Michigan, May 2024. MMWR Morb Mortal Wkly Rep. 2025;74:615. DOIPubMedGoogle Scholar
  8. Frye  EA, Nooruzzaman  M, Cronk  B, Laverack  M, de Oliveira  PSB, Caserta  LC, et al. Isolation of highly pathogenic avian influenza A(H5N1) virus from cat urine after raw milk ingestion, United States. Emerg Infect Dis. 2025;31:16369. DOIPubMedGoogle Scholar
  9. Kang  YM, Heo  GB, An  SH, Lee  H, Park  E, Cha  RM, et al. Highly pathogenic avian influenza A(H5N1) virus infection in cats, South Korea, 2023. Emerg Infect Dis. 2024;30:251020. DOIPubMedGoogle Scholar
  10. Wang  H, Wu  X, Cheng  Y, An  Y, Ning  Z. Tissue distribution of human and avian type sialic acid influenza virus receptors in domestic cat. Acta Vet Hung. 2013;61:53746.PubMedGoogle Scholar
  11. Lee  CT, Slavinski  S, Schiff  C, Merlino  M, Daskalakis  D, Liu  D, et al. Influenza A(H7N2) Response Team. Outbreak of influenza A(H7N2) among cats in an animal shelter with cat-to-human transmission—New York City, 2016. Clin Infect Dis. 2017;65:19279. DOIPubMedGoogle Scholar
  12. Poirot  E, Levine  MZ, Russell  K, Stewart  RJ, Pompey  JM, Chiu  S, et al. Detection of avian influenza A(H7N2) virus infection among animal shelter workers using a novel serological approach—New York City, 2016–2017. J Infect Dis. 2019;219:168896. DOIPubMedGoogle Scholar
  13. Vaughan  A, Joyce  A, Traub  E, Jae  M, Beeler  E, Paiva  E, et al. Serologic evidence of highly pathogenic avian influenza A(H5N1) virus infection in a veterinary professional exposed to an infected domestic cat—Los Angeles County, California, December 2024–January 2025. MMWR Morb Mortal Wkly Rep. 2026;75:21520. DOIPubMedGoogle Scholar
  14. Chothe  SK, Srinivas  S, Misra  S, Nallipogu  NC, Gilbride  E, LaBella  L, et al. Marked neurotropism and potential adaptation of H5N1 clade 2.3.4.4.b virus in naturally infected domestic cats. Emerg Microbes Infect. 2025;14:2440498. DOIPubMedGoogle Scholar
  15. Gray  GC, Warren  CJ, Webby  RJ, Bowman  AS. Why we must vaccinate US dairy cattle against HPAI H5N1. J Infect Dis. 2026;•••:jiag183. DOIPubMedGoogle Scholar

Top

Figures

Top

Suggested citation for this article: Bemis IG, Shittu I, Gomez JF, Fadaka EA, Perez S, Gray GC, et al. Seroprevalence of influenza A(H5N1) virus in domestic cats at epicenter of dairy cattle outbreaks, California, USA, 2024–2026. Emerg Infect Dis. 2026 Sep [date cited]. https://doi.org/10.3201/eid3209.260785

DOI: 10.3201/eid3209.260785

Original Publication Date: July 28, 2026

Table of Contents – Volume 32, Number 9—September 2026

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Kristen K. Coleman, University of Maryland School of Public Health, 4200 Valley Dr, College Park, MD 20742, USA

Send To

10000 character(s) remaining.

Top

Page created: July 21, 2026
Page updated: July 28, 2026
Page reviewed: July 28, 2026
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external