Only one virus, Avipox, has been documented in wild birds in Hawaii. Here, using immunohistochemistry and PCR, we found that two native threatened Hawaiian geese, one with multicentric histiocytoma and another with toxoplasmosis and one Laysan albatross with avian pox were infected with reticuloendotheliosis virus (REV). The virus was isolated from one of the geese by cell culture. PCR surveys of other Hawaiian geese with various pathologies, avian pox cases, and pox viral isolates failed to reveal REV suggesting the virus is uncommon, at least in samples examined. The full genome of the Gag, Pol, and Env genes were sequenced for all three infected birds and revealed geographic divergence of the Pol gene suggesting it to be under strong selective pressure. Our finding of REV in Hawaii makes this only the second virus documented in native Hawaiian birds associated with pathology. Moreover, the presence of REV in a pelagic seabird is unusual. Future surveys should seek the reservoir of the virus in efforts to trace its origins.

Data sets containing: (1) sample collection and influenza A virus (IAV) screening information for wild ducks, (2) water temperature data for six North American wetlands, (3) water quality measurement from those wetlands, (4) laboratory-based study of viral viability using Minnesota wetland water, (5) naive mallards challenged experimentally with IAVs identified from the field experiment, and (6) genetic sequence data for IAVs recovered from the challenge study.

Data sets containing: (1) sample collection and influenza A virus (IAV) screening information for wild ducks, (2) water temperature data for six North American wetlands, (3) water quality measurement from those wetlands, (4) laboratory-based study of viral viability using Minnesota wetland water, (5) naive mallards challenged experimentally with IAVs identified from the field experiment, and (6) genetic sequence data for IAVs recovered from the challenge study.

This data set contains three spreadsheets with results of Influenza A Virus (IAV) screening in blood from Pacific, Red-throated, and Yellow-billed Loons at three locations in Alaska. Loons were captured along the Beaufort Sea Coast, Chukchi Sea Coast, and Yukon-Kuskokwim Delta from 2008-2017. Three different tests were used and the results are presented in separate spreadsheets. All serum samples were screened for IAV antibodies using a blocking enzyme-linked immunosorbent assay (bELISA). A subsample were screened using agar gel immunodiffusion (AGID), and hemagglutination inhibition assays (HI).

This data set contains three spreadsheets with results of Influenza A Virus (IAV) screening in blood from Pacific, Red-throated, and Yellow-billed Loons at three locations in Alaska. Loons were captured along the Beaufort Sea Coast, Chukchi Sea Coast, and Yukon-Kuskokwim Delta from 2008-2017. Three different tests were used and the results are presented in separate spreadsheets. All serum samples were screened for IAV antibodies using a blocking enzyme-linked immunosorbent assay (bELISA). A subsample were screened using agar gel immunodiffusion (AGID), and hemagglutination inhibition assays (HI).

Data sets containing: (1) sample collection and influenza A virus (IAV) screening information for wild ducks, (2) water temperature data from four wetlands within the Izembek National Wildlife Refuge in Alaska, USA (3) water quality measurement from four wetlands within the Izembek National Wildlife Refuge in Alaska, USA, (4) genetic sequence data for IAVs recovered from replicate samples of wild ducks.

Data sets containing: (1) sample collection and influenza A virus (IAV) screening information for wild ducks, (2) water temperature data from four wetlands within the Izembek National Wildlife Refuge in Alaska, USA (3) water quality measurement from four wetlands within the Izembek National Wildlife Refuge in Alaska, USA, (4) genetic sequence data for IAVs recovered from replicate samples of wild ducks.

This dataset includes epidemiology, clinical signs, gross and microscopic pathology, and virology data from two red foxes (Vulpes vulpes) and one fisher (Pekania pennanti) submitted to the USGS-National Wildlife Health Center for cause-of-death determination and confirmed positive for highly pathogenic avian influenza (HPAI) H5N1 by USDA’s National Veterinary Services Laboratories. The foxes were juveniles from North Dakota and the fisher was an adult from Wisconsin. Clinical signs included neurological deficits such as ataxia, lethargy, or paralysis. Gross and microscopic lesions included myocardial pallor, pulmonary and hepatic congestion, meningoencephalitis, interstitial pneumonia, myocardial necrosis, and hepatic necrosis. Highly pathogenic avian influenza H5N1 2.3.4.4 was detected in swabs and/or organ tissues by PCR; genotype B3.1 was identified in the foxes and B3.2 was identified in the fisher. Death of all three animals was attributed to HPAI.

This dataset includes epidemiology, clinical signs, gross and microscopic pathology, and virology data from two red foxes (Vulpes vulpes) and one fisher (Pekania pennanti) submitted to the USGS-National Wildlife Health Center for cause-of-death determination and confirmed positive for highly pathogenic avian influenza (HPAI) H5N1 by USDA’s National Veterinary Services Laboratories. The foxes were juveniles from North Dakota and the fisher was an adult from Wisconsin. Clinical signs included neurological deficits such as ataxia, lethargy, or paralysis. Gross and microscopic lesions included myocardial pallor, pulmonary and hepatic congestion, meningoencephalitis, interstitial pneumonia, myocardial necrosis, and hepatic necrosis. Highly pathogenic avian influenza H5N1 2.3.4.4 was detected in swabs and/or organ tissues by PCR; genotype B3.1 was identified in the foxes and B3.2 was identified in the fisher. Death of all three animals was attributed to HPAI.

This data set is comprised of four files related to the biosurveillance of low pathogenic avian influenza viruses (LPAIV) in migratory waterfowl at 20 locations in the Delmarva Peninsula in fall/winter of 2013-2014. Two files contain data related to the species, age, and AIV prevalence for all birds sampled (1 data file, 1 definitions file). The other two files contain data related to the primers and standards used in bioassays for AIVs (1 data file, 1 definitions file).