Safety of and Antibody Response to West Nile Virus Vaccination in Captive Sea Otters (Enhydra lutris)
Abstract
Encephalitis and associated morbidity from West Nile virus (WNV) has been confirmed in several species of marine mammals including sea otters (Enhydra lutris).1-4 A killed WNV vaccine (Fort Dodge West Nile Innovator©) was evaluated in 9 captive sea otters to determine vaccine safety and antibody response. The vaccine was administered intramuscularly at day 0 and again at day 30. Animals were monitored daily for adverse effects and titers measured at days 0, 30, and 90 post-vaccination. All samples were screened with a modification of Ebel's wild bird WNV enzyme immunoassay (EIA) using anti-dog IgG, as well as a duplicate series of plaque reduction serum neutralization tests (PRNT) performed at the USGS National Wildlife Health Center and the Cornell Animal Health Diagnostic Center.5,6 None of the animals included in the study had measurable titers at day 0. Vaccination resulted in neutralizing antibody production in 5 of the 9 vaccinated animals (55%) at day 30 and 90. The level of neutralizing antibodies produced was between 1:20 and 1:40 with a plaque reduction of 80%. Other types of vaccines such as a recombinant canary pox-vectored vaccine may produce higher levels of neutralizing antibodies; however, reactions to live and modified live vaccines have been noted in sea otters. No adverse reactions to vaccination were noted. Protective efficacy of the WNV vaccination in sea otters was not evaluated. Vaccination of sea otters against WNV may be warranted in high risk areas or in rehabilitation situations, such as during oil spill response situations, combined with management practices aimed at limiting exposures to potential vectors.7,8
Acknowledgements
The Seattle Aquarium would like to thank the Monterey Bay Aquarium and the Minnesota Zoo for their generous support of this study. We would like to thank Dr. Hendrink Nollens and Dr. David Jessup for their assistance with project design.
* Presenting author
Literature Cited
1. Miller DL, Ewing RY, Bossart GD. Emerging and resurging diseases. In: Dierauf LA, Gulland FMD, eds. CRC Handbook of Marine Mammal Medicine. 2nd ed. Boca Raton, FL: CRC Press; 2001: 15–30.
2. Pier F, Stremme D, Habecker P, Cantile C. West Nile flavivirus polioencephalomyelitis in a harbor seal (Phoca vitulina). Veterinary Pathology. 2006;43(1):58–61.
3. Schaefer AM, Reif JS, Goldstein JD, Ryan CN, Fair PA, Bossart GD. Serological evidence of exposure to selected viral, bacterial, and protozoal pathogens in free-ranging Atlantic bottlenose dolphins (Tursiops truncatus) from the Indian River Lagoon, Florida, and Charleston, South Carolina. Aquatic Mammals. 2009;35:163–170.
4. St. Leger J, Wu G, Anderson M, Dalton L, Nilson E, et al. 2011. West Nile virus infection in killer whale, Texas, USA, 2007. Emerging Infectious Diseases. 2011;17(8):1531–1533.
5. Ebel GD, Dupuis AP, Nicholas D, Young D, Maffei J, Kramer LD. Detection by enzyme-linked immunosorbent assay of antibodies to West Nile virus in birds. Emerging Infectious Diseases. 2002;8:979–982.
6. Beaty B, Calisher C, Shope R. Arboviruses. In: Schmidt N, Emmons R, eds. Diagnostic Procedures for Viral, Rickettsial and Chlamydial Infections. Washington, DC: American Public Health Association; 1989: 797–855.
7. Goldstein T, Gill V, Tuomi P, Monson D, Burdin A, et al. 2011. Assessment of clinical pathology and pathogen exposure in sea otters (Enhydra lutris) bordering the threatened population in Alaska. Journal of Wildlife Diseases. 2011;47(3):579–592.
8. Levin M, Leibrecht C, Mori C, Jessup D, De Guise S. Immunomodulatory effects of organochlorine mixtures upon in vitro exposure of peripheral blood leukocytes differ between free-ranging and captive southern sea otters (Enhydra lutris). Vet Immunology and Immunopathology. 2007;119:269–277.