Causes of Mortality of Northern Sea Otters (Enhydra lutris kenyoni) in Alaska from 2002–2012
IAAAM 2021
Kathy A. Burek Huntington1*; Verena A. Gill2,3; Amanda M. Berrian4; Tracey Goldstein5; Pam Tuomi6; Barbara A. Byrne7; Kristin Worman3; Jonna Mazet5
1Alaska Veterinary Pathology Services, Eagle River, AK, USA; 2NOAA Fisheries, Anchorage, AK, USA; 3U.S Fish & Wildlife Service, Anchorage, AK, USA; 4Department of Veterinary Preventive Medicine, The Ohio State University, Columbus, OH, USA; 5Karen C. Draver Wildlife Health Center & One Health Institute, University of California, Davis, CA, USA; 6Alaska SeaLife Center, Seward, AK, USA; 7Pathology, Microbiology, and Immunology, University of California Davis, School of Veterinary Medicine, Davis, CA, USA

Abstract

Most of the world’s sea otters reside in Alaska; however, there has never been an assessment of long-term mortality patterns for this keystone predator. Prior studies examining the health and disease of northern sea otters in Alaska have been limited in their timeline and scope with most examining the effects of the 1989 Exxon Valdez oil spill in Prince William Sound and found that environmental disasters can have long-term impacts on survival rates and mortality.1,2 Other studies have compared Northern sea otters in Alaska to southern sea otters in California showing low exposure to most potential marine and terrestrial pathogens but 40% exposure to PDV.3,4

We examined data collected from 780 northern sea otter (Enhydra lutris kenyoni) carcasses recovered in Alaska from 2002–2012 to evaluate the causes of mortality and risk factors associated with death. A subset of fresh non-frozen carcasses (n=144, 18%) were included in a detailed mortality analysis. From this analysis, 44% of these freshly dead otters were determined to have died from infectious endocarditis, meningoencephalitis, and/or septicemia due to systemic streptococcosis (“Strep syndrome”).5 Streptococcus lutetiensis, a member of the Streptococcus bovis/equinus (SB/E) group was most commonly isolated, although other members of the SB/E group were identified. There were fewer cases where S. phocae and other streptococci were isolated. A regression analysis revealed age and location risk factors for Strep syndrome. Subadults were the highest risk age group, and otters recovered from the Kachemak Bay region were 3.6 times (95% CI: 2.2–5.9) more likely to die from Strep syndrome than otters recovered elsewhere. Diagnosis of this Strep syndrome has not been reported in sea otters outside of Alaska or other marine mammals in Alaska. Other causes of death for the fresh otters included neurologic disease (10%), trauma (8%), nutritional causes and cardiovascular diseases (7%), gastrointestinal disease/parasites (6%), undetermined (5%), and septicemia and neoplasia (3%). All other causes of death (oiling, hepatobiliary disease, fungal, marine biotoxins, pulmonary disease) were at or below 1%. Twenty percent of tested fresh animals were positive for phocine distemper virus (PDV) by polymerase chain reaction (PCR, 11/55) and 18% seropositive for PDV (7/38). Paramyxovirus-like particles were demonstrated by electron microscopy within inclusion bodies from one animal. Related studies suggest PDV may be emerging in the Pacific correlated to changes in sea ice cover6 and our study provides the first pathologic data. Low concentrations of the harmful algal bloom toxins domoic acid and saxitoxin were also detected in 26% and 22% of fresh animals, respectively as has been reported previously.7 Protozoal disease was very rare. These patterns of disease differ from sea otters in other regions such as Washington and Oregon8 and California9 and possible reasons and significance are discussed.

Acknowledgements

We appreciate the many members of the volunteer Alaska marine mammal stranding network as well as interns and biologists that assisted us on the beaches and in the laboratory, they are too numerous to list. Special thanks go to all the staff at the Alaska SeaLife Center. We are indebted to veterinarians Carrie Goertz, Joanne Hill, and Marc Kramer, for their help with multiple necropsies and to veterinary pathologists Jennifer Chilton, David Rotstein, and Melissa Miller for their help with histology and interpretation. The WARRN-west laboratory with Dr. Kathi Lefebvre and Maryjean Willis provided DA and SXT analysis and Dr. Patricia Conrad and UCDavis Protozoal laboratory provided the analyses for Toxoplasma, Sarcocystis and Neospora. Carcasses and samples were collected under MMPA permit No. MA041309-5 issued to VAG in the U.S. Fish and Wildlife’s Marine Mammals Management office. Funding sources include the Oiled Wildlife Care Network and the Minnesota Zoo Conservation Fund and the U.S. Fish and Wildlife Service. The findings and conclusions in this article are those of the authors(s) and do not necessarily represent the views of the U.S. Fish and Wildlife Service.

*Presenting author

Literature Cited

1.  Monson, DH, Doak, DF, Ballachey, BE, Johnson, A, Bodkin, JL. 2000. Long-term impacts of the Exxon Valdez oil spill on sea otters, assessed through age-dependent mortality patterns. Proc Natl Acad Sci 97:6562–6567.

2.  Miles AK, Bowen L, Ballachey B, Bodkin JL, Murray M, Estes J, Keister RA, Stott JL. 2012. Variations of transcript profiles between sea otters Enhydra lutris from Prince William Sound, Alaska, and clinically normal reference otters. Mar Ecol Prog Ser 451:201–212.

3.  Hanni KD, Mazet JAK, Gulland FMD, Estes J, Staedler M, Murray MJ, Miller M, Jessup DA. 2003. Clinical pathology and assessment of pathogen exposure in southern and Alaskan sea otters. J Wildl Dis 39:837–850.

4.  Goldstein T, Gill VA, Tuomi P, Monson D, Burdin A, Conrad PA, Dunn JL, Field C, Johnson C, Jessup DA, Bodkin J. 2011. Assessment of clinical pathology and pathogen exposure in sea otters (Enhydra lutris) bordering the threatened population in Alaska. J Wildl Dis 47:579–592.

5.  Williams, BH, Burek-Huntington, KA, Miller M. 2018. “Mustelidae” Chapter 11 In: Terio K, McAloose D, St. Leger J, editors. Pathology of wildlife and zoo animals. London (UK): Academic Press. p 287–304.

6.  VanWormer E, Mazet JA, Hall A, Gill VA, Boveng PL, London JM, Gelatt T, Fadely BS, Lander ME, Sterling J, Burkanov VN. 2019. Viral emergence in marine mammals in the North Pacific may be linked to Arctic sea ice reduction. Sci Rep 9:1–11.

7.  Lefebvre KA, Quakenbush L, Frame E, Burek Huntington K, Sheffield G, Stimmelmayr R, Bryan A, Kendrick P, Ziel H, Goldstein T, Snyder JA, Gelatt T, Gulland F, Dickerson B, Gill V. 2016. Prevalence of algal toxins in Alaskan marine mammals foraging in a changing arctic and subarctic environment. Harmful Algae. 55:13–24.

8.  White CL, Lankau EW, Lynch D, Knowles S, Schuler KL, Dubey JP, Shearn-Bochsler VI, Isidoro-Ayza M, Thomas NJ. 2018. Mortality trends in northern sea otters (Enhydra lutris kenyoni) collected from the coasts of Washington and Oregon, USA (2002–15). J Wildl Dis 54:238–247.

9.  Miller MA, Moriarty ME, Henkel L, Tinker MT, Burgess TL, Batac FI, Dodd E, Young C, Harris MD, Jessup DA, Ames J. 2020. Predators, disease, and environmental change in the nearshore ecosystem: Mortality in southern sea otters (Enhydra lutris nereis) from 1998–2012. Front Mar Sci 7:582.

 

Speaker Information
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Kathy Burek-Huntington
Alaska Veterinary Pathology Services
Eagle River, AK, USA


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