Diagnosis and seroprevalence of leptospirosis in California sea lions from coastal California

Angela M. Colagross-Schouten, Jonna A Mazet, Frances M D Gulland, Melissa A. Miller, Sharon Hietala

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

The sensitivity and specificity of the microscopic agglutination test (MAT) as a method for detection of exposure to Leptospira spp. in California sea lions (Zalophus californianus) were determined. Sera came from individuals that demonstrated clinical signs of renal disease, had lesions suggestive of leptospirosis at necropsy, and had visible leptospires in silver stained kidney sections as positive controls. Sera from unexposed captive individuals were used as negative controls. The test was 100% sensitive at 1:3,200 for confirming renal infection and 100% specific at negative < 1:100 for detection of Leptospira interrogans serovar pomona antibodies by MAT in California sea lions. Leptospira interrogans serovar pomona was used as a screening serovar because it has been isolated previously from the kidneys and placentas of California sea lions, and there appears to be cross-reactivity between serovar pomona and other serovars. Sera from 225 free-ranging California sea lions presented to one of three participating California (USA) coastal marine mammal rehabilitation centers in 1996 were then evaluated for antibodies to serovar pomona using the MAT. The overall seroprevalence was 38.2% (86/225), although the prevalence varied among locations from 100% (38/38) in animals at the Marine Mammal Care Center (Fort MacArthur, California, USA) to 0% (0/14) at SeaWorld California (San Diego, California). At The Marine Mammal Center (Sausalito, California) [prevalence 27.8% (48/173)], the majority of seropositive animals were subadults and adults, and males were 4.7 times more likely to be seropositive to serovar pomona than females. When combining results from all three centers, subadult and adult animals were more likely to be seropositive than pups and juvenile sea lions, and the highest proportion of seropositive animals presented during the autumn months. Serum elevations of blood urea nitrogen, creatinine, phosphorus, and/or calcium were associated with seropositivity to serovar pomona. We found no association between potassium or sodium levels and seropositivity.

Original languageEnglish (US)
Pages (from-to)7-17
Number of pages11
JournalJournal of Wildlife Diseases
Volume38
Issue number1
StatePublished - Jan 2002

Fingerprint

Sea Lions
Leptospirosis
pinniped
leptospirosis
Seroepidemiologic Studies
seroprevalence
serotypes
serum
marine mammal
Agglutination Tests
Leptospira interrogans serovar pomona
animal
Kidney
Mammals
agglutination tests
marine mammals
antibody
Serum
Leptospira interrogans
kidneys

Keywords

  • California sea lion
  • Leptospira interrogans pomona
  • Leptospirosis
  • Microscopic agglutination test
  • Seroprevalence
  • Warthin-Starry stain
  • Zalophus californianus

ASJC Scopus subject areas

  • veterinary(all)

Cite this

Colagross-Schouten, A. M., Mazet, J. A., Gulland, F. M. D., Miller, M. A., & Hietala, S. (2002). Diagnosis and seroprevalence of leptospirosis in California sea lions from coastal California. Journal of Wildlife Diseases, 38(1), 7-17.

Diagnosis and seroprevalence of leptospirosis in California sea lions from coastal California. / Colagross-Schouten, Angela M.; Mazet, Jonna A; Gulland, Frances M D; Miller, Melissa A.; Hietala, Sharon.

In: Journal of Wildlife Diseases, Vol. 38, No. 1, 01.2002, p. 7-17.

Research output: Contribution to journalArticle

Colagross-Schouten, AM, Mazet, JA, Gulland, FMD, Miller, MA & Hietala, S 2002, 'Diagnosis and seroprevalence of leptospirosis in California sea lions from coastal California', Journal of Wildlife Diseases, vol. 38, no. 1, pp. 7-17.
Colagross-Schouten, Angela M. ; Mazet, Jonna A ; Gulland, Frances M D ; Miller, Melissa A. ; Hietala, Sharon. / Diagnosis and seroprevalence of leptospirosis in California sea lions from coastal California. In: Journal of Wildlife Diseases. 2002 ; Vol. 38, No. 1. pp. 7-17.
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