Cross-sectional study of canine leptospirosis in animal shelter populations in mainland Australia.

OBJECTIVE: To measure the prevalence of canine leptospirosis in Queensland and to detect infection, if present, in New South Wales, Victoria, South Australia, Western Australia and the Northern Territory by measuring the serological titres of dogs held in animal shelters. PROCEDURE: Samples were collected through stratified sampling from multiple dog shelters in Queensland and New South Wales, and from one dog shelter located in close proximity to a major urban area in Victoria, South Australia, the Northern Territory and Western Australia. All samples were analysed using the microscopic agglutination test at the WHO/FAO/OIE Collaborating Centre for Reference & Research on Leptospirosis, Queensland Health Scientific Services in Brisbane, Queensland. RESULTS: Of a total of 956 samples submitted, 18 (1.9%) had positive leptospirosis titres. True prevalence measured in Queensland was estimated to be 2.5%, and the true prevalence in New South Wales, Victoria, South Australia, Western Australia and the Northern Territory was estimated to be 2.3%, 2.8%, 0%, 1% and 1.1% respectively. An association was found between seropositive status and female dogs (odds ratio (OR) 1.92) and seropositive status and the age group 1 to < 3 years (OR 1.41). Although 11 different serovars were detected, Leptospira interrogans serovar Copenhageni was the most prevalent and was found in 4 of the 18 positive dogs as a single infection. CONCLUSION: Serological evidence of canine leptospirosis in five states in mainland Australia indicates that the disease is more broadly distributed than previously thought.

Molecular subtyping of feline immunodeficiency virus from domestic cats in Australia.

OBJECTIVE: To determine the prevalent subtypes of feline immunodeficiency virus (FIV) present in the domestic cat population of Australia. METHOD: Blood samples were collected from 41 FIV antibody positive cats from four cities across Australia. Following DNA extraction, polymerase chain reaction (PCR) was performed to amplify the variable V3-V5 region of the envelope (env) gene. Genotypes were assessed by direct sequencing of PCR products and comparison with previously reported FIV sequences. Phylogenetic analysis allowed classification of the Australian sequences into the appropriate subtype. RESULTS: Of the 41 FIV samples, 40 were found to cluster with previously reported subtype A isolates, whilst the remaining sample grouped within subtype B. CONCLUSIONS: Subtype A was found to be the predominant FIV subtype present in Australia, although subtype B was also found. These results broaden our knowledge of the genetic diversity of FIV and the associated implications for preventative, diagnostic and therapeutic approaches.