The aim of this dissertation was to investigate the role of M. canis infection in dogs with urogenital diseases and with fertility problems. The clinical study included 52 dogs; 7 dogs with urogenital disease symptoms, 14 dogs with fertility problems, and 31 healthy dogs.
The pathogen was detected by PCR (polymerase chain reaction) method on vaginal and preputial swabs. Swab samples were analysed to determine the full bacterial spectrum, and these analyses were extended by metagenomic analysis. The presence of antibodies was tested by the Dot-immunobinding assay (DIBA) method, while the results were confirmed by the Western Blot method. In addition to clinical signs, we looked for abnormalities in haematological and biochemical parameters in blood, urinalysis, and specific parameters of fertility disorders, and compared the groups with each other.
M. canis was detected by PCR method in 3/7 (43 %) patients with urogenital disorders, in 6/14 (43 %) patients with fertility disorders, and in a statistically significantly lower proportion of healthy dogs in the control group (6/31, 19 %). Metagenomic analysis of bacterial composition showed no significant differences between the groups.
The DIBA method showed the presence of specific antibodies against at least one of the five selected strains in 54/55 samples (98 %). With all patients, except two from the control group, we detected a reaction to the M. canis Larissa strain. The results of the DIBA test were confirmed by the Western Blot method.
The results of the thesis will help us to select appropriate diagnostic methods and treatment plan and to monitor the response to treatment in canine patients with chronic urinary tract diseases or fertility disorders. The results show that serological screening tests are useful at least for patients with fertility disorders. The specific PCR method is the most suitable for the detection of M. canis infections.
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