Aim:This study was conducted to determine the role of Staphylococcus in the formation of subclinical mastitis in cows and to isolate the phage against isolated Staphylococcus aureus strains.Materials and Methods:In this study, 400 milk cows were screened by California Mastitis Test (CMT) for subclinical mastitis and 235 udders of 96 cows, which were determined to be positive, were evaluated for Staphylococcus. Milk samples were evaluated using conventional and molecular methods. In addition, phage isolation studies were performed against S. aureus strains causing mastitis.Results:At the result of cultural examination, of 235 milk samples that were found as positive for mastitis by CMT, a total of 117 (49.7%) Staphylococcus spp. were isolated as a distribution of 74 (63.24%) coagulase-positive staphylococci and 43 (36.75%) coagulase-negative staphylococci. Of these isolates, 76 (64.95%) were characterized as S. aureus both conventional and molecular techniques. Lytic bacteriophages against two S. aureus strains which were isolated from mastitic milk samples were obtained from wastewater samples.Conclusion:The results of this study show that a significant portion of subclinical mastitis was formed by staphylococci. In addition, phage isolation against S. aureus strains isolated can be considered as one of the steps to be applied in the prophylaxis and treatment of such infections.

The stability of the plasmid-mediated virulence factors of Bacillus anthracis, a tripartite toxin located on pXO1 and an antiphagocytic capsule encoded by genes located on pXO2, following long-term storage was investigated. A collection of 159 isolates of B. anthracis were collected from the Kars region of Turkey between 2000 and 2013 and stored at -20°C in Brucella broth supplemented with 20% glycerine. A total of 142 isolates were recovered of which one failed to express a capsule upon primary culture. A further 35 isolates yielded a mixture of mucoid and non-mucoid colonies; the majority of which had lost the pXO2 plasmid as determined by PCR analysis. Results would suggest that pXO2 is more unstable than pXO1 and that this instability increases with the length of storage. It is possible that the pXO2-deficient isolates of B. anthracis described here could be developed into a vaccine to treat at risk animals in the Kars region as many animal vaccines are based upon pXO2 deficiency.

Though the main route of tularemia outbreaks is water-borne in Turkey, it was determined that people whose occupations bring them into contact with animals are at risk. Similar studies are recommended in order to further clarify the epidemiology of the disease in the northeast of Turkey.

Paratuberculosis, caused by Mycobacterium avium subsp. paratuberculosis (Map), is one of the most prevalent and costly infectious diseases of livestock, particularly sheep and cattle herds. The aim of this study was to estimate true animal, within-herd, and between-herd prevalence of Map antibodies in sheep herds of the Kars Region in the Northeast part of Turkey. A seroprevalence study was carried out using a commercial ELISA kit. Twenty six sheep herds, non-vaccinated against Map, were randomly selected in different regions and in total 450 sheep aged 24 months and more were sampled. Herds were declared positive if one or more sheep in the herd tested positive for Map antibodies. The animal, within-herd, and between-herd apparent prevalences were calculated as 6.2% (95% CI = 4.3 to 8.8%), 10.2% (95 CI = 7.1 to 14.3%) and 57.7% (95% CI = 38.9 to 74.5%), respectively. True prevalences were estimated by conversion from apparent prevalences via the Rogan-Gladen estimator. True animal, within-herd, and between-herd prevalences were calculated as 8.3% (95% CI = 4.7 to 11.8), 14.6% (95 CI = 8.9 to 20.2) and 90% (95 CI = 59.8 to 120.1), respectively. The results provide useful information regarding the prevalence of Map infection in sheep herds in the Kars Region and will hopefully attract the special attention of veterinarians and promote the establishment of an efficient control programme.

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