Haematopinus Infestations and Mycoplasma Infections of Water Buffalo (Bubalus bubalis) Herds in National Parks of Hungary

The biology, epidemiology and pathology of sucking louse infestation and Mycoplasma infection of water buffalo (Bubalus bubalis) herds in Hungarian national parks were studied between 19 December 2011 and 4 May 2012. A total of 333 water buffaloes were examined in buffalo stocks of the Balaton Uplands, Fertő-Hanság and Kiskunság National Parks. The objective was to determine the prevalence and rate of sucking louse infestation and mycoplasma infection among water buffaloes. Always an area of identical size (2 cm2) was examined on the right or left side of the middle part of the animals' neck. A total of 3106 eggs, 10 nymphs and 105 adults of the sucking louse Haematopinus tuberculatus were identified with the help of a Conrad USB microscopic camera and a Wild-Leitz-Leica M420 photomacroscope. The data were evaluated using the Quantitative Parasitology software QP 3.0. The prevalence of mycoplasmas was determined in 20 randomly selected buffaloes of two national parks with the help of sterile nasal and vaginal transport swabs (Sarstedt). All of the 10 nasal swabs collected from buffaloes in the Balaton Uplands National Park contained Mycoplasma bovirhinis and three swab samples yielded M. bovis as well. Mycoplasma bovirhinis was cultured from 8 out of 10 swabs taken from the vagina, and three vaginal samples also yielded M. bovis. Similar results were obtained by testing samples collected from buffaloes in the Kiskunság National Park (Mórahalom). All ten nasal swab samples yielded M. bovirhinis. From two samples a mixture of M. bovirhinis and M. bovis was cultured. Nine out of the 10 vaginal swabs yielded M. bovirhinis while two showed a combined infection by M. bovis and M. bovirhinis

Clinical study of the disease of calves associated with Mycoplasma bovis infection

Clinical, bacteriological and serological examination of 35 calves from the age of 5 to 26 days was performed in a Holstein-Friesian dairy herd endemically infected with Mycoplasma bovis. M. bovis was isolated from 48.6% of nasal swabs taken from the calves at the age of 5 days, and from 91.4% of the same calves at the age of 26 days, indicating the gradual spread of infection. The isolation rate of Pasteurella multocida did not change much, and varied from 28.6 to 25.7%. No P. haemolytica could be detected. In addition to M. bovis and P. multocida, the herd was also infected with different viruses (including bovine viral diarrhoea virus, infectious bovine rhinotracheitis virus, bovine adenoviruses, parainfluenza-3 virus, and bovine respiratory syncytial virus) as a large proportion of the sera of newborn calves contained colostral antibodies against these viruses. In most of the newborn calves severe clinical signs (fever, depression, inappetence, hyperventilation, dyspnoea, nasal discharge and coughing) due to M. bovis infection developed. The clinical signs appeared already on the fifth day of life, and their incidence was the highest at the age of 10 to 15 days. Three calves (8.6%) died as a result of severe serofibrinous pneumonia. The surviving calves showed very poor weight gain (ranging from 1.5 to 3.5 kg) during the first two weeks of life

Screening of Hungarian cattle herds for Mycoplasma mycoides subspecies mycoides small colony infection with negative results

At abattoirs and farms, 1248 sera were collected from animals representing 121 farms, and examined by complement fixation test using Mycoplasma mycoides subspecies mycoides small colony type (MmmSC) antigen. All sera were negative except seven from four farms, giving ++ reactions in the serum dilution of 1:10. On retesting, these sera and additional 30 sera collected repeatedly in both farms gave negative results. In isolation attempts, 953 lung samples collected from slaughtered cattle at the same abattoirs, and 326 nasal swabs collected from 11 herds proved to be negative for the presence of MmmSC, but M. bovis was isolated frequently. In the small farms 23.95% of the animals had pleurisy and/or pneumonia while in the large herds 34.69% had lesions. DNA extracted from 50 nasal swabs and 430 lung samples was examined by polymerase chain reaction (PCR) using M. mycoides cluster-specific primers. DNA from further 325 lung samples was tested by the more specific M. mycoides subspecies mycoides small colony/large colony/capri specific primers and 196 samples by nested PCR specific for MmmSC. All gave negative results. The detection level of cluster-specific primers and the more specific primers was 33.4 pg of DNA, whereas that of nested PCR was 0.33 pg

Examination of the role of Mycoplasma bovis in bovine pneumonia and a mathematical model for its evaluation

The authors screened 34 large cattle herds for the presence of Mycoplasma bovis infection by examining slaughtered cattle for macroscopic lung lesions, by culturing M. bovis from lung lesions and at the same time by testing sera for the presence of antibodies against M. bovis. Among the 595 cattle examined, 33.9% had pneumonic lesions, mycoplasmas were isolated from 59.9% of pneumonic lung samples, and 10.9% of sera from those animals contained antibodies to M.bovis. In 25.2% of the cases M. bovis was isolated from lungs with no macroscopic lesions. The proportion of seropositive herds was 64.7%. The average seropositivity rate of individuals was 11.3% but in certain herds it exceeded 50%. A probability model was developed for examining the relationship among the occurrence of pneumonia, the isolation of M. bovis from the lungs and the presence of M. bovis specific antibodies in sera