Clinico-physiological effects of Xylazine - Ketamine were evaluated in 12 clinical cases of uremic buffalo calves having urolithiasis. In group A, Xylazine -Ketamine were used at the dose rate of 0.05 mg/kg body weight and 2.5 mg/kg body weight respectively to create regional spinal anesthesia at the lumbosacral space in 6 buffalo calves. In group B, Xylazine and Ketamine at the same dose rates were used intramuscularly in 6 buffalo calves. Analgesia was then recorded at different regions by the pin prick method and scored on a scale and motor incoordination, sedation, complete duration of anesthesia, complete recovery and physiological parameters (heart rate, respiration rate and rectal temperature) were evaluated in both the groups at various intervals of time throughout the duration of surgery of Tube cystotomy. It was found that the animals of group B achieved a safer physiological peak values than animals of group A.

Survivability of Listeria monocytogenes in clay loam soil was examined at 30° C for a period of 35 days. The microorganism inoculated in soil steadily declined from 3.5 × 10 6 g -1 to 3.9 × 10 4 g -1 (P = 0.05) on 35 th days. Destruction of normal soil microflora by heat treatment resulted in marginal rise in 3.3 × 10 6 g -1 of L. monocytogenes to 4.2 × 10 6 g -1 during the first 7 days, followed by steady decline to 5.6 × 10 4 g -1 on 35 th days. Heat treated soil inoculated with lower concentration of L. monocytogenes (3.6 × 10 4 g -1 ) supported sharp rise in its population to 4.8 × 10 6 g -1 (P=0.05) during the first weak which gradually declined, but remained higher (6.1 × 10 4 g -1 ) than the initial load even on 35 th days. In non-sterile soil, the rise was less appreciable but L. monocytogenes maintained its levels (10 4 g -1 ) during the experimental period. Survivability of the microorganisms was also observed in the soil with added chicken manure, cattle manure or sheep/goat manure.

Ground fresh green leaves of Lucas aspera and Parthenium hysterophorus were screened for their molluscicidal property at dilutions of 1,000,2,500,5,000 and 10,000 ppm in water against fresh water snail, Indoplanorbis exustus at 6, 24 and 48 hr of exposure. Cent percent mortality of snails was noticed in all dilutions except the first one for each exposure time.

The present study reports the concentration of Copper, Zinc, Iron and Manganese in the blood plasma of male kutchi camels during their breeding season. The respective concentrations of the plasma trace minerals were 112.94 ±O.44, 105.65±2.08, 117.65±1.72 and 160.29±0.75 µ/dl.

Abortion, still birth, premature birth and mortality of cross bred dairy cattle (Jersey × Tharparkar/Red Sindhi) were noticed in the organized dairy farm of National Dairy Research Institute, Eastern Regional Station, Kalyani, Nadia, situated in hot and humid climatic area nearer to the river Ganges of West Bengal, India. The history of the farm revealed newly introduction of pure bred dairy cattle and outbreak of FMD during mid March to mid April, affected about 34% cross bred cows. During investigation, intermittent rise of temperature (104°F -108°F), anorexia, rapid respiration, progressive deterioration of health of animals and loss of milk production were also noticed. On the basis of past history, twenty suspected animals were taken for disease investigation. Repeated visit of the farm and repeated examinations of blood smears were done to observe any haemoprotozoan infections. Twenty to thirty percent of those suspected animals were found positive for Brucella antibodies by STAT, plate agglutination test and MRT. After a massive screening of blood smears, during the visit of third time, ultimately one animal (Identification number JT614) was found positive for the presence of Trypanosoma evansi infections in Giemsa stained blood smears. The infected and all suspected animals were successfully treated with single injection of a mixture of quinapyramine sulphate and chloride @ 7.4 mg/kg body weight subcutaneously. As a prophylactic measure, a mixture of quinapyramine sulphate and chloride @ 7.4 mg/kg body weight subcutaneously were also administered to all suspected animals prevented further occurrence of the disease in this dairy farm. It can be concluded that the iAfection with T. evansi in this farm has happened in a condition of intercurrent diseases with environmental stresses.

One hundred thirty one samples (nasal, faecal, soil, tissue from dead foal) were tested for presence of Rhodococcus equi. These samples included 58 nasal swabs including 45 from foals with respiratory problem and 13 from in contact apparently healthy foals. Faecal samples were 54 including 41 from foals with respiratory problem and 13 from in contact apparently healthy foals. Faecal and nasal samples were from same foals, soil samples from infected premises were 15, besides tissues from foals (4) which died due to respiratory problems. Fourteen isolates of Rhodococcus equi were obtained from foals with respiratory problems, which were subjected to in vitro antibiotic sensitivity testing to 17 antimicrobial agents which were amoxycillin, gentamycin, ampicillin, trimethoprim, chloramphenicol, sulphadiazine, cloxacin, oxytetracycline, amikacin, streptomycin, cotrimoxazole, cephalexin, kanamycin erythromycin, ciprofloxacin, neomycin and rifampicin. All the isolates were found sensitive to chloramphenicol, erythromycin, oxytetracycline, ciprofloxacin, neomycin and rifampicin.

A total of six clinical cases of snake bite were examined clinico-haematologically. The clinical examination revealed the normal rectal temperature but increased respiration as well as heart rates. The hematological values showed decreased Hb and PCV but increase in polymorphonuclear cells. All these snake bite dogs had been successfully treated with slow i.v. administration of antivenin along with corticosteroids i.m., adrenaline (1: 10,000 dilution in i.v. fluid), inj. DNS (5%), i.m. administration of antibiotic(s) and local antiseptic dressing with povidone Iodine after irrigation or washing the affected area(s) with soap water. Out of six dogs, four dogs survived and two died even after treatment.

A total of 253 samples from cattle (52), buffalo (51), sheep (50), goat (50) and chicken (50) were screened for the presence of Pasteurella multocida. Out of these, 17 samples were found positive by species specific PCR (PM-PCR) with ~460 bp amplified product. Overall prevalence of P. multocida was found to be 6.7%. Out of 17 PM-PCR positive samples, 12 (70%) were found positive by capsular type-B specific (HSB-PCR) and multiplex PCR assays with amplification of ~620 bp product in both the cases. A total of 5 isolates of P. multocida were obtained in 17 PM-PCR positive samples of which 4 were of serotype B:2 and 1 was of serotype A:3. The PM-PCR and HSB-PCR assays can be performed directly on clinical samples from animals with reproducible results without any non-specific amplification. Multiplex PCR further reduces the time for the species and type specific detection of P. multocida.

The study found out the chemical and microbial quality of various milk samples collected from different sources of milk procured from rural areas of Tirupati. Thefat, SNF and protein percentages of milk samples collected from Dairy Experimental Station were higher than the other milk samples collected from commercial dairies of Sangam, Balaji and Heritage and local vendors. The milk samples collected from local vendors showed lower fat, SNF and protein percentages. No significant difference was observed in the milk samples collected from commercial dairies of Sangam, Balaji and Heritage with regard to fat, SNF and protein percentages. None of the milk samples collected from Dairy Experimental Station were found to be adulterated with water, whereas higher percentage of water was observed in the milk samples of local vendors. The Standard Plate Count of milk from local vendors is higher followed by Dairy Experimental Station. Presence of E.coli organisms in the milk samples collected from local vendors and Dairy Experimental Station indicated the extraneous contamination and unhygienic conditions of milking barn.

A total of 128 faecal samples of dogs suspected for canine parvovirus infection were examined by Haemagglutination (HA) and Haemagglutination inhibition (HI) tests. The prevalence of canine parvovirus infection was 45.30% (58/128) and the age wise maximum (70.20%) prevalence was found in dogs upto 6 month. The breed wise maximum (56.90%) prevalence was in Non-descript dogs and sex wise prevalence revealed no significant difference in male (45.9%) and female (43.3%).