The present study was conducted in buffaloes to determine the occurrence of subclinical mastitis and its diagnosis in relation to milk SCC and biochemical composition. The results showed that taking quarter foremilk (QFM) somatic cell count (SCC) threshold limit of LT 200*10**(3) cell for defining healthy quarters, 16.48 percent of buffaloes and 5.79 percent of quarters were positive for specific subclinical mastitis. In total, 57/363 (15.70 percent)of quarters were bacteriological positive with 21 (5.79 percent) representing specific and 36 (9.92 percent) latent infections. The major pathogen isolated were 28 (49 percent) coagulase-negative staphylococci followed by 16 (28 percent) S. aureus, 09 (16 percent) Streptococcus and 4(7 percent) Corynebacterium spp. The average QFM SCC was found as 52.50*10**(3) cells /ml for the quarter with no bacteria, and 356.51*10**(3) cell /ml for the quarters infected with one or the other bacteria (p LT 0.05). The milk electrical conductivity (EC), Fat and Lactoseshowed significant alterations with the quarter infection, the EC and Fat increased while Lactose decreased in infected quarters (p LT 0.05). The California mastitis test CMT) at cut off score of GT 0.5 for diseased quarters showed 68.75 percent sensitivity with 99.09 percent specificity. The EC with 87.50 percent sensitivity and 74.02 percent specificity and Lactose with 84.37 percent sensitivity and 66.16 percent specificity also showed significant (p LT 0.01) discrimination ability to differentiate healthy and mastitis quarters in buffaloes. The milk pH was not found to be a good parameter to identify diseased quarters.

The present study was designed to correlate the milk pH, somatic cell count (SCC), lactate dehydrogenase (LDH) and alkaline phosphatase (ALP) activities in buffalo milk with the udder health status. A total of 60 (Sixty) buffaloes were randomly selected irrespective of their age, breed, feeding practice, stage and season of lactation from the herd belonging to Purnadhadi buffalo unit, PGIVAS, Teaching Veterinary Clinical complex, PGIVAS, Veterinary Polyclinic, Akola and also buffaloes of farmers in and around Akola. After thorough clinical examination of each udder, about 30 ml of milk was collected in sterilized, clean, dry plastic bottles and after careful screening by CMT, categorized in normal, sub- clinical (1+), sub- clinical (2+), sub- clinical (3+) and clinical group containing 12 animals in each group. The pH was measured using a digital pH meter (E.I. Model 101E) and SCC was calculated in freshly collected milk. LDH and ALP activities were measured by spectrophotometric method. The milk pH, SCC, LDH and ALP activities were found proportional to the severity of the udder infection as detected by the CMT reactions.