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Mastitis, most often udder infection of dairy animals attracted concerns due to heavy economic loss to dairy industry and public health. This study was conducted to determine the cultivable bacterial species associated with bovine clinical mastitis and their resistance patterns to different antimicrobials. The milk samples from 272 quarters of cows suffering from clinical mastitis were investigated. A total of 110 bacterial isolates belonging to 14 different genera were isolated and identi ed. Aminoglycosides and Quinolones were found to be most effective antibiotics. We demonstrated Extended Spectrum β Lactamases (ESBL), Cephalosporins, Tetracyclines, Vancomycin and Chloramphenicol resistant Grampositive and Gram-negative bacteria along with Vancomycin Resistant Enterococci (VRE), Multiple Drug Resistant Gram-Negative Rods (MDR-GNR), MDR-Pseudomonas (MDR-P) and MDR Acinetobacter (MDR-A). The ESBLs and cephalosporins resistant S. aureus isolates showed resistance to Vancomycin. Wide spread of resistance among Streptococcus uberis against ESBLs and Cephalosporins, widely used antibiotics in bovine mastitis, was documented. Variable MDR patterns were recorded for every species. MDR transfer from non-pathogens to emerging foodborne and established mastitis pathogens could be potential problem to dairy industry as well as public health.

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Background: The avian reoviruses have emerged to induce various manifestations in chickens. They are associated with disease conditions including malabsorption syndrome, tenosynovitis etc. Reoviruses are an important cause of suboptimum performance in broilers, resulting in poor growth performance. Poultry industry in India is facing a catastrophe due to such infections which go unnoticed in field due to masking of the symptoms by secondary infections and commonly observed nutritional disorders. Aim: To investigate the effect of reovirus infection on overall performance of broiler birds. Material and Methods: The broiler birds were challenged with homologous strains of malabsorption syndrome and tenosynovitis syndrome of reovirus. The growth performance was recorded. Results and conclusion: The growth performance and immune response to NDV did not differ in the birds challenged with tenosynovitis syndrome strain of reo virus as compared to un challenged birds. However, poor live body weight, feed intake, FCR, PE and BPEI and better serum NDV titres were found in chicks challenged with malabsorption syndrome strain of reo virus as compared to the chicks from control group.

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Mastitis, most often udder infection of dairy animals attracted concerns due to heavy economic loss to dairy industry and public health. This study was conducted to determine the cultivable bacterial species associated with bovine clinical mastitis and their resistance patterns to different antimicrobials. The milk samples from 272 quarters of cows suffering from clinical mastitis were investigated. A total of 110 bacterial isolates belonging to 14 different genera were isolated and identified. Aminoglycosides and Quinolones were found to be most effective antibiotics. We demonstrated Extended Spectrum β Lactamases (ESBL), Cephalosporins, Tetracyclines, Vancomycin and Chloramphenicol resistant Gram-positive and Gram-negative bacteria along with Vancomycin Resistant Enterococci (VRE), Multiple Drug Resistant Gram-Negative Rods (MDR-GNR), MDR-Pseudomonas (MDR-P) and MDR Acinetobacter (MDR-A). The ESBLs and cephalosporins resistant S. aureus isolates showed resistance to Vancomycin. Wide spread of resistance among Streptococcus uberis against ESBLs and Cephalosporins, widely used antibiotics in bovine mastitis, was documented. Variable MDR patterns were recorded for every species. MDR transfer from non-pathogens to emerging foodborne and established mastitis pathogens could be potential problem to dairy industry as well as public health.

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| The presence of Salmonella spp in collected faecal samples was assessed by performing the pre-enrichment and enrichment culture, followed by PCR assay. The primer was selected from the invA gene, specific for the detection of Salmonella spp. It was observed that 28% (10/35) of Salmonella were isolated by the conventional method. All Salmonella isolates thus obtained were subjected to PCR for the invA gene and all were found positive. In order to provide a more accurate profile of the prevalence of Salmonella spp in faecal samples, it was pertinent to use invA gene specific PCR method that could be considered as rapid technique for identification of Salmonella spp.