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The study was designed to isolate predominance contamination of Pseudomonas aeruginosa in marketed raw buffalo milk (n=122) samples, collected from private dairy farms from different places of south Gujarat, India. Pre-enrichment of 1 ml of each sample was done with inoculation in 9 ml tryptone soya broth and incubated at 37ºC for 24 hrs. A loopful of culture was taken from broth and streaked on selective Pseudomonas agar F plates and incubated at 37ºC for 24 hrs, after completion of incubation period, the colonies characteristics were studied and further confirmed by various biochemical tests and found 14 samples contaminated with P. aeruginosa, were further more biochemical testes are used and give positive results with IMViC, Motility test, catalase and sugar fermentation confirm at 37ºC for 24 hrs incubation. All biochemically conformed isolates were further subjected for molecular characterization and were also tested for antimicrobial susceptibility by using various antibiotics discs such as vancomycin, penicillin, tylosin, cefixime, chloramphenicol, kanamycin, ceftriaxone, cefixime, tetracycline, streptomycin, ciprofloxacin, enrofloxacin, oxytetracycline and gentamicin, which has shown multi drug resistant ranging from seven to nine antimicrobials and Multiple Antibiotic Resistance (MAR) index ranges from 0.50 to 0.64.The isolates of P. aeruginosa in the present study are extremely resistant to vancomycin, penicillin, tylosin, cefixime, chloramphenicol and maximum sensitive to ciprofloxacin and enrofloxacin followed by gentamicin. Further statistical analysis of antibiotics wise zone diameter interpretative standard (mm) reveled susceptibility phenotypes under significant of difference at P≤0.05 in one way ANOVA using Duncan’s multiple range test and found ciprofloxacin having maximum sensitivity among antibiotic tested and it could be considered as a drug of choice for controlling P. aeruginosa mediated animal and human infections in the studied regions for insuring food safety as well.

The n- Hexane, ethyl acetate, methanol and distilled water Leaf, Stem, Flower and Fruit extracts of Moringa oleifera were evaluated for their antibacterial activity against six Gram-Negative and Gram-Positive bacteria and antifungal activity against seven fungal strains using Ciprofloxacin, Doxycycline, Fluconazole and Ketacozole as positive control. The activity was analyzed by well diffusion and two-fold serial broth dilution method of different extract. The study revealed that all the extracts irrespective of their types, in different concentrations inhibited growth of the test pathogens to varying degrees. Ethyl acetate extract showed maximum activity against all the bacterial strains followed in descending order by methanol, n-.Hexane and distilled water extracts. Ethyl acetate extract showed high antibacterial activity against Serratia marcescens (22mm) Methanol and n-Hexane extract were effective against Enterococcus faecalis and Bacillus subtilis (10mm) respectively. Aqueous extract showed maximum number of inhibition against Staphylococcus aureus (27mm) and Micrococcus luteus (18mm). Ethyl acetate extract showed maximum inhibition against Trichoderma harzianum (16mm) than other extracts were ineffective against selected fungus. MIC values were recorded as 0.125 to 4mg/ml. The phytochemical screening revealed the presence of phenols and flavonoids. Expression to these results it may be concluded that M. oleifera may be a potential source for the curing of various infectious diseases caused by the resistant microbes

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