Background: Newcastle disease (ND) in spite of the availability of vaccines remains a constant threat to poultry producers worldwide. It is prevalent in Indian subcontinent and leads to economic losses. The present study was aimed with isolate and identify virulent Newcastle disease virus (NDV) in layer poultry from field outbreaks.Methods: Total 47 samples consisting of nasal (05), oropharyngeal (13) and cloacal swabs (11) and tissue samples consisting of trachea (07), lungs (06), larynx (05) were collected from layer birds. For isolation of NDV swab and tissue samples were inoculated in 9-11 days old embryonated eggs via allantoic cavity route. After preparing the viral inoculum, 47 suspected samples (29 swab and 18 tissue samples) were inoculated in 141 embryonated eggs to isolate the virus.Result: Out of 47 samples 10 (21.27%) samples were positive for HA activity. All the 10 isolates showing HA activity subjected to Reverse-Transcriptase PCR of F gene and 6 were found positive in RT-PCR for F1 gene. The PCR amplified product showed amplicon at 356 bp and 254 bp positive for F1 and F2 gene, respectively. On basis of F gene, 06 (50%) isolates were considered as virulent Newcastle Disease Virus. One isolate sequence was submitted at NCBI with accession MT890653 On phylogenetic analysis MT890653 designated as Class II/ genotype II/ virulent strain and had the motif 112R-R-R-K-R-F117 at the cleavage site of the fusion protein.
Background: Methicillin resistant Staphylococcus aureus (MRSA) refers to a group of gram-positive bacteria that are genetically distinct from other strains of Staphylococcus aureus that has developed, through horizontal gene transfer, natural selection and multiple drug resistance to beta lactam antibiotics and thus causing many severe diseases which are very problematic to treat as they are resistant to different antibiotics. The above situation is further aggravated by the formation of biofilms which are structured aggregation of surface attached microbes encased in an extracellular matrix. Thus, the time required to develop biofilms becomes an important point to study. Methods: In the present study, detection of the extent of biofilm formation by MRSA isolates, was performed using the Microtitre Plate Assay. The test was performed in triplicates and was continued for a time period of 7 days to detect the extent of biofilm formation with increase in incubation interval.
Result: On comparing the biofilm forming ability of different isolates from Day 1 to Day 7, it could be clearly observed that the biofilm forming capacity of isolates gradually increased with increase in incubation time and most of the isolates became strong biofilm producers from Day 4.
Background: Drug resistant bacteria related health problems are major concern globally and search for newer and most effective antibacterial agents is the urgent need to combat with these challenges. The study was undertaken with the aim of isolating and identifying endophytic fungi associated with Carica papaya and assessing their potential as antibacterial agents.Methods: Carica papaya plants were collected from different locations and endophytic fungi were isolated and characterized phenotypically and genotypically by microscopy, colonial characteristics and ITS gene sequencing, respectively. Antibacterial activity of endophyte was assessed against Escherichia coli, Klebsiella pneumonia, Salmonella Typhimurium, Bacillus cereus, Staphylococcus aureus and Streptococcus pyogenes, using the agar plate diffusion assay method with Ciprofloxacin as a positive control.Result: Thirty four (34) fungal endophytes of two genera Fusarium and Penicillium were recovered from 60 samples of Carica papaya and they showed the antibacterial activity against Staphylococcus aureus. Thus, the endophytic fungi have the potential to be used as an antibacterial agent.
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