tailieunhanh - Molecular detection of virulence associated genes in salmonella Serovars isolated from raw pork of Aizawl and Imphal

The study was aimed to detect virulence associated genes of Salmonella serovars, which were isolated from raw pork samples of unorganised butcher shops of Aizawl and Imphal. A total of 5 Salmonella isolates (Aizawl=2, Imphal=3), belonging to Salmonella vircho (n=4), and Salmonella typhimurium (n=1), were obtained from 200 samples (100= Aizawl and 100= Imphal) and screened for five virulence associated genes, namely invA, stn, pefA, sefC, spvC by Polymerase Chain Reaction (PCR) technique. All Salmonella serovars detected positive for invA and stn genes, spvC and pefA gene was found positive in Salmonella typhimurium and one Salmonella Vircho of Aizawl origin (overall 40%). sefA was absent in all isolates. All the Salmonella serovars possessed invasive gene (invA) and enterotoxin gene (stn), which make them capable for producing gastroenteritis in human. Presence of Salmonella typhimurium positive with 4 virulence associated genes in Aizawl is a matter of worry from hygienic point of view. | Molecular detection of virulence associated genes in salmonella Serovars isolated from raw pork of Aizawl and Imphal

• Sinh học
• Molecular detection
• Virulence associated genes
• Salmonella Serovars isolated
• Raw pork of Aizawl and Imphal
• Worry from hygienic point
• Prevalence and molecular detection
• Blood protozoa
• Domestic pigeon
• Haemoprotozoan infection
• Brucella spp
• Molecular detection of Brucella spp
• Reproductive disorders
• Vaginal mucus
• Brucella abortus
• Real time PCR
• Molecular detection of Brucella abortus
• Buffaloes in Gujarat
• Japanese encephalitis
• Pigs and punjab
• Serological and molecular detection
• Molecular detection of japanese encephalitis
• Naturally infected pigs
• Molecular protocol
• Establishing a molecular protocol
• Detection of EGFR mutations
• Non small cell lung cancer
• The molecular protocol constructed
• Multidrug resistant
• Molecular detection of Rifampicin
• Molecular detection of Isoniazid
• Mycobacterium Tuberculosis complex
• Using line probe assay
• Molecular detection of brucella organism
• Brucella organism
• Brucella organism from milk
• Milk products
• Ehrlichia canis
• Nested PCR
• Canine monocytic ehrlichiosis
• Molecular detection of canine monocytic ehrlichiosis
• Pathomorphological and molecular detection
• Black spot
• Asperisporium caricae
• Incited byasperisporium caricae
• Detection and molecular characterization
• Virusfree garlic
• Bulb associated potyviruses in garlic
• Field response
• Molecular detection of bulb associated potyviruses
• Garlic through molecular diagnosis
• BMC Veterinary Research
• Pig brucellosis
• Molecular evidence
• Systematically quantify and identify
• Molecular techniques
• Listeria monocytogenes
• Antibiotic sensitivity
• Antibiotic sensitivity profile
• Cattle sources of aizawl
• Ziehl Neelsen stain
• Rapid molecular detection
• Mycobacterium tuberculosis
• Comparison to other conventional methods
• Conventional methods
• Polymerase chain reaction assays
• Brucella abortus from cattle
• Brucella abortus from buffalo
• DNA extraction
• Major streptococcus spp
• Antimicrobial resistance
• Bovine mastitis
• Antimicrobial resistance pattern
• Vibrio alginolyticus
• Isothermal amplification
• Recombinase polymerase amplification
• Lateral flow dipstick
• Clinico seroepidemiology
• Molecular characterization of brucellosis
• Brucellosis in animals
• Brucella antibodies by RBPT
• Chili pepper
• Molecular marker
• Resistant chili pepper cultivars
• Anthracnose resistance associated molecular markers
• Resistant chili pepper cultivars in Vietnam
• Cinnamon witches’ broom
• Identification of a phytoplasma associated
• Cinnamomum cassia B
• Phyllody phytoplasma
• Characterization of Niger
• Cymbopogon citratus
• Leaf phytoplasma
• Khasi mandarin
• Candidatus liberibacter asiaticus
• Khasi mandarin orchards
• Total DNA was extracted
• Papaya ring spot virus
• Papaya ring spot virus disease
• NCBI Genebank
• PRSV in the plants
• China aster
• Molecular and detection
• Characterization of china aster
• 16S rII phytoplasmal group
• Latex agglutination test
• Group a rotaviruses
• Bhandara and Chandrapur district
• Circulating rotaviruses