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Molecular Characterization of Fowl Pox Virus Isolates from Backyard Poultry

机译:后院家禽禽痘病毒分离株的分子表征

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With the aim of characterizing the fowl pox field isolates with molecular techniques, scab materials (of comb, wattle and skin of the face) were collected from ten (10) clinically affected backyard chickens from two different agro–climatic zones of West Bengal state, India, viz. Red latterite (Jhargram, District– Paschim Medinipur) and Coastal saline (Kakdwip, District– South 24 Parganas).Viral DNA was extracted from the collected scabs and was subjected to fowl pox virus (FPV) specific Polymerase chain reaction (PCR) for amplification of 4b core protein gene for confirmation of the presence of virus in clinically positive samples. In PCR, an expected amplicon of 578 bp was obtained in all the ten clinically positive samples and in vaccine strain as positive control. Restriction endonuclease analysis (REA) of PCR products with EcoR V and Mse I showed similar restriction patterns among the FPV isolates. Nucleotide sequence analysis of the amplified fragments revealed 99–100% nucleotide similarity with pox virus of other avian species. The present study revealed the molecular characteristics of FPV, circulating in backyard poultry in eastern Indian state West Bengal that was not reported earlier
机译:为了通过分子技术表征禽痘场分离株,从西孟加拉邦两个不同农业气候区的十(10)只受临床影响的后院鸡中收集了结ab材料(梳子,鸡冠和面部皮肤),印度,即红红土(Jhargram,Paschim Medinipur区)和沿海盐水(Kakdwip,Southern Parganas区24)。从收集的sc中提取病毒DNA,并进行禽痘病毒(FPV)特异性聚合酶链反应(PCR)扩增4b核心蛋白基因的鉴定,用于确认临床阳性样品中病毒的存在。在PCR中,在所有十个临床阳性样品中和作为阳性对照的疫苗株中均获得了578 bp的预期扩增子。对带有EcoR V和Mse I的PCR产物进行的限制性核酸内切酶分析(REA)显示,FPV分离株中的限制性酶切模式相似。扩增片段的核苷酸序列分析显示与其他禽痘病毒的99-100%核苷酸相似性。本研究揭示了FPV的分子特征,该特征在印度东部西孟加拉邦的后院家禽中循环传播,这一点以前未曾报道过。

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