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基于简并引物的逆转录聚合酶链反应对新城疫病毒毒株的鉴别检测

Differential detection of Newcastle disease virus strains by degenerate primers based RT-PCR.

作者信息

Tiwari A K, Kataria R S, Nanthakumar T, Dash B B, Desai G

机构信息

National Biotechnology Centre, Indian Veterinary Research Institute, Izatnagar 243 122 (UP), India.

出版信息

Comp Immunol Microbiol Infect Dis. 2004 May;27(3):163-9. doi: 10.1016/j.cimid.2003.09.002.

Abstract

Degenerate primers based RT-PCR (previously described by [Avian Dis 26 (1997) 837]) has been used for the detection and differentiation of Newcastle disease (ND) viruses. Two sets of primers (A+B and A+C), with common forward primer and distinct reverse degenerate primers, designed from fusion protein gene encoding for cleavage site, could differentiate virulent and avirulent Newcastle disease viruses (NDV). Both sets of primers amplified "F" gene sequence of virulent (velogenic and mesogenic) viruses, whereas in avirulent strains, amplification was only with primer set A+C. Total 10 NDV isolates and two clinical samples including both known and unknown pathotypes, were checked. Based on amplification results 5 viruses were found to be virulent type and 6 as avirulent with one of the two clinical samples, earlier positive by RT-PCR using non-degenerate "F" gene specific primers was found negative in this study. The technique has been found to be a simple and quick for the detection and differentiation of virulent and avirulent NDV, which is important for control of the disease in the events of the outbreaks.

摘要

基于简并引物的逆转录聚合酶链反应(先前由[《禽病》26(1997)837]描述)已用于新城疫(ND)病毒的检测和鉴别。两组引物(A + B和A + C),具有共同的正向引物和不同的反向简并引物,从编码裂解位点的融合蛋白基因设计而来,可区分强毒和无毒新城疫病毒(NDV)。两组引物均扩增了强毒(速发型和中发型)病毒的“F”基因序列,而在无毒株中,仅用引物组A + C进行扩增。共检测了10株NDV分离株和两个临床样本,包括已知和未知致病型。根据扩增结果,发现5种病毒为强毒型,6种为无毒型,两个临床样本中的一个,在本研究中,先前使用非简并“F”基因特异性引物进行逆转录聚合酶链反应呈阳性,现发现为阴性。已发现该技术对于检测和区分强毒和无毒NDV简单快速,这对于疫情爆发时疾病的控制很重要。

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