Development of loop-mediated isothermal amplification and SYBR green real-time PCR methods for the detection of Citrus yellow mosaic badnavirus in citrus species

被引:18
|
作者
Johnson, A. M. Anthony [1 ]
Dasgupta, I. [2 ]
Gopal, D. V. R. Sai [1 ]
机构
[1] Sri Venkateswara Univ, Dept Virol, Tirupati 517502, Andhra Pradesh, India
[2] Univ Delhi South Campus, Dept Plant Mol Biol, New Delhi 110021, India
关键词
Citrus; Badnavirus; LAMP; PCR; Real-time PCR; RAPID DETECTION; QUANTITATIVE DETECTION; MOTTLE-VIRUS; DNA; LAMP; EXTRACTION; SEQUENCES; DISEASE; INDIA; ASSAY;
D O I
10.1016/j.jviromet.2014.03.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Citrus yellow mosaic badnavirus (CMBV) is an important pathogen in southern India spread by infected citrus propagules. One of the measures to arrest the spread of CMBV is to develop methods to screen and certify citrus propagules as CMBV-free. The methods loop-mediated isothermal amplification (LAMP) and SYBR green real-time PCR (SGRTPCR) have been developed for the efficient detection of CMBV in citrus propagules. This paper compares the sensitivities of LAMP and SGRTPCR with polymerase chain reaction (PCR) for the detection of CMBV. Whereas PCR and LAMP were able to detect CMBV from a minimum of 10 ng of total DNA of infected leaf samples, SGRTPCR could detect the same from 1 ng of total DNA. Using SGRTPCR, the viral titres were estimated to be the highest in rough lemon and lowest in Nagpur Mandarin of the five naturally infected citrus species tested. The results will help in designing suitable strategies for the sensitive detection of CMBV from citrus propagules. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:9 / 14
页数:6
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