Madhu Kovileri Midhuna, Nair Smita, Loius Vimi
Centre for Plant Biotechnology and Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala 680656 India.
Banana Research Station, Kerala Agricultural University, Kannara P.O., Marakkal, Thrissur, Kerala 680652 India.
3 Biotech. 2023 May;13(5):131. doi: 10.1007/s13205-023-03550-x. Epub 2023 Apr 13.
The banana bract mosaic virus (BBrMV) is a major virus affecting bananas and plantains. Banana being propagated vegetatively, there arises a high risk of virus transmission through planting materials. Available molecular detection technique like the Reverse Transcriptase Polymerase Chain Reaction needs post-amplification sample handling, predisposing to sample cross contamination. A one-step Reverse Transcription-LoopMediated Isothermal Amplification (RT-LAMP) assay coupled with colorimetric detection was optimised for easy and quick detection of BBrMV in banana. The viral coat protein gene was amplified under isothermal conditions at 65 ºC. The RT-LAMP assay was optimised with respect to concentrations of MgSO, dNTP, polymerase enzyme and HNB dye. The total RNA purified from symptomatic samples was directly amplified under isothermal conditions by including 100 U M-MLV reverse transcriptase and 20 U RNasin® plus RNase inhibitor in the reaction. With the addition of 120 µM of Hydroxy Naphthol Blue (HNB) dye in the RT-LAMP reaction, the BBrMV-positive samples had a colour change from violet to sky blue after the reaction. The RT-LAMP assay detected BBrMV in 0.1 pg of total RNA isolated from symptomatic plants. Molecular characterisation of RT-LAMP products was done using restriction profiling and sequence analysis. The RT-LAMP assay was validated using field-collected banana leaf samples. The assay successfully detected the virus from symptomatic samples while the healthy samples showed no amplification. Samples sourced from banana plants with symptoms of banana bunchy top virus, banana streak virus and cucumber mosaic virus tested negative in the RT-LAMP assay, thus ensuring the specificity of the assay.
香蕉苞片花叶病毒(BBrMV)是一种影响香蕉和大蕉的主要病毒。由于香蕉通过营养繁殖,通过种植材料传播病毒的风险很高。现有的分子检测技术,如逆转录聚合酶链反应,需要进行扩增后样品处理,容易导致样品交叉污染。为了便于快速检测香蕉中的BBrMV,优化了一种一步法逆转录环介导等温扩增(RT-LAMP)检测方法并结合比色检测。在65℃等温条件下扩增病毒外壳蛋白基因。对RT-LAMP检测方法在MgSO、dNTP、聚合酶和HNB染料浓度方面进行了优化。从有症状样品中纯化的总RNA在等温条件下直接扩增,反应中加入100 U M-MLV逆转录酶和20 U RNasin® Plus核糖核酸酶抑制剂。在RT-LAMP反应中加入120µM羟基萘酚蓝(HNB)染料后,BBrMV阳性样品反应后颜色从紫色变为天蓝色。RT-LAMP检测方法能检测出从有症状植物中分离的0.1 pg总RNA中的BBrMV。使用限制性图谱分析和序列分析对RT-LAMP产物进行分子特征分析。使用田间采集的香蕉叶样品对RT-LAMP检测方法进行验证。该检测方法成功地从有症状样品中检测到病毒,而健康样品未显示扩增。从有香蕉束顶病毒、香蕉条纹病毒和黄瓜花叶病毒症状的香蕉植株采集的样品在RT-LAMP检测中呈阴性,从而确保了该检测方法的特异性。