Department of Plant Pathology, Centre for Plant Protection studies, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu 641003, India.
Department of Plant Pathology, Centre for Plant Protection studies, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu 641003, India.
Pestic Biochem Physiol. 2020 Jun;166:104570. doi: 10.1016/j.pestbp.2020.104570. Epub 2020 Apr 23.
Tomato is an important vegetable crop which is severely affected by Groundnut bud necrosis virus (GBNV). Until now effective antiviral agents have not been reported for the management of necrosis disease caused by GBNV. Therefore, a study was undertaken to manage the necrosis disease caused by GBNV using culture filtrate of basidiomycetous fungi viz., Coprinopsiscinerea, Ganoderma lucidum and Lentinula edodes. In vitro studies were conducted in the indicator host cowpea and primary host tomato in glasshouse under insect proof condition; co-inoculation spraying of culture filtrate of Ganoderma lucidum at 0.1% concentration reduced the lesion numbers and inhibited the virus population build-up when compared to inoculated control in the indicator host cowpea upto 77.83%. DAC-ELISA test was performed to quantify the virus titre, indicated reduced virus titre in co- inoculation spray of culture filtrate of G. lucidum treated cowpea with OD value 0.17 ± 0.01 at 405 nm and in tomato plants 0.14 ± 0.01 respectively. The viral copy numbers were quantified by qPCR. About 2.0 × 10 viral copy numbers were observed in tomato plants treated with G. lucidum (co-inoculation) which was lesser than untreated inoculated control plants (2.4 × 10). In order to identify the antiviral properties of G. lucidum, GCMS analysis was carried out and we found the triterpenoid compound Squalene. This is the first study to analyse and confirm the antiviral activity of G. lucidum against a plant virus.
番茄是一种重要的蔬菜作物,严重受到花生芽坏死病毒(GBNV)的影响。到目前为止,还没有报道有效的抗病毒剂来管理由 GBNV 引起的坏死病。因此,进行了一项研究,使用担子菌培养滤液来管理由 GBNV 引起的坏死病,这些担子菌包括糙皮侧耳、灵芝和香菇。在防虫温室条件下,在指示宿主豇豆和原宿主番茄中进行了体外研究;与接种对照相比,在指示宿主豇豆中以 0.1%浓度共同接种灵芝培养滤液可减少病变数量并抑制病毒种群的建立,达到 77.83%。DAC-ELISA 测试用于定量病毒滴度,指示在共同接种灵芝培养滤液处理的豇豆中病毒滴度降低,OD 值为 0.17 ± 0.01 在 405nm 处,在番茄植物中分别为 0.14 ± 0.01。通过 qPCR 定量病毒拷贝数。在用灵芝(共同接种)处理的番茄植物中观察到约 2.0×10 个病毒拷贝数,少于未经处理的接种对照植物(2.4×10)。为了鉴定灵芝的抗病毒特性,进行了 GCMS 分析,我们发现了三萜化合物角鲨烯。这是首次分析和确认灵芝对植物病毒的抗病毒活性的研究。