Intana Warin, Wonglom Prisana, Suwannarach Nakarin, Sunpapao Anurag
School of Agricultural Technology and Food Industry, Walailak University, Nakhon Si Thammarat 80161, Thailand.
Faculty of Technology and Community Development, Phatthalung Campus, Thaksin University, Songkhla 93110, Thailand.
J Fungi (Basel). 2022 Feb 4;8(2):156. doi: 10.3390/jof8020156.
Gummy stem blight caused by is the most destructive disease of muskmelon cultivation. This study aimed to induce disease resistance against gummy stem blight in muskmelon by PSU-P1. This study was arranged into two crops. Spore suspension at a concentration of 1 × 10 spores/mL of PSU-P1 was applied to muskmelon to investigate gene expression. The expression of PR genes including chitinase () and β-1,3-glucanase () were determined by reverse transcription quantitative polymerase chain reaction (RT-qPCR), and enzyme activity was assayed by the DNS method. The effects of PSU-P1 on growth, yield, and postharvest quality of muskmelon fruit were measured. A spore suspension at a concentration of 1 × 10 spore/mL of PSU-P1 and was applied to muskmelons to determine the reduction in disease severity. The results showed that the expression of and genes in PSU-P1-treated muskmelon plants was 7-10-fold higher than that of the control. The enzyme activities of chitinase and β-1,3-glucanase were 0.15-0.284 and 0.343-0.681 U/mL, respectively, which were higher than those of the control (pathogen alone). Scanning electron microscopy revealed crude metabolites extracted from PSU-P1-treated muskmelon plants caused wilting and lysis of hyphae, confirming the activity of cell-wall-degrading enzymes (CWDEs). Application of PSU-P1 increased fruit weight and fruit width; sweetness and fruit texture were not significantly different among treated muskmelons. Application of PSU-P1 reduced the disease severity scale of gummy stem blight to 1.10 in both crops, which was significantly lower than that of the control (2.90 and 3.40, respectively). These results revealed that application of PSU-P1 reduced disease severity against gummy stem blight by overexpressed PR genes and elevated enzyme activity in muskmelon plants.
由[未提及病原菌名称]引起的蔓枯病是甜瓜种植中最具毁灭性的病害。本研究旨在通过PSU - P1诱导甜瓜对蔓枯病的抗病性。本研究分为两季作物。将浓度为1×10⁶孢子/mL的PSU - P1孢子悬浮液施用于甜瓜以研究基因表达。通过逆转录定量聚合酶链反应(RT - qPCR)测定包括几丁质酶([未提及具体基因名称])和β - 1,3 - 葡聚糖酶([未提及具体基因名称])在内的病程相关(PR)基因的表达,并通过DNS法测定酶活性。测定了PSU - P1对甜瓜果实生长、产量和采后品质的影响。将浓度为1×10⁶孢子/mL的PSU - P1和[未提及病原菌名称]的孢子悬浮液施用于甜瓜以确定病害严重程度的降低情况。结果表明,PSU - P1处理的甜瓜植株中[未提及具体基因名称]和[未提及具体基因名称]基因的表达比对照高7 - 10倍。几丁质酶和β - 1,3 - 葡聚糖酶的酶活性分别为0.15 - 0.284和0.343 - 0.681 U/mL,高于对照(仅病原菌处理)。扫描电子显微镜显示,从PSU - P1处理的甜瓜植株中提取的粗代谢产物导致[未提及病原菌名称]菌丝枯萎和裂解,证实了细胞壁降解酶(CWDEs)的活性。施用PSU - P1增加了果实重量和果实宽度;处理后的甜瓜在甜度和果实质地方面没有显著差异。在两季作物中,施用PSU - P1均将蔓枯病的病害严重程度等级降低至1.10,显著低于对照(分别为2.90和3.40)。这些结果表明,施用PSU - P1通过过表达病程相关基因和提高甜瓜植株中的酶活性降低了对蔓枯病的病害严重程度。