一种新的绿僵菌菌株通过破坏关键的生理系统来抑制果夜蛾(鳞翅目:夜蛾科)。

Piumalee Isurika Damithri Wellabada Hewage Don, Yun Meng, Dun Wang
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引用次数: 0

摘要

秋粘虫(Spodoptera frugiperda, J.E. Smith, 1797)是一种高度多食性害虫,全球对农业生产日益增长的需求正受到秋粘虫(FAW)的威胁。生物防治这种害虫比化学防治有益。摘要从湖南衡山分离到一株新绿僵菌(Driver & Milner)(次creale: Clavicipitaceae) ML。通过实验室生物测定评估ML对FAW的生物防治潜力,同时通过组织病理学检测检测生理效应。采用酶活性测定法评估真菌酶活性水平,采用RT-qPCR分析真菌毒力相关基因的相对表达水平。本研究发现菌株ML在1 × 109孢子/ ML时幼虫死亡率高达97.92%,LC50为1.26 × 104孢子/ ML。1 × 108孢子/ml时,蛹死亡率为87.5%,ST50为8.33 d。结果表明,高毒力与真菌毒力相关基因和酶的表达升高有关。组织病理学分析证实,ML广泛的菌丝入侵破坏了幼虫的角质层、表皮、血淋巴、脂肪体和肌肉等组织,损害了呼吸、消化和排泄系统。几丁质酶(35.82µg/h/g)、蛋白酶(3,844.02 nmol/min/g)和脂肪酶(2,288.50 nmol/min/g)活性的升高与整个感染过程中异戊二酮弹性酶样丝氨酸蛋白酶基因(MLpr1)、几丁质酶基因(Mlchit1)、分泌脂肪酶基因(MlSecL)和脂肪酶A基因(MlLIPA)的表达协同作用。这些研究结果为揭示M. lepidiotae对FAW高毒力的病理机制提供了有价值的见解,为可持续的生物防治提供了潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new Metarhizium strain suppresses Spodoptera frugiperda (Lepidoptera: Noctuidae) by disrupting key physiological systems.

The increasing global demand for agricultural production is threatened by fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith, 1797), a highly polyphagous pest. The biocontrol of this pest is beneficial over chemical control. The new Metarhizium lepidiotae (Driver & Milner) (Hypocreales: Clavicipitaceae), strain ML was isolated from Mount Heng, Hunan Province in China. The biocontrol potential of ML on FAW was evaluated through laboratory bioassays, while physiological effects were examined via histopathological assays. Enzyme activity assays were conducted to assess fungal enzyme activity levels, and the relative expression levels of fungal virulence-related genes were analyzed using RT-qPCR. This study explored that the strain ML caused a high larval mortality of 97.92% at 1 × 109 spores/ml, with an LC50 of 1.26 × 104 spores/ml. The pupal mortality was 87.5% at 1 × 108 spores/ml, with an ST50 of 8.33 d. The results showed that the high virulence was driven by elevated expression of fungal virulence-related genes and enzymes. The histopathological assays proved that the extensive hyphal invasion by ML disrupted larval tissues such as cuticle, epidermis, hemolymph, fat body, and muscles, damaging the respiratory, digestive, and excretory systems. The elevated levels of chitinase (35.82 µg/h/g), protease (3,844.02 nmol/min/g), and lipase (2,288.50 nmol/min/g) activities were synergized with the expression of M. lepidiotae elastase-like serine protease gene (MLpr1), chitinase gene (Mlchit1), secreted lipase gene (MlSecL), and lipase A gene (MlLIPA) throughout the infection. These findings provided valuable insights into the pathological mechanisms driving the high virulence of M. lepidiotae against FAW, offering potential for sustainable biocontrol.

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