Perumal Vivekanandhan, Kannan Swathy, Alford Lucy, Pittarate Sarayut, Geedi Ruchika, Elangovan Dilipan, Marimuthu Ramachandran, Krutmuang Patcharin
Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, Thailand.
Department of Physiology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, Tamil Nadu, India.
Front Microbiol. 2023 Mar 2;14:1104079. doi: 10.3389/fmicb.2023.1104079. eCollection 2023.
Entomopathogenic fungi from microbial sources are a powerful tool for combating insecticide resistance in insect pests. The purpose of the current study was to isolate, identify, and evaluate bag-formulated entomopathogenic fungal conidial virulence against insect pests. We further investigated the enzymatic responses induced by the entomopathogenic fungi as well as the effect on a non-target species. Entomopathogenic fungi were isolated from the Palamalai Hills, India, using the insect bait method, and the (MK418990.1) entomopathogen was identified using biotechnological techniques (genomic DNA isolation and 18S rDNA amplification). Bag-formulated fungal conidial efficacy (2.5 × 10, 2.5 × 10, 2.5 × 10, 2.5 × 10, and 2.5 × 10 conidia/ml) was evaluated against third instar larvae of at 3, 6, 9, and 12 days of treatment, and acid and alkaline phosphatases, catalase, and superoxide dismutase enzymatic responses were evaluated at 3 days post-treatment. After 12 days of treatment, non-target assays on the earthworm were performed using an artificial soil assay. Results of the bag formulated fungal conidial treatment showed that had high susceptibility rates at higher concentrations (2.5 × 10 conidia/ml) of . Lower concentration of 2.5 × 10 conidia/ml caused 68.6% mortality, while 2.5 × 10 conidia/ml caused 100% mortality at 9 days post treatment. Investigation into enzymatic responses revealed that at 3 days post conidia exposure (2.5 × 10 conidia/ml), insect enzyme levels had significantly changed, with acid and alkaline phosphatases, and catalase enzymes significantly reduced and superoxide dismutase enzymes significantly raised relative to the control. After 12 days of treatment, no sublethal effects of conidia were observed on , with no observed damage to gut tissues including lumen and epithelial cells, the nucleus, setae, coelom, mitochondria, and muscles. This study offers support for the use of fungal conidia in the target-specific control of insect pests.
来自微生物源的昆虫病原真菌是对抗害虫抗药性的有力工具。本研究的目的是分离、鉴定和评估袋装昆虫病原真菌分生孢子对害虫的毒力。我们进一步研究了昆虫病原真菌诱导的酶促反应以及对非靶标物种的影响。采用昆虫诱饵法从印度帕拉马莱山分离昆虫病原真菌,并利用生物技术(基因组DNA分离和18S rDNA扩增)鉴定昆虫病原体(MK418990.1)。在处理后3、6、9和12天,评估袋装真菌分生孢子效力(2.5×10、2.5×10、2.5×10、2.5×10和2.5×10分生孢子/ml)对[昆虫名称未给出]三龄幼虫的影响,并在处理后3天评估酸性和碱性磷酸酶、过氧化氢酶和超氧化物歧化酶的酶促反应。处理12天后,使用人工土壤试验对蚯蚓[蚯蚓名称未给出]进行非靶标测定。袋装真菌分生孢子处理结果表明,[昆虫名称未给出]在较高浓度(2.5×10分生孢子/ml)的[真菌名称未给出]下具有较高的易感性。较低浓度2.5×10分生孢子/ml在处理后9天导致68.6%的死亡率,而2.5×10分生孢子/ml导致100%的死亡率。酶促反应研究表明,在暴露于[真菌名称未给出]分生孢子(2.5×10分生孢子/ml)后3天,昆虫酶水平发生了显著变化,相对于对照组,酸性和碱性磷酸酶以及过氧化氢酶显著降低,超氧化物歧化酶显著升高。处理12天后,未观察到[真菌名称未给出]分生孢子对[蚯蚓名称未给出]的亚致死效应,未观察到对包括肠腔和上皮细胞、细胞核、刚毛、体腔、线粒体和肌肉在内的肠道组织的损害。本研究为在害虫的靶标特异性防治中使用真菌分生孢子提供了支持。