Departamento de Veterinária, Universidade Federal de Viçosa, Viçosa-MG, CEP 36570-000 Vicosa, Brazil.
Exp Parasitol. 2011 Aug;128(4):460-3. doi: 10.1016/j.exppara.2011.05.013. Epub 2011 May 24.
The continued maintenance of nematophagous fungi predatory activity under laboratory conditions is one of the basic requirements for a successful biological control. The purpose of this study was to evaluate the influence of time on the preservation of the fungus Duddingtonia flagrans (AC001 and CG722) stored in silica-gel for 7 years and their subsequent predatory activity on cyathostomin L(3) larvae in 2% water-agar medium (2% WA). Samples of the isolates AC001 and CG722, originating from vials containing grains of silica-gel sterilized and stored for 7 years, were used. After obtaining fungal conidia, the predation test was conducted over 7 days on the surface of 9.0 cm Petri dishes filled with 2% WA. In the treated groups each Petri dish contained 500 cyathostomin L(3) and conidia of fungal isolates in 2% WA. In the control group (without fungi) the plates contained 500 L(3) in 2% WA. The experimental results showed that isolated AC001 and CG722 were efficient in preying on cyathostomin L(3) (p<0.01) compared to control (without fungus). However, no difference was observed (p>0.01) in the predatory activity of the fungal isolates tested. Comparing the groups, there was a significant reductions of cyathostomin L(3) (p<0.01) of 88.6% and 78.4% on average recovered from the groups treated with the isolates AC001 and CG722, respectively, after 7 days. The results of this test showed that the fungus D. flagrans (AC001 and CG722) stored in silica-gel for at least 7 years maintained its predatory activity on cyathostomin L(3).
在实验室条件下维持食线虫真菌的捕食活性是成功进行生物防治的基本要求之一。本研究旨在评估时间对保藏在硅胶中 7 年的真菌 Duddingtonia flagrans(AC001 和 CG722)及其随后在 2%水琼脂培养基(2%WA)中对 Cyathostomin L(3)幼虫的捕食活性的影响。使用了来自含有经消毒和保藏 7 年的硅胶颗粒的小瓶的分离株 AC001 和 CG722 的样品。获得真菌分生孢子后,在填充有 2%WA 的 9.0cm 培养皿表面上进行了为期 7 天的捕食试验。在处理组中,每个培养皿中含有 500 个 Cyathostomin L(3)和真菌分离物的分生孢子在 2%WA 中。在对照组(无真菌)中,平板中含有 500 个 L(3)在 2%WA 中。实验结果表明,与对照组(无真菌)相比,分离株 AC001 和 CG722 对 Cyathostomin L(3)的捕食效率更高(p<0.01)。然而,测试的真菌分离物的捕食活性没有差异(p>0.01)。比较各组,用分离株 AC001 和 CG722 处理的组中,Cyathostomin L(3)的数量分别平均减少了 88.6%和 78.4%,差异有统计学意义(p<0.01)。经过 7 天。该试验结果表明,保藏在硅胶中至少 7 年的真菌 D. flagrans(AC001 和 CG722)保持了对 Cyathostomin L(3)的捕食活性。