首页> 美国卫生研究院文献>other >Inhibitory Effects of Macrotetrolides from Streptomyces spp. On Zoosporogenesis and Motility of Peronosporomycete Zoospores Are Likely Linked with Enhanced ATPase Activity in Mitochondria
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Inhibitory Effects of Macrotetrolides from Streptomyces spp. On Zoosporogenesis and Motility of Peronosporomycete Zoospores Are Likely Linked with Enhanced ATPase Activity in Mitochondria

机译:链霉菌大环内酯的抑制作用。关于Peronosporomycete游动孢子的游动发生和运动性可能与线粒体中增强的ATPase活性有关。

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摘要

The release of zoospores from sporangia and motility of the released zoospores are critical in the disease cycle of the Peronosporomycetes that cause devastating diseases in plants, fishes, animals and humans. Disruption of any of these asexual life stages eliminates the possibility of pathogenesis. In the course of screening novel bioactive secondary metabolites, we found that extracts of some strains of marine Streptomyces spp. rapidly impaired motility and caused subsequent lysis of zoospores of the grapevine downy mildew pathogen Plasmopara viticola at 10 μg/ml. We tested a number of secondary metabolites previously isolated from these strains and found that macrotetrolide antibiotics such as nonactin, monactin, dinactin and trinactin, and nactic acids such as (+)-nonactic acid, (+)-homonactic acid, nonactic acid methyl ester, homonactic acid methyl ester, bonactin and feigrisolide C impaired motility and caused subsequent lysis of P. viticola zoospores in a dose- and time-dependent manners with dinactin being the most active compound (MIC 0.3 μg/ml). A cation channel-forming compound, gramicidin, and a carrier of monovalent cations, nigericin also showed similar biological activities. Among all 12 compounds tested, gramicidin most potently arrested the motility of zoospores at concentrations starting from 0.1 μg/ml. All macrotetrolide antibiotics also displayed similar motility impairing activities against P. viticola, Phytophthora capsici, and Aphanomyces cochlioides zoospores indicating non-specific biological effects of these compounds toward peronosporomyctes. Furthermore, macrotetrolide antibiotics and gramicidin also markedly suppressed the release of zoospores from sporangia of P. viticola in a dose-dependent manner. As macrotetrolide antibiotics and gramicidin are known as enhancers of mitochondrial ATPase activity, inhibition of zoosporogenesis and motility of zoospores by these compounds are likely linked with hydrolysis of ATP through enhanced ATPase activity in mitochondria. This is the first report on motility inhibitory and lytic activities of macrotetrolide antibiotics and nactic acids against the zoospores of peronosporomycete phytopathogens.
机译:孢子囊从孢子囊中释放出来,释放出来的游动孢子的运动性在引起植物,鱼类,动物和人类破坏性疾病的Peronosporomycetes的疾病周期中至关重要。这些无性生活阶段中任何一个的中断都消除了发病的可能性。在筛选新型生物活性次生代谢产物的过程中,我们发现了一些海洋链霉菌属菌株的提取物。迅速削弱了运动能力,并随后溶解了10μg/ ml的葡萄霜霉病病原体Plasmopara viticola游动孢子。我们测试了先前从这些菌株中分离出来的许多次生代谢产物,发现大四环内酯类抗生素例如nonactin,monactin,dinactin和trinactin,以及乳酸例如(+)-非乳酸,(+)-高乳酸,非乳酸甲酯,高乳酸甲酯,bonactin和feigrisolide C损害了运动能力,并随后以剂量和时间依赖性方式溶解了葡萄球菌的游动孢子,其中dinactin是活性最高的化合物(MIC 0.3μg/ ml)。形成阳离子通道的化合物,短杆菌肽和一价阳离子的载体,尼日利亚霉素也显示出相似的生物活性。在所有测试的12种化合物中,短杆菌肽最有效地阻止游动孢子的运动,浓度从0.1μg/ ml开始。所有大四环内酯类抗生素还表现出相似的运动能力,削弱了对葡萄球菌,疫霉菌和拟球孢子虫的游动孢子的活动,表明这些化合物对孢子囊菌具有非特异性生物学作用。此外,大环内酯类抗生素和短杆菌肽还以剂量依赖的方式显着抑制了葡萄球菌孢子囊中游动孢子的释放。由于大环内酯类抗生素和短杆菌肽被认为是线粒体ATPase活性的增强剂,因此这些化合物对游动孢子发生和游动孢子运动的抑制作用可能是通过线粒体中ATPase活性增强而与ATP水解相关的。这是关于大环内酯类抗生素和乳酸针对过孔孢子菌植物病原菌游动孢子的运动抑制和裂解活性的首次报道。

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