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Putative Antiparasite Defensive System Involving Ribosomal and Nonribosomal Oligopeptides in Cyanobacteria of the Genus Planktothrix

机译:推定的寄生虫防御系统涉及核糖体和非核糖体寡肽在蓝藻属蓝藻属中。

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Parasitic chytrid fungi can inflict significant mortality on cyanobacteria but frequently fail to keep cyanobacterial dominance and bloom formation in check. Our study tested whether oligopeptide production, a common feature in many cyanobacteria, can be a defensive mechanism against chytrid parasitism. The study employed the cyanobacterial strain Planktothrix NIVA-CYA126/8 and its mutants with knockout mutations for microcystins, anabaenopeptins, and microviridins, major oligopeptide classes to be found in NIVA-CYA126/8. Four chytrid strains were used as parasite models. They are obligate parasites of Planktothrix and are unable to exploit alternative food sources. All chytrid strains were less virulent to the NIVA-CYA126/8 wild type than to at least one of its oligopeptide knockout mutants. One chytrid strain even failed to infect the wild type, while exhibiting considerable virulence to all mutants. It is therefore evident that producing microcystins, microviridins, and/or anabaenopeptins can reduce the virulence of chytrids to Planktothrix , thereby increasing the host's chance of survival. Microcystins and anabaenopeptins are nonribosomal oligopeptides, while microviridins are produced ribosomally, suggesting that Planktothrix resists chytrids by relying on metabolites that are produced via distinct biosynthetic pathways. Chytrids, on the other hand, can adapt to the oligopeptides produced by Planktothrix in different ways. This setting most likely results in an evolutionary arms race, which would probably lead to Planktothrix and chytrid population structures that closely resemble those actually found in nature. In , the findings of the present study suggest oligopeptide production in Planktothrix to be part of a defensive mechanism against chytrid parasitism.
机译:寄生的壶菌属真菌可对蓝细菌造成极大的死亡率,但常常无法保持蓝细菌的优势和水华的形成。我们的研究测试了寡肽的生产是否是许多蓝细菌的共同特征,它是否可以作为抵抗糜蛋白酶寄生的防御机制。这项研究使用了蓝藻菌株Planktothrix NIVA-CYA126 / 8及其突变体,这些突变体具有微囊藻毒素,阿那贝肽素和微病毒素的敲除突变,这是NIVA-CYA126 / 8中的主要寡肽类别。四种糜蛋白酶菌株被用作寄生虫模型。他们是浮游生物的专性寄生虫,无法利用其他食物来源。所有chytrid菌株对NIVA-CYA126 / 8野生型的毒性要比对至少一种寡肽敲除突变体的毒性低。一种糜蛋白酶菌株甚至未能感染野生型,同时对所有突变体均表现出相当的毒力。因此,很明显,产生微囊藻毒素,微viridins和/或Anabaenopeptins可以降低糜蛋白酶对Planktothrix的毒力,从而增加宿主的存活机会。微囊藻毒素和anabaenopeptins是非核糖体寡肽,而微病毒素是通过核糖体产生的,这表明Planktothrix通过依赖于通过独特的生物合成途径产生的代谢产物来抵抗糜蛋白酶。另一方面,壶菌可以不同的方式适应普兰克菌丝产生的寡肽。这种设置极有可能导致一场进化军备竞赛,这很可能导致浮游生物和壶菌的种群结构与自然界中的实际情况极为相似。在中,本研究的发现表明,Planktothrix中的寡肽产生是针对糜蛋白酶寄生的防御机制的一部分。

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