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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Synergistic action of Galleria mellonella apolipophorin III and lysozyme against Gram-negative bacteria
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Synergistic action of Galleria mellonella apolipophorin III and lysozyme against Gram-negative bacteria

机译:梅勒菌载脂蛋白III和溶菌酶对革兰氏阴性菌的协同作用

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摘要

Insect immune response relies on the humoral and cellular mechanisms of innate immunity. The key factors are the antimicrobial polypeptides that act in concert against invading pathogens. Several such components, e.g. apolipophorin III (apoLp-III), lysozyme, and anionic peptide 2, are present constitutively in the hemolymph of non-challenged Galleria mellonella larvae. In the present study, we demonstrate an evidence for a synergistic action of G. mellonella lysozyme and apoLp-III against Gram-negative bacteria, providing novel insights into the mode of action of these proteins in insect antimicrobial defense. It was found that the muramidase activity of G. mellonella lysozyme considerably increased in the presence of apoLp-III. Moreover, apoLp-III enhanced the permeabilizing activity of lysozyme toward Escherichia coli cells. As shown using non-denaturing PAGE, the proteins did not form intermolecular complexes in vivo and in vitro, indicating that the effect observed was not connected with the intermolecular interactions between the proteins. Analysis of AFM images of E. coli cells exposed to G. mellonella lysozyme and/or apoLp-III revealed evident alterations in the bacterial surface structure accompanied by the changes in their biophysical properties. The bacterial cells demonstrated significant differences in elasticity, reflected by Young's modulus, as well as in adhesive forces and roughness values in comparison to the control ones. The constitutive presence of these two defense molecules in G. mellonella hemolymph and the fact that apoLp-III enhances lysozyme muramidase and perforating activities indicate that they can be regarded as important antibacterial factors acting at the early stage of infection against Gram-negative as well as Gram-positive bacteria.
机译:昆虫免疫应答依赖于先天免疫的体液和细胞机制。关键因素是协同作用于入侵病原体的抗菌多肽。几个这样的组件,例如载脂蛋白III(apoLp-III),溶菌酶和阴离子肽2组成型地存在于非挑战性马勒菌幼虫的血淋巴中。在本研究中,我们证明了G. mellonella溶菌酶和apoLp-III对革兰氏阴性细菌有协同作用的证据,为这些蛋白质在昆虫抗菌防御中的作用方式提供了新见解。已经发现,在apoLp-III存在的情况下,梅勒氏菌溶菌酶的muramidase活性显着增加。此外,apoLp-III增强了溶菌酶对大肠杆菌细胞的透化活性。如使用非变性PAGE所示,蛋白质在体内和体外均未形成分子间复合物,表明观察到的作用与蛋白质之间的分子间相互作用无关。对暴露于G. mellonella溶菌酶和/或apoLp-III的大肠杆菌细胞进行AFM图像分析发现,细菌表面结构发生了明显变化,并伴有其生物物理特性的变化。与对照组相比,细菌细胞在弹性上表现出显着差异,由杨氏模量反映出来,在粘附力和粗糙度值上也是如此。这两个防御分子在G. mellonella血淋巴中的组成性存在以及apoLp-III增强溶菌酶muramidase和穿孔活性的事实表明,它们可以被视为重要的抗菌因子,在感染早期针对革兰氏阴性菌以及革兰氏阳性细菌。

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