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Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH Ionic Strength and Temperature and Implications for Adhesion to Surfaces

机译:代表诺如病毒的病毒样颗粒的二级和三级结构的稳定性:pH离子强度和温度的影响以及对表面粘附的影响

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摘要

Loss of ordered molecular structure in proteins is known to increase their adhesion to surfaces. The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and temperature conditions studied correspond to those prevalent in the principal vehicles of viral transmission (vomit and feces) and in the food processing and handling environment (pasteurization and refrigeration). The structures of virus-like particles representing GI.1, GII.4, and feline calicivirus (FCV) were studied using circular dichroism and intrinsic UV fluorescence. The particles were remarkably stable under most of the conditions. However, heating to 65°C caused losses of β-strand structure, notably in GI.1 and FCV, while at 75°C the α-helix content of GII.4 and FCV decreased and tertiary structures unfolded in all three cases. Combining temperature with pH or ionic strength caused variable losses of structure depending on the particle type. Regardless of pH, heating to pasteurization temperatures or higher would be required to increase GII.4 and FCV adhesion, while either low or high temperatures would favor GI.1 adhesion. Regardless of temperature, increased ionic strength would increase GII.4 adhesion but would decrease GI.1 adhesion. FCV adsorption would be greater at refrigeration, pasteurization, or high temperature combined with a low salt concentration or at a higher NaCl concentration regardless of temperature. Norovirus adhesion mediated by hydrophobic interaction may depend on hydrophobic residues normally exposed on the capsid surface at pH 3, pH 8, physiological ionic strength, and low temperature, while at pasteurization temperatures it may rely more on buried hydrophobic residues exposed upon structural rearrangement.
机译:已知蛋白质中有序分子结构的丧失会增加其与表面的附着力。这项工作的目的是研究诺如病毒二级和三级结构的稳定性及其对病毒与新鲜食品和农业食品表面粘附的影响。研究的pH,离子强度和温度条件与病毒传播的主要媒介(呕吐物和粪便)以及食品加工和处理环境(巴氏灭菌和冷藏)中普遍存在的pH,离子强度和温度条件相对应。使用圆二色性和固有的紫外荧光研究了代表GI.1,GII.4和猫杯状病毒(FCV)的病毒样颗粒的结构。在大多数条件下,颗粒都非常稳定。然而,加热至65°C会导致β​​链结构的损失,特别是在GI.1和FCV中,而在75°C时,这三种情况下GII.4和FCV的α-螺旋含量均下降并且三级结构展开。温度与pH值或离子强度的结合会导致结构损失,具体取决于颗粒类型。无论pH值如何,都需要加热至巴氏灭菌温度或更高温度以提高GII.4和FCV的粘附力,而低温或高温都将有利于GI.1粘附力。无论温度如何,增加的离子强度都会增加GII.4的附着力,但会降低GI.1的附着力。不论温度如何,在冷藏,巴氏灭菌或高温,低盐浓度或高NaCl浓度下,FCV的吸附都会更大。由疏水相互作用介导的诺如病毒粘附可能取决于通常在pH 3,pH 8,生理离子强度和低温下暴露于衣壳表面的疏水残基,而在巴氏灭菌温度下,它可能更多地依赖于结构重排而暴露的掩埋疏水残基。

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