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基于口蹄疫病毒颗粒的灭活疫苗具有保留的免疫原性且稳定性提高。

Preserved immunogenicity of an inactivated vaccine based on foot-and-mouth disease virus particles with improved stability.

作者信息

Caridi Flavia, Vázquez-Calvo Ángela, Borrego Belén, McCullough Kenneth, Summerfield Artur, Sobrino Francisco, Martín-Acebes Miguel A

机构信息

Department of Virology and Microbiology, Centro de Biología Molecular "Severo Ochoa" (CSIC-UAM), 28049 Madrid, Spain.

Centro de Investigación en Sanidad Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Valdeolmos, 28130 Madrid, Spain.

出版信息

Vet Microbiol. 2017 May;203:275-279. doi: 10.1016/j.vetmic.2017.03.031. Epub 2017 Mar 30.

Abstract

Foot-and-mouth disease virus (FMDV) is the etiological agent of a highly contagious disease that affects important livestock species. Vaccines based on inactivated FMDV virions provide a useful tool for the control of this pathogen. However, long term storage at 4°C (the temperature for vaccine storage) or ruptures of the cold chain, provoke the dissociation of virions, reducing the immunogenicity of the vaccine. An FMDV mutant carrying amino acid replacements VP1 N17D and VP2 H145Y isolated previously rendered virions with increased resistance to dissociation at 4°C. We have evaluated the immunogenicity in swine (a natural FMDV host) of a chemically inactivated vaccine based on this mutant. The presence of these amino acid substitutions did not compromise the immunological potential, including its ability to elicit neutralizing antibodies. These results support the feasibility of this kind of mutants with increased capsid stability as suitable viruses for producing improved FMDV vaccines.

摘要

口蹄疫病毒(FMDV)是一种影响重要家畜物种的高度传染性疾病的病原体。基于灭活FMDV病毒粒子的疫苗为控制这种病原体提供了一种有用的工具。然而,在4°C(疫苗储存温度)下长期储存或冷链破裂会导致病毒粒子解离,降低疫苗的免疫原性。先前分离出的携带氨基酸替换VP1 N17D和VP2 H145Y的FMDV突变体使病毒粒子在4°C下对解离的抵抗力增强。我们评估了基于这种突变体的化学灭活疫苗在猪(FMDV天然宿主)中的免疫原性。这些氨基酸取代的存在并未损害其免疫潜力,包括引发中和抗体的能力。这些结果支持了这种衣壳稳定性增强的突变体作为生产改良FMDV疫苗的合适病毒的可行性。

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