对新型 NADC-34 类猪繁殖与呼吸综合征病毒(PRRSV)分离株 YC-2020 的计算抗原学见解

IF 1.4 3区 农林科学 Q4 IMMUNOLOGY
Maria Karolaynne da Silva , Jonas Galileu Ferreira de Aquino , Claudio Bruno Silva de Oliveira , João Firmino Rodrigues-Neto , Miadur Rahman , Shahina Akter , Umberto Laino Fulco , Yousef A. Bin Jardan , Samir Ibenmoussa , Jonas Ivan Nobre Oliveira
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引用次数: 0

摘要

在这项计算研究中,我们进一步了解了与兽医病理学相关的猪繁殖与呼吸综合征病毒(PRRSV)NADC-34 相似分离物(名为 YC-2020)的抗原特性。我们对 M 蛋白和 N 蛋白进行了序列比较分析,将它们与 NADC34 蛋白进行比较,确定了大量氨基酸同源性,从而突出了保守表位和关键变体。通过使用 Clustal Omega 进行多序列比对,以及使用 Vaxijen 和 AllerTOP 等平台预测抗原性和致敏性潜力,我们的分析揭示了表位保护和变异的重要见解,这对于开发有效的诊断工具和疫苗至关重要。我们的研究结果与最初的实验研究相一致,强调了这些表位在开发有针对性的免疫诊断平台中的重要性,并大大有助于PRRSV的管理和控制。然而,还需要进一步的研究来验证对这种新病毒分离物抗原性的计算预测。这种方法强调了计算模型在持续监测和控制猪 PRRSV 演变方面的潜力。虽然本研究通过计算分析为新型 PRRSV 分离物 YC-2020 的抗原特性提供了宝贵的见解,但必须承认硅预测固有的局限性,特别是缺乏实验室验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computational antigenic insights into the novel NADC-34-like Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) isolate YC-2020

In this computational study, we advanced the understanding of the antigenic properties of the NADC-34-like isolate of the Porcine Reproductive and Respiratory Syndrome Virus (PRRSV), named YC-2020, relevant in veterinary pathology. We utilized sequence comparison analyses of the M and N proteins, comparing them with those of NADC34, identifying substantial amino acid homology that allowed us to highlight conserved epitopes and crucial variants. Through the application of Clustal Omega for multiple sequence alignment and platforms like Vaxijen and AllerTOP for predicting antigenic and allergenic potential, our analyses revealed important insights into the conservation and variation of epitopes essential for the development of effective diagnostic tools and vaccines. Our findings, aligned with initial experimental studies, underscore the importance of these epitopes in the development of targeted immunodiagnostic platforms and significantly contribute to the management and control of PRRSV. However, further studies are required to validate the computational predictions of antigenicity for this new viral isolate. This approach underscores the potential of computational models to enable ongoing monitoring and control of PRRSV evolution in swine. While this study provides valuable insights into the antigenic properties of the novel PRRSV isolate YC-2020 through computational analysis, it is important to acknowledge the limitations inherent to in silico predictions, specifically, the absence of laboratory validation.

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来源期刊
CiteScore
3.40
自引率
5.60%
发文量
79
审稿时长
70 days
期刊介绍: The journal reports basic, comparative and clinical immunology as they pertain to the animal species designated here: livestock, poultry, and fish species that are major food animals and companion animals such as cats, dogs, horses and camels, and wildlife species that act as reservoirs for food, companion or human infectious diseases, or as models for human disease. Rodent models of infectious diseases that are of importance in the animal species indicated above,when the disease requires a level of containment that is not readily available for larger animal experimentation (ABSL3), will be considered. Papers on rabbits, lizards, guinea pigs, badgers, armadillos, elephants, antelope, and buffalo will be reviewed if the research advances our fundamental understanding of immunology, or if they act as a reservoir of infectious disease for the primary animal species designated above, or for humans. Manuscripts employing other species will be reviewed if justified as fitting into the categories above. The following topics are appropriate: biology of cells and mechanisms of the immune system, immunochemistry, immunodeficiencies, immunodiagnosis, immunogenetics, immunopathology, immunology of infectious disease and tumors, immunoprophylaxis including vaccine development and delivery, immunological aspects of pregnancy including passive immunity, autoimmuity, neuroimmunology, and transplanatation immunology. Manuscripts that describe new genes and development of tools such as monoclonal antibodies are also of interest when part of a larger biological study. Studies employing extracts or constituents (plant extracts, feed additives or microbiome) must be sufficiently defined to be reproduced in other laboratories and also provide evidence for possible mechanisms and not simply show an effect on the immune system.
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