Artificial intelligence-driven reverse vaccinology for Neisseria gonorrhoeae vaccine: Prioritizing epitope-based candidates.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2024-08-13 eCollection Date: 2024-01-01 DOI:10.3389/fmolb.2024.1442158
Ravi Kant, Mohd Shoaib Khan, Madhu Chopra, Daman Saluja
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Abstract

Neisseria gonorrhoeae is the causative agent of the sexually transmitted disease gonorrhea. The increasing prevalence of this disease worldwide, the rise of antibiotic-resistant strains, and the difficulties in treatment necessitate the development of a vaccine, highlighting the significance of preventative measures to control and eradicate the infection. Currently, there is no widely available vaccine, partly due to the bacterium's ability to evade natural immunity and the limited research investment in gonorrhea compared to other diseases. To identify distinct vaccine candidates, we chose to focus on the uncharacterized, hypothetical proteins (HPs) as our initial approach. Using the in silico method, we first carried out a comprehensive assessment of hypothetical proteins of Neisseria gonorrhoeae, encompassing assessments of physicochemical properties, cellular localization, secretary pathways, transmembrane regions, antigenicity, toxicity, and prediction of B-cell and T-cell epitopes, among other analyses. Detailed analysis of all HPs resulted in the functional annotation of twenty proteins with a great degree of confidence. Further, using the immuno-informatics approach, the prediction pipeline identified one CD8+ restricted T-cell epitope, seven linear B-cell epitopes, and seven conformational B-cell epitopes as putative epitope-based peptide vaccine candidates which certainly require further validation in laboratory settings. The study accentuates the promise of functional annotation and immuno-informatics in the systematic design of epitope-based peptide vaccines targeting Neisseria gonorrhoeae.

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人工智能驱动的淋病奈瑟菌疫苗反向疫苗学:基于表位的候选者优先排序。
淋病奈瑟菌是性传播疾病淋病的病原体。这种疾病在全球范围内的发病率越来越高,抗生素耐药菌株增多,治疗困难,因此有必要开发一种疫苗,这突出了采取预防措施控制和根除感染的重要性。目前还没有广泛使用的疫苗,部分原因是淋病菌能够逃避天然免疫,而且与其他疾病相比,淋病的研究投入有限。为了确定独特的候选疫苗,我们选择将未表征的假定蛋白(HPs)作为最初的研究方向。我们首先使用硅学方法对淋病奈瑟菌的假定蛋白进行了全面评估,包括理化性质、细胞定位、秘书途径、跨膜区、抗原性、毒性以及 B 细胞和 T 细胞表位预测等方面的评估。通过对所有 HPs 的详细分析,对 20 个蛋白质进行了功能注释,并取得了很高的可信度。此外,利用免疫信息学方法,预测管道确定了一个 CD8+ 限制性 T 细胞表位、七个线性 B 细胞表位和七个构象 B 细胞表位,作为基于表位的多肽疫苗候选物,这些候选物当然需要在实验室环境中进一步验证。这项研究强调了功能注释和免疫信息学在系统设计以淋病奈瑟菌为靶标的表位肽疫苗方面的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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