Immunoinformatic analysis for identifying immunogenic antigens from the complete proteome of Giardia lamblia.

IF 2.5 4区 医学 Q2 PARASITOLOGY
Memorias do Instituto Oswaldo Cruz Pub Date : 2026-04-17 eCollection Date: 2026-01-01 DOI:10.1590/0074-02760250216
David Ortega-Tirado, Carlos A Velazquez-Valdez, Thania Garzon, Leslie Bracamontes-Picos, Gloria Lopez-Romero, Carlos Velazquez
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Abstract

Background: Giardia lamblia is a parasite that infects humans. To date, there is no vaccine available for human giardiasis. Thus, discovering new immunogenic antigens is crucial for the rational design of a vaccine.

Objectives: This study aimed to identify the main immunogenic antigens of G. lamblia from its entire proteome using immunoinformatic and data science techniques. To our knowledge, this is the first study to systematically identify immunogenic antigens of G. lamblia across its complete proteome, providing a comprehensive map of potential immunogenic antigens.

Methods: Briefly, FASTA sequences of G. lamblia isolates WB and GS were submitted to the NetMHCII 2.3 predictor. The analysis was conducted for five murine major histocompatibility complex (MHC)-II molecules: I-Ab, I-Ad, I-Ed, I-Ak, and I-Ek. Python 3.9 was used to develop custom code for data processing and analysis.

Findings: We identified 414 potential immunogenic polypeptides for isolate WB and 350 for isolate GS. For both isolates, most polypeptides contained peptides with high affinity for I-Ab and I-Ek. Notably, no polypeptides with high affinity for I-Ak were detected. Homologous potential immunogenic antigens (129 polypeptides) were identified in both isolates. The analysis revealed that 12 potential immunogenic polypeptides from isolate WB and 10 from isolate GS are part of the Giardia secretome. Additionally, promiscuous polypeptides that bind to at least two different MHC-II molecules were found in both isolates.

Main conclusions: These findings lay a valuable foundation for the rational development of a vaccine against human giardiasis and show a computational strategy that can be applied to the study of other pathogens.

从兰氏贾第鞭毛虫完整蛋白质组中鉴定免疫原性抗原的免疫信息学分析。
背景:贾第鞭毛虫是一种感染人类的寄生虫。迄今为止,还没有针对人贾第虫病的疫苗。因此,发现新的免疫原性抗原对于疫苗的合理设计至关重要。目的:利用免疫信息学和数据科学技术,从兰氏螺旋体整个蛋白质组中鉴定其主要免疫原性抗原。据我们所知,这是第一次系统地识别兰氏螺旋体完整蛋白质组的免疫原性抗原的研究,提供了潜在免疫原性抗原的全面图谱。方法:简单地将兰螺旋体分离物WB和GS的FASTA序列提交NetMHCII 2.3预测器。分析了5种小鼠主要组织相容性复合体(MHC)-II分子:I-Ab、I-Ad、I-Ed、I-Ak和I-Ek。Python 3.9用于开发用于数据处理和分析的自定义代码。结果:我们为WB分离物鉴定了414个潜在的免疫原性多肽,为GS分离物鉴定了350个。对于这两个分离株,大多数多肽都含有对I-Ab和I-Ek具有高亲和力的肽。值得注意的是,没有检测到对I-Ak具有高亲和力的多肽。在两个分离株中鉴定出同源的潜在免疫原性抗原(129多肽)。分析结果显示,贾第鞭毛虫分泌组中有12个可能具有免疫原性的多肽和10个可能具有免疫原性的多肽。此外,在两个分离株中发现了至少结合两种不同MHC-II分子的混杂多肽。主要结论:这些发现为合理开发人贾第虫病疫苗奠定了宝贵的基础,并展示了一种可应用于其他病原体研究的计算策略。
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
CiteScore
5.00
自引率
3.60%
发文量
91
审稿时长
3-8 weeks
期刊介绍: Memórias do Instituto Oswaldo Cruz is a journal specialized in microbes & their vectors causing human infections. This means that we accept manuscripts covering multidisciplinary approaches and findings in the basic aspects of infectious diseases, e.g. basic in research in prokariotes, eukaryotes, and/or virus. Articles must clearly show what is the main question to be answered, the hypothesis raised, and the contribution given by the study. Priority is given to manuscripts reporting novel mechanisms and general findings concerning the biology of human infectious prokariotes, eukariotes or virus. Papers reporting innovative methods for diagnostics or that advance the basic research with these infectious agents are also welcome. It is important to mention what we do not publish: veterinary infectious agents research, taxonomic analysis and re-description of species, epidemiological studies or surveys or case reports and data re-analysis. Manuscripts that fall in these cases or that are considered of low priority by the journal editorial board, will be returned to the author(s) for submission to another journal.
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