Vinícius Andrade-Silva , Jéssica Waldman , Maria Aparecida Juliano , Lucas Tirloni , Itabajara da Silva Vaz Jr.
{"title":"蜱虫控制肽基疫苗潜在b细胞表位鉴定的Pepscan和生物信息学策略","authors":"Vinícius Andrade-Silva , Jéssica Waldman , Maria Aparecida Juliano , Lucas Tirloni , Itabajara da Silva Vaz Jr.","doi":"10.1016/j.molbiopara.2025.111692","DOIUrl":null,"url":null,"abstract":"<div><div>The cattle tick <em>Rhipicephalus microplus</em> poses a major problem to the livestock industry worldwide, with acaricides resistance presenting an increasing challenge. On other hand, vaccination has been suggested as a better strategy for tick control, and peptide-based vaccines could be developed to target multiple tick antigens. Nevertheless, there are still limitations to the identification of epitopes in tick candidate antigens, as the bioinformatics tools currently available were developed almost exclusively based on mammalian genomes. Therefore, improving the performance of B-cell epitope predictor algorithms is essential to achieve an effective multi-epitope vaccine for tick control. The aim of this study was to reduce costs and increase the efficacy in identifying epitopes in tick antigens. We first evaluated the performance of B-cell epitope predictor algorithms in replicating the results of an <em>in vitro</em> epitope mapping result for the tick salivary serpin RmS-17 as a “benchmark”. Then the algorithm with the best performance was employed to predict epitopes for the tick salivary serpin RmS-6, and we screened the candidate epitopes based on predictions that were close to the reactive center loop (RCL), the region of the serpin that interacts with the target protease. Antibodies raised against p1RmS-6 and p3RmS-6 neutralize RmS-6 activity. Using this strategy, we were able to adjust an <em>in silico</em> algorithm predictor based on a Pepscan result to identify epitopes in another serpin. Our strategy offers a cost-effective way to identify neutralizing epitopes in serpins. Furthermore, this strategy can be applied to identify epitopes in serpins and other proteins from other tick species, potentially leading to the development of a peptide-based anti-tick vaccine.</div></div>","PeriodicalId":18721,"journal":{"name":"Molecular and biochemical parasitology","volume":"263 ","pages":"Article 111692"},"PeriodicalIF":1.5000,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pepscan and bioinformatic strategies for identification of potential B-cell epitopes for a peptide-based vaccine for tick control\",\"authors\":\"Vinícius Andrade-Silva , Jéssica Waldman , Maria Aparecida Juliano , Lucas Tirloni , Itabajara da Silva Vaz Jr.\",\"doi\":\"10.1016/j.molbiopara.2025.111692\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The cattle tick <em>Rhipicephalus microplus</em> poses a major problem to the livestock industry worldwide, with acaricides resistance presenting an increasing challenge. On other hand, vaccination has been suggested as a better strategy for tick control, and peptide-based vaccines could be developed to target multiple tick antigens. Nevertheless, there are still limitations to the identification of epitopes in tick candidate antigens, as the bioinformatics tools currently available were developed almost exclusively based on mammalian genomes. Therefore, improving the performance of B-cell epitope predictor algorithms is essential to achieve an effective multi-epitope vaccine for tick control. The aim of this study was to reduce costs and increase the efficacy in identifying epitopes in tick antigens. We first evaluated the performance of B-cell epitope predictor algorithms in replicating the results of an <em>in vitro</em> epitope mapping result for the tick salivary serpin RmS-17 as a “benchmark”. Then the algorithm with the best performance was employed to predict epitopes for the tick salivary serpin RmS-6, and we screened the candidate epitopes based on predictions that were close to the reactive center loop (RCL), the region of the serpin that interacts with the target protease. Antibodies raised against p1RmS-6 and p3RmS-6 neutralize RmS-6 activity. Using this strategy, we were able to adjust an <em>in silico</em> algorithm predictor based on a Pepscan result to identify epitopes in another serpin. Our strategy offers a cost-effective way to identify neutralizing epitopes in serpins. Furthermore, this strategy can be applied to identify epitopes in serpins and other proteins from other tick species, potentially leading to the development of a peptide-based anti-tick vaccine.</div></div>\",\"PeriodicalId\":18721,\"journal\":{\"name\":\"Molecular and biochemical parasitology\",\"volume\":\"263 \",\"pages\":\"Article 111692\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular and biochemical parasitology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0166685125000283\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular and biochemical parasitology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166685125000283","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Pepscan and bioinformatic strategies for identification of potential B-cell epitopes for a peptide-based vaccine for tick control
The cattle tick Rhipicephalus microplus poses a major problem to the livestock industry worldwide, with acaricides resistance presenting an increasing challenge. On other hand, vaccination has been suggested as a better strategy for tick control, and peptide-based vaccines could be developed to target multiple tick antigens. Nevertheless, there are still limitations to the identification of epitopes in tick candidate antigens, as the bioinformatics tools currently available were developed almost exclusively based on mammalian genomes. Therefore, improving the performance of B-cell epitope predictor algorithms is essential to achieve an effective multi-epitope vaccine for tick control. The aim of this study was to reduce costs and increase the efficacy in identifying epitopes in tick antigens. We first evaluated the performance of B-cell epitope predictor algorithms in replicating the results of an in vitro epitope mapping result for the tick salivary serpin RmS-17 as a “benchmark”. Then the algorithm with the best performance was employed to predict epitopes for the tick salivary serpin RmS-6, and we screened the candidate epitopes based on predictions that were close to the reactive center loop (RCL), the region of the serpin that interacts with the target protease. Antibodies raised against p1RmS-6 and p3RmS-6 neutralize RmS-6 activity. Using this strategy, we were able to adjust an in silico algorithm predictor based on a Pepscan result to identify epitopes in another serpin. Our strategy offers a cost-effective way to identify neutralizing epitopes in serpins. Furthermore, this strategy can be applied to identify epitopes in serpins and other proteins from other tick species, potentially leading to the development of a peptide-based anti-tick vaccine.
期刊介绍:
The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are:
• the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances
• intermediary metabolism and bioenergetics
• drug target characterization and the mode of action of antiparasitic drugs
• molecular and biochemical aspects of membrane structure and function
• host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules.
• analysis of genes and genome structure, function and expression
• analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance.
• parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules
• parasite programmed cell death, development, and cell division at the molecular level.