N. López-Ureña, R. Calero-Bernal, Břetislav Koudela, S. Cherchi, A. Possenti, Fabio Tosini, Sandra Klein, Carmen San Juan-Casero, Silvia Jara-Herrera, P. Jokelainen, J. Regidor-Cerrillo, L. Ortega-Mora, F. Spano, Frank Seeber, G. Álvarez‐García
{"title":"当前和新的硅学预测的弓形虫卵囊特异性蛋白在来源归因血清学中的价值有限","authors":"N. López-Ureña, R. Calero-Bernal, Břetislav Koudela, S. Cherchi, A. Possenti, Fabio Tosini, Sandra Klein, Carmen San Juan-Casero, Silvia Jara-Herrera, P. Jokelainen, J. Regidor-Cerrillo, L. Ortega-Mora, F. Spano, Frank Seeber, G. Álvarez‐García","doi":"10.3389/fpara.2023.1292322","DOIUrl":null,"url":null,"abstract":"Toxoplasma gondii is a zoonotic parasite infecting all warm-blooded animals, including humans. The contribution of environmental contamination by T. gondii oocysts to infections is understudied. The aim of the current work was to explore T. gondii serology as a means of attributing the source of infection using a robust stepwise approach. We identified in silico thirty-two promising oocyst-specific antigens from T. gondii ´omics data, recombinantly expressed and purified them and validated whether serology based on these proteins could discriminate oocyst- from tissue cyst-driven experimental infections. For this, three well-characterized serum panels, sampled from 0 to 6 weeks post-infection, from pigs and sheep experimentally infected with T. gondii oocysts or tissue cysts, were used. Candidate proteins were initially screened by Western blot with sera from pigs or sheep, infected for different times, either with oocysts or tissue cysts, as well as non-infected animals. Only the recombinant proteins TgCCp5A and TgSR1 provoked seroconversion upon infection and appeared to discriminate between oocyst- and tissue cyst-driven infections with pig sera. They were subsequently used to develop an enzyme-linked immunosorbent assay test for pigs. Based on this assay and Western blot analyses, a lack of stage specificity and low antigenicity was observed with all pig sera. The same was true for proteins TgERP, TgSporoSAG, TgOWP1 and TgOWP8, previously described as source-attributing antigens, when analyzed using the whole panels of sera. We conclude that there is currently no antigen that allows the discrimination of T. gondii infections acquired from either oocysts or tissue cysts by serological tests. This work provides robust new knowledge that can inform further research and development toward source-attributing T. gondii serology.","PeriodicalId":73098,"journal":{"name":"Frontiers in parasitology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Limited value of current and new in silico predicted oocyst-specific proteins of Toxoplasma gondii for source-attributing serology\",\"authors\":\"N. López-Ureña, R. Calero-Bernal, Břetislav Koudela, S. Cherchi, A. Possenti, Fabio Tosini, Sandra Klein, Carmen San Juan-Casero, Silvia Jara-Herrera, P. Jokelainen, J. Regidor-Cerrillo, L. Ortega-Mora, F. Spano, Frank Seeber, G. 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引用次数: 0
摘要
弓形虫是一种人畜共患寄生虫,可感染包括人类在内的所有温血动物。关于弓形虫卵囊对环境污染造成的感染,研究还不够深入。当前工作的目的是探索用淋病双球菌血清学作为一种手段,采用稳健的逐步法确定感染源。我们从基因组学数据中确定了 32 种有希望的卵囊特异性抗原,重组表达并纯化了这些抗原,并验证了基于这些蛋白的血清学是否能区分卵囊和组织囊肿驱动的实验感染。为此,我们使用了三组特征明确的血清样本,取样时间为感染后 0 至 6 周,样本来自实验性感染了淋病双球菌卵囊或组织囊肿的猪和羊。用来自不同时间感染过卵囊或组织囊肿的猪或羊以及未感染动物的血清进行 Western 印迹初步筛选候选蛋白。只有重组蛋白 TgCCp5A 和 TgSR1 能在感染时引起血清转换,并能在猪血清中区分卵囊感染和组织囊肿感染。它们随后被用于开发猪用酶联免疫吸附试验。根据这种检测方法和 Western 印迹分析,观察到所有猪血清都缺乏阶段特异性和低抗原性。在使用整组血清进行分析时,之前被描述为来源归因抗原的蛋白质 TgERP、TgSporoSAG、TgOWP1 和 TgOWP8 也是如此。我们的结论是,目前还没有一种抗原可以通过血清学检测来区分从卵囊或组织囊中获得的淋病双球菌感染。这项工作提供了有力的新知识,可为进一步研究和开发源归因淋球菌血清学提供依据。
Limited value of current and new in silico predicted oocyst-specific proteins of Toxoplasma gondii for source-attributing serology
Toxoplasma gondii is a zoonotic parasite infecting all warm-blooded animals, including humans. The contribution of environmental contamination by T. gondii oocysts to infections is understudied. The aim of the current work was to explore T. gondii serology as a means of attributing the source of infection using a robust stepwise approach. We identified in silico thirty-two promising oocyst-specific antigens from T. gondii ´omics data, recombinantly expressed and purified them and validated whether serology based on these proteins could discriminate oocyst- from tissue cyst-driven experimental infections. For this, three well-characterized serum panels, sampled from 0 to 6 weeks post-infection, from pigs and sheep experimentally infected with T. gondii oocysts or tissue cysts, were used. Candidate proteins were initially screened by Western blot with sera from pigs or sheep, infected for different times, either with oocysts or tissue cysts, as well as non-infected animals. Only the recombinant proteins TgCCp5A and TgSR1 provoked seroconversion upon infection and appeared to discriminate between oocyst- and tissue cyst-driven infections with pig sera. They were subsequently used to develop an enzyme-linked immunosorbent assay test for pigs. Based on this assay and Western blot analyses, a lack of stage specificity and low antigenicity was observed with all pig sera. The same was true for proteins TgERP, TgSporoSAG, TgOWP1 and TgOWP8, previously described as source-attributing antigens, when analyzed using the whole panels of sera. We conclude that there is currently no antigen that allows the discrimination of T. gondii infections acquired from either oocysts or tissue cysts by serological tests. This work provides robust new knowledge that can inform further research and development toward source-attributing T. gondii serology.