在SARS-CoV-2疫苗接种小鼠中补充假丝酵母增强免疫反应并调节肠道微生物组

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Renan E A Piraine, Neida L Conrad, Vitória S Gonçalves, Jeferson V Ramos, Júlia L Froldi, Fausto Almeida, Fábio P L Leite
{"title":"在SARS-CoV-2疫苗接种小鼠中补充假丝酵母增强免疫反应并调节肠道微生物组","authors":"Renan E A Piraine, Neida L Conrad, Vitória S Gonçalves, Jeferson V Ramos, Júlia L Froldi, Fausto Almeida, Fábio P L Leite","doi":"10.3390/jof11090685","DOIUrl":null,"url":null,"abstract":"<p><p>Non-<i>Saccharomyces</i> yeasts are emerging as promising new probiotics with a beneficial effect equal to or greater than the reference probiotic yeast, <i>Saccharomyces boulardii</i>. <i>Candida intermedia</i>, a non-<i>albicans</i> species not considered a common human pathogen, previously demonstrated probiotic potential. In this work, our objective was to evaluate the immunomodulatory effects of <i>C. intermedia</i> ORQ001 in mice vaccinated with inactivated SARS-CoV-2, seeking further evidence of its probiotic activity. Murine macrophages were stimulated with <i>C. intermedia</i>, followed by mRNA transcription analysis via qPCR. Mice were supplemented with <i>C. intermedia</i> prior to SARS-CoV-2 vaccination. Antibody production was assessed by ELISA, and fecal microbiomes were analyzed using next-generation sequencing. <i>C. intermedia</i> significantly increased <i>Il4</i> and <i>Il13</i> expression while decreasing <i>Stat3</i> in macrophages. Splenocytes from supplemented mice exhibited elevated transcription levels of <i>Tnf</i>, <i>Ifng</i>, <i>Il4</i>, <i>Bcl6</i>, and <i>Stat3</i> after exposure to stimulatory molecules. These mice showed increased levels of anti-SARS-CoV-2 IgG and sIgA isotypes, along with higher abundances of <i>Bacteroides</i> spp. and <i>Clostridium</i> spp. in their gut microbiome. In conclusion, <i>C. intermedia</i> supplementation modulated the expression of key immune-related genes and enhanced humoral responses in mice. Furthermore, its influence on gastrointestinal microbiota suggests a synergistic effect on vaccine immunogenicity. These findings support the potential of <i>C. intermedia</i> as a novel probiotic candidate with immunomodulatory properties applicable to vaccine adjuvanticity.</p>","PeriodicalId":15878,"journal":{"name":"Journal of Fungi","volume":"11 9","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12470568/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>Candida intermedia</i> Supplementation Enhances Immune Response and Modulates the Gut Microbiome in SARS-CoV-2 Vaccinated Mice.\",\"authors\":\"Renan E A Piraine, Neida L Conrad, Vitória S Gonçalves, Jeferson V Ramos, Júlia L Froldi, Fausto Almeida, Fábio P L Leite\",\"doi\":\"10.3390/jof11090685\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Non-<i>Saccharomyces</i> yeasts are emerging as promising new probiotics with a beneficial effect equal to or greater than the reference probiotic yeast, <i>Saccharomyces boulardii</i>. <i>Candida intermedia</i>, a non-<i>albicans</i> species not considered a common human pathogen, previously demonstrated probiotic potential. In this work, our objective was to evaluate the immunomodulatory effects of <i>C. intermedia</i> ORQ001 in mice vaccinated with inactivated SARS-CoV-2, seeking further evidence of its probiotic activity. Murine macrophages were stimulated with <i>C. intermedia</i>, followed by mRNA transcription analysis via qPCR. Mice were supplemented with <i>C. intermedia</i> prior to SARS-CoV-2 vaccination. Antibody production was assessed by ELISA, and fecal microbiomes were analyzed using next-generation sequencing. <i>C. intermedia</i> significantly increased <i>Il4</i> and <i>Il13</i> expression while decreasing <i>Stat3</i> in macrophages. Splenocytes from supplemented mice exhibited elevated transcription levels of <i>Tnf</i>, <i>Ifng</i>, <i>Il4</i>, <i>Bcl6</i>, and <i>Stat3</i> after exposure to stimulatory molecules. These mice showed increased levels of anti-SARS-CoV-2 IgG and sIgA isotypes, along with higher abundances of <i>Bacteroides</i> spp. and <i>Clostridium</i> spp. in their gut microbiome. In conclusion, <i>C. intermedia</i> supplementation modulated the expression of key immune-related genes and enhanced humoral responses in mice. Furthermore, its influence on gastrointestinal microbiota suggests a synergistic effect on vaccine immunogenicity. These findings support the potential of <i>C. intermedia</i> as a novel probiotic candidate with immunomodulatory properties applicable to vaccine adjuvanticity.</p>\",\"PeriodicalId\":15878,\"journal\":{\"name\":\"Journal of Fungi\",\"volume\":\"11 9\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12470568/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fungi\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/jof11090685\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fungi","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/jof11090685","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

非酵母菌正在成为一种有前途的新型益生菌,其有益效果等于或大于参考益生菌酵母菌博拉迪酵母菌。中间假丝酵母是一种非白色念珠菌,不被认为是一种常见的人类病原体,以前曾显示出益生菌的潜力。在这项工作中,我们的目的是评估C. intermedia ORQ001在灭活的SARS-CoV-2疫苗接种小鼠中的免疫调节作用,寻求其益生菌活性的进一步证据。用C. intermedia刺激小鼠巨噬细胞,通过qPCR分析mRNA转录。小鼠在SARS-CoV-2疫苗接种前补充中间芽胞杆菌。ELISA检测抗体产生,下一代测序检测粪便微生物组。C. intermedia显著提高巨噬细胞中Il4和Il13的表达,降低Stat3的表达。小鼠脾细胞暴露于刺激分子后,Tnf、Ifng、Il4、Bcl6和Stat3的转录水平升高。这些小鼠显示出抗sars - cov -2 IgG和sIgA同型水平的增加,以及肠道微生物组中拟杆菌和梭状芽孢杆菌的丰度更高。综上所述,添加C. intermedia可调节小鼠关键免疫相关基因的表达,增强体液应答。此外,其对胃肠道微生物群的影响表明其对疫苗免疫原性有协同作用。这些发现支持中间芽胞杆菌作为一种具有免疫调节特性的新型候选益生菌的潜力,适用于疫苗佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Candida intermedia Supplementation Enhances Immune Response and Modulates the Gut Microbiome in SARS-CoV-2 Vaccinated Mice.

Non-Saccharomyces yeasts are emerging as promising new probiotics with a beneficial effect equal to or greater than the reference probiotic yeast, Saccharomyces boulardii. Candida intermedia, a non-albicans species not considered a common human pathogen, previously demonstrated probiotic potential. In this work, our objective was to evaluate the immunomodulatory effects of C. intermedia ORQ001 in mice vaccinated with inactivated SARS-CoV-2, seeking further evidence of its probiotic activity. Murine macrophages were stimulated with C. intermedia, followed by mRNA transcription analysis via qPCR. Mice were supplemented with C. intermedia prior to SARS-CoV-2 vaccination. Antibody production was assessed by ELISA, and fecal microbiomes were analyzed using next-generation sequencing. C. intermedia significantly increased Il4 and Il13 expression while decreasing Stat3 in macrophages. Splenocytes from supplemented mice exhibited elevated transcription levels of Tnf, Ifng, Il4, Bcl6, and Stat3 after exposure to stimulatory molecules. These mice showed increased levels of anti-SARS-CoV-2 IgG and sIgA isotypes, along with higher abundances of Bacteroides spp. and Clostridium spp. in their gut microbiome. In conclusion, C. intermedia supplementation modulated the expression of key immune-related genes and enhanced humoral responses in mice. Furthermore, its influence on gastrointestinal microbiota suggests a synergistic effect on vaccine immunogenicity. These findings support the potential of C. intermedia as a novel probiotic candidate with immunomodulatory properties applicable to vaccine adjuvanticity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信