Nicholas Naidovski, Sarah K T Chong, Fang Liu, Stephen M Riordan, Michael C Wehrhahn, Christopher Yuwono, Li Zhang
{"title":"人巨噬细胞对新出现的肠道病原体维罗氏气单胞菌的反应:炎症、凋亡和组蛋白下调。","authors":"Nicholas Naidovski, Sarah K T Chong, Fang Liu, Stephen M Riordan, Michael C Wehrhahn, Christopher Yuwono, Li Zhang","doi":"10.1080/21505594.2024.2440554","DOIUrl":null,"url":null,"abstract":"<p><p>This study investigated the pathogenic mechanisms of <i>Aeromonas veronii</i> in macrophages. THP-1 derived macrophages were used as a human macrophage model and were treated with <i>A. veronii</i> strain AS1 isolated from intestinal biopsies of an IBD patient, or <i>Escherichia coli</i> strain K-12. RNA was extracted and subjected to RNA sequencing and comparative transcriptomic analyses. Protein levels of IL-8, IL-1β, IL-18, and TNFα were measured using ELISA, and apoptosis was assessed using caspase 3/7 assays. Both <i>A. veronii</i> AS1 and <i>E. coli</i> K-12 significantly upregulated the expression of many genes involving inflammation. At the protein level, <i>A. veronii</i> AS1 induced significantly higher levels of IL-8, TNFα, mature IL-18 and IL-1β than <i>E. coli</i> K-12, and led to greater elevation of caspase 3/7 activities. Both <i>A. veronii</i> AS1 and <i>E. coli</i> K-12 upregulated the expression of <i>CASP5</i>, but not other caspase genes. <i>A. veronii</i> AS1 significantly downregulated the expression of 20 genes encoding histone proteins that <i>E. coli</i> K-12 did not. The more profound pathogenic effects of <i>A. veronii</i> in inducing inflammation and apoptosis in macrophages than <i>E. coli</i> K-12 are consistent with its role as a human enteric pathogen. The upregulated expression of <i>CASP5</i> and increased release of IL-1β and IL-18 support the role of <i>CASP5</i> in activation of non-canonical inflammasome. The downregulation of histone genes by <i>A. veronii</i> suggests a unique impact on host cell gene expression, which may represent a novel virulence strategy. These findings advance the understanding of pathogenic mechanisms of the emerging human enteric pathogen <i>A. veronii.</i></p>","PeriodicalId":23747,"journal":{"name":"Virulence","volume":" ","pages":"2440554"},"PeriodicalIF":5.5000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Human macrophage response to the emerging enteric pathogen <i>Aeromonas veronii</i>: Inflammation, apoptosis, and downregulation of histones.\",\"authors\":\"Nicholas Naidovski, Sarah K T Chong, Fang Liu, Stephen M Riordan, Michael C Wehrhahn, Christopher Yuwono, Li Zhang\",\"doi\":\"10.1080/21505594.2024.2440554\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This study investigated the pathogenic mechanisms of <i>Aeromonas veronii</i> in macrophages. THP-1 derived macrophages were used as a human macrophage model and were treated with <i>A. veronii</i> strain AS1 isolated from intestinal biopsies of an IBD patient, or <i>Escherichia coli</i> strain K-12. RNA was extracted and subjected to RNA sequencing and comparative transcriptomic analyses. Protein levels of IL-8, IL-1β, IL-18, and TNFα were measured using ELISA, and apoptosis was assessed using caspase 3/7 assays. Both <i>A. veronii</i> AS1 and <i>E. coli</i> K-12 significantly upregulated the expression of many genes involving inflammation. At the protein level, <i>A. veronii</i> AS1 induced significantly higher levels of IL-8, TNFα, mature IL-18 and IL-1β than <i>E. coli</i> K-12, and led to greater elevation of caspase 3/7 activities. Both <i>A. veronii</i> AS1 and <i>E. coli</i> K-12 upregulated the expression of <i>CASP5</i>, but not other caspase genes. <i>A. veronii</i> AS1 significantly downregulated the expression of 20 genes encoding histone proteins that <i>E. coli</i> K-12 did not. The more profound pathogenic effects of <i>A. veronii</i> in inducing inflammation and apoptosis in macrophages than <i>E. coli</i> K-12 are consistent with its role as a human enteric pathogen. The upregulated expression of <i>CASP5</i> and increased release of IL-1β and IL-18 support the role of <i>CASP5</i> in activation of non-canonical inflammasome. The downregulation of histone genes by <i>A. veronii</i> suggests a unique impact on host cell gene expression, which may represent a novel virulence strategy. 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Human macrophage response to the emerging enteric pathogen Aeromonas veronii: Inflammation, apoptosis, and downregulation of histones.
This study investigated the pathogenic mechanisms of Aeromonas veronii in macrophages. THP-1 derived macrophages were used as a human macrophage model and were treated with A. veronii strain AS1 isolated from intestinal biopsies of an IBD patient, or Escherichia coli strain K-12. RNA was extracted and subjected to RNA sequencing and comparative transcriptomic analyses. Protein levels of IL-8, IL-1β, IL-18, and TNFα were measured using ELISA, and apoptosis was assessed using caspase 3/7 assays. Both A. veronii AS1 and E. coli K-12 significantly upregulated the expression of many genes involving inflammation. At the protein level, A. veronii AS1 induced significantly higher levels of IL-8, TNFα, mature IL-18 and IL-1β than E. coli K-12, and led to greater elevation of caspase 3/7 activities. Both A. veronii AS1 and E. coli K-12 upregulated the expression of CASP5, but not other caspase genes. A. veronii AS1 significantly downregulated the expression of 20 genes encoding histone proteins that E. coli K-12 did not. The more profound pathogenic effects of A. veronii in inducing inflammation and apoptosis in macrophages than E. coli K-12 are consistent with its role as a human enteric pathogen. The upregulated expression of CASP5 and increased release of IL-1β and IL-18 support the role of CASP5 in activation of non-canonical inflammasome. The downregulation of histone genes by A. veronii suggests a unique impact on host cell gene expression, which may represent a novel virulence strategy. These findings advance the understanding of pathogenic mechanisms of the emerging human enteric pathogen A. veronii.
期刊介绍:
Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication.
Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.