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<p>Gene expression heterogeneity has an impact on human bacterial pathogens responses, including antimicrobial resistance genes expression. Promoter region variability in resistance genes may include different regulatory boxes involved in metabolic processes essential for bacterial survival. In this study, a molecular tool was developed to characterize promoter region variability and resistance gene expression. For these, 46 bacterial clinical isolates were used. Sequence analysis of resistance genes promoter region showed the existence of different variants for each promoter and identified gene-specific regulatory boxes. Using a fluorescent transcriptional reporter, we analysed the most common promoter variants of the most prevalent acquired resistance genes in clinical isolates (<i>qnrA</i>, <i>qnrB, bla</i><sub>OXA-48</sub>, <i>bla</i><sub>KPC-3</sub> and <i>bla</i><sub>VIM-1</sub>, <i>aac(6’)-Ib-cr</i>, and <i>fosA</i>). Gene expression fluctuations were found to be dependent on culture medium used. Specific gene promoter variants showed lower expression levels in poor (M9) medium (<i>p</i> &lt; 0.0001) and an induction of expression under antimicrobials presence (tetracycline, quinolones and beta-lactams). <i>qnrB1</i> genes were regulated by <i>phoB</i> and <i>lexA</i> boxes; <i>bla</i><sub>OXA-48</sub> was regulated by the <i>argR</i> box or <i>fnr</i> and <i>arcA</i> boxes. Differences in regulation of resistance gene promoter variants observed in this study suggest heterogeneity in expression under different bacterial culture conditions and a new link between metabolism and acquired resistance.</p>

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Implications of gene expression heterogeneity in the interplay between acquired resistance and bacterial metabolism

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年7月22日

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  • María Romero-Muñoz,
  • Marina R. Pulido,
  • Esther Recacha,
  • Sara Díaz-Díaz,
  • Marina Murillo-Torres,
  • Fernando Docobo-Pérez,
  • José Manuel Rodríguez-Martínez

摘要

Gene expression heterogeneity has an impact on human bacterial pathogens responses, including antimicrobial resistance genes expression. Promoter region variability in resistance genes may include different regulatory boxes involved in metabolic processes essential for bacterial survival. In this study, a molecular tool was developed to characterize promoter region variability and resistance gene expression. For these, 46 bacterial clinical isolates were used. Sequence analysis of resistance genes promoter region showed the existence of different variants for each promoter and identified gene-specific regulatory boxes. Using a fluorescent transcriptional reporter, we analysed the most common promoter variants of the most prevalent acquired resistance genes in clinical isolates (qnrA, qnrB, blaOXA-48, blaKPC-3 and blaVIM-1, aac(6’)-Ib-cr, and fosA). Gene expression fluctuations were found to be dependent on culture medium used. Specific gene promoter variants showed lower expression levels in poor (M9) medium (p < 0.0001) and an induction of expression under antimicrobials presence (tetracycline, quinolones and beta-lactams). qnrB1 genes were regulated by phoB and lexA boxes; blaOXA-48 was regulated by the argR box or fnr and arcA boxes. Differences in regulation of resistance gene promoter variants observed in this study suggest heterogeneity in expression under different bacterial culture conditions and a new link between metabolism and acquired resistance.