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Background <p>Competence for natural transformation enables bacteria to acquire extracellular DNA and incorporate it into their genome, driving genetic diversification, DNA repair, and adaptation. While the regulatory mechanisms of competence development are well characterized in model organisms such as <i>Bacillus subtilis</i> and <i>Streptococcus pneumoniae</i>, little is known about how this process is controlled in <i>Actinomycetota</i>. Here, we investigate competence development in <i>Micrococcus luteus</i>, a high-GC Gram-positive species historically recognized for natural transformation.</p> Results <p>Using transformation frequency assays, transcriptional reporters, single-cell flow cytometry, and fluorescence microscopy, we show that in this actinobacterial model competence is consistent with a probabilistic regulatory strategy that integrates cell density, nutrient-limitation-responsive signals, and physiological state. Peak transformation occurs during exponential growth in minimal medium at moderate inoculation densities, whereas both low and high starting densities suppress competence. Although transcription of the late competence genes <i>comEA/EC</i> is induced under competence-promoting conditions, this activation does not always correlate with transformability, indicating additional post-transcriptional or physiological regulation. Single-cell analyses revealed that promoter activity develops gradually and heterogeneously across the population, lacking the bistability or strong population-level coordination observed in other well-studied Gram-positive model systems.</p> Conclusions <p>These data characterize competence induction dynamics in <i>M. luteus</i> and expand our understanding of the diversity of competence regulation across bacteria. While these observations constrain plausible regulatory models—supporting density- and nutrient-sensitive, probabilistic induction with heterogeneous single-cell activation—the upstream signal(s) or regulatory cascade controlling competence in <i>M. luteus</i> remain to be identified. Together, the results suggest that high-GC Gram-positive <i>Actinomycetota</i> may employ distinct, potentially bet-hedging-like strategies to balance growth, stress responses, and horizontal gene transfer.</p>

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Cell density and single-cell heterogeneity reveal distinct competence induction dynamics in the high-GC Gram-positive Micrococcus luteus

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月22日

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  • Antoni Lichev,
  • Angel Angelov,
  • Wolfgang Liebl

摘要

Background

Competence for natural transformation enables bacteria to acquire extracellular DNA and incorporate it into their genome, driving genetic diversification, DNA repair, and adaptation. While the regulatory mechanisms of competence development are well characterized in model organisms such as Bacillus subtilis and Streptococcus pneumoniae, little is known about how this process is controlled in Actinomycetota. Here, we investigate competence development in Micrococcus luteus, a high-GC Gram-positive species historically recognized for natural transformation.

Results

Using transformation frequency assays, transcriptional reporters, single-cell flow cytometry, and fluorescence microscopy, we show that in this actinobacterial model competence is consistent with a probabilistic regulatory strategy that integrates cell density, nutrient-limitation-responsive signals, and physiological state. Peak transformation occurs during exponential growth in minimal medium at moderate inoculation densities, whereas both low and high starting densities suppress competence. Although transcription of the late competence genes comEA/EC is induced under competence-promoting conditions, this activation does not always correlate with transformability, indicating additional post-transcriptional or physiological regulation. Single-cell analyses revealed that promoter activity develops gradually and heterogeneously across the population, lacking the bistability or strong population-level coordination observed in other well-studied Gram-positive model systems.

Conclusions

These data characterize competence induction dynamics in M. luteus and expand our understanding of the diversity of competence regulation across bacteria. While these observations constrain plausible regulatory models—supporting density- and nutrient-sensitive, probabilistic induction with heterogeneous single-cell activation—the upstream signal(s) or regulatory cascade controlling competence in M. luteus remain to be identified. Together, the results suggest that high-GC Gram-positive Actinomycetota may employ distinct, potentially bet-hedging-like strategies to balance growth, stress responses, and horizontal gene transfer.