Abstract

Natural competence allows bacteria to respond to environmental and nutritional cues by taking up free DNA from their surroundings, thus gaining both nutrients and genetic information. In the Gram-negative bacterium Haemophilus influenzae, the genes needed for DNA uptake are induced by the CRP and Sxy transcription factors in response to lack of preferred carbon sources and nucleotide precursors. Here we show that one of these genes, HI0659, encodes the antitoxin of a competence-regulated toxin-antitoxin operon (‘toxTA’), likely acquired by horizontal gene transfer from a Streptococcus species. Deletion of the putative toxin (HI0660) restores uptake to the antitoxin mutant. The full toxTA operon was present in only 17 of the 181 strains we examined; complete deletion was seen in 22 strains and deletions removing parts of the toxin gene in 142 others. In addition to the expected Sxy- and CRP-dependent-competence promoter, HI0659/660 transcript analysis using RNA-seq identified an internal antitoxin-repressed promoter whose transcription starts within toxT and will yield nonfunctional protein. We propose that the most likely effect of unopposed toxin expression is non-specific cleavage of mRNAs and arrest or death of competent cells in the culture. Although the high frequency of toxT and toxTA deletions suggests that this competence-regulated toxin-antitoxin system may be mildly deleterious, it could also facilitate downregulation of protein synthesis and recycling of nucleotides under starvation conditions. Although our analyses were focused on the effects of toxTA, the RNA-seq dataset will be a useful resource for further investigations into competence regulation.

Highlights

  • Bacterial toxin-antitoxin gene pairs were originally discovered on plasmids, where they function to promote plasmid persistence by killing any daughter cells that have not inherited the plasmid

  • The HI0659 protein is annotated in NCBI as containing a helix-turn-helix-XRE DNA-binding domain, which is commonly found in promoterbinding antitoxins [14]

  • The Phyre2 modelling software predicts that the best match of known structure for HI0660 is the HigB toxin of Streptococcus pneumoniae (100% confidence across 95% of the protein sequence), and the best match for HI0659 is the HigA antitoxin of Streptococcus pneumoniae (99.9% confidence across 92% of the protein sequence) [15]

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Summary

Introduction

Bacterial toxin-antitoxin gene pairs were originally discovered on plasmids, where they function to promote plasmid persistence by killing any daughter cells that have not inherited the plasmid. The resulting rise in cyclic AMP (cAMP) activates the transcription factor CRP, and the CRP/cAMP complex stimulates transcription of genes with canonical CRP-promoter elements (CRP-N genes) Most of these genes help the cell to use alternative carbon sources, but one encodes the competence-specific transcriptional activator Sxy. efficient translation of sxy mRNA occurs only when purine pools are depleted [9,10]. Efficient translation of sxy mRNA occurs only when purine pools are depleted [9,10] If both signals are active, Sxy acts with CRP at the promoters of competence genes, stimulating their transcription and leading to DNA uptake and natural transformation. As is common in competence systems, only some of the cells in the population become competent (typically 10–50%)

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