Acquisition, co-option, and duplication of the rtx toxin system and the emergence of virulence in Kingella

Daniel P. Morreale, Eric A. Porsch, Brad K. Kern, Joseph W. Geme and Paul J. Planet ()
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Daniel P. Morreale: University of Pennsylvania
Eric A. Porsch: Children’s Hospital of Philadelphia
Brad K. Kern: University of Pennsylvania
Joseph W. Geme: University of Pennsylvania
Paul J. Planet: University of Pennsylvania

Nature Communications, 2023, vol. 14, issue 1, 1-15

Abstract: Abstract The bacterial genus Kingella includes two pathogenic species, namely Kingella kingae and Kingella negevensis, as well as strictly commensal species. Both K. kingae and K. negevensis secrete a toxin called RtxA that is absent in the commensal species. Here we present a phylogenomic study of the genus Kingella, including new genomic sequences for 88 clinical isolates, genotyping of another 131 global isolates, and analysis of 52 available genomes. The phylogenetic evidence supports that the toxin-encoding operon rtxCA was acquired by a common ancestor of the pathogenic Kingella species, and that a preexisting type-I secretion system was co-opted for toxin export. Subsequent genomic reorganization distributed the toxin machinery across two loci, with 30-35% of K. kingae strains containing two copies of the rtxA toxin gene. The rtxA duplication is largely clonal and is associated with invasive disease. Assays with isogenic strains show that a single copy of rtxA is associated with reduced cytotoxicity in vitro. Thus, our study identifies key steps in the evolutionary transition from commensal to pathogen, including horizontal gene transfer, co-option of an existing secretion system, and gene duplication.

Date: 2023
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DOI: 10.1038/s41467-023-39939-8

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