| Literature DB >> 32366575 |
Adam M Pickrum1, Orlando DeLeon1, Aaron Dirck1, Maxx H Tessmer1, Molly O Riegert1, Julie A Biller2, Nathan A Ledeboer3, John R Kirby1, Dara W Frank4.
Abstract
Achromobacter xylosoxidans is increasingly recognized as a colonizer of cystic fibrosis (CF) patients, but the role that A. xylosoxidans plays in pathology remains unknown. This knowledge gap is largely due to the lack of model systems available to study the toxic potential of this bacterium. Recently, a phospholipase A2 (PLA2) encoded by a majority of A. xylosoxidans genomes, termed AxoU, was identified. Here, we show that AxoU is a type III secretion system (T3SS) substrate that induces cytotoxicity to mammalian cells. A tissue culture model was developed showing that a subset of A. xylosoxidans isolates from CF patients induce cytotoxicity in macrophages, suggestive of a pathogenic or inflammatory role in the CF lung. In a toxic strain, cytotoxicity is correlated with transcriptional activation of axoU and T3SS genes, demonstrating that this model can be used as a tool to identify and track expression of virulence determinants produced by this poorly understood bacterium.Entities:
Keywords: Achromobacter pathogenesis; T3SS; cystic fibrosis; cytotoxicity; phagocytic cells
Year: 2020 PMID: 32366575 PMCID: PMC7309624 DOI: 10.1128/IAI.00136-20
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441