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DksA is a conserved master regulator of stress response in Acinetobacter baumannii. | LitMetric

AI Article Synopsis

  • - The study focuses on how bacteria, specifically Acinetobacter baumannii, survive in tough environments and cause infections, despite lacking a key stress response regulator called RpoS, which is found in other bacteria like E. coli.
  • - Researchers discovered that a different regulator, DksA, plays a crucial role in helping A. baumannii manage various stresses and boost its ability to infect hosts, impacting everything from ribosomal protein synthesis to antibiotic resistance.
  • - DksA is highly conserved among related bacterial families, indicating its importance, and this research provides a foundation for understanding its role in stress responses and pathogenicity in A. baumannii.

Article Abstract

Coordination of bacterial stress response mechanisms is critical for long-term survival in harsh environments for successful host infection. The general and specific stress responses of well-studied Gram-negative pathogens like Escherichia coli are controlled by alternative sigma factors, archetypically RpoS. The deadly hospital pathogen Acinetobacter baumannii is notoriously resistant to environmental stresses, yet it lacks RpoS, and the molecular mechanisms driving this incredible stress tolerance remain poorly defined. Here, using functional genomics, we identified the transcriptional regulator DksA as a master regulator for broad stress protection and virulence in A. baumannii. Transcriptomics, phenomics and in vivo animal studies revealed that DksA controls ribosomal protein expression, metabolism, mutation rates, desiccation, antibiotic resistance, and host colonization in a niche-specific manner. Phylogenetically, DksA was highly conserved and well-distributed across Gammaproteobacteria, with 96.6% containing DksA, spanning 88 families. This study lays the groundwork for understanding DksA as a major regulator of general stress response and virulence in this important pathogen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325922PMC
http://dx.doi.org/10.1093/nar/gkad341DOI Listing

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