RpoN (sigma factor 54) contributes to bacterial fitness during tracheal colonization of Bordetella bronchiseptica.
Xingyan MaDendi Krisna NugrahaYukihiro HiramatsuYasuhiko HoriguchiPublished in: Microbiology and immunology (2023)
The Gram-negative pathogenic bacterium Bordetella bronchiseptica is a respiratory pathogen closely related to Bordetella pertussis, the causative agent of whooping cough. Despite sharing homologous virulence factors, B. bronchiseptica infects a broad range of mammalian hosts, including some experimental animals, whereas B. pertussis is strictly adapted to humans. Therefore, B. bronchiseptica is often used as a representative model to explore the pathogenicity of Bordetella in infection experiments with laboratory animals. Although Bordetella virulence factors, including toxins and adhesins have been studied well, our recent study implied that unknown virulence factors are involved in tracheal colonization and infection. Here, we investigated bacterial genes contributing to tracheal colonization by high-throughput transposon sequencing (Tn-seq). After the screening, we picked up 151 candidate genes of various functions and found that a rpoN-deficient mutant strain was defective in tracheal colonization when co-inoculated with the wild-type strain. rpoN encodes σ 54 , a sigma factor that regulates the transcription of various genes, implying its contribution to various bacterial activities. In fact, we found RpoN of B. bronchiseptica is involved in bacterial motility and initial biofilm formation. From these results, we propose that RpoN supports bacterial colonization by regulating various bacteriological functions.
Keyphrases
- biofilm formation
- pseudomonas aeruginosa
- staphylococcus aureus
- candida albicans
- escherichia coli
- wild type
- gram negative
- high throughput
- genome wide
- single cell
- multidrug resistant
- cystic fibrosis
- physical activity
- dna damage
- antimicrobial resistance
- dna methylation
- cross sectional
- rna seq
- body composition
- health information
- mass spectrometry
- genome wide identification