Within-host adaptation mutations associated with persistent colonization of Pseudomonas aeruginosa in a silicosis patient
Year: 2026
Type: article
Abstract: Pseudomonas aeruginosa is a notorious opportunistic pathogen that causes life-threatening infections in immunocompromised individuals. In this study, we isolated two mucoid imipenem-resistant P. aeruginosa strains, SCPa14 and SCPa16, from a single silicosis patient. Whole-genome sequencing revealed that these two strains are homologous, both of which belong to the epidemic high-risk clone ST274. Gene sequence analysis identified a deletion mutation (ΔG 433) of the mucA gene and a premature stop mutation in the oprD gene in SCPa14 and SCPa16; these mutations are assumed to be responsible for their mucoid phenotype and imipenem resistance, respectively. Compared to the reference strain PAO1, both strains showed slow growth, reduced cell motility, increased pyocyanin production, and enhanced H 2 O 2 resistance, which may collectively aid their adaptation to the respiratory tract environment. SCPa14 had impaired biofilm formation, which may be attributed to a premature termination mutation in its relA gene. In contrast, SCPa16 exhibited enhanced biofilm formation—a trait that may explain its persistence within the host. However, both strains showed poor growth under iron-restriction stress, which likely results from their lack of pyoverdine genes; they also exhibited impaired resistance to the antimicrobial peptide LL-37 and serum complement. Consistent with these traits, SCPa14 and SCPa16 were identified as low-virulence strains using the G. mellonella infection experiment. Overall, these data improve understanding of the adaptive strategies and fitness costs of P. aeruginosa during chronic infection in the silicosis patient, which offers new insights for antimicrobial therapy.
Institution: Southwest Medical University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,801
Award: G8476175517
OpenAlex ID: W7129339952