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. 2025 Apr 9;25(1):203.
doi: 10.1186/s12866-025-03920-w.

Unveiling the molecular epidemiology of Pseudomonas aeruginosa in lung infections among cystic fibrosis patients in the Brazilian Amazon

Affiliations

Unveiling the molecular epidemiology of Pseudomonas aeruginosa in lung infections among cystic fibrosis patients in the Brazilian Amazon

Maria Isabel Montoril Gouveia et al. BMC Microbiol. .

Abstract

Background: Pseudomonas aeruginosa is a major pathogen in cystic fibrosis (CF), where chronic and intermittent infections significantly affect patient outcomes. This study aimed to investigate the molecular epidemiology of P. aeruginosa in CF patients from the Brazilian Amazon, focusing on genotypic diversity, resistance profiles, and virulence factors.

Methods: A cross-sectional study included 72 P. aeruginosa isolates from 44 CF patients treated at a regional reference center between 2018 and 2019. Antimicrobial susceptibility patterns were determined using VITEK-2 system and Kirby-Bauer disk diffusion. Virulotypes were defined by molecular detection of exoS, exoU, exoT, exoY, algU, and algD genes. Genetic diversity was assessed using multilocus sequence typing (MLST). Demographic data, clinical severity, and spirometry results were also collected.

Results: Among the patients, 54.55% experienced intermittent infections, while 45.45% had chronic infections. Chronic infections were associated with older age, lower FEV1, and reduced Shwachman-Kulczycki scores. Multidrug resistance was observed in 15.3% of isolates, particularly against ciprofloxacin and piperacillin/tazobactam. The exoU gene was present in 55.56% of isolates, an uncommon finding in CF populations. High genetic diversity was evident, with 37 sequence types (STs), including 14 novel STs. High-risk clones (HRCs) constituted 25% of isolates, with ST274 being the most prevalent (12.5%). Longitudinal analysis revealed transient colonization in intermittent infections, while chronic infections were dominated by stable clones.

Conclusion: This study highlights the molecular and clinical dynamics of P. aeruginosa in CF patients from the Brazilian Amazon. Chronic infections were linked to severe lung impairment , while intermittent infections were dominated by HRCs. These findings underscore the need for robust genotypic surveillance to mitigate the burden of P. aeruginosa in CF populations.

Keywords: Pseudomonas aeruginosa; Antimicrobial Resistance; Brazil; Genotyping; Virulence.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: The samples included in this study were obtained during routine laboratory procedures at the CF reference center. Consent for participation was obtained from all included patients upon written signature of informed consent form. All data collection and experiments related to this study were performed in accordance with Brazilian guidelines and regulations (Resolution CNS nº 196/96), as well as the Declaration of Helsinki. This study was approved by the Ethics Committee of the HUJBB/UFPA (Approval no. 1.910.716) and was registered with the National System for the Management of Genetic Heritage and Associated Traditional Knowledge (SisGen; registration no. AF44CCB). Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
goeBURST full MST of P. aeruginosa isolated from CF patients demonstrating unique STs and clonal complexes. Each node represents a unique ST and node size is proportional to the isolates related with that ST. Solid lines between STs shaded in grey represents SLVs and belong to CCs, and dashed lines between STs represents double locus variants DLVs
Fig. 2
Fig. 2
Longitudinal distribution of P. aeruginosa Sequence Types (STs) in CF patients with intermittent and chronic infections. Legend: ST: sequence type; Virulotype. V1: exoS ( +); exoU ( +); exoT ( +); exoY ( +); algD ( +); algU ( +); V2: exoS ( +); exoU (-); exoT ( +); exoY ( +); algD ( +); algU ( +); V3: exoS ( +); exoU (-); exoT (-); exoY ( +); algD ( +); algU ( +). Resistance pattern: MultiS: Multi susceptive; ModR: Moderate resistant; MDR: Multidrug resistant

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