AI Article Synopsis

  • MABS, a pathogenic bacterium linked to severe lung infections, particularly in cystic fibrosis patients, has smooth and rough morphotypes influenced by glycopeptidolipids (GPLs) on its surface.
  • This study aimed to explore the relationship between MABS morphotypes, GPL levels, and infectivity by analyzing strains from cystic fibrosis patients, revealing that about 50% had mixed morphologies and that smooth strains exhibited a consistent GPL-morphotype relationship.
  • Findings showed that rough clinical strains replicated more effectively in macrophages compared to smooth strains, with a higher rate of infection, indicating significant differences between clinical and laboratory strains in terms of infectivity, underscoring the complexity of MABS

Article Abstract

(MABS) is a pathogenic bacterium that can cause severe lung infections, particularly in individuals with cystic fibrosis. MABS colonies can exhibit either a smooth (S) or rough (R) morphotype, influenced by the presence or absence of glycopeptidolipids (GPLs) on their surface, respectively. Despite the clinical significance of these morphotypes, the relationship between GPL levels, morphotype and the pathogenesis of MABS infections remains poorly understood. The mechanisms and implications of GPL production and morphotypes in clinical MABS infections are unclear. There is a gap in understanding their correlation with infectivity and pathogenicity, particularly in patients with underlying lung disease. This study aimed to investigate the correlation between MABS morphology, GPL and infectivity by analysing strains from cystic fibrosis patients' sputum samples. MABS was isolated from patient sputum samples and categorized by morphotype, GPL profile and replication rate in macrophages. A high-content ex vivo infection model using THP-1 cells assessed the infectivity of both clinical and laboratory strains. Our findings revealed that around 50 % of isolates displayed mixed morphologies. GPL analysis confirmed a consistent relationship between GPL content and morphotype that was only found in smooth isolates. Across morphotype groups, no differences were observed , yet clinical R strains were observed to replicate at higher levels in the THP-1 infection model. Moreover, the proportion of infected macrophages was notably higher among clinical R strains compared to their S counterparts at 72 h post-infection. Clinical variants also infected THP-1 cells at significantly higher rates compared to laboratory strains, highlighting the limited translatability of lab strain infection data to clinical contexts. Our study confirmed the general correlation between morphotype and GPL levels in smooth strains yet unveiled more variability within morphotype groups than previously recognized, particularly during intracellular infection. As the R morphotype is the highest clinical concern, these findings contribute to the expanding knowledge base surrounding MABS infections, offering insights that can steer diagnostic methodologies and treatment approaches.

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Source
http://dx.doi.org/10.1099/jmm.0.001869DOI Listing

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