The diversity of clinical Mycobacterium abscessus isolates in morphology, glycopeptidolipids and infection rates in a macrophage model

Author:

Pichler Virginia12ORCID,Dalkilic Lara2,Shoaib Ghazaleh2,Shapira Tirosh2ORCID,Rankine-Wilson Leah2ORCID,Boudehen Yves-Marie1ORCID,Chao Joseph D.2ORCID,Sexton Danielle2,Prieto Miguel3,Quon Bradley S.3ORCID,Tocheva Elitza I.2ORCID,Kremer Laurent1ORCID,Hsiao William4ORCID,Av-Gay Yossef23ORCID

Affiliation:

1. INSERM, IRIM, 34293 Montpellier, France

2. Department of Microbiology and Immunology, Life Sciences Institute, University of British Columbia, Vancouver, Canada

3. Department of Medicine, University of British Columbia, Vancouver, Canada

4. Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, Canada

Abstract

Introduction. Mycobacterium abscessus (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. Gap statement. 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. Aim. This study aimed to investigate the correlation between MABS morphology, GPL and infectivity by analysing strains from cystic fibrosis patients’ sputum samples. Methodology. 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. Results. 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 in vitro, 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. Conclusion. 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.

Funder

University of British Columbia

Cystic Fibrosis Canada

Agence Nationale de la Recherche

Publisher

Microbiology Society

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