Virginia Pichler, Lara Dalkilic, Ghazaleh Shoaib, Tirosh Shapira, Leah Rankine-Wilson, Yves-Marie Boudehen, Joseph D Chao, Danielle Sexton, Miguel Prieto, Bradley S Quon, Elitza I Tocheva, Laurent Kremer, William Hsiao, Yossef Av-Gay
{"title":"临床脓肿分枝杆菌分离物在形态、糖肽类脂和巨噬细胞模型感染率方面的多样性。","authors":"Virginia Pichler, Lara Dalkilic, Ghazaleh Shoaib, Tirosh Shapira, Leah Rankine-Wilson, Yves-Marie Boudehen, Joseph D Chao, Danielle Sexton, Miguel Prieto, Bradley S Quon, Elitza I Tocheva, Laurent Kremer, William Hsiao, Yossef Av-Gay","doi":"10.1099/jmm.0.001869","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction.</b> <i>Mycobacterium abscessus</i> (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.<b>Gap statement.</b> 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.<b>Aim.</b> This study aimed to investigate the correlation between MABS morphology, GPL and infectivity by analysing strains from cystic fibrosis patients' sputum samples.<b>Methodology.</b> 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.<b>Results.</b> 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 <i>in vitro</i>, 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.<b>Conclusion.</b> 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.</p>","PeriodicalId":94093,"journal":{"name":"Journal of medical microbiology","volume":"73 8","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The diversity of clinical <i>Mycobacterium abscessus</i> isolates in morphology, glycopeptidolipids and infection rates in a macrophage model.\",\"authors\":\"Virginia Pichler, Lara Dalkilic, Ghazaleh Shoaib, Tirosh Shapira, Leah Rankine-Wilson, Yves-Marie Boudehen, Joseph D Chao, Danielle Sexton, Miguel Prieto, Bradley S Quon, Elitza I Tocheva, Laurent Kremer, William Hsiao, Yossef Av-Gay\",\"doi\":\"10.1099/jmm.0.001869\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction.</b> <i>Mycobacterium abscessus</i> (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.<b>Gap statement.</b> 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.<b>Aim.</b> This study aimed to investigate the correlation between MABS morphology, GPL and infectivity by analysing strains from cystic fibrosis patients' sputum samples.<b>Methodology.</b> 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.<b>Results.</b> 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 <i>in vitro</i>, 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.<b>Conclusion.</b> 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. 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引用次数: 0
摘要
导言。脓肿分枝杆菌(MABS)是一种致病细菌,可引起严重的肺部感染,尤其是在囊性纤维化患者中。脓肿分枝杆菌的菌落可呈现光滑(S)或粗糙(R)形态,这分别受其表面是否存在糖肽类脂(GPL)的影响。尽管这些形态具有临床意义,但人们对 GPL 水平、形态与 MABS 感染发病机制之间的关系仍然知之甚少。临床 MABS 感染中 GPL 生成和形态类型的机制和影响尚不清楚。对其与感染性和致病性的相关性,尤其是在有潜在肺部疾病的患者中的相关性的理解还存在差距。本研究旨在通过分析囊性纤维化患者痰液样本中的菌株,研究 MABS 形态、GPL 和感染性之间的相关性。从患者痰液样本中分离出 MABS,并根据形态、GPL 特征和在巨噬细胞中的复制率对其进行分类。使用 THP-1 细胞建立的高浓度体外感染模型评估了临床菌株和实验室菌株的感染性。我们的研究结果表明,约 50% 的分离株显示出混合形态。GPL 分析证实了 GPL 含量与形态之间的一致关系,这种关系只存在于光滑的分离株中。各形态组在体外未观察到差异,但在 THP-1 感染模型中观察到临床 R 型菌株的复制水平较高。此外,在感染后 72 小时,临床 R 型菌株感染巨噬细胞的比例明显高于 S 型菌株。与实验室菌株相比,临床变异株感染 THP-1 细胞的比例也明显更高,这突出表明实验室菌株感染数据在临床环境中的可转化性有限。我们的研究证实了平滑菌株中形态与 GPL 水平之间的普遍相关性,但也揭示了形态组内的变异性比以前认识到的更大,尤其是在细胞内感染期间。由于 R 形态是临床上最关注的问题,这些发现有助于扩大有关 MABS 感染的知识库,提供了可指导诊断方法和治疗方法的见解。
The diversity of clinical Mycobacterium abscessus isolates in morphology, glycopeptidolipids and infection rates in a macrophage model.
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.