Role of viable but non culturable cells in patients with cystic fibrosis in the era of highly effective modulator therapy

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM Journal of Cystic Fibrosis Pub Date : 2024-11-01 DOI:10.1016/j.jcf.2024.02.013
Natalia Cirilli , Valentina Schiavoni , Valentina Tagliabracci , Rosaria Gesuita , Luca Tiano , Benedetta Fabrizzi , Anastasia D'Antuono , Arianna Peruzzi , Nicholas Cedraro , Flavia Carle , Marco Moretti , Luigi Ferrante , Carla Vignaroli , Francesca Biavasco , Gianmarco Mangiaterra
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Abstract

Background

Lung infections antibiotic treatment in Cystic Fibrosis patients (pwCF) is often complicated by bacterial persisters, including the so-called Viable but Non Culturable (VBNC) forms, live cells undetected by the routine cultural microbiological methods. This study investigated the occurrence of VBNC cells of five CF bacterial pathogens in 94 pwCF over one year and the possible associations with the patients’ clinical features.

Methods

Sputum samples, recovered at routine visits and during exacerbation episodes, were analyzed for the presence of the five pathogens by both routine culture-based assays and species-specific qPCR. VBNC cells were estimated as the difference between molecular and cultural counts and their presence was matched with the clinical data in particular the therapeutic regimens.

Results

All but ten pwCF showed the presence of VBNC cells at least once during the study. Pseudomonas aeruginosa and methicillin-susceptible Staphylococcus aureus were the species most frequently found in the VBNC state. Only the former showed a significant association between chronic infection and VBNC cells presence; VBNC-MSSA positive patients significantly increased overtime. The presence of non culturable bacteria was generally concurrent with poor lung functionality and more frequent pulmonary exacerbations. No significant association with modulator treatment was evidenced.

Conclusions

The obtained data demonstrated the overwhelming occurrence of bacterial VBNC cells in CF lung infections, warranting a constant monitoring of pwCF and underlining the need of implementing the routine culture-based assays with culture-independent techniques. This is pivotal to understand the CF bacterial population dynamics and to efficiently contrast the lung infection progression and worsening.
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高效调节剂疗法时代囊性纤维化患者体内可存活但不可培养的细胞的作用。
背景:囊性纤维化患者(pwCF)的肺部感染抗生素治疗通常会因细菌持久存在而变得复杂,包括所谓的 "可存活但不可培养(VBNC)"形式,即常规微生物培养方法无法检测到的活细胞。本研究调查了 94 名儿童肺结核患者一年内五种 CF 细菌病原体 VBNC 细胞的发生情况,以及与患者临床特征的可能关联:方法: 通过常规培养法和物种特异性 qPCR 分析在常规就诊和病情加重期间采集的痰液样本中是否存在五种病原体。VBNC 细胞是根据分子计数和培养计数的差值估算的,它们的存在与临床数据特别是治疗方案相匹配:结果:除 10 例 pwCF 外,其他所有 pwCF 在研究期间至少出现过一次 VBNC 细胞。铜绿假单胞菌和对甲氧西林敏感的金黄色葡萄球菌是在 VBNC 状态下最常发现的菌种。只有前者显示出慢性感染与 VBNC 细胞存在之间的显著关联;VBNC-MSSA 阳性患者随时间推移显著增加。不可培养细菌的存在通常与肺功能低下和更频繁的肺部恶化同时存在。结论:获得的数据表明,细菌 VBNC 细胞在 CF 肺部感染中的发生率极高,因此有必要对 pwCF 进行持续监测,并强调有必要使用独立于培养的技术进行常规培养检测。这对于了解 CF 细菌种群动态、有效对比肺部感染进展和恶化至关重要。
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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
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