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囊性纤维化呼吸道样本中非结核分枝杆菌的非培养鉴定

Culture-Independent Identification of Nontuberculous Mycobacteria in Cystic Fibrosis Respiratory Samples.

作者信息

Caverly Lindsay J, Carmody Lisa A, Haig Sarah-Jane, Kotlarz Nadine, Kalikin Linda M, Raskin Lutgarde, LiPuma John J

机构信息

Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.

Department of Civil & Environmental Engineering, University of Michigan, Ann Arbor, Michigan, United States of America.

出版信息

PLoS One. 2016 Apr 19;11(4):e0153876. doi: 10.1371/journal.pone.0153876. eCollection 2016.

Abstract

Respiratory tract infections with nontuberculous mycobacteria (NTM) are increasing in prevalence and are a significant cause of lung function decline in individuals with cystic fibrosis (CF). NTM have been detected in culture-independent analyses of CF airway microbiota at lower rates than would be expected based on published prevalence data, likely due to poor lysing of the NTM cell wall during DNA extraction. We compared a standard bacterial lysis protocol with a modified method by measuring NTM DNA extraction by qPCR and NTM detection with bacterial 16S rRNA gene sequencing. The modified method improved NTM DNA recovery from spiked CF sputum samples by a mean of 0.53 log10 copies/mL for M. abscessus complex and by a mean of 0.43 log10 copies/mL for M. avium complex as measured by qPCR targeting the atpE gene. The modified method also improved DNA sequence based NTM detection in NTM culture-positive CF sputum and bronchoalveolar lavage samples; however, both qPCR and 16S rRNA gene sequencing remained less sensitive than culture for NTM detection. We highlight the limitations of culture-independent identification of NTM from CF respiratory samples, and illustrate how alterations in the bacterial lysis and DNA extraction process can be employed to improve NTM detection with both qPCR and 16S rRNA gene sequencing.

摘要

非结核分枝杆菌(NTM)引起的呼吸道感染患病率正在上升,是囊性纤维化(CF)患者肺功能下降的重要原因。在对CF气道微生物群进行的非培养分析中,检测到NTM的比率低于根据已发表的患病率数据预期的比率,这可能是由于DNA提取过程中NTM细胞壁裂解不佳所致。我们通过qPCR测量NTM DNA提取量,并使用细菌16S rRNA基因测序检测NTM,将标准细菌裂解方案与改良方法进行了比较。改良方法使加标的CF痰液样本中脓肿分枝杆菌复合群的NTM DNA回收率平均提高了0.53 log10拷贝/mL,通过靶向atpE基因的qPCR测量,鸟分枝杆菌复合群的NTM DNA回收率平均提高了0.43 log10拷贝/mL。改良方法还提高了NTM培养阳性的CF痰液和支气管肺泡灌洗样本中基于DNA序列的NTM检测率;然而,qPCR和16S rRNA基因测序在检测NTM方面仍然比培养法敏感性低。我们强调了从CF呼吸道样本中进行NTM非培养鉴定的局限性,并说明了如何通过改变细菌裂解和DNA提取过程,利用qPCR和16S rRNA基因测序来提高NTM检测率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a75f/4836755/faa88956ca9f/pone.0153876.g001.jpg

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