Department of Surgery, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9160, USA.
Surg Infect (Larchmt). 2013 Jun;14(3):275-82. doi: 10.1089/sur.2012.095. Epub 2013 May 6.
We examined the microbiota of bronchoalveolar lavage (BAL) samples with next-generation sequencing (NGS) technology to determine whether its results correlate with those of standard culture methods or affect patient outcome or both.
We collected BAL samples in the surgical intensive care unit (SICU) as part of the standard of care for intubated individuals who had a Clinical Pulmonary Infection Score (CPIS)≥6 points. A portion of the BAL fluid was sequenced for the 16S region of ribosomal deoxyribonucleic acid (rDNA) with the Roche 454 FLX Titanium sequencer. Sequences were analyzed through a data-analysis pipeline to identify the appropriate taxonomic designation (∼species) of each 16s sequence. The bacterial microbiota of each BAL sample was compared with the bacteria identified in the sample through standard culture methods. Correlations between the taxonomic diversity of the microbiota and clinical outcome were examined through linear regression and Pearson correlation.
Bronchoalveolar lavage samples from 12 individuals in the SICU who had a CPIS≥6 points were examined through 454 pyrosequencing. The number of phylotypes (∼species) in the samples ranged from 15 to 129. The number of phyla in the BAL samples ranged from 3 to 14. There was little correlation between the bacteria identified by NGS and those identified with standard culture methods. The same predominant bacterial strain was identified by both culture and sequencing in only a single sample. The correlation between patient days on a ventilator and the number of species in BAL samples was significant (r=0.7435, p=0.0056; r2=0.5528).
Increasing diversity of the bacterial microbiota in BAL samples correlates with the duration of mechanical ventilation. Bacteria identified through standard culture methods were not well correlated with the findings of NGS.
我们使用下一代测序(NGS)技术检查支气管肺泡灌洗液(BAL)样本中的微生物群,以确定其结果是否与标准培养方法相关,或者是否影响患者的预后,或者两者兼而有之。
我们在外科重症监护病房(SICU)收集 BAL 样本,作为对 CPIS≥6 分的插管患者的标准护理的一部分。BAL 液体的一部分用 Roche 454 FLX Titanium 测序仪对核糖体脱氧核糖核酸(rDNA)的 16S 区进行测序。通过数据分析管道对序列进行分析,以确定每个 16s 序列的适当分类指定(约物种)。通过标准培养方法鉴定的细菌与每个 BAL 样本的细菌微生物群进行比较。通过线性回归和 Pearson 相关性分析来检查微生物群的分类多样性与临床结果之间的相关性。
对 SICU 中 CPIS≥6 分的 12 名患者的 BAL 样本进行了 454 焦磷酸测序。样本中的菌型(约物种)数量从 15 到 129 不等。BAL 样本中的菌门数量从 3 到 14 不等。NGS 鉴定的细菌与标准培养方法鉴定的细菌之间几乎没有相关性。只有一个样本通过培养和测序同时鉴定出相同的主要细菌菌株。患者在呼吸机上的天数与 BAL 样本中的物种数量之间存在显著相关性(r=0.7435,p=0.0056;r2=0.5528)。
BAL 样本中细菌微生物群的多样性增加与机械通气的持续时间相关。通过标准培养方法鉴定的细菌与 NGS 的结果相关性不佳。