Department of Civil & Environmental Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan, USA.
mBio. 2018 Feb 13;9(1):e02354-17. doi: 10.1128/mBio.02354-17.
Nontuberculous mycobacteria (NTM) frequently detected in drinking water (DW) include species associated with human infections, as well as species rarely linked to disease. Methods for improved the recovery of NTM DNA and high-throughput identification of NTM are needed for risk assessment of NTM infection through DW exposure. In this study, different methods of recovering bacterial DNA from DW were compared, revealing that a phenol-chloroform DNA extraction method yielded two to four times as much total DNA and eight times as much NTM DNA as two commercial DNA extraction kits. This method, combined with high-throughput, single-molecule real-time sequencing of NTM genes, allowed the identification of NTM to the species, subspecies, and (in some cases) strain levels. This approach was applied to DW samples collected from 15 households serviced by a chloraminated distribution system, with homes located in areas representing short (<24 h) and long (>24 h) distribution system residence times. Multivariate statistical analysis revealed that greater water age (i.e., combined distribution system residence time and home plumbing stagnation time) was associated with a greater relative abundance of subsp. , one of the most prevalent NTM causing infections in humans. DW from homes closer to the treatment plant (with a shorter water age) contained more diverse NTM species, including and Overall, our approach allows NTM identification to the species and subspecies levels and can be used in future studies to assess the risk of waterborne infection by providing insight into the similarity between environmental and infection-associated NTM. An extraction method for improved recovery of DNA from nontuberculous mycobacteria (NTM), combined with single-molecule real-time sequencing (PacBio) of NTM genes, was used for high-throughput characterization of NTM species and in some cases strains in drinking water (DW). The extraction procedure recovered, on average, eight times as much NTM DNA and three times as much total DNA from DW as two widely used commercial DNA extraction kits. The combined DNA extraction and sequencing approach allowed high-throughput screening of DW samples to identify NTM, revealing that the relative abundance of subsp. increased with water age. Furthermore, the two-step barcoding approach developed as part of the PacBio sequencing method makes this procedure highly adaptable, allowing it to be used for other target genes and species.
非结核分枝杆菌(NTM)经常在饮用水(DW)中检测到,包括与人类感染相关的物种,以及与疾病很少相关的物种。为了通过 DW 暴露评估 NTM 感染的风险,需要改进 NTM DNA 的回收方法和高通量鉴定 NTM 的方法。在这项研究中,比较了从 DW 中回收细菌 DNA 的不同方法,结果表明,酚-氯仿 DNA 提取方法比两种商业 DNA 提取试剂盒分别多提取 2 到 4 倍的总 DNA 和 8 倍的 NTM DNA。这种方法与 NTM 基因的高通量单分子实时测序相结合,可以鉴定 NTM 到种、亚种(在某些情况下)和菌株水平。该方法应用于由加氯分配系统服务的 15 户家庭的 DW 样本采集,家庭位于代表短(<24 小时)和长(>24 小时)分配系统停留时间的区域。多变量统计分析表明,更大的水龄(即,组合分配系统停留时间和家庭管道停滞时间)与相对丰度较高的 亚种有关,这是人类感染最常见的 NTM 之一。来自离处理厂更近的家庭(水龄更短)的 DW 含有更多不同的 NTM 物种,包括 和 。总体而言,我们的方法可以鉴定 NTM 到种和亚种水平,并可用于未来的研究,通过提供对环境和感染相关 NTM 之间相似性的深入了解,评估水传播感染的风险。一种用于从非结核分枝杆菌(NTM)中提高 DNA 回收率的提取方法,结合 NTM 基因的单分子实时测序(PacBio),用于高通量鉴定饮用水(DW)中的 NTM 物种,在某些情况下还可以鉴定菌株。该提取程序从 DW 中平均提取了 8 倍的 NTM DNA 和 3 倍的总 DNA,而两种广泛使用的商业 DNA 提取试剂盒。结合 DNA 提取和测序方法可以高通量筛选 DW 样本以鉴定 NTM,结果表明,水龄与 亚种的相对丰度增加有关。此外,作为 PacBio 测序方法的一部分开发的两步条形码方法使该程序具有高度的适应性,允许它用于其他目标基因和物种。