Seattle Children's Hospital, Seattle, WA, United States.
Department of Pediatrics, University of Washington, Seattle, WA, United States.
Front Cell Infect Microbiol. 2021 Aug 20;11:699506. doi: 10.3389/fcimb.2021.699506. eCollection 2021.
Understanding the etiology of cerebrospinal fluid (CSF) shunt infections and reinfections requires detailed characterization of associated microorganisms. Traditionally, identification of bacteria present in the CSF has relied on culture methods, but recent studies have used high throughput sequencing of 16S rRNA genes. Here we evaluated the method of shotgun DNA sequencing for its potential to provide additional genomic information. CSF samples were collected from 3 patients near the beginning and end of each of 2 infection episodes. Extracted total DNA was sequenced by: (1) whole genome amplification followed by shotgun sequencing (WGA) and (2) high-throughput sequencing of the 16S rRNA V4 region (16S). Taxonomic assignments of sequences from WGA and 16S were compared with one another and with conventional microbiological cultures. While classification of bacteria was consistent among the 3 approaches, WGA provided additional insights into sample microbiological composition, such as showing relative abundances of microbial versus human DNA, identifying samples of questionable quality, and detecting significant viral load in some samples. One sample yielded sufficient non-human reads to allow assembly of a high-quality genome, denoted CLIMB1, which we characterized in terms of its MLST profile, gene complement (including putative antimicrobial resistance genes), and similarity to other annotated genomes. Our results demonstrate that WGA directly applied to CSF is a valuable tool for the identification and genomic characterization of dominant microorganisms in CSF shunt infections, which can facilitate molecular approaches for the development of better diagnostic and treatment methods.
了解脑脊液 (CSF) 分流感染和再感染的病因需要对相关微生物进行详细的特征描述。传统上,CSF 中存在的细菌的鉴定依赖于培养方法,但最近的研究已经使用了 16S rRNA 基因的高通量测序。在这里,我们评估了 shotgun DNA 测序方法在提供额外基因组信息方面的潜力。从 3 名患者的 CSF 样本在每个感染发作的开始和结束时收集。提取的总 DNA 进行测序:(1)全基因组扩增后进行 shotgun 测序 (WGA) 和 (2) 16S rRNA V4 区 (16S) 的高通量测序。WGA 和 16S 的序列的分类分配彼此进行了比较,并与传统微生物培养进行了比较。虽然细菌的分类在这 3 种方法中是一致的,但 WGA 提供了有关样本微生物组成的更多见解,例如显示微生物与人类 DNA 的相对丰度、确定样本质量可疑,以及在一些样本中检测到显著的病毒载量。一个样本产生了足够的非人类读数,允许组装一个高质量的基因组,称为 CLIMB1,我们根据其 MLST 图谱、基因组成 (包括假定的抗生素耐药基因) 和与其他注释基因组的相似性对其进行了特征描述。我们的结果表明,直接应用于 CSF 的 WGA 是识别和基因组表征 CSF 分流感染中主要微生物的有价值工具,这有助于开发更好的诊断和治疗方法的分子方法。