Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, New York, USA.
Department of Medicine, Infectious Diseases, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York, USA.
mBio. 2018 Oct 23;9(5):e02007-18. doi: 10.1128/mBio.02007-18.
We report a platform that increases the sensitivity of high-throughput sequencing for detection and characterization of bacteria, virulence determinants, and antimicrobial resistance (AMR) genes. The system uses a probe set comprised of 4.2 million oligonucleotides based on the Pathosystems Resource Integration Center (PATRIC) database, the Comprehensive Antibiotic Resistance Database (CARD), and the Virulence Factor Database (VFDB), representing 307 bacterial species that include all known human-pathogenic species, known antimicrobial resistance genes, and known virulence factors, respectively. The use of bacterial capture sequencing (BacCapSeq) resulted in an up to 1,000-fold increase in bacterial reads from blood samples and lowered the limit of detection by 1 to 2 orders of magnitude compared to conventional unbiased high-throughput sequencing, down to a level comparable to that of agent-specific real-time PCR with as few as 5 million total reads generated per sample. It detected not only the presence of AMR genes but also biomarkers for AMR that included both constitutive and differentially expressed transcripts. BacCapSeq is a method for differential diagnosis of bacterial infections and defining antimicrobial sensitivity profiles that has the potential to reduce morbidity and mortality, health care costs, and the inappropriate use of antibiotics that contributes to the development of antimicrobial resistance.
我们报告了一个平台,该平台提高了高通量测序检测和鉴定细菌、毒力决定因素和抗生素耐药性(AMR)基因的灵敏度。该系统使用了基于 Pathosystems Resource Integration Center(PATRIC)数据库、Comprehensive Antibiotic Resistance Database(CARD)和 Virulence Factor Database(VFDB)的探针集,包含 420 万个寡核苷酸,分别代表 307 种细菌,其中包括所有已知的人类致病菌、已知的抗生素耐药基因和已知的毒力因子。使用细菌捕获测序(BacCapSeq)可使血液样本中的细菌读数增加 1000 倍,与传统的非靶向高通量测序相比,检测下限降低了 1 到 2 个数量级,低至与每个样本生成的总读数低至 500 万时,与特定于试剂的实时 PCR 相当。它不仅可以检测 AMR 基因的存在,还可以检测 AMR 的生物标志物,包括组成型和差异表达的转录本。BacCapSeq 是一种用于细菌感染的鉴别诊断和定义抗生素敏感性特征的方法,具有降低发病率和死亡率、医疗保健成本以及减少导致抗生素耐药性发展的抗生素不合理使用的潜力。