Esoteric Testing/R&D Laboratory, Tampa General Hospital, Tampa, Florida.
Esoteric Testing/R&D Laboratory, Tampa General Hospital, Tampa, Florida.
J Mol Diagn. 2020 Dec;22(12):1419-1429. doi: 10.1016/j.jmoldx.2020.09.003. Epub 2020 Sep 19.
Bacterial whole-genome sequencing (WGS) provides clinical and public health laboratories an unprecedented level of information on species identification, antimicrobial resistance, and epidemiologic typing. However, multiple barriers to widespread adoption still exist. This research describes bacterial WGS using the Illumina iSeq 100 instrument to overcome some of these barriers. Using an in-house, high-quality single-nucleotide polymorphism analysis pipeline and a commercial whole-genome multilocus sequence typing program, the sequencing of Acinetobacter baumannii, Burkholderia cepacia, Clostridioides difficile, Enterococcus faecalis, Escherichia coli, Pseudomonas aeruginosa, Serratia marcescens, and Staphylococcus aureus isolates was validated. The genome coverage range was 17× to 149×, with a mean of 59×. The limit of detection for single-nucleotide polymorphisms was 30×. Overall platform base calling accuracy was >99.999%. Reproducibility and repeatability of base calling inferred from whole-genome multilocus sequence typing was species dependent and ranged from >97% similarity for P. aeruginosa to >99.9% similarity for S. aureus. Resistance gene and multilocus sequence typing allele identification was 100% concordant with expected results. A simple, modified library preparation reduces the per-sample cost by half to give overall theoretical sample costs ranging from approximately $50 to $100 for library preparation and sequencing. The iSeq 100 provides a cost-effective and easy-to-use platform for clinical and public health laboratories to sequence bacterial isolates for a wide range of potential applications.
细菌全基因组测序(WGS)为临床和公共卫生实验室提供了前所未有的物种鉴定、抗菌药物耐药性和流行病学分型信息。然而,广泛采用仍然存在多种障碍。本研究描述了使用 Illumina iSeq 100 仪器进行细菌 WGS 的方法,以克服其中的一些障碍。使用内部高质量的单核苷酸多态性分析管道和商业全基因组多位点序列分型程序,对鲍曼不动杆菌、洋葱伯克霍尔德菌、艰难梭菌、粪肠球菌、大肠杆菌、铜绿假单胞菌、粘质沙雷氏菌和金黄色葡萄球菌分离株的测序进行了验证。基因组覆盖范围为 17×至 149×,平均为 59×。单核苷酸多态性的检测限为 30×。总体平台碱基调用准确率>99.999%。基于全基因组多位点序列分型推断的碱基调用的重现性和可重复性取决于物种,铜绿假单胞菌的相似度>97%,金黄色葡萄球菌的相似度>99.9%。耐药基因和多位点序列分型等位基因的鉴定与预期结果完全一致。一种简单的改良文库制备方法将每个样本的成本降低了一半,理论上每个样本的文库制备和测序成本约为 50 至 100 美元。iSeq 100 为临床和公共卫生实验室提供了一种具有成本效益且易于使用的平台,可用于对各种潜在应用的细菌分离物进行测序。