4.7 Article

Optimized Method for Bacterial Nucleic Acid Extraction from Positive Blood Culture Broth for Whole-Genome Sequencing, Resistance Phenotype Prediction, and Downstream Molecular Applications

期刊

JOURNAL OF CLINICAL MICROBIOLOGY
卷 60, 期 11, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/jcm.01012-22

关键词

blood culture broth; DNA extraction; host DNA depletion; Illumina; Nanopore; real-time PCR

资金

  1. Pathology Queensland Study, Education and Research Committee (SERC) [SERC 5891_HarrisP]
  2. Royal Brisbane and Women's Hospital Foundation
  3. National Health andMedical Research Council [GNT1157530]

向作者/读者索取更多资源

The application of direct metagenomic sequencing from positive blood culture broth holds promise in solving the challenges of sequencing low-bacterial-load blood samples in sepsis patients. This study compared the identification of species and prediction of susceptibility using metagenomic sequencing and a machine-learning algorithm to conventional methods and other diagnostic platforms. The results showed that direct metagenomic sequencing from blood cultures is feasible for pathogen detection and susceptibility prediction, and further optimization is needed for uncommon species and complex resistance genotypes.
The application of direct metagenomic sequencing from positive blood culture broth may solve the challenges of sequencing from low-bacterial-load blood samples in patients with sepsis. Forty prospectively collected blood culture broth samples growing Gram-negative bacteria were extracted using commercially available kits to achieve high-quality DNA. Species identification via metagenomic sequencing and susceptibility prediction via a machine-learning algorithm (AREScloud) were compared to conventional methods and other rapid diagnostic platforms (Accelerate Pheno and blood culture identification [BCID] panel). A two-kit method (using MolYsis Basic and Qiagen DNeasy UltraClean kits) resulted in optimal extractions. Taxonomic profiling by direct metagenomic sequencing matched conventional identification in 38/40 (95%) samples. In two polymicrobial samples, a second organism was missed by sequencing. Prediction models were able to accurately infer susceptibility profiles for 6 common pathogens against 17 antibiotics, with an overall categorical agreement (CA) of 95% (increasing to >95% for 5/6 of the most common pathogens, if Klebsiella oxytoca was excluded). The performance of whole-genome sequencing (WGS)-antimicrobial susceptibility testing (AST) was suboptimal for uncommon pathogens (e.g., Elizabethkingia) and some 0-lactamase inhibitor antibiotics (e.g, ticarcillin-clavulanate). The time to pathogen identification was the fastest with BCID (1 h from blood culture positivity). Accelerate Pheno provided a susceptibility result in approximately 8 h. IIlumina-based direct sequencing methods provided results in time frames similar to those of conventional culture-based methods. Direct metagenomic sequencing from blood cultures for pathogen detection and susceptibility prediction is feasible. Additional work is required to optimize algorithms for uncommon species and complex resistance genotypes as well as to streamline methods to provide more rapid results.

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