Young E L, Roach D J, Martinsen M A, McGrath Geg, Holbrook N R, Cho H E, Seyoum E Y, Pierce V M, Bhattacharyya R P
The Broad Institute of MIT and Harvard, Boston, MA, USA.
Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA, USA.
medRxiv. 2024 Jul 10:2024.07.10.24310021. doi: 10.1101/2024.07.10.24310021.
Antimicrobial resistance is a growing health threat, but standard methods for determining antibiotic susceptibility are slow and can delay optimal treatment, which is especially consequential in severe infections such as bacteremia. Novel approaches for rapid susceptibility profiling have emerged that characterize either bacterial response to antibiotics (phenotype) or detect specific resistance genes (genotype). GoPhAST-R is a novel assay, performed directly on positive blood cultures, that integrates rapid transcriptional response profiling with detection of key resistance gene transcripts, thereby providing simultaneous data on both phenotype and genotype. Here, we performed the first clinical pilot of GoPhAST-R on 42 positive blood cultures: 26 growing , 15 growing , and 1 with both. An aliquot of each positive blood culture was exposed to 9 different antibiotics, lysed, then underwent rapid transcriptional profiling on the NanoString platform; results were analyzed using an in-house susceptibility classification algorithm. GoPhAST-R achieved 95% overall agreement with standard antimicrobial susceptibility testing methods, with the highest agreement for beta-lactams (98%) and the lowest for fluoroquinolones (88%). Epidemic resistance genes including the extended spectrum beta-lactamase and the carbapenemase were also detected within the population. This study demonstrates the clinical feasibility of using transcriptional response profiling for rapid resistance determination, although further validation with larger and more diverse bacterial populations will be essential in future work. GoPhAST-R represents a promising new approach for rapid and comprehensive antibiotic susceptibility testing in clinical settings.
抗菌药物耐药性对健康的威胁日益增大,但用于确定抗生素敏感性的标准方法耗时较长,可能会延误最佳治疗时机,这在诸如菌血症等严重感染中后果尤为严重。目前已出现了一些用于快速药敏分析的新方法,这些方法可对细菌对抗生素的反应(表型)进行特征分析,或检测特定的耐药基因(基因型)。GoPhAST-R是一种直接在阳性血培养物上进行的新型检测方法,它将快速转录反应分析与关键耐药基因转录本的检测相结合,从而同时提供表型和基因型数据。在此,我们对42份阳性血培养物进行了GoPhAST-R的首次临床试点:其中26份培养出 ,15份培养出 ,1份同时培养出这两种细菌。将每份阳性血培养物的一部分分别暴露于9种不同的抗生素,进行裂解,然后在NanoString平台上进行快速转录分析;使用内部药敏分类算法对结果进行分析。GoPhAST-R与标准抗菌药敏测试方法的总体一致性达到95%,其中对β-内酰胺类药物的一致性最高(98%),对氟喹诺酮类药物的一致性最低(88%)。在这些样本中还检测到了包括超广谱β-内酰胺酶 和碳青霉烯酶 在内的流行耐药基因。本研究证明了使用转录反应分析进行快速耐药性测定的临床可行性,不过在未来的工作中,对更大规模且更多样化的细菌群体进行进一步验证至关重要。GoPhAST-R代表了一种在临床环境中进行快速、全面抗生素药敏测试的有前景的新方法。