Blood culture-free ultra-rapid antimicrobial susceptibility testing

IF 50.5 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Nature Pub Date : 2024-07-24 DOI:10.1038/s41586-024-07725-1
Tae Hyun Kim, Junwon Kang, Haewook Jang, Hyelyn Joo, Gi Yoon Lee, Hamin Kim, Untack Cho, Hyeeun Bang, Jisung Jang, Sangkwon Han, Dong Young Kim, Chan Mi Lee, Chang Kyung Kang, Pyoeng Gyun Choe, Nam Joong Kim, Myoung-don Oh, Taek Soo Kim, Inho Kim, Wan Beom Park, Sunghoon Kwon
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Abstract

Treatment assessment and patient outcome for sepsis depend predominantly on the timely administration of appropriate antibiotics1–3. However, the clinical protocols used to stratify and select patient-specific optimal therapy are extremely slow4. In particular, the major hurdle in performing rapid antimicrobial susceptibility testing (AST) remains in the lengthy blood culture procedure, which has long been considered unavoidable due to the limited number of pathogens present in the patient’s blood. Here we describe an ultra-rapid AST method that bypasses the need for traditional blood culture, thereby demonstrating potential to reduce the turnaround time of reporting drug susceptibility profiles by more than 40–60 h compared with hospital AST workflows. Introducing a synthetic beta-2-glycoprotein I peptide, a broad range of microbial pathogens are selectively recovered from whole blood, subjected to species identification or instantly proliferated and phenotypically evaluated for various drug conditions using a low-inoculum AST chip. The platform was clinically evaluated by the enrolment of 190 hospitalized patients suspected of having infection, achieving 100% match in species identification. Among the eight positive cases, six clinical isolates were retrospectively tested for AST showing an overall categorical agreement of 94.90% with an average theoretical turnaround time of 13 ± 2.53 h starting from initial blood processing. An ultra-rapid antimicrobial susceptibility testing method is introduced that bypasses the need for traditional blood culture, demonstrating the potential to significantly reduce the turnaround time of reporting drug susceptibility profiles.

Abstract Image

Abstract Image

无需血液培养的超快速抗菌药物药敏试验。
脓毒症的治疗评估和患者预后主要取决于是否能及时使用适当的抗生素1-3。然而,用于对患者进行分层和选择特定最佳疗法的临床方案却极为缓慢4。特别是,进行快速抗菌药物敏感性检测(AST)的主要障碍仍然是冗长的血液培养过程,由于患者血液中的病原体数量有限,长期以来血液培养一直被认为是不可避免的。在这里,我们介绍了一种超快速 AST 方法,这种方法无需进行传统的血液培养,因此与医院的 AST 工作流程相比,有可能将药物敏感性分析报告的周转时间缩短 40-60 小时以上。通过引入合成的 beta-2 糖蛋白 I 肽,可从全血中选择性地回收多种微生物病原体,并利用低接种量 AST 芯片进行物种鉴定或瞬时增殖和各种药物条件下的表型评估。通过对 190 名疑似感染的住院病人进行登记,对该平台进行了临床评估,物种鉴定匹配率达到 100%。在 8 个阳性病例中,对 6 个临床分离物进行了 AST 回顾性检测,结果显示总体分类吻合度为 94.90%,从最初的血液处理开始,平均理论周转时间为 13±2.53 小时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nature
Nature 综合性期刊-综合性期刊
CiteScore
90.00
自引率
1.20%
发文量
3652
审稿时长
3 months
期刊介绍: Nature is a prestigious international journal that publishes peer-reviewed research in various scientific and technological fields. The selection of articles is based on criteria such as originality, importance, interdisciplinary relevance, timeliness, accessibility, elegance, and surprising conclusions. In addition to showcasing significant scientific advances, Nature delivers rapid, authoritative, insightful news, and interpretation of current and upcoming trends impacting science, scientists, and the broader public. The journal serves a dual purpose: firstly, to promptly share noteworthy scientific advances and foster discussions among scientists, and secondly, to ensure the swift dissemination of scientific results globally, emphasizing their significance for knowledge, culture, and daily life.
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