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基于显微镜成像分析的阳性血培养物直接快速抗菌药物敏感性检测。

Direct, rapid antimicrobial susceptibility test from positive blood cultures based on microscopic imaging analysis.

机构信息

QuantaMatrix Inc., Medical Innovation Center, Seoul National University Hospital, Seoul, 03080, Republic of Korea.

Institutes of Entrepreneurial BioConvergence, Seoul National University, Seoul, 08826, Republic of Korea.

出版信息

Sci Rep. 2017 Apr 25;7(1):1148. doi: 10.1038/s41598-017-01278-2.

Abstract

For the timely treatment of patients with infections in bloodstream and cerebrospinal fluid, a rapid antimicrobial susceptibility test (AST) is urgently needed. Here, we describe a direct and rapid antimicrobial susceptibility testing (dRAST) system, which can determine the antimicrobial susceptibility of bacteria from a positive blood culture bottle (PBCB) in six hours. The positive blood culture sample is directly mixed with agarose and inoculated into a micropatterned plastic microchip with lyophilized antibiotic agents. Using microscopic detection of bacterial colony formation in agarose, the total time to result from a PBCB for dRAST was only six hours for a wide range of bacterial concentrations in PBCBs. The results from the dRAST system were consistent with the results from a standard AST, broth microdilution test. In tests of clinical isolates (n = 206) composed of 16 Gram-negative species and seven Gram-positive species, the dRAST system was accurate compared to the standard broth microdilution test, with rates of 91.11% (2613/2868) categorical agreement, 6.69% (192/2868) minor error, 2.72% (50/1837) major error and 1.45% (13/896) very major error. Thus, the dRAST system can be used to rapidly identify appropriate antimicrobial agents for the treatment of blood stream infection (BSI) and antibiotic-resistant strain infections.

摘要

为了及时治疗血液和脑脊液感染患者,迫切需要快速的抗菌药敏试验(AST)。在这里,我们描述了一种直接快速抗菌药敏试验(dRAST)系统,它可以在六小时内确定阳性血培养瓶(PBCB)中细菌的抗菌药敏性。将阳性血培养样本直接与琼脂糖混合,并接种到带有冻干抗生素的微图案塑料微芯片中。通过琼脂中细菌菌落形成的显微镜检测,可以在六小时内从 PBCB 获得 dRAST 的总结果,而 PBCB 中的细菌浓度范围很广。dRAST 系统的结果与标准 AST、肉汤微量稀释试验的结果一致。在由 16 种革兰氏阴性菌和 7 种革兰氏阳性菌组成的临床分离株(n=206)测试中,与标准肉汤微量稀释试验相比,dRAST 系统具有较高的准确性,分类一致性为 91.11%(2613/2868),次要误差率为 6.69%(192/2868),主要误差率为 2.72%(50/1837),非常大的误差率为 1.45%(13/896)。因此,dRAST 系统可用于快速鉴定治疗血流感染(BSI)和抗生素耐药菌株感染的合适抗菌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3674/5430693/6d83b832a3c5/41598_2017_1278_Fig1_HTML.jpg

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