基于适配体的超灵敏金属-有机框架-金属-有机框架平台临床检测KPC-2肺炎克雷伯菌和耐多药鲍曼不动杆菌。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Dandan Shi, Ruiwen Li, Shaoning Yu and Guoqing Qian*, 
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引用次数: 0

摘要

医院获得性耐多药(MDR)感染危机不断升级,尤其是表达碳青霉烯酶2的肺炎克雷伯菌(KPC-2 KP)和耐多药鲍曼不动杆菌(AB),需要快速诊断解决方案。我们开发了一种利用级联放大机制的双纳米酶比色传感器,一种具有过氧化物酶样活性的金属-有机框架(MOF)- MOF纳米结构。Cu-MOF@PMOF(Fe)整合了类似儿茶酚氧化酶的活性,Cu-MOF核心氧化儿茶酚生成H2O2, PMOF(Fe)外壳利用H2O2氧化TMB底物,在370和652nm产生双波长信号,用于超灵敏检测。该系统具有病原体特异性适体功能,可在40分钟内实现选择性细菌捕获,定量10-108 CFU/mL,检测限KPC-2 KP为7 CFU/mL, MDR-AB为6 CFU/mL。脑脊液、腹膜液、血清和胆汁样品的临床验证表明,在复杂基质中具有良好的性能(回收率为91.2-112.2%)。因此,这个平台提供了一个快速的(
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasensitive Aptamer-Based Metal–Organic Framework-on-Metal–Organic Framework Platform for Clinical Detection of KPC-2 Klebsiella pneumoniae and Multidrug-Resistant Acinetobacter baumannii

Ultrasensitive Aptamer-Based Metal–Organic Framework-on-Metal–Organic Framework Platform for Clinical Detection of KPC-2 Klebsiella pneumoniae and Multidrug-Resistant Acinetobacter baumannii

The escalating crisis of hospital-acquired multidrug-resistant (MDR) infections, particularly Klebsiella pneumoniae carbapenemase 2-expressing K. pneumoniae (KPC-2 KP) and MDR-Acinetobacter baumannii (AB), demands rapid diagnostic solutions. We developed a dual nanozyme-powered colorimetric aptasensor leveraging a cascade amplification mechanism, a metal–organic framework (MOF)-on-MOF nanostructure with peroxidase-like activity. Cu-MOF@PMOF(Fe) integrates catechol oxidase-like activity, with the Cu-MOF core oxidizing catechol to generate H2O2, and the PMOF(Fe) shell utilizes H2O2 to oxidize the TMB substrate, producing dual-wavelength signals at 370 and 652 nm for ultrasensitive detection. Functionalized with pathogen-specific aptamers, the system achieves selective bacterial capture within 40 min, quantifying 10–108 CFU/mL with detection limits of 7 CFU/mL for KPC-2 KP and 6 CFU/mL for MDR-AB. Clinical validation using cerebrospinal fluid, peritoneal fluid, serum, and bile samples demonstrated robust performance in complex matrices (91.2–112.2% recovery rates). Therefore, this platform provides a rapid (<1 h), sensitive, and clinically adaptable solution for combating MDR bacterial infections, bridging advanced materials with diagnostic microbiology.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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