Dandan Shi, Ruiwen Li, Shaoning Yu and Guoqing Qian*,
{"title":"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。","authors":"Dandan Shi, Ruiwen Li, Shaoning Yu and Guoqing Qian*, ","doi":"10.1021/acsinfecdis.5c00349","DOIUrl":null,"url":null,"abstract":"<p >The escalating crisis of hospital-acquired multidrug-resistant (MDR) infections, particularly <i><i>Klebsiella pneumoniae</i></i> carbapenemase 2-expressing <i><i>K. pneumoniae</i></i> (KPC-2 KP) and MDR-<i><i>Acinetobacter baumannii</i></i> (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 H<sub>2</sub>O<sub>2</sub>, and the PMOF(Fe) shell utilizes H<sub>2</sub>O<sub>2</sub> 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 10–10<sup>8</sup> 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.</p>","PeriodicalId":17,"journal":{"name":"ACS Infectious Diseases","volume":"11 9","pages":"2491–2499"},"PeriodicalIF":3.8000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrasensitive Aptamer-Based Metal–Organic Framework-on-Metal–Organic Framework Platform for Clinical Detection of KPC-2 Klebsiella pneumoniae and Multidrug-Resistant Acinetobacter baumannii\",\"authors\":\"Dandan Shi, Ruiwen Li, Shaoning Yu and Guoqing Qian*, \",\"doi\":\"10.1021/acsinfecdis.5c00349\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The escalating crisis of hospital-acquired multidrug-resistant (MDR) infections, particularly <i><i>Klebsiella pneumoniae</i></i> carbapenemase 2-expressing <i><i>K. pneumoniae</i></i> (KPC-2 KP) and MDR-<i><i>Acinetobacter baumannii</i></i> (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 H<sub>2</sub>O<sub>2</sub>, and the PMOF(Fe) shell utilizes H<sub>2</sub>O<sub>2</sub> 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 10–10<sup>8</sup> 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.</p>\",\"PeriodicalId\":17,\"journal\":{\"name\":\"ACS Infectious Diseases\",\"volume\":\"11 9\",\"pages\":\"2491–2499\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-08-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsinfecdis.5c00349\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsinfecdis.5c00349","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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.
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.