A dual nanozyme-enabled colorimetric aptasensor detects KPC-2 and MDR pathogens in clinical samples, suggesting improvements in rapid diagnostics for MDR infections.
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.
No takes yet. Share an insight, caveat, or question.
Shi et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: