摘要：AbstractThe worldwide emergence of multidrug‐resistant (MDR) bacteria is associated with significant morbidity, mortality, and healthcare costs. Rapid and accurate diagnostic methods to detect antibiotic resistance are critical for antibiotic stewardship and infection control measurements. Here a cantilever nanosensor‐based diagnostic assay is shown to detect single nucleotide polymorphisms (SNPs) and genes associated with antibiotic resistance in Gram negative (Pseudomonas aeruginosa) and positive (Enterococcus faecium) bacteria, representing frequent causes for MDR infections. Highly specific RNA capture probes for SNPs (ampRD135GorampRG154R) or resistance genes (vanA,vanB, andvanD) allow to detect the binding of bacterial RNA within less than 5 min. Serial dilutions of bacterial RNA indicate an unprecedented sensitivity of 10 fg µL−1total RNA corresponding to less than ten bacterial cells for SNPs and 1 fg µL−1total RNA forvanDdetection equivalent to single bacterial cell sensitivity.A new nanosensor array method is presented to investigate antibiotic resistances in bacteria. Single nucleotide polymorphisms in ampicillin resistance markers from gram negativePseudomonas aeruginosaand vancomycin resistance genes in gram positiveEnterococcus faeciumare studied. The method shows unprecedented sensitivity and specificity (1 bacterial cell) as well as drastically reduced times to obtain a diagnosis, compared to standard procedures.
