| Literature DB >> 33552553 |
François Huber1, Hans Peter Lang1, Daniela Lang2, Daniel Wüthrich2, Vladimira Hinić2, Christoph Gerber1, Adrian Egli2, Ernst Meyer1.
Abstract
The 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 (ampRD135G or ampRG154R ) or resistance genes (vanA, vanB, and vanD) 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-1 total RNA corresponding to less than ten bacterial cells for SNPs and 1 fg µL-1 total RNA for vanD detection equivalent to single bacterial cell sensitivity.Entities:
Keywords: MRSA; bacterial antibiotic resistances; diagnostics; nanosensors; single nucleotide polymorphisms
Year: 2020 PMID: 33552553 PMCID: PMC7857129 DOI: 10.1002/gch2.202000066
Source DB: PubMed Journal: Glob Chall ISSN: 2056-6646