Rapid and Ultrasensitive Detection of Mutations and Genes Relevant to Antimicrobial Resistance in Bacteria.
François HuberHans Peter LangDaniela LangDaniel WüthrichVladimira HinićChristoph GerberAdrian EgliErnst MeyerPublished in: Global challenges (Hoboken, NJ) (2020)
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.
Keyphrases
- multidrug resistant
- gram negative
- genome wide
- loop mediated isothermal amplification
- acinetobacter baumannii
- antimicrobial resistance
- healthcare
- drug resistant
- nucleic acid
- pseudomonas aeruginosa
- induced apoptosis
- label free
- cystic fibrosis
- small molecule
- type diabetes
- stem cells
- oxidative stress
- mass spectrometry
- single cell
- signaling pathway
- escherichia coli
- cardiovascular events
- risk factors
- binding protein
- high throughput
- photodynamic therapy
- cardiovascular disease
- real time pcr
- bioinformatics analysis
- biofilm formation
- sensitive detection
- liquid chromatography