Nanoparticle-Mediated Capture and Electrochemical Detection of Methicillin-Resistant Staphylococcus aureus

Carine R. Nemr, Sarah J. Smith, Wenhan Liu, Adam H. Mepham, Reza M. Mohamadi, Mahmoud Labib, Shana O. Kelley*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

75 Scopus citations

Abstract

The spread of antibiotic-resistant bacteria poses a global threat to public health. Conventional bacterial detection and identification methods often require pre-enrichment and/or sample preprocessing and purification steps that can prolong diagnosis by days. Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most widespread antibiotic-resistant bacteria and is the leading cause of hospital-acquired infections. Here, we have developed a method to specifically capture and detect MRSA directly from patient nasal swabs with no prior culture and minimal processing steps using a microfluidic device and antibody-functionalized magnetic nanoparticles. Bacteria are captured based on antibody recognition of a membrane-bound protein marker that confers β-lactam antibiotic resistance. MRSA identification is then achieved by the use of a strain-specific antibody functionalized with alkaline phosphatase for electrochemical detection. This approach ensures that only those bacteria of the target strain and resistance profile are measured. The method has a limit of detection of 845 CFU/mL and excellent discrimination against high concentrations of common nontarget nasal flora with a turnaround time of under 4.5 h. This detection method was successfully validated using clinical nasal swab specimens (n = 30) and has the potential to be tailored to various bacterial targets.

Original languageEnglish (US)
Pages (from-to)2847-2853
Number of pages7
JournalAnalytical Chemistry
Volume91
Issue number4
DOIs
StatePublished - Feb 19 2019

Funding

C.R.N. acknowledges support from the Walter C. Sumner Memorial Fellowship and the Natural Sciences and Engineering Research Council (Postgraduate Scholarship-Doctoral Program). Research reported in this publication was supported in part by the Canadian Institutes of Health Research (Grant No. FDN-148415) and the Natural Sciences and Engineering Research Council of Canada (Grant No. RGPIN-2016-06090). The authors wish to thank Dr. Tony Mazzulli at Mount Sinai Hospital for access to clinical samples.

ASJC Scopus subject areas

  • Analytical Chemistry

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