Literature DB >> 34541168

Detection of Pathogens and Ampicillin-resistance Genes Using Multiplex Padlock Probes.

Rick Conzemius1, Ivan Barišić1.   

Abstract

Diagnostic assays for pathogen identification and characterization are limited either by the number of simultaneously detectable targets, which rely on multiplexing methods, or by time constraints due to cultivation-based techniques. We recently presented a 100-plex method for human pathogen characterization to identify 75 bacterial and fungal species as well as 33 clinically relevant β-lactamases ( Barišić et al., 2016 ). By using 16S rRNA gene sequences as barcode elements in the padlock probes, and two different fluorescence channels for species and antibiotic resistance identification, we managed to cut the number of microarray probes needed by half. Consequently, we present here the protocol of an assay with a runtime of approx. 8 h and a detection limit of 105 cfu ml-1. A total of 89% of β-lactamases and 93.7% of species were identified correctly.
Copyright © 2017 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Antibiotic resistance identification; Human pathogens; Multiplex detection; Padlock probes; Species identification

Year:  2017        PMID: 34541168      PMCID: PMC8413525          DOI: 10.21769/BioProtoc.2504

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


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  1 in total

1.  Padlock Probe-Based Generation of DNAzymes for the Colorimetric Detection of Antibiotic Resistance Genes.

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  1 in total

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