Abstract

PCR-based techniques are widely used to identify disease causing bacterial and viral pathogens, especially in point-of-care or near-patient clinical settings that require rapid results and sample-to-answer workflows. However, such techniques often fail to differentiate between closely related species that have highly variable genomes. Here, a homogenous (closed-tube) pathogen identification and classification method is described that combines PCR amplification, array-based amplicon sequence verification, and real-time detection using an inverse fluorescence fluorescence-resonance energy transfer technique. The amplification is designed to satisfy the inclusivity criteria and create ssDNA amplicons, bearing a nonradiating quencher moiety at the 5ʹ-terminus, for all the related species. The array includes fluorescent-labeled probes which preferentially capture the variants of the amplicons and classify them through solid-phase thermal denaturing (melt curve) analysis. Systematic primer and probe design algorithms and empirical validation methods are presented and successfully applied to the challenging example of identification of, and differentiation between, closely related human rhinovirus and human enterovirus strains.

Details

Title
An array-based melt curve analysis method for the identification and classification of closely related pathogen strains
Author
Hassibi, Arjang 1 ; Ebert, Jessica 1 ; Bolouki, Sara 1 ; Anemogiannis, Alexander 1 ; Mazarei, Gelareh 1 ; Li, Yuan 1 ; Johnson, Kirsten A 1 ; Tran, Van 1 ; Mantina, Pallavi 1 ; Gharooni, Taraneh 1 ; Jirage, Kshama 1 ; Pei, Lei 1 ; Sinha, Ruma 1 ; Manickam, Arun 1 ; Amin Zia 1 ; Naraghi-Arani, Pejman 1 ; Schoolnik, Gary 1 ; Kuimelis, Robert G 1 

 InSilixa, Inc., 1000 Hamlin Court, Sunnyvale, CA 94089, USA 
Publication year
2018
Publication date
2018
Publisher
Oxford University Press
e-ISSN
23968923
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3169468822
Copyright
© The Author(s) 2018. Published by Oxford University Press. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.