Real-Time Continuous Identification of Greenhouse Plant Pathogens Based on Recyclable Microfluidic Bioassay System

ACS Appl Mater Interfaces. 2017 Sep 20;9(37):31568-31575. doi: 10.1021/acsami.7b10116. Epub 2017 Sep 11.

Abstract

The development of a real-time continuous analytical platform for the pathogen detection is of great scientific importance for achieving better disease control and prevention. In this work, we report a rapid and recyclable microfluidic bioassay system constructed from oligonucleotide arrays for selective and sensitive continuous identification of DNA targets of fungal pathogens. We employ the thermal denaturation method to effectively regenerate the oligonucleotide arrays for multiple sample detection, which could considerably reduce the screening effort and costs. The combination of thermal denaturation and laser-induced fluorescence detection technique enables real-time continuous identification of multiple samples (<10 min per sample). As a proof of concept, we have demonstrated that two DNA targets of fungal pathogens (Botrytis cinerea and Didymella bryoniae) can be sequentially analyzed using our rapid microfluidic bioassay system, which provides a new paradigm in the design of microfluidic bioassay system and will be valuable for chemical and biomedical analysis.

Keywords: DNA; greenhouse plant pathogens; hybridization; microchannel; multiple samples detection; real time.

MeSH terms

  • Ascomycota
  • Biological Assay
  • Botrytis
  • Microfluidic Analytical Techniques*
  • Microfluidics
  • Plants