Affiliations 

  • 1 Institute of Advanced Technology, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia; Biotechnology & Nanotechnology Research Centre, Malaysian Agricultural Research and Development Institute, Persiaran MARDI-UPM, 43400, Serdang, Selangor, Malaysia
  • 2 Institute of Advanced Technology, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia; Department of Chemistry, Faculty of Science, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia. Electronic address: jafar@upm.edu.my
  • 3 Biotechnology & Nanotechnology Research Centre, Malaysian Agricultural Research and Development Institute, Persiaran MARDI-UPM, 43400, Serdang, Selangor, Malaysia
  • 4 Paddy & Rice Research Centre, Malaysian Agricultural Research and Development Institute, MARDI Seberang Perai, Beg Berkunci No.203, Pejabat Pos Kepala Batas, 13200, Seberang Perai, Pulau Pinang, Malaysia
  • 5 Institute of Advanced Technology, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia; Department of Chemistry, Faculty of Science, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia
  • 6 Department of Bioprocess Technology, Faculty of Biotechnology and Biomolecule Science, University of Putra Malaysia, 43400, Serdang, Selangor, Malaysia
Anal Biochem, 2020 12 01;610:113876.
PMID: 32750357 DOI: 10.1016/j.ab.2020.113876

Abstract

The identification of rice bacterial leaf blight disease requires a simple, rapid, highly sensitive, and quantitative approach that can be applied as an early detection monitoring tool in rice health. This paper highlights the development of a turn-off fluorescence-based immunoassay for the early detection of Xanthomonas oryzae pv. oryzae (Xoo), a gram-negative bacterium that causes rice bacterial leaf blight disease. Antibodies against Xoo bacterial cells were produced as specific bio-recognition molecules and the conjugation of these antibodies with graphene quantum dots and gold nanoparticles was performed and characterized, respectively. The combination of both these bio-probes as a fluorescent donor and metal quencher led to changes in the fluorescence signal. The immunoreaction between AntiXoo-GQDs, Xoo cells, and AntiXoo-AuNPs in the immuno-aggregation complex led to the energy transfer in the turn-off fluorescence-based quenching system. The change in fluorescence intensity was proportional to the logarithm of Xoo cells in the range of 100-105 CFU mL-1. The limit of detection was achieved at 22 CFU mL-1 and the specificity test against other plant disease pathogens showed high specificity towards Xoo. The detection of Xoo in real plant samples was also performed in this study and demonstrated satisfactory results.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.