| Literature DB >> 31179687 |
Rajesh Paul, Amanda C Saville, Jeana C Hansel, Yanqi Ye1, Carmin Ball, Alyssa Williams, Xinyuan Chang2, Guojun Chen1, Zhen Gu1, Jean B Ristaino, Qingshan Wei.
Abstract
In-field molecular diagnosis of plant diseases via nucleic acid amplification is currently limited by cumbersome protocols for extracting and isolating pathogenic DNA from plant tissues. To address this challenge, a rapid plant DNA extraction method was developed using a disposable polymeric microneedle (MN) patch. By applying MN patches on plant leaves, amplification-assay-ready DNA can be extracted within a minute from different plant species. MN-extracted DNA was used for direct polymerase chain reaction amplification of plant plastid DNA without purification. Furthermore, using this patch device, extraction of plant pathogen DNA ( Phytophthora infestans) from both laboratory-inoculated and field-infected leaf samples was performed for detection of late blight disease in tomato. MN extraction achieved 100% detection rate of late blight infections for samples after 3 days of inoculation when compared to the conventional gold standard cetyltrimethylammonium bromide (CTAB)-based DNA extraction method and 100% detection rate for all blind field samples tested. This simple, cell-lysis-free, and purification-free DNA extraction method could be a transformative approach to facilitate rapid sample preparation for molecular diagnosis of various plant diseases directly in the field.Entities:
Keywords: DNA extraction; microneedle patch; nucleic acid amplification; plant disease; point-of-care diagnostics
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Year: 2019 PMID: 31179687 DOI: 10.1021/acsnano.9b00193
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881