Quick Plant Sample Preparation Methods Using a Micro-Homogenizer for the Detection of Multiple Citrus Pathogens

被引:0
|
作者
Liu, Chia-Wei [1 ]
Bodaghi, Sohrab [2 ]
Vidalakis, Georgios [2 ]
Tsutsui, Hideaki [1 ,3 ]
机构
[1] Univ Calif Riverside, Dept Mech Engn, Riverside, CA 92521 USA
[2] Univ Calif Riverside, Dept Microbiol & Plant Pathol, Riverside, CA 92521 USA
[3] Univ Calif Riverside, Dept Bioengn, Riverside, CA 92521 USA
基金
美国食品与农业研究所; 美国国家科学基金会;
关键词
sample preparation; nucleic acid extraction; micro-homogenizer; paper disk; citrus diseases; NUCLEIC-ACID EXTRACTION; TRISTEZA-VIRUS; PCR INHIBITION; IDENTIFICATION; DNA;
D O I
10.3390/chemosensors12060105
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Effective pathogen detection is essential for plant disease control. However, plant sample preparation for downstream assays, such as quantitative polymerase chain reaction (qPCR), is challenging to perform outside of a laboratory. This paper reports two sample preparation methods featuring chemical and mechanical lysis and nucleic acid extraction using a micro-homogenizer, followed by serial dilution or nucleic acid purification with a paper disk before assay. Five minutes of lysis and extraction resulted in DNA and RNA yields of up to 76.5% and 63.3%, respectively, compared to mortar and pestle controls. Crude lysates were unsuitable for direct use in qPCR assays; however, serial dilution or quick wash using chromatography paper rendered samples ready for such assays. Additionally, the nucleic acids stored on paper disks under various storage conditions remained stable for one month. These methods can facilitate the in-field preparation of citrus samples and allow for both onsite and mail-in diagnostics for growers.
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页数:20
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