Rapid colorimetric detection of citrus tristeza virus combining portable sample preparation and reverse transcription-loop mediated isothermal amplification
Liu, C.-W.; Bodaghi, S.; Keremane, M. L.; Kalish, B.; Vidalakis, G.; Tsutsui, H.
Show abstract
AbstractsA sensing platform combining semi-automated sample preparation protocol and one-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) is reported for rapid colorimetric detection of citrus tristeza virus (CTV) in a greenhouse. An OmniLyse micro-homogenizer and cellulose paper disks were integrated for quick sample preparation of total nucleic acids (<15 min). RT-LAMP assays were optimized in terms of primers concentrations and minimization of false positives for both CTV and cytochrome oxidase (COX) detections. Specifically, the optimal reaction time for lab-based RT-LAMP assays was determined as 40 minutes with the detection limits of CTV and COX as 43 copies/L (equivalent to 86 copies/mg of tissue) and 5 copies/L (equivalent to 10 copies/mg of tissue), respectively. Additionally, an in-greenhouse colorimetric RT-LAMP assay with lyophilized reaction mix for endpoint CTV detection was successfully conducted in 35 minutes without a false response in either colorimetric or fluorometric assays. Overall, this quick sample preparation protocol integrated with the lyophilized RT-LAMP assays showed high efficiency and reliability in plant pathogen detection in a greenhouse. This strategy holds great potential to be integrated into a portable, autonomous system and be universally adopted for in-field diagnosis of different pathogens.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Probing Loop-Mediated Isothermal Amplification (LAMP) targeting two gene-fragments of rose rosette virus 97%
- Development and evaluation of a loop-mediated isothermal amplification (LAMP) assay for the detection of Tomato brown rugose fruit virus (ToBRFV) 97%
- Multiplex detection of "Candidatus Liberibacter asiaticus" and Spiroplasma citri by qPCR and droplet digital PCR 96%
Similar papers in this journal
- Improved performance of nucleic acid-based assays for genetically diverse norovirus surveillance 92%
- Heat-treated virus inactivation rate depends strongly on treatment procedure: illustration with SARS-CoV-2 92%
- Lessons and considerations for the creation of universal primers targeting non-conserved, horizontally mobile genes 91%
Similar papers in this journal
- Cas12a-based on-site and rapid nucleic acid detection of African swine fever 94%
- Pixel-based machine learning and image reconstitution for dot-ELISA pathogen serodiagnosis 93%
- Disinfection performance of a drinking water bottle system with a UVC LED cap against waterborne pathogens and heterotrophic contaminants 92%
Similar papers in this journal
- A Paper-based Loop-Mediated Isothermal Amplification (LAMP) Assay for Highly Pathogenic Avian Influenza 97%
- Development and validation of cost-effective one-step multiplex RT-PCR assay for detecting the SARS-CoV-2 infection using SYBR Green melting curve analysis 95%
- A multiplexed RT-PCR Assay for Nanopore Whole Genome Sequencing of Tilapia lake virus (TiLV) 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.