Literature DB >> 33420312

LAMP-based foldable microdevice platform for the rapid detection of Magnaporthe oryzae and Sarocladium oryzae in rice seed.

M K Prasannakumar1, P Buela Parivallal2, Devanna Pramesh3, H B Mahesh4, Edwin Raj5.   

Abstract

Rice blast (caused by Magnaporthe oryzae) and sheath rot diseases (caused by Sarocladium oryzae) are the most predominant seed-borne pathogens of rice. The detection of both pathogens in rice seed is essential to avoid production losses. In the present study, a microdevice platform was designed, which works on the principles of loop-mediated isothermal amplification (LAMP) to detect M. oryzae and S. oryzae in rice seeds. Initially, a LAMP, polymerase chain reaction (PCR), quantitative PCR (qPCR), and helicase dependent amplification (HDA) assays were developed with primers, specifically targeting M. oryzae and S. oryzae genome. The LAMP assay was highly efficient and could detect the presence of M. oryzae and S. oryzae genome at a concentration down to 100 fg within 20 min at 60 °C. Further, the sensitivity of the LAMP, HDA, PCR, and qPCR assays were compared wherein; the LAMP assay was highly sensitive up to 100 fg of template DNA. Using the optimized LAMP assay conditions, a portable foldable microdevice platform was developed to detect M. oryzae and S. oryzae in rice seeds. The foldable microdevice assay was similar to that of conventional LAMP assay with respect to its sensitivity (up to 100 fg), rapidity (30 min), and specificity. This platform could serve as a prototype for developing on-field diagnostic kits to be used at the point of care centers for the rapid diagnosis of M. oryzae and S. oryzae in rice seeds. This is the first study to report a LAMP-based foldable microdevice platform to detect any plant pathogens.

Entities:  

Year:  2021        PMID: 33420312      PMCID: PMC7794292          DOI: 10.1038/s41598-020-80644-z

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  20 in total

Review 1.  Molecular diagnostics for fungal plant pathogens.

Authors:  H Alastair McCartney; Simon J Foster; Bart A Fraaije; Elaine Ward
Journal:  Pest Manag Sci       Date:  2003-02       Impact factor: 4.845

Review 2.  Comparison of isothermal helicase-dependent amplification and PCR for the detection of Mycobacterium tuberculosis by an electrochemical genomagnetic assay.

Authors:  Susana Barreda-García; Rebeca Miranda-Castro; Noemí de-Los-Santos-Álvarez; Arturo J Miranda-Ordieres; M Jesús Lobo-Castañón
Journal:  Anal Bioanal Chem       Date:  2016-04-07       Impact factor: 4.142

3.  Direct detection of various pathogens by loop-mediated isothermal amplification assays on bacterial culture and bacterial colony.

Authors:  Muxia Yan; Weidong Li; Zhenwen Zhou; Hongxia Peng; Ziyan Luo; Ling Xu
Journal:  Microb Pathog       Date:  2016-11-09       Impact factor: 3.738

4.  Pyrophosphate as a selective inhibitor of macromolecule synthesis in normal and leukemic leukocytes.

Authors:  J Laszlo; O E Brown; D S Miller; P Ove
Journal:  Biochem Pharmacol       Date:  1969-06       Impact factor: 5.858

5.  Development of a LAMP assay with a portable device for real-time detection of begomoviruses under field conditions.

Authors:  Fariha Wilisiani; Aika Tomiyama; Hiroshi Katoh; Sedyo Hartono; Yutaro Neriya; Hisashi Nishigawa; Tomohide Natsuaki
Journal:  J Virol Methods       Date:  2018-10-12       Impact factor: 2.014

6.  The use of conventional and quantitative real-time PCR assays for Polymyxa graminis to examine host plant resistance, inoculum levels and intraspecific variation.

Authors:  Elaine Ward; Kostya Kanyuka; Juliet Motteram; Dmitry Kornyukhin; Michael J Adams
Journal:  New Phytol       Date:  2005-03       Impact factor: 10.151

7.  Comparison among the Quantification of Bacterial Pathogens by qPCR, dPCR, and Cultural Methods.

Authors:  Matteo Ricchi; Cristina Bertasio; Maria B Boniotti; Nadia Vicari; Simone Russo; Michela Tilola; Marco A Bellotti; Barbara Bertasi
Journal:  Front Microbiol       Date:  2017-06-28       Impact factor: 5.640

8.  Development of a single-tube one-step RT-LAMP assay to detect the Chikungunya virus genome.

Authors:  Benjamin Lopez-Jimena; Stefanie Wehner; Graham Harold; Mohammed Bakheit; Sieghard Frischmann; Michaël Bekaert; Oumar Faye; Amadou Alpha Sall; Manfred Weidmann
Journal:  PLoS Negl Trop Dis       Date:  2018-05-29

Review 9.  Helicase-dependent isothermal amplification: a novel tool in the development of molecular-based analytical systems for rapid pathogen detection.

Authors:  Susana Barreda-García; Rebeca Miranda-Castro; Noemí de-Los-Santos-Álvarez; Arturo J Miranda-Ordieres; María Jesús Lobo-Castañón
Journal:  Anal Bioanal Chem       Date:  2017-09-20       Impact factor: 4.142

10.  Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of yellow head virus in shrimp.

Authors:  Tohru Mekata; Raja Sudhakaran; Tomoya Kono; Kittichon U-taynapun; Kidchakan Supamattaya; Yoshihiro Suzuki; Masahiro Sakai; Toshiaki Itami
Journal:  J Virol Methods       Date:  2009-07-29       Impact factor: 2.014

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  3 in total

1.  The Classification of Rice Blast Resistant Seed Based on Ranman Spectroscopy and SVM.

Authors:  Yan He; Wei Zhang; Yongcai Ma; Jinyang Li; Bo Ma
Journal:  Molecules       Date:  2022-06-25       Impact factor: 4.927

Review 2.  Loop-Mediated Isothermal Amplification for Detection of Plant Pathogens in Wheat (Triticum aestivum).

Authors:  Sandra V Gomez-Gutierrez; Stephen B Goodwin
Journal:  Front Plant Sci       Date:  2022-03-15       Impact factor: 5.753

3.  Colorimetric loop-mediated isothermal amplification assay for detection and ecological monitoring of Sarocladium oryzae, an important seed-borne pathogen of rice.

Authors:  Prassan Choudhary; Sanjay Kumar Goswami; Hillol Chakdar; Shaloo Verma; Shobit Thapa; Alok Kumar Srivastava; Anil Kumar Saxena
Journal:  Front Plant Sci       Date:  2022-08-18       Impact factor: 6.627

  3 in total

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