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Rapid real-time quantitative colorimetric LAMP methodology for field detection of Verticillium dahliae in crude olive-plant samples
by
Papadakis, George
, Gizeli, Electra
, Patsis, Georgios
, Paplomatas, Epaminondas J.
, Megariti, Maria
, Tzima, Aliki K.
, Panagou, Alexandra
, Markakis, Emmanouil A.
, Pantazis, Alexandros K.
in
Analysis
/ Biological Techniques
/ Biomedical and Life Sciences
/ chemical control
/ colorimetry
/ cross reaction
/ Defoliating pathotype
/ detection limit
/ Diseases and pests
/ DNA
/ Field-based detection
/ Fungi
/ genes
/ Genetic screening
/ Health aspects
/ host range
/ internal transcribed spacers
/ Life Sciences
/ Loop mediated isothermal amplification
/ Methodology
/ Methods
/ Molecular diagnostics
/ Olive
/ olives
/ pathogens
/ Plant Sciences
/ portable equipment
/ prototypes
/ RNA
/ Soilborne pathogens
/ Verticillium dahliae
/ Verticillium wilt
/ wood
2024
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Rapid real-time quantitative colorimetric LAMP methodology for field detection of Verticillium dahliae in crude olive-plant samples
by
Papadakis, George
, Gizeli, Electra
, Patsis, Georgios
, Paplomatas, Epaminondas J.
, Megariti, Maria
, Tzima, Aliki K.
, Panagou, Alexandra
, Markakis, Emmanouil A.
, Pantazis, Alexandros K.
in
Analysis
/ Biological Techniques
/ Biomedical and Life Sciences
/ chemical control
/ colorimetry
/ cross reaction
/ Defoliating pathotype
/ detection limit
/ Diseases and pests
/ DNA
/ Field-based detection
/ Fungi
/ genes
/ Genetic screening
/ Health aspects
/ host range
/ internal transcribed spacers
/ Life Sciences
/ Loop mediated isothermal amplification
/ Methodology
/ Methods
/ Molecular diagnostics
/ Olive
/ olives
/ pathogens
/ Plant Sciences
/ portable equipment
/ prototypes
/ RNA
/ Soilborne pathogens
/ Verticillium dahliae
/ Verticillium wilt
/ wood
2024
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Rapid real-time quantitative colorimetric LAMP methodology for field detection of Verticillium dahliae in crude olive-plant samples
by
Papadakis, George
, Gizeli, Electra
, Patsis, Georgios
, Paplomatas, Epaminondas J.
, Megariti, Maria
, Tzima, Aliki K.
, Panagou, Alexandra
, Markakis, Emmanouil A.
, Pantazis, Alexandros K.
in
Analysis
/ Biological Techniques
/ Biomedical and Life Sciences
/ chemical control
/ colorimetry
/ cross reaction
/ Defoliating pathotype
/ detection limit
/ Diseases and pests
/ DNA
/ Field-based detection
/ Fungi
/ genes
/ Genetic screening
/ Health aspects
/ host range
/ internal transcribed spacers
/ Life Sciences
/ Loop mediated isothermal amplification
/ Methodology
/ Methods
/ Molecular diagnostics
/ Olive
/ olives
/ pathogens
/ Plant Sciences
/ portable equipment
/ prototypes
/ RNA
/ Soilborne pathogens
/ Verticillium dahliae
/ Verticillium wilt
/ wood
2024
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Rapid real-time quantitative colorimetric LAMP methodology for field detection of Verticillium dahliae in crude olive-plant samples
Journal Article
Rapid real-time quantitative colorimetric LAMP methodology for field detection of Verticillium dahliae in crude olive-plant samples
2024
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Overview
Background
Verticilium dahliae
is the most important wilt pathogen of olive trees with a broad host range causing devastating diseases currently without any effective chemical control. Traditional detection methodologies are based on symptoms-observation or lab-detection using time consuming culturing or molecular techniques. Therefore, there is an increasing need for portable tools that can detect rapidly
V. dahliae
in the field.
Results
In this work, we report the development of a novel method for the rapid, reliable and on-site detection of
V. dahliae
using a newly designed isothermal LAMP assay and crude extracts of olive wood. For the detection of the fungus, LAMP primers were designed targeting the internal transcribed spacer (ITS) region of the rRNA gene. The above assay was combined with a purpose-built prototype portable device which allowed real time quantitative colorimetric detection of
V. dahliae
in 35 min. The limit of detection of our assay was found to be 0.8 fg/μl reaction and the specificity 100% as indicated by zero cross-reactivity to common pathogens found in olive trees. Moreover, detection of
V. dahliae
in purified DNA gave a sensitivity of 100% (Ct < 30) and 80% (Ct > 30) while the detection of the fungus in unpurified crude wood extracts showed a sensitivity of 80% when multisampling was implemented. The superiority of the LAMP methodology regarding robustness and sensitivity was demonstrated when only LAMP was able to detect
V. dahliae
in crude samples from naturally infected trees with very low infection levels, while nested PCR and SYBR qPCR failed to detect the pathogen in an unpurified form.
Conclusions
This study describes the development of a new real time LAMP assay, targeting the ITS region of the rRNA gene of
V. dahliae
in olive trees combined with a 3D-printed portable device for field testing using a tablet. The assay is characterized by high sensitivity and specificity as well as ability to operate using directly crude samples such as woody tissue or petioles. The reported methodology is setting the basis for the development of an on-site detection methodology for
V. dahliae
in olive trees, but also for other plant pathogens.
Publisher
BioMed Central,BioMed Central Ltd,BMC
Subject
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