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A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses
Thrips palmi (Thysanoptera: Thripidae) is an important pest of vegetables, ornamentals, and legumes worldwide. Besides damage caused by feeding, it transmits several tospoviruses. Identification of T. palmi at an early stage is crucial in implementing appropriate pest management strategies. Morpho-t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541097/ https://www.ncbi.nlm.nih.gov/pubmed/33046966 http://dx.doi.org/10.1007/s10340-020-01284-w |
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author | Priti Jangra, Sumit Baranwal, V. K. Dietzgen, Ralf G. Ghosh, Amalendu |
author_facet | Priti Jangra, Sumit Baranwal, V. K. Dietzgen, Ralf G. Ghosh, Amalendu |
author_sort | Priti |
collection | PubMed |
description | Thrips palmi (Thysanoptera: Thripidae) is an important pest of vegetables, ornamentals, and legumes worldwide. Besides damage caused by feeding, it transmits several tospoviruses. Identification of T. palmi at an early stage is crucial in implementing appropriate pest management strategies. Morpho-taxonomic identification of T. palmi based on the adult stage is time-consuming and needs taxonomic expertise. Here, we report a rapid, on-site, field-based assay for identification of T. palmi based on recombinase polymerase amplification (RPA), its first application in insects. RPA primers designed based on 3′ polymorphisms of the Internal Transcribed Spacer 2 region efficiently discriminated T. palmi without any cross-reactivity to other predominant thrips species. RPA was performed with crude DNA, extracted from single T. palmi simply by crushing in sterile distilled water and could be completed within 20 min by holding the reaction tubes in the hand. The assay was further simplified by using fluorescent as well as colorimetric dyes thus eliminating the gel-electrophoresis steps. The presence of T. palmi was visualized by a change in color from dark blue to sky blue. The assay was validated with known thrips specimens and found to be effective in diagnosing the presence of T. palmi in natural vegetation. This on-site, rapid assay for diagnosis of T. palmi can be used by non-expert personnel in the field of quarantine and pest management. |
format | Online Article Text |
id | pubmed-7541097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75410972020-10-08 A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses Priti Jangra, Sumit Baranwal, V. K. Dietzgen, Ralf G. Ghosh, Amalendu J Pest Sci (2004) Rapid Communication Thrips palmi (Thysanoptera: Thripidae) is an important pest of vegetables, ornamentals, and legumes worldwide. Besides damage caused by feeding, it transmits several tospoviruses. Identification of T. palmi at an early stage is crucial in implementing appropriate pest management strategies. Morpho-taxonomic identification of T. palmi based on the adult stage is time-consuming and needs taxonomic expertise. Here, we report a rapid, on-site, field-based assay for identification of T. palmi based on recombinase polymerase amplification (RPA), its first application in insects. RPA primers designed based on 3′ polymorphisms of the Internal Transcribed Spacer 2 region efficiently discriminated T. palmi without any cross-reactivity to other predominant thrips species. RPA was performed with crude DNA, extracted from single T. palmi simply by crushing in sterile distilled water and could be completed within 20 min by holding the reaction tubes in the hand. The assay was further simplified by using fluorescent as well as colorimetric dyes thus eliminating the gel-electrophoresis steps. The presence of T. palmi was visualized by a change in color from dark blue to sky blue. The assay was validated with known thrips specimens and found to be effective in diagnosing the presence of T. palmi in natural vegetation. This on-site, rapid assay for diagnosis of T. palmi can be used by non-expert personnel in the field of quarantine and pest management. Springer Berlin Heidelberg 2020-10-08 2021 /pmc/articles/PMC7541097/ /pubmed/33046966 http://dx.doi.org/10.1007/s10340-020-01284-w Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Rapid Communication Priti Jangra, Sumit Baranwal, V. K. Dietzgen, Ralf G. Ghosh, Amalendu A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title | A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title_full | A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title_fullStr | A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title_full_unstemmed | A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title_short | A rapid field-based assay using recombinase polymerase amplification for identification of Thrips palmi, a vector of tospoviruses |
title_sort | rapid field-based assay using recombinase polymerase amplification for identification of thrips palmi, a vector of tospoviruses |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541097/ https://www.ncbi.nlm.nih.gov/pubmed/33046966 http://dx.doi.org/10.1007/s10340-020-01284-w |
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