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A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies
SIMPLE SUMMARY: Rapid diagnostic tools are critical for the management and eradication of boll weevil, Anthonomus grandis grandis. Here, we present the development and validation of a novel qPCR assay that enables same-day identification of Anthonomus grandis subspecies. ABSTRACT: Rapid and accurate...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671495/ https://www.ncbi.nlm.nih.gov/pubmed/37999044 http://dx.doi.org/10.3390/insects14110845 |
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author | Raszick, Tyler Jay Perkin, Lindsey C. Godoy, Alejandra Shirley, Xanthe A. Wright, Karen Martin, Paxton T. Suh, Charles P. -C. Ruiz-Arce, Raul Sword, Gregory A. |
author_facet | Raszick, Tyler Jay Perkin, Lindsey C. Godoy, Alejandra Shirley, Xanthe A. Wright, Karen Martin, Paxton T. Suh, Charles P. -C. Ruiz-Arce, Raul Sword, Gregory A. |
author_sort | Raszick, Tyler Jay |
collection | PubMed |
description | SIMPLE SUMMARY: Rapid diagnostic tools are critical for the management and eradication of boll weevil, Anthonomus grandis grandis. Here, we present the development and validation of a novel qPCR assay that enables same-day identification of Anthonomus grandis subspecies. ABSTRACT: Rapid and accurate identification of Anthonomus grandis subspecies is crucial for effective management and eradication. Current diagnostic methods have limitations in terms of time to diagnosis (up to seven days) and can yield ambiguous results. Here, we present the validation of a custom TaqMan SNP Genotyping Assay for the rapid and accurate identification of A. grandis grandis (boll weevil) and A. g. thurberiae (thurberia weevil) subspecies. To validate the assay, we conducted three main experiments: (1) a sensitivity test to determine the DNA concentration range at which the assay performs, (2) a non-target specificity test to ensure no amplification in non-target weevils (false positives), and (3) an accuracy test comparing the results of the new assay to previously established methods. These experiments were carried out in parallel at three independent facilities to confirm the robustness of the assay to variations in equipment and personnel. We used DNA samples from various sources, including field-collected specimens, museum specimens, and previously isolated DNA. The assay demonstrated high sensitivity (PCR success with ≥0.05 ng/µL DNA template), specificity (0.02 false positive rate), and accuracy (97.7%) in diagnosing boll weevil and thurberia weevil subspecies. The entire workflow, including DNA extraction, assay preparation, PCR run time, and data analysis, can be completed within a single workday (7–9 h) by a single technician. The deployment of this assay as a diagnostic tool could benefit boll weevil management and eradication programs by enabling same-day diagnosis of trap-captured or intercepted weevil specimens. Furthermore, it offers a more reliable method for identifying unknown specimens, contributing to the overall effectiveness of boll weevil research and control efforts. |
format | Online Article Text |
id | pubmed-10671495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106714952023-10-31 A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies Raszick, Tyler Jay Perkin, Lindsey C. Godoy, Alejandra Shirley, Xanthe A. Wright, Karen Martin, Paxton T. Suh, Charles P. -C. Ruiz-Arce, Raul Sword, Gregory A. Insects Article SIMPLE SUMMARY: Rapid diagnostic tools are critical for the management and eradication of boll weevil, Anthonomus grandis grandis. Here, we present the development and validation of a novel qPCR assay that enables same-day identification of Anthonomus grandis subspecies. ABSTRACT: Rapid and accurate identification of Anthonomus grandis subspecies is crucial for effective management and eradication. Current diagnostic methods have limitations in terms of time to diagnosis (up to seven days) and can yield ambiguous results. Here, we present the validation of a custom TaqMan SNP Genotyping Assay for the rapid and accurate identification of A. grandis grandis (boll weevil) and A. g. thurberiae (thurberia weevil) subspecies. To validate the assay, we conducted three main experiments: (1) a sensitivity test to determine the DNA concentration range at which the assay performs, (2) a non-target specificity test to ensure no amplification in non-target weevils (false positives), and (3) an accuracy test comparing the results of the new assay to previously established methods. These experiments were carried out in parallel at three independent facilities to confirm the robustness of the assay to variations in equipment and personnel. We used DNA samples from various sources, including field-collected specimens, museum specimens, and previously isolated DNA. The assay demonstrated high sensitivity (PCR success with ≥0.05 ng/µL DNA template), specificity (0.02 false positive rate), and accuracy (97.7%) in diagnosing boll weevil and thurberia weevil subspecies. The entire workflow, including DNA extraction, assay preparation, PCR run time, and data analysis, can be completed within a single workday (7–9 h) by a single technician. The deployment of this assay as a diagnostic tool could benefit boll weevil management and eradication programs by enabling same-day diagnosis of trap-captured or intercepted weevil specimens. Furthermore, it offers a more reliable method for identifying unknown specimens, contributing to the overall effectiveness of boll weevil research and control efforts. MDPI 2023-10-31 /pmc/articles/PMC10671495/ /pubmed/37999044 http://dx.doi.org/10.3390/insects14110845 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Raszick, Tyler Jay Perkin, Lindsey C. Godoy, Alejandra Shirley, Xanthe A. Wright, Karen Martin, Paxton T. Suh, Charles P. -C. Ruiz-Arce, Raul Sword, Gregory A. A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title | A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title_full | A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title_fullStr | A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title_full_unstemmed | A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title_short | A New qPCR Assay for the Rapid Diagnosis of Anthonomus grandis Subspecies |
title_sort | new qpcr assay for the rapid diagnosis of anthonomus grandis subspecies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671495/ https://www.ncbi.nlm.nih.gov/pubmed/37999044 http://dx.doi.org/10.3390/insects14110845 |
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