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Development and Validation of One-Step Reverse Transcription-Droplet Digital PCR for Plum Pox Virus Detection and Quantification from Plant Purified RNA and Crude Extract
Plum pox virus (PPV) is the etiological agent of sharka, the most important viral disease of stone fruit worldwide. In this study, a one-step reverse transcription real-time PCR test (RT-qPCR) was modified and translated as a one-step RT-droplet digital PCR (RT-ddPCR) for sensitive, direct, and accu...
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Published in: | Plants (Basel) 2024-11, Vol.13 (23), p.3276 |
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description | Plum pox virus (PPV) is the etiological agent of sharka, the most important viral disease of stone fruit worldwide. In this study, a one-step reverse transcription real-time PCR test (RT-qPCR) was modified and translated as a one-step RT-droplet digital PCR (RT-ddPCR) for sensitive, direct, and accurate detection and quantification of PPV. The modified RT-qPCR and RT-ddPCR PPV detection tests were validated using both plant purified total RNA (TRNA) and crude extract as templates. The proposed tests were sensitive, specific, selective, repeatable, and reproducible in detecting PPV from fresh, lyophilized, and
plant samples. RT-ddPCR was more sensitive than RT-qPCR in detecting PPV using purified TRNA while showing the same sensitivity using crude extract. This work highlights the robustness, time-saving, and cost-effective nature of the proposed one-step RT-ddPCR test, offering a potential reduction in resources for PPV detection and quantification even with raw extracts. |
doi_str_mv | 10.3390/plants13233276 |
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plant samples. RT-ddPCR was more sensitive than RT-qPCR in detecting PPV using purified TRNA while showing the same sensitivity using crude extract. This work highlights the robustness, time-saving, and cost-effective nature of the proposed one-step RT-ddPCR test, offering a potential reduction in resources for PPV detection and quantification even with raw extracts.</description><identifier>ISSN: 2223-7747</identifier><identifier>EISSN: 2223-7747</identifier><identifier>DOI: 10.3390/plants13233276</identifier><identifier>PMID: 39683069</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Costs ; Droplets ; Flowers & plants ; Genetic transcription ; Methods ; Pay-per-view television ; Plant extracts ; Plant virus diseases ; Plant viruses ; Plum pox ; plum pox virus ; PPV strains ; Prunus spp ; Real time ; real-time PCR ; Reproducibility ; Reverse transcription ; RNA viruses ; RT-ddPCR ; sharka ; Temperature ; Transfer RNA ; tRNA ; Viral diseases ; Viruses</subject><ispartof>Plants (Basel), 2024-11, Vol.13 (23), p.3276</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3541-6ea2c791c95008aedc85133464ae5e259c99e494257a805ee7e48d60e7cddf443</cites><orcidid>0000-0003-0609-9876 ; 0000-0002-4186-4687 ; 0000-0003-0016-9239 ; 0000-0002-0048-7942 ; 0000-0003-3657-1158</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3144140772/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3144140772?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39683069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bertinelli, Giorgia</creatorcontrib><creatorcontrib>Tizzani, Lorenza</creatorcontrib><creatorcontrib>Luigi, Marta</creatorcontrib><creatorcontrib>Monticelli, Simona</creatorcontrib><creatorcontrib>Ilardi, Vincenza</creatorcontrib><title>Development and Validation of One-Step Reverse Transcription-Droplet Digital PCR for Plum Pox Virus Detection and Quantification from Plant Purified RNA and Crude Extract</title><title>Plants (Basel)</title><addtitle>Plants (Basel)</addtitle><description>Plum pox virus (PPV) is the etiological agent of sharka, the most important viral disease of stone fruit worldwide. In this study, a one-step reverse transcription real-time PCR test (RT-qPCR) was modified and translated as a one-step RT-droplet digital PCR (RT-ddPCR) for sensitive, direct, and accurate detection and quantification of PPV. The modified RT-qPCR and RT-ddPCR PPV detection tests were validated using both plant purified total RNA (TRNA) and crude extract as templates. The proposed tests were sensitive, specific, selective, repeatable, and reproducible in detecting PPV from fresh, lyophilized, and
plant samples. RT-ddPCR was more sensitive than RT-qPCR in detecting PPV using purified TRNA while showing the same sensitivity using crude extract. 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In this study, a one-step reverse transcription real-time PCR test (RT-qPCR) was modified and translated as a one-step RT-droplet digital PCR (RT-ddPCR) for sensitive, direct, and accurate detection and quantification of PPV. The modified RT-qPCR and RT-ddPCR PPV detection tests were validated using both plant purified total RNA (TRNA) and crude extract as templates. The proposed tests were sensitive, specific, selective, repeatable, and reproducible in detecting PPV from fresh, lyophilized, and
plant samples. RT-ddPCR was more sensitive than RT-qPCR in detecting PPV using purified TRNA while showing the same sensitivity using crude extract. This work highlights the robustness, time-saving, and cost-effective nature of the proposed one-step RT-ddPCR test, offering a potential reduction in resources for PPV detection and quantification even with raw extracts.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39683069</pmid><doi>10.3390/plants13233276</doi><orcidid>https://orcid.org/0000-0003-0609-9876</orcidid><orcidid>https://orcid.org/0000-0002-4186-4687</orcidid><orcidid>https://orcid.org/0000-0003-0016-9239</orcidid><orcidid>https://orcid.org/0000-0002-0048-7942</orcidid><orcidid>https://orcid.org/0000-0003-3657-1158</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Costs Droplets Flowers & plants Genetic transcription Methods Pay-per-view television Plant extracts Plant virus diseases Plant viruses Plum pox plum pox virus PPV strains Prunus spp Real time real-time PCR Reproducibility Reverse transcription RNA viruses RT-ddPCR sharka Temperature Transfer RNA tRNA Viral diseases Viruses |
title | Development and Validation of One-Step Reverse Transcription-Droplet Digital PCR for Plum Pox Virus Detection and Quantification from Plant Purified RNA and Crude Extract |
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