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Title:The influence of storage conditions and DNA extraction protocol on the results of molecular analysis of the European spruce bark beetle (Ips typographus L.)
Authors:ID Devetak, Zina (Author)
ID Kavčič, Andreja (Author)
ID De Groot, Maarten (Author)
ID Piškur, Barbara (Author)
Files:URL URL - Source URL, visit https://doi.org/10.20315/ASetL.132.3
 
.pdf PDF - Presentation file, download (1,17 MB)
MD5: 4EBCAA87DBDD1FC548C5FED00E88F063
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo SciVie - Slovenian Forestry Institute
Abstract:One of the key steps of the molecular identification of bark beetles is obtaining a sufficient quantity of high-quality DNA extract. In this study, we investigated the influence of different storage procedures for Ips typographus (L.) specimens and various DNA extraction protocols on the quantity and quality of DNA intended for use in molecular diagnostics. Adult beetles were frozen at -20 °C, either dry or in ethanol. We tested four different protocols for DNA extraction. We compared the quantity of extracted DNA and assessed its quality with PCR and Sanger sequencing. Different storage protocols had no significant effect on the quantity of DNA extracted. However, freezing specimens in ethanol provided higher-quality DNA for molecular applications. Only two of the extraction protocols produced sequenceable amplicons, and the difference in the amount of extracted DNA between them was not significant. We propose the optimal combination of storing specimens in ethanol at -20°C and using the Nucleospin Insect DNA extraction kit from Macherey Nagel, enabling a timeefficient identification process.
Keywords:early detection, specimen storage, total DNA extraction, PCR, polymerase chain reaction, Sanger sequencing, molecular diagnostics
Publication version:Version of Record
Publication date:01.01.2023
Year of publishing:2023
Number of pages:str. 29-38
Numbering:Vol. 132
PID:20.500.12556/DiRROS-18084-753714a3-81a7-cc37-5a95-de9e0459aa34 New window
UDC:630*14:630*13(045)=111
ISSN on article:2335-3112
DOI:10.20315/ASetL.132.3 New window
COBISS.SI-ID:180304131 New window
Publication date in DiRROS:02.02.2024
Views:429
Downloads:132
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Record is a part of a journal

Title:Acta Silvae et Ligni
Publisher:Gozdarski inštitut Slovenije, založba Silva Slovenica, Biotehniška fakulteta, Oddelek za gozdarstvo in obnovljive gozdne vire, Biotehniška fakulteta, Oddelek za lesarstvo
ISSN:2335-3112
COBISS.SI-ID:266761216 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P4-0107-2020
Name:Gozdna biologija, ekologija in tehnologija

Funder:Other - Other funder or multiple funders
Funding programme:Ministrstvo za kmetijstvo, gozdarstvo in prehrano
Project number:JGS
Name:Javna gozdarska služba
Acronym:JGS

Licences

License:CC BY-SA 4.0, Creative Commons Attribution-ShareAlike 4.0 International
Link:http://creativecommons.org/licenses/by-sa/4.0/
Description:This Creative Commons license is very similar to the regular Attribution license, but requires the release of all derivative works under this same license.

Secondary language

Language:Slovenian
Title:Vpliv postopkov shranjevanja in ekstrakcije celokupne DNA na rezultate molekularne analize osmerozobega smrekovega lubadarja (Ips typographus L.)
Abstract:Za uspeh molekularne identifikacije podlubnikov je ključna zadostna količina kakovostnega ekstrakta DNA. Pri raziskavi vrste smo se osredotočili na vpliv različnih postopkov shranjevanja osebkov Ips typographus(L.) in različnih protokolov ekstrakcije DNA na količino in kakovost DNA, namenjene za uporabo v molekularni diagnostiki. Odrasle hrošče smo zamrznili pri -20 °C na dva načina, v etanolu in na suho. Ekstrakcije smo opravili po štirih različnih postopkih. Primerjali smo količino pridobljene DNA. Kakovost ekstrahirane DNA smo ocenili s polimerazno verižno reakcijo in sekvenciranjem po Sangerju. Način shranjevanja ni statistično značilno vplival na količino pridobljene DNA. DNA višje kakovosti smo pridobili iz hroščev, ki so bili zamrznjeni v etanolu. Le dva postopka ekstrakcije DNA sta dala DNA, uporabno za sekvenciranje. V količini pridobljene DNA se pri sekvenciranju uspešna postopka nista pomembno razlikovala. Določili smo optimalno kombinacijo postopkov shranjevanja v etanolu pri -20 °C in ekstrakcije celokupne DNA z ekstrakcijskim kitom Nucleospin Insect DNA proizvajalca Macherey Nagel, ki omogoča časovno učinkovito identifikacijo.
Keywords:zgodnje zaznavanje, shranjevanje osebkov, ekstrakcijski postopek, polimerazna verižna reakcija, PCR, sekvenciranje po Sangerju, molekularna diagnostika


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  1. Acta Silvae et Ligni

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