Literature DB >> 24093923

Exploitation of FTA cartridges for the sampling, long-term storage, and DNA-based analyses of plant-parasitic nematodes.

Martin Marek, Miloslav Zouhar, Ondřej Douda, Marie Maňasová, Pavel Ryšánek.   

Abstract

The use of DNA-based analyses in molecular plant nematology research has dramatically increased over recent decades. Therefore, the development and adaptation of simple, robust, and cost-effective DNA purification procedures are required to address these contemporary challenges. The solid-phase-based approach developed by Flinders Technology Associates (FTA) has been shown to be a powerful technology for the preparation of DNA from different biological materials, including blood, saliva, plant tissues, and various human and plant microbial pathogens. In this work, we demonstrate, for the first time, that this FTA-based technology is a valuable, low-cost, and time-saving approach for the sampling, long-term archiving, and molecular analysis of plant-parasitic nematodes. Despite the complex structure and anatomical organization of the multicellular bodies of nematodes, we report the successful and reliable DNA-based analysis of nematode high-copy and low-copy genes using the FTA technology. This was achieved by applying nematodes to the FTA cards either in the form of a suspension of individuals, as intact or pestle-crushed nematodes, or by the direct mechanical printing of nematode-infested plant tissues. We further demonstrate that the FTA method is also suitable for the so-called "one-nematode-assay", in which the target DNA is typically analyzed from a single individual nematode. More surprisingly, a time-course experiment showed that nematode DNA can be detected specifically in the FTA-captured samples many years after initial sampling occurs. Collectively, our data clearly demonstrate the applicability and the robustness of this FTA-based approach for molecular research and diagnostics concerning phytonematodes; this research includes economically important species such as the stem nematode (Ditylenchus dipsaci), the sugar beet nematode (Heterodera schachtii), and the Northern root-knot nematode (Meloidogyne hapla).

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Year:  2014        PMID: 24093923     DOI: 10.1094/PHYTO-03-13-0067-R

Source DB:  PubMed          Journal:  Phytopathology        ISSN: 0031-949X            Impact factor:   4.025


  3 in total

1.  Rapid, simple and direct detection of Meloidogyne hapla from infected root galls using loop-mediated isothermal amplification combined with FTA technology.

Authors:  Huan Peng; Haibo Long; Wenkun Huang; Jing Liu; Jiangkuan Cui; Lingan Kong; Xianqi Hu; Jianfeng Gu; Deliang Peng
Journal:  Sci Rep       Date:  2017-04-03       Impact factor: 4.379

2.  Evaluation of DNA Extraction Methods on Individual Helminth Egg and Larval Stages for Whole-Genome Sequencing.

Authors:  Stephen R Doyle; Geetha Sankaranarayanan; Fiona Allan; Duncan Berger; Pablo D Jimenez Castro; James Bryant Collins; Thomas Crellen; María A Duque-Correa; Peter Ellis; Tegegn G Jaleta; Roz Laing; Kirsty Maitland; Catherine McCarthy; Tchonfienet Moundai; Ben Softley; Elizabeth Thiele; Philippe Tchindebet Ouakou; John Vianney Tushabe; Joanne P Webster; Adam J Weiss; James Lok; Eileen Devaney; Ray M Kaplan; James A Cotton; Matthew Berriman; Nancy Holroyd
Journal:  Front Genet       Date:  2019-09-20       Impact factor: 4.599

3.  Caenorhabditis nematodes colonize ephemeral resource patches in neotropical forests.

Authors:  Solomon A Sloat; Luke M Noble; Annalise B Paaby; Max Bernstein; Audrey Chang; Taniya Kaur; John Yuen; Sophia C Tintori; Jacqueline L Jackson; Arielle Martel; Jose A Salome Correa; Lewis Stevens; Karin Kiontke; Mark Blaxter; Matthew V Rockman
Journal:  Ecol Evol       Date:  2022-07-24       Impact factor: 3.167

  3 in total

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