Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The protocol describes the in vivo and in vitro pinewood nematode infection of Pinus pinaster and their volatilome analysis through Gas Chromatography (GC) and GC coupled to Mass Spectrometry (GC-MS).

Abstract

The pinewood nematode (PWN) is a phytoparasite that causes pine wilt disease (PWD) in conifer species. This plant parasitic nematode has heavily contributed to pine deforestation in Asian countries, e.g., Japan, China, and Korea. Over the last two decades, in Europe, Portugal and Spain have been greatly affected. Research on the mechanisms of PWN infection and/or PWD progression in susceptible host species relies on the controlled infection of pine seedlings under greenhouse conditions. This technique is laborious and mobilizes substantial economic and human resources. Additionally, it can be prone to variability that results from the genetic diversity associated with some pine species but also from the interference of external factors. As an alternative, in vitro co-cultures of pine with PWNs offer a more advantageous system for studying biochemical changes since they a) allow controlling single environmental or nutritional variables, b) occupy less space, c) require less time to obtain, and d) are free from contamination or from host genetic variation. The following protocol details the standard in vivo PWN infection of Pinus pinaster, the maritime pine, and the establishment of the novel in vitro co-cultures of pine shoots with the PWN as an improved methodology to study this phytoparasite influence on pine volatiles. PWN-induced volatiles are extracted from in vivo and in vitro infected pines by hydrodistillation and distillation-extraction, and the emitted volatiles are captured by solid phase microextraction (SPME), using fiber or packed column techniques.

Introduction

The pinewood nematode (PWN), Bursaphelenchus xylophilus (Steiner & Bührer 1934) Nickle 1970, is a plant parasitic nematode that mainly parasitizes Pinus species. This phytoparasite is vectored by insects of the genus Monochamus into trees of susceptible pine species during the insect's maturation feeding. The PWN kills the tree by attacking its resin canals and reducing resin flow, and by damaging its vascular tissue, causing interruptions in the water column. Lack of water at the tree canopy induces the first visible symptoms of pine wilt disease (PWD), i.e., the pine needles become chlorotic after the cessation of photosy....

Protocol

1. Growing in vitro pinewood nematode

NOTE: Pinewood nematodes are grown by feeding on the fungal mycelium of a non-sporulating strain of Botrytis cinerea (de Bary) Whetzel11.

  1. For routine sub-culture, transfer a culture plug (0.5 cm diameter) from the outermost border of the fungal colony onto a plate of sterile potato dextrose agar (PDA) and keep at 25 ± 1 °C for 7 to 10 days, or until the fungal colony .......

Representative Results

The PWN reproduces quickly under optimal conditions, and generation times can be as low as 4 days, with each female lying about 80 eggs during her life28. Using the methodology described above, large amounts of PWNs can be obtained depending on fungal growth. Within an 8-day growth period, PWNs can have a 100-fold increase in population numbers (Figure 1). To increase the consistency in the amounts of PWNs, use sterilized PWNs since contamination with unknown bacteria.......

Discussion

The protocol presented here outlines an enhanced methodology to analyze volatile compounds in maritime pine infected by the PWN, where environmental and genetic variability is reduced and does not influence the outcomes. Using pure lines of in vitro maritime pine genotypes, extracted and emitted volatiles can be analyzed as a host response to one of the most damaging biotic threats to pine forests.

Maintenance of reference cultures or the growth of large amounts of PWNs is easily perf.......

Acknowledgements

This research was partly funded by the EU under the PurPest project through grant agreement 101060634, and by Fundação para a Ciência e a Tecnologia (FCT), through projects NemACT, DOI 10.54499/2022.00359.CEECIND/CP1737/CT0002; NemaWAARS, DOI 10.54499/PTDC/ASP-PLA/1108/2021; CESAM UIDP/50017/2020+UIDB/50017/2020+ LA/P/0094/2020; CE3C, DOI 10.54499/UIDB/00329/2020; GREEN-IT, DOI 10.54499/UIDB/04551/2020 and 10.54499/UIDP/04551/2020.

....

Materials

NameCompanyCatalog NumberComments
38 mesh test sieveRetsch60.131.000038
6-Benzylaminopurine (6-BAP)Duchefa BiochemieB0904
Charcoal activatedDuchefa BiochemieC1302
Clevenger apparatusWINZER Laborglastechnik25-000-02
Hydrogen peroxide solutionSigma-AldrichH1009-500ML
Indole-3-butyric acid (IBA)Duchefa BiochemieI0902
Likens-Nickerson apparatusVitriLab LDA.c/IN29/32
Microbox round containersSac O2O118/80+OD118
n-PentaneSigma-Aldrich1.00882
PARAFILM M sealing filmBRANDHS234526B-1EA
Phyto agarDuchefa BiochemieP1003
Potato Dextrose AgarBD DIFCO213400
Scalpel blade no. 24Romed HollandBLADE24
Schenk & Hildebrandt Basal salt mediumDuchefa BiochemieS0225
Schenk & Hildebrandt vitamin mixtureDuchefa BiochemieS0411
SPME fiber assembly Polydimethylsiloxane (PDMS)Supelco57300-U
SPME Fiber HolderSupelco57330-U
SucroseDuchefa BiochemieS0809
Tenax TA- stainless steel tubes- conditioned + cappedMarkes InternationalC1-AAXX-5003

References

  1. Back, M. A., Bonifácio, L., Inácio, M. L., Mota, M., Boa, E. Pine wilt disease: A global threat to forestry. Plant Pathol. 73 (5), 1026-1041 (2024).
  2. Mumm, R., Hilker, M. Direct and indirect chemical defence of pine against f....

Explore More Articles

Biology

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved