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Volatile compounds as potential bio-fumigants against plant-parasitic nematodes – a mini review

Hung Xuan Bui
Hung Xuan Bui
 und 
Johan A. Desaeger
Johan A. Desaeger
   | 01. Jan. 2021
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Online veröffentlicht: 01. Jan. 2021
Seitenbereich: 1 - 12
DOI: https://doi.org/10.21307/jofnem-2021-014
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© 2021 Authors, published by Sciendo.
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Overview of studies investigating the effect of plant volatile compounds on different plant-parasitic nematodes.

Volatile compound producers Identified volatile compounds Experiment conditions Target plant-parasitic nematodes References
Brassica Glucosinolates and isothiocyanates Field biofumigation Meloidogyne incognita, M. javanica, Heterodera schachtii, Pratylenchus neglectus, Paratrichodorus allius Thierfelder and Friedt (1995), Potter et al. (1998), Lord et al. (2011)
White mustard (Sinapis alba) Methyl sulfide, dimethyl disulfide Field biofumigation Tylenchulus semipenetrans Wang et al. (2009)
Brassica leaf 2-propenyl glucosinolate Field biofumigation Globodera pallida Lord et al. (2011)
Brassica juncea, Azadirachta indica, Canavalia ensiformis, Mucuna pruriens, and Cajanus cajan Alcohols and esters and sulfur containing compounds (mainly isothiocyanates) In vitro and greenhouse M. incognita Barros et al. (2014)
Camellia seed cake 18 compounds were identified In vitro M. javanica Yang et al. (2015)
Eruca sativa (Z)-3-hexenyl acetate, (Z)-3-hexen-1-ol and erucin In vitro M. incognita Aissani et al. (2015)
Cottonseed meal 2-methyl-1-butanol, 3-methyl-1-butanol, phenyl-ethylalcohol, benzene-1-ethyl-4methoxy (p-ethylanisole), and 4-ethyl-1,2-dimethoxybenzene In vitro and greenhouse M. incognita Estupiñan-López et al. (2017)
Castor bean cake Phenol, 4-methylphenol, γ-decalactone, and skatole In vitro and greenhouse M. incognita Pedroso et al. (2019)
Citronella (Cymbopogon nardus L.) or black pepper (Piper nigrum L.) leaves, broccoli shoots (Brassica oleracea L.) and Brazil nuts (Bertholletia excelsa Bonpl.) Dimethyl disulfide and 3-pentanol In vitro and greenhouse M. incognita Silva et al. (2018), da Silva et al. (2019)
Watercress (Nasturtium officinale) leaves and passion fruit (Passiflora edulis) seeds 26 and 12 compounds were identified. 1-octanol had strong nematicidal activity In vitro and greenhouse M. incognita Silva et al. (2020)
Seeds of papaya fruit (Carica papaya) Vinyl acetate, phenylacetaldehyde and benzylacetonitrile In vitro and greenhouse M. incognita Gomes et al. (2020)
Cymbopogon nardus and Dysphania ambrosioides Ascaridole and citronellal In vitro and greenhouse M. incognita de Freitas Silva et al. (2020)

Overview of studies investigating the effect of bacterial volatile compounds on different plant-parasitic nematodes.

Volatile compound producers Identified volatile compounds Experiment conditions Target plant-parasitic nematodes References
Bacillus simplex, B. subtilis, B. weihenstephanensis, Stenotrophomonas maltophilia and Serratia marcescens Terpineol, benzeneethanol, propanone, phenyl ethanone and nonane In vitro B. xylophilus Gu et al. (2007)
Bacillus megaterium YFM3.25 Benzeneacetaldehyde, 2-nonanone, decanal, 2-undecanone and dimethyl disulphide,phenyl ethanone, nonane, phenol, 3,5-dimethoxytoluene, 2,3-dimethyl- butanedinitrile and 1-thenyl-4-methoxy- benzene In vitro and greenhouse M. incognita Huang et al. (2010)
Pseudomonas putida, Microbacterium sp., Bacillus methylotrophicus, Bacillus pumilus and Bacillus pumilus Unidentified In vitro M. exigua Costa et al. (2015)
Pseudomonas putida BP25 As 1-Undecene; Disulfide dimethyl; Pyrazine, methyl-Pyrazine, 2,5-dimethyl-; Isoamyl alcohol; Pyrazine,methyl-; Dimethyl trisulfide In vitro Radopholus similis Sheoran et al. (2015), Agisha et al. (2019)
Pseudochrobactrum saccharolyticum, Wautersiella falsenii, Proteus hauseri, Arthrobacter nicotianae, and Achromobacter xylosoxidans Acetophenone, S-methyl thiobutyrate, dimethyl disulfide, ethyl 3,3-dimethylacrylate, nonan-2 one, 1-methoxy-4-methylbenzene, and butyl isovalerate In vitro M. incognita Xu et al. (2015)
Paenibacillus polymyxa KM 2501 Acetone, 2-heptanone, benzaldehyde, 2-nonanone, 2-nonanol, cyclopentasiloxane, decamethyl-, 11-dodecen-2-one, 2-decanone, 2-decanol, 4-acetylbenzoic acid, furfural acetone, 2-undecanone, Acetic acid, [bis[(trimethylsilyl)oxy]phosphinyl]-, trimethylsilyl ester, 2-undecanol In vitro M. incognita Cheng et al. (2017)
Pseudomonas putida 1A00316 Dimethyl disulfide, 1-undecene, 2- nonanone, 2-octanone, (Z)-hexen-1-ol acetate, 2-undecanone, and 1-(ethenyloxy)- octadecane. Of these, dimethyl disulfide, 2-nonanone, 2-octanone, (Z)-hexen-1-ol acetate, and 2-undecanone In vitro M. incognita Zhai et al. (2018)
Bacillus sp., Paenibacillus sp. and Xanthomonas sp. Unidentified In vitro and greenhouse M. graminicola Bui et al. (2020)

Overview of studies investigating the effect of fungal volatile compounds on different plant-parasitic nematodes.

Volatile compound producers Identified volatile compounds Experiment conditions Target plant-parasitic nematodes References
Muscodor albus Unidentified In vitro Meloidogyne chitwoodi, M. hapla, Paratrichodorus allius, and P. penetrans Riga et al. (2008)
Trichoderma sp. YMF 1.00416 1β-vinylcyclopentane-1α,3α-diol, 6-pentyl-2H-pyran-2-one and 4-(2-hydroxyethyl) phenol In vitro Bursaphelenchus xylophilus Yang et al. (2012)
Fusarium oxysporum and Fusarium solani Dioctyl disulfide (2-propyldecan-1-ol or 1-(2-hydroxyethoxy) tridecane); caryophyllene; 4-methyl-2,6-di-tert-butylphenol; and acoradiene In vitro and greenhouse M. incognita Freire et al. (2012)
Fusarium oxysporum Unidentified In vitro M. exigua Costa et al. (2015)
Endophytic fungus Daldinia cf. concentrica 3-methyl-1-butanol, (±)-2-methyl-1-butanol, 4-heptanone, and isoamyl acetate, In vitro and greenhouse M. javanica Liarzi et al. (2016)
Epicoccum nigrum and Schizophyllum commune Alcohols, esters, terpenes, and ketones In vitro and greenhouse M. incognita Pimenta et al. (2017)
Fusarium oxysporum strain 21 More than 28 volatile organic compounds were identified. In vitro and greenhouse M. incognita Terra et al. (2017)
Fusarium oxysporum strain 21 2-methylbutyl acetate, 3-methylbutyl acetate, ethyl acetate, and 2-methylpropyl acetate In vitro and greenhouse M. incognita Terra et al. (2018)
Fusarium oxysporum and Fusarium solani 23 compounds belong to esters, alcohols, phenols, aldehydes, carboxylic acids and sesquiterpenes In vitro and greenhouse M. incognita Estupiñan-López et al. (2018)
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