| Title: | "Caenorhabditis elegans susceptibility to Daldinia cf. concentrica bioactive volatiles is coupled with expression activation of the stress-response transcription factor daf-16, a part of distinct nematicidal action" |
| Author(s): | Sanadhya P; Bucki P; Liarzi O; Ezra D; Gamliel A; Braun Miyara S; |
| Address: | "Department of Entomology and the Nematology and Chemistry Units, Agricultural Research Organization (ARO), the Volcani Center, Rishon Lezion, Israel. Department of Plant Pathology and Weed Research, ARO, the Volcani Center, Rishon Lezion, Israel. Agricultural Engineering, Growing, Production and Environmental Engineering, Laboratory for Pest Management Research, ARO, the Volcani Center, Rishon Lezion, Israel" |
| DOI: | 10.1371/journal.pone.0196870 |
| ISSN/ISBN: | 1932-6203 (Electronic) 1932-6203 (Linking) |
| Abstract: | "The bionematicidal effect of a synthetic volatile mixture (SVM) of four volatile organic compounds (VOCs) emitted by the endophytic fungus Daldinia cf. concentrica against the devastating plant-parasitic root-knot nematode Meloidogyne javanica has been recently demonstrated in both in vitro and greenhouse experiments. However, the mode of action governing the observed irreversible paralysis of J2 larvae upon exposure to SVM is unknown. To unravel the mechanism underlying the anthelmintic and nematicidal activities, we used the tractable model worm Caenorhabditis elegans. C. elegans was also susceptible to both the fungal VOCs and SVM. Among compounds comprising SVM, 3-methyl-1-butanol, (+/-)-2-methyl-1-butanol, and 4-heptanone showed significant nematicidal activity toward L1, L4 and young adult stages. Egg hatching was only negatively affected by 4-heptanone. To determine the mechanism underlying this activity, we examined the response of C. elegans mutants for glutamate-gated chloride channel and acetylcholine transporter, targets of the nematicidal drugs ivermectin and aldicarb, respectively, to 4-heptanone and SVM. These aldicarb- and ivermectin-resistant mutants retained susceptibility upon exposure to 4-heptanone and SVM. Next, we used C. elegans TJ356 strain zIs356 (daf-16::GFP+rol-6), LD1 ldIs7 [skn-1B/C::GFP + pRF4(rol-6(su1006))], LD1171 ldIs3 [gcs-1p::gfp; rol-6(su1006))], CL2166 dvIs19 (gst-4p::GFP) and CF1553 muIs84 (sod-3p::GFP+rol-6), which have mutations in genes regulating multiple stress responses. Following exposure of L4 larvae to 4-heptanone or SVM, there was clear nuclear translocation of DAF-16::GFP, and SKN-1::GFP indicating that their susceptibility involves DAF-16 and SKN1 regulation. Application of 4-heptanone, but not SVM, induced increased expression of, gcs-1::GFP and gst-4::GFP compared to controls. In contrast, application of 4-heptanone or SVM to the sod-3::GFP line elicited a significant decline in overall fluorescence intensity compared to controls, indicating SOD-3 downregulation and therefore overall reduction in cellular redox machinery. Our data indicate that the mode of action of SVM and 4-heptanone from D. cf. concentrica differs from that of currently available nematicides, potentially offering new solutions for nematode management" |
| Keywords: | Aldicarb/pharmacology Animals Anthelmintics/isolation & purification/*pharmacology Caenorhabditis elegans/*drug effects/genetics/growth & development/metabolism Caenorhabditis elegans Proteins/agonists/*genetics/metabolism DNA-Binding Proteins/genetics/me; |
| Notes: | "MedlineSanadhya, Payal Bucki, Patricia Liarzi, Orna Ezra, David Gamliel, Abraham Braun Miyara, Sigal eng Research Support, Non-U.S. Gov't 2018/05/04 PLoS One. 2018 May 3; 13(5):e0196870. doi: 10.1371/journal.pone.0196870. eCollection 2018" |
