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Systemic deterrence of aphid probing and feeding by novel β-damascone analogues

β-Damascone appeared a weak attractant close to not active to Myzus persicae, but modifications of its structure caused the avoidance of treated leaves by aphids during settling and reluctance to probe in simple choice- and no-choice experiments in previous studies. Here, the electrical penetration...

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Autores principales: Gabryś, Beata, Dancewicz, Katarzyna, Gliszczyńska, Anna, Kordan, Bożena, Wawrzeńczyk, Czesław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539356/
https://www.ncbi.nlm.nih.gov/pubmed/26300715
http://dx.doi.org/10.1007/s10340-014-0635-x
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author Gabryś, Beata
Dancewicz, Katarzyna
Gliszczyńska, Anna
Kordan, Bożena
Wawrzeńczyk, Czesław
author_facet Gabryś, Beata
Dancewicz, Katarzyna
Gliszczyńska, Anna
Kordan, Bożena
Wawrzeńczyk, Czesław
author_sort Gabryś, Beata
collection PubMed
description β-Damascone appeared a weak attractant close to not active to Myzus persicae, but modifications of its structure caused the avoidance of treated leaves by aphids during settling and reluctance to probe in simple choice- and no-choice experiments in previous studies. Here, the electrical penetration graph (EPG) technique, which allows monitoring of aphid probing within plant tissues, was applied to explore the biological background and localisation in plant tissues of the deterrent activities of β-damascone and its analogues. Activity of β-damascone and β-damascone-derived compounds depended on their substituents, which was manifested in the variation in the potency of the behavioural effect and differences in aphid probing phases that were affected. β-Damascone appeared a behaviourally inactive compound. The moderately active β-damascone ester affected aphid activities only during the phloem phase. The highly active deterrents—dihydro-β-damascol, β-damascone acetate, δ-bromo-γ-lactone, and unsaturated γ-lactone—affected pre-phloem and phloem aphid probing activities. The most effective structural modification that evoked the strongest negative response from M. persicae was the transformation of β-damascone into δ-bromo-γ-lactone. The behavioural effect of this transformation was demonstrated in frequent interruption of probing in peripheral tissues, which caused repeated failures in finding sieve elements, and reduction in the ingestion time during the phloem phase in favour of watery salivation. The inhibition of aphid probing at both the pre-phloem and phloem levels reveals the passage of the compounds studied through the plant surface and their distribution within plant tissues in a systemic way, which may reduce the risk of the transmission of non-persistent and persistent viruses.
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spelling pubmed-45393562015-08-19 Systemic deterrence of aphid probing and feeding by novel β-damascone analogues Gabryś, Beata Dancewicz, Katarzyna Gliszczyńska, Anna Kordan, Bożena Wawrzeńczyk, Czesław J Pest Sci (2004) Original Paper β-Damascone appeared a weak attractant close to not active to Myzus persicae, but modifications of its structure caused the avoidance of treated leaves by aphids during settling and reluctance to probe in simple choice- and no-choice experiments in previous studies. Here, the electrical penetration graph (EPG) technique, which allows monitoring of aphid probing within plant tissues, was applied to explore the biological background and localisation in plant tissues of the deterrent activities of β-damascone and its analogues. Activity of β-damascone and β-damascone-derived compounds depended on their substituents, which was manifested in the variation in the potency of the behavioural effect and differences in aphid probing phases that were affected. β-Damascone appeared a behaviourally inactive compound. The moderately active β-damascone ester affected aphid activities only during the phloem phase. The highly active deterrents—dihydro-β-damascol, β-damascone acetate, δ-bromo-γ-lactone, and unsaturated γ-lactone—affected pre-phloem and phloem aphid probing activities. The most effective structural modification that evoked the strongest negative response from M. persicae was the transformation of β-damascone into δ-bromo-γ-lactone. The behavioural effect of this transformation was demonstrated in frequent interruption of probing in peripheral tissues, which caused repeated failures in finding sieve elements, and reduction in the ingestion time during the phloem phase in favour of watery salivation. The inhibition of aphid probing at both the pre-phloem and phloem levels reveals the passage of the compounds studied through the plant surface and their distribution within plant tissues in a systemic way, which may reduce the risk of the transmission of non-persistent and persistent viruses. Springer Berlin Heidelberg 2014-11-25 2015 /pmc/articles/PMC4539356/ /pubmed/26300715 http://dx.doi.org/10.1007/s10340-014-0635-x Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Gabryś, Beata
Dancewicz, Katarzyna
Gliszczyńska, Anna
Kordan, Bożena
Wawrzeńczyk, Czesław
Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title_full Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title_fullStr Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title_full_unstemmed Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title_short Systemic deterrence of aphid probing and feeding by novel β-damascone analogues
title_sort systemic deterrence of aphid probing and feeding by novel β-damascone analogues
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539356/
https://www.ncbi.nlm.nih.gov/pubmed/26300715
http://dx.doi.org/10.1007/s10340-014-0635-x
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