Literature DB >> 28311805

The watercress glucosinolate-myrosinase system: a feeding deterrent to caddisflies, snails and amphipods.

Raymond M Newman1, Zac Hanscom2, W Charles Kerfoot3.   

Abstract

Watercress (Nasturtium officinale) possesses the glucosinolate-myrosinase system. This system is regarded as a classic example of chemical defense for terrestrial crucifers. Damage of watercress initiates myrosinase-mediated hydrolysis of phenylethyl glucosinolate to a toxic endproduct, phenylethyl isothiocyanate. In multiple choice tests, the amphipod Gammarus pseudolimnaeus, the limnephilid caddisflies Hesperophylax designatus and Limnephilus sp., and the physid snail Physella sp. all strongly preferred (10X) yellowed senescent watercress (FY) over fresh green watercress (FG), despite the 2X higher nitrogen content of green watercress (6.9% for FG vs 3.8% for FY). Green watercress contained 10-40 X more glucosinolate than FY watercress (6.4-8.5 mg/g wet for FG vs 0.2-0.7 mg/g wet for FY). However, when the watercress was heated (ca 70°C), to deactivate the myrosinase enzyme, multiple choice tests showed that these species shift their preferences to heated green watercress (HG). Heating deactivated the deterrent effect and overall preference (consumption) was HG ≥ HY > FY ≫ FG for Gammarus. HG > HY ≥ FY ≫ FG for Hesperophylax, HG > FY ≥HY ≥ FG for Limnephilus, and HG ≥ FY > HY ≥ FG for Physella. Thus heating resulted in a shift in preference from the low glucosinolate, but low nitrogen, unheated yellowed tissue to the high nitrogen green tissue. These results suggest that deactivation of the myrosinase enzyme, and hence isothiocyanate production, results in a shift in preference. Preliminary results with Hesperophylax indicate that addition of myrosinase to the test water, which resulted in the formation of isothiocyanate, results in a significant decrease in HG consumption from control levels (p < 0.001) and no change in preference for HY watercress. With Gammarus, myrosinase resulted in reduced consumption of both green and yellowed watercress, but no significant differential effect. These results provide evidence that the glucosinolate-myrosinase system, recognized as the principle deterrent system of terrestrial crucifers, is the feeding deterrent in watercress and also suggest that in the absence of a functioning deterrent system, nitrogen content may influence consumption.

Entities:  

Keywords:  Chemical defense; Crucifer; Feeding deterrent; Freshwater; Streams

Year:  1992        PMID: 28311805     DOI: 10.1007/BF00317255

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  7 in total

1.  Ecological patterns in the glucosinolate content of a native mustard,Cardamine cordifolia, in the rocky mountains.

Authors:  S M Louda; J E Rodman
Journal:  J Chem Ecol       Date:  1983-03       Impact factor: 2.626

2.  Analysis of feeding preference experiments.

Authors:  C H Peterson; P E Renaud
Journal:  Oecologia       Date:  2013-03-13       Impact factor: 3.225

3.  Developmental profile of sinalbin (p-hydroxybenzyl glucosinolate) in mustard seedlings,Sinapis alba L., and its relationship to insect resistance.

Authors:  R P Bodnaryk
Journal:  J Chem Ecol       Date:  1991-08       Impact factor: 2.626

4.  Watercress and amphipods Potential chemical defense in a spring stream macrophyte.

Authors:  R M Newman; W C Kerfoot; Z Hanscom
Journal:  J Chem Ecol       Date:  1990-01       Impact factor: 2.626

5.  Glucosinolate levels in cotyledons of mustard,Brassica juncea L. and rape,B. napus L. do not determine feeding rates of flea beetle,Phyllotreta cruciferae (Goeze).

Authors:  R P Bodnaryk; P Palaniswamy
Journal:  J Chem Ecol       Date:  1990-09       Impact factor: 2.626

6.  Isolation and characterization of glucocapparin inIsomeris arborea nutt.

Authors:  M J Blua; Z Hanscom
Journal:  J Chem Ecol       Date:  1986-06       Impact factor: 2.626

7.  Allylglucosinolate and herbivorous caterpillars: a contrast in toxicity and tolerance.

Authors:  P A Blau; P Feeny; L Contardo; D S Robson
Journal:  Science       Date:  1978-06-16       Impact factor: 47.728

  7 in total
  8 in total

1.  Activated chemical defenses suppress herbivory on freshwater red algae.

Authors:  Keri M Goodman; Mark E Hay
Journal:  Oecologia       Date:  2012-09-26       Impact factor: 3.225

2.  Induction and Priming of Plant Defense by Root-Associated Insect-Pathogenic Fungi.

Authors:  Joana Carvalho Cachapa; Nicolai Vitt Meyling; Meike Burow; Thure Pavlo Hauser
Journal:  J Chem Ecol       Date:  2020-11-12       Impact factor: 2.626

3.  Prevalence of chemical defenses among freshwater plants.

Authors:  Anne C Prusak; Jennifer O'Neal; Julia Kubanek
Journal:  J Chem Ecol       Date:  2005-05       Impact factor: 2.626

4.  Changes in the glucosinolate-myrosinase defense system in Brassica juncea cotyledons during seedling development.

Authors:  S K Wallace; Sanford D Eigenbrode
Journal:  J Chem Ecol       Date:  2002-02       Impact factor: 2.626

5.  Effects of light and nutrient availability on the growth, allocation, carbon/nitrogen balance, phenolic chemistry, and resistance to herbivory of two freshwater macrophytes.

Authors:  Greg Cronin; David M Lodge
Journal:  Oecologia       Date:  2003-06-19       Impact factor: 3.225

Review 6.  Plant defense against insect herbivores.

Authors:  Joel Fürstenberg-Hägg; Mika Zagrobelny; Søren Bak
Journal:  Int J Mol Sci       Date:  2013-05-16       Impact factor: 5.923

7.  Do metal-rich plants deter herbivores? A field test of the defence hypothesis.

Authors:  Nausicaa Noret; Pierre Meerts; Mathieu Vanhaelen; Anabelle Dos Santos; José Escarré
Journal:  Oecologia       Date:  2007-01-10       Impact factor: 3.298

8.  Tritrophic metabolism of plant chemical defenses and its effects on herbivore and predator performance.

Authors:  Ruo Sun; Xingcong Jiang; Michael Reichelt; Jonathan Gershenzon; Sagar Subhash Pandit; Daniel Giddings Vassão
Journal:  Elife       Date:  2019-12-16       Impact factor: 8.140

  8 in total

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