Ubiquitous Water-Soluble Molecules in Aquatic Plant Exudates Determine Specific Insect Attraction

被引:11
|
作者
Serandour, Julien [1 ]
Reynaud, Stephane [1 ]
Willison, John [2 ]
Patouraux, Joelle [1 ]
Gaude, Thierry [1 ]
Ravanel, Patrick [1 ]
Lemperiere, Guy [1 ]
Raveton, Muriel [1 ]
机构
[1] Univ Grenoble 1, Lab Ecol Alpine, Equipe Perturbat Environm & Xenobiot, CNRS,UMR 5553, Grenoble, France
[2] CEA Grenoble, Inst Rech Technol Sci Vivant, UJF, CEA, CNRS, UMR 5249,Lab Chim Biol Metaux, Grenoble, France
来源
PLOS ONE | 2008年 / 3卷 / 10期
关键词
D O I
10.1371/journal.pone.0003350
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plants produce semio-chemicals that directly influence insect attraction and/or repulsion. Generally, this attraction is closely associated with herbivory and has been studied mainly under atmospheric conditions. On the other hand, the relationship between aquatic plants and insects has been little studied. To determine whether the roots of aquatic macrophytes release attractive chemical mixtures into the water, we studied the behaviour of mosquito larvae using olfactory experiments with root exudates. After testing the attraction on Culex and Aedes mosquito larvae, we chose to work with Coquillettidia species, which have a complex behaviour in nature and need to be attached to plant roots in order to obtain oxygen. This relationship is non-destructive and can be described as commensal behaviour. Commonly found compounds seemed to be involved in insect attraction since root exudates from different plants were all attractive. Moreover, chemical analysis allowed us to identify a certain number of commonly found, highly water-soluble, low-molecular-weight compounds, several of which ( glycerol, uracil, thymine, uridine, thymidine) were able to induce attraction when tested individually but at concentrations substantially higher than those found in nature. However, our principal findings demonstrated that these compounds appeared to act synergistically, since a mixture of these five compounds attracted larvae at natural concentrations (0.7 nM glycerol, <0.5 nM uracil, 0.6 nM thymine, 2.8 nM uridine, 86 nM thymidine), much lower than those found for each compound tested individually. These results provide strong evidence that a mixture of polyols (glycerol), pyrimidines (uracil, thymine), and nucleosides (uridine, thymidine) functions as an efficient attractive signal in nature for Coquillettidia larvae. We therefore show for the first time, that such commonly found compounds may play an important role in plant-insect relationships in aquatic eco-systems.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] WATER-SOLUBLE PLANT ROOT EXUDATES: ROLE AND SIGNIFICANCE OF THEIR STUDY
    Vranova, Valerie
    Rejsek, Klement
    Formanek, Pavel
    LISTY CUKROVARNICKE A REPARSKE, 2012, 128 (11): : 350 - 353
  • [2] WATER-SOLUBLE PLANT GUM EXUDATES .1. GUM ARABIC
    ANDERSON, DMW
    PROCESS BIOCHEMISTRY, 1977, 12 (10) : 24 - +
  • [3] WATER-SOLUBLE PLANT GUM EXUDATES .2. COMBRETUM GUMS
    ANDERSON, DMW
    PROCESS BIOCHEMISTRY, 1978, 13 (07) : 3 - +
  • [4] Qualitative and quantitative analysis of water-soluble root exudates in relation to plant species and development
    Gransee, A
    Wittenmayer, L
    JOURNAL OF PLANT NUTRITION AND SOIL SCIENCE, 2000, 163 (04) : 381 - 385
  • [5] Water-soluble carbohydrates in dried plant
    Kerepesi, I
    Toth, M
    Boross, L
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1996, 44 (10) : 3235 - 3239
  • [6] The water-soluble plant food of soils
    Snyder, H
    SCIENCE, 1904, 19 : 0834 - 0835
  • [7] PERMEABILITY OF DOG MESENTERY TO WATER-SOLUBLE MOLECULES
    SEPULVEDA, FV
    ROBINSON, JWL
    MIRKOVITCH, V
    EXPERIENTIA, 1976, 32 (06): : 762 - 762
  • [8] WATER-SOLUBLE PORPHYRINS WITH 4 SUGAR MOLECULES
    ONO, N
    BOUGAUCHI, M
    MARUYAMA, K
    TETRAHEDRON LETTERS, 1992, 33 (12) : 1629 - 1632
  • [9] Synthesis and properties of water-soluble asterisk molecules
    Menger, FM
    Azov, VA
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (37) : 11159 - 11166
  • [10] Synthesis and properties of water-soluble asterisk molecules
    Menger, F.M. (menger@emory.edu), 1600, American Chemical Society (124):