» Articles » PMID: 15365181

Selective Transport Systems Mediate Sequestration of Plant Glucosides in Leaf Beetles: a Molecular Basis for Adaptation and Evolution

Overview
Specialty Science
Date 2004 Sep 15
PMID 15365181
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Chrysomeline larvae respond to disturbance and attack by everting dorsal glandular reservoirs, which release defensive secretions. The ancestral defense is based on the de novo synthesis of monoterpene iridoids. The catabolization of the host-plant O-glucoside salicin into salicylaldehyde is a character state that evolved later in two distinct lineages, which specialized on Salicaceae. By using two species producing monoterpenes (Hydrothassa marginella and Phratora laticollis) and two sequestering species (Chrysomela populi and Phratora vitellinae), we studied the molecular basis of sequestration by feeding the larvae structurally different thioglucosides resembling natural O-glucosides. Their accumulation in the defensive systems demonstrated that the larvae possess transport systems, which are evolutionarily adapted to the glycosides of their host plants. Minor structural modifications in the aglycon result in drastically reduced transport rates of the test compounds. Moreover, the ancestral iridoid-producing leaf beetles already possess a fully functional import system for an early precursor of the iridoid defenses. Our data confirm an evolutionary scenario in which, after a host-plant change, the transport system of the leaf beetles may play a pivotal role in the adaptation on new hosts by selecting plant-derived glucosides that can be channeled to the defensive system.

Citing Articles

Metabolic enhancement contributed by horizontal gene transfer is essential for dietary specialization in leaf beetles.

Zhang Y, Tu C, Bai J, Li X, Sun Z, Xu L Proc Natl Acad Sci U S A. 2025; 122(1):e2415717122.

PMID: 39793087 PMC: 11725898. DOI: 10.1073/pnas.2415717122.


2-Methoxybenzaldehyde effectively repels ants.

Kay T, Siegenthaler G, Kench T, Keller L J Econ Entomol. 2023; 117(1):24-33.

PMID: 38070195 PMC: 10860152. DOI: 10.1093/jee/toad225.


Rapid and Selective Absorption of Plant Defense Compounds From the Gut of a Sequestering Insect.

Yang Z, Seitz F, Grabe V, Nietzsche S, Richter A, Reichelt M Front Physiol. 2022; 13:846732.

PMID: 35309070 PMC: 8928188. DOI: 10.3389/fphys.2022.846732.


Lineage-specific duplication and adaptive evolution of bitter taste receptor genes in bats.

Jiao H, Wang Y, Zhang L, Jiang P, Zhao H Mol Ecol. 2018; 27(22):4475-4488.

PMID: 30230081 PMC: 8381267. DOI: 10.1111/mec.14873.


Three-way interaction among plants, bacteria, and coleopteran insects.

Wielkopolan B, Obrepalska-Steplowska A Planta. 2016; 244(2):313-32.

PMID: 27170360 PMC: 4938854. DOI: 10.1007/s00425-016-2543-1.


References
1.
Weibel D, Oldham N, Feld B, Glombitza G, Dettner K, Boland W . Iridoid biosynthesis in staphylinid rove beetles (Coleoptera: Staphylinidae, Philonthinae). Insect Biochem Mol Biol. 2001; 31(6-7):583-91. DOI: 10.1016/s0965-1748(00)00163-6. View

2.
Dyer L, Bowers M . The importance of sequestered iridoid glycosides as a defense against an ant predator. J Chem Ecol. 2013; 22(8):1527-39. DOI: 10.1007/BF02027729. View

3.
Frick C, Wink M . Uptake and sequestration of ouabain and other cardiac glycosides inDanaus plexippus (Lepidoptera: Danaidae): Evidence for a carrier-mediated process. J Chem Ecol. 2013; 21(5):557-75. DOI: 10.1007/BF02033701. View

4.
Soe A, Bartram S, Gatto N, Boland W . Are iridoids in leaf beetle larvae synthesized de novo or derived from plant precursors? A methodological approach. Isotopes Environ Health Stud. 2004; 40(3):175-80. DOI: 10.1080/10256010410001674994. View

5.
Bruckmann M, Termonia A, Pasteels J, Hartmann T . Characterization of an extracellular salicyl alcohol oxidase from larval defensive secretions of Chrysomela populi and Phratora vitellinae (Chrysomelina). Insect Biochem Mol Biol. 2003; 32(11):1517-23. DOI: 10.1016/s0965-1748(02)00072-3. View