Reverse genetics demonstrate the role of mucosal C-type lectins in food particle selection in the oyster Crassostrea virginica

Author:

Pales Espinosa Emmanuelle1,Allam Bassem1

Affiliation:

1. School of Marine and Atmospheric Sciences, State University of New York, Stony Brook, NY 11794, USA

Abstract

Prey selection governs species interactions and regulates physiological energetics of individuals and populations. Suspension-feeding bivalves represent key species in coastal and estuarine systems for their ecological and economic value. These animals are able to sort and selectively ingest nutritious microalgae from dilute and composite mixtures of particulate matter. This aptitude was suggested to be mediated by interactions between carbohydrates associated with the surface of microalgae and C-type lectins present in mucus covering the feeding organs although a direct, unequivocal, role of lectins in food sorting in bivalves remains elusive. This study was designed to identify and characterize mucosal C-type lectins from oysters and manipulate the expression of these proteins in order to obtain decisive information regarding their involvement in food choice. Thus, 2 mucosal C-type lectins (CvML3912 and CvML3914) were identified based on transcriptomic and proteomic information. Transcripts of these lectins were detected in the feeding organs and their expression was upregulated following starvation. Recombinant lectin (rCvML3912) competitively inhibited the binding of commercial mannose/glucose-specific lectins to microalgae. Short DsiRNA targeting these two lectins were designed and used to evaluate the effect of gene silencing on food particle sorting. As a result, the abundance of the two cognate transcripts significantly decreased and food sorting ability was significantly reduced among silenced oysters as compared to control animals. Overall, these findings propose a novel concept establishing the role of carbohydrate-protein interactions to provide an efficient food particle sorting, and establish a new dimension for the role of evolutionarily-conserved mannose/glucose-binding proteins in the metazoan.

Funder

National Science Foundation

Publisher

The Company of Biologists

Subject

Insect Science,Molecular Biology,Animal Science and Zoology,Aquatic Science,Physiology,Ecology, Evolution, Behavior and Systematics

Reference77 articles.

1. RNA interference: biology, mechanism, and applications;Agrawal;Microbiol. Mol. Biol. Rev.,2003

2. Mucosal immunity in mollusks. In Mucosal Health in Aquaculture (ed. B. H. Beck and E. Peatman);Allam;New York: Academic Press,2015

3. Characteristics, dynamics and significance of marine snow;Alldredge;Prog. Oceanogr.,1988

4. Studies of the biology of freshwater mussels - experimental studies of the food relations of certain Unionidae;Allen;Biol. Bull.,1921

5. Mussel beds: limiting or promoting phytoplankton?;Asmus;J. Exp. Mar. Biol. Ecol.,1991

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3