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Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei

Biofouling mediated by byssus adhesion in invasive bivalves has become a global environmental problem in aquatic ecosystems, resulting in negative ecological and economic consequences. Previous studies suggested that mechanisms responsible for byssus adhesion largely vary among bivalves, but it is p...

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Autores principales: Li, Shiguo, Xia, Zhiqiang, Chen, Yiyong, Gao, Yangchun, Zhan, Aibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911496/
https://www.ncbi.nlm.nih.gov/pubmed/29713291
http://dx.doi.org/10.3389/fphys.2018.00418
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author Li, Shiguo
Xia, Zhiqiang
Chen, Yiyong
Gao, Yangchun
Zhan, Aibin
author_facet Li, Shiguo
Xia, Zhiqiang
Chen, Yiyong
Gao, Yangchun
Zhan, Aibin
author_sort Li, Shiguo
collection PubMed
description Biofouling mediated by byssus adhesion in invasive bivalves has become a global environmental problem in aquatic ecosystems, resulting in negative ecological and economic consequences. Previous studies suggested that mechanisms responsible for byssus adhesion largely vary among bivalves, but it is poorly understood in freshwater species. Understanding of byssus structure and protein composition is the prerequisite for revealing these mechanisms. Here, we used multiple methods, including scanning electron microscope, liquid chromatography–tandem mass spectrometry, transcriptome sequencing, real-time quantitative PCR, inductively coupled plasma mass spectrometry, to investigate structure, and protein composition of byssus in the highly invasive freshwater mussel Limnoperna fortunei. The results indicated that the structure characteristics of adhesive plaque, proximal and distal threads were conducive to byssus adhesion, contributing to the high biofouling capacity of this species. The 3,4-dihydroxyphenyl-α-alanine (Dopa) is a major post-transnationally modification in L. fortunei byssus. We identified 16 representative foot proteins with typical repetitive motifs and conserved domains by integrating transcriptomic and proteomic approaches. In these proteins, Lfbp-1, Lffp-2, and Lfbp-3 were specially located in foot tissue and highly expressed in the rapid byssus formation period, suggesting the involvement of these foot proteins in byssus production and adhesion. Multiple metal irons, including Ca(2+), Mg(2+), Zn(2+), Al(3+), and Fe(3+), were abundant in both foot tissue and byssal thread. The heavy metals in these irons may be directly accumulated by L. fortunei from surrounding environments. Nevertheless, some metal ions (e.g., Ca(2+)) corresponded well with amino acid preferences of L. fortunei foot proteins, suggesting functional roles of these metal ions by interacting with foot proteins in byssus adhesion. Overall, this study provides structural and molecular bases of adhesive mechanisms of byssus in L. fortunei, and findings here are expected to develop strategies against biofouling by freshwater organisms.
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spelling pubmed-59114962018-04-30 Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei Li, Shiguo Xia, Zhiqiang Chen, Yiyong Gao, Yangchun Zhan, Aibin Front Physiol Physiology Biofouling mediated by byssus adhesion in invasive bivalves has become a global environmental problem in aquatic ecosystems, resulting in negative ecological and economic consequences. Previous studies suggested that mechanisms responsible for byssus adhesion largely vary among bivalves, but it is poorly understood in freshwater species. Understanding of byssus structure and protein composition is the prerequisite for revealing these mechanisms. Here, we used multiple methods, including scanning electron microscope, liquid chromatography–tandem mass spectrometry, transcriptome sequencing, real-time quantitative PCR, inductively coupled plasma mass spectrometry, to investigate structure, and protein composition of byssus in the highly invasive freshwater mussel Limnoperna fortunei. The results indicated that the structure characteristics of adhesive plaque, proximal and distal threads were conducive to byssus adhesion, contributing to the high biofouling capacity of this species. The 3,4-dihydroxyphenyl-α-alanine (Dopa) is a major post-transnationally modification in L. fortunei byssus. We identified 16 representative foot proteins with typical repetitive motifs and conserved domains by integrating transcriptomic and proteomic approaches. In these proteins, Lfbp-1, Lffp-2, and Lfbp-3 were specially located in foot tissue and highly expressed in the rapid byssus formation period, suggesting the involvement of these foot proteins in byssus production and adhesion. Multiple metal irons, including Ca(2+), Mg(2+), Zn(2+), Al(3+), and Fe(3+), were abundant in both foot tissue and byssal thread. The heavy metals in these irons may be directly accumulated by L. fortunei from surrounding environments. Nevertheless, some metal ions (e.g., Ca(2+)) corresponded well with amino acid preferences of L. fortunei foot proteins, suggesting functional roles of these metal ions by interacting with foot proteins in byssus adhesion. Overall, this study provides structural and molecular bases of adhesive mechanisms of byssus in L. fortunei, and findings here are expected to develop strategies against biofouling by freshwater organisms. Frontiers Media S.A. 2018-04-16 /pmc/articles/PMC5911496/ /pubmed/29713291 http://dx.doi.org/10.3389/fphys.2018.00418 Text en Copyright © 2018 Li, Xia, Chen, Gao and Zhan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Li, Shiguo
Xia, Zhiqiang
Chen, Yiyong
Gao, Yangchun
Zhan, Aibin
Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title_full Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title_fullStr Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title_full_unstemmed Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title_short Byssus Structure and Protein Composition in the Highly Invasive Fouling Mussel Limnoperna fortunei
title_sort byssus structure and protein composition in the highly invasive fouling mussel limnoperna fortunei
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911496/
https://www.ncbi.nlm.nih.gov/pubmed/29713291
http://dx.doi.org/10.3389/fphys.2018.00418
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