FN Archimer Export Format PT J TI Molecular diversity of antimicrobial effectors in the oyster Crassostrea gigas BT AF SCHMITT, Paulina GUEGUEN, Yannick DESMARAIS, Erick BACHERE, Evelyne DE LORGERIL, Julien AS 1:1;2:1,3;3:2;4:1;5:1; FF 1:PDG-DOP-DCM-BOME-LALR;2:PDG-DOP-DCOP-AQUAPOL-LBQP;3:;4:PDG-DOP-DCM-BOME;5:PDG-DOP-DCM-BOME-LALR; C1 Univ Montpellier 2, CNRS, UMR Ecosyst Lagunaires 5119, IFREMER,IRD, F-34095 Montpellier 5, France. Univ Montpellier 2, CNRS, UMR 5554, Inst Sci Evolut, F-34095 Montpellier, France. Ctr Oceanol Pacifique, IFREMER, Tahiti 98719, Fr Polynesia. C2 UNIV MONTPELLIER, FRANCE UNIV MONTPELLIER, FRANCE IFREMER, FRANCE SI MONTPELLIER TAHITI PALAVAS SE PDG-DOP-DCM-BOME-LALR PDG-DOP-DCOP-AQUAPOL-LBQP PDG-DOP-DCM-BOME IN WOS Ifremer jusqu'en 2018 copubli-france copubli-univ-france IF 3.702 TC 50 UR https://archimer.ifremer.fr/doc/00001/11182/6691.pdf LA English DT Article AB Background: To gain insight into the molecular diversity of antimicrobial peptides and proteins in the oyster Crassostrea gigas, we characterized and compared the sequence polymorphism of the antimicrobial peptides (AMPs), Cg-Defensins (Cg-Defs) and Cg-Proline Rich peptide (Cg-Prp), and of the bactericidal permeability increasing protein, Cg-BPI. For that, we analyzed genomic and transcript sequences obtained by specific PCR amplification and in silico searches. Results: High diversification among the three antimicrobial effectors was evidenced by this polymorphism survey. On the basis of sequence phylogenies, each AMP aggregates into clearly defined groups of variants and is the product of a multigenic family displaying a variety of gene structures. In contrast, Cg-bpi forms a single group and is encoded by a single gene copy. Moreover, we identified for both AMPs several genetic mechanisms of diversification such as recombination, parallel mutations leading to phylogenetic homoplasy and indel events. In addition, the non synonymous to synonymous substitutions ratio by codon (dN/dS) revealed several negatively and positively selected sites for both AMPs, suggesting that directional selection pressures have shaped their sequence variations. Conclusions: This study shows for the first time in a mollusc that antimicrobial peptides and proteins have been subject to distinct patterns of diversification and we evidence the existence of different evolutionary routes leading to such sequence variability. PY 2010 PD JAN SO Bmc Evolutionary Biology SN 1471-2148 PU Biomed Central Ltd VL 10 UT 000274623800001 DI 10.1186/1471-2148-10-23 ID 11182 ER EF