Association between the polymorphism of CfPGRP-S gene and disease susceptibility/resistance of zhikong scallop (Chlamys farreri) to Listonella anguillarum challenge
文献类型：期刊论文
| 作者 | Siva, Vinu S.1,2; Yang, Chuanyan1,2; Yang, Jialong1,2; Wang, Lingling1; Wang, Leilei1,2; Zhou, Zhi1,2; Qiu, Limei1; Song, Linsheng1 |
| 刊名 | FISH & SHELLFISH IMMUNOLOGY
 |
| 出版日期 | 2012-10-01 |
| 卷号 | 33期号:4页码:736-742 |
| 关键词 | Zhikong scallop Chlamys farreri Peptidoglycan recognition protein Single nucleotide polymorphism Pathogen-associated molecular patterns (PAMP) binding Antimicrobial activity |
| ISSN号 | 1050-4648 |
| 通讯作者 | Wang, LL (reprint author), Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, 7 Nanhai Rd, Qingdao 266071, Peoples R China. |
| 英文摘要 | Peptidoglycan recognition protein (PGRP) is a pattern recognition receptor, playing important roles in the innate immune response against invasive pathogens. The single nucleotide polymorphism (SNP) loci in scallop PGRP gene (CfPGRP) were screened from Chlamys farreri to investigate their association with disease resistance of scallop against Listonella anguillarum. Thirteen SNP sites were identified in PGRP domain of CfPGRP, and two of them at positions 4407 and 4408 which are located in the same codon resulted in a nonsynonymous substitution. The genotype frequency of CG/CG in the resistant stock was significantly lower than that in susceptible stock (0% vs 32.4%), while that of CG/TA in the resistant stock was significantly higher than that in susceptible stock (P < 0.01). The pathogen-associated molecular patterns (PAMP) binding activity of two recombinant proteins, rCfPGRP-S1 (R) with CG variant in 4407 -4408 site, rCfPGRP-S1 (Y) with TA variant in 4407-4408 site, were elucidated by examining their P/N value at 405 nm with ELISA assay. The in vitro binding activities of the two rCfPGRP-S1 variants to both lipopolysaccharide (LPS) and peptidoglycan (PGN) varied (P < 0.05) in a dose-dependent manner, and rCfPRPP-S1(Y) exhibited significantly higher affinity to PGN and LPS than that of rCfPGRP-S1(R) (P < 0.05). The growth inhibition assay was conducted to find the antibacterial activities of the two variants. Both rCfPGRP-S1(R) and rCfPGRP-S1 (Y) displayed obvious activity to suppress the growth of Escherichia coli, but there was no significant difference in suppression activity of two variants (P > 0.05). The results suggested that the polymorphism at locus 4407-4408 of CfPGRP-S1 considerably affected its PAMP binding activity, and the SNP locus 4407-4408 CG/TA was associated with disease resistance of scallop against L anguillarum infection, which could be used as a candidate marker for future selection in zhikong scallop breeding program. (C) 2012 Elsevier Ltd. All rights reserved. |
| 学科主题 | Fisheries ; Immunology ; Marine & Freshwater Biology ; Veterinary Sciences |
| 收录类别 | SCI |
| 原文出处 | 10.1016/j.fsi.2012.06.016 |
| 语种 | 英语 |
| WOS记录号 | WOS:000310185800008 |
| 公开日期 | 2013-09-24 |
| 源URL | [http://ir.qdio.ac.cn/handle/337002/12287]  |
| 专题 | 海洋研究所_实验海洋生物学重点实验室 |
| 作者单位 | 1.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China 2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China |
| 推荐引用方式 GB/T 7714 | Siva, Vinu S.,Yang, Chuanyan,Yang, Jialong,et al. Association between the polymorphism of CfPGRP-S gene and disease susceptibility/resistance of zhikong scallop (Chlamys farreri) to Listonella anguillarum challenge[J]. FISH & SHELLFISH IMMUNOLOGY,2012,33(4):736-742. |
| APA | Siva, Vinu S..,Yang, Chuanyan.,Yang, Jialong.,Wang, Lingling.,Wang, Leilei.,...&Song, Linsheng.(2012).Association between the polymorphism of CfPGRP-S gene and disease susceptibility/resistance of zhikong scallop (Chlamys farreri) to Listonella anguillarum challenge.FISH & SHELLFISH IMMUNOLOGY,33(4),736-742. |
| MLA | Siva, Vinu S.,et al."Association between the polymorphism of CfPGRP-S gene and disease susceptibility/resistance of zhikong scallop (Chlamys farreri) to Listonella anguillarum challenge".FISH & SHELLFISH IMMUNOLOGY 33.4(2012):736-742. |
入库方式： OAI收割
来源：海洋研究所
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