Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Rd., Qingdao 266071, China.
Fish Shellfish Immunol. 2012 Oct;33(4):736-42. doi: 10.1016/j.fsi.2012.06.016. Epub 2012 Jul 15.
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.
肽聚糖识别蛋白(PGRP)是一种模式识别受体,在对抗入侵病原体的先天免疫反应中发挥重要作用。本研究从栉孔扇贝中筛选出扇贝 PGRP 基因(CfPGRP)的单核苷酸多态性(SNP)位点,探讨其与栉孔扇贝对鳗弧菌抗性的关系。在 CfPGRP 的 PGRP 结构域中鉴定出 13 个 SNP 位点,其中位于同一密码子的 4407 和 4408 位的两个 SNP 导致非同义突变。在抗性品系中,CG/CG 基因型的频率显著低于易感品系(0%对 32.4%),而 CG/TA 基因型的频率显著高于易感品系(P<0.01)。通过 ELISA 试验测定两个重组蛋白 rCfPGRP-S1(R)(4407-4408 位 CG 变异)和 rCfPGRP-S1(Y)(4407-4408 位 TA 变异)的 P/N 值,阐明了它们与两种模式识别分子(PAMP)的结合活性。两种 rCfPGRP-S1 变体与脂多糖(LPS)和肽聚糖(PGN)的体外结合活性呈剂量依赖性变化(P<0.05),rCfPGRP-S1(Y)与 PGN 和 LPS 的亲和力明显高于 rCfPGRP-S1(R)(P<0.05)。进行抑菌活性试验以发现两种变体的抗菌活性。rCfPGRP-S1(R)和 rCfPGRP-S1(Y)对大肠杆菌的生长均有明显抑制作用,但两种变体的抑制活性无显著差异(P>0.05)。结果表明,CfPGRP-S1 基因座 4407-4408 处的多态性显著影响其 PAMP 结合活性,SNP 基因座 4407-4408 的 CG/TA 与栉孔扇贝对鳗弧菌感染的抗性有关,可作为未来栉孔扇贝选育计划的候选标记。