菲律宾蛤仔在不同浓度鳗弧菌二次感染后相关酶活性和基因表达的影响

SECONDARY INFECTION WITH VIBRIO ANGUILLARUM AT DIFFERENT CONCENTRATIONS ON ENZYME ACTIVITIES AND GENE EXPRESSION IN RUDITAPES PHILIPPINARUM

  • 摘要: 为了探究不同浓度鳗弧菌二次感染菲律宾蛤仔时免疫增强的机制, 本研究记录了菲律宾蛤仔二次感染不同浓度鳗弧菌后的存活率, 探究了溶菌酶和SOD酶的活性的变化趋势, 分析了二次感染下肝胰腺组织中6种免疫基因mRNA的表达情况。五个实验组分别是二次注射了浓度为5×105、5×106、5×107、5×108和5×109 CFU/mL的鳗弧菌悬浮液的van1、van2、van3、van4、van5组, 和注射鳗弧菌浓度为5×107 CFU/mL的初次感染组van (对照组)。结果表明, van1组存活率最高(85.3%), van5组存活率最低(17.5%)。酶活性测定显示, 对照组van和二次感染组van1、van2、van3溶菌酶活性在24h达到峰值(P<0.05), 而二次感染组van4和van5的溶菌酶活性在72h达到峰值(P<0.05); 24—96h时二次感染组van3、van4、van5的SOD酶活性显著高于初次感染组(对照组van; P<0.05), 48h、72h时二次感染组van1和van2的SOD活性显著低于初次感染组(对照组van; P<0.05)。此外, 荧光定量PCR (qPCR)分析发现二次感染鳗弧菌显著诱导了C型甘露糖受体2 (MRC2)、泛素样蛋白ATG12 (Atg12)、Toll 样受体4 (TLR4)和溶菌酶(Lysozyme)等免疫基因的表达(P<0.05), 揭示了这些基因在菲律宾蛤仔二次感染鳗弧菌的免疫防御过程中发挥了重要作用。本研究探究了不同浓度鳗弧菌二次感染后对菲律宾蛤仔免疫反应的剂量依赖性影响, 为新型疫苗开发和免疫研究提供新思路。

     

    Abstract: To investigate the immunoenhancement mechanism in Ruditapes philippinarum during secondary infection by Vibrio anguillarum at varying concentrations. In this study, we documented survival rates of R. philippinarum following secondary infection with varying concentrations of V. anguillarum, investigated dynamic changes in lysozyme and superoxide dismutase (SOD) activities, and analyzed mRNA expression levels of six immune-related genes in hepatopancreatic tissues under secondary infection conditions. Results indicated that the van1 group injected with V. anguillarum at a concentration of 5×105 CFU/mL exhibited the highest survival rate (85.3%), while the van5 group injected with V. anguillarum at a concentration of 5×109 CFU/mL showed the lowest (17.5%). Lysozyme activity peaked at 24h in the control group (van) and secondary infection groups van1, van2, and van3 (P<0.05), whereas peaked at 72h in groups van4 and van5 (P<0.05). Between 24h and 96h, SOD activity in groups van3, van4, and van5 was significantly higher than that in the primary infection group (control van) (P<0.05), whereas, at 48h and 72h, SOD activity in groups van1 and van2 was significantly lower (P<0.05). Furthermore, quantitative Real-time PCR (qPCR) analysis revealed that secondary infection with V. anguillarum significantly upregulated the expression of immune-related genes, including mannose receptor C-type 2 (MRC2), ubiquitin-like protein ATG12 (Atg12), Toll-like receptor 4 (TLR4), and lysozyme (P<0.05). The study reveals that these genes play a critical role in the immune defense mechanism of R. philippinarum against secondary infection with V. anguillarum.

     

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