Department of Pathology and Microbiology, Atlantic Veterinary College, University of Prince Edward Island, 550 University Avenue, Charlottetown, PE, Canada.
Dev Comp Immunol. 2010 Jul;34(7):710-4. doi: 10.1016/j.dci.2010.02.006. Epub 2010 Feb 23.
Immune function gene expression in Mya arenaria haemocytes was evaluated following in vivo infection with Vibrio splendidus LGP32-GFP and 7SHRW. Elongation factor 1alpha (EF-1alpha) with 2 (EF-2), after challenge with LGP32-GFP, and EF-1alpha with the ribosomal protein S-18, after challenge with 7SHRW, were found to be the most stable housekeeping genes. Using these internal controls and comparing the regulation induced by both strains, up-regulation of gamma-actin, down-regulation of TLR-2 and up-regulation of IRAK-4 was significantly higher after challenge with LGP32-GFP (p<0.001, p=0.001 and p<0.05, respectively). These results suggest specific responses at a molecular level modulated by the bacterial strains. LGP32-GFP induced marked responses which coincide with a similar trend previously found on phenotypic responses under our experimental model.
在体内感染灿烂弧菌 LGP32-GFP 和 7SHRW 后,评估了美洲帘蛤血细胞中免疫功能基因的表达。在受到 LGP32-GFP 挑战后,延伸因子 1α(EF-1α)与 2(EF-2),以及在受到 7SHRW 挑战后,核糖体蛋白 S-18 的 EF-1α,被发现是最稳定的管家基因。使用这些内参基因,并比较两种菌株诱导的调控,在受到 LGP32-GFP 挑战后,γ-肌动蛋白的上调、TLR-2 的下调和 IRAK-4 的上调显著更高(p<0.001、p=0.001 和 p<0.05,分别)。这些结果表明,细菌菌株在分子水平上调节了特定的反应。LGP32-GFP 诱导的反应与我们实验模型中表型反应的相似趋势一致。