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采用抑制性消减杂交结合微阵列分析技术研究牙鲆白细胞在迟钝爱德华氏菌和病毒性出血性败血症病毒感染过程中差异表达基因。

Suppression subtractive hybridization coupled with microarray analysis to examine differential expression of genes in Japanese flounder Paralichthys olivaceus leucocytes during Edwardsiella tarda and viral hemorrhagic septicemia virus infection.

机构信息

National Research Institute of Aquaculture, Fisheries Research Agency, Minami-Ise, Mie 516-0193, Japan.

出版信息

Fish Shellfish Immunol. 2011 Oct;31(4):524-32. doi: 10.1016/j.fsi.2011.06.015. Epub 2011 Jun 23.

Abstract

Transcriptional changes in the peripheral blood leucocytes (PBL) of Japanese flounder Paralichthys olivaceus challenged by Edwardsiella tarda and viral hemorrhagic septicemia virus (VHSV) were investigated using suppression subtractive hybridization (SSH) coupled with cDNA microarray analysis. First, we constructed an SSH cDNA library using mRNA samples isolated from PBL of P. olivaceus that had been experimentally infected with E. tarda. We then examined the transcriptional changes occurring in the PBL due to E. tarda and VHSV infection using a cDNA microarray produced using clones produced from the SSH library. A total of 565 and 180 cDNA sequences corresponding to mRNA species that are either up- or down-regulated by E. tarda infection were isolated by SSH. While host gene expression responses in response to E. tarda and VHSV infection share several response elements, distinct patterns of gene expression were also observed. Specifically, E. tarda infection enhanced the expression of cell adhesion molecules while VHSV enhanced the expression of interferon and proteasome-related genes. In challenge trials of the two infectious agents, expression profiles of chemokines were also observed to differ. The results indicated that distinguishing between viral and bacterial infection is possible based on the RNA expression profiles of PBL from infected fish.

摘要

采用抑制性消减杂交(SSH)结合 cDNA 微阵列分析技术,研究了牙鲆外周血白细胞(PBL)在迟钝爱德华氏菌和病毒性出血性败血症病毒(VHSV)感染后的转录变化。首先,我们使用从已用迟钝爱德华氏菌感染的牙鲆 PBL 中分离的 mRNA 样本构建了 SSH cDNA 文库。然后,我们使用从 SSH 文库产生的克隆制作的 cDNA 微阵列检查了 PBL 因迟钝爱德华氏菌和 VHSV 感染而发生的转录变化。通过 SSH 分离了总共 565 和 180 个 cDNA 序列,这些序列分别对应于 mRNA 种类的上调或下调。尽管宿主基因表达对迟钝爱德华氏菌和 VHSV 感染的反应有几个共同的反应元件,但也观察到了不同的基因表达模式。具体而言,迟钝爱德华氏菌感染增强了细胞粘附分子的表达,而 VHSV 增强了干扰素和蛋白酶体相关基因的表达。在两种感染性病原体的挑战试验中,还观察到趋化因子的表达谱不同。结果表明,根据感染鱼的 PBL 的 RNA 表达谱,可以区分病毒和细菌感染。

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