Findly R Craig, Niagro Frank D, Dickerson Harry W
Department of Infectious Diseases, College of Veterinary Medicine, The University of Georgia, Athens, GA 30602, USA.
Dev Comp Immunol. 2017 Mar;68:26-33. doi: 10.1016/j.dci.2016.11.010. Epub 2016 Nov 10.
We analyzed by high-throughput sequencing T cell receptor beta CDR3 repertoires expressed by αβ T cells in outbred channel catfish before and after an immunizing infection with the parasitic protozoan Ichthyophthirius multifiliis. We compared CDR3 repertoires in caudal fin before infection and at three weeks after infection, and in skin, PBL, spleen and head kidney at seven and twenty-one weeks after infection. Public clonotypes with the same CDR3 amino acid sequence were expressed by αβ T cells that underwent clonal expansion following development of immunity. These clonally expanded αβ T cells were primarily located in spleen and skin, which is a site of infection. Although multiple DNA sequences were expected to code for each public clonotype, each public clonotype was predominately coded by an identical CDR3 DNA sequence in combination with the same J gene in all fish. The processes underlying this shared use of CDR3 DNA sequences are not clear.
我们通过高通量测序分析了杂交鲶鱼在感染寄生原生动物多子小瓜虫前后,αβ T细胞所表达的T细胞受体β链互补决定区3(CDR3)库。我们比较了感染前和感染后三周尾鳍中的CDR3库,以及感染后七周和二十一周时皮肤、外周血淋巴细胞(PBL)、脾脏和头肾中的CDR3库。具有相同CDR3氨基酸序列的公共克隆型由免疫发育后经历克隆扩增的αβ T细胞表达。这些克隆扩增的αβ T细胞主要位于脾脏和皮肤,即感染部位。尽管预计每个公共克隆型由多个DNA序列编码,但在所有鱼类中,每个公共克隆型主要由相同的CDR3 DNA序列与相同的J基因组合编码。这种CDR3 DNA序列共享使用的潜在机制尚不清楚。