Molecular modeling and expression of the Litopenaeus vannamei proliferating cell nuclear antigen (PCNA) after white spot syndrome virus shrimp infection

Results in immunology Pub Date : 2011-05-01 Epub Date: 2011-07-26 DOI:10.1016/j.rinim.2011.07.001
Enrique de-la-Re-Vega , Adriana Muhlia-Almazan , Aldo A. Arvizu-Flores , Maria A. Islas-Osuna , Gloria Yepiz-Plascencia , Luis G. Brieba , Rogerio R. Sotelo-Mundo
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引用次数: 5

Abstract

Proliferating cell nuclear antigen (PCNA) is the eukaryotic sliding clamp that tethers DNA polymerase to DNA during replication. The full-length cDNA of the Pacific white shrimp Litopenaeus vannamei PCNA (LvPCNA) was cloned and encoded a protein of 260 amino acids that is highly similar to other Crustacean PCNAs. The theoretical shrimp PCNA structure has all the domains that are necessary for its interaction with template DNA and DNA polymerase. RT-PCR analysis showed that LvPCNA is expressed mainly in muscle and hemocytes and much less in hepatopancreas and gills. LvPCNA mRNA levels are not statistically different in muscle from healthy and challenged shrimp with the white spot syndrome virus (WSSV). In contrast, the mRNA levels of the viral DNA polymerase show a biphasic pattern with expression at 6 h post-infection and later at 24 and 48 h. These results suggest that in shrimp muscle LvPCNA levels are steadily kept to allow viral replication and that WSSV DNA polymerase (WSSV-DNApol) is more responsive towards later stages of infection. More knowledge of the DNA replication machinery would result in a better understanding of the mechanism and components of viral replication, since the WSSV genome does not have all the components required for assembly of a fully functional replisome.

虾感染白斑综合征病毒后凡纳滨对虾增殖细胞核抗原(PCNA)的分子模拟与表达
增殖细胞核抗原(PCNA)是真核生物在复制过程中将DNA聚合酶拴在DNA上的滑动钳。克隆了凡纳滨对虾(Litopenaeus vannamei) PCNA (LvPCNA)的全长cDNA,并编码了一个与其他甲壳类动物PCNA高度相似的260个氨基酸的蛋白。虾的理论PCNA结构具有与模板DNA和DNA聚合酶相互作用所必需的所有结构域。RT-PCR分析显示LvPCNA主要在肌肉和血细胞中表达,在肝胰腺和鱼鳃中表达较少。正常和感染白斑综合征病毒(WSSV)的对虾肌肉中LvPCNA mRNA水平无统计学差异。相比之下,病毒DNA聚合酶的mRNA水平呈现双相模式,在感染后6小时表达,然后在24和48小时表达。这些结果表明,在虾肌中,LvPCNA水平稳定保持以允许病毒复制,并且WSSV DNA聚合酶(WSSV- dnapol)对感染后期反应更强。对DNA复制机制的更多了解将有助于更好地理解病毒复制的机制和组成部分,因为WSSV基因组不具备组装功能齐全的复制体所需的所有组成部分。
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