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从沙氏游动球菌中鉴定出一种诱导黑头软口鲦细胞凋亡的细胞壁肽酶(NlpC/P60)。

Identification of a cell-wall peptidase (NlpC/P60) from Nocardia seriolae which induces apoptosis in fathead minnow cells.

机构信息

Guangdong Provincial Engineering Research Center for Aquatic Animal Health Assessment, Shenzhen Public Service Platform for Evaluation of Marine Economic Animal Seedings, Shenzhen Institute of Guangdong Ocean University, Shenzhen, China.

Guangdong Provincial Key Laboratory of Pathogenic Biology and Epidemiology for Aquatic Economic Animals, College of Fisheries, Guangdong Ocean University, Zhanjiang, China.

出版信息

J Fish Dis. 2020 May;43(5):571-581. doi: 10.1111/jfd.13154. Epub 2020 Mar 20.

Abstract

Nocardia seriolae, a Gram-positive bacterium, is the main pathogen of fish nocardiosis. Protein NlpC/P60 is a cell-wall peptidase and a potential virulence factor of N. seriolae. Subcellular localization research revealed that both NlpC/P60-GFP and NlpC/P60Δsig-GFP fusion proteins were evenly distributed in the whole cell of fathead minnow (FHM) cells. Furthermore, typical apoptotic features, such as nuclear pyrosis and apoptotic bodies, were observed in the transfected FHM cells and grouper spleen cells by the overexpression of protein NlpC/P60. Then, quantitative assays of mitochondrial membrane potential (ΔΨm) value, caspase-3 activity and apoptosis-related gene (Bax, BNIP3, TNF1 and TNF6) mRNA expression were conducted. The results showed that ΔΨm was decreased, caspase-3 was significantly activated, and the mRNA expression of pro-apoptotic genes (Bax and BNIP3) and tumour necrosis factors (TNF1 and TNF6) was up-regulated in NlpC/P60-overexpressed cells. Taken together, the results indicated that the protein NlpC/P60 of N. seriolae might involve in apoptosis regulation. This study may lay the foundation for further study on the function of N. seriolae NlpC/P60 and promote the understanding of the virulence factors and pathogenic mechanism of N. seriolae.

摘要

海洋分枝杆菌是一种革兰氏阳性细菌,是鱼类诺卡氏菌病的主要病原体。蛋白 NlpC/P60 是一种细胞壁肽酶,也是海洋分枝杆菌的潜在毒力因子。亚细胞定位研究表明,NlpC/P60-GFP 和 NlpC/P60Δsig-GFP 融合蛋白均均匀分布在肥头鲦(FHM)细胞的整个细胞中。此外,在转染的 FHM 细胞和石斑鱼脾脏细胞中过表达蛋白 NlpC/P60 后,观察到典型的凋亡特征,如核质肿胀和凋亡小体。然后,进行线粒体膜电位(ΔΨm)值、caspase-3 活性和凋亡相关基因(Bax、BNIP3、TNF1 和 TNF6)mRNA 表达的定量测定。结果表明,ΔΨm 降低,caspase-3 显著激活,并且过表达细胞中促凋亡基因(Bax 和 BNIP3)和肿瘤坏死因子(TNF1 和 TNF6)的 mRNA 表达上调。总之,这些结果表明海洋分枝杆菌的蛋白 NlpC/P60 可能参与细胞凋亡的调控。本研究可为进一步研究海洋分枝杆菌 NlpC/P60 的功能奠定基础,并促进对海洋分枝杆菌毒力因子和致病机制的理解。

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