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柔嫩艾美耳球虫自噬标志物ATG8的鉴定与特性分析

Identification and Characterization of the ATG8, a Marker of Eimeria tenella Autophagy.

作者信息

Qi Nanshan, Liao Shenquan, Li Juan, Wu Caiyan, Lv Minna, Liu Yunqiu, Mohiuddin Mudassar, Lin Xuhui, Hu Junjing, Cai Haiming, Yu Linzeng, Xiao Wenwan, Sun Mingfei, Li Guoqing

机构信息

Key Laboratory of Livestock Disease Prevention of Guangdong Province, Maoming Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Scientific Observation and Experiment Station of Veterinary Drugs and Diagnostic Techniques of Guangdong Province, Ministry of Agriculture, Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, Guangdong, P. R. China.

College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, Guangdong, P R China.

出版信息

Rev Bras Parasitol Vet. 2021 Mar 12;30(1):e017020. doi: 10.1590/S1984-29612021002. eCollection 2021.

Abstract

Autophagy plays an important role in maintaining cell homeostasis through degradation of denatured proteins and other biological macromolecules. In recent years, many researchers focus on mechanism of autophagy in apicomplexan parasites, but little was known about this process in avian coccidia. In our present study. The cloning, sequencing and characterization of autophagy-related gene (Etatg8) were investigated by quantitative real-time PCR (RT-qPCR), western blotting (WB), indirect immunofluorescence assays (IFAs) and transmission electron microscopy (TEM), respectively. The results have shown 375-bp ORF of Etatg8, encoding a protein of 124 amino acids in E. tenella, the protein structure and properties are similar to other apicomplexan parasites. RT-qPCR revealed Etatg8 gene expression during four developmental stages in E. tenella, but their transcriptional levels were significantly higher at the unsporulated oocysts stage. WB and IFA showed that EtATG8 was lipidated to bind the autophagosome membrane under starvation or rapamycin conditions, and aggregated in the cytoplasm of sporozoites and merozoites, however, the process of autophagosome membrane production can be inhibited by 3-methyladenine. In conclusion, we found that E. tenella has a conserved autophagy mechanism like other apicomplexan parasites, and EtATG8 can be used as a marker for future research on autophagy targeting avian coccidia.

摘要

自噬通过降解变性蛋白质和其他生物大分子在维持细胞内稳态中发挥重要作用。近年来,许多研究人员关注顶复门寄生虫中自噬的机制,但对禽球虫的这一过程了解甚少。在我们目前的研究中,分别通过定量实时PCR(RT-qPCR)、蛋白质免疫印迹法(WB)、间接免疫荧光分析(IFA)和透射电子显微镜(TEM)对自噬相关基因(Etatg8)进行了克隆、测序和表征。结果显示,柔嫩艾美耳球虫中Etatg8的开放阅读框为375 bp,编码一个124个氨基酸的蛋白质,其蛋白质结构和特性与其他顶复门寄生虫相似。RT-qPCR显示Etatg8基因在柔嫩艾美耳球虫的四个发育阶段均有表达,但其转录水平在未孢子化卵囊阶段显著更高。WB和IFA表明,在饥饿或雷帕霉素条件下,EtATG8被脂化以结合自噬体膜,并在子孢子和裂殖子的细胞质中聚集,然而,自噬体膜的产生过程可被3-甲基腺嘌呤抑制。总之,我们发现柔嫩艾美耳球虫与其他顶复门寄生虫一样具有保守的自噬机制,并且EtATG8可作为未来针对禽球虫自噬研究的一个标志物。

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