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对与维罗纳气单胞菌C4的小蛋白B和替代核糖体拯救因子A相互作用并抑制它们的肽适配体进行基因筛选。

Genetic Selection of Peptide Aptamers That Interact and Inhibit Both Small Protein B and Alternative Ribosome-Rescue Factor A of Aeromonas veronii C4.

作者信息

Liu Peng, Chen Yong, Wang Dan, Tang Yanqiong, Tang Hongqian, Song Haichao, Sun Qun, Zhang Yueling, Liu Zhu

机构信息

Department of Biology, College of Sciences, Shantou University Shantou, China.

Hainan Key Laboratory for Sustainable Utilization of Tropical Bioresources, College of Agriculture, Hainan University Haikou, China.

出版信息

Front Microbiol. 2016 Aug 18;7:1228. doi: 10.3389/fmicb.2016.01228. eCollection 2016.

Abstract

Aeromonas veronii is a pathogenic gram-negative bacterium, which infects a variety of animals and results in mass mortality. The stalled-ribosome rescues are reported to ensure viability and virulence under stress conditions, of which primarily include trans-translation and alternative ribosome-rescue factor A (ArfA) in A. veronii. For identification of specific peptides that interact and inhibit the stalled-ribosome rescues, peptide aptamer library (pTRG-SN-peptides) was constructed using pTRG as vector and Staphylococcus aureus nuclease (SN) as scaffold protein, in which 16 random amino acids were introduced to form an exposed surface loop. In the meantime both Small Protein B (SmpB) which acts as one of the key components in trans-translation, and ArfA were inserted to pBT to constitute pBT-SmpB and pBT-ArfA, respectively. The peptide aptamer PA-2 was selected from pTRG-SN-peptides by bacterial two-hybrid system (B2H) employing pBT-SmpB or pBT-ArfA as baits. The conserved sites G133K134 and D138K139R140 of C-terminal SmpB were identified by interacting with N-terminal SN, and concurrently the residue K62 of ArfA was recognized by interacting with the surface loop of the specific peptide aptamer PA-2. The expression plasmids pN-SN or pN-PA-2, which combined the duplication origin of pRE112 with the neokanamycin promoter expressing SN or PA-2, were created and transformed into A. veronii C4, separately. The engineered A. veronii C4 which endowing SN or PA-2 expression impaired growth capabilities under stress conditions including temperatures, sucrose, glucose, potassium chloride (KCl) and antibiotics, and the stress-related genes rpoS and nhaP were down-regulated significantly by Quantitative Real-time PCR (qRT-PCR) when treating in 2.0% KCl. Thus, the engineered A. veronii C4 conferring PA-2 expression might be potentially attenuated vaccine, and also the peptide aptamer PA-2 could develop as anti-microbial drugs targeted to the ribosome rescued factors in A. veronii.

摘要

维氏气单胞菌是一种致病性革兰氏阴性菌,可感染多种动物并导致大量死亡。据报道,停滞核糖体拯救机制可确保细菌在应激条件下的生存能力和毒力,其中主要包括维氏气单胞菌中的反式翻译和替代核糖体拯救因子A(ArfA)。为了鉴定与停滞核糖体拯救机制相互作用并抑制其功能的特定肽段,构建了以pTRG为载体、金黄色葡萄球菌核酸酶(SN)为支架蛋白的肽适配体文库(pTRG-SN-肽段),其中引入了16个随机氨基酸以形成一个暴露的表面环。同时,将作为反式翻译关键组分之一的小蛋白B(SmpB)和ArfA分别插入pBT中,构建成pBT-SmpB和pBT-ArfA。以pBT-SmpB或pBT-ArfA为诱饵,通过细菌双杂交系统(B2H)从pTRG-SN-肽段中筛选出肽适配体PA-2。通过与N端SN相互作用鉴定出C端SmpB的保守位点G133K134和D138K139R140,同时通过与特定肽适配体PA-2的表面环相互作用识别出ArfA的K62残基。构建了将pRE112的复制起点与表达SN或PA-2的新霉素启动子相结合的表达质粒pN-SN或pN-PA-2,并分别将其转入维氏气单胞菌C4中。赋予SN或PA-2表达的工程化维氏气单胞菌C4在包括温度、蔗糖、葡萄糖、氯化钾(KCl)和抗生素在内的应激条件下生长能力受损,并且在2.0% KCl处理时,通过定量实时PCR(qRT-PCR)检测发现应激相关基因rpoS和nhaP显著下调。因此,赋予PA-2表达的工程化维氏气单胞菌C4可能是一种潜在的减毒疫苗,并且肽适配体PA-2可开发成为针对维氏气单胞菌核糖体拯救因子的抗菌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8dc/4988972/6015aea4f10a/fmicb-07-01228-g0001.jpg

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