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首页> 外文期刊>Fish & Shellfish Immunology >Defense involvement of piscidin from striped murrel Channa striatus and its peptides CsRG12 and CsLC11 involvement in an antimicrobial and antibiofilm activity
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Defense involvement of piscidin from striped murrel Channa striatus and its peptides CsRG12 and CsLC11 involvement in an antimicrobial and antibiofilm activity

机译:Piscidin的防御涉及条纹梅雷尔通道纹状体及其肽CSRG12和CSLC11参与抗菌剂和抗生素活性

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摘要

In this study, we have evaluated bioinformatics characterization and antimicrobial role of two piscidin (Pi) peptide identified from the established transcriptome of striped murrel Channa striatus (Cs). The identified CsPi cDNA contains 256 nucleotides encode a protein with 70 amino acids in length which has two antimicrobial peptides and named CsRG12 and CsLC11. The gene expression analysis with various immune stimulants indicated an induced expression pattern of CsPi. Antibiogram showed that CsRG12 and CsLC11 was active against Staphylococcus aureus ATCC 33592, a major multi-drug resistant (MDR) bacterial pathogen and Bacillus cereus ATCC 2106. The minimum inhibitory concentration (MIC) and antibiofilm assays were conducted to observe the activity of pathogenic bacteria with these derived antimicrobial peptides. Flow cytometry analysis noticed that the CsRG12 and CsLC11 disrupt the membrane formation of S. aureus and B. cereus, which was further assured by scanning electron microscopic (SEM) images that bleb formation leads to disruption around the bacterial membrane. Overall, it is reported that CsPi is involved in innate immunity as the gene expression plays a remarkable role in up and down regulation during infection. In addition, the involvement of peptides in anti-biofilm formation and bacterial membrane disruption support its immune character. This study leads to a possibility for the development of therapeutics in aquaculture biotechnology.
机译:在这项研究中,我们已经评估了从已建立的脐带通道纹状体(CS)的已建立的转录组中鉴定的两种皮蛋白(PI)肽的生物信息学表征和抗微生物作用。所识别的CSPI cDNA含有256个核苷酸编码具有70个氨基酸的蛋白质,其长度具有两个抗微生物肽和命名为CSRG12和CSLC11。具有各种免疫刺激剂的基因表达分析表明了CSPI的诱导表达模式。抗诊断表明,CSRG12和CSLC11对葡萄球菌ATCC 33592有效,主要多药物抗性(MDR)细菌病原体和芽孢杆菌ATCC 2106。进行最小抑制浓度(MIC)和抗抗氧化铝测定以观察病原体细菌的活性用这些衍生的抗微生物肽。流式细胞术分析注意到CSRG12和CSLC11扰乱了金黄色葡萄球菌和B.培养物的膜形成,其通过扫描电子显微镜(SEM)图像进一步确保BLEB形成导致细菌膜中断。总的来说,据报道,由于基因表达在感染期间在上下调节中起着显着作用,CSPI涉及先天免疫力。此外,肽在抗生物膜形成和细菌膜中断的累积支持其免疫特征。本研究导致水产养殖生物技术在水产病患者中发展的可能性。

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