SRM Research Institute, SRM Institute of Science and Technology, Kattankulathur, 603 203, Chennai, Tamil Nadu, India.
Department of Biotechnology, School of Bioengineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, 603 203, Chennai, Tamil Nadu, India.
Fish Shellfish Immunol. 2020 Apr;99:368-378. doi: 10.1016/j.fsi.2020.02.027. Epub 2020 Feb 17.
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 antibiofilm formation and bacterial membrane disruption support its immune character. This study leads to a possibility for the development of therapeutics in aquaculture biotechnology.
在这项研究中,我们评估了从已建立的条纹𬶐(Channa striatus)转录组中鉴定出的两种鱼抗菌肽(Pi)的生物信息学特征和抗菌作用。鉴定出的 CsPi cDNA 包含 256 个核苷酸,编码一个长度为 70 个氨基酸的蛋白质,其中包含两个抗菌肽,分别命名为 CsRG12 和 CsLC11。用各种免疫刺激剂进行的基因表达分析表明,CsPi 表现出诱导表达模式。抗生素图谱显示,CsRG12 和 CsLC11 对金黄色葡萄球菌 ATCC 33592(一种主要的多药耐药(MDR)细菌病原体)和蜡状芽孢杆菌 ATCC 2106 具有活性。进行最小抑菌浓度(MIC)和抗生物膜测定,以观察这些衍生的抗菌肽对致病菌的活性。流式细胞术分析注意到,CsRG12 和 CsLC11 破坏了金黄色葡萄球菌和蜡状芽孢杆菌的膜形成,扫描电子显微镜(SEM)图像进一步证实了这一点,即小泡形成导致细菌膜周围的破坏。总的来说,据报道,CsPi 参与先天免疫,因为基因表达在感染过程中起着显著的上调和下调作用。此外,肽在抗生物膜形成和细菌膜破坏中的参与支持其免疫特性。这项研究为水产养殖生物技术中的治疗方法的开发提供了可能性。