Pellino-1 derived cationic antimicrobial prawn peptide: Bactericidal activity, toxicity and mode of action. (October 2016)
- Record Type:
- Journal Article
- Title:
- Pellino-1 derived cationic antimicrobial prawn peptide: Bactericidal activity, toxicity and mode of action. (October 2016)
- Main Title:
- Pellino-1 derived cationic antimicrobial prawn peptide: Bactericidal activity, toxicity and mode of action
- Authors:
- Ravichandran, Gayathri
Kumaresan, Venkatesh
Arasu, Mariadhas Valan
Al-Dhabi, Naif Abdullah
Ganesh, Munuswamy-Ramanujam
Mahesh, Arun
Dhayalan, Arunkumar
Pasupuleti, Mukesh
Arockiaraj, Jesu - Abstract:
- Highlights: Pellino-1 plays a major role in innate immune function of M. rosenbergii. . A cationic antimicrobial peptide ( Mr DN) has been derived. Mr DN found to have broad range of antibacterial activity. Mr DN doesn't show any cytotoxicity and hemolytic activity. Mode of action of Mr DN determined to be membrane targeting along with DNA binding. Abstract: The antimicrobial peptides (AMPs) are multifunctional molecules which represent significant roles in the innate immune system. These molecules have been well known for decades because of their role as natural antibiotics in both invertebrates and vertebrates. The development of multiple drug resistance against conventional antibiotics brought a greater focus on AMPs in recent years. The cationic peptides, in particular, proven as host defense peptides and are considered as effectors of innate immunity. Among the various innate immune molecules, functions of pellino-1 (Peli-1) have been recently studied for its remarkable role in specific immune functions. In our study, we have identified Peli-1 from the cDNA library of freshwater prawn Macrobrachium rosenbergii ( Mr ) and analyzed its features using various in-silico methods. Real time PCR analysis showed an induced expression of Mr Peli-1 during white spot syndrome virus (WSSV), bacteria ( Vibrio harveyi ) and lipopolysaccharide (LPS) from Escherichia coli challenge. Also, a cationic AMP named Mr DN was derived from Mr Peli-1 protein sequence and its activity wasHighlights: Pellino-1 plays a major role in innate immune function of M. rosenbergii. . A cationic antimicrobial peptide ( Mr DN) has been derived. Mr DN found to have broad range of antibacterial activity. Mr DN doesn't show any cytotoxicity and hemolytic activity. Mode of action of Mr DN determined to be membrane targeting along with DNA binding. Abstract: The antimicrobial peptides (AMPs) are multifunctional molecules which represent significant roles in the innate immune system. These molecules have been well known for decades because of their role as natural antibiotics in both invertebrates and vertebrates. The development of multiple drug resistance against conventional antibiotics brought a greater focus on AMPs in recent years. The cationic peptides, in particular, proven as host defense peptides and are considered as effectors of innate immunity. Among the various innate immune molecules, functions of pellino-1 (Peli-1) have been recently studied for its remarkable role in specific immune functions. In our study, we have identified Peli-1 from the cDNA library of freshwater prawn Macrobrachium rosenbergii ( Mr ) and analyzed its features using various in-silico methods. Real time PCR analysis showed an induced expression of Mr Peli-1 during white spot syndrome virus (WSSV), bacteria ( Vibrio harveyi ) and lipopolysaccharide (LPS) from Escherichia coli challenge. Also, a cationic AMP named Mr DN was derived from Mr Peli-1 protein sequence and its activity was confirmed against various pathogenic bacteria. The mode of action of Mr DN was determined to be its membrane permeabilization ability against Bacillus cereus ATCC 2106 as well as its DNA binding ability. Further, scanning electron microscopic (SEM) images showed the membrane disruption and leakage of cellular components of B. cereus cells induced by Mr DN. The toxicity of Mr DN against normal cells (HEK293 cells) was demonstrated by MTT and hemolysis assays. Overall, the results demonstrated the innate immune function of Mr Peli-1 with a potential cationic AMP in prawn. … (more)
- Is Part Of:
- Molecular immunology. Volume 78(2016:Oct.)
- Journal:
- Molecular immunology
- Issue:
- Volume 78(2016:Oct.)
- Issue Display:
- Volume 78 (2016)
- Year:
- 2016
- Volume:
- 78
- Issue Sort Value:
- 2016-0078-0000-0000
- Page Start:
- 171
- Page End:
- 182
- Publication Date:
- 2016-10
- Subjects:
- Pellino -- Peptide -- Prawn -- Membrane permeabilization -- Electrophoretic mobility
Immunochemistry -- Periodicals
Molecular biology -- Periodicals
Immunochemistry -- Periodicals
Allergy and Immunology -- Periodicals
Molecular Biology -- Periodicals
Immunochimie -- Périodiques
Biologie moléculaire -- Périodiques
Immunochemistry
Molecular biology
Periodicals
Electronic journals
571.96 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01615890 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molimm.2016.09.015 ↗
- Languages:
- English
- ISSNs:
- 0161-5890
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 388.xml