Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii

Background: Now a day, antibiotic resistance is a global problem. A way to solve this problem is production of alternative drugs. In this regard, today so many researches on antimicrobial peptides against pathogens are being done. LL-37 peptide is one of these peptides that is cationic and has antib...

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Main Authors: Ehsan Zarei-Mehrvarz, Ehsanollah Ghaznavi-Rad, Shohreh Fahimi-Rad, Hamid Abtahi
Format: Article
Language:fas
Published: Vesnu Publications 2017-10-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/8383
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spelling doaj-3ca96887a5324bbc88d43fd0682d94312020-11-25T01:01:27ZfasVesnu Publications مجله دانشکده پزشکی اصفهان1027-75951735-854X2017-10-01354419549602607Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter BaumanniiEhsan Zarei-Mehrvarz0Ehsanollah Ghaznavi-Rad1Shohreh Fahimi-Rad2Hamid Abtahi3MSc Student, Department of Medical Biotechnology, School of Medicine, Arak University of Medical Sciences, Arak, IranAssociate Professor, Molecular and Medicine Research Center, Arak University of Medical Sciences, Arak, IranDepartment of Agricultural Biotechnology, School of Agriculture and Natural Resources, University of Tehran, Karaj, IranAssociate Professor, Molecular and Medicine Research Center, Arak University of Medical Sciences, Arak, IranBackground: Now a day, antibiotic resistance is a global problem. A way to solve this problem is production of alternative drugs. In this regard, today so many researches on antimicrobial peptides against pathogens are being done. LL-37 peptide is one of these peptides that is cationic and has antibacterial, antiviral, and anticancer activity. This project aimed to study the antimicrobial effectiveness of peptide LL-37 on multiple-drug-resistant (MDR) Acinetobacter baumannii. Methods: First, the LL-37 gene was linked to the pET-32a vector; then, recombinant DNA was transformed into the host bacteria and inducted to produce proteins. After the production and purification of recombinant proteins, to activate the protein, dialysis was performed in phosphate buffered saline (PBS). Then, the efficiency of peptide LL-37 on multiple-drug-resistant Acinetobacter baumannii was tested using common laboratory tests such as minimum inhibitory concentration (MIC). Findings: The minimum inhibitory concentration of LL-37 on Acinetobacter baumannii ATCC19606 was 1.5 µg/ml. In addition, the activity test showed that the recombinant proteins could inhibit the growth and decay the bacteria. Conclusion: The results of this study show that LL-37 protein, in comparison to other peptides and drugs in other studies, is more efficient and in low concentration can cause destruction of bacteria. This can herald a bright future for the treatment of infections caused by multiple-drug-resistant Acinetobacter baumannii.http://jims.mui.ac.ir/index.php/jims/article/view/8383LL-37 antibacterial peptideAntimicrobial drug resistanceAcinetobacter baumannii
collection DOAJ
language fas
format Article
sources DOAJ
author Ehsan Zarei-Mehrvarz
Ehsanollah Ghaznavi-Rad
Shohreh Fahimi-Rad
Hamid Abtahi
spellingShingle Ehsan Zarei-Mehrvarz
Ehsanollah Ghaznavi-Rad
Shohreh Fahimi-Rad
Hamid Abtahi
Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
مجله دانشکده پزشکی اصفهان
LL-37 antibacterial peptide
Antimicrobial drug resistance
Acinetobacter baumannii
author_facet Ehsan Zarei-Mehrvarz
Ehsanollah Ghaznavi-Rad
Shohreh Fahimi-Rad
Hamid Abtahi
author_sort Ehsan Zarei-Mehrvarz
title Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
title_short Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
title_full Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
title_fullStr Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
title_full_unstemmed Cloning, Expression, and Purification of Antimicrobial Peptide LL-37 and Assessment of its Antimicrobial Effectiveness on Multiple-Drug-Resistant Acinetobacter Baumannii
title_sort cloning, expression, and purification of antimicrobial peptide ll-37 and assessment of its antimicrobial effectiveness on multiple-drug-resistant acinetobacter baumannii
publisher Vesnu Publications
series مجله دانشکده پزشکی اصفهان
issn 1027-7595
1735-854X
publishDate 2017-10-01
description Background: Now a day, antibiotic resistance is a global problem. A way to solve this problem is production of alternative drugs. In this regard, today so many researches on antimicrobial peptides against pathogens are being done. LL-37 peptide is one of these peptides that is cationic and has antibacterial, antiviral, and anticancer activity. This project aimed to study the antimicrobial effectiveness of peptide LL-37 on multiple-drug-resistant (MDR) Acinetobacter baumannii. Methods: First, the LL-37 gene was linked to the pET-32a vector; then, recombinant DNA was transformed into the host bacteria and inducted to produce proteins. After the production and purification of recombinant proteins, to activate the protein, dialysis was performed in phosphate buffered saline (PBS). Then, the efficiency of peptide LL-37 on multiple-drug-resistant Acinetobacter baumannii was tested using common laboratory tests such as minimum inhibitory concentration (MIC). Findings: The minimum inhibitory concentration of LL-37 on Acinetobacter baumannii ATCC19606 was 1.5 µg/ml. In addition, the activity test showed that the recombinant proteins could inhibit the growth and decay the bacteria. Conclusion: The results of this study show that LL-37 protein, in comparison to other peptides and drugs in other studies, is more efficient and in low concentration can cause destruction of bacteria. This can herald a bright future for the treatment of infections caused by multiple-drug-resistant Acinetobacter baumannii.
topic LL-37 antibacterial peptide
Antimicrobial drug resistance
Acinetobacter baumannii
url http://jims.mui.ac.ir/index.php/jims/article/view/8383
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