» Articles » PMID: 31438823

Expression of Thanatin in HEK293 Cells and Investigation of Its Antibacterial Effects on Some Human Pathogens

Overview
Specialty Biochemistry
Date 2019 Aug 24
PMID 31438823
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Thanatin is the smallest member of Beta-hairpin class of cationic peptide derived from insects with vast activities against various pathogens.

Objective: In this study, the antimicrobial activity of this peptide against some species of human bacterial pathogens as well as its toxicity on NIH cells were evaluated.

Methods: Thanatin DNA sequence was cloned into pcDNA3.1+ vector and transformed into a DH5α bacterial strain. Then the recombinant plasmids were transfected into HEK-293 cells by calcium phosphate co-precipitation. After applying antibiotic treatment, the supernatant medium containing thanatin was collected. The peptide quantity was estimated by SDS-PAGE and GelQuant software. The antimicrobial activity of this peptide was performed with Minimum Inhibitory Concentration (MIC) method. In addition, its toxicity on NIH cells were evaluated by MTT assay.

Results: The peptide quantity was estimated approximately 164.21 µmolL-1. The antibacterial activity of thanatin was estimated between 0.99 and 31.58 µmolL-1 using MIC method. The result of cytotoxicity test on NIH cell line showed that the peptide toxicity up to the concentration of 394.10 µmolL-1 and for 48 hours, was not statistically significant from negative control cells (P>0.05). The antimicrobial assay demonstrated that thanatin had an antibacterial effect on some tested microorganisms. The results obtained in this study also showed that thanatin had no toxicity on mammalian cell lines including HEK293 and NIH.

Conclusion: Antimicrobial peptides such as thanatin are considered to be appropriate alternatives to conventional antibiotics in treating various human pathological diseases bacteria.

Citing Articles

CRISPR-edited, cell-based future-proof meat and seafood to enhance global food security and nutrition.

Chandrababu A, Puthumana J Cytotechnology. 2024; 76(6):619-652.

PMID: 39435422 PMC: 11490478. DOI: 10.1007/s10616-024-00645-y.


Thanatin: A Promising Antimicrobial Peptide Targeting the Achilles' Heel of Multidrug-Resistant Bacteria.

Liu Q, Wu Q, Xu T, Malakar P, Zhu Y, Liu J Int J Mol Sci. 2024; 25(17).

PMID: 39273441 PMC: 11395501. DOI: 10.3390/ijms25179496.


A Natural Bioactive Peptide from Pearls Can Be Used as a Potential Inhibitor of the Interaction between SARS-CoV-2 and ACE2 against COVID-19.

Wang Y, Wang Q, Chen X, Li B, Zhang Z, Yao L Int J Mol Sci. 2024; 25(14).

PMID: 39063143 PMC: 11277083. DOI: 10.3390/ijms25147902.


GlmS plays a key role in the virulence factor expression and biofilm formation ability of promoted by advanced glycation end products.

Ni L, Shen R, Luo H, Li X, Zhang X, Huang L Virulence. 2024; 15(1):2352476.

PMID: 38741276 PMC: 11095574. DOI: 10.1080/21505594.2024.2352476.


Upregulation of Nrf2 in myocardial infarction and ischemia-reperfusion injury of the heart.

Zuberi S, Rafi H, Hussain A, Hashmi S PLoS One. 2024; 19(3):e0299503.

PMID: 38489253 PMC: 10942075. DOI: 10.1371/journal.pone.0299503.


References
1.
Bechinger B . Structure and functions of channel-forming peptides: magainins, cecropins, melittin and alamethicin. J Membr Biol. 1997; 156(3):197-211. DOI: 10.1007/s002329900201. View

2.
Wang L, Yu B, Han G, He J, Chen D . Design, expression and characterization of recombinant hybrid peptide Attacin-Thanatin in Escherichia coli. Mol Biol Rep. 2009; 37(7):3495-501. DOI: 10.1007/s11033-009-9942-3. View

3.
Sinha S, Zheng L, Mu Y, Ng W, Bhattacharjya S . Structure and Interactions of A Host Defense Antimicrobial Peptide Thanatin in Lipopolysaccharide Micelles Reveal Mechanism of Bacterial Cell Agglutination. Sci Rep. 2017; 7(1):17795. PMC: 5736615. DOI: 10.1038/s41598-017-18102-6. View

4.
Wu G, Fan X, Li L, Wang H, Ding J, Hongbin W . Interaction of antimicrobial peptide s-thanatin with lipopolysaccharide in vitro and in an experimental mouse model of septic shock caused by a multidrug-resistant clinical isolate of Escherichia coli. Int J Antimicrob Agents. 2010; 35(3):250-4. DOI: 10.1016/j.ijantimicag.2009.11.009. View

5.
Simmaco M, Mignogna G, Barra D, Bossa F . Antimicrobial peptides from skin secretions of Rana esculenta. Molecular cloning of cDNAs encoding esculentin and brevinins and isolation of new active peptides. J Biol Chem. 1994; 269(16):11956-61. View