» Articles » PMID: 32765010

Evaluation of the Anti-Leishmanial Effect of Recombinant α-Toxin

Overview
Publisher Dove Medical Press
Date 2020 Aug 9
PMID 32765010
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Leishmaniasis is an infectious disease common in tropical and subtropical regions caused by the genus , which is transmitted by the bite of female sandflies. In this study, we evaluate the anti-leishmanial effect of recombinant α-toxin protein alone and the combination with glucantime through in vitro and in vivo.

Materials And Methods: Production, expression, and purification of recombinant α-toxin were evaluated by SDS-PAGE and Western blotting techniques. The antileishmanial activities of the purified α-toxin plus and without glucantime were examined in vitro and in vivo.

Results: The results indicated successful expression of α-toxin as a 48 kDa band on SDS-PAGE and Western blot methods. Also, evaluation of α-toxin IC showed the strong fatal effect of it, and glucantime on medium proliferated promastigotes at lower concentrations compared with glucantime or α-toxin alone. Moreover, in vivo surveys showed that at the end of treatment courses, the mean of lesion size diminished in glucantime plus α-toxin treated mice versus negative control groups (p < 0.001). Also, there was a significant difference in the parasite burden of the spleen and liver of the control versus the test groups (p < 0.001).

Conclusion: The results showed recombinant α-toxin has synergistic effects with glucantime in destroying parasites.

Citing Articles

Anti-tumor Effects of Recombinant Clostridium α-Toxin on Breast Cancer: An and Study.

Rezaei Khozani N, Shayesteh Pour M, Yekani M, Hejazi S, Saffari M Int J Mol Cell Med. 2025; 13(4):404-416.

PMID: 39895919 PMC: 11786122. DOI: 10.22088/IJMCM.BUMS.13.4.404.


A novel inhibitory strategy of using and killer toxins.

Zolfaghari A, Beheshti-Maal K, Ahadi A, Monajemi R Future Microbiol. 2024; 20(3):189-199.

PMID: 39704759 PMC: 11812320. DOI: 10.1080/17460913.2024.2443329.


Genetic diversity of strains isolated from and in western Iran based on minicircle kDNA.

Khoshnood S, Tavalla M, Mohaghegh M, Khamesipour F, Hejazi S J Parasit Dis. 2021; 45(3):838-844.

PMID: 34475667 PMC: 8368947. DOI: 10.1007/s12639-021-01369-y.

References
1.
Gordon V, Benz R, Fujii K, Leppla S, Tweten R . Clostridium septicum alpha-toxin is proteolytically activated by furin. Infect Immun. 1997; 65(10):4130-4. PMC: 175594. DOI: 10.1128/iai.65.10.4130-4134.1997. View

2.
Hickey M, Kwan R, Awad M, Kennedy C, Young L, Hall P . Molecular and cellular basis of microvascular perfusion deficits induced by Clostridium perfringens and Clostridium septicum. PLoS Pathog. 2008; 4(4):e1000045. PMC: 2275794. DOI: 10.1371/journal.ppat.1000045. View

3.
Inoue M, Kikuchi M, Komoriya T, Watanabe K, Kouno H . [Cloning of Clostridium perfringens alpha-toxin gene and extracellular expression in Escherichia coli]. Rinsho Biseibutshu Jinsoku Shindan Kenkyukai Shi. 2007; 18(2):127-35. View

4.
Melton J, Parker M, Rossjohn J, Buckley J, Tweten R . The identification and structure of the membrane-spanning domain of the Clostridium septicum alpha toxin. J Biol Chem. 2004; 279(14):14315-22. DOI: 10.1074/jbc.M313758200. View

5.
Sellman B, Kagan B, Tweten R . Generation of a membrane-bound, oligomerized pre-pore complex is necessary for pore formation by Clostridium septicum alpha toxin. Mol Microbiol. 1997; 23(3):551-8. DOI: 10.1046/j.1365-2958.1997.d01-1876.x. View