Cloning of Clostridium perfringens Iota Toxin Gene in Escherichia coli

Document Type : Original Articles

Authors

1 Department of Biology, Islamic Azad University, Urmia branch, Urmia, Iran

2 Department of Biology, Islamic Azad University,Urmia branch, Urmia, Iran

3 Specialized Clostridia reseach laboratory, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Alborz, Karaj, Iran.

Abstract

Iota toxin is produced by Clostridium perfringens type E. This toxin causes antibiotic-associated enterotoxemia in lambs and calves. Iota toxin is a binary toxin that has two components including Ia (the enzyme component) and Ib (the binding component). Ib binds to the surface receptor of target cells and translocate Ia into the cytosol of cells. The aim of this study was to clone toxigenic epitope of iota a gene in E. coli strain Top10. In this study, the phenol–chloroform method was used for the extraction of the whole genomic DNA. The toxigenic epitope of iota a gene was amplified by polymerase chain reaction (PCR). The PCR product was ligated into the pTZ57R/T vector cloning site. Then, based on the TA-cloning method, the product was cloned in competent E. coli strain Top10. Colony PCR was used to screen bacterial colonies transformed with recombinant plasmids. The presence of 446-bp fragment on agarose gel showed that the toxigenic epitope of iota a gene of C. perfringens has been cloned in E. coli strain Top10.

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Main Subjects


Article Title [French]

Clonage du gène iota-toxine du Clostridium perfringens chez

Abstract [French]

Iota-toxine est produite par le Clostridium perfringens de type E. Cette toxine provoque une entérotoxémie associée aux antibiotiques chez les agneaux et les veaux. L'iota-toxine est une toxine binaire qui a deux composants dont Ia (le composant enzymatique) et Ib (le composant de liaison). Ib se lie au récepteur de surface des cellules cibles et translocation Ia dans le cytosol des cellules. Le but de cette recherche était le clonage de l'épitope toxigénique du gène iota a dans la souche d’E. coli Top10. Dans ce travail de recherche, la méthode phénol-chloroforme a été utilisée pour l'extraction de l'ADN entier. L'épitope toxigénique de iota est un gène amplifié par PCR. Le produit de PCR a été ligaturé dans le clonage du vecteur pTZ57R / T et a été ensuite cloné dans E. colistrain Top10 selon la méthode de clonage TA,. L’analyse PCR des colonies a été utilisée pour cribler des colonies bactériennes qui ont été transformées avec des plasmides recombinants. La présence d'un fragment de 446 pb sur legel d'agarose a montré que l'épitope toxigénique de iota, un gène de C. perfringens, a été cloné dans la souche d’E. coli Top10.

Keywords [French]

  • Clonage
  • Clostridium perfringens
  • iota-toxine
  • E. coli
  • TA-clonage
Aktories, K.; Wegner, A., 1989.ADP-ribosylation of actin by clostridial toxins. J Cell Biol 109, 1385–1387.
Aziminia, P., Pilehchian-Langroudi, R., Esmaeilnia, K., 2016. Cloning and expression of Clostridium perfringens type D vaccine strain epsilon toxin gene in E. coli as a recombinant vaccine candidate. Iranian J Microbiol 8, 226-231.
Bakhshi, F., Pilehchian-Langroudi, R., Golestani, Eimani, B., 2016. Enhanced expression of recombinant beta toxin of Clostridium perfringens type B using a commercially available Escherichia coli strain. Onderstepoort J Vet Res 30; 83(1):a1136.
Barth, H., Aktories, K., Popoff, M.R., Stiles, B.G., 2004. Binary bacterial toxins: Biochemistry, biology, and applications of common Clostridium and Bacillus proteins. Microbiol. Mol Biol Rev 68, 373–402.
Barth, H., K. Aktories, M. R. Popoff, and B. G. Stiles. 2004. Binary bacterial toxins: biochemistry, biology, and applications of common Clostridium and Bacillus proteins. Microbiol. Mol Biol Rev 68:373–402.
Blöcker, D., Behlke, J., Aktories, K., Barth, H., 2001. Cellular uptake of the Clostridium perfringens binary iota-toxin. Infect Immun 69(5):2980-7.
Brynestad, S., Synstad, B., Granum, P.E., 1997.Th e Clostridiumperfringensenterotoxin gene is on a transposable element in type A human food poisoning strains. Microbiology 143: 2109-2115.
Czeczulin, J.R., Collie, R.E., McClane, B.A., 1996. Regulated expression of Clostridium perfringens enterotoxin in naturally cpe-negative type A, B, and C isolates of C. perfringens. Infec Immun 64: 3301-3309.
Hale, M. L., J. C. Marvaud, M. R. Popoff, and B. G. Stiles. 2004. Detergentresistant membrane microdomains facilitate Ib oligomer formation and biological activity of Clostridium perfringens iota-toxin. Infect Immun 72: 2186–2193.
McDonel, J.L., 1986. Pharmacology of Bacterial Toxins; Pergamon Press: New York, NY, USA, pp. 477–517.
Ming-Yi Zhou and Celso E. Gomez-Sanchez., 2000.Universal TA Cloning.Curr. Mol Biol 2(1): 1-7.
Nagahama, M., Umezaki, M., Oda, M., Kobayashi, K., Tone, S, Suda, T., Ishidoh, K., Sakurai, J., 2011. Clostridium perfringens iota-toxin binducesrapidcellnecrosis. Infect Immun 79(11):4353-60.
Nijland R, Lindner C, Hartskamp M, Hamoen L, Kuipers OP., 2007 Heterologous production and secretion of Clostridium perfringens β-toxoid in closelyrelated Gram-positive hosts. J Biotechnol 127:361-372.
Perelle S, Scalzo S, Kochi S, Mock M, Popoff MR., 1997. Immunological and functional comparison between Clostridium perfringens iota toxin, C. spiroforme toxin, and anthrax toxins. FEMS Microbiol Lett 146(1):117-21.
Petit, L., Gibert, M., Popoff, M.R., 1999. Clostridium perfringens: toxinotype and genotype. Trends. Microbiol 7: 104-110.
PilehchianLangroudi R, Shamsara M, Aghaiypour K., 2013. Expression of Clostridium perfringens epsilon-beta fusion toxin gene in E. coli and its immunologic studies in mouse.Vaccine 11; 31 (32):3295-9.
PilehchianLangroudi R., 2015. Isolation, Specification, Molecular Biology Assessment and Vaccine Development of Clostridium in Iran: A Review. Int J Enteric Pathog 3(4): e28979.
Sakurai J, Nagahama M, Oda M, Tsuge H, Kobayashi K., 2009. Clostridium perfringens iota-toxin: structure and function. Toxins (Basel) 1(2):208-28.
Sakurai, J., Nagahama. M., Ochi, S., 1997.Major toxins of Clostridium perfringens. J Toxicol Toxin Rev 16, 195–214.
Stiles BG, Hale ML, Marvaud JC, Popoff MR., 2002. Clostridium perfringens iotatoxin: characterization of the cell-associatediotab complex. Biochem J 367(Pt 3):801-8.
Vandekerckhove J, Schering B, Bärmann M, Aktories K., 1987. Clostridium perfringens iota toxin ADP-ribosylates skeletal muscle actin in Arg-177.FEBS Lett 225(1-2):48-52.
Hadjeb, N. and Berkowitz, G.A., 1996. Preparation of T-overhang vectors with high PCR product cloning efficiency. BioTechniques 20: 20-22.
Rashtchian, A., 1995. Novel methods for cloning and engineering genes using the polymerase chain reaction. Curr Opin Biotech 6: 30-36.