Cover image of the article: Cloning and Expression of Brucella Cyclic ?-1, 2 Glucan Transporter Gene (cgt)

Image Credit:Arch Clin Infect Dis

Cloning and Expression of Brucella Cyclic ?-1, 2 Glucan Transporter Gene (cgt)

Authors

Mojgan Bandehpour1, Narges Abdali2, Farzaneh Sadeghi3, Kazem Parivar2, Zarrin Sharifnia1, Hossein Ryahi3, Ali Haghighi4, Bahram KazemiBahram Kazemi ORCID1,*
1Cellular and Molecular Biology Research Center, Shahid Beheshti University, M.C., Tehran, IR Iran
2Islamic Azad University, Research and Science Campus, Tehran, IR Iran
3Department of Biology, Shahid Beheshti University, M.C., Tehran, IR Iran
4Department of Parasitology, Shahid Beheshti University, M.C., Tehran, IR Iran
*Corresponding Author: Cellular and Molecular Biology Research Center, Shahid Beheshti University, M.C., Tehran, IR Iran. Email:, kazemi@sbmu.ac.ir. Email: kazemi@sbmu.ac.ir

Archives of Clinical Infectious Diseases:Vol. 4, issue 1; 3-7
Published online:Jan 31, 2009
Article type:Research Article
How to Cite:Bandehpour M, Abdali N, Sadeghi F, Parivar K, Sharifnia Z, et al. Cloning and Expression of Brucella Cyclic ?-1, 2 Glucan Transporter Gene (cgt). Arch Clin Infect Dis. 2009;4(1):. doi:

Abstract

Background:

Brucellosis is an important cosmopolitan infection disease caused by organisms belonging to the genus Brucella. The cgt gene (cyclic ?-1, 2 glucan transporter gene) is a virulent factor in Brucella genus. The present study was conducted with the aim of cloning and expression of Brucella cgt gene.

Materials and methods:

Brucella melitensis cgt gene was amplified from extracted chromosomal DNA by PCR, then

PCR product was cloned into pTZ57R and subcloned into pGEMEX-1 expression vector, then expressed in JM109 E.coli strain. Recombinant protein was confirmed by western blot analysis using patient's serum.

Results:

The PCR product was cloned in pTZ57R plasmid via T/A cloning method. Recombinant plasmid was digested by BamHI and SacI restriction enzymes, the released band was purified and subcloned into pGEMEX-1 expression vector. Then, sample cells were lysed using lyses buffer and sonicated, then electrophoresed on SDS-PAGE. Protein bands were transferred on nitrocellulose membrane and reacted by patient's serum and detected by HRP conjugated anti

human antibody.

Conclusion:

We cloned and expressed Brucella abortus cyclic -1, 2-glucan transporter gene (cgt) which is an important agent in brucellosis. Using cgt gene mutant may be an effective way for inhibiting or decreasing the pathogenicity of bacteria

Highlights

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Copyright

© 2009, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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