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

Author(s):
Mojgan BandehpourMojgan Bandehpour1, Narges AbdaliNarges Abdali2, Farzaneh SadeghiFarzaneh Sadeghi3, Kazem ParivarKazem Parivar2, Zarrin SharifniaZarrin Sharifnia1, Hossein RyahiHossein Ryahi3, Ali HaghighiAli Haghighi4, Bahram KazemiBahram 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


Archives of Clinical Infectious Diseases:Vol. 4, issue 1; 3-7
Article type:Research Article
How to Cite:Mojgan BandehpourNarges AbdaliFarzaneh SadeghiKazem ParivarZarrin SharifniaHossein RyahiAli HaghighiBahram Kazemiet al.Cloning and Expression of Brucella Cyclic ?-1, 2 Glucan Transporter Gene (cgt).Arch Clin Infect Dis.4(1):3-7.

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

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

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

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