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Reports of Biochemistry and Molecular Biology
rbmb.net
Basic Sciences
http://rbmb.net
1
admin
2322-3480
2322-3480
10.61882/rbmb
en
jalali
1396
7
1
gregorian
2017
10
1
6
1
online
1
fulltext
en
Construction of Mtb72F Plasmid as a DNA Vaccine Candidate for Mycobacterium tuberculosis
میکروب شناسی
Microbiology
مقالات اصلی
Original Article
<p style="text-align: justify;"><strong><em>Background:</em></strong> With one-third of the world’s population infected, tuberculosis<strong> (</strong>TB) is one of the most common infectious diseases and a major public health problem, especially in developing countries. The efficacy of the BCG vaccine for controlling the disease in adults is poor. The development of an effective TB vaccine is a global objective. An effective tuberculosis vaccine should stimulate cellular immunity. DNA vaccines are a new generation of vaccines with the potential to achieve this goal. The aim of this study was to produce a DNA vaccine of Mtb72F. </p>
<p style="text-align: justify;"><strong><em>Methods:</em></strong> <em>mtb32C</em>, <em>mtb39, </em>and <em>mtb32N</em> were cloned into pcDNA3.1 using restriction enzyme digestion and <em>T4 DNA ligase</em>. Colony-PCR and restriction enzyme digestion were performed to detect transformed bacteria. DNA sequencing confirmed the desired gene insertion into the vector. A Chinese hamster ovary (CHO) cell line was transfected with the recombinant plasmid and RT-PCR was performed to assess gene expression.</p>
<p style="text-align: justify;"><strong><em>Results:</em></strong> Gel electrophoresis showed the expected amplified gene fragments of 429, 614, and 1200 base pairs (bps) for <em>mtb32C</em>, <em>mtb32N</em>, and <em>mtb39</em>, respectively. Enzyme digestion and gel electrophoresis showed the expected fragments, indicating the desired gene position and orientation in the recombinant plasmid. This finding was verified by DNA sequencing, and RT-PCR demonstrated gene expression in the CHO cell line.</p>
<p style="text-align: justify;"><strong><em>Conclusions:</em></strong> An Mtb72F DNA plasmid was successfully constructed. This plasmid may be a candidate for animal immunizations.</p>
Cloning, DNA vaccine, mtb32C, mtb32N, mtb39, Mycobacterium tuberculosis.
95
101
http://rbmb.net/browse.php?a_code=A-10-69-2&slc_lang=en&sid=1
Maryam Sadat
Nabavinia
10031947532846002263
10031947532846002263
No
Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Mohammad
Ramezani
10031947532846002264
10031947532846002264
No
Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
Aida
Gholoobi
10031947532846002265
10031947532846002265
No
Department of Modern Sciences and Technologies, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Mahboubeh
Naderinasab
10031947532846002266
10031947532846002266
No
Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
Zahra
Meshkat
meshkatz@mums.ac.ir
10031947532846002267
10031947532846002267
Yes
Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran