Expression and epitope prediction of MPT64 recombinant proteins from clinical isolates of Mycobacterium tuberculosis as immunoserodiagnostic candidates

被引:3
作者
Fihiruddin, Fihiruddin [1 ,2 ]
Inayati, Nurul [1 ]
Jannah, Raudatul [3 ]
Unsunnidhal, Lalu [4 ,5 ]
Kusumawati, Asmarani [6 ]
机构
[1] Politeknik Kesehatan Mataram, Dept Med Lab Technol, Praburangkasari St, Mataram, Indonesia
[2] Politeknik Kesehatan Mataram, Ctr Excellent, Praburangkasari St, Mataram, Indonesia
[3] STIKES Yarsi Mataram, Midwifery Study Program, Mataram 83361, West Nusa Tengg, Indonesia
[4] Univ Mataram, Fac Food Technol & Agroind, Food Technol Study Program, Mataram 83125, Indonesia
[5] STIKES Yarsi Mataram, Nursing Study Program, Biomed Field, Mataram 83361, West Nusa Tengg, Indonesia
[6] Univ Gadjah Mada, Fac Vet Med, Dept Reprod & Obstet, Yogyakarta 55281, Indonesia
关键词
Escherichia coli; immune response; lymphocytes; tuberculosis; JEMBRANA DISEASE VIRUS; FUSION PROTEIN; ESAT-6; GENE;
D O I
10.14202/vetworld.2022.2376-2383
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Background and Aim: The success in the handling and prevention of tuberculosis (TB) cases is highly dependent on their rapid detection, monitoring, and treatment. The efficacy of the Bacille Calmette-Guerin (BCG) vaccine is inconclusive in eastern Indonesia. The RV1980c gene ofMycobacterium tuberculosis encodes an antigenic protein that is considered to be a virulence factor, as it can stimulate the immune response in patients with TB. This study aimed to study the expression and epitope indicator of MPT64 recombinant proteins from clinical isolates of M. tuberculosis as immunoserodiagnostic candidates for pET SUMO plasmids from clinical isolates as candidates for serodiagnostic tests and recombinant vaccines.Materials and Methods: The polymerase chain reaction (PCR) product of the RV1980c gene was inserted into the SUMO pET plasmid, which was then transformed into Escherichia coli BL21 (DE3) cells and expressed in Luria Bertani media induced by 1.0 M IPTG. Subsequently, sequencing was performed and the results were analyzed using the ClustalW and National Center for Biotechnology Information BLAST software. The T-cell epitope prognosis was then explained by GENETYX version 8.0., for the prediction of B-cell epitope, as assessed using an Immune Epitope Database analysis.Results: The PCR product of the RV1980c gene had a length of 619 bp. Moreover, SDS- polyacrylamide gel electrophoresis and Western blotting revealed that the protein encoded by the Rv1980c gene weighed 36 kDa. We gained nine specific T-cell epitopes according to Iad Pattern position and eight epitopes according to Rothbard/Taylor Pattern Position; furthermore, we detected five B-cell epitopes in the RV1980c gene.Conclusion: The MPT64 protein encoded by the RV1980c gene carries epitopes that are realized by lymphocytes and represent potential immunoserodiagnostic candidates in diagnostic immunology.
引用
收藏
页码:2376 / 2383
页数:8
相关论文
共 35 条
[1]   Association of ESAT-6/CFP-10-induced IFN-, TNF- and IL-10 with clinical tuberculosis: evidence from cohorts of pulmonary tuberculosis patients, household contacts and community controls in an endemic setting [J].
Abebe, F. ;
Belay, M. ;
Legesse, M. ;
Mihret, A. ;
Franken, K. S. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2017, 189 (02) :241-249
[2]  
Ahmad A., 2019, J PHYS C SER, V1341, P1
[3]  
Bahar E, 2019, IOP C SER EARTH ENV, V217, P1, DOI [DOI 10.1088/1755-1315/217/1/012061, 10.1088/1755-1315/217/1/012061]
[4]   Cloning, expression, and characterization of human brain acetylcholinesterase in Escherichia coli using a SUMO fusion tag [J].
Ceylan, Hamid ;
Erdogan, Orhan .
TURKISH JOURNAL OF BIOLOGY, 2017, 41 (01) :77-87
[5]   Early Secreted Antigen ESAT-6 of Mycobacterium tuberculosis Promotes Protective T Helper 17 Cell Responses in a Toll-Like Receptor-2-dependent Manner [J].
Chatterjee, Samit ;
Dwivedi, Ved Prakash ;
Singh, Yogesh ;
Siddiqui, Imran ;
Sharma, Pawan ;
Van Kaer, Luc ;
Chattopadhyay, Debprasad ;
Das, Gobardhan .
PLOS PATHOGENS, 2011, 7 (11)
[6]  
Dinesh B.R., 2018, J MED MICROBIOL DIAG, V7, P282
[7]   CLONING, EXPRESSION AND T CELL EPITOPE PREDICTION OF FBPA AND FBPB GENES OF MYCOBACTERIUM TUBERCULOSIS CLINICAL ISOLATES [J].
Fihiruddin ;
Artama, Wayan Tunas ;
Wibawa, Tri ;
Mertaniasih, Ni Made .
JOURNAL OF MICROBIOLOGY BIOTECHNOLOGY AND FOOD SCIENCES, 2020, 9 (05) :998-1002
[8]   Virulence factors of the Mycobacterium tuberculosis complex [J].
Forrellad, Marina A. ;
Klepp, Laura I. ;
Gioffre, Andrea ;
Sabio y Garcia, Julia ;
Morbidoni, Hector R. ;
de la Paz Santangelo, Mara ;
Cataldi, Angel A. ;
Bigi, Fabiana .
VIRULENCE, 2013, 4 (01) :3-66
[9]   Strategies for the Production of Recombinant Protein in Escherichia coli [J].
Gopal, Gopal Jee ;
Kumar, Awanish .
PROTEIN JOURNAL, 2013, 32 (06) :419-425
[10]   Perspectives on TB patients' care and support: a qualitative study conducted in Accra Metropolis, Ghana [J].
Gyimah, Faustina Twumwaa ;
Dako-Gyeke, Phyllis .
GLOBALIZATION AND HEALTH, 2019, 15 (1)