Antibody Reactivity to Mycobacterium tuberculosis-specific Regions of Differences 1 and Regions of Differences 9 Proteins and Peptides in Rabbits, Mice, and Humans

被引:0
作者
Hanif, Shumaila N. M. [1 ]
Al-Attiyah, R. [2 ]
Mustafa, A. S. [2 ]
机构
[1] Univ Pikeville, Kentucky Coll Osteopath Med, Dept Biomed Sci, Coal Bldg,Off 718,147 Sycamore St, Pikeville, KY 41501 USA
[2] KUWAIT UNIV, FAC MED, Dept Microbiol, Kuwait, Kuwait
关键词
Antibodies; antigens; enzyme-linked immunosorbent assays; Mycobacterium tuberculosis; regions of differences; CELLULAR IMMUNE-RESPONSES; DNA VACCINE CONSTRUCTS; GENOMIC REGIONS; MCE3; OPERON; IN-VITRO; ANTIGENS; GENES; IDENTIFICATION; PURIFICATION; RECOMBINANT;
D O I
10.4103/ijmy.ijmy_157_23
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background:The major antigens encoded by Mycobacterium tuberculosis-specific genomic regions of differences (RDs) could be useful in the development of new vaccines and/or diagnostic reagents using T-cell and/or antibody assays. In particular, RD1 proteins PE35, PPE68, ESXA, ESXB, and RD9 protein ESXV and their peptides have been identified as major T-cell antigens. However, little is known about their antibody reactivities in different mammalian species. This study aims to determine the antigen-specific antibody reactivities to the above antigens and their peptides in three different mammalian species, i.e., rabbits, mice, and humans.Methods:Sera were obtained from (i) rabbits immunized with purified recombinant proteins PE35, PPE68, ESXA, ESXB, and ESXV; (ii) mice immunized with recombinant DNA vaccine constructs of pUMVC6 and pUMVC7 containing RD1 and RD9 genes; and (iii) tuberculosis (TB) patients and healthy humans. Enzyme-linked immunosorbent assays (ELISAs) were performed with the sera to determine the antibody reactivity to purified recombinant proteins, peptide pools, and individual peptides of RD1 and RD9 proteins.Results:The ELISA results with sera from rabbits immunized with pure recombinant proteins showed positive antibody reactivity with all of the immunizing proteins and their synthetic peptide pools. Testing of the sera with individual peptides showed positive antibody reactivity with PE35 peptides P1 (aa 1-25), P2 (aa 16-40), P5 (aa 61-85), and P6 (aa 76-99); PPE68 peptides P9 (aa 121-145), P11 (aa 151-175), P14 (aa 196-220), P22 (aa 316-340), P23 (aa 331-355), and P24 (aa 346-371); all peptides (P1 to P6) of ESXA and ESXB; and ESXV peptides P1 (aa 1-25), P2 (aa 16-40), P3 (aa 31-55), P5 (aa 61-85), and P6 (aa 76-94). The sera from mice immunized with DNA vaccine constructs showed antibody reactivity to all proteins and the peptide P6 (aa 76-99) of PE35 and peptides P19 (aa 271-295) and P24 (aa 346-371) of PPE68. In humans, the peptides P11 (aa 151-175), P14 (aa 196-220), P22 (aa 316-340), P23 (aa 331-355), and P24 (aa 346-371) of PPE68 and the peptides P4 (aa 46-70), P5 (aa 61-85), and P6 (aa 76-94) of ESXV showed positive reactivity with sera from TB patients and healthy controls.Conclusion:The results demonstrate the presence of several antibody epitopes in each protein, but variations in the epitopes recognized were observed among mice, rabbits, and humans, which could be due to mammalian species differences and/or mode of antigen delivery.
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页码:448 / 458
页数:11
相关论文
共 45 条
[1]   Synergy between Th1 and Th2 responses during Mycobacterium tuberculosis infection: A review of current understanding [J].
Abebe, Fekadu .
INTERNATIONAL REVIEWS OF IMMUNOLOGY, 2019, 38 (04) :172-179
[2]   The six mammalian cell entry proteins (Mce3A-F) encoded by the mce3 operon are expressed during in vitro growth of Mycobocterium tuberculosis [J].
Ahmad, S ;
El-Shazly, S ;
Mustafa, AS ;
Al-Attiyah, R .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2005, 62 (01) :16-24
[3]   Mammalian cell-entry proteins encoded by the mce3 operon of Mycobacterium tuberculosis are expressed during natural infection in humans [J].
Ahmad, S ;
El-Shazly, S ;
Mustafa, AS ;
Al-Attiyah, R .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2004, 60 (04) :382-391
[4]   Construction of a modified vector for efficient purification of recombinant Mycobacterium tuberculosis proteins expressed in Escherichia coli [J].
Ahmad, S ;
Ali, MM ;
Mustafa, AS .
PROTEIN EXPRESSION AND PURIFICATION, 2003, 29 (02) :167-175
[5]  
Ahmad S, 1999, SCAND J IMMUNOL, V50, P510
[6]   Characterization of human cellular immune responses to novel Mycobacterium tuberculosis antigens encoded by genomic regions absent in Mycobacterium bovis BCG [J].
Al-Attiyah, R. ;
Mustafa, A. S. .
INFECTION AND IMMUNITY, 2008, 76 (09) :4190-4198
[7]   Identification, Diagnostic Potential, and Natural Expression of Immunodominant Seroreactive Peptides Encoded by Five Mycobacterium tuberculosis-Specific Genomic Regions [J].
Al-Khodari, Noora Y. ;
Al-Attiyah, Rajaa ;
Mustafa, Abu S. .
CLINICAL AND VACCINE IMMUNOLOGY, 2011, 18 (03) :477-482
[8]  
[Anonymous], 2013, TUBERCULOSIS
[9]   Optimization of HIV-1 Envelope DNA Vaccine Candidates within Three Different Animal Models, Guinea Pigs, Rabbits and Cynomolgus Macaques [J].
Borggren, Marie ;
Vinner, Lasse ;
Andresen, Betina Skovgaard ;
Grevstad, Berit ;
Repits, Johanna ;
Melchers, Mark ;
Elvang, Tara Laura ;
Sanders, Rogier W. ;
Martinon, Frederic ;
Dereuddre-Bosquet, Nathalie ;
Bowles, Emma Joanne ;
Stewart-Jones, Guillaume ;
Biswas, Priscilla ;
Scarlatti, Gabriella ;
Jansson, Marianne ;
Heyndrickx, Leo ;
Le Grand, Roger ;
Fomsgaard, Anders .
VACCINES, 2013, 1 (03) :305-327
[10]   Experimental animal modelling for TB vaccine development [J].
Cardona, Pere-Joan ;
Williams, Ann .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2017, 56 :268-273