کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3416456 1593700 2015 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Expression and immunological characteristics of the surface-localized pyruvate kinase in Mycoplasma gallisepticum
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروب شناسی
پیش نمایش صفحه اول مقاله
Expression and immunological characteristics of the surface-localized pyruvate kinase in Mycoplasma gallisepticum
چکیده انگلیسی


• M. gallisepticum pyruvate kinase fusion protein (PykF) was expressed in a pET system.
• Recombinant M. gallisepticum PykF catalyzed the conversion of NADH to NAD+.
• PykF was identified as an immunogenic protein on the M. gallisepticum cell surface.
• M. gallisepticum PykF was identified as a potential protective antigen.
• M. gallisepticum PykF participated in the bacterial adhesion to DF-1 cells.

The widespread avian pathogen Mycoplasma gallisepticum is a causative agent of respiratory disease. The wall-less prokaryotes lack some tricarboxylic acid cycle enzymes, therefore, the glycolysis metabolic pathway is of great importance to these organisms. Pyruvate kinase (PK) is one of the key enzymes of the glycolytic pathway, and its immunological characteristics in Mycoplasma are not well known. In this study, the M. gallisepticum pyruvate kinase fusion protein (PykF) was expressed in a pET system. The full-length of the gene was subcloned into the expression vector pET28a(+) to construct the pET28a-rMGPykF plasmid, which was then transformed into Escherichia coli strain BL21 (DE3) cells. The expression of the 62 kDa recombinant protein of rMGPykF in E. coli strain BL21 (DE3) was confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis with Coomassie blue staining. Purified rMGPykF exhibited PK catalytic activity, which could reflect the conversion of NADH to NAD+. Mouse anti-PykF antibodies were generated by immunization of mice with rMGPykF. Immunoblot and immunoelectron microscopy assays identified PykF as an immunogenic protein expressed on the surface of M. gallisepticum cells. Bactericidal assay showed that anti-rMGPykF antiserum killed 70.55% of M. gallisepticum cells, suggesting the protective potential of PykF. Adherence inhibition assay on immortalized chicken fibroblasts (DF-1) cells revealed more than 39.31% inhibition of adhesion in the presence of anti-rMGPykF antiserum, suggesting that PykF of M. gallisepticum participates in bacterial adhesion to DF-1 cells.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Microbial Pathogenesis - Volume 89, December 2015, Pages 161–168
نویسندگان
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