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Expression and confirmation of the surface display of C. <t>hepaticus</t> mimotopes as a fusion with OmpC in E. coli DH5α Δ ompC and APEC PSUO78 Δ aroA Δ asd double mutant strains. ( A ) Coomassie brilliant blue–stained gel picture showing the outer membrane proteins extracted from the recombinant E. coli DH5α Δ ompC strains. The arrow indicates the position of OmpC (30 KDa). ( B ) Western blot image showing the recombinant His-tagged OmpC protein extracted from the E. coli DH5α Δ ompC strain. The arrow indicates the 48 kDa OmpC + mimotope fusion (lanes 4 and 5 in ( A )). ( C ) The western blot showing the recombinant outer membrane protein fractions extracted from APEC PSUO78 Δ aroA Δ asd carrying three different mimotopes. The arrow indicates the 48 kDa OmpC+ mimotope.
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Expression and confirmation of the surface display of C. <t>hepaticus</t> mimotopes as a fusion with OmpC in E. coli DH5α Δ ompC and APEC PSUO78 Δ aroA Δ asd double mutant strains. ( A ) Coomassie brilliant blue–stained gel picture showing the outer membrane proteins extracted from the recombinant E. coli DH5α Δ ompC strains. The arrow indicates the position of OmpC (30 KDa). ( B ) Western blot image showing the recombinant His-tagged OmpC protein extracted from the E. coli DH5α Δ ompC strain. The arrow indicates the 48 kDa OmpC + mimotope fusion (lanes 4 and 5 in ( A )). ( C ) The western blot showing the recombinant outer membrane protein fractions extracted from APEC PSUO78 Δ aroA Δ asd carrying three different mimotopes. The arrow indicates the 48 kDa OmpC+ mimotope.
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Expression and confirmation of the surface display of C. <t>hepaticus</t> mimotopes as a fusion with OmpC in E. coli DH5α Δ ompC and APEC PSUO78 Δ aroA Δ asd double mutant strains. ( A ) Coomassie brilliant blue–stained gel picture showing the outer membrane proteins extracted from the recombinant E. coli DH5α Δ ompC strains. The arrow indicates the position of OmpC (30 KDa). ( B ) Western blot image showing the recombinant His-tagged OmpC protein extracted from the E. coli DH5α Δ ompC strain. The arrow indicates the 48 kDa OmpC + mimotope fusion (lanes 4 and 5 in ( A )). ( C ) The western blot showing the recombinant outer membrane protein fractions extracted from APEC PSUO78 Δ aroA Δ asd carrying three different mimotopes. The arrow indicates the 48 kDa OmpC+ mimotope.
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Expression and confirmation of the surface display of C. hepaticus mimotopes as a fusion with OmpC in E. coli DH5α Δ ompC and APEC PSUO78 Δ aroA Δ asd double mutant strains. ( A ) Coomassie brilliant blue–stained gel picture showing the outer membrane proteins extracted from the recombinant E. coli DH5α Δ ompC strains. The arrow indicates the position of OmpC (30 KDa). ( B ) Western blot image showing the recombinant His-tagged OmpC protein extracted from the E. coli DH5α Δ ompC strain. The arrow indicates the 48 kDa OmpC + mimotope fusion (lanes 4 and 5 in ( A )). ( C ) The western blot showing the recombinant outer membrane protein fractions extracted from APEC PSUO78 Δ aroA Δ asd carrying three different mimotopes. The arrow indicates the 48 kDa OmpC+ mimotope.

Journal: Vaccines

Article Title: Identification and Expression of Immunogenic Mimotopes of C. hepaticus Using an E. coli -Based Surface Display System

doi: 10.3390/vaccines14040298

Figure Lengend Snippet: Expression and confirmation of the surface display of C. hepaticus mimotopes as a fusion with OmpC in E. coli DH5α Δ ompC and APEC PSUO78 Δ aroA Δ asd double mutant strains. ( A ) Coomassie brilliant blue–stained gel picture showing the outer membrane proteins extracted from the recombinant E. coli DH5α Δ ompC strains. The arrow indicates the position of OmpC (30 KDa). ( B ) Western blot image showing the recombinant His-tagged OmpC protein extracted from the E. coli DH5α Δ ompC strain. The arrow indicates the 48 kDa OmpC + mimotope fusion (lanes 4 and 5 in ( A )). ( C ) The western blot showing the recombinant outer membrane protein fractions extracted from APEC PSUO78 Δ aroA Δ asd carrying three different mimotopes. The arrow indicates the 48 kDa OmpC+ mimotope.

Article Snippet: Furthermore, the peptides were searched via BLASTP and PHI-BLAST against the National Center for Biotechnology Information (NCBI BLAST+ suite, version 2.16.0) C. hepaticus -encoded open reading frame (ORF) database to identify highly similar proteins, which were then subjected to subcellular localization prediction for further selection.

Techniques: Expressing, Mutagenesis, Staining, Membrane, Recombinant, Western Blot

Comparison of C. hepaticus loads in liver and cecal samples across the experimental groups by quantitative real-time PCR. Group-4 (Mimotope-2, FliK), group-6 (mimotope-4, flagellin A), group-7 (mimotope-5, MOMP), and the control group (positive control: unvaccinated-challenged control group). ns: p > 0.05 (not significant), and **: p ≤ 0.01 (moderately/highly significant).

Journal: Vaccines

Article Title: Identification and Expression of Immunogenic Mimotopes of C. hepaticus Using an E. coli -Based Surface Display System

doi: 10.3390/vaccines14040298

Figure Lengend Snippet: Comparison of C. hepaticus loads in liver and cecal samples across the experimental groups by quantitative real-time PCR. Group-4 (Mimotope-2, FliK), group-6 (mimotope-4, flagellin A), group-7 (mimotope-5, MOMP), and the control group (positive control: unvaccinated-challenged control group). ns: p > 0.05 (not significant), and **: p ≤ 0.01 (moderately/highly significant).

Article Snippet: Furthermore, the peptides were searched via BLASTP and PHI-BLAST against the National Center for Biotechnology Information (NCBI BLAST+ suite, version 2.16.0) C. hepaticus -encoded open reading frame (ORF) database to identify highly similar proteins, which were then subjected to subcellular localization prediction for further selection.

Techniques: Comparison, Real-time Polymerase Chain Reaction, Control, Positive Control