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Image Search Results
Journal: mBio
Article Title: Increased Production of Outer Membrane Vesicles by Salmonella Interferes with Complement-Mediated Innate Immune Attack
doi: 10.1128/mBio.00869-21
Figure Lengend Snippet: Serum resistance assay for Salmonella mutants grown under PhoPQ-activating conditions. (A) Survival of Salmonella deletion mutants in 25% NHS incubated at 37°C for 1 h. Deletion of Δ pgtE , Δ rck (used as positive controls), Δ phoP , and Δ pagC made the bacteria susceptible to complement-mediated killing. (B) A comparison of serum resistance between Salmonella Δ pagC , Δ rck , and Δ ompX single, double, and triple mutants. (C) Quantitative RT-PCR-based analysis of gene expression ratio of pagC , rck , and ompX (relative to housekeeping gene rpoB ) in wild-type Salmonella grown in LB or under PhoPQ-activating conditions (5.8L) showed the expression of pagC increased significantly under PhoPQ-activating conditions. (D) Resistance to serum-mediated attack was restored in single Salmonella mutants complemented with plasmids induced to express PagC, Rck, and OmpX in the corresponding mutants. Plasmids expressing Rck or PagC complemented best the triple mutant compared with mutants containing empty vector (pRS1). The data represent one of three separate, reproducible experiments, expressed as mean ± SEM. Statistical significance was calculated using one-way ANOVA multiple-comparison test and set at a P value of <0.05 (*, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001; and ns, P > 0.05).
Article Snippet: For analyzing the sensitivity of Salmonella to serum-mediated killing, bacteria (∼1 × 10 5 CFU grown in 5.8L N-minimal media (optical density at 600 nm [OD 600 ], 0.5) were incubated with 25%
Techniques: Incubation, Bacteria, Comparison, Quantitative RT-PCR, Gene Expression, Expressing, Mutagenesis, Plasmid Preparation
Journal: mBio
Article Title: Increased Production of Outer Membrane Vesicles by Salmonella Interferes with Complement-Mediated Innate Immune Attack
doi: 10.1128/mBio.00869-21
Figure Lengend Snippet: Serum protection assay by OMV produced under PhoPQ-activating conditions. (A) Survival of WT and Δ pagC Salmonella incubated with 25% NHS in the presence of sterile culture medium, OMV-depleted culture supernatants, or OMV-containing culture supernatants showed that bacteria incubated with OMV-containing culture supernatants from PagC-expressing bacteria (WT, Δ pagC + p pagC , and PhoP C ) were significantly more resistant to serum-mediated attack than bacteria incubated with sterile culture medium or culture supernatant from the Δ pagC mutant. Bacterial survival in sterile culture medium was comparable to the survival in OMV-depleted spent culture supernatants. (B) Survival of WT and Δ pagC Salmonella incubated with 25% NHS in the presence of purified OMVs at indicated concentrations (0 to 10 5 OMVs), isolated from bacteria grown under PhoPQ-activating (5.8L; solid line) or nonactivating (7.6H; dashed line) conditions. OMVs from bacteria expressing PagC (WT) grown under PhoPQ-activating conditions were more protective than OMVs from bacteria grown under nonactivating conditions. The data represent one of three separate, reproducible experiments, expressed as mean ± SEM. Statistical significance was calculated using Student’s t test and set at a P value of <0.05 (*, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001; and ns, P > 0.05).
Article Snippet: For analyzing the sensitivity of Salmonella to serum-mediated killing, bacteria (∼1 × 10 5 CFU grown in 5.8L N-minimal media (optical density at 600 nm [OD 600 ], 0.5) were incubated with 25%
Techniques: Produced, Incubation, Sterility, Bacteria, Expressing, Mutagenesis, Purification, Isolation
Journal: mBio
Article Title: Increased Production of Outer Membrane Vesicles by Salmonella Interferes with Complement-Mediated Innate Immune Attack
doi: 10.1128/mBio.00869-21
Figure Lengend Snippet: Blocking of complement activation by OMVs from PagC-expressing bacteria. (A) Survival of WT Salmonella incubated with 25% NHS treated with 5 mM EGTA or EDTA, in the presence or absence of 1 × 10 9 purified OMVs from WT or Δ pagC mutant. OMVs from PagC-expressing WT bacteria block the alternative pathway of the complement more efficiently than the OMVs from the Δ pagC mutant. Statistical significance was calculated using Student’s t test. (B) Schematic representation of C3 and its cleavage products C3b and iC3b (molecular weight [MW] of the α and β chain and the cleaved or uncleaved products is indicated in the brackets). (C) WT OMVs (10 8 to 10 10 OMVs) incubated with 5% NHS, when immunoblotted with anti-C3 antibody, showed bands for C3b inactivation at 68 kDa (iC3bα′) and 46 kDa (iC3bα″) in OMV pellet and supernatant fractions, respectively. No C3b inactivation bands were found when Δ pagC OMVs were incubated with NHS, suggesting that WT OMVs bind to C3b and inactivate C3b into iC3b in a dose-dependent manner. The Western blot image was spliced to remove an empty lane in between pellet and supernatant fractions. The panel on the right represents relative protein band densities (WT versus Δ pagC OMVs) as analyzed by NIH ImageJ software from 3 separate, reproducible experiments, expressed as mean ± SEM. Statistical significance was calculated using Student’s t test. (D) WT or Δ pagC mutant incubated with C3/C4-depleted human serum (gray bars) survived significantly better than the bacteria incubated with NHS (black bars). Presence of OMV-containing culture supernatant (+ OMV) contributed to bacterial survival when incubated with NHS, compared with bacteria incubated in the presence of OMV-depleted culture supernatants (− OMV). (E) Incubation of the Δ pagC Δ rck Δ ompX Δ pgtE mutant with NHS in the presence of OMV-containing culture supernatant prevented C3b deposition on bacterial cell surfaces. OMVs from the quadruple mutant expressing PagC prevented C3 deposition most significantly. The bar graph below the blot represents relative protein band densities as analyzed by NIH ImageJ software from 3 separate, reproducible experiments, expressed as mean ± SEM. For iC3bα′, relative protein densities were calculated for bacteria incubated in sterile culture medium (−) with no OMVs versus bacteria incubated with OMV-containing spent culture supernatant. Statistical significance was calculated using the one-way ANOVA multiple-comparison test. The data represent one of three separate, reproducible experiments, expressed as mean ± SEM (*, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001; and ns, P > 0.05).
Article Snippet: For analyzing the sensitivity of Salmonella to serum-mediated killing, bacteria (∼1 × 10 5 CFU grown in 5.8L N-minimal media (optical density at 600 nm [OD 600 ], 0.5) were incubated with 25%
Techniques: Blocking Assay, Activation Assay, Expressing, Bacteria, Incubation, Purification, Mutagenesis, Molecular Weight, Western Blot, Software, Sterility, Comparison