Journal: Microorganisms

Article Title: A Plasmid-Encoded FetMP-Fls Iron Uptake System Confers Selective Advantages to Salmonella enterica Serovar Typhimurium in Growth under Iron-Restricted Conditions and for Infection of Mammalian Host Cells

doi: 10.3390/microorganisms8050630

Figure Lengend Snippet: Invasion of epithelial HeLa cells ( A ) and replication within RAW264.7 macrophages ( B ) by wild-type S. Typhimurium LSP 146/02, its Δ fetMP - flsDA isogenic derivative, and the latter strain complemented with the cloned fetMP - flsDA genes (LSP 146/02 Δ fetMP - flsDA C ). The data shown are the mean values ± standard deviations of three biological replicates. Statistical significance (**** p < 0.0001; *** p < 0.001; ** p < 0.01; * p < 0.05; n.s., not significant) was determined by one-way ANOVA and the Tukey´s post-test.

Article Snippet: HeLa and RAW264.7 cells (Cell Lines Service (CLS), Heidelberg, Germany) were propagated in a high-glucose (4.5 g/L) Dulbecco’s modified Eagle’s medium (DMEM) containing 4 mM glutamine (PAA, Cölbe, Germany) and 10% (HeLa) or 6% (RAW264.7) inactivated fetal calf serum (iFCS) (Sigma), at 37 °C in an atmosphere of 5% CO 2 .

Techniques: Clone Assay

Journal: Microorganisms

Article Title: A Plasmid-Encoded FetMP-Fls Iron Uptake System Confers Selective Advantages to Salmonella enterica Serovar Typhimurium in Growth under Iron-Restricted Conditions and for Infection of Mammalian Host Cells

doi: 10.3390/microorganisms8050630

Figure Lengend Snippet: Invasion of epithelial HeLa cells by S. Typhimurium ATCC 14028 harboring the cloned fetMP - flsDA genes (ATCC 14028 fetMP - flsDA T ) ( A ) and replication of the same strain within RAW264.7 macrophages ( B ). The data are the mean values ± standard deviations of three biological replicates. Statistical significance (**** p < 0.0001; *** p < 0.001; ** p < 0.01) was determined by one-way ANOVA and the Tukey´s post-test.

Article Snippet: HeLa and RAW264.7 cells (Cell Lines Service (CLS), Heidelberg, Germany) were propagated in a high-glucose (4.5 g/L) Dulbecco’s modified Eagle’s medium (DMEM) containing 4 mM glutamine (PAA, Cölbe, Germany) and 10% (HeLa) or 6% (RAW264.7) inactivated fetal calf serum (iFCS) (Sigma), at 37 °C in an atmosphere of 5% CO 2 .

Techniques: Clone Assay

Journal: NPJ Biofilms and Microbiomes

Article Title: In silico identification of two peptides with antibacterial activity against multidrug-resistant Staphylococcus aureus

doi: 10.1038/s41522-022-00320-0

Figure Lengend Snippet: Inhibitory action of HG2 and HG4 on LPS or LTA-driven inflammation in murine macrophages: eLUCidate™ Raw 264.7 NF-kB reporter cell line was used to measure the inhibitory action of HG2 and HG4 on LPS ( a ) or LTA ( b ) -mediated inflammation as explained in the Materials and Methods’ section. Data were plotted using GraphPad® Prism 7 software. Results are expressed as means ± standard deviation. Representative images of toxicity assay of peptides ( c ) — ( i ) HG2 and ( ii ) HG4 in G. mellonella 120 h post-treatment with 3x MIC concentrations. The larvae remained alive and without melanisation. Virulence assay of MRSA USA300 in G. mellonella using a lethal dose inoculum of 10 6 CFU/per larvae—( iii ) 24 h post-infection: some larvae were dead and partial melanisation was observed. ( iv ). 48 h post-infection: most larvae were dead and complete melanisation was evident. The experiment was done with three experimental replicates, each containing groups of 10 larvae. d Kaplan–Meier survival curves of G. mellonella infected with a lethal dose (LD 50 ) of S. aureus (2.25 × 10 6 CFU/larvae) and treated with peptides HG2 and HG4 at 1x and 3x MIC concentrations and uninfected larvae treated with peptides in PBS at 3x MIC (placebo showing a 100% larvae survival rate).

Article Snippet: The inhibitory activity of HG2, HG4 and comparator compounds against LPS and LTA was assessed using eLUCidate™ Raw 264.7 NF-kB reporter cell line (AMSBIO) as previously described .

Techniques: Software, Standard Deviation, Infection

Journal: PLoS Pathogens

Article Title: Capsule carbohydrate structure determines virulence in Acinetobacter baumannii

doi: 10.1371/journal.ppat.1009291

Figure Lengend Snippet: (2A) RAW 264.7 cells were co-incubated with NIH1 (left) and ATCC 17978 (right) isogenic wild-type strains and Δ gtr6 mutants. (2B) RAW 264.7 cells were co-incubated with ATCC 17978, the HUMC1:: gtr6 mutant strain with repaired gtr6 , or wild-type HUMC1. (2C) RAW 264.7 cells were co-incubated with ATCC 17978 wild type, Δ gtr6 , Δ gtr6 /pSC1a (the knockout mutant with a plasmid-borne functional copy) in the presence of complement-active serum, and Δ gtr6 /pSC1a in the presence of heat-inactivated serum. *p < 0.001. (2D) Gentamicin protection assay with RAW 264.7 cells and wild-type ATCC 17978 (black bars) or ATCC 17978 Δ gtr6 (white bars). Cytochalasin D was added as an inhibitor of phagocytosis. Total bacteria plated for CFUs and expressed as a proportion of initial bacterial inoculum. * = significant vs. bacteria-only group, ⸸ = significant vs. bacteria + RAW 264.7 cell group. *,⸸ = p < 0.01 (2E) RAW 264.7 cells were incubated with ATCC 17978, HUMC1, ATCC 17978 Δ gtr6 , and HUMC1:: gtr6 . Stained with Wright-Giemsa stain, total magnification is 1000x. Results are from two repeat experiments with duplicate samples in each. White arrows denote adherent or internalized bacteria.

Article Snippet: Bacterial strains were grown in Tryptic Soy Broth (TSB) (VWR, Radnor, PA USA #90000–372) overnight at 37°C with shaking at 200 rpm, sub-cultured to logarithmic phase, washed three times in PBS, diluted to 2×10 8 CFUs/mL based on OD 600 measurements, and added to RAW 264.7 cells at a multiplicity of infection of 20:1 in Hanks’ Balanced Salt Solution (HBSS) (VWR, #45001–101) supplemented with 10% complement-active CD-1 mouse serum (Innovative Research Inc., Novi, MI USA).

Techniques: Incubation, Mutagenesis, Knock-Out, Plasmid Preparation, Functional Assay, Staining, Giemsa Stain

Journal: PLoS Pathogens

Article Title: Capsule carbohydrate structure determines virulence in Acinetobacter baumannii

doi: 10.1371/journal.ppat.1009291

Figure Lengend Snippet: ( 4A ) 2.0×10 8 CFU of ATCC 1778 and HUMC1 had total capsule carbohydrate capsule extracted in parallel and total carbohydrate content measured via phenol-sulfuric acid colorimetry. ( 4B ) Incubation of macrophages and bacteria with purified capsule from gtr6 + (ATCC 17978, 15827) and gtr6 - (HUMC1, ATCC 17978 Δ gtr6 ) strains. Extract-free uptake was used as a control. * p < 0.0001 (4C) RAW 264.7 cells were pre-incubated with soluble mannan (0.5mg/mL), laminarin (0.5mg/mL), and dextran sulfate (0.1mg/mL) or an untreated control prior to co-incubation with ATCC 17978. *p < 0.0001. Two biological replicates for in vitro . Wide bars denote median, error bars denote IQR.

Article Snippet: Bacterial strains were grown in Tryptic Soy Broth (TSB) (VWR, Radnor, PA USA #90000–372) overnight at 37°C with shaking at 200 rpm, sub-cultured to logarithmic phase, washed three times in PBS, diluted to 2×10 8 CFUs/mL based on OD 600 measurements, and added to RAW 264.7 cells at a multiplicity of infection of 20:1 in Hanks’ Balanced Salt Solution (HBSS) (VWR, #45001–101) supplemented with 10% complement-active CD-1 mouse serum (Innovative Research Inc., Novi, MI USA).

Techniques: Colorimetric Assay, Incubation, Purification, In Vitro

Journal: PLoS Pathogens

Article Title: Capsule carbohydrate structure determines virulence in Acinetobacter baumannii

doi: 10.1371/journal.ppat.1009291

Figure Lengend Snippet: (5A) RAW 264.7 cells were pre-incubated with anti-Dectin-1, anti-CR3, anti-MR neutralizing monoclonal antibodies or an isotype control prior to co-incubation with ATCC 17978. *p < 0.0005, * *p < 0.0001 (5B) Knockdown of Dectin-1 and/or CR3 in RAW 264.7 cells followed by incubation with ATCC 17978. *p < 0.0001 (5C) Primary peritoneally-elicited macrophages from C57BL/6 mice followed by phagocytosis assays with ATCC 17978. *p < 0.05, * *p < 0.0001 (5D) Phagocytosis assays of ATCC 17978 with peritoneal neutrophils from wild-type mice with disruption of phagocytosis upon the addition of heat-inactivated serum (HI-S) or complement-active serum (CA-S). *p < 0.0001 (5E) Phagocytosis assays with RAW 264.7 macrophages with gtr6 + and capsule-free strains (ATCC 17978 WT, 15827, ATCC 17978 ΔitrA ), and gtr6 - strains (ATCC 17978 Δgtr6 , HUMC1), with complement active (CA-S) or heat-inactivated (HI-S) serum. *p < 0.0001. Experiments repeated once with two biological replicates. Wide bars denote median, error bars denote IQR.

Article Snippet: Bacterial strains were grown in Tryptic Soy Broth (TSB) (VWR, Radnor, PA USA #90000–372) overnight at 37°C with shaking at 200 rpm, sub-cultured to logarithmic phase, washed three times in PBS, diluted to 2×10 8 CFUs/mL based on OD 600 measurements, and added to RAW 264.7 cells at a multiplicity of infection of 20:1 in Hanks’ Balanced Salt Solution (HBSS) (VWR, #45001–101) supplemented with 10% complement-active CD-1 mouse serum (Innovative Research Inc., Novi, MI USA).

Techniques: Incubation

Journal: PLoS Pathogens

Article Title: Capsule carbohydrate structure determines virulence in Acinetobacter baumannii

doi: 10.1371/journal.ppat.1009291

Figure Lengend Snippet: (6A) Incubation of RAW 264.7 cells with ATCC 17978 in the presence of 100μg/mL GlcNAc (NAG), a CR3 lectin domain inhibitor. (6B) Serial two-fold dilutions of complement-active mouse serum in a RAW 264.7 cell phagocytosis assay with ATCC 17978. *p < 0.0001 (6C) Male C57BL/6 mice aged 10 weeks were infected intravenously with 2.0×10 8 CFUs of 15827, with or without administration of 15μg cobra venom factor (CVF) 48 h prior to infection. *p < 0.001. Experiments repeated once, n = 5 per group for in vivo and two technical replicates for in vitro .

Article Snippet: Bacterial strains were grown in Tryptic Soy Broth (TSB) (VWR, Radnor, PA USA #90000–372) overnight at 37°C with shaking at 200 rpm, sub-cultured to logarithmic phase, washed three times in PBS, diluted to 2×10 8 CFUs/mL based on OD 600 measurements, and added to RAW 264.7 cells at a multiplicity of infection of 20:1 in Hanks’ Balanced Salt Solution (HBSS) (VWR, #45001–101) supplemented with 10% complement-active CD-1 mouse serum (Innovative Research Inc., Novi, MI USA).

Techniques: Incubation, Phagocytosis Assay, Infection, Combined Bisulfite Restriction Analysis Assay, In Vivo, In Vitro