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The ATCC 6919 is a laboratory equipment product offered by the American Type Culture Collection. It is a device designed for the culturing and maintenance of microbial cell lines. The core function of the ATCC 6919 is to provide a controlled environment for the growth and preservation of various microorganisms.

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6 protocols using atcc 6919

1

Cultivation of P. acnes Isolate

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The P. acnes isolate was obtained from the American Type Culture Collection (ATCC® 6919™). The strain was streaked from freezer stock onto Tryptic soy agar plates (TSA) supplemented with 5% sheep blood (BD, Franklin Lakes, NJ) and incubated at 37°C for 72 h prior to making liquid cultures in brain heart infusion (BHI) broth (BD, Franklin Lakes, NJ) supplemented with 1% dextrose (Fisher Scientific, Waltham, MA) (additional 72 h incubation) for use in the below described assays. All cultures were grown in anaerobic chambers using the EZ Anaerobe Chamber (BD, Franklin Lakes, NJ) and GasPak EZ Anaerobe container sachets (BD, Franklin Lakes, NJ).
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2

Cultivation and Storage of C. acnes and S. epidermidis

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C. acnes standard strain ATCC 6919 was obtained from the American Type Culture Collection (ATCC) (Manassas, VA, USA), while S. epidermidis DSM 28319 (equivalent to ATCC 35984) was obtained from the German Collection of Microorganisms (Braunschweig, Germany). C. acnes was cultured anaerobically on RCM agar (Oxoid Limited, Basingstoke, United Kingdom (UK) and incubated for 48 h at 37 °C under ~5% CO2 using an anaerobic jar and anaerobic atmosphere generation bags (Sigma–Aldrich, St. Louis, MO, USA). Isolated colonies of C. acnes were sub-cultured in an RCM broth for 48 h at 37 °C under anaerobic conditions. For S. epidermidis, the bacteria were cultured aerobically on brain heart infusion (BHI) agar (LAB M limited, Lancashire, UK) and incubated at 37 °C for 18 h. Isolated colonies of S. epidermidis were sub-cultured in BHI broth and incubated at 37 °C for 18 h aerobically. Glycerol stock of each bacterial strain were prepared using their appropriate media supplemented with 25% glycerol and stored in a −70 °C freezer (Thermo Fisher Scientific, Waltham, MA, USA).
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3

Isolation and Characterization of Probiotic Lactobacillus

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Samples of kimchi soup were used to inoculated de Man-Rogosa-Sharpe (MRS) agar plate medium (cat. No.: HB0384, Hope Bio-Technology Co., Ltd) and incubated under aerobic conditions at 37°C for 72 h (31 (link)). A lactic acid bacterium was isolated and designated as L. plantarum VHProbi® E15 based on polyphasic analysis (32 (link)). C. acnes ATCC 11827 and ATCC 6919 were purchased from American Type Culture Collection, (Manassas, VA, USA). C. acnes ATCC 11827 and ATCC 6919 were maintained on a Reinforced Clostridial Medium (RCM, cat. no.: HB0316, Hope Bio-Technology Co., Ltd) and incubated in an anaerobic jar (Sigma-Aldrich®) with an oxygen absorber CO2 generator (AnaeroPack C-1, MGC®, Japan) at 37°C for 48 h.
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4

Bacterial Stimulation of Cell Lines

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Propionibacterium acnes (P. acnes) strain ATCC 6919 was purchased from American Type Culture Collection (ATCC) and cultured on Columbia blood agar plates under anaerobic conditions at 37 °C. Escherichia coli (E. coli) DH5α were cultured in Luria-Bertani broth using an orbital shaker incubator at 37 °C. GC cell lines and THP-1 derived macrophages were then stimulated with live P. acnes (MOI = 30) and E. coli DH5α (MOI = 1000), respectively.
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5

Isolation and Characterization of P. acnes Strains

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P. acnes strain ATCC 6919 was obtained from American Type Culture Collections (Manassas, VA). Clinical isolates were obtained from Biodefense and Emerging Infections Research Resources Repository (BEI Resources) and from nasal skin microcomedones from patients attending the Division of Dermatology outpatient clinic at UCLA, after signed written informed consent as approved by the Institutional Review Board at UCLA in accordance with the Declaration of Helsinki Principles. The level of endotoxin contaminating the P. acnes was quantified with a Limulus Amoebocyte Lysate assay (BioWhittaker, Radnor, PA) and found to be <0.1 ng ml−1. P. acnes cultures were grown as previously described (Agak et al., 2014 (link)). P. acnes strains and clinical isolates used in the study are summarized in Table 1.
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6

Isolation and Characterization of P. acnes Strains

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P. acnes strain ATCC 6919 was obtained from American Type Culture Collections (Manassas, VA). Clinical isolates were obtained from Biodefense and Emerging Infections Research Resources Repository (BEI Resources) and from nasal skin microcomedones from patients attending the Division of Dermatology outpatient clinic at UCLA, after signed written informed consent as approved by the Institutional Review Board at UCLA in accordance with the Declaration of Helsinki Principles. The level of endotoxin contaminating the P. acnes was quantified with a Limulus Amoebocyte Lysate assay (BioWhittaker, Radnor, PA) and found to be <0.1 ng ml−1. P. acnes cultures were grown as previously described (Agak et al., 2014 (link)). P. acnes strains and clinical isolates used in the study are summarized in Table 1.
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