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    Name:
    Enterococcus faecium LRA 55 03 77 API SA
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    Catalog Number:
    35667
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    ATCC e faecium atcc 35667 strains
    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus <t>faecium</t> ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    https://www.bioz.com/result/e faecium atcc 35667 strains/product/ATCC
    Average 94 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    e faecium atcc 35667 strains - by Bioz Stars, 2020-08
    94/100 stars

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    1) Product Images from "Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains"

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    Journal: BMC Microbiology

    doi: 10.1186/s12866-018-1321-6

    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min
    Figure Legend Snippet: Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Techniques Used: Activity Assay, Incubation, Fluorescence

    Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)
    Figure Legend Snippet: Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Techniques Used: Staining, Incubation, Standard Deviation

    2) Product Images from "Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains"

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    Journal: BMC Microbiology

    doi: 10.1186/s12866-018-1321-6

    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min
    Figure Legend Snippet: Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Techniques Used: Activity Assay, Incubation, Fluorescence

    Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)
    Figure Legend Snippet: Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Techniques Used: Staining, Incubation, Standard Deviation

    Related Articles

    Incubation:

    Article Title: Mechanisms of Resistance to Daptomycin in Enterococcus faecium ▿
    Article Snippet: .. When isolates were tested in triplicate (Fig. ), no daptomycin inactivation was observed after 2, 4, 8, or 24 h of incubation with isolates 1 and 8 or E. faecium ATCC 35667. ..

    other:

    Article Title: DNA Sequence Signatures for Rapid Detection of Six Target Bacterial Pathogens Using PCR Assays
    Article Snippet: Microbial strains Microbial strain E. faecalis (ATCC 29212), E. faecium (ATCC 35667), S. aureus (ATCC 25923), C. perfringens (ATCC 3628, ATCC 13124), and C. difficile (ATCC 17857, ATCC 43255) were obtained from American Type Cell Collection (ATCC).

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    ATCC e faecium atcc 35667
    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus <t>faecium</t> ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min
    E Faecium Atcc 35667, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 31 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e faecium atcc 35667/product/ATCC
    Average 94 stars, based on 31 article reviews
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    e faecium atcc 35667 - by Bioz Stars, 2020-08
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    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Journal: BMC Microbiology

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    doi: 10.1186/s12866-018-1321-6

    Figure Lengend Snippet: Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Article Snippet: Both E. faecium strains had the lowest biofilm mass in MHB compared with other tested strains, with an average of 0.149 for E. faecium ATCC 35667 (Fig. ) and 0.109 for vancomycin resistant E. faecium (VRE) ATCC 700221 (Fig. ).

    Techniques: Activity Assay, Incubation, Fluorescence

    Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Journal: BMC Microbiology

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    doi: 10.1186/s12866-018-1321-6

    Figure Lengend Snippet: Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Article Snippet: Both E. faecium strains had the lowest biofilm mass in MHB compared with other tested strains, with an average of 0.149 for E. faecium ATCC 35667 (Fig. ) and 0.109 for vancomycin resistant E. faecium (VRE) ATCC 700221 (Fig. ).

    Techniques: Staining, Incubation, Standard Deviation

    Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Journal: BMC Microbiology

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    doi: 10.1186/s12866-018-1321-6

    Figure Lengend Snippet: Assessment of metabolic activity of biofilm cells by resazurin. Quantification of biofilm production of six bacterial strains, using three concentrations of resazurin solution (2, 4 and 8 μg/mL): ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212, ( F ) Enterococcus faecalis VRE ATCC 51575, incubated at 25 °C and 37 °C. Relative fluorescence measurements were taken at 20, 40, 60 and 80 min

    Article Snippet: E. faecium ATCC 35667, showed a 2-fold lower linezolid MBIC than its respective MIC.

    Techniques: Activity Assay, Incubation, Fluorescence

    Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Journal: BMC Microbiology

    Article Title: Defining conditions for biofilm inhibition and eradication assays for Gram-positive clinical reference strains

    doi: 10.1186/s12866-018-1321-6

    Figure Lengend Snippet: Assessment of biofilm biomass by crystal violet staining and cell enumeration by colony count. Biofilm production analysis through crystal violet staining (OD 570 nm, bars) and cell enumeration (log 10 CFU/mL, lines) of six bacterial strains: ( a ) Staphylococcus aureus ATCC 29213, ( b ) Staphylococcus aureus MRSA ATCC 43300, ( c ) Enterococcus faecium ATCC 35667, ( d ) Enterococcus faecium VRE ATCC 700221, ( e ) Enterococcus faecalis ATCC 29212 and ( f ) Enterococcus faecalis VRE ATCC 51575, incubated in six different media: Mueller Hinton (MH), Tryptic Soy (TS), Tryptic Soy supplemented with 1% glucose (TSG), Tryptic Soy supplemented with 2% glucose (TS2G), Brain Heart Infusion (BHI) and Brain Heart Infusion supplemented with 1% glucose (BHIG). Error bars represent standard deviation of two independent experiments in triplicate. Lowercase letters indicate significant differences amongst media used for biofilm production. Similar letters denote no significant difference ( P > 0.05)

    Article Snippet: E. faecium ATCC 35667, showed a 2-fold lower linezolid MBIC than its respective MIC.

    Techniques: Staining, Incubation, Standard Deviation

    Representative conventional PCR testing of species-specific primer sets (Elf6, Efm12, Cp14, Cd3, Ct3, and Sa2) using 5 pg, 500 fg, 50 fg, and 5 fg of purified target genomic DNA (lanes 1–4 without human DNA and lanes 5–8 with 5 ng of human DNA, respectively, for E. faecalis , E. faecium , C. clostridium , C. difficile , and C. tetani ; lanes 45–48 without human DNA and lanes 49–52 with 5 ng of human DNA for S. aureus ) and 5 ng of purified DNA from respective nontarget species: S. pyogenes , Streptococcus dysgalactiae Group G, Streptococcus agalactiae Group B, Streptococcus dysgalactiae Group C, Streptococcus sp. strain H60R Group F, Streptococcus viridans , Streptococcus equi Group C, Streptococcus gallolyticus , Streptococcus mutans , Streptococcus uberis , Streptococcus salivarius , Streptococcus thermophilus , Streptococcus pneumoniae , Staphylococcus epidermis , Listeria monocytogenes , Corynebacterium sp., Bacillus subtilis , Bacillus cereus , Bacillus circulans , Bacillus polymyxa , Bacillus megaterium , Bacillus sphaericus , Bacillus thuringiensis , Bacillus coagulans , Bacillus alvei , Escherichia coli , Salmonella typhimurium , Salmonella sp. Group D, Pseudomonas fluorescens , Shigella sonnei , Enterobacter aerogenes , Klebsiella pneumoniae , Morganella morganii , Proteus mirabilis , Alcaligenes odorans , Stenotrophomonas maltophilia , C. albicans , C. tropicalis , C. parapsilosis , human being, and a no template control.

    Journal: Microbiology Insights

    Article Title: DNA Sequence Signatures for Rapid Detection of Six Target Bacterial Pathogens Using PCR Assays

    doi: 10.4137/MBI.S29736

    Figure Lengend Snippet: Representative conventional PCR testing of species-specific primer sets (Elf6, Efm12, Cp14, Cd3, Ct3, and Sa2) using 5 pg, 500 fg, 50 fg, and 5 fg of purified target genomic DNA (lanes 1–4 without human DNA and lanes 5–8 with 5 ng of human DNA, respectively, for E. faecalis , E. faecium , C. clostridium , C. difficile , and C. tetani ; lanes 45–48 without human DNA and lanes 49–52 with 5 ng of human DNA for S. aureus ) and 5 ng of purified DNA from respective nontarget species: S. pyogenes , Streptococcus dysgalactiae Group G, Streptococcus agalactiae Group B, Streptococcus dysgalactiae Group C, Streptococcus sp. strain H60R Group F, Streptococcus viridans , Streptococcus equi Group C, Streptococcus gallolyticus , Streptococcus mutans , Streptococcus uberis , Streptococcus salivarius , Streptococcus thermophilus , Streptococcus pneumoniae , Staphylococcus epidermis , Listeria monocytogenes , Corynebacterium sp., Bacillus subtilis , Bacillus cereus , Bacillus circulans , Bacillus polymyxa , Bacillus megaterium , Bacillus sphaericus , Bacillus thuringiensis , Bacillus coagulans , Bacillus alvei , Escherichia coli , Salmonella typhimurium , Salmonella sp. Group D, Pseudomonas fluorescens , Shigella sonnei , Enterobacter aerogenes , Klebsiella pneumoniae , Morganella morganii , Proteus mirabilis , Alcaligenes odorans , Stenotrophomonas maltophilia , C. albicans , C. tropicalis , C. parapsilosis , human being, and a no template control.

    Article Snippet: Microbial strains Microbial strain E. faecalis (ATCC 29212), E. faecium (ATCC 35667), S. aureus (ATCC 25923), C. perfringens (ATCC 3628, ATCC 13124), and C. difficile (ATCC 17857, ATCC 43255) were obtained from American Type Cell Collection (ATCC).

    Techniques: Polymerase Chain Reaction, Purification

    Diameter of zone of inhibition as a function of incubation time with different E. faecium strains. No significant difference was observed between the strains tested and the control solution with daptomycin and tryptic soy broth. For isolate 1, the daptomycin MIC was 4 μg/ml; for isolate 8, the MIC was 16 μg/ml; and for E. faecium ATCC 35667, the MIC was 1 μg/ml).

    Journal: Antimicrobial Agents and Chemotherapy

    Article Title: Mechanisms of Resistance to Daptomycin in Enterococcus faecium ▿

    doi: 10.1128/AAC.00774-07

    Figure Lengend Snippet: Diameter of zone of inhibition as a function of incubation time with different E. faecium strains. No significant difference was observed between the strains tested and the control solution with daptomycin and tryptic soy broth. For isolate 1, the daptomycin MIC was 4 μg/ml; for isolate 8, the MIC was 16 μg/ml; and for E. faecium ATCC 35667, the MIC was 1 μg/ml).

    Article Snippet: When isolates were tested in triplicate (Fig. ), no daptomycin inactivation was observed after 2, 4, 8, or 24 h of incubation with isolates 1 and 8 or E. faecium ATCC 35667.

    Techniques: Inhibition, Incubation