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s aureus strains usa300 je2  (ATCC)


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    Structured Review

    ATCC s aureus strains usa300 je2
    S Aureus Strains Usa300 Je2, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 250 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/baa+1717/Staphylococcus+aureus+subsp%2E+aureus+Rosenbach/pm42885928-344-11-16
    Average 97 stars, based on 250 article reviews
    s aureus strains usa300 je2 - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    other:

    Article Title: A small-molecule membrane fluidizer re-sensitizes methicillin-resistant Staphylococcus aureus (MRSA) to β-lactam antibiotics
    Article Snippet: S. aureus strains 29213, BAA-1683, BAA-1717, BAA-1720, 43300, 33591, 33592, and 700789; K. pneumoniae strain 700603; A. baumannii strain BAA-1605; P. aeruginosa strain 27853; and E. coli strain 25922 were purchased from American Type Culture Collection, and E. coli strain CGSC 4213(ΔlptD) was obtained from Coli Genetic Stock Center.

    Article Title: Mechanistic and functional aspects of the Ruminococcin C sactipeptide isoforms
    Article Snippet: Methicillin-resistant Staphylococcus aureus , ATCC BAA-1717 , 10.4 , R , 50 , 66.6 , 12.5.

    Incubation:

    Article Title: New polyphenolic glycosides from the stems of Caesalpinia cucullata and their inhibitory effect on methicillin-resistant Staphylococcus aureus with different ways.
    Article Snippet: Anti-virulence strategy represents an emerging alternative strategy in the war against increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) due to its milder selection pressure on bacterial resistance.. Sortase A (SrtA), as an important virulence factor, is a membrane-localized cysteine transpeptidase which anchors cell surface proteins to the cell wall.. Natural products in medicinal plants are the source of targeting bacterial virulence factors.

    Inhibition:

    Article Title: New polyphenolic glycosides from the stems of Caesalpinia cucullata and their inhibitory effect on methicillin-resistant Staphylococcus aureus with different ways.
    Article Snippet: Anti-virulence strategy represents an emerging alternative strategy in the war against increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) due to its milder selection pressure on bacterial resistance.. Sortase A (SrtA), as an important virulence factor, is a membrane-localized cysteine transpeptidase which anchors cell surface proteins to the cell wall.. Natural products in medicinal plants are the source of targeting bacterial virulence factors.

    Infection:

    Article Title: Immunostimulatory DNA Hydrogel Enhances Protective Efficacy of Nanotoxoids against Bacterial Infection.
    Article Snippet: While vaccines have been highly successful in protecting against various infections, there are still many high-priority pathogens for which there are no clinically approved formulations.. To overcome this challenge, researchers have explored the use of nanoparticulate strategies for more effective antigen delivery to the immune system.. Along these lines, nanotoxoids are a promising biomimetic platform that leverages cell membrane coating technology to safely deliver otherwise toxic bacterial antigens in their native form for antivirulence vaccination.

    Cell Culture:

    Article Title: Immunostimulatory DNA Hydrogel Enhances Protective Efficacy of Nanotoxoids against Bacterial Infection.
    Article Snippet: While vaccines have been highly successful in protecting against various infections, there are still many high-priority pathogens for which there are no clinically approved formulations.. To overcome this challenge, researchers have explored the use of nanoparticulate strategies for more effective antigen delivery to the immune system.. Along these lines, nanotoxoids are a promising biomimetic platform that leverages cell membrane coating technology to safely deliver otherwise toxic bacterial antigens in their native form for antivirulence vaccination.

    Isolation:

    Article Title: 7,8-Dihydroxyflavone attenuates the virulence of Staphylococcus aureus by inhibiting alpha-hemolysin.
    Article Snippet: Staphylococcus aureus (S. aureus), a Gram-positive bacteria, is an incurable cause of hospital and community-acquired infections.. Inhibition bacterial virulence is a viable strategy against S. aureus infections based on the multiple virulence factors secreted by S. aureus.. Alpha-hemolysin (Hla) plays a crucial role in bacteria virulence without affecting bacterial viability.



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    ATCC staphylococcus aureus atcc 43300
    (A) Efficacy of Fc-CHAP-LSN constructs against in vitro formed biofilms. Bacterial quantification of 24 h-cultivated biofilms of S. aureus <t>ATCC</t> <t>43300</t> after 24 h exposure to SOC antibiotics or lysins. Concentrations indicated in µg/mL. Statistical analysis was performed using Graphpad’s one-way ANOVA with Dunnett’s correction for multiple comparisons; ****: P<0.0001; ***: P=0.001; **: P<0.01 ns: not significant (B) Graphical representation of the tested lysins in this assay. Cli: clindamycin; Dapto: daptomycin; LOQ: limit of quantification at 500 CFU/mL; Rif: rifampicin; Untr.: untreated control; Van: vancomycin;
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    (A) Efficacy of Fc-CHAP-LSN constructs against in vitro formed biofilms. Bacterial quantification of 24 h-cultivated biofilms of S. aureus ATCC 43300 after 24 h exposure to SOC antibiotics or lysins. Concentrations indicated in µg/mL. Statistical analysis was performed using Graphpad’s one-way ANOVA with Dunnett’s correction for multiple comparisons; ****: P<0.0001; ***: P=0.001; **: P<0.01 ns: not significant (B) Graphical representation of the tested lysins in this assay. Cli: clindamycin; Dapto: daptomycin; LOQ: limit of quantification at 500 CFU/mL; Rif: rifampicin; Untr.: untreated control; Van: vancomycin;

    Journal: bioRxiv

    Article Title: A chimeric, half-life extended lysin with a unique mode of action

    doi: 10.64898/2026.05.13.724763

    Figure Lengend Snippet: (A) Efficacy of Fc-CHAP-LSN constructs against in vitro formed biofilms. Bacterial quantification of 24 h-cultivated biofilms of S. aureus ATCC 43300 after 24 h exposure to SOC antibiotics or lysins. Concentrations indicated in µg/mL. Statistical analysis was performed using Graphpad’s one-way ANOVA with Dunnett’s correction for multiple comparisons; ****: P<0.0001; ***: P=0.001; **: P<0.01 ns: not significant (B) Graphical representation of the tested lysins in this assay. Cli: clindamycin; Dapto: daptomycin; LOQ: limit of quantification at 500 CFU/mL; Rif: rifampicin; Untr.: untreated control; Van: vancomycin;

    Article Snippet: The following strains were used for this study: Staphylococcus aureus ATCC 43300 (ATCC), BAA-1717 (ATCC), NCTC 8178 (NCTC), Staphylococcus epidermidis DSM3269 (DSMZ), S. epidermidis RP62A (ATCC), Staphylococcus lugdunensis DSM4804 (DSMZ), Staphylococcus haemolyticus DSM20263 (DSMZ) and Staphylococcus haemolyticus DSM20265 (DSMZ).

    Techniques: Construct, In Vitro, Control

    Efficacy of Fc-CHAP-LSN against in vivo formed biofilms and in sepsis model. (A) Catheters with in vivo formed biofilms of S. aureus ATCC 43300 were explanted from CD1 mice 3 dpi and treated with either 50 µg/mL or 100 µg/mL Fc-L1-CHAP opt -LSN HEKa for 24 h at 37 °C. Rifampicin (10 µg/mL) was used as comparator. (B) Datapoints represent the biofilm bacterial burden in each catheter (n=6). Horizontal bars indicate the median burden for each group. When burden is below LOQ, half a value of LOQ is assigned for graphical and statistical purposes. Brown Forsythe ANOVA with Welch’s correction (GraphPad Prism) was used to calculate statistical significance against vehicle. dpi: days post infection; LOQ: limit of quantification at 10 CFU/catheter. (C) Lysin efficacy in mouse IV sepsis: Immunocompetent male CD1 mice were challenged with 3.23 × 10 7 CFU/mouse of S. aureus NCTC 8178, IV. Lysins were administered IV, twice (1 hpi and 25 hpi) at dose of either 100 µg/mouse or 500 µg/mouse. Vancomycin (Van) was dosed at 25 mg/kg, IV, q12 h, starting from 1 hpi. (D) Points on the graph represent CFU counts in individual mice (n=6), with horizontal lines indicating median CFU burden and interquartile range. Open circles indicate animals that needed to be terminated before planned endpoint due to clinical symptoms. Brown-Forsythe ANOVA with Welch’s correction was used to calculate the significance compared to vehicle group on log transformed data, with P values indicated in the graph. hpi: hours post infection; CFU: colony forming units; LOQ: limit of quantification at 54 CFU/g; For graphical and statistical purposes, values under LOQ were assigned half of the LOQ value.

    Journal: bioRxiv

    Article Title: A chimeric, half-life extended lysin with a unique mode of action

    doi: 10.64898/2026.05.13.724763

    Figure Lengend Snippet: Efficacy of Fc-CHAP-LSN against in vivo formed biofilms and in sepsis model. (A) Catheters with in vivo formed biofilms of S. aureus ATCC 43300 were explanted from CD1 mice 3 dpi and treated with either 50 µg/mL or 100 µg/mL Fc-L1-CHAP opt -LSN HEKa for 24 h at 37 °C. Rifampicin (10 µg/mL) was used as comparator. (B) Datapoints represent the biofilm bacterial burden in each catheter (n=6). Horizontal bars indicate the median burden for each group. When burden is below LOQ, half a value of LOQ is assigned for graphical and statistical purposes. Brown Forsythe ANOVA with Welch’s correction (GraphPad Prism) was used to calculate statistical significance against vehicle. dpi: days post infection; LOQ: limit of quantification at 10 CFU/catheter. (C) Lysin efficacy in mouse IV sepsis: Immunocompetent male CD1 mice were challenged with 3.23 × 10 7 CFU/mouse of S. aureus NCTC 8178, IV. Lysins were administered IV, twice (1 hpi and 25 hpi) at dose of either 100 µg/mouse or 500 µg/mouse. Vancomycin (Van) was dosed at 25 mg/kg, IV, q12 h, starting from 1 hpi. (D) Points on the graph represent CFU counts in individual mice (n=6), with horizontal lines indicating median CFU burden and interquartile range. Open circles indicate animals that needed to be terminated before planned endpoint due to clinical symptoms. Brown-Forsythe ANOVA with Welch’s correction was used to calculate the significance compared to vehicle group on log transformed data, with P values indicated in the graph. hpi: hours post infection; CFU: colony forming units; LOQ: limit of quantification at 54 CFU/g; For graphical and statistical purposes, values under LOQ were assigned half of the LOQ value.

    Article Snippet: The following strains were used for this study: Staphylococcus aureus ATCC 43300 (ATCC), BAA-1717 (ATCC), NCTC 8178 (NCTC), Staphylococcus epidermidis DSM3269 (DSMZ), S. epidermidis RP62A (ATCC), Staphylococcus lugdunensis DSM4804 (DSMZ), Staphylococcus haemolyticus DSM20263 (DSMZ) and Staphylococcus haemolyticus DSM20265 (DSMZ).

    Techniques: In Vivo, Infection, Transformation Assay

    LSN-induced LSN-release from Fc-CHAP-LSN. (a) Purified LSN HEKa was incubated at increasing concentrations in 80% human serum and in presence of 10 8 CFU/mL S. aureus ATCC 43300 with (circles) or without (boxes) a fixed concentration of Fc-L1-CHAP opt -LSN HEK (1 µM) for 3h at 37°C. Samples were analyzed by SDS-PAGE followed by Western Blotting to quantify the amounts of free LSN in each reaction (x-axis). The remainder of the reaction was subjected to quantitative plating to determine the log10 CFU reduction relative to a growth control lacking lysins (y-axis). (B) Concentrations of spiked-in purified LSN are plotted against free LSN detected by Western blotting in the experiment described in panel (A).

    Journal: bioRxiv

    Article Title: A chimeric, half-life extended lysin with a unique mode of action

    doi: 10.64898/2026.05.13.724763

    Figure Lengend Snippet: LSN-induced LSN-release from Fc-CHAP-LSN. (a) Purified LSN HEKa was incubated at increasing concentrations in 80% human serum and in presence of 10 8 CFU/mL S. aureus ATCC 43300 with (circles) or without (boxes) a fixed concentration of Fc-L1-CHAP opt -LSN HEK (1 µM) for 3h at 37°C. Samples were analyzed by SDS-PAGE followed by Western Blotting to quantify the amounts of free LSN in each reaction (x-axis). The remainder of the reaction was subjected to quantitative plating to determine the log10 CFU reduction relative to a growth control lacking lysins (y-axis). (B) Concentrations of spiked-in purified LSN are plotted against free LSN detected by Western blotting in the experiment described in panel (A).

    Article Snippet: The following strains were used for this study: Staphylococcus aureus ATCC 43300 (ATCC), BAA-1717 (ATCC), NCTC 8178 (NCTC), Staphylococcus epidermidis DSM3269 (DSMZ), S. epidermidis RP62A (ATCC), Staphylococcus lugdunensis DSM4804 (DSMZ), Staphylococcus haemolyticus DSM20263 (DSMZ) and Staphylococcus haemolyticus DSM20265 (DSMZ).

    Techniques: Purification, Incubation, Concentration Assay, SDS Page, Western Blot, Control