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s spartinae atcc 18866  (ATCC)


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    ATCC s spartinae atcc 18866
    S Spartinae Atcc 18866, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/18866/Scheffersomyces+spartinae+(Ahearn+et+al)+Kurtzman+et+Suzuki/10__1128_slash_mra__00652___21-28-21-23
    Average 92 stars, based on 4 article reviews
    s spartinae atcc 18866 - by Bioz Stars, 2026-09
    92/100 stars

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    MAC-dependent increase in sensitivity and susceptibility of multidrug-resistant Gc to frontline antibiotics. (A–C) H041 Gc was pre-incubated with anti-Gc IgM followed by incubation with 2% (A, C) or indicated concentration (B) of IgG/M-depleted human serum, with or without heat inactivation (HI). Gc was then incubated with the indicated antibiotic, and CFUs were enumerated. Where indicated, serum was first incubated with the C5 inhibitor OMCI (20 µg/mL) or vehicle. Error bars are standard error of the mean. Significance was determined by one-way ANOVA with Tukey’s multiple comparisons on log 10 -transformed data. ** P < 0.01 and **** P < 0.0001. Dotted line represents minimum reportable CFUs. (D, E) FA19 Gc (D) or H041 Gc (E) were assayed via 16 h minimum inhibitory concentration (MIC) broth microdilution assays over a range of azithromycin or ceftriaxone concentrations in GCBL alone, or supplemented with 2.5% IgG/M-depleted human serum.

    Journal: mBio

    Article Title: Terminal complement complexes with or without C9 potentiate antimicrobial activity against Neisseria gonorrhoeae

    doi: 10.1128/mbio.00141-25

    Figure Lengend Snippet: MAC-dependent increase in sensitivity and susceptibility of multidrug-resistant Gc to frontline antibiotics. (A–C) H041 Gc was pre-incubated with anti-Gc IgM followed by incubation with 2% (A, C) or indicated concentration (B) of IgG/M-depleted human serum, with or without heat inactivation (HI). Gc was then incubated with the indicated antibiotic, and CFUs were enumerated. Where indicated, serum was first incubated with the C5 inhibitor OMCI (20 µg/mL) or vehicle. Error bars are standard error of the mean. Significance was determined by one-way ANOVA with Tukey’s multiple comparisons on log 10 -transformed data. ** P < 0.01 and **** P < 0.0001. Dotted line represents minimum reportable CFUs. (D, E) FA19 Gc (D) or H041 Gc (E) were assayed via 16 h minimum inhibitory concentration (MIC) broth microdilution assays over a range of azithromycin or ceftriaxone concentrations in GCBL alone, or supplemented with 2.5% IgG/M-depleted human serum.

    Article Snippet: Ceftriaxone , Cayman , 18866 , , , , .

    Techniques: Incubation, Concentration Assay, Transformation Assay

    Minimum inhibitory concentrations of antimicrobials against E. faecalis 3143 and P. mirabilis HI4320 cultured in TSB-glucose.

    Journal: Pathogens

    Article Title: Enterococcus faecalis Polymicrobial Interactions Facilitate Biofilm Formation, Antibiotic Recalcitrance, and Persistent Colonization of the Catheterized Urinary Tract

    doi: 10.3390/pathogens9100835

    Figure Lengend Snippet: Minimum inhibitory concentrations of antimicrobials against E. faecalis 3143 and P. mirabilis HI4320 cultured in TSB-glucose.

    Article Snippet: Antimicrobials were diluted as per manufacturer specifications and stored at -20 °C until needed, and included trimethoprim (Cayman Chemical 16473), ceftriaxone sodium salt (Cayman Chemical 18866), nitrofurantoin (TCI Chemicals N0883), ampicillin sodium salt (Research Products International A40040), and daptomycin (Cayman Chemical 15651).

    Techniques: Cell Culture

    E. faecalis and P. mirabilis polymicrobial biofilms provide additional antimicrobial resistance to both species. Static biofilms were established on 24 well plates in TSB-G for 20 h, then treated with the following antimicrobials for 24 h: ampicillin-clavulanate ( A ), ceftriaxone ( B ), or trimethoprim ( C ). Data represent the mean log 10 CFU/mL ± SD of P. mirabilis HI4320 (black) or E. faecalis 3143 (white) for single-species biofilms (solid bars) or co-culture biofilms (diagonal lines) from three independent experiments. *** P < 0.001 by Student’s t test.

    Journal: Pathogens

    Article Title: Enterococcus faecalis Polymicrobial Interactions Facilitate Biofilm Formation, Antibiotic Recalcitrance, and Persistent Colonization of the Catheterized Urinary Tract

    doi: 10.3390/pathogens9100835

    Figure Lengend Snippet: E. faecalis and P. mirabilis polymicrobial biofilms provide additional antimicrobial resistance to both species. Static biofilms were established on 24 well plates in TSB-G for 20 h, then treated with the following antimicrobials for 24 h: ampicillin-clavulanate ( A ), ceftriaxone ( B ), or trimethoprim ( C ). Data represent the mean log 10 CFU/mL ± SD of P. mirabilis HI4320 (black) or E. faecalis 3143 (white) for single-species biofilms (solid bars) or co-culture biofilms (diagonal lines) from three independent experiments. *** P < 0.001 by Student’s t test.

    Article Snippet: Antimicrobials were diluted as per manufacturer specifications and stored at -20 °C until needed, and included trimethoprim (Cayman Chemical 16473), ceftriaxone sodium salt (Cayman Chemical 18866), nitrofurantoin (TCI Chemicals N0883), ampicillin sodium salt (Research Products International A40040), and daptomycin (Cayman Chemical 15651).

    Techniques: Co-Culture Assay