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Apollo Scientific Ltd daptomycin lipopeptide
Daptomycin Lipopeptide, supplied by Apollo Scientific Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Antimicrobial resistance pattern of the 95 GAS isolates by the Sensititre® STP6F system.
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Apollo Scientific Ltd daptomycin lipopeptide
Antimicrobial resistance pattern of the 95 GAS isolates by the Sensititre® STP6F system.
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Antibacterial efficacy by SCF in the absence or presence of valine. ( A ) Percent survival of MRSA2 in the presence of the indicated antibiotics with or without 5 mM valine. SCF, cefoperazone sodium and <t>sulbactam</t> sodium; ASPC, amoxicillin sodium clavulanate potassium. Antibiotic doses are as follows: 200 µg/mL for SCF; 300 µg/mL for ceftriaxone, cefradine, ceftazidime, cefazolin; 150 µg/mL for vancomycin; and 400 µg/mL for the others. ( B ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of SCF plus 5 mM valine. ( C ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of valine plus 200 µg/mL SCF. ( D ) Percent survival of MRSA2 in the absence or presence of the indicated incubation time with 5 mM valine and 200 µg/mL SCF. ( E ) Percent survival of 18 MRSA isolates (2.5 × 10 7 CFU/mL) in the absence or presence of 5 mM valine, 200 µg/mL SCF, and both. ( F ) Bacterial load of liver, kidney, and spleen of mice infected with MRSA2. Mice were intraperitoneally infected with 2.5 × 10 6 CFU of MRSA2 and divided into four groups, four male Balb/c mice per group. The four groups were separately intravenously injected with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both in an hour later. Spleen, kidney, and liver of these treated mice were collected at 24 h and homogenized for spot plate counting. ( G ) Percent survival of mice in the absence or presence of the indicated dose of SCF or/and the indicated dose of valine. Mice were intraperitoneally infected with 2.5 × 10 7 CFU of MRSA2 and divided into eight (sub)groups to be treated as the indicated post 1 h of infection, 10 mice per group. Survival of mice was monitored for 7 days. ( H ) Bacterial load of mouse thigh infected with MRSA2. Mice were intramuscularly infected with 2.8 × 10 5 CFU of MRSA2 and divided into four groups. The four groups were separately treated with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both post 2 h infection. The thigh muscle infected was collected at 26 h and homogenized for spot plate counting. ( I ) Percent survival of MRSA2 in the absence or presence of 5 mM leucine or isoleucine plus 200 µg/mL SCF. Data are mean ± SD from three biological replicates. *, P < 0.05; **, P < 0.01.
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Antibacterial efficacy by SCF in the absence or presence of valine. ( A ) Percent survival of MRSA2 in the presence of the indicated antibiotics with or without 5 mM valine. SCF, cefoperazone sodium and <t>sulbactam</t> sodium; ASPC, amoxicillin sodium clavulanate potassium. Antibiotic doses are as follows: 200 µg/mL for SCF; 300 µg/mL for ceftriaxone, cefradine, ceftazidime, cefazolin; 150 µg/mL for vancomycin; and 400 µg/mL for the others. ( B ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of SCF plus 5 mM valine. ( C ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of valine plus 200 µg/mL SCF. ( D ) Percent survival of MRSA2 in the absence or presence of the indicated incubation time with 5 mM valine and 200 µg/mL SCF. ( E ) Percent survival of 18 MRSA isolates (2.5 × 10 7 CFU/mL) in the absence or presence of 5 mM valine, 200 µg/mL SCF, and both. ( F ) Bacterial load of liver, kidney, and spleen of mice infected with MRSA2. Mice were intraperitoneally infected with 2.5 × 10 6 CFU of MRSA2 and divided into four groups, four male Balb/c mice per group. The four groups were separately intravenously injected with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both in an hour later. Spleen, kidney, and liver of these treated mice were collected at 24 h and homogenized for spot plate counting. ( G ) Percent survival of mice in the absence or presence of the indicated dose of SCF or/and the indicated dose of valine. Mice were intraperitoneally infected with 2.5 × 10 7 CFU of MRSA2 and divided into eight (sub)groups to be treated as the indicated post 1 h of infection, 10 mice per group. Survival of mice was monitored for 7 days. ( H ) Bacterial load of mouse thigh infected with MRSA2. Mice were intramuscularly infected with 2.8 × 10 5 CFU of MRSA2 and divided into four groups. The four groups were separately treated with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both post 2 h infection. The thigh muscle infected was collected at 26 h and homogenized for spot plate counting. ( I ) Percent survival of MRSA2 in the absence or presence of 5 mM leucine or isoleucine plus 200 µg/mL SCF. Data are mean ± SD from three biological replicates. *, P < 0.05; **, P < 0.01.
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Antimicrobial resistance pattern of the 95 GAS isolates by the Sensititre® STP6F system.

Journal: Heliyon

Article Title: A survey of antibiotic resistance patterns among Group A Streptococcus isolated from invasive and non-invasive infections in Cape Town, South Africa

doi: 10.1016/j.heliyon.2024.e33694

Figure Lengend Snippet: Antimicrobial resistance pattern of the 95 GAS isolates by the Sensititre® STP6F system.

Article Snippet: The antibiogram of 20 antibiotics belonging to 10 different classes including β-lactams (penicillin, amoxicillin/clavulanic acid, cefuroxime, cefotaxime, ceftriaxone, cefepime, meropenem, ertapenem), macrolides (erythromycin, azithromycin), oxazolidinones (linezolid), lincosamides (clindamycin), fluoroquinolones (levofloxacin, moxifloxacin), phenicols (chloramphenicol), lipopeptide (daptomycin), glycopeptide (vancomycin), cyclines (tetracycline, tigecycline), sulfonamides (sulfamethoxazole/trimethoprim) was performed using the Sensititre® STP6F system (ThermoFisher Scientific) following the guidelines of the manufacturer.

Techniques:

Antibacterial efficacy by SCF in the absence or presence of valine. ( A ) Percent survival of MRSA2 in the presence of the indicated antibiotics with or without 5 mM valine. SCF, cefoperazone sodium and sulbactam sodium; ASPC, amoxicillin sodium clavulanate potassium. Antibiotic doses are as follows: 200 µg/mL for SCF; 300 µg/mL for ceftriaxone, cefradine, ceftazidime, cefazolin; 150 µg/mL for vancomycin; and 400 µg/mL for the others. ( B ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of SCF plus 5 mM valine. ( C ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of valine plus 200 µg/mL SCF. ( D ) Percent survival of MRSA2 in the absence or presence of the indicated incubation time with 5 mM valine and 200 µg/mL SCF. ( E ) Percent survival of 18 MRSA isolates (2.5 × 10 7 CFU/mL) in the absence or presence of 5 mM valine, 200 µg/mL SCF, and both. ( F ) Bacterial load of liver, kidney, and spleen of mice infected with MRSA2. Mice were intraperitoneally infected with 2.5 × 10 6 CFU of MRSA2 and divided into four groups, four male Balb/c mice per group. The four groups were separately intravenously injected with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both in an hour later. Spleen, kidney, and liver of these treated mice were collected at 24 h and homogenized for spot plate counting. ( G ) Percent survival of mice in the absence or presence of the indicated dose of SCF or/and the indicated dose of valine. Mice were intraperitoneally infected with 2.5 × 10 7 CFU of MRSA2 and divided into eight (sub)groups to be treated as the indicated post 1 h of infection, 10 mice per group. Survival of mice was monitored for 7 days. ( H ) Bacterial load of mouse thigh infected with MRSA2. Mice were intramuscularly infected with 2.8 × 10 5 CFU of MRSA2 and divided into four groups. The four groups were separately treated with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both post 2 h infection. The thigh muscle infected was collected at 26 h and homogenized for spot plate counting. ( I ) Percent survival of MRSA2 in the absence or presence of 5 mM leucine or isoleucine plus 200 µg/mL SCF. Data are mean ± SD from three biological replicates. *, P < 0.05; **, P < 0.01.

Journal: mSystems

Article Title: Valine potentiates cefoperazone-sulbactam to kill methicillin-resistant Staphylococcus aureus

doi: 10.1128/msystems.01244-24

Figure Lengend Snippet: Antibacterial efficacy by SCF in the absence or presence of valine. ( A ) Percent survival of MRSA2 in the presence of the indicated antibiotics with or without 5 mM valine. SCF, cefoperazone sodium and sulbactam sodium; ASPC, amoxicillin sodium clavulanate potassium. Antibiotic doses are as follows: 200 µg/mL for SCF; 300 µg/mL for ceftriaxone, cefradine, ceftazidime, cefazolin; 150 µg/mL for vancomycin; and 400 µg/mL for the others. ( B ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of SCF plus 5 mM valine. ( C ) Percent survival of MRSA2 in the absence or presence of the indicated concentrations of valine plus 200 µg/mL SCF. ( D ) Percent survival of MRSA2 in the absence or presence of the indicated incubation time with 5 mM valine and 200 µg/mL SCF. ( E ) Percent survival of 18 MRSA isolates (2.5 × 10 7 CFU/mL) in the absence or presence of 5 mM valine, 200 µg/mL SCF, and both. ( F ) Bacterial load of liver, kidney, and spleen of mice infected with MRSA2. Mice were intraperitoneally infected with 2.5 × 10 6 CFU of MRSA2 and divided into four groups, four male Balb/c mice per group. The four groups were separately intravenously injected with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both in an hour later. Spleen, kidney, and liver of these treated mice were collected at 24 h and homogenized for spot plate counting. ( G ) Percent survival of mice in the absence or presence of the indicated dose of SCF or/and the indicated dose of valine. Mice were intraperitoneally infected with 2.5 × 10 7 CFU of MRSA2 and divided into eight (sub)groups to be treated as the indicated post 1 h of infection, 10 mice per group. Survival of mice was monitored for 7 days. ( H ) Bacterial load of mouse thigh infected with MRSA2. Mice were intramuscularly infected with 2.8 × 10 5 CFU of MRSA2 and divided into four groups. The four groups were separately treated with saline solution, 200 mg/kg SCF, 200 mg/kg valine, or both post 2 h infection. The thigh muscle infected was collected at 26 h and homogenized for spot plate counting. ( I ) Percent survival of MRSA2 in the absence or presence of 5 mM leucine or isoleucine plus 200 µg/mL SCF. Data are mean ± SD from three biological replicates. *, P < 0.05; **, P < 0.01.

Article Snippet: All antibiotics tested, including vancomycin (glycopeptides), cefoperazone sodium and sulbactam sodium (cephalosporins), daptomycin (cyclic lipopeptides), oxacillin (penicillins) were purchased from Sangon Biotech (BBI) Limited (Shanghai, China).

Techniques: Incubation, Infection, Injection, Saline

List of AMP in clinical trials and Food and Drug Administration (FDA) approved AMP for various human infections and diseases [ <xref ref-type= 5 , 6 , 42 ]." width="100%" height="100%">

Journal: Molecules

Article Title: S100 Proteins as Novel Therapeutic Targets in Psoriasis and Other Autoimmune Diseases

doi: 10.3390/molecules27196640

Figure Lengend Snippet: List of AMP in clinical trials and Food and Drug Administration (FDA) approved AMP for various human infections and diseases [ 5 , 6 , 42 ].

Article Snippet: Daptomycin (lipopeptide) , Streptomyces roseosporus , Complicated skin infections caused by susceptible strains of Gram-positive microorganisms , Intravenous injection , 2003 , Cubist Pharmaceuticals LLC (Merck & Co.).

Techniques: Clinical Proteomics, Formulation, Glycoproteomics, Virus, Injection, Ointment, Derivative Assay, Infection, Cream