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5 protocols using vancomycin

1

Antimicrobial Susceptibility of Staphylococcus aureus

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In vitro antimicrobial susceptibility testing determined by Kirby-Bauer disk diffusion according to the CLSI guidelines [13 ]. The 10 antimicrobial disks tested included: cefoxitin (FOX, 30 μg), clindamycin (CD, 2 μg), ciprofloxacin (CIP, 5 μg), cotrimaxazole (TS, 25 μg), rifampicin (RP, 5 μg), teicoplanin (TEC, 30 μg), tetracycline (T, 10 μg), erythromycin (E, 15 μg), quinupristin/dalfopristin (SYN, 15 μg), and linezolid (LZD, 30 μg) [MAST Diagnostics, Merseyside UK]..Also, vancomycin susceptibility testing was performed by vancomycin agar screen method with brain heart infusion agar containing 6 μg/ml. Finally, the minimum inhibitory concentration (MIC) of vancomycin was determined with the broth microdilution method according to CLSI 2016 instructions [13 ]. The vancomycin powder was purchased from Sigma (USA) Company. S. aureus ATCC 29213 and ATCC 33591 were used as methicillin-sensitive and resistant control strains, respectively.
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2

Antimicrobial Resistance Profiling of Pneumococci

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Isolates primarily identified as pneumococci with M phenotype were subsequently tested for resistance against tetracycline (30 µg), oxacillin (1 µg), clindamycin (2 µg), cotrimoxazole (1.25/23.75 µg), vancomycin (30 µg), and chloramphenicol (30 µg) (Mast Diagnostics Ltd) by employing the disc diffusion agar method.
Minimum inhibitory concentrations (MICs) of erythromycin were determined by the Etest (Liofilchem, Via Scozia, Italy) method on Mueller-Hinton agar with 5% defibrinated sheep blood according to the manufacturer's instructions. All plates were incubated at 37℃ for 20 hr. The MICs for penicillin for all isolates with the M phenotype were also determined by the Etest method. MIC results were interpreted according to the guidelines of the Clinical and Laboratory Standard Institute [13 ].
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Antimicrobial Susceptibility Testing of S. pseudintermedius

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All S. pseudintermedius isolates were tested for their antimicrobial susceptibility by disk diffusion method according to the guidelines of the French Society for Microbiology (CA-SFM 2). Antibiotics tested were cefovecin 30 μg (which was used as the phenotypic marker of methicillin resistance), penicillin 6 μg, fusidic acid 10 μg, kanamycin 30 μg, gentamicin 15 μg, tobramycin 10 μg, erythromycin 15 μg, spiramycin 100 μg, lincomycin 15 μg, tetracycline 30 μg, chloramphenicol 30 μg, florfenicol 30 μg, enrofloxacin 5 μg, vancomycin 30 μg, and teicoplanin 30 μg (Mast Diagnostics, Amiens, France). Bacteria were classified as susceptible, intermediate or resistant according to the clinical breakpoints approved by the veterinary part of the CA-SFM. Staphylococcus aureus ATCC 25923 was used as the quality control strain.
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Antimicrobial Susceptibility Testing for S. aureus

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Antimicrobial susceptibility test was confirmed by the ANSES laboratory using the disk diffusion method and interpreted according to the guidelines of the Antibiogram Committee of the French Society for Microbiology3. S. aureus ATCC 25923 was used as quality control. In addition, 16 antibiotics of veterinary and/or human interest were tested: penicillin G, cefoxitin, cefovecine, kanamycin, gentamicin, tobramycin, tetracycline, erythromycin, spiramycin, lincomycin, chloramphenicol, florfenicol, fusidic acid, enrofloxacin, vancomycin, teicoplanin (Mast Diagnostics, Amiens, France).
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5

Antimicrobial Activity of Camel Lactoferrins

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Standard discs of 17 antibiotics were obtained from Mast Diagnostics (Merseyside, Liverpool, UK) to be used in this assay; amikacin (30 µg), ampicillin (10 µg), augmentin (30 µg), aztreonam (30 µg), cefoxitin (30 µg), cefepime (30 µg), ceftazidime (30 µg), cephalothin (30 µg), chloramphenicol (30 µg), ciprofloxacin (5 µg), cotrimoxazole (25 µg), fucidic acid (10 µg), gentamicin (10 µg), imipenem (10 µg), oxacillin (1 µg), piperacillin (100 µg), and vancomycin (30 µg).
Antimicrobial activity of four cLfs isolated from milk of four different breeds of Saudi camels (cLf1, cLf2, cLf3, and cLf4), bLf, hLf, and the standard antibiotics against S. typhimurium and S. sonnei was tested by agar disc-diffusion technique. Plates of Mueller-Hinton (MH) agar were overlaid with 2 × 106 CFU/ml of Salmonella typhimurium LT2 and Shigella sonnei. Wells of about 5 mm diameter were made on inoculated plates then different concentrations of lactoferrins (0.00, 0.125, 0.250, 0.50, 0.750, 1, 1.5, 2, 2.5, and 3 mg/ml) were added, and left to diffuse in agar at 4 °C for 2 h before plates finally incubated overnight at 37 °C. The diameters of clear inhibition zones were measured in millimeters. Antibacterial effects of different lactoferrins on growth of S. typhimurium and S. sonnei after 1, 3, 6, 12, and 24 h of incubation at 37 °C were monitored spectrophotometrically (measuring OD at 620 nm).
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