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14 protocols using lincomycin

1

Antimicrobial Resistance Profiling of MRSA

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The pattern of antimicrobial resistance was studied using the simple disk diffusion technique. The Mueller–Hinton agar (Merck, Germany) medium was used for this purpose. Antibiotic resistance of the MRSA strains against 18 commonly used antibiotics was determined using the instructions provided by the Clinical and Laboratory Standards Institute guidelines (18 ). Susceptibility of MRSA isolates was tested against ampicillin (10 µg/disk), gentamycin (10 µg/disk), lincomycin (2 µg/disk), cephalothin (30 µg/disk), imipenem (30 µg/disk), tetracycline (30 µg/disk), vancomycin (5 µg/disk), ciprofloxacin (5 µg/disk), norfloxacin (30 µg/disk), cotrimoxazole (30 µg/disk), clindamycin (2 µg/disk), trimethoprim-sulfamethoxazole (25 μg/disk), penicillin (10 µg/disk), oxacillin (1 µg/disk), erythromycin (15 µg/disk), azithromycin (15 µg/disk), ceftriaxone (30 µg/disk) and cefixime (5 µg/disk) antibiotic agents (Oxoid, UK). The plates containing the discs were allowed to stand for at least 30 minutes before incubation at 35°C for 24 hours. The diameter of the zone of inhibition produced by each antibiotic disc was measured and interpreted using the CLSI zone diameter interpretative standards (18 ). Staphylococcus aureus ATCC 25923 and Escherichia coli (E. coli) ATCC 25922 were used as quality control organisms in antimicrobial susceptibility determination.
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2

Antimicrobial Susceptibility of Enterococcus faecalis

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The antimicrobial susceptibility of the 76 E. faecalis isolates was tested by broth microdilution using 13 antimicrobials. Susceptibility to vancomycin (0.25–128 mg l−1), linezolid (0.25–128 mg l−1), penicillin (0.25–128 mg l−1), ampicillin (0.125–64 mg l−1), gentamicin (2–1024 mg l−1), streptomycin (4–2,048 mg l−1), kanamycin (4–2,048 mg l−1), tetracycline (0.25–128 mg l−1), tigecycline (0.03–2 mg l−1), erythromycin (0.125–64 mg l−1), lincomycin (0.5-256 mg l−1), ciprofloxacin (0.125-64 mg l−1), and chloramphenicol (0.25–128 mg l−1) (Oxoid, UK) was determined. E. faecalis ATCC 29212 was used as a quality control strain.
Susceptibility tests were performed according to recommendations by the Clinical and Laboratory Standards Institute (CLSI, 2015a ). MICs (minimal inhibitory concentrations) were evaluated based on the interpretative criteria of CLSI (CLSI, 2015c ) supplement VET01S for vancomycin, penicillin, ampicillin, erythromycin, tetracycline, doxycycline, and chloramphenicol for Enterococcus spp.; CLSI (CLSI, 2015b ) document M100-S25 for ciprofloxacin for Enterococcus spp.; and Comité de l´antibiogramme de la Société Française de Microbiologie (CA-SFM) (CA-SFM, 2015 ) for lincomycin and all aminoglycosides for Streptococcus spp.
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3

Antibiotic Susceptibility Testing Protocol

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The following 8 antibiotic agents of 5 different groups; macrolides, fluoroquinolones, tetracyclines, lincosamide, and pleuromutilins were used for the susceptibility tests: tylvalosin (Pharmgate Animal Health Canada, Inc), tilmicosin (ELANCO, Geneva), tylosin (ELANCO, USA), enrofloxacin (INVESA, Spain), doxycycline (Oxoid, UK), chlortetracycline (Oxoid, UK), lincomycin (Oxoid, UK), and tiamulin (Sandoz GmbH, Basel, Switzerland).
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4

In Vitro Antibiotic Sensitivity of Clostridium perfringens

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Thirty-two C. perfringens isolates were examined in vitro against eight antibiotics, which included streptomycin (10 μg), amoxicillin (10 μg), ampicillin (10 μg), ciprofloxacin (5 μg), lincomycin (30 μg), cefotaxime (30 μg), rifampicin (5 μg), and trimethoprim-sulfamethoxazole (1.25 + 23.75 μg) (Oxoid, UK). The test was carried out using the agar disc diffusion test, (17, 26). The isolates were cultured anaerobically at 37° for 24 h in 10% neomycin sheep blood agar, then suspended in 0.9% NaCl to a 0.5 McFarland standard. Every isolate was inoculated onto Mueller-Hinton agar plates (Remel, USA) and the antibiotic discs were applied. The plates were incubated anaerobically at 37° for 24 h. The interpretation of the results was performed according to CLSI, 2012 (8 ).
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5

Antibiotic Susceptibility of S. aureus

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All S. aureus detected at culture and identification step of samples were subjected to antimicrobial susceptibility test using the disk diffusion method (Price et al., 2012 ). Eleven antibiotics of veterinary and/or human interest were examined: penicillin G, cefoxitin, kanamycin, gentamicin, tetracycline, erythromycin, spiramycin, lincomycin, chloramphenicol, enrofloxacin and vancomycin (Oxoid, United Kingdom). The result was interpretated according to CLSI (CLSI 2015 ).
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6

Antibiotic Susceptibility Testing on Muller-Hinton Agar

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Antibiotic susceptibility was determined using the disk-diffusion method on Muller–Hinton agar at 30 °C for 24 h based on the guidelines of the Clinical and Laboratory Standards Institute [30 ]. Eight types of antibiotic disks containing chloramphenicol (30 μg), clindamycin (10 μg), erythromycin (15 μg), gentamicin (30 μg), lincomycin (15 μg), streptomycin (300 μg), tetracycline (30 μg), and vancomycin (30 μg) were purchased from Oxoid (Basingstoke, Hants, UK).
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7

Antimicrobial Susceptibility of Streptococcus agalactiae

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Antimicrobial susceptibility test was conducted to further understand the exposure of the strain toward antibiotics by standard antibiotics disc and disc diffusion technique [20 (link)]. A suspension (100 µl) of fresh cultured of S. agalactiae <24 h on TSB, diluted to a turbidity equivalent to a MacFarland No. 0.5 standard solution, was spread onto triplicate Mueller–Hinton agar (Oxoid, England) plates, and tested against 18 chemotherapeutic agent discs namely nitrofurantoin (F - 50 µg), flumequine (UB - 30 µg), florfenicol (FFC - 30 µg), amoxylin (AML - 25 µg), doxycycline (DO - 30 µg), oleandomycin (OL - 15 µg), tetracycline (TE - 30 µg), ampicillin (AMP - 10 µg), lincomycin (MY - 15 µg), colistin sulfate (CT - 25 µg), oxolinic acid (OA - 2 µg), novobiocin (NV - 30 µg), spiramycin (SP - 100 µg), erythromycin (E - 15 µg), fosfomycin (FOS - 50 µg), neomycin (N - 10 µg), gentamicin (GM - 10 µg), and polymyxin B (PB - 30 µg) (Oxoid, England). The susceptibility test agars were incubated at 37°C for 24 h and the diameter of inhibition zones around the discs was measured and compared to the standard table for antimicrobial susceptibility provided by CLSI [21 ].
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8

Antimicrobial Susceptibility of Campylobacter Isolates

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All the recovered CP isolates were in vitro tested for their antimicrobial susceptibility using the agar disc diffusion according to the standards of the Clinical and Laboratory Standards Institute method (CLSI, 2017 ). Eleven commercial antibiotic disks: Tetracycline (TET; 10 μg), lincomycin (L; 15 μg), norfloxacin (NOR; 10 μg), erythromycin (E; 30 μg), ampicillin (AM; 10 μg), penicillin (P; 10 μg), chloramphenicol (C; 30 μg), amoxicillin clavulanic acid (AMX; 25μg), gentamycin (CEN; 10 μg), cefotaxime (CTX; 30 μg), and ciprofloxacin (CIP; 5 μg); Oxoid, Cambridge, UK; were evaluated and then the results were interpreted according to Gomaa et al. (2023 (link)).
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9

Identification and Antibiotic Resistance of S. aureus in Milk

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Milk samples were cultured on mannitol salt agar (MSA) plates, with 50 μl of each sample spread on the plate, and incubated for 24 hours at 37°C. Staphylococci were identified according to standard microbiological procedures, with isolates that were mannitol fermenters, Gram-positive cocci (grape-like clusters), producing catalase, DNase and positive to tube coagulase tests (producing coagulase) with human plasma, considered S. aureus [13 ]. Further confirmation of S. aureus was done by polymerase chain reaction (PCR) detecting the nuc gene.
Antibiotic susceptibility was assessed using standard Clinical and Laboratory Standards Institute guidelines for antimicrobial disk diffusion using the following sixteen antibiotics: ampicillin (AM), amoxicillin (AX), lincomycin (L2), ceftazidime (CAZ), azithromycin (AZM), ceftriaxone (CRO), norfloxacin (NOR), cefoxitin (FOX), gentamicin (CN), erythromycin (E), tetracycline (TE), doxycycline (DO), clindamycin (DA), trimethoprim/sulfamethoxazole (SXT), rifampin (RA), and linezolid (LZN) (Oxoid, UK).
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10

Inducibility of MLS-B Antibiotic Resistance

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The inducibility of resistance to MLS-B antibiotics was performed with the use of disc diffusion (DD) D-shape zone method with erythromycin (E, 15 μg), clindamycin (DA, 2 μg), and lincomycin (MY, 15 μg) (Oxoid), according to the EUCAST guidelines [28 ,51 ].
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