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. Author manuscript; available in PMC: 2022 Sep 1.
Published in final edited form as: J Glob Antimicrob Resist. 2021 May 25;26:84–90. doi: 10.1016/j.jgar.2021.04.029

Table 1.

Minimum inhibitory concentrations (MICs) and interpretations for Campylobacter jejuni isolates from Patient #1, Patient #2 and the puppy belonging to Patient #1

Antibiotic class Antibiotic MIC (Mμ/mL)
Patient #1
Patient #2 Puppy Intermediate range (μg/mL) Resistant range (μg/mL)

Aminoglycosides Gentamicina >32 >32 >32 N/A ≥4
Tobramycin b, c >4 >4 > 4 8 ≥16
β- Amoxicillin/clavulanic acid b 4/2 4/2 4/2 16/8 ≥32/16
Lactam Ampicillin/sulbactam b, c >8/4 >8/4 > 8/4 16/8 ≥32/16
combinations Piperacillin/tazobactamb 64/2 64/2 64/2 32/4–64/4 ≥ 128/4
Carbapenems Ertapenemb 0.25 <0.12 <0.12 1 ≥ 2
Imipenemb 0.12 0.12 0.12 2 ≥4
Meropenemb 0.06 0.06 0.06 2 ≥4
Cephems Cefuroximeb, c, d >4 >4 > 4 8–16 ≥32
Cefotaximeb 4 4 4 2 ≥4
Ceftazidimeb 16 8 8 8 ≥16
Ceftriaxoneb 16 16 16 2 ≥4
Cefepimeb 1 1 1 4–8 ≥16
Folate pathway antagonists Trimethoprim/sulfamethoxazoleb >4/76 >4/76 >4/76 N/A ≥4/76
Glycylcyclines Tigecycline ≤0.008 ≤0.008 ≤0.008 N/A N/A
Ketolides Telithromycin a >8 >8 > 8 N/A ≥8
Lincosamides Clindamycin a 4 8 8 N/A ≥1
Macrolides Azithromycin a >64 >64 > 64 N/A ≥0.5
Erythromycin a >64 >64 > 64 N/A ≥8
Tylosin >16 >16 > 16 N/A N/A
Monobactams Aztreonamb >16 >16 > 16 8 ≥16
Nitroimidazoles Metronidazole e >16 >16 > 16 16 ≥32
Phenicols Chloramphenicol a ≤2 ≤2 ≤2 N/A ≥32
Florfenicol a 1 1 1 N/A ≥8
Quinolones Ciprofloxacin a 16 16 16 N/A ≥1
Levofloxacinb >4 >4 > 4 1 ≥2
Moxifloxacin e 2 2 2 4 ≥8
Nalidixic acid a >64 >64 > 64 N/A ≥32
Tetracyclines Minocyclineb 2 2 4 8 ≥16
Tetracycline a >64 >64 > 64 N/A ≥2

N/A, not applicable; CLSI; Clinical and Laboratory Standards Institute.

NOTE: MICs at or above the intermediate or resistant MIC ranges are shown in boldface.

a

Resistant range for these agents was defined by MICs above the epidemiological cut-off values (ECOFFs) established by the European Committee on Antimicrobial Susceptibility Testing (EUCAST) [19]. EUCAST uses the terms ‘wild-type’ and ‘non-wild-type’ instead of susceptible and resistant; ECOFFs should not be used to predict clinical efficacy.

b

Intermediate and resistant ranges for these agents were defined based on CLSI breakpoints for Enterobacterales [21] and should not be used to predict clinical efficacy.

c

It is not possible to distinguish whether the isolate MICs fall into the intermediate or resistant range based on the dilutions tested.

d

Intermediate and resistant ranges differ based on the route of transmission; these values are for oral administration.

e

Intermediate and resistant ranges for these agents were defined based on CLSI breakpoints for anaerobes [21] from the CLSI M100Ed30 and should not be used to predict clinical efficacy.