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. 2023 Mar 8;14:1125531. doi: 10.3389/fmicb.2023.1125531

Table 1.

The association of antimicrobial susceptibilities with CRISPR-Cas systems in clinical isolates of Klebsiella pneumoniae.

CRISPR-Cas system [Number of susceptible isolates (%)]
Type I-E* (n = 111) Type I-E (n = 54) Absent (n = 533) p-value
Amikacin 98 (88.3) 49 (90.7) 346 (64.9) <0.001 <0.001
Aztreonam 72 (64.9) 39 (72.2) 208 (39.0) <0.001 <0.001
Cefotaxime 65 (58.6) 35 (64.8) 171 (32.1) <0.001 <0.001
Cefoxitin 83 (74.8) 35 (64.8) 232 (43.5) <0.001 <0.001
Ceftazidime 74 (66.7) 38 (70.4) 214 (40.2) <0.001 <0.001
Ceftazidime-avibactam 110 (99.1) 53 (98.1) 508 (95.3) 0.067 0.499
Chloramphenicol 71 (64.0) 29 (53.7) 218 (40.9) <0.001 0.082
Ciprofloxacin 66 (59.5) 28 (51.9) 158 (29.6) <0.001 0.001
Colistin 109 (98.2) 54 (100.0) 506 (94.9) 0.205 0.161
Ertapenem 96 (86.5) 47 (87.0) 278 (52.2) <0.001 <0.001
Fosfomycin 80 (72.1) 34 (63.0) 248 (46.5) <0.001 0.021
Imipenem 100 (90.1) 48 (88.9) 296 (55.5) <0.001 <0.001
Meropenem 98 (88.3) 50 (92.6) 305 (57.2) <0.001 <0.001
Minocycline 35 (31.5) 16 (29.6) 152 (28.5) 0.525 0.863
Tigecycline 95 (85.6) 45 (83.3) 432 (81.1) 0.282 0.855
Trimethoprim-sulfamethoxazole 49 (44.1) 17 (31.5) 147 (27.6) 0.001 0.543

p-values are shown as CRISPR-negative isolates compared with type I-E* isolates and CRISPR-negative isolates compared with type I-E isolates. The bold p-values were statistically significant.