In vitro interactions of combinations of colistin with meropenem, rifampicin and tigecycline in colistin-resistant, biofilm-forming Klebsiella pneumoniae

被引:0
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作者
Muderris, Tuba [1 ]
Manyasli, Guelden Dursun [2 ]
Kaya, Selcuk [1 ]
Yurtsever, Suereyya Gul [1 ]
机构
[1] Izmir Katip Celebi Univ, Fac Med, Dept Med Microbiol, Izmir, Turkiye
[2] Minist Hlth Cizre Dr Selahattin Cizrelioglu State, Dept Med Microbiol, Sirnak, Turkiye
关键词
Klebsiella pneumoniae; Antimicrobial synergy; Biofilm; Antibiofilm effects; Biofilm inhibitory concentration; ACINETOBACTER-BAUMANNII; PSEUDOMONAS-AERUGINOSA; SUSCEPTIBILITY; VIRULENCE; GENTAMICIN; THERAPY; SYNERGY;
D O I
10.1016/j.diagmicrobio.2024.116408
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In this study, it was aimed to reveal the in vitro interactions of combinations of colistin with meropenem, rifampicin and tigecycline in colistin-resistant, biofilm-forming Klebsiella pneumonia. A total of 30 isolates, 15 of which formed biofilms and 15 did not form biofilms, were randomly selected from K. pneumoniae isolates growing in blood samples. The synergy rates of colistin-meropenem, colistin-tigecycline, colistin-rifampicin combinations in planktonic/sessile bacteria are; It was determined as 83,3%/73,3%, 66,6%/33,3%, 100%/ 60% respectively. Biofilm inhibitory concentration (BIC) of colistin, meropenem, tigecycline, and rifampicin significantly increased after biofilm formation. The synergistic activity seen in the sessile form was independent of the planktonic form. Although a high synergistic effect was observed in the meropenem-colistin combination on sessile bacteria, colistin had very high BIC in all combinations. Large-scale studies are needed in which the number of isolates studied is large, bacterial resistance profiles are evaluated genomically, and various antimicrobial groups are included.
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