Ciprofloxacin-susceptible but levofloxacin-resistant Pseudomonas aeruginosa clinical strains with Vitek®2: which mechanism involved and consequences in case of fluoroquinolone treatment?

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES European Journal of Clinical Microbiology & Infectious Diseases Pub Date : 2025-03-01 Epub Date: 2024-12-20 DOI:10.1007/s10096-024-05006-3
Manon Robert, Louise Ruffier d'Epenoux, Axelle Paquin, David Boutoille, Aurélie Guillouzouic, Stéphane Corvec
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Abstract

Purpose: Pseudomonas aeruginosa clinical strains isolated harbored sometimes an atypical phenotype using the automated Vitek2®: ciprofloxacin-susceptibility but levofloxacin-resistance according to 2019 CA-SFM criteria. The aims of this study are to investigate the resistance mechanism(s) involved and to identify the consequences on fluoroquinolone treatment.

Methods: Strain resistance profile, patient's data were recovered and reviewed from the database. Minimum inhibitory concentrations of levofloxacin, ciprofloxacin, moxifloxacin and delafloxacin were determined by using a concentration gradient strip. gyrA, gyrB, parC, parE and mexR genes were PCR amplified and sequenced. A PFGE analysis was performed for strains, recovered in a short period of time from the same patient.

Results: 46 strains were studied. A couple of seldom mutations were detected in gyrA, gyrB, parC and parE genes. Phenotypically, most of the strains (91%) were resistant to ticarcillin/ clavulanic acid combination and aztreonam suggesting a MexAB-OprM efflux-pump overexpression. mexR sequencing demonstrated either a deletion, a mutation or a premature stop codon appearance leading to amino acid substitution for 75% of the strains. Interestingly, four patients presented successively a fully fluoroquinolone susceptible isolate, thereafter a ciprofloxacin-susceptible but levofloxacin-resistant isolate (discordant phenotype) and finally a fluoroquinolone-resistant isolate. Molecular typing of these strains highlighted a strong relatedness between those isolates.

Conclusion: The phenotype detected by the automate Vitek2® is linked to a likely efflux-pump overexpression mechanism and not fluoroquinolone-target mutation. Regarding this discordant phenotype, an alert should be provided to clinicians concerning the high risk of selecting a fluoroquinolone-resistant mutant.

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环丙沙星敏感但左氧氟沙星耐药的铜绿假单胞菌临床菌株Vitek®2:氟喹诺酮治疗的机制和后果?
目的:根据2019年CA-SFM标准,铜绿假单胞菌临床分离菌株有时具有非典型表型:环丙沙星敏感性,但左氧氟沙星耐药。本研究的目的是调查所涉及的耐药机制,并确定氟喹诺酮治疗的后果。方法:从数据库中检索菌株耐药谱和患者资料。采用浓度梯度条法测定左氧氟沙星、环丙沙星、莫西沙星和德拉沙星的最低抑菌浓度。对gyrA、gyrB、parC、parE和mexR基因进行PCR扩增和测序。对同一患者短时间内恢复的菌株进行PFGE分析。结果:研究了46株菌株。在gyrA、gyrB、parC和parE基因中检测到少量突变。表型上,大多数菌株(91%)对替卡西林/克拉维酸联合用药和氨曲南耐药,提示MexAB-OprM外排泵过表达。mexR测序显示,75%的菌株存在缺失、突变或过早终止密码子出现,导致氨基酸替代。有趣的是,4例患者先后出现了完全氟喹诺酮敏感的分离株,随后出现了环丙沙星敏感但左氧氟沙星耐药的分离株(表型不一致),最后出现了氟喹诺酮耐药分离株。这些菌株的分子分型突出了这些分离株之间的强烈亲缘关系。结论:自动化Vitek2®检测到的表型可能与外排泵过表达机制有关,而不是氟喹诺酮靶向突变。关于这种不一致的表型,应向临床医生提出警告,注意选择氟喹诺酮耐药突变体的高风险。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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