Heteroresistance associated with the production of fosfomycin-resistant inner colonies during disk diffusion testing among a geographically diverse collection of Klebsiella pneumoniae clinical isolates.

IF 3.7 Q2 INFECTIOUS DISEASES
JAC-Antimicrobial Resistance Pub Date : 2025-02-20 eCollection Date: 2025-02-01 DOI:10.1093/jacamr/dlaf013
Morgan L Bixby, Lindsey B Collins, Ellora C Daley, Jenna M Salay, Sofia Oliver, Alexandra L Bryson, Elizabeth B Hirsch
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Abstract

Background: Fosfomycin susceptibility breakpoints apply only to Escherichia coli despite clinical use against Klebsiella pneumoniae. EUCAST and CLSI have different breakpoints and guidelines for disk diffusion (DD) interpretation that are frequently extrapolated to K. pneumoniae. Guidelines differ in interpreting inner colonies (IC) that grow within the zone of inhibition, but specificity to E. coli leaves knowledge gaps when extrapolating to other uropathogens.

Objectives: To examine the frequency and MIC of K. pneumoniae IC during fosfomycin DD testing and to determine potential relationships between IC production, heteroresistance and fosA presence.

Methods: A collection of K. pneumoniae clinical isolates (n = 262) and their IC (n = 116) underwent broth microdilution testing. Heteroresistance screening and PCR for fosA was performed on susceptible isolates that either never produced (NP) IC (n = 14) or produced ≥5 resistant IC (n = 43).

Results: The MIC range (≤2 to >256 mg/L) of clinical isolates increased to 32 to >1024 mg/L for the IC collection with a median MIC increase of three, 2-fold dilutions. IC producers had 1.71 greater odds (P < 0.01) of a positive heteroresistance screen compared to NP isolates. No relationship was found between fosA presence and either IC production or heteroresistance.

Conclusions: Production of ≥5 IC among clinical K. pneumoniae isolates was frequent and often resulted in an increased IC isolate MIC. Significantly greater odds of heteroresistance among IC producers were found when compared to NP isolates. Thus, presence of IC during fosfomycin DD testing should prompt avoidance of fosfomycin treatment.

在不同地理位置收集的肺炎克雷伯菌临床分离株的磁盘扩散试验期间,异耐药与磷霉素耐药内菌落的产生相关。
背景:磷霉素敏感性断点仅适用于大肠杆菌,尽管临床用于肺炎克雷伯菌。EUCAST和CLSI有不同的断点和磁盘扩散(DD)解释指南,经常推断为肺炎克雷布菌。指南在解释生长在抑制区内的内菌落(IC)方面有所不同,但在推断其他泌尿系统病原体时,对大肠杆菌的特异性留下了知识空白。目的:在磷霉素DD检测中检测肺炎克雷伯菌IC的频率和MIC,并确定IC产生、异源耐药和fosA存在之间的潜在关系。方法:收集临床分离的肺炎克雷伯菌262株及其IC 116株进行肉汤微量稀释试验。对从未产生(NP) IC (n = 14)或产生≥5个耐药IC (n = 43)的敏感分离株进行fosA异耐药筛选和PCR。结果:临床分离株的MIC范围(≤2 ~ >256 mg/L)增加到32 ~ >1024 mg/L,中位MIC增加了3,2倍稀释。IC生产者的P - sa存在和IC生产或异源抗性的几率比P - sa高1.71。结论:临床肺炎克雷伯菌分离株中IC≥5的产生是常见的,并且经常导致IC分离株MIC升高。与NP分离株相比,IC生产者之间的异源抗性明显更大。因此,在磷霉素DD试验中出现IC应提示避免磷霉素治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
0.00%
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审稿时长
16 weeks
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