产碳青霉烯酶肺炎克雷伯菌的基因型和表型抗菌谱的比较。

Arcadia Del Rio, Mariangela Puci, Narcisa Muresu, Illari Sechi, Laura Saderi, Luigi Cugia, Giovanni Sotgiu, Andrea Piana
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引用次数: 0

摘要

背景和目的:及时给予适当的抗生素治疗对改善疗效至关重要,尤其是在多药耐药菌株的情况下。尽管表型抗微生物药敏试验(AST)是解决抗生素治疗问题的金标准,但获得负担得起的结果所需的长时间可能会对预后产生负面影响。相反,快速基因型AST为治疗和监测计划提供了必要的信息。为了评估在临床常规中采用快速AST的可能性,我们比较了不同肺炎克雷伯菌菌株的基因型和表型抗菌谱,其特征是碳青霉烯酶编码基因的不同表达。方法:采用Vitek II全自动系统对109株Cr-Kp菌株进行抗菌药物检测,同时采用Etest对新组合的β-内酰胺酶/β-内酶抑制剂(BL/BLI)进行抗菌药物的检测。计算每个菌株的抗微生物耐药性指数(ARI),根据观察到的耐药性/易感性为每个菌株分配1或0分,并将总数除以测试的抗生素数量。Kruskal-Wallis检验,然后是Dunn的事后检验(Bonferroni校正),用于比较抗性基因亚组之间的定量变量。结果:我们在KPC/OXA-48菌株中观察到较高的ARI评分,在单独的KPC和KPC/CTX-M组中观察到相似的情况,在不产生碳青霉烯酶的组中观察出显著较低的耐药性。在BL/BLI的AST中也观察到了同样的趋势。结论:这些初步结果表明基因型和表型AST之间存在密切联系,支持在严重感染病例中采用快速AST,确保节省时间并提供MDR菌株的监测和改进管理计划。
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Comparison of genotypic and phenotypic antimicrobial profile in carbapenemases producing Klebsiella pneumoniae.

Background and aim: Prompt administration of appropriate antibiotic therapy is crucial in improving outcomes, particularly in cases sustained by multi-drug resistant strains. Although phenotypic antimicrobial susceptibility testing (AST) represents the gold standard to address antibiotics treatment, the long time required to obtained affordable results could negatively affect the prognosis. In contrast, rapid genotypic AST provide essential information for treatment and surveillance program. In order to evaluate the potential adoption of rapid AST in clinical routine, we compared the genotypic and phenotypic antimicrobial profiles of different K.pneumoniae strains, characterized by different expression of carbapenemases-encoding genes.

Methods: A set of 109 strains of Cr-Kp were tested for the antimicrobial drugs by the automatized Vitek II system and, in parallel, to the new combination of β-lactams/β-lactamases inhibitors (BL/BLI) by Etest. An antimicrobial resistance index (ARI) was calculated for each strain, assigning each 1 or 0 points based on observed resistance/susceptibility, and dividing the total by the number of antibiotics tested. Kruskal-Wallis test, followed by Dunn's post hoc test (Bonferroni correction), were used to compare quantitative variables among resistance gene subgroups.

Results: We observed a higher ARI score in KPC/OXA-48 strains, similar profile in KPC alone and KPC/CTX-M groups and a significant lower resistance in no-carbapenemases-producing group. Same trend was observed in AST for BL/BLI.

Conclusions: These preliminary results showed a close link between genotypic and phenotypic AST, supporting the adoption of rapid AST in cases of severe infections, ensuring to saving time and providing, the surveillance of MDR strains and improving stewardship programs.

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