Cross-resistance to 14-, 15- and 16-membered ring macrolides in Salmonella and Campylobacter.

IF 3.9 2区 医学 Q1 INFECTIOUS DISEASES
Ruby Singh, Sampa Mukherjee, Lucas B Harrision, Patrick F McDermott, Beilei Ge, Jeffrey M Gilbert, Cong Li, Jean M Whichard, Gamola Z Fortenberry, Uday Dessai, Shaohua Zhao
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引用次数: 0

Abstract

Objectives: This study aimed to gain a better understanding of how resistance determinants in Salmonella and Campylobacter contribute to 14-, 15- and 16-membered ring macrolide resistance phenotypes.

Methods: A total of 126 azithromycin-resistant (AziR) and -susceptible (AziS) [Salmonella (n = 45) and Campylobacter (n = 81)] isolates were selected for antimicrobial susceptibility testing (AST) and WGS.

Results: Seven functional macrolide resistance determinants, including erm(42), mef(C), mph(A), mph(E), mph(G), msr(E) and one point mutation (acrB_R717L) were previously identified in AziR  Salmonella. These determinants resulted in an 8- and 16-fold 15-membered ring gamithromycin and azithromycin MIC50 increase, respectively, compared with AziS isolates, with a maximum MIC increase of up to 256. The same isolates also exhibited up to a 32-fold 14-membered ring erythromycin MIC50 increase. Salmonella with erm(42) or acrB_R717L showed up to 128-fold 16-membered ring macrolide tildipirosin MIC increase, compared with isolates that were susceptible or carrying other macrolide resistance genes. In Campylobacter, all AziR isolates had an MIC50 ranging from 32 to 4096 mg/L of the various membered ring macrolides, whereases all susceptible Campylobacter isolates had significantly lower MIC50 values, ranging from 0.25 to 4 mg/L. The MIC50 of the various ring macrolides for AziR  Campylobacter isolates was 16- to 4096-fold higher when compared with AziS  Campylobacter.

Conclusions: Our study has revealed that the function of macrolide resistance genes in Salmonella can be associated with specific macrolide ring structures, whereas the single 23S rRNA mutation in Campylobacter results in significantly elevated MICs of all macrolides. for the various ring macrolides.

沙门氏菌和弯曲杆菌对14、15和16元环大环内酯的交叉抗性。
目的:本研究旨在更好地了解沙门氏菌和弯曲杆菌的耐药决定因素如何促进14-,15-和16元环大环内酯耐药表型。方法:选取126株阿奇霉素耐药(AziR)和敏感(AziS)[沙门氏菌(n = 45)和弯曲杆菌(n = 81)]进行药敏试验(AST)和WGS。结果:先前在AziR沙门氏菌中鉴定出7个功能性大环内酯类耐药决定因素,包括erm(42)、mef(C)、mph(A)、mph(E)、mph(G)、msr(E)和一个点突变(acrB_R717L)。与AziS分离株相比,这些决定因素导致加霉素和阿奇霉素15元环MIC50分别增加8倍和16倍,最大MIC增加高达256倍。同样的分离株也表现出高达32倍的14元环红霉素MIC50增加。与易感或携带其他大环内酯类耐药基因的沙门氏菌相比,携带erm(42)或acrB_R717L的沙门氏菌对大环内酯类替地吡醇的MIC增加了128倍。在弯曲杆菌中,所有AziR分离株的MIC50值在32 ~ 4096 mg/L之间,而所有敏感弯曲杆菌分离株的MIC50值均显著降低,在0.25 ~ 4 mg/L之间。不同环型大环内酯类化合物在AziR弯曲杆菌中的MIC50值是AziS弯曲杆菌的16 ~ 4096倍。结论:我们的研究表明沙门氏菌中大环内酯类耐药基因的功能可能与特定的大环内酯环结构有关,而弯曲杆菌中单个23S rRNA突变导致所有大环内酯类药物的mic显著升高。对于各种环型大环内酯。
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
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
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