Fernández Javier, Karau Melissa J, Cunningham Scott A, Greenwood-Quaintance Kerryl E, Patel Robin
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA Department of Functional Biology, Section of Microbiology, University of Oviedo, Oviedo, Spain Service of Microbiology, Hospital Universitario Central de Asturias, Oviedo, Spain.
Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Antimicrob Agents Chemother. 2016 Jul 22;60(8):4793-8. doi: 10.1128/AAC.00671-16. Print 2016 Aug.
Ureaplasma urealyticum and Ureaplasma parvum are pathogens involved in urogenital tract and intrauterine infections and also in systemic diseases in newborns and immunosuppressed patients. There is limited information on the antimicrobial susceptibility and clonality of these species. In this study, we report the susceptibility of 250 contemporary isolates of Ureaplasma (202 U. parvum and 48 U. urealyticum isolates) recovered at Mayo Clinic, Rochester, MN. MICs of doxycycline, azithromycin, ciprofloxacin, tetracycline, erythromycin, and levofloxacin were determined by broth microdilution, with MICS of the last three interpreted according to CLSI guidelines. Levofloxacin resistance was found in 6.4% and 5.2% of U. parvum and U. urealyticum isolates, respectively, while 27.2% and 68.8% of isolates, respectively, showed ciprofloxacin MICs of ≥4 μg/ml. The resistance mechanism of levofloxacin-resistant isolates was due to mutations in parC, with the Ser83Leu substitution being most frequent, followed by Glu87Lys. No macrolide resistance was found among the 250 isolates studied; a single U. parvum isolate was tetracycline resistant. tet(M) was found in 10 U. parvum isolates, including the single tetracycline-resistant isolate, as well as in 9 isolates which had low tetracycline and doxycycline MICs. Multilocus sequence typing (MLST) performed on a selection of 46 isolates showed high diversity within the clinical Ureaplasma isolates studied, regardless of antimicrobial susceptibility. The present work extends previous knowledge regarding susceptibility to antimicrobial agents, resistance mechanisms, and clonality of Ureaplasma species in the United States.
解脲脲原体和微小脲原体是涉及泌尿生殖道和宫内感染以及新生儿和免疫抑制患者全身性疾病的病原体。关于这些菌种的抗菌药敏性和克隆性的信息有限。在本研究中,我们报告了在明尼苏达州罗切斯特市梅奥诊所分离出的250株当代脲原体菌株(202株微小脲原体和48株解脲脲原体菌株)的药敏情况。通过肉汤微量稀释法测定了多西环素、阿奇霉素、环丙沙星、四环素、红霉素和左氧氟沙星的最低抑菌浓度(MIC),根据临床和实验室标准协会(CLSI)指南解释后三种药物的MIC。分别在6.4%的微小脲原体菌株和5.2%的解脲脲原体菌株中发现了左氧氟沙星耐药,而分别有27.2%和68.8%的菌株显示环丙沙星MIC≥4μg/ml。左氧氟沙星耐药菌株的耐药机制是由于parC基因突变,其中Ser83Leu替换最为常见,其次是Glu87Lys。在所研究的250株菌株中未发现大环内酯类耐药;有1株微小脲原体菌株对四环素耐药。在10株微小脲原体菌株中发现了tet(M),包括这株对四环素耐药的单一菌株,以及9株四环素和多西环素MIC较低的菌株。对46株菌株进行的多位点序列分型(MLST)显示,在所研究的临床脲原体菌株中具有高度多样性,无论其抗菌药敏性如何。目前的工作扩展了关于美国脲原体菌种对抗菌药物的敏感性、耐药机制和克隆性的先前知识。