Joshua T Waites, Donna M Crabb, Amy E Ratliff, Ken B Waites, Li Xiao
{"title":"Antimicrobial susceptibility and genetic mechanisms of resistance of <i>Ureaplasma</i> isolates in North America between 2012 and 2023.","authors":"Joshua T Waites, Donna M Crabb, Amy E Ratliff, Ken B Waites, Li Xiao","doi":"10.1128/aac.01868-24","DOIUrl":null,"url":null,"abstract":"<p><p>We analyzed antimicrobial susceptibilities of 415 <i>Ureaplasma</i> isolates from various sample types derived from different regions of the United States and Canada from 2012 to 2023 and investigated the genetic mechanisms of antimicrobial resistance. Minimum inhibitory concentration (MIC) ranges for erythromycin, tetracycline, and levofloxacin were 0.063-256, 0.016-64, and 0.063-32 µg/mL, respectively. MIC<sub>50</sub> values for erythromycin, tetracycline, and levofloxacin were 2, 0.25, and 1 µg/mL, and MIC<sub>90</sub> values were 4, 1, and 2 µg/mL, respectively. According to Clinical and Laboratory Standards Institute breakpoints, there were 61 (14.7%) isolates resistant to one or more drugs, and resistance rates for erythromycin, tetracycline, and levofloxacin were 2.4% (10/415), 6.5% (27/413), and 6.7% (28/415), respectively. Four isolates (1.0%) were resistant to two drugs. Mutations in domain V of 23S rRNA, mainly A2058G (<i>Escherichia coli</i> numbering), and/or in the <i>rpl</i>D gene encoding ribosomal protein L4 were identified in most erythromycin-resistant isolates. <i>Tet</i>(M) was detected in all isolates with tetracycline MIC ≥4 µg/mL but absent in 64.7% (11/17) of isolates with MIC of 2 µg/mL. For fluoroquinolone-resistant isolates, C248T (S83L) and G259A (E87K) mutations in <i>parC</i> were identified in most cases (23/26). In summary, erythromycin, tetracycline, and levofloxacin are still effective <i>in vitro</i> against most <i>Ureaplasma</i> isolates in North America.</p>","PeriodicalId":8152,"journal":{"name":"Antimicrobial Agents and Chemotherapy","volume":" ","pages":"e0186824"},"PeriodicalIF":4.1000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antimicrobial Agents and Chemotherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1128/aac.01868-24","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/5 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
We analyzed antimicrobial susceptibilities of 415 Ureaplasma isolates from various sample types derived from different regions of the United States and Canada from 2012 to 2023 and investigated the genetic mechanisms of antimicrobial resistance. Minimum inhibitory concentration (MIC) ranges for erythromycin, tetracycline, and levofloxacin were 0.063-256, 0.016-64, and 0.063-32 µg/mL, respectively. MIC50 values for erythromycin, tetracycline, and levofloxacin were 2, 0.25, and 1 µg/mL, and MIC90 values were 4, 1, and 2 µg/mL, respectively. According to Clinical and Laboratory Standards Institute breakpoints, there were 61 (14.7%) isolates resistant to one or more drugs, and resistance rates for erythromycin, tetracycline, and levofloxacin were 2.4% (10/415), 6.5% (27/413), and 6.7% (28/415), respectively. Four isolates (1.0%) were resistant to two drugs. Mutations in domain V of 23S rRNA, mainly A2058G (Escherichia coli numbering), and/or in the rplD gene encoding ribosomal protein L4 were identified in most erythromycin-resistant isolates. Tet(M) was detected in all isolates with tetracycline MIC ≥4 µg/mL but absent in 64.7% (11/17) of isolates with MIC of 2 µg/mL. For fluoroquinolone-resistant isolates, C248T (S83L) and G259A (E87K) mutations in parC were identified in most cases (23/26). In summary, erythromycin, tetracycline, and levofloxacin are still effective in vitro against most Ureaplasma isolates in North America.
期刊介绍:
Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.