在法国,对用于副猪脲原体、尿解脲原体和人型支原体抗菌药物敏感性检测和确定抗菌药物耐药性流行率的商用定制微量稀释板进行评估。

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-07-16 Epub Date: 2024-06-04 DOI:10.1128/jcm.00226-24
Sabine Pereyre, Nadège Hénin, Amandine Dolzy, Jennifer Guiraud, Cécile Laurier-Nadalié, Marie Gardette, Cécile Bébéar
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引用次数: 0

摘要

使用微量稀释法对人类支原体进行抗菌药敏感性检测(AST)非常耗时。在这项研究中,我们比较了 MICRONAUT-S 菌落总数计数板(Biocentric-Bruker)与临床与实验室标准协会(CLSI)参考方法的性能。然后,我们调查了 2020 年和 2021 年法国四环素类、氟喹诺酮类和大环内酯类药物耐药性的流行情况和机制。我们使用 60 株菌株对两种方法进行了比较。在耐药性流行率研究中,22 个法国诊断实验室每年收集一个月的副猪脲菌、尿脲菌和人疟原虫阳性临床标本。使用 MICRONAUT-S 菌落总数计数板测定 MIC。使用 PCR 筛选 tet(M) 基因,使用 PCR 和 Sanger 测序筛选氟喹诺酮类药物耐药性相关突变。比较两种方法,使用 MICRONAUT-S 菌落总数计数板获得的 MIC 值与使用 CLSI 参考方法获得的 MIC 值一致率为 99.5%(679/680)。对于 90 株人乳头瘤病毒分离物,四环素、左氧氟沙星和莫西沙星耐药率分别为 11.1%、2.2% 和 2.2%,无克林霉素耐药。在 248 个 U. parvum 分离物中,对左氧氟沙星和莫西沙星的耐药率分别为 5.2% 和 0.8%;在 68 个 U. urealyticum 分离物中,对左氧氟沙星和莫西沙星的耐药率分别为 2.9% 和 1.5%。U. urealyticum(11.8%)对四环素的耐药性明显(P < 0.001)高于 U. parvum(1.2%)。未发现大环内酯类耐药性。总之,定制的 MICRONAUT-S 菌落总数计数板是一种可靠、方便的人类支原体检测工具。在法国,四环素和氟喹诺酮类药物的耐药性仍然有限。然而,从 2010 年到 2015 年,左氧氟沙星和莫西沙星耐药性在解脲支原体中的流行率显著上升,需要进行监测:使用 CLSI 参考肉汤微量稀释法对人类泌尿生殖道支原体进行抗菌药物敏感性检测非常耗时,而且需要费力地制备抗菌药物储备溶液。在这里,我们验证了可靠、方便的抗菌药敏感性检测板的使用方法,它可以同时测定八种相关抗生素的 MICs。然后,我们调查了 2020 年和 2021 年法国境内这些细菌对四环素类、氟喹诺酮类和大环内酯类药物的耐药性流行情况和机制。我们发现,从 2010 年到 2015 年,左氧氟沙星和莫西沙星耐药性在解脲脲原体中的流行率显著上升,需要持续监测。
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Evaluation of commercial, customized microdilution plates for Ureaplasma parvum, Ureaplasma urealyticum, and Mycoplasma hominis antimicrobial susceptibility testing and determination of antimicrobial resistance prevalence in France.

Antimicrobial susceptibility testing (AST) of human mycoplasmas using microdilution is time-consuming. In this study, we compared the performance of MICRONAUT-S plates (Biocentric-Bruker) designed for AST of Ureaplasma parvum, Ureaplasma urealyticum, and Mycoplasma hominis with the results using the Clinical & Laboratory Standards Institute (CLSI) reference method. Then, we investigated the prevalence and mechanisms of resistance to tetracyclines, fluoroquinolones, and macrolides in France in 2020 and 2021. The two methods were compared using 60 strains. For the resistance prevalence study, U. parvum-, U. urealyticum-, and M. hominis-positive clinical specimens were collected for 1 month each year in 22 French diagnostic laboratories. MICs were determined using the MICRONAUT-S plates. The tet(M) gene was screened using PCR, and fluoroquinolone resistance-associated mutations were screened using PCR and Sanger sequencing. Comparing the methods, 99.5% (679/680) MICs obtained using the MICRONAUT-S plates concurred with those obtained using the CLSI reference method. For 90 M. hominis isolates, the tetracycline, levofloxacin, and moxifloxacin resistance rates were 11.1%, 2.2%, and 2.2%, respectively, with no clindamycin resistance. For 248 U. parvum isolates, the levofloxacin and moxifloxacin resistance rates were 5.2% and 0.8%, respectively; they were 2.9% and 1.5% in 68 U. urealyticum isolates. Tetracycline resistance in U. urealyticum (11.8%) was significantly (P < 0.001) higher than in U. parvum (1.2%). No macrolide resistance was observed. Overall, the customized MICRONAUT-S plates are a reliable, convenient tool for AST of human mycoplasmas. Tetracycline and fluoroquinolone resistance remain limited in France. However, the prevalence of levofloxacin and moxifloxacin resistance has increased significantly in Ureaplasma spp. from 2010 to 2015 and requires monitoring.

Importance: Antimicrobial susceptibility testing of human urogenital mycoplasmas using the CLSI reference broth microdilution method is time-consuming and requires the laborious preparation of antimicrobial stock solutions. Here, we validated the use of reliable, convenient plates designed for antimicrobial susceptibility testing that allows the simultaneous determination of the MICs of eight antibiotics of interest. We then investigated the prevalence and mechanisms of resistance of each of these bacteria to tetracyclines, fluoroquinolones, and macrolides in France in 2020 and 2021. We showed that the prevalence of levofloxacin and moxifloxacin resistance has increased significantly in Ureaplasma spp. from 2010 to 2015 and requires ongoing monitoring.

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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
期刊最新文献
Characterization of carbapenem-resistant Enterobacterales and Pseudomonas aeruginosa carrying multiple carbapenemase genes-Antimicrobial Resistance Laboratory Network, 2018-2022. A simplified pyrazinamidase test for Mycobacterium tuberculosis pyrazinamide antimicrobial susceptibility testing. Retrospective analysis of antimicrobial susceptibility profiles of non-diphtheriae Corynebacterium species from a tertiary hospital and reference laboratory, 2012-2023. Performance evaluation of the Specific Reveal system for rapid antibiotic susceptibility testing from positive blood cultures containing Gram-negative pathogens. Evaluation of the KPC/IMP/NDM/VIM/OXA-48 Combo Test Kit and Carbapenem-Resistant K.N.I.V.O. Detection K-Set in detecting KPC variants.
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