Pedace Carolina Salgado, Arbeit Robert D, Dos Santos Simeão Fernanda Cristina, Gallo Juliana Failde, de Souza Andréia Rodrigues, Chimara Erica
Bacteriology Center, Adolfo Lutz Institute, São Paulo/SP, Brazil.
Division of Infectious Diseases, Tufts Medical Center, Boston, MA, USA.
J Med Microbiol. 2025 Apr;74(4). doi: 10.1099/jmm.0.002005.
Infections caused by , an environmentally prevalent, rapidly growing mycobacteria, are increasingly frequent in developed countries. To analyse the drug susceptibility profiles of isolated in the state of São Paulo from 2008 to 2024. Of the 2,402 . isolates identified during those 17 years, 558 (23.2%) met the American Thoracic Society's microbiologic and clinical criteria for drug susceptibility testing (DST), which was performed for five agents - clarithromycin, amikacin, cefoxitin, ciprofloxacin, and doxycycline. Clarithromycin showed a dramatic increase in resistance phenotype from ≤10% in the early period to 73-90% over the last 8 years. Over half those isolates demonstrated inducible resistance. Resistance to amikacin was found in fewer than 5% of isolates from 2016 to 2021. In 2022, that result increased to 13%, but for 2023 and 2024, it had fallen back to 2%. Over the past decade, cefoxitin DST has reported the majority of isolates as intermediate, a problematic result in . group (MAG) infections, which typically require long-term treatment for successful outcomes. Since 2018, the annual susceptibility rate has been ≤18%, and in five of the 7 years, ≤7%. Ciprofloxacin was typically assessed as susceptible from 2009 to 2011, then decreased sharply to ≤20% over the next several years, and since 2018, the rate has been less than 5%. Through the entire study, doxycycline resistance has remained consistently high; in the years since 2018, ≤6% of isolates have been susceptible. This study demonstrates wide variation among MAG clinical isolates in the frequency of susceptibility, both across different agents and within individual agents over time. These results emphasize the importance of performing high-quality DST on MAG clinical isolates and suggest the need to consider revising the standard panel of drugs tested.
由一种在环境中普遍存在、生长迅速的分枝杆菌引起的感染在发达国家越来越常见。为分析2008年至2024年在圣保罗州分离出的[该分枝杆菌名称未给出]的药敏谱。在这17年中鉴定出的2402株[该分枝杆菌名称未给出]分离株中,558株(23.2%)符合美国胸科学会的药敏试验(DST)微生物学和临床标准,对克拉霉素、阿米卡星、头孢西丁、环丙沙星和多西环素这五种药物进行了药敏试验。克拉霉素耐药表型从早期的≤10%急剧上升至过去8年的73 - 90%。超过一半的分离株表现出诱导性耐药。2016年至2021年,对阿米卡星耐药的分离株不到5%。2022年,这一结果升至13%,但2023年和2024年又回落至2%。在过去十年中,头孢西丁DST报告大多数分离株为中介,这在[该分枝杆菌名称未给出]组(MAG)感染中是个问题,这类感染通常需要长期治疗才能成功治愈。自2018年以来,年度药敏率≤18%,在7年中的5年里≤7%。环丙沙星在2009年至2011年通常被评估为敏感,随后在接下来几年急剧下降至≤20%,自2018年以来,该比率一直低于5%。在整个研究过程中,多西环素耐药率一直居高不下;自2018年以来,≤6%的分离株敏感。这项研究表明,MAG临床分离株在药敏频率上存在广泛差异,无论是在不同药物之间还是在单个药物随时间的变化上。这些结果强调了对MAG临床分离株进行高质量DST的重要性,并表明有必要考虑修订标准的药敏检测药物组合。