Aronin Steven I, Huband Michael D, Becker Holly, Fedler Kelley A, Dunne Michael W
Iterum Therapeutics, Old Saybrook, CT, USA.
Element Materials Technology, North Liberty, IA, USA.
J Glob Antimicrob Resist. 2025 Jun 22;44:152-159. doi: 10.1016/j.jgar.2025.06.013.
Sulopenem is a thiopenem antibacterial with an oral and parenteral formulation. Sulopenem etzadroxil/probenecid, the oral formulation, was recently approved by the United States Food and Drug Administration for the treatment of women with uncomplicated urinary tract infection (UTI). This study evaluated the in vitro activity of sulopenem and comparator agents against contemporary Enterobacterales clinical isolates predominantly from patients with UTIs.
A contemporary collection of 1086 community- and nosocomial-acquired Enterobacterales isolates was assembled from US medical centres. Isolates were susceptibility tested using the Clinical and Laboratory Standards Institute broth microdilution reference method.
Sulopenem demonstrated potent in vitro antimicrobial activity (MIC, 0.03/0.25 mg/L) against Enterobacterales isolates regardless of infection type, inhibiting 98.0% of isolates at ≤0.5 mg/L. This activity was conserved against resistant phenotypes, including extended-spectrum β-lactamase (ESBL)-phenotype Escherichia coli (MIC, 0.03/0.06 mg/L) and ESBL-phenotype Klebsiella pneumoniae (MIC, 0.06/0.12 mg/L). As would be expected, cross-resistance was found with imipenem and meropenem to a lesser extent. Sulopenem maintained activity against ciprofloxacin-, nitrofurantoin-, and trimethoprim/sulfamethoxazole-non-susceptible subsets, including urinary isolates from patients in the community (MIC 0.03-0.12/0.12-0.5 mg/L). Sulopenem also maintained activity against community-acquired ESBL-producing Enterobacterales urinary isolates non-susceptible to two or more oral antimicrobial agents commonly used to treat UTIs.
The potent in vitro activity of sulopenem against this large collection of contemporary Enterobacterales clinical isolates from multiple infection types supports its use in the treatment of uncomplicated UTI, as well as its further clinical evaluation in the treatment of other common bacterial infections demonstrating resistant phenotypes.
舒洛培南是一种具有口服和胃肠外给药制剂的硫代青霉烯类抗菌药物。舒洛培南乙酯/丙磺舒口服制剂最近获得美国食品药品监督管理局批准,用于治疗非复杂性尿路感染(UTI)的女性患者。本研究评估了舒洛培南及对照药物对主要来自UTI患者的当代肠杆菌科临床分离株的体外活性。
从美国医疗中心收集了1086株社区获得性和医院获得性肠杆菌科分离株。采用临床和实验室标准协会肉汤微量稀释参考方法对分离株进行药敏试验。
无论感染类型如何,舒洛培南对肠杆菌科分离株均表现出强大的体外抗菌活性(MIC,0.03/0.25mg/L),在≤0.5mg/L时可抑制98.0%的分离株。这种活性在耐药表型中保持,包括产超广谱β-内酰胺酶(ESBL)表型的大肠埃希菌(MIC,0.03/0.06mg/L)和产ESBL表型的肺炎克雷伯菌(MIC,0.06/0.12mg/L)。不出所料,在较小程度上发现与亚胺培南和美罗培南存在交叉耐药。舒洛培南对环丙沙星、呋喃妥因和甲氧苄啶/磺胺甲恶唑不敏感亚组保持活性,包括社区患者的尿液分离株(MIC 0.03-0.12/0.12-0.5mg/L)。舒洛培南对社区获得性产ESBL肠杆菌科尿液分离株也保持活性,这些分离株对两种或更多种常用于治疗UTI的口服抗菌药物不敏感。
舒洛培南对大量来自多种感染类型的当代肠杆菌科临床分离株具有强大的体外活性,支持其用于治疗非复杂性UTI,以及在治疗表现出耐药表型的其他常见细菌感染方面进行进一步的临床评估。