Sader Helio S, Mendes Rodrigo E, Carvalhaes Cecilia G, Kimbrough John H, Castanheira Mariana
JMI Laboratories, North Liberty, Iowa, USA.
Open Forum Infect Dis. 2023 Jan 31;10(2):ofad046. doi: 10.1093/ofid/ofad046. eCollection 2023 Feb.
As the frequency of metallo-β-lactamase (MBL)-producing Enterobacterales is increasing worldwide, effective antimicrobials to treat the infections caused by these organisms are urgently needed.
The activity of aztreonam-avibactam and comparators were evaluated against 27 834 Enterobacterales isolates collected from 74 US medical centers in 2019-2021. Isolates were susceptibility tested by broth microdilution. An aztreonam-avibactam pharmacokinetic/pharmacodynamic breakpoint of ≤8 mg/L was applied for comparison. Antimicrobial susceptibility and the frequency of key resistance phenotypes were assessed then stratified by year and infection type. Carbapenem-resistant Enterobacterales (CRE) were screened for carbapenemase (CPE) genes by whole genome sequencing.
Aztreonam-avibactam inhibited >99.9% of Enterobacterales at ≤8 mg/L. Only 3 isolates (0.01%) had an aztreonam-avibactam minimum inhibitory concentration (MIC) >8 mg/L. The CRE rates were 0.8%, 0.9%, and 1.1% in 2019, 2020, and 2021, respectively; 99.6% (260 of 261) of CRE isolates were inhibited at an aztreonam-avibactam MIC of ≤8 mg/L. The CRE susceptibility to meropenem-vaborbactam decreased from 91.7% in 2019 to 83.1% in 2020 and 76.5% in 2021 (82.1% overall). The CRE, multidrug-resistant, and extensively drug-resistant phenotypes were markedly higher among isolates from pneumonia compared with other infections. The most common carbapenemase among CRE was carbapenemase (65.5% of CRE), followed by New Delhi metallo-β-lactamase (11.1%), oxacillinase (OXA)-48-like (4.6%), enzyme (2.3%), and imipenemase (1.5%). Among non-CPE-producing CRE isolates ( = 44; 16.9% of CRE), 97.7% were inhibited at ≤8 mg/L aztreonam-avibactam and 85.4% were meropenem-vaborbactam susceptible.
The frequencies of MBL and OXA-48-type producers increased markedly. Aztreonam-avibactam demonstrated potent and consistent activity against Enterobacterales across infection types and over time.
随着产金属β-内酰胺酶(MBL)的肠杆菌科细菌在全球范围内的出现频率不断增加,迫切需要有效的抗菌药物来治疗由这些微生物引起的感染。
对2019 - 2021年从美国74个医疗中心收集的27834株肠杆菌科细菌分离株评估氨曲南-阿维巴坦及对照药物的活性。分离株通过肉汤稀释法进行药敏试验。应用≤8mg/L的氨曲南-阿维巴坦药代动力学/药效学折点进行比较。评估抗菌药物敏感性和关键耐药表型的频率,然后按年份和感染类型分层。通过全基因组测序对耐碳青霉烯类肠杆菌(CRE)进行碳青霉烯酶(CPE)基因筛查。
氨曲南-阿维巴坦在≤8mg/L时可抑制>99.9%的肠杆菌科细菌。仅有3株分离株(0.01%)的氨曲南-阿维巴坦最低抑菌浓度(MIC)>8mg/L。2019年、2020年和2021年的CRE发生率分别为0.8%、0.9%和1.1%;99.6%(261株中的260株)的CRE分离株在氨曲南-阿维巴坦MIC≤8mg/L时被抑制。CRE对美罗培南-巴罗巴坦的敏感性从2019年的91.7%降至2020年的83.1%和2021年的76.5%(总体为82.1%)。与其他感染相比,肺炎分离株中CRE、多重耐药和广泛耐药表型明显更高。CRE中最常见的碳青霉烯酶是碳青霉烯酶(占CRE的65.5%),其次是新德里金属β-内酰胺酶(11.1%)、氧青霉烯酶(OXA)-48样酶(4.6%)、酶(2.3%)和亚胺培南酶(1.5%)。在非产CPE的CRE分离株(n = 44;占CRE的16.9%)中,97.7%在氨曲南-阿维巴坦≤8mg/L时被抑制,85.4%对美罗培南-巴罗巴坦敏感。
MBL和OXA-48型产生菌的频率显著增加。氨曲南-阿维巴坦在不同感染类型和时间段内对肠杆菌科细菌均表现出强大且一致的活性。