Molecular drivers of resistance to sulbactam-durlobactam in contemporary clinical isolates of Acinetobacter baumannii

被引:11
作者
Moussa, Samir H. [1 ]
Shapiro, Adam B. [1 ]
Mcleod, Sarah M. [1 ]
Iyer, Ramkumar [1 ,3 ]
Carter, Nicole M. [1 ]
Tsai, Yu-Kuo [2 ]
Siu, L. Kristopher [2 ]
Miller, Alita A. [1 ,4 ]
机构
[1] Entasis Therapeut Inc, Innov Specialty Therapeut Inc, Waltham, MA 02451 USA
[2] Kemyth Biotech Co Ltd, Taipei, Taiwan
[3] Global Alliance TB Drug Dev, New York, NY USA
[4] Design Therapeut, Carlsbad, CA USA
关键词
Acinetobacter; sulbactam; durlobactam; surveillance studies; resistance; ETX2514; ACINETOBACTER-BAUMANNII; MULTIDRUG-RESISTANCE; VITRO ACTIVITY; ADEABC; SULBACTAM/DURLOBACTAM; CARBAPENEMS; INFECTIONS; SYSTEM;
D O I
10.1128/aac.00665-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Acinetobacter baumannii-calcoaceticus complex (ABC) causes severe infections that are difficult to treat due to pre-existing antibiotic resistance. Sulbactam-durlobactam (SUL-DUR) is a targeted beta-lactam/beta-lactamase inhibitor combination antibiotic designed to treat serious infections caused by Acinetobacter, including multidrug- and carbapenem-resistant strains. In a recent global surveillance study of 5,032 ABC clinical isolates collected from 2016 to 2021, less than 2% of ABC isolates had SUL-DUR MIC values >4 mu g/mL. Molecular characterization of these isolates confirmed the primary drivers of resistance are metallo-beta-lactamases or penicillin-binding protein 3 (PBP3) mutations, as previously described. In addition, this study shows that certain common PBP3 variants, such as A515V, are insufficient to confer sulbactam resistance and that the efflux of durlobactam by AdeIJK is likely to play a role in a subset of strains.
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页数:15
相关论文
共 40 条
  • [1] Barnes MD, 2019, MBIO, V10, DOI [10.1128/mBio.00159-19, 10.1128/mbio.00159-19]
  • [2] INTERACTION OF AZTHREONAM AND RELATED MONOBACTAMS WITH BETA-LACTAMASES FROM GRAM-NEGATIVE BACTERIA
    BUSH, K
    FREUDENBERGER, JS
    SYKES, RB
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1982, 22 (03) : 414 - 420
  • [3] Multidrug Resistant Acinetobacter baumannii: Resistance by Any Other Name Would Still be Hard to Treat
    Butler, David A.
    Biagi, Mark
    Tan, Xing
    Qasmieh, Samah
    Bulman, Zackery P.
    Wenzler, Eric
    [J]. CURRENT INFECTIOUS DISEASE REPORTS, 2019, 21 (12)
  • [4] Clinical Laboratory and Standards Institute (CLSI), 2018, Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically
  • [5] Approved Standard Eleventh Edition
  • [6] CLSI, 2023, Performance Standards for Antimicrobial Susceptibility Testing, V33rd ed.
  • [7] Efflux-Mediated Antibiotic Resistance in Acinetobacter spp.
    Coyne, Sebastien
    Courvalin, Patrice
    Perichon, Bruno
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) : 947 - 953
  • [8] Overexpression of Resistance-Nodulation-Cell Division Pump AdeFGH Confers Multidrug Resistance in Acinetobacter baumannii
    Coyne, Sebastien
    Rosenfeld, Nicolas
    Lambert, Thierry
    Courvalin, Patrice
    Perichon, Bruno
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (10) : 4389 - 4393
  • [9] ETX2514 is a broad-spectrum β-lactamase inhibitor for the treatment of drug-resistant Gram-negative bacteria including Acinetobacter baumannii
    Durand-Reville, Thomas F.
    Guler, Satenig
    Comita-Prevoir, Janelle
    Chen, Brendan
    Bifulco, Neil
    Hoan Huynh
    Lahiri, Sushmita
    Shapiro, Adam B.
    McLeod, Sarah M.
    Carter, Nicole M.
    Moussa, Samir H.
    Velez-Vega, Camilo
    Olivier, Nelson B.
    McLaughlin, Robert
    Gao, Ning
    Thresher, Jason
    Palmer, Tiffany
    Andrews, Beth
    Giacobbe, Robert A.
    Newman, Joseph V.
    Ehmann, David E.
    de Jonge, Boudewijn
    O'Donnell, John
    Mueller, John P.
    Tommasi, Ruben A.
    Miller, Alita A.
    [J]. NATURE MICROBIOLOGY, 2017, 2 (09):
  • [10] Entasis Therapeutics, 2023, XACDURO (sulbactam for injection