Increasing frequency of OXA-48-producing Enterobacterales worldwide and activity of ceftazidime/avibactam, meropenem/vaborbactam and comparators against these isolates

被引:40
|
作者
Castanheira, Mariana [1 ]
Doyle, Timothy B. [1 ]
Collingsworth, Timothy D. [1 ]
Sader, Helio S. [1 ]
Mendes, Rodrigo E. [1 ]
机构
[1] JMI Labs, North Liberty, IA 52317 USA
关键词
READ ALIGNMENT; CARBAPENEMASES;
D O I
10.1093/jac/dkab306
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To investigate the increase in the rates of OXA-48-like-producing isolates during 3years of global surveillance. Methods: Among 55162 Enterobacterales isolates, 354 carbapenem-resistant isolates carried genes encoding OXA-48-like enzymes. Isolates were susceptibility tested for ceftazidime/avibactam and comparators by broth microdilution methods. Analysis of beta-lactam resistance mechanisms and MLST was performed in silico using WGS data. Results: OXA-48-like-producing isolates increased from 0.5% (94/18656) in 2016 to 0.9% (169/18 808) in 2018. OXA-48 was the most common variant; isolates primarily were Klebsiella pneumoniae (318/354 isolates) from Europe and adjacent countries. MLST analysis revealed a diversity of STs, but K. pneumoniae belonging to ST395, ST23 and ST11 were observed most frequently. Thirty-nine isolates harboured MBLs and were resistant to most agents tested. The presence of bla(CTX-M-15) (258 isolates), OmpK35 nonsense mutations (232) and OmpK36 alterations (316) was common among OXA-48 producers. Ceftazidime, cefepime and aztreonam susceptibility rates, when applying CLSI breakpoints, were 12%-15% lower for isolates carrying ESBLs alone and with either or both OmpK35 stop codons and OmpK36 alterations. Meropenem and, remarkably, meropenem/vaborbactam were affected by specific OmpK36 alterations when a deleterious mutation also was observed in OmpK35. These mechanisms caused a decrease of 12%-42% in the susceptibility rates for meropenem and meropenem/vaborbactam. Ceftazidime/avibactam susceptibility rates were >98.9%, regardless of the presence of additional beta-lactam resistance mechanisms. Conclusions: Guidelines for the treatment of infections caused by OXA-48-producing isolates are scarce and, as the dissemination of these isolates continues, studies are needed to help physicians understand treatment options for these infections.
引用
收藏
页码:3125 / 3134
页数:10
相关论文
共 50 条
  • [31] In Vitro Efficacy of Ceftazidime-avibactam Against blaOXA-48-producing Klebsiella pneumoniae Isolates
    Cag, Yasemin
    Kocoglu, Muecahide Esra
    Caskurlu, Hulya
    Haciseyitoglu, Demet
    Mirza, Hasan Cenk
    Guclu, Aylin Uskudar
    Cetinkaya, Riza Aytac
    Vahaboglu, Haluk
    MEDITERRANEAN JOURNAL OF INFECTION MICROBES AND ANTIMICROBIALS, 2023, 12
  • [32] Clonal dissemination of Klebsiella pneumoniae resistant to cefiderocol, ceftazidime/avibactam, meropenem/vaborbactam and imipenem/relebactam co-producing KPC and OXA-181 carbapenemase
    Bovo, Federica
    Amadesi, Stefano
    Palombo, Marta
    Lazzarotto, Tiziana
    Ambretti, Simone
    Gaibani, Paolo
    JAC-ANTIMICROBIAL RESISTANCE, 2023, 5 (04):
  • [33] Activity of mecillinam against OXA-48-like carbapenemase-producing Enterobacterales
    Tsakris, Athanasios
    Koumaki, Vasiliki
    Baka, Stavroula
    Balakrishnan, Indran
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2022, 77 (02) : 537 - 538
  • [34] Antimicrobial activities of ceftazidime/avibactam, ceftolozane/tazobactam, imipenem/relebactam, meropenem/vaborbactam, and comparators against Pseudomonas aeruginosa from patients with skin and soft tissue infections
    Sader, Helio S.
    Castanheira, Mariana
    Duncan, Leonard R.
    Mendes, Rodrigo E.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2021, 113 : 279 - 281
  • [35] In Vitro Synergism of Azithromycin Combination with Antibiotics against OXA-48-Producing Klebsiella pneumoniae Clinical Isolates
    Singkham-in, Uthaibhorn
    Muhummudaree, Netchanok
    Chatsuwan, Tanittha
    ANTIBIOTICS-BASEL, 2021, 10 (12):
  • [36] Evolution of ceftazidime/avibactam resistance and plasmid dynamics in OXA-48-producing Klebsiella spp. during long-term patient colonization
    Salud Rodríguez-Pallares
    María Alejandra Mateo-Vargas
    Manuel Antonio Rodríguez-Iglesias
    Jorge Arca-Suárez
    Fátima Galán-Sánchez
    European Journal of Clinical Microbiology & Infectious Diseases, 2025, 44 (4) : 807 - 817
  • [37] Antimicrobial activity of ceftazidime-avibactam against KPC-2-producing Enterobacterales: a cross-combination and dose-escalation titration study with relebactam and vaborbactam
    Kang, Min Seo
    Baek, Jin Yang
    Ko, Jae-Hoon
    Cho, Sun Young
    Lee, Keon Young
    Lee, Young Ho
    Yang, Jinyoung
    Kim, Tae Yeul
    Huh, Hee Jae
    Lee, Nam Yong
    Huh, Kyungmin
    Kang, Cheol-In
    Chung, Doo Ryeon
    Peck, Kyong Ran
    MICROBIOLOGY SPECTRUM, 2024, 12 (06):
  • [38] An innovative population pharmacokinetic/pharmacodynamic strategy for attaining aggressive joint PK/PD target of continuous infusion ceftazidime/avibactam against KPC- and OXA-48-producing Enterobacterales and preventing resistance development in critically ill patients
    Cojutti, Pier Giorgio
    Pai, Manjunath P.
    Gatti, Milo
    Rinaldi, Matteo
    Ambretti, Simone
    Viale, Pierluigi
    Pea, Federico
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2024,
  • [39] In vitro activity of ceftazidime/avibactam, imipenem/relebactam and meropenem/vaborbactam alone or in combination with polymyxin B against carbapenem resistant Acinetobacter baumannii
    Rongxin Liang
    Dongxing Wang
    Mingjin Hu
    Yuxia Gu
    Meijun Wang
    Dan Hu
    Mingan Zhu
    Meng Wang
    The Journal of Antibiotics, 2023, 76 : 540 - 547
  • [40] In vitro activity of ceftazidime/avibactam against clinical isolates of ESBL-producing Enterobacteriaceae in Italy
    Viaggi, Valentina
    Pini, Beatrice
    Tonolo, Silvia
    Luzzaro, Francesco
    Principe, Luigi
    JOURNAL OF CHEMOTHERAPY, 2019, 31 (04) : 195 - 201