In Vitro Activities of β-Lactam-β-Lactamase Inhibitor Antimicrobial Agents against Cystic Fibrosis Respiratory Pathogens

被引:29
作者
Caverly, Lindsay J. [1 ]
Spilker, Theodore [1 ]
Kalikin, Linda M. [1 ]
Stillwell, Terri [1 ]
Young, Carol [2 ]
Huang, David B. [3 ,4 ]
LiPuma, John J. [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pediat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[3] Motif BioSci, Princeton, NJ USA
[4] Rutgers New Jersey Med Sch, Trenton, NJ USA
基金
美国国家卫生研究院;
关键词
cystic fibrosis; respiratory tract infection; ceftazidime-avibactam; ceftolozane-tazobactam; meropenem-vaborbactam; IDENTIFICATION; EPIDEMIOLOGY; GENE;
D O I
10.1128/AAC.01595-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We tested the in vitro activities of ceftazidime-avibactam, ceftolozane-tazobactam, meropenem-vaborbactam, piperacillin-tazobactam, and 11 other antimicrobial agents against 420 Burkholderia, Achromobacter, Stenotrophomonas, and Pandoraea strains, 89% of which were cultured from respiratory specimens from persons with cystic fibrosis. Among the beta-lactam-beta-lactamase inhibitor agents, meropenem-vaborbactam had the greatest activity against Burkholderia and Achromobacter, including multidrug-resistant and extensively-drug-resistant strains. None of the newer beta-lactam-beta-lactamase combination drugs showed increased activity compared to that of the older agents against Stenotrophomonas maltophilia or Pandoraea spp.
引用
收藏
页数:4
相关论文
共 14 条
[1]  
[Anonymous], 2018, PERFORMANCE STANDARD
[2]   Past and Present Perspectives on β-Lactamases [J].
Bush, Karen .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (10)
[3]   Cystic fibrosis respiratory microbiota: unraveling complexity to inform clinical practice [J].
Caverly, Lindsay J. ;
LiPuma, John J. .
EXPERT REVIEW OF RESPIRATORY MEDICINE, 2018, 12 (10) :857-865
[4]  
Coenye T, 2002, FEMS MICROBIOL LETT, V208, P15
[5]   Comparative assessment of genotyping methods for epidemiologic study of Burkholderia cepacia genomovar III [J].
Coenye, T ;
Spilker, T ;
Martin, A ;
LiPuma, JJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (09) :3300-3307
[6]   Effect of β-Lactamase inhibitors on in vitro activity of β-Lactam antibiotics against Burkholderia cepacia complex species [J].
Everaert, Annelien ;
Coenye, Tom .
ANTIMICROBIAL RESISTANCE AND INFECTION CONTROL, 2016, 5
[7]   The Changing Microbial Epidemiology in Cystic Fibrosis [J].
LiPuma, John J. .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (02) :299-+
[8]   Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance [J].
Magiorakos, A. -P. ;
Srinivasan, A. ;
Carey, R. B. ;
Carmeli, Y. ;
Falagas, M. E. ;
Giske, C. G. ;
Harbarth, S. ;
Hindler, J. F. ;
Kahlmeter, G. ;
Olsson-Liljequist, B. ;
Paterson, D. L. ;
Rice, L. B. ;
Stelling, J. ;
Struelens, M. J. ;
Vatopoulos, A. ;
Weber, J. T. ;
Monnet, D. L. .
CLINICAL MICROBIOLOGY AND INFECTION, 2012, 18 (03) :268-281
[9]   Overcoming an Extremely Drug Resistant (XDR) Pathogen: Avibactam Restores Susceptibility to Ceftazidime for Burkholderia cepacia Complex Isolates from Cystic Fibrosis Patients [J].
Papp-Wallace, Krisztina M. ;
Becka, Scott A. ;
Zeiser, Elise T. ;
Ohuchi, Nozomi ;
Mojica, Maria F. ;
Gatta, Julian A. ;
Falleni, Monica ;
Tosi, Delfina ;
Borghi, Elisa ;
Winkler, Marisa L. ;
Wilson, Brigid M. ;
LiPuma, John J. ;
Nukaga, Michiyoshi ;
Bonomo, Robert A. .
ACS INFECTIOUS DISEASES, 2017, 3 (07) :502-511
[10]   Development of a recA gene-based identification approach for the the entire Burkholderia genus [J].
Payne, GW ;
Vandamme, P ;
Morgan, SH ;
LiPuma, JJ ;
Coenye, T ;
Weightman, AJ ;
Jones, TH ;
Mahenthiralingam, E .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (07) :3917-3927