In-vitro activity of tigecycline against clinical isolates of Acinetobacter baumannii in Taiwan determined by the broth microdilution and disk diffusion methods

2008 ◽  
Vol 32 ◽  
pp. S192-S196 ◽  
Author(s):  
Chun-Hsing Liao ◽  
Hsiang-Chi Kung ◽  
Gwo-Jong Hsu ◽  
Po-Liang Lu ◽  
Yung-Ching Liu ◽  
...  
2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S281-S281
Author(s):  
Andrew Walkty ◽  
James Karlowsky

Abstract Background There are limited options available for the treatment of infections caused by Enterobacteriaceae that produce an NDM metallo-β-lactamase. The purpose of this study was to compare the in vitro activity of aztreonam in combination with three different β-lactam/β-lactamase inhibitors (ceftazidime–avibactam, amoxicillin-clavulanate, piperacillin–tazobactam) vs. NDM-positive Enterobacteriaceae clinical isolates. Methods Seven Escherichia coli and three Klebsiella pneumoniae clinical isolates (all NDM-positive by PCR) were included in this study. The in vitro activities of ceftazidime–avibactam, amoxicillin-clavulanate, piperacillin–tazobactam, and aztreonam were determined by disk diffusion as described by CLSI. For synergy testing, disks containing a β-lactamase inhibitor (ceftazidime–avibactam, amoxicillin-clavulanate, piperacillin tazobactam) were applied to Mueller–Hinton agar plates inoculated with the test organisms, and the plates were incubated for 1 hour. The disks were then removed and aztreonam disks were dropped on the previous disk sites. The plates were then incubated as per standard CLSI recommendations for disk diffusion testing. Results All ten isolates demonstrated phenotypic resistance to aztreonam, amoxicillin-clavulanate, and piperacillin–tazobactam, and eight were resistant to ceftazidime–avibactam (CLSI breakpoints). The zone diameter observed for aztreonam in combination with ceftazidime–avibactam was greater than for either antimicrobial on its own for nine isolates. Seven isolates (70%) had susceptibility to aztreonam restored (zone diameter ≥21 mm) in the presence of avibactam. Aztreonam in combination with amoxicillin-clavulanate demonstrated in increase in zone diameter for all isolates relative to the zone for each antimicrobial alone, but only two (20%) had aztreonam susceptibility restored. Aztreonam susceptibility was not restored for any of the isolates in combination with piperacillin–tazobactam. Conclusion Of the three β-lactam/β-lactamase inhibitor-aztreonam combinations evaluated, ceftazidime–avibactam plus aztreonam demonstrated the greatest in vitro activity vs. NDM-producing Enterobacteriaceae. Disclosures All authors: No reported disclosures.


Chemotherapy ◽  
2003 ◽  
Vol 49 (1-2) ◽  
pp. 24-26 ◽  
Author(s):  
Felipe Fernández-Cuenca ◽  
Luis Martínez-Martínez ◽  
Alvaro Pascual ◽  
Evelio J. Perea

2007 ◽  
Vol 29 ◽  
pp. S476
Author(s):  
A. Stylianakis ◽  
A. Koutsoukou ◽  
S. Tsiplakou ◽  
S. Sardiniari ◽  
A. Vourtsi ◽  
...  

2009 ◽  
Vol 34 (3) ◽  
pp. 265-267 ◽  
Author(s):  
Sara Marti ◽  
Javier Sánchez-Céspedes ◽  
Paula Espinal ◽  
Jordi Vila

2020 ◽  
Vol 75 (7) ◽  
pp. 1833-1839 ◽  
Author(s):  
Qiwen Yang ◽  
Yingchun Xu ◽  
Peiyao Jia ◽  
Ying Zhu ◽  
Jingjia Zhang ◽  
...  

Abstract Background Durlobactam is a broad-spectrum inhibitor of class A, C and D β-lactamases. Sulbactam is a generic β-lactam most commonly used as a β-lactamase inhibitor in combination with ampicillin; however, it has a unique property in that it has selective intrinsic activity against Acinetobacter baumannii. Currently, there is widespread resistance caused by multiple β-lactamases including class A carbapenemases and class C and class D enzymes. The addition of durlobactam to sulbactam restores in vitro activity against MDR A. baumannii that possess multiple β-lactamases. Objectives Previously, susceptibility data for sulbactam/durlobactam were limited to isolates from patients in Western countries. This study was undertaken to determine the activity of sulbactam/durlobactam against A. baumannii isolated from patients in mainland China. Methods Nine hundred and eighty-two recent A. baumannii clinical isolates were collected from 22 sites across mainland China during 2016–18. The isolates were collected from lower respiratory tract, intra-abdominal, urinary tract and skin and skin structure infections. The in vitro activities of sulbactam/durlobactam and comparators were determined by broth microdilution. Results The addition of durlobactam restored the activity of sulbactam against the majority of the strains tested. The MIC90 of sulbactam/durlobactam was 2 mg/L for all A. baumannii, compared with 64 mg/L for sulbactam alone. The MIC90 of sulbactam/durlobactam of 2 mg/L remained unchanged for 831 carbapenem-resistant isolates. Colistin was the only comparator with comparable activity (MIC90 = 1 mg/L). Conclusions This study demonstrated the potential utility of sulbactam/durlobactam for the treatment of infections caused by A. baumannii in China.


2008 ◽  
Vol 32 ◽  
pp. S188-S191 ◽  
Author(s):  
Jien-Wei Liu ◽  
Lih-Shinn Wang ◽  
Yu-Jen Cheng ◽  
Gwo-Jong Hsu ◽  
Po-Liang Lu ◽  
...  

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