Interactions of colistin and rifampin on multidrug-resistant Acinetobacter baumannii.

Diagn Microbiol Infect Dis

4th Department of Internal Medicine, University of Athens, Medical School, Greece.

Published: July 2001

The increased incidence of nosocomial infections by multidrug-resistant Acinetobacter spp creates demand on the application of some combinations of older antimicrobials on that species. The in vitro activities of colistin and of rifampin and of their interaction were tested on 39 nosocomial isolates of Acinetobacter baumannii. All isolates were resistant to ampicillin/sulbactam, to 3(rd) and 4(th) generation cephalosporins, to amikacin and to ciprofloxacin. MICs were determined by a microdilution technique and interactive studies between 1x or 4x MIC of colistin and rifampin were performed by the time-kill assay. Rifampin was applied at a concentration of 2 microg/mL which is equal to its mean serum level. All isolates were inhibited by colistin and only 15.2% by rifampin. Synergy between 1x MIC of colistin and rifampin was detected in 15.4% of isolates at 6 h of growth and in 51.3% of isolates at 24 h of growth. Synergy between 4x MIC of colistin and rifampin was detected in 15.4% of isolates at 6 h of growth and in 66.7% of isolates at 24 h of growth. It is concluded that colistin is highly active on multidrug-resistant Acinetobacter spp and its activity on A.baumannii is increased in the presence of rifampin, so that their administration might be proposed for nosocomial infections by these isolates.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0732-8893(01)00258-9DOI Listing

Publication Analysis

Top Keywords

colistin rifampin
20
isolates growth
16
multidrug-resistant acinetobacter
12
mic colistin
12
rifampin
8
acinetobacter baumannii
8
nosocomial infections
8
acinetobacter spp
8
isolates
8
synergy mic
8

Similar Publications

Synergistic effects of colistin-rifampin-based triple antimicrobial combination therapy against Carbapenem-resistant Pseudomonas aeruginosa: a time-kill assay.

J Antimicrob Chemother

December 2024

Division of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul 06351, South Korea.

Background: Our research aimed to investigate the potential of in vitro triple antimicrobial synergism against carbapenem-resistant Pseudomonas aeruginosa (CRPA) as a strategy to overcome antimicrobial resistance.

Methods: We used 12 CRPA blood isolates stocked in the Asian Bacterial Bank between 2016 and 2018. All isolates were tested by multi-locus sequencing and carbapenemase multiplex PCR.

View Article and Find Full Text PDF
Article Synopsis
  • The study explores the use of Caspofungin acetate (CAS) as an antibiotic adjuvant to enhance the effectiveness of existing antibiotics against Gram-negative bacteria (GNB), which are known for their resistance to treatments.
  • CAS was identified from a large screening of FDA-approved drugs, showing the ability to boost the activity of rifampin and colistin against various GNB strains, even in multidrug-resistant cases.
  • The research highlights that CAS works by disrupting the bacterial cell envelope and inhibiting biofilm formation, with PgaC identified as its target, suggesting a promising approach to tackle antimicrobial resistance.
View Article and Find Full Text PDF

Carbapenem-resistant Klebsiella pneumoniae (CRKP) infections are a major public health problem, requiring the use of last-resort antibiotics such as colistin. However, there is concern regarding the emergence of isolates resistant to this agent. The report describes two patients with urinary tract infection (UTI) and ventilator-associated pneumonia (VAP) infection caused by CRKP strains.

View Article and Find Full Text PDF

In this study, it was aimed to reveal the in vitro interactions of combinations of colistin with meropenem, rifampicin and tigecycline in colistin-resistant, biofilm-forming Klebsiella pneumonia. A total of 30 isolates, 15 of which formed biofilms and 15 did not form biofilms, were randomly selected from K. pneumoniae isolates growing in blood samples.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!