2009
DOI: 10.1128/jcm.02380-08
|View full text |Cite
|
Sign up to set email alerts
|

Rapid Determination of Quinolone Resistance in Acinetobacter spp

Abstract: In the treatment of serious bacterial infections, the rapid institution of appropriate antimicrobial chemotherapy may be lifesaving. Choosing the correct antibiotic or combination of antibiotics is becoming very important, as multidrug resistance is found in many pathogens. Using a collection of 75 well-characterized multidrug-resistant (MDR) Acinetobacter sp. isolates, we show that PCR followed by electrospray ionization mass spectrometry (PCR/ESI-MS) and base composition analysis of PCR amplification product… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

2
39
0
1

Year Published

2011
2011
2018
2018

Publication Types

Select...
7
2
1

Relationship

2
8

Authors

Journals

citations
Cited by 69 publications
(42 citation statements)
references
References 29 publications
2
39
0
1
Order By: Relevance
“…Many A. baumannii isolates manifest high levels of resistance (36) to antibiotics such as ampicillin-sulbactam (6), carbapenems (28,29), aminoglycosides (10,26), tetracyclines (15,17), and quinolones (8,16). Of particular concern is the emergence of A. baumannii strains resistant to all commonly used antibiotics, including colistin (13,30), polymyxin B (27), or tigecycline (25).…”
mentioning
confidence: 99%
“…Many A. baumannii isolates manifest high levels of resistance (36) to antibiotics such as ampicillin-sulbactam (6), carbapenems (28,29), aminoglycosides (10,26), tetracyclines (15,17), and quinolones (8,16). Of particular concern is the emergence of A. baumannii strains resistant to all commonly used antibiotics, including colistin (13,30), polymyxin B (27), or tigecycline (25).…”
mentioning
confidence: 99%
“…Using a hydrolysis reaction to identify ␤-lactamases and carbapenemases, MALDI-TOF is able to accurately report the presence of carbapenemases. PCR followed by electrospray ionization mass spectrometry (PCR/ESI-MS) quickly identifies Gram-negative bacteria and can target identification of common resistance genes such as gyrA, parC, and bla KPC with Ͼ96% sensitivity and specificity (4,6). Both of these applications are awaiting large-scale trials in the clinical arena.…”
mentioning
confidence: 99%
“…lates was established as the simultaneous mutations resulting in changes at codon 83 for gyrA and at codon 80 for parC (10,20,21).…”
Section: Resultsmentioning
confidence: 99%