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Comparison of methods for the detection of in vitro synergy in multidrug-resistant gram-negative bacteria

Authors :
Juliana Januario Gaudereto
Lauro Vieira Perdigão Neto
Gleice Cristina Leite
Evelyn Patricia Sanchez Espinoza
Roberta Cristina Ruedas Martins
Gladys Villas Boa Prado
Flavia Rossi
Thais Guimarães
Anna Sara Levin
Silvia Figueiredo Costa
Source :
BMC Microbiology, Vol 20, Iss 1, Pp 1-7 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Background The use of combined antibiotic therapy has become an option for infections caused by multidrug-resistant (MDR) bacteria. The time-kill (TK) assay is considered the gold standard method for the evaluation of in vitro synergy, but it is a time-consuming and expensive method. The purpose of this study was to evaluate two methods for testing in vitro antimicrobial combinations: the disk diffusion method through disk approximation (DA) and the agar gradient diffusion method via the MIC:MIC ratio. The TK assay was included as the gold standard. MDR Gram-negative clinical isolates (n = 62; 28 Pseudomonas aeruginosa, 20 Acinetobacter baumannii, and 14 Serratia marcescens) were submitted to TK, DA, and MIC:MIC ratio synergy methods. Results Overall, the agreement between the DA and TK assays ranged from 20 to 93%. The isolates of A. baumannii showed variable results of synergism according to TK, and the calculated agreement was statistically significant in this species against fosfomycin with meropenem including colistin-resistant isolates. The MIC:MIC ratiometric agreed from 35 to 71% with TK assays. The kappa test showed good agreement for the combination of colistin with amikacin (K = 0.58; P = 0.04) among the colistin-resistant A. baumannii isolates. Conclusions The DA and MIC:MIC ratiometric methods are easier to perform and might be a more viable tool for clinical microbiology laboratories.

Details

Language :
English
ISSN :
14712180
Volume :
20
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Microbiology
Publication Type :
Academic Journal
Accession number :
edsdoj.63625db8197a41a6bff5bb82e0b26cda
Document Type :
article
Full Text :
https://doi.org/10.1186/s12866-020-01756-0