Screening of antibiotics resistance to Enterobacteriaceae, Pseudomonas aeruginosa, and Acinetobacter baumannii by an advanced expert system

• Published in: Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2005-12, Vol.11 (6), p.288-292
• Main Authors: Nakamura, Tatsuya, Takahashi, Hakuo
• Format: Article
• Language: English
• Subjects: Acinetobacter baumannii; Acinetobacter baumannii - drug effects; Anti-Bacterial Agents - pharmacology; beta-Lactam Resistance; beta-Lactams - pharmacology; Drug resistance; Enterobacteriaceae; Enterobacteriaceae - drug effects; Humans; Mass Screening; Microbial Sensitivity Tests - instrumentation; Microbial Sensitivity Tests - methods; Minimum inhibitory concentration; Phenotype; Providencia rettgeri; Pseudomonas aeruginosa; Pseudomonas aeruginosa - drug effects; Serratia marcescens
• ISSN: 1341-321X; 1437-7780
• DOI: 10.1007/s10156-005-0415-X

The VITEK2 advanced expert system (AES) gives information about the antibiotics-resistance mechanisms based on the biological validation derived from the VITEK2 susceptibility result. In this study, we investigated whether or not this system correctly categorized the β-lactamase resistance mechanism data derived from the VITEK2 susceptibility result using the testing card, AST-N025, with Enterobacteriaceae, Pseudomonas aeruginosa, and Acinetobacter baumannii. We used 131 strains, and their phenotypes were determined according to the biological and genetic screening. The AES analysis result matched the phenotype testing in 120 (91.6%) of the 131 strains. Incorrect findings were found in six strains, including three strains of Serratia marcescens. The resistance mechanism could not be determined in five strains, including three strains of Providencia rettgeri. The analysis of those phenotypes agreed in 34 (97.1%) among 35 strains with extended spectrum β-lactamase (ESBL), and in 27 (96.4%) among 28 strains with high-level cephalosporinase. The agreement ratio in the phenotype was very high as we expected. The incorrect and nondeterminable samples were strains with relatively high cephalosporinase that has variation of outer membrane protein. The AES was able to detect the phenotype for carbapenemase. The AES is a clinically useful system that allows taking prompt measures to treat patients because it can provide information about the resistance mechanism in less than half a day after starting the analysis.