Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa
Carbapenems are the primary choice of treatment for severe Pseudomonas aeruginosa infection. However, the emergence of carbapenem resistance due to the production of metallo-β-lactamases (MBLs) is of global concern. In this study, 90 imipenem- (IPM- or IP-) resistant P. aeruginosa (IRPA) isolates, i...
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2012-01-01
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Online Access: | http://dx.doi.org/10.1100/2012/654939 |
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author | Yalda Khosravi Mun Fai Loke Eng Guan Chua Sun Tee Tay Jamuna Vadivelu |
author_facet | Yalda Khosravi Mun Fai Loke Eng Guan Chua Sun Tee Tay Jamuna Vadivelu |
author_sort | Yalda Khosravi |
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description | Carbapenems are the primary choice of treatment for severe Pseudomonas aeruginosa infection. However, the emergence of carbapenem resistance due to the production of metallo-β-lactamases (MBLs) is of global concern. In this study, 90 imipenem- (IPM- or IP-) resistant P. aeruginosa (IRPA) isolates, including 32 previously tested positive and genotyped for MBL genes by PCR, were subjected to double-disk synergy test (DDST), combined disk test (CDT), and imipenem/imipenem-inhibitor (IP/IPI) E-test to evaluate their MBLs detection capability. All three methods were shown to have a sensitivity of 100%. However, DDST was the most specific of the three (96.6%), followed by IP/IPI E-test interpreted based on the single criteria of IP/IPI ≥8 as positive (62.1%), and CDT was the least specific (43.1%). Based on the data from this evaluation, we propose that only IRPA with IP MIC >16 μg/mL and IP/IPI ≥8 by IP/IPI E-test should be taken as positive for MBL activity. With the new dual interpretation criteria, the MBL IP/IPI E-test was shown to achieve 100% sensitivity as well as specificity for the IRPA in this study. Therefore, the IP/IPI E-test is a viable alternative phenotypic assay to detect MBL production in IRPA in our population in circumstances where PCR detection is not a feasible option. |
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institution | Kabale University |
issn | 1537-744X |
language | English |
publishDate | 2012-01-01 |
publisher | Wiley |
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series | The Scientific World Journal |
spelling | doaj-art-7edd793b86e24ba7b9378325864ff5c82025-02-03T01:31:27ZengWileyThe Scientific World Journal1537-744X2012-01-01201210.1100/2012/654939654939Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosaYalda Khosravi0Mun Fai Loke1Eng Guan Chua2Sun Tee Tay3Jamuna Vadivelu4Department of Medical Microbiology, University of Malaya, 50603 Kuala Lumpur, MalaysiaFaculty of Medicine, University of Malaya, 50603 Kuala Lumpur, MalaysiaDepartment of Medical Microbiology, University of Malaya, 50603 Kuala Lumpur, MalaysiaDepartment of Medical Microbiology, University of Malaya, 50603 Kuala Lumpur, MalaysiaDepartment of Medical Microbiology, University of Malaya, 50603 Kuala Lumpur, MalaysiaCarbapenems are the primary choice of treatment for severe Pseudomonas aeruginosa infection. However, the emergence of carbapenem resistance due to the production of metallo-β-lactamases (MBLs) is of global concern. In this study, 90 imipenem- (IPM- or IP-) resistant P. aeruginosa (IRPA) isolates, including 32 previously tested positive and genotyped for MBL genes by PCR, were subjected to double-disk synergy test (DDST), combined disk test (CDT), and imipenem/imipenem-inhibitor (IP/IPI) E-test to evaluate their MBLs detection capability. All three methods were shown to have a sensitivity of 100%. However, DDST was the most specific of the three (96.6%), followed by IP/IPI E-test interpreted based on the single criteria of IP/IPI ≥8 as positive (62.1%), and CDT was the least specific (43.1%). Based on the data from this evaluation, we propose that only IRPA with IP MIC >16 μg/mL and IP/IPI ≥8 by IP/IPI E-test should be taken as positive for MBL activity. With the new dual interpretation criteria, the MBL IP/IPI E-test was shown to achieve 100% sensitivity as well as specificity for the IRPA in this study. Therefore, the IP/IPI E-test is a viable alternative phenotypic assay to detect MBL production in IRPA in our population in circumstances where PCR detection is not a feasible option.http://dx.doi.org/10.1100/2012/654939 |
spellingShingle | Yalda Khosravi Mun Fai Loke Eng Guan Chua Sun Tee Tay Jamuna Vadivelu Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa The Scientific World Journal |
title | Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa |
title_full | Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa |
title_fullStr | Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa |
title_full_unstemmed | Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa |
title_short | Phenotypic Detection of Metallo-β-Lactamase in Imipenem-Resistant Pseudomonas aeruginosa |
title_sort | phenotypic detection of metallo β lactamase in imipenem resistant pseudomonas aeruginosa |
url | http://dx.doi.org/10.1100/2012/654939 |
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