TY - JOUR
T1 - mCIM test as a reliable assay for the detection of CRE in the Gulf region
AU - Al Musawi, Safiya
AU - Ur Rahman, Jawad
AU - Aljaroodi, Salma Ali
AU - AlShammari, Lateefah
AU - Itbaileh, Ahmed
AU - Mohammed, Hessa
AU - Saeed, Nermin
AU - Abdalhamid, Baha
AU - Alkharsah, Khaled R.
AU - Aljindan, Reem Y.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021
Y1 - 2021
N2 - Introduction. Carbapenem resistant Enterobacterales (CRE) are one of the leading causes of systemic and nosocomial infections and are multidrug-resistant organisms producing different carbapenemases. There are many genotypic and phenotypic methods for detecting the carbapenemases; however, there is a limitation for each. Modified carbapenem inactivation method (mCIM) assay is a recent phenotypic method which has been published by the Clinical and Laboratory Standards Institute. Hypothesis / Gap Statement. mCIM assay could provide a reliable method for the detection of carbapenemases in CRE. Aim. Evaluation of the mCIM assay performance for the detection of carbapenemases in Enterobacterales and the identification of the common carbapenemase genes at Eastern Province of Saudi Arabia and Kingdom of Bahrain. Methodology. A collection of 197 non-duplicate carbapenem resistant Enterobacterales clinical isolates, were evaluated with the mCIM test comparing its performance to multiplex PCR. The minimum inhibitory concentration susceptibility testing was done by the Etest method for imipenem, meropenem, and ertapenem. Results. The sensitivity of the mCIM assay was 94% (95% CI, (89.3-97.1)). In Saudi Arabia and Bahrain, OXA-48 was the most prevalent carbapenemase gene followed by NDM. Coexistence of multiple carbapenemase genes is reported in eleven cases. Conclusion. These findings indicate that the mCIM test is a reliable and simple assay for detecting the activity of carbapenemase in Enterobacterales, especially in resource-limited laboratories.
AB - Introduction. Carbapenem resistant Enterobacterales (CRE) are one of the leading causes of systemic and nosocomial infections and are multidrug-resistant organisms producing different carbapenemases. There are many genotypic and phenotypic methods for detecting the carbapenemases; however, there is a limitation for each. Modified carbapenem inactivation method (mCIM) assay is a recent phenotypic method which has been published by the Clinical and Laboratory Standards Institute. Hypothesis / Gap Statement. mCIM assay could provide a reliable method for the detection of carbapenemases in CRE. Aim. Evaluation of the mCIM assay performance for the detection of carbapenemases in Enterobacterales and the identification of the common carbapenemase genes at Eastern Province of Saudi Arabia and Kingdom of Bahrain. Methodology. A collection of 197 non-duplicate carbapenem resistant Enterobacterales clinical isolates, were evaluated with the mCIM test comparing its performance to multiplex PCR. The minimum inhibitory concentration susceptibility testing was done by the Etest method for imipenem, meropenem, and ertapenem. Results. The sensitivity of the mCIM assay was 94% (95% CI, (89.3-97.1)). In Saudi Arabia and Bahrain, OXA-48 was the most prevalent carbapenemase gene followed by NDM. Coexistence of multiple carbapenemase genes is reported in eleven cases. Conclusion. These findings indicate that the mCIM test is a reliable and simple assay for detecting the activity of carbapenemase in Enterobacterales, especially in resource-limited laboratories.
KW - Carbapenem resistant Enterobacterales
KW - Gulf region prevalence
KW - Modified carbapenem inactivation method
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U2 - 10.1099/JMM.0.001381
DO - 10.1099/JMM.0.001381
M3 - Article
C2 - 34232118
AN - SCOPUS:85111249339
SN - 0022-2615
VL - 70
JO - Journal of Medical Microbiology
JF - Journal of Medical Microbiology
IS - 7
M1 - 001381
ER -