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Reduction of the Carbapenemase Inactivation Method (CIM) assay time by real-time PCR.
Haque, F; Fisseha, S; Athamanolap, P; Tower, R; Ortega, J; Dominguez, C; Maruca, T; Torpey, D; Myers, R; Laksanalamai, P.
Affiliation
  • Haque F; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Fisseha S; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Athamanolap P; Department of Biomedical Engineering, Faculty of Engineering, Mahidol University, 999 Phuttamonthon4 Road, Salaya, Nakhon Pathom 73170, Thailand.
  • Tower R; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Ortega J; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Dominguez C; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Maruca T; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Torpey D; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Myers R; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America.
  • Laksanalamai P; Maryland Department of Health, Laboratories Administration, 1770 Ashland Ave., Baltimore, MD 21205, United States of America. Electronic address: pongpan.laksanalamai@maryland.gov.
J Microbiol Methods ; 178: 106072, 2020 Oct 06.
Article in En | MEDLINE | ID: mdl-33031896
ABSTRACT
Carbapenemase Inactivation Method (CIM) is a test to detect presence of the carbapenemase in Gram-negative bacteria. Determination of the carbapenemase production by inactivation of meropenem requires that a zone of control E. coli inhibition be measured approximately 6-24 h after plating. We have modified the CIM test by developing a rapid method which instead measures the growth of E. coli indicator strain ATCC 25922 using real-time PCR, referred to as a nucleic acid testing CIM (natCIM). Our natCIM, therefore reduces the detecting time from 6 to 24 h to approximately 4 h.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Microbiol Methods Year: 2020 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Microbiol Methods Year: 2020 Document type: Article Affiliation country: Estados Unidos