Evaluating the accuracy of the MBT Lipid Xtract Kit for assessing colistin resistance in comparison to broth microdilution

Author:

Lo Calvin Ka-Fung1ORCID,Ritchie Gordon21ORCID,Bilawka Jennifer2,Gowland Leah2,Chorlton Samuel D.3ORCID,Jang Willson2,Matic Nancy21ORCID,Romney Marc G.21ORCID,Stefanovic Aleksandra21ORCID,Lowe Christopher F.12ORCID

Affiliation:

1. Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada

2. Division of Medical Microbiology and Virology, Providence Health Care, St. Paul’s Hospital, Vancouver, British Columbia, Canada

3. BugSeq Bioinformatics, Vancouver, British Columbia, Canada

Abstract

Colistin resistance testing methods such as broth microdilution (BMD) are time-consuming and labour intensive for clinical laboratories. MBT Lipid Xtract Kit on MALDI Biotyper Sirius System (Bruker, Billerica, MA, USA) utilizes lipidomic analysis to identify specific cell wall modifications associated with colistin resistance. We compared MBT to BMD (ComASP Colistin, Liofilchem) across 36 Gram-negative isolates (non-resistant MIC ≤2 µg ml−1, resistant MIC ≥4 µg ml−1). All samples were tested twice on MBT with discrepant results repeated before assessing categorical agreement between MBT and BMD. 44.4% (16/36) of isolates were colistin resistant via BMD. MBT Lipid Xtract had 80.6% agreement (29/36) with BMD, with 5/7 discrepancies corrected to match upon repeat testing. There was 100% agreement for Escherichia coli isolates (n=16). The whole-genome sequencing was completed on the two discrepant Klebsiella pneumoniae isolates, with variants within colistin resistance-associated loci identified (MIC 0.5 µg ml−1: arnC S30T, pmrB T246A, lapB N212T, lpxM S253G, crrB Q287K and MIC >16 µg ml−1: arnC S30T, pmrB R90insRN, pmrB T246A, pmrA E57G, lpxM S253G). Further evaluation, particularly for non-E. coli, of MBT is required prior to implementation in clinical laboratories.

Publisher

Microbiology Society

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