Lateral Flow Immunoassay and the EDTA-Colistin Broth Disk Elution for mcr-1 gene detection in colistin-resistant E. coli and K. pneumoniae
Keywords:
Edetic Acid, Enterobacteriaceae, Genes, Immunoassay, PlasmidsAbstract
Introduction: The global emergence of colistin-resistant Enterobacterales, especially strains carrying plasmid-mediated mcr genes, poses a significant threat to public health. Rapid detection of mcr-mediated resistance is critical for timely clinical management and infection control, particularly in resource-limited settings such as Southeast Asia.
Objectives: To evaluate the performance of the lateral flow immunoassay (NG-Test MCR-1) in comparison with the combined reference method of EDTA-Colistin Broth Disk Elution (CBDE/EDTA) and polymerase chain reaction (PCR) for detecting mcr-mediated colistin.
Methods: A cross-sectional study was conducted at Cho Ray Hospital, Ho Chi Minh City, Vietnam. A total of 160 clinical isolates of Klebsiella pneumoniae (n = 128) and Escherichia coli (n = 32), along with 2 additional E. coli strains carrying the mcr-1 gene, were tested for colistin resistance using Broth Microdilution (BMD) combined with the NG-Test MCR-1 in comparison with the CBDE/EDTA combined with PCR detection of mcr-1 to mcr-10.
Results: Among 32/160 colistin-resistant isolates, only 2 E. coli strains were confirmed to carry mcr-1 by both NG-Test MCR-1 and PCR, while no K. pneumoniae isolates tested positive for mcr genes. The NG-Test MCR-1 showed perfect agreement with the CBDE/EDTA method combined with PCR. Furthermore, it achieved 100% PPA and NPA, with wide 95% confidence intervals due to the limited number of mcr-positive isolates.
Conclusions: NG Test MCR-1 provides rapid, specific detection of mcr-1, while CBDE/EDTA is a cost-effective screening tool but less definitive. Combining these methods is recommended to improve mcr-mediated colistin resistance detection.
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