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Identifying Antimicrobial Resistance Genes with DNA Microarrays

By Douglas R. Call, Marlene K. Bakko, Melissa J. Krug and Marilyn C. Roberts


We developed and tested a glass-based microarray suitable for detecting multiple tetracycline (tet) resistance genes. Microarray probes for 17 tet genes, the β-lactamase blaTEM-1 gene, and a 16S ribosomal DNA gene (Escherichia coli) were generated from known controls by PCR. The resulting products (ca. 550 bp) were applied as spots onto epoxy-silane-derivatized, Teflon-masked slides by using a robotic spotter. DNA was extracted from test strains, biotinylated, hybridized overnight to individual microarrays at 65°C, and detected with Tyramide Signal Amplification, Alexa Fluor 546, and a microarray scanner. Using a detection threshold of 3× the standard deviation, we correctly identified tet genes carried by 39 test strains. Nine additional strains were not known to harbor any genes represented on the microarray, and these strains were negative for all 17 tet probes as expected. We verified that R741a, which was originally thought to carry a novel tet gene, tet(I), actually harbored a tet(G) gene. Microarray technology has the potential for screening a large number of different antibiotic resistance genes by the relatively low-cost methods outlined in this paper

Topics: Mechanisms of Resistance
Publisher: American Society for Microbiology
Year: 2003
DOI identifier: 10.1128/AAC.47.10.3290-3295.2003
OAI identifier: oai:pubmedcentral.nih.gov:201141
Provided by: PubMed Central
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