Development of a Multiplex Real-Time PCR Assay for Rapid Detection of Tigecycline Resistance Gene (X) Variants from Bacterial, Fecal, and Environmental Samples
Overview
Affiliations
We developed a multiplex real-time SYBR green-based PCR assay for rapid detection of (X) and its variants, including (X1) and (X2) and high-level tigecycline resistance genes (X3), (X4), and (X5). We showed that the real-time PCR assay developed had high linearity ( ≥ 0.996), sensitivity (low detection limit), and specificity (only the target gene could be amplified significantly) and further evaluated it using bacterial, fecal, and environmental samples.
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