Development of a Multiplex Real-Time PCR Assay for Rapid Detection of Tigecycline Resistance Gene tet(X) Variants from Bacterial, Fecal, and Environmental Samples.

Abstract:

:We developed a multiplex real-time SYBR green-based PCR assay for rapid detection of tet(X) and its variants, including tet(X1) and tet(X2) and high-level tigecycline resistance genes tet(X3), tet(X4), and tet(X5). We showed that the real-time PCR assay developed had high linearity (R2 ≥ 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.

authors

Fu Y,Liu D,Song H,Liu Z,Jiang H,Wang Y

doi

10.1128/AAC.02292-19

subject

Has Abstract

pub_date

2020-03-24 00:00:00

issue

4

eissn

0066-4804

issn

1098-6596

pii

AAC.02292-19

journal_volume

64

pub_type

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