Harnessing efficient multiplex PCR methods to detect the expanding Tet(X) family of tigecycline resistance genes

Virulence. 2020 Dec;11(1):49-56. doi: 10.1080/21505594.2019.1706913.

Abstract

A growing number of tet(X)-type tigecycline resistance determinants [tet(X1) to tet(X5)] constitutes an expanding family of tetracycline-inactivating enzymes, posing a potential risk to global public health. Here, we report the development of an efficient multiplex PCR method to detect the family of tet(X) variants. This method is successfully applied in the screen and validation of tet(X) genes in the field and clinic bacterial samples. In addition, we found that the formerly proposed tet(X1) is a premature truncated version by the inappropriate annotation, and fixed this error. Overall, it might be the first genetic tool for the detection of different Tet(X) members.

Keywords: Antimicrobial resistance; Multiplex PCR; Tet(X); Tet(X1); Tet(X2); Tet(X3); Tet(X4); Tet(X5); Tigecycline resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacterial Proteins / genetics
  • Genes, Bacterial / genetics*
  • Multiplex Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity
  • Tetracycline Resistance / genetics*
  • Tigecycline

Substances

  • Bacterial Proteins
  • Tet M resistance protein, Bacteria
  • Tigecycline

Grants and funding

This work was supported by the National Natural Science Foundation of China [31830001, 81772142 & 31570027, for YF; 31760437, for CJ] and National Key R&D Program of China [2017YFD0500202]. Dr. Feng is a recipient of the national “Young 1000 Talents” Award of China.