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Identification of the Novel Lincosamide Resistance Gene lnu (E) Truncated by ISEnfa5-cfr-IS Enfa5 Insertion in Streptococcus suis: De Novo Synthesis and Confirmation of Functional Activity in Staphylococcus aureus
Author(s) -
Qin Zhao,
Sarah Wendlandt,
Hui Li,
Jun Li,
Congming Wu,
Jianzhong Shen,
Štefan Schwarz,
Yang Wang
Publication year - 2013
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.02007-13
Subject(s) - lincomycin , biology , streptococcus suis , shuttle vector , gene , lincosamides , microbiology and biotechnology , genetics , staphylococcus aureus , bacteria , vector (molecular biology) , antibiotics , recombinant dna , virulence
The novel lincosamide resistance gene lnu(E), truncated by insertion of an ISEnfa5-cfr-ISEnfa5 segment, was identified in Streptococcus suis. The gene lnu(E) encodes a 173-amino-acid protein with ≤69.4% identity to other lincosamide nucleotidyltransferases. The lnu(E) gene and its promoter region were de novo synthesized, and Staphylococcus aureus RN4220 carrying a shuttle vector with the cloned lnu(E) gene showed a 16-fold increase in the lincomycin MIC. Mass spectrometry experiments demonstrated that Lnu(E) catalyzed the nucleotidylation of lincomycin.

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