Affiliation:
1. Department of Bacteriology
2. Department of Infection Control Science
3. Faculty of Medicine, Juntendo University, 2-1-1 Bunkyo-Ku, Tokyo 113-8421, Japan
Abstract
ABSTRACT
We have previously reported the establishment of a
Staphylococcus aureus
laboratory strain, 10*3d1, having reduced susceptibility to daptomycin and heterogeneous vancomycin-intermediate
S. aureus
(VISA) phenotype. The strain was generated
in vitro
by serial daptomycin selection (Camargo, I. L., H. M. Neoh, L. Cui, and K. Hiramatsu, Antimicrob. Agents Chemother. 52:4289-4299, 2008). Here we explored the genetic mechanism of resistance in the strain by whole-genome sequencing and by producing gene-replaced strains. By genome comparison between 10*3d1 and its parent methicillin-resistant
Staphylococcus aureus
(MRSA) strain N315ΔIP, we identified five nonsynonymous single nucleotide polymorphisms (SNPs). One of the five mutations was found in the
rpoB
gene encoding the RNA polymerase β subunit. The mutation at nucleotide position 1862 substituted the 621st alanine by glutamic acid. The replacement of the intact
rpoB
with the mutated
rpoB
, designated
rpoB(A621E)
, conferred N315ΔIP with the phenotypes of reduced susceptibility to daptomycin and hetero-VISA. The
rpoB(A621E)
-mediated resistance conversion was accompanied by a thickened cell wall and reduction of the cell surface negative charge. Being consistent with these phenotypic changes, microarray data showed that the expression of the
dlt
operon, which increases the cell surface positive charge, was enhanced in the
rpoB(A621E)
mutant. Other remarkable findings of microarray analysis of the
rpoB(A621E)
mutant included repression of metabolic pathways of purine, pyrimidine, arginine, the urea cycle, and the
lac
operon, enhancement of the biosynthetic pathway of vitamin B2, K1, and K2, and cell wall metabolism. Finally, mutations identified in
rplV
and
rplC
, encoding 50S ribosomal proteins L22 and L3, respectively, were found to be associated with the slow growth, but not with the phenotype of decreased susceptibility to vancomycin and daptomycin, of 10*3d1.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology