Affiliation:
1. Department of Clinical Microbiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
2. Department of Microbiology, Faculty of Pharmacy, Meijo University, Nagoya, Japan
Abstract
The presence of
Haemophilus influenzae
strains with low susceptibility to quinolones has been reported worldwide. However, the emergence and dissemination mechanisms remain unclear. In this study, a total of 14 quinolone-low-susceptible
H. influenzae
isolates were investigated phylogenetically and
in vitro
resistance transfer assay in order to elucidate the emergence and dissemination mechanisms.
The phylogenetic analysis based on
gyrA
sequences showed that strains with the same sequence type determined by multilocus sequence typing were classified into different clusters, suggesting that
H. influenzae
quinolone resistance emerges not only by point mutation, but also by the horizontal transfer of mutated
gyrA
. Moreover, the
in vitro
resistance transfer assay confirmed the horizontal transfer of quinolone resistance and indicated an active role of extracellular DNA in the resistance transfer. Interestingly, the horizontal transfer of
parC
only occurred in those cells that harbored a GyrA with amino acid substitutions, suggesting a possible mechanism of quinolone resistance in clinical settings. Moreover, the uptake signal and uptake-signal-like sequences located downstream of the quinolone resistant-determining regions of
gyrA
and
parC
, respectively, contributed to the horizontal transfer of resistance in
H. influenzae
.
Our study demonstrates that the quinolone resistance of
H. influenzae
could emerge due to the horizontal transfer of
gyrA
and
parC
via recognition of an uptake signal sequence or uptake-signal-like sequence. Since the presence of quinolone-low-susceptible
H. influenzae
with amino acid substitutions in GyrA have been increasing in recent years, it is necessary to focus our attention to the acquisition of further drug resistance in these isolates.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
6 articles.
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