机构:[1]Department of Clinical Laboratory, The Second Affiliated Hospital of Soochow University, Suzhou 215004, Jiangsu, People’s Republic of China[2]Public Health Research Institute Center, New Jersey Medical School, Rutgers University, Newark, NJ 07103, USA
Bacterial antimicrobial resistance has been associated with the up regulation of genes encoding efflux pumps and the down regulation of genes encoding outer membrane proteins (OMPs). Gene expression in bacteria is primarily initiated by sigma factors (sigma factors) such as RpoE, which plays an important role in responding to many environmental stresses. Here, we report the first observation that RpoE serves as an antibiotic resistance regulator in Salmonella enteric serovar Typhi (S. Typhi). In this study, we found that the rpoE mutant (Delta rpoE) of S. Typhi GIFU10007 has elevated resistance to several antimicrobial agents, including beta-lactams, quinolones, and aminoglycosides. Genomic DNA microarray analysis was used to investigate the differential gene expression profiles between a wild type and rpoE mutant in response to ampicillin. The results showed that a total of 57 genes displayed differential expression (two-fold increase or decrease) in Delta rpoE versus the wild-type strain. The expressions of two outer membrane protein genes, ompF and ompC, were significantly down-regulated in Delta rpoE (six and seven-fold lower in comparison to wild-type strain) and RamA, a member of the efflux pump AraC/XylS family, was up-regulated about four-fold in the Delta rpoE. Our results suggest RpoE is a potential antimicrobial regulator in S. Typhi, controlling both the down regulation of the OMP genes and up-regulating the efflux system.
基金:
This study was supported by the National Natural
Science Foundation of China (No. 81572032), Jiangsu Key
Laboratory of Medical Science and Laboratory Medicine (JSKLM-
2014-015) and the startup fund of the Second Affiliated Hospital of
Soochow University (No. SDFEYGJ1301). This study was partially
supported by a grant (to B.N.K.) from the National Institutes of
Health (1R01AI090155).