TY - JOUR
T1 - Identification and molecular characterisation of CmeB, a Campylobacter jejuni multidrug efflux pump
AU - Pumbwe, Lilian
AU - Piddock, Laura
PY - 2002/1/1
Y1 - 2002/1/1
N2 - A multidrug efflux pump gene (cmeB) was identified from the published Campylobacter jejuni genome sequence. Secondary structural analysis showed that the gene encoded a protein belonging to the resistance nodulation cell division (RND) family of efflux transporters. The gene was inactivated by insertional mutagenesis. Compared with the wild-type strain (NCTC 11168), the resultant knockout strain (NCTC 11168-cmeB::kan(r)) displayed increased susceptibility to a range of antibiotics including beta-lactams, fluoroquinolones, macrolides, chloramphenicol, tetracycline, ethidium bromide, the dye acridine orange and the detergent sodium dodecyl sulfate. Accumulation of ciprofloxacin was increased in the knockout mutant, but carbonyl cyanide m-chlorophenyl hydrazone, a proton motive force inhibitor, had less effect upon ciprofloxacin accumulation in the knockout mutant compared with NCTC 11168. These data show that the identified gene encodes an RND-type multi-substrate efflux transporter, which contributes to intrinsic resistance to a range of structurally unrelated compounds in C. jejuni. This efflux pump has been named CmeB (for Campylobacter multidrug efflux).
AB - A multidrug efflux pump gene (cmeB) was identified from the published Campylobacter jejuni genome sequence. Secondary structural analysis showed that the gene encoded a protein belonging to the resistance nodulation cell division (RND) family of efflux transporters. The gene was inactivated by insertional mutagenesis. Compared with the wild-type strain (NCTC 11168), the resultant knockout strain (NCTC 11168-cmeB::kan(r)) displayed increased susceptibility to a range of antibiotics including beta-lactams, fluoroquinolones, macrolides, chloramphenicol, tetracycline, ethidium bromide, the dye acridine orange and the detergent sodium dodecyl sulfate. Accumulation of ciprofloxacin was increased in the knockout mutant, but carbonyl cyanide m-chlorophenyl hydrazone, a proton motive force inhibitor, had less effect upon ciprofloxacin accumulation in the knockout mutant compared with NCTC 11168. These data show that the identified gene encodes an RND-type multi-substrate efflux transporter, which contributes to intrinsic resistance to a range of structurally unrelated compounds in C. jejuni. This efflux pump has been named CmeB (for Campylobacter multidrug efflux).
KW - multiple antibiotic resistance
KW - Campylobacter jejuni
KW - Campylobacter multidrug efflux B
KW - efflux
UR - http://www.scopus.com/inward/record.url?scp=0037050288&partnerID=8YFLogxK
U2 - 10.1111/j.1574-6968.2002.tb11007.x
DO - 10.1111/j.1574-6968.2002.tb11007.x
M3 - Article
C2 - 11814661
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
SN - 1574-6968
VL - 206
SP - 185
EP - 189
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 2
ER -