TY - JOUR
T1 - aadA Confers Streptomycin Resistance in Borrelia burgdorferi
AU - Frank, Kristi L.
AU - Bundle, Sharyl F.
AU - Kresge, Michele E.
AU - Eggers, Christian H.
AU - Samuels, D. Scott
PY - 2003/11
Y1 - 2003/11
N2 - To enhance genetic manipulation of the Lyme disease spirochete Borrelia burgdorferi, we assayed the aadA gene for the ability to confer resistance to the antibiotics spectinomycin and streptomycin. Using the previously described pBSV2 as a backbone, a shuttle vector, termed pKFSS1, which carries the aadA open reading frame fused to the B. burgdorferi flgb promoter was constructed. The hybrid flgb promoter-aadA cassette confers resistance to spectinomycin and streptomycin in both B. burgdorferi and Escherichia coli. pKFSS1 has a replication origin derived from the 9-kb circular plasmid and can be comaintained in B. burgdorferi with extant shuttle vector pCE320, which has a replication origin derived from a 32-kb circular plasmid, or pBSV2, despite the fact that pKFSS1 and pBSV2 have the same replication origin. Our results demonstrate the availability of a new selectable marker and shuttle vector for genetically dissecting B. burgdorferi at the molecular level.
AB - To enhance genetic manipulation of the Lyme disease spirochete Borrelia burgdorferi, we assayed the aadA gene for the ability to confer resistance to the antibiotics spectinomycin and streptomycin. Using the previously described pBSV2 as a backbone, a shuttle vector, termed pKFSS1, which carries the aadA open reading frame fused to the B. burgdorferi flgb promoter was constructed. The hybrid flgb promoter-aadA cassette confers resistance to spectinomycin and streptomycin in both B. burgdorferi and Escherichia coli. pKFSS1 has a replication origin derived from the 9-kb circular plasmid and can be comaintained in B. burgdorferi with extant shuttle vector pCE320, which has a replication origin derived from a 32-kb circular plasmid, or pBSV2, despite the fact that pKFSS1 and pBSV2 have the same replication origin. Our results demonstrate the availability of a new selectable marker and shuttle vector for genetically dissecting B. burgdorferi at the molecular level.
UR - http://www.scopus.com/inward/record.url?scp=0242407459&partnerID=8YFLogxK
U2 - 10.1128/JB.185.22.6723-6727.2003
DO - 10.1128/JB.185.22.6723-6727.2003
M3 - Article
C2 - 14594849
AN - SCOPUS:0242407459
SN - 0021-9193
VL - 185
SP - 6723
EP - 6727
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 22
ER -