In vivo expression technology identifies a novel virulence factor critical for Borrelia burgdorferi persistence in mice.
Ontology highlight
ABSTRACT: Analysis of the transcriptome of Borrelia burgdorferi, the causative agent of Lyme disease, during infection has proven difficult due to the low spirochete loads in the mammalian tissues. To overcome this challenge, we have developed an In Vivo Expression Technology (IVET) system for identification of B. burgdorferi genes expressed during an active murine infection. Spirochetes lacking linear plasmid (lp) 25 are non-infectious yet highly transformable. Mouse infection can be restored to these spirochetes by expression of the essential lp25-encoded pncA gene alone. Therefore, this IVET-based approach selects for in vivo-expressed promoters that drive expression of pncA resulting in the recovery of infectious spirochetes lacking lp25 following a three week infection in mice. Screening of app
SUBMITTER: Ellis TC
PROVIDER: S-EPMC3757035 | biostudies-literature | 2013
REPOSITORIES: biostudies-literature
ACCESS DATA