, 2007). Subsequently, Pal and co-workers demonstrated that Lmp1-deficient spirochetes were severely defective in their ability to persist in murine tissues, especially in the heart, and that Lmp1
deficiency increased B. burgdorferi susceptibility to the bactericidal effects of immune sera in vitro (Yang et al., 2009). Interestingly, Lmp1 mutants survived and persisted in SCID murine tissues, suggesting that Lmp1 is needed to help Alpelisib mw B. burgdorferi resist or evade the host-adaptive immune response (Yang et al., 2009). Lmp1 is a relatively large, 128-kDa surface-exposed protein predicted to contain three distinct domains of similar length: an N-terminal region (Lmp1-N) with no known conserved structural motifs, a middle domain (Lmp1-M) containing seven unique 54-residue repeats, and a C-terminal domain (Lmp1-C) rich in tetratricopeptide (TPR) repeats (Yang et al., 2009). Preliminary studies indicate that the membrane-imbedded region is contained in the N-terminal domain, and in comparison with Lmp1-M and Lmp1-C domains, the immunogenic Lmp1-N domain may be most important for spirochete survival in the murine host (Yang et al., 2010). The functions of the other two Lmp1 domains are currently not well understood, and the significance of the unique Lmp1-M repeats and of the Lmp1-C TPRs is unclear. TPR structures are ubiquitous in prokaryotic and eukaryotic proteins, and they
are specifically involved in protein–protein interactions (Sikorski et al., 1990; D’Andrea & Regan, 2003). Interestingly, IFA data suggest that Lmp1-C, in addition to Lmp1-N, is surface exposed, https://www.selleckchem.com/products/Erlotinib-Hydrochloride.html suggesting that
the C-terminal TPRs may be interacting with host proteins at the B. burgdorferi surface to aid in spirochete survival during mammalian infection. In silico analyses identified BesC (Borrelia efflux system protein C) as a chromosomally encoded ortholog of the E. coli OM channel protein TolC (Bunikis et al., 2008). Protein products of besC (ORF bb0142) and the co-transcribed upstream genes dipyridamole besA (bb0141) and besB (bb0140) are predicted to form a bacterial resistance-nodulation-division (RND)-type protein export system known to be involved in multidrug resistance (Yen et al., 2002; Nikaido, 2003). RND complexes are composed of three protein components: an inner membrane (IM)-localized antiporter protein, a periplasmic membrane fusion protein (MFP), and an OM channel protein, also known as OM factor (OMF; Yen et al., 2002; Nikaido, 2003; Nikaido & Takatsuka, 2009). Bunikis et al. (2008) demonstrated that B. burgdorferi BesC deletion mutants were 2- to 64-fold more sensitive than the wild-type strain to various antimicrobial agents when tested for susceptibility in vitro. Additionally, BesC was found to possess channel-forming activity, with a large conductance of 11 nS in 1 M KCl (Bunikis et al., 2008).