Lyme disease is a major public health problem worldwide and is the most common arthropod- borne infection in the United States. Borrelia burgdorferi, which is the cause of Lyme disease in North America, is an extracellular pathogen that has the unique ability to evade the host immune response and infect individuals for years to decades. To gain a better understanding of how this organism persists in the infected mammal, many laboratories, including our own, have focused on identifying and characterizing outer surface proteins of B. burgdorferi. Since the interface between B. burgdorferi and its mammalian host is its outer surface, proteins localized in the outer membrane must play an important role in dissemination, virulence, tissue tropism, and, ultimately, immune evasion. Over the last funding period, we have identified and focused on several outer surface lipoproteins (Osps) from B. burgdorferi. We have determined the role of numerous surface lipoproteins in pathogenesis and examined their potential as vaccine candidates. While we continue to be very productive in characterizing surface lipoproteins that are capable of binding factor H to help aid the spirochete in evading serum-mediated killing during the acute stage of infection, we have yet to identify a specific lipoprotein that could work as a potential vaccine candidate for Lyme disease. The lack of good vaccine efficacy for the various lipoproteins we have been characterizing over the last funding period prompted us to start identifying integral, membrane spanning, outer membrane proteins (OMPs) that could be used as more viable potential vaccine candidates for Lyme disease. These more recent studies also led us to discover the protein machinery required for chaperoning and assembling OMPs into the B. burgdorferi outer membrane. Although the mechanism of outer membrane biogenesis is poorly understood in spirochetes, our recent studies have indicated that a heterooligomeric OM protein beta-barrel assembly machine (BAM) complex is required for proper assembly of OMPs into the borrelial OM. The B. burgdorferi BAM complex is made up of the integral outer membrane protein BamA, and two additional periplasmic lipoproteins located in the inner leaflet of the outer membrane, BB0324 and BB0028. We have shown that the borrelial BAM complex is required for inserting OMPs into the borrelial outer membrane. The studies we propose in this revised, renewal application will allow us to characterize the BAM complex and examine in detail its role in export and translocation of OMPs to the surface of this spirochetal pathogen. A better understanding of the basic mechanisms by which the BAM complex chaperones and exports OMPs to the surface of B. burgdorferi will also allow us, for the first time, to begin elucidating the complete outer surface integral OMP content of B. burgdorferi. Additionally, since the BAM system is a conserved pathway for OMP export and localization among all Gram-negative bacteria, the studies outlined here could lead to the development of novel antibacterial compounds that could have an impact not only against pathogenic spirochetes such as B. burgdorferi and Treponema pallidum, but could potentially be widely applicable against other important human pathogens, such as E. coli, Salmonella, Vibrio, Pseudomonas, Neisseria, Helicobacter and others.
Our long-term goal is to characterize the Borrelia burgdorferi outer surface protein export machine, which we recently discovered. These initial mechanistic studies will allow us to then identify novel outer membrane proteins and other potential mechanisms that could be used to generate a new vaccine or disease modulating therapeutic for Lyme disease. Given that the integral outer membrane protein export machine we will be examining in B. burgdorferi is conserved, at some level, among all proteobacteria, our studies also could greatly benefit public health worldwide by identifying novel broad-spectrum antibacterials that could be used to treat many different devastating and important diseases in the United States and abroad.
|Kenedy, Melisha R; Scott 2nd, Edgar J; Shrestha, Binu et al. (2016) Consensus computational network analysis for identifying candidate outer membrane proteins from Borrelia spirochetes. BMC Microbiol 16:141|
|Dunn, Joshua P; Kenedy, Melisha R; Iqbal, Henna et al. (2015) Characterization of the Î²-barrel assembly machine accessory lipoproteins from Borrelia burgdorferi. BMC Microbiol 15:70|
|Kenedy, Melisha R; Luthra, Amit; Anand, Arvind et al. (2014) Structural modeling and physicochemical characterization provide evidence that P66 forms a *-barrel in the Borrelia burgdorferi outer membrane. J Bacteriol 196:859-72|
|Lenhart, Tiffany R; Kenedy, Melisha R; Yang, Xiuli et al. (2012) BB0324 and BB0028 are constituents of the Borrelia burgdorferi Î²-barrel assembly machine (BAM) complex. BMC Microbiol 12:60|
|Kenedy, Melisha R; Lenhart, Tiffany R; Akins, Darrin R (2012) The role of Borrelia burgdorferi outer surface proteins. FEMS Immunol Med Microbiol 66:1-19|
|Kenedy, Melisha R; Akins, Darrin R (2011) The OspE-related proteins inhibit complement deposition and enhance serum resistance of Borrelia burgdorferi, the lyme disease spirochete. Infect Immun 79:1451-7|
|Caimano, Melissa J; Kenedy, Melisha R; Kairu, Toru et al. (2011) The hybrid histidine kinase Hk1 is part of a two-component system that is essential for survival of Borrelia burgdorferi in feeding Ixodes scapularis ticks. Infect Immun 79:3117-30|
|Yang, Xiuli; Lenhart, Tiffany R; Kariu, Toru et al. (2010) Characterization of unique regions of Borrelia burgdorferi surface-located membrane protein 1. Infect Immun 78:4477-87|
|Lenhart, Tiffany R; Akins, Darrin R (2010) Borrelia burgdorferi locus BB0795 encodes a BamA orthologue required for growth and efficient localization of outer membrane proteins. Mol Microbiol 75:692-709|
|Kenedy, Melisha R; Vuppala, Santosh R; Siegel, Corinna et al. (2009) CspA-mediated binding of human factor H inhibits complement deposition and confers serum resistance in Borrelia burgdorferi. Infect Immun 77:2773-82|
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