Upon transmission by a vector tick, Lyme disease spirochetes can establish a local skin infection, then may disseminate further to multiple tissues. Interactions with mammalian cells and extracellular matrix (ECM) are critical for colonization of diverse sites, and many B. burgdorferi adhesins that bind to cells or extracellular matrix (ECM) have been identified. The large number of adhesins, as well as the sequence variability of some, is likely to promote chronic multisystem disease and contribute to the noted diversity of human Lyme disease. Understanding this infection is complicated by the diversity of target tissues, multifunctionality of adhesins, and complexity of colonization (e.g. bloodstream survival, vascular adherence, tissue invasion, and escape from immune surveillance). To organize the plethora of receptor-ligand interactions into a framework for understanding the multisystem nature of Lyme disease, the three collaborators have taken multi-faceted genetic, biochemical and imaging approaches to fully characterize known B. burgdorferi adhesins, to discover and validate new adhesins, and to probe the functions of the full repertoire of B. burgdorferi adhesins using in vitro and in vivo models. These approaches led to important new insights into the known adhesins DbpA, BBK32, and P66, and defined new adhesive functions for the OspF subfamily and for OspC, which was previously shown to be essential for full infectivity. We showed that DbpA and OspC variants are associated with different tissue tropisms, so strain-specific differences in the repertoire of adhesins may contribute to corresponding differences in clinical manifestations. We found that BBK32 and P66 have roles in vascular adherence and joint invasion, and the interactions they mediate with the vascular endothelium may reflect sequential activities analogous to those involved in lymphocyte transmigration. We hypothesize that B. burgdorferi utilizes a multitude of adhesins with distinct activities to negotiate successie steps in a multiphasic and multisystem infection. In addition, sequence variation of a subset of adhesins may promote colonization of distinct sites and contribute to strain-specific differences in tissue tropism and disease. To gain a detailed understanding of how the diverse host cell interactions mediated by the complex repertoire of B. burgdorferi adhesins coordinate vascular attachment, tissue invasion and long-term colonization of diverse tissues, we will use the power of B. burgdorferi genetic systems and diverse mouse infection models. We will expand and fully characterize B. burgdorferi adhesins that promote interactions with endothelium to define the adhesin-ligand interactions that are required for dissemination and long-term colonization of mouse tissues. We will also characterize the role of each of these interactions in promoting the multiple steps required to attach to the vascular endothelium, to transmigrate across this barrier to stably colonize tissue. The proposed work will organize complex adhesive pathways into functional groups that mediate discrete steps in the infectious processes that together result in systemic Lyme borreliosis and disseminated, persistent infection in the mouse.

Public Health Relevance

Lyme disease is the most prevalent vector-borne illness in the northern hemisphere, is continuing to expand in geographic range and case numbers, and is a significant burden on the health system in endemic regions. The causative organism, Borrelia burgdorferi, produces a complex array of proteins (adhesins) that bind to mammalian tissue components and that contribute to the ability of the bacteria to cause infection in mice. The three principal investigators of this application together are a team with unique expertise that wil allow comprehensive investigations of the functions of these B. burgdorferi adhesins. Each adhesin has unique biochemical activities that affect tissue targeting by the bacteria and therefore may be excellent candidates for development as vaccines or as targets for therapeutic interventions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI118799-03
Application #
9402006
Study Section
Bacterial Pathogenesis Study Section (BACP)
Program Officer
Ilias, Maliha R
Project Start
2016-01-15
Project End
2020-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
937639060
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Caine, Jennifer A; Lin, Yi-Pin; Kessler, Julie R et al. (2017) Borrelia burgdorferi outer surface protein C (OspC) binds complement component C4b and confers bloodstream survival. Cell Microbiol 19: