Lyme disease is the most prevalent tick-borne disease in the USA and affects the heart, joints, skin, musculoskeletal and nervous systems. Recently, the reported cases in the USA have increased to e20,000 per year. The causative agent, Borrelia burgdorferi, often persists in the face of a strong immune response and can result in incapacitating chronic disease manifestations, such as arthritis or neuroborreliosis. My long-term goal is to describe the host-bacterial interactions essential for establishment of the bacterial infection and consequently Lyme disease. Colonization of various tissues by many microbial pathogens requires attachment to cells or extracellular matrix (ECM). Glycosaminoglycans (GAGs) are carbohydrate units of proteoglycans, which are ubiquitously expressed ECM components on mammalian cells. Our extensive studies show that GAG-binding is a major adherence mechanism of B. burgdorferi. Indeed, we have shown that B. burgdorferi produces several GAG- binding adhesins, including, (i) DbpA and DbpB, (ii) Borrelia GAG-binding Protein (Bgp), and (iii) BBK32. Consistent with the multiplicity of GAG-binding adhesins, mutants lacking one or two documented adhesins of Lyme spirochetes retain some degree of infectivity. B. burgdorferi dbpA-dbpB double deletion mutants, generated in a variety of strain backgrounds, our B. burgdorferi bgp mutants, and bbk32 mutants remain infectious in immunocompetent mice. At least first three of these exhibit colonization defect. Bgp also exhibits 5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase activity. However, it is not known if the colonization defect of the bgp mutant is related to its GAG-binding activity, its nucleosidase activity, or both. To determine if the defect in colonization by a bgp mutant is related to its GAG-binding, its enzymatic activity, or both, and whether Bgp displays partial functional redundancy with other GAG-binding adhesins, the following aims will be pursued. (1). Delineate the GAG-binding and MTA/SAH nucleosidase activities of Bgp. (2). Define the activity of Bgp required for colonization during infection. (3). Assess the functional redundancy of Bgp with other GAG-binding adhesins during colonization. Significance. We first recognized Bgp as a multifunctional surface protein, observed its role in tissue colonization during mouse infection, and determined it to be a target of novel drugs. This study will genetically delineate two activities of Bgp to assess if one or both activities are required during infection. We will also determine if defect in Bgp and DbpA-DbpB production is additive or each contribute to the tissue- specific colonization by B. burgdorferi. Such an understanding of the spirochete-GAG interactions involving Bgp, DbpA and DbpB, on Lyme pathogenesis and of the role of Bgp as a metabolic enzyme could help design better diagnostic tests and facilitate the development of novel treatment strategies, especially for the later stages of Lyme disease.

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Glycosamioglycan-mediated adherence of Lyme spirochetes to various mammalian cells appears to be a critical initial step during infection and also plays an important contribution in tissue colonization. Bgp is a GAG-binding adhesin that also exhibits 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase activity. We will evaluate importance of these two activities of Bgp for infection in the mouse model and determine if Bgp-DbpA and DbpB are the major GAG-binding proteins required for B. burgdorferi pathogenesis.

National Institute of Health (NIH)
National Institute of Allergy and Infectious Diseases (NIAID)
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Bacterial Pathogenesis Study Section (BACP)
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Breen, Joseph J
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University of Medicine & Dentistry of NJ
Schools of Medicine
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Schlachter, Samantha; Seshu, Janakiram; Lin, Tao et al. (2018) The Borrelia burgdorferi Glycosaminoglycan Binding Protein Bgp in the B31 Strain Is Not Essential for Infectivity despite Facilitating Adherence and Tissue Colonization. Infect Immun 86:
Bhanot, Purnima; Parveen, Nikhat (2018) Investigating disease severity in an animal model of concurrent babesiosis and Lyme disease. Int J Parasitol :
Primus, Shekerah; Akoolo, Lavoisier; Schlachter, Samantha et al. (2018) Efficient detection of symptomatic and asymptomatic patient samples for Babesia microti and Borrelia burgdorferi infection by multiplex qPCR. PLoS One 13:e0196748
Djokic, Vitomir; Akoolo, Lavoisier; Parveen, Nikhat (2018) Babesia microti Infection Changes Host Spleen Architecture and Is Cleared by a Th1 Immune Response. Front Microbiol 9:85
Primus, Shekerah; Akoolo, Lavoisier; Schlachter, Samantha et al. (2018) Screening of patient blood samples for babesiosis using enzymatic assays. Ticks Tick Borne Dis 9:302-306
Schlachter, Samantha; Chan, Kamfai; Marras, Salvatore A E et al. (2017) Detection and Differentiation of Lyme Spirochetes and Other Tick-Borne Pathogens from Blood Using Real-Time PCR with Molecular Beacons. Methods Mol Biol 1616:155-170
Chan, Kamfai; Alter, Laura; Barthold, Stephen W et al. (2015) Disruption of bbe02 by Insertion of a Luciferase Gene Increases Transformation Efficiency of Borrelia burgdorferi and Allows Live Imaging in Lyme Disease Susceptible C3H Mice. PLoS One 10:e0129532
Chan, Kamfai; Marras, Salvatore A E; Parveen, Nikhat (2013) Sensitive multiplex PCR assay to differentiate Lyme spirochetes and emerging pathogens Anaplasma phagocytophilum and Babesia microti. BMC Microbiol 13:295
Chan, Kamfai; Awan, Mehwish; Barthold, Stephen W et al. (2012) Comparative molecular analyses of Borrelia burgdorferi sensu stricto strains B31 and N40D10/E9 and determination of their pathogenicity. BMC Microbiol 12:157
Chan, Kamfai; Casjens, Sherwood; Parveen, Nikhat (2012) Detection of established virulence genes and plasmids to differentiate Borrelia burgdorferi strains. Infect Immun 80:1519-29