Despite considerable advances in our understanding of borrelial differential gene expression, the molecular interactions and regulatory events that enable Borrelia burgdorferi to cycle between its arthropod vector and mammal host are not well understood. The studies presented in this proposal are predicated on the notion that a more thorough analysis of Bb within infected ticks will provide valuable insight into the virulence-related processes involved in spirochete transmission. Our preliminary studies using a GFP+ strain 297 isolate challenge the conventional thinking of how Bb migrate out of the nymphal midgut during feeding. During the bloodmeal, Bb replicate within the tick midgut as non-motile networks, gaining access to the basement membrane by taking advantage of the weakness created by midgut remodeling. Bb then undergo a dramatic transition from the non-motile networks to individual motile organisms that are able to penetrate through the MG epithelium into the hemocoel, migrate to the salivary glands, and ultimately, infect mammalian host tissues. In this application, we propose using a combination of molecular, genetic and microscopic imaging methodologies to more precisely delineate the interactions that occur between the Lyme disease spirochete and its arthropod vector throughout the feeding process. By refining our understanding of the interplay between spirochetal and tick factors, we will further our long-term objective to identify borrelial, as well as ixodid, gene products and regulatory pathways that promote spirochete dissemination within both ticks and mammals. By identifying key components acting at the pathogen-vector interface, we will be setting the stage for the development of novel therapeutic strategies, including vaccine candidates capable of blocking transmission to, as well as dissemination within, the human host.

Public Health Relevance

Borrelia burgdorferi (Bb), the causative agent of Lyme disease (LD), is maintained within nature by an enzootic life cycle that involves an Ixodes tick vector and a mammalian host, typically wild rodents. The studies presented in this proposal are predicated on the notion that a more thorough analysis of spirochetes within ticks will provide valuable insight into how Bb is transmitted to its reservoir host and humans. By refining our understanding of the interplay between Bb and the tick midgut epithelium, we will further our long-term objective to identify borrelial, as well as tick, gene products and regulatory pathways that promote maintenance of Bb within its tick-mouse infectious cycle.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
1R03AI085248-01A1
Application #
7990585
Study Section
Vector Biology Study Section (VB)
Program Officer
Breen, Joseph J
Project Start
2010-06-04
Project End
2012-05-31
Budget Start
2010-06-04
Budget End
2011-05-31
Support Year
1
Fiscal Year
2010
Total Cost
$76,500
Indirect Cost
Name
University of Connecticut
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030
Miller, Daniel P; Oliver Jr, Lee D; Tegels, Brittney K et al. (2016) The Treponema denticola FhbB Protein Is a Dominant Early Antigen That Elicits FhbB Variant-Specific Antibodies That Block Factor H Binding and Cleavage by Dentilisin. Infect Immun 84:2051-2058
Caimano, Melissa J; Dunham-Ems, Star; Allard, Anna M et al. (2015) Cyclic di-GMP modulates gene expression in Lyme disease spirochetes at the tick-mammal interface to promote spirochete survival during the blood meal and tick-to-mammal transmission. Infect Immun 83:3043-60
Iyer, Radha; Caimano, Melissa J; Luthra, Amit et al. (2015) Stage-specific global alterations in the transcriptomes of Lyme disease spirochetes during tick feeding and following mammalian host adaptation. Mol Microbiol 95:509-38
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Miller, D P; McDowell, J V; Rhodes, D V et al. (2013) Sequence divergence in the Treponema denticola FhbB protein and its impact on factor H binding. Mol Oral Microbiol 28:316-30
Salman-Dilgimen, Aydan; Hardy, Pierre-Olivier; Radolf, Justin D et al. (2013) HrpA, an RNA helicase involved in RNA processing, is required for mouse infectivity and tick transmission of the Lyme disease spirochete. PLoS Pathog 9:e1003841
Radolf, Justin D; Caimano, Melissa J; Stevenson, Brian et al. (2012) Of ticks, mice and men: understanding the dual-host lifestyle of Lyme disease spirochaetes. Nat Rev Microbiol 10:87-99
Dunham-Ems, Star M; Caimano, Melissa J; Eggers, Christian H et al. (2012) Borrelia burgdorferi requires the alternative sigma factor RpoS for dissemination within the vector during tick-to-mammal transmission. PLoS Pathog 8:e1002532
Harman, Michael W; Dunham-Ems, Star M; Caimano, Melissa J et al. (2012) The heterogeneous motility of the Lyme disease spirochete in gelatin mimics dissemination through tissue. Proc Natl Acad Sci U S A 109:3059-64
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

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