The proposed collaborative project is based collectively on investigations of the pathogenesis and epidemiology of Lyme disease, the ecology, vector biology, and population genetics of vector-borne diseases, the molecular biology of Borrelia burgdorferi, and vaccine development. The emphases of the proposed studies are the evolutionary biology of B. burgdorferi and new strategies for Lyme disease prevention. The long term goals are the following: (1) To significantly reduce the risk of Lyme disease among humans and domestic animals by vaccine intervention in the natural maintenance cycle of B. burgdorferi in a highly endemic area. (2) To study the evolution of B. burgdorferi as an infectious agent through controlled intervention studies in a highly endemic area. (3)To provide for a vaccine that is highly effective and that can be expeditiously, safely, and inexpensively administered in the field. The hypotheses for the project are the following: (A) A high prevalence of anti-OspA antibodies among Peromyscus leucopus and/or other mammalian reservoirs in the field will reduce the transmission rate between reservoir hosts and vector ticks, thereby reducing the prevalence of B. burgdorferi infection in ticks. (B) Immunization of reservoirs in the field will not alter the population structure of B. burgdorferi at the vaccine field sites in comparison to the control sites. (C) Transmission-blocking immunity among P. leucopus and/or other mammalian reservoirs can be achieved by oral as well as by parenteral immunization with a single immunogen or combined immunogens.
The specific aims are the following: (1) Field studies of the effect of immunization of P. leucopus on the rate of transmission of B. burgdorferi between reservoir host and vector ticks. (2) Assessment of the effects of vaccine intervention in the field on the population structure of B. burgdorferi in ticks and in vertebrate reservoirs. (3) Further development of single-vaccination and orally-delivered field vaccines and evaluation of second, supplementary antigens. The proposed studies may provide insights as molecular, organismal, and population levels about B. burgdorferi, its transmission, and reservoir host immunize responses. The results may also have relevance for the control of other vector-bone zoonotic diseases and perhaps for development of novel methods for vaccine delivery.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI037248-08
Application #
6510576
Study Section
Special Emphasis Panel (ZRG1-SSS-K (03))
Program Officer
Baker, Phillip J
Project Start
1994-09-30
Project End
2005-04-30
Budget Start
2002-05-01
Budget End
2003-04-30
Support Year
8
Fiscal Year
2002
Total Cost
$291,879
Indirect Cost
Name
University of California Irvine
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Barbour, Alan G; Bunikis, Jonas; Fish, Durland et al. (2015) Association between body size and reservoir competence of mammals bearing Borrelia burgdorferi at an endemic site in the northeastern United States. Parasit Vectors 8:299
Elfving, Karin; Olsen, Bjorn; Bergstrom, Sven et al. (2010) Dissemination of spotted fever rickettsia agents in Europe by migrating birds. PLoS One 5:e8572
Barbour, Alan G; Bunikis, Jonas; Travinsky, Bridgit et al. (2009) Niche partitioning of Borrelia burgdorferi and Borrelia miyamotoi in the same tick vector and mammalian reservoir species. Am J Trop Med Hyg 81:1120-31
Hanincova, Klara; Kurtenbach, Klaus; Diuk-Wasser, Maria et al. (2006) Epidemic spread of Lyme borreliosis, northeastern United States. Emerg Infect Dis 12:604-11
Ornstein, Katharina; Barbour, Alan G (2006) A reverse transcriptase-polymerase chain reaction assay of Borrelia burgdorferi 16S rRNA for highly sensitive quantification of pathogen load in a vector. Vector Borne Zoonotic Dis 6:103-12
Comstedt, Par; Bergstrom, Sven; Olsen, Bjorn et al. (2006) Migratory passerine birds as reservoirs of Lyme borreliosis in Europe. Emerg Infect Dis 12:1087-95
Bunikis, Jonas; Barbour, Alan G (2005) Third Borrelia species in white-footed mice. Emerg Infect Dis 11:1150-1
Becker, Michael; Bunikis, Jonas; Lade, Barbara D et al. (2005) Structural investigation of Borrelia burgdorferi OspB, a bactericidal Fab target. J Biol Chem 280:17363-70
Zhong, Jianmin; Barbour, Alan G (2004) Cross-species hybridization of a Borrelia burgdorferi DNA array reveals infection- and culture-associated genes of the unsequenced genome of the relapsing fever agent Borrelia hermsii. Mol Microbiol 51:729-48
Bunikis, Jonas; Garpmo, Ulf; Tsao, Jean et al. (2004) Sequence typing reveals extensive strain diversity of the Lyme borreliosis agents Borrelia burgdorferi in North America and Borrelia afzelii in Europe. Microbiology 150:1741-55

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