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Related post: October 1, 1989, to September 30, 1990 TITLE OF PROJECT (SO character* or tea*. THIt Buy Cheap Isoptin Sr mutt ft on ont tint bttwttn tht bordtra.) Molecular Basis for Infection by Borrelia burgdorferi PRINCIPAL INVESTIGATOR (List other professional personnel below the Principal Investigator.) (Name, title, laboratory, and institute affiliation) PI: Tom G. Schwan Sr. Staff Fellow LVP, NIAID OTHERS: W. J. Simpson Visiting Associate LVP, NIAID K. L Gage IRTA Fellow LVP, NIAID W. Burgdorfer Scientist Emeritus LVP, NIAID S. Czub Visiting Fellow LVP, NIAID M. E. Schrumpf Bio. Lab. Tech. (Micro) LVP, NIAID R. H. Karstens Bio. Lab. Tech. (Micro) LVP, NIAID cooperating vms (» tny) Southampton Hospital, Southampton, NY (A. MacDonald), CDC, Fort Collins (J. Piesman), Tufts University, Boston (K. Georgilis and M. Klempner), LMSF, RML (P. Rosa), Texas H. D., Austin (J. Rawlings) lab/branch Laboratory of Vectors and Pathogens SECTION Arthropod-borne Diseases Section INSTITUTE AND LOCATION NIAID, NIH, Bethesda, MD TOTAL MAN-YEARS: 3.9 PROFESSIONAL 2.1 OTHER: 1.8 CHECK APPROPRIATE BOX(ES) □ (a) Human subjects □ (a1) Minors D (a2) Interviews E (b) Human tissues D (c) Neither SUMMARY OF WORK (Utt tttndtrd unrtductd typt. Do not txcttd tht tptct provided..) The objectives of this project are to (1) determine if genes present on plasmid DNA of Buy Isoptin Sr Online Borrelia burgdorferi, the causative agent of Lyme disease, control infectivity, (2) characterize these plasmids, (3) clone the infectivity genes and express those components that promote Borrelia infection in mammals, and (4) determine immunogenic properties of components responsible for infection, and (5) use recombinant DNA techniques to express B. burgdorferi-specific antigens to improve the serodiagnosis of Lyme disease. The reduction in the number of detectable plasmids with the loss of infectivity suggests that gene(s), encoding for components related to infectivity, may be present on one or Buy Isoptin Sr more of these extrachromosomal elements. A 8.4 kilobase (kb) pair circular plasmid was first identified as a strong candidate for regulating infection. Numerous fresh strains of B. burgdorferi were examined for their infectivity and presence of the 8.4 kb plasmid, two strains that were infectious lacked this plasmid or sequences similar to it elsewhere in their genomes. Thirteen strains of B. burgdorferi were cloned by limiting dilution from the low passage Sh-2-82 and examined for their infectivity, plasmid profile, and reactivity with anti-OspB monoclonal antibodies. One clone was noninfectious and had a unique and deficient plasmid profile compared to the other 12 clones. Investigations concerning in vivo antigenic changes in white-footed mice, the natural reservoir for B. burgdorferi, and white mice are continuing and have demonstrated that antigenic variation during infection is significant and may play an important role in the spirochete's ability to maintain persistent infections in spite of a pronounced humoral immune response by the host. PHS 6040 |Hw 1/3*) 18-10 DEPARTMENT OF HEALTH AND HUMAN SERVICES • PUBLIC HEALTH SERVICE NOTICE OF INTRAMURAL RESEARCH PROJECT PROJECT NUMBER Z01 Al 00552-02 LVP PERIOD COVERED October 1 , 1989, to September 30, 1990 TITLE OF PROJECT (80 chancers or less. THIe must * on one Urte between the borders.) Immunopathobiology of Bacterial Toxins PRINCIPAL INVESTIGATOR (Ust other professional personnel botow the Principal Investigator.) (Name, tltla, laboratory, and Institute affiliation) PI: Witold Cieplak, Jr. Sr. Staff Fellow LVP, MAID OTHERS: Christopher Guff IRTA Fellow LVP, MAID Susan G. Smith Microbiologist LVP, MAID Marius G. Peacock Microbiologist
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