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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Flavell, R. A. Fikrig, E. Barthold, S. W. Kantor, F. S. Tao, H. |
| Description | Author Affiliation: Fikrig E ( Section of Immunobiology, Yale University School of Medicine, New Haven, CT 06510.); |
| Abstract | We analyzed variability in outer surface protein B (OspB) from Borrelia burgdorferi (Bb), the causative agent of Lyme disease, to determine how Bb escapes immune destruction. We have shown that vaccination with OspB from Bb strain B31 protected mice from infection with Bb B31 but not against Bb N40. The present study demonstrates that Bb N40 spirochetes which evade vaccination immunity to OspB have a truncated form of OspB, due to a TAA stop codon at nucleotide 577. In contrast, Bb N40 spirochetes that express full-length OspB are unable to infect mice immunized with OspB, analogous to our previous studies with Bb B31. Mapping of the OspB antibody response shows that epitopes in the C terminus of OspB are surface-exposed and bind protective monoclonal and polyclonal antibodies. This suggests that the C terminus of OspB is important for eliciting a protective immune response to OspB. Truncation or modification of outer surface proteins that do not bind protective antibody may be a means by which Bb evades host defenses. |
| ISSN | 00278424 |
| e-ISSN | 10916490 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Issue Number | 9 |
| Volume Number | 90 |
| Language | English |
| Publisher | National Academy of Sciences |
| Publisher Date | 1993-06-01 |
| Publisher Place | United States |
| Access Restriction | Open |
| Subject Keyword | Antigens, Bacterial Antigens, Surface Immunology Bacterial Outer Membrane Proteins Borrelia Burgdorferi Group Lyme Disease Amino Acid Sequence Animals Antibodies Antibodies, Monoclonal Biosynthesis Genetics Cloning, Molecular Codon Epitopes Escherichia Coli Fluorescent Antibody Technique Genes, Bacterial Prevention & Control Mice Mice, Inbred C3H Polymerase Chain Reaction Recombinant Fusion Proteins Recombinant Proteins Restriction Mapping Microbiology Vaccines, Synthetic Viral Vaccines Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Multidisciplinary |
| Content Type | Text |
| Resource Type | Article |
| Subject | Multidisciplinary |
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