NYMC Faculty Publications
Multipartite Genome of Lyme Disease
Author Type(s)
Faculty
DOI
10.21775/cimb.042.409
Journal Title
Current Issues in Molecular Biology
First Page
409
Last Page
454
Document Type
Article
Publication Date
1-2021
Department
Pathology, Microbiology and Immunology
Abstract
All members of the Borrelia genus that have been examined harbour a linear chromosome that is about 900 kbp in length, as well as a plethora of both linear and circular plasmids in the 5-220 kbp size range. Genome sequences for 27 Lyme disease Borrelia isolates have been determined since the elucidation of the B. burgdorferi B31 genome sequence in 1997. The chromosomes, which carry the vast majority of the housekeeping genes, appear to be very constant in gene content and organization across all Lyme disease Borrelia species. The content of the plasmids, which carry most of the genes that encode the differentially expressed surface proteins that interact with the spirochete's arthropod and vertebrate hosts, is much more variable. Lyme disease Borrelia isolates carry between 7-21 different plasmids, ranging in size from 5-84 kbp. All strains analyzed to date harbor three plasmids, cp26, lp54 and lp17. The plasmids are unusual, as compared to most bacterial plasmids, in that they contain many paralogous sequences, a large number of pseudogenes, and, in some cases, essential genes. In addition, a number of the plasmids have features indicating that they are prophages. Numerous methods have been developed for Lyme disease Borrelia strain typing. These have proven valuable for clinical and epidemiological studies, as well as phylogenomic and population genetic analyses. Increasingly, these approaches have been displaced by whole genome sequencing techniques. Some correlations between genome content and pathogenicity have been deduced, and comparative whole genome analyses promise future progress in this arena.
Recommended Citation
Schwartz, I., Margos, G., Casjens, S. R., Qiu, W., & Eggers, C. H. (2021). Multipartite Genome of Lyme Disease. Current Issues in Molecular Biology, 42, 409-454. https://doi.org/10.21775/cimb.042.409