Cargando…

Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids

Lyme disease is the most common tick-borne human illness in North America. In order to understand the molecular pathogenesis, natural diversity, population structure and epizootic spread of the North American Lyme agent, Borrelia burgdorferi sensu stricto, a much better understanding of the natural...

Descripción completa

Detalles Bibliográficos
Autores principales: Casjens, Sherwood R., Mongodin, Emmanuel F., Qiu, Wei-Gang, Luft, Benjamin J., Schutzer, Steven E., Gilcrease, Eddie B., Huang, Wai Mun, Vujadinovic, Marija, Aron, John K., Vargas, Levy C., Freeman, Sam, Radune, Diana, Weidman, Janice F., Dimitrov, George I., Khouri, Hoda M., Sosa, Julia E., Halpin, Rebecca A., Dunn, John J., Fraser, Claire M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3303823/
https://www.ncbi.nlm.nih.gov/pubmed/22432010
http://dx.doi.org/10.1371/journal.pone.0033280
_version_ 1782226800675389440
author Casjens, Sherwood R.
Mongodin, Emmanuel F.
Qiu, Wei-Gang
Luft, Benjamin J.
Schutzer, Steven E.
Gilcrease, Eddie B.
Huang, Wai Mun
Vujadinovic, Marija
Aron, John K.
Vargas, Levy C.
Freeman, Sam
Radune, Diana
Weidman, Janice F.
Dimitrov, George I.
Khouri, Hoda M.
Sosa, Julia E.
Halpin, Rebecca A.
Dunn, John J.
Fraser, Claire M.
author_facet Casjens, Sherwood R.
Mongodin, Emmanuel F.
Qiu, Wei-Gang
Luft, Benjamin J.
Schutzer, Steven E.
Gilcrease, Eddie B.
Huang, Wai Mun
Vujadinovic, Marija
Aron, John K.
Vargas, Levy C.
Freeman, Sam
Radune, Diana
Weidman, Janice F.
Dimitrov, George I.
Khouri, Hoda M.
Sosa, Julia E.
Halpin, Rebecca A.
Dunn, John J.
Fraser, Claire M.
author_sort Casjens, Sherwood R.
collection PubMed
description Lyme disease is the most common tick-borne human illness in North America. In order to understand the molecular pathogenesis, natural diversity, population structure and epizootic spread of the North American Lyme agent, Borrelia burgdorferi sensu stricto, a much better understanding of the natural diversity of its genome will be required. Towards this end we present a comparative analysis of the nucleotide sequences of the numerous plasmids of B. burgdorferi isolates B31, N40, JD1 and 297. These strains were chosen because they include the three most commonly studied laboratory strains, and because they represent different major genetic lineages and so are informative regarding the genetic diversity and evolution of this organism. A unique feature of Borrelia genomes is that they carry a large number of linear and circular plasmids, and this work shows that strains N40, JD1, 297 and B31 carry related but non-identical sets of 16, 20, 19 and 21 plasmids, respectively, that comprise 33–40% of their genomes. We deduce that there are at least 28 plasmid compatibility types among the four strains. The B. burgdorferi ∼900 Kbp linear chromosomes are evolutionarily exceptionally stable, except for a short ≤20 Kbp plasmid-like section at the right end. A few of the plasmids, including the linear lp54 and circular cp26, are also very stable. We show here that the other plasmids, especially the linear ones, are considerably more variable. Nearly all of the linear plasmids have undergone one or more substantial inter-plasmid rearrangements since their last common ancestor. In spite of these rearrangements and differences in plasmid contents, the overall gene complement of the different isolates has remained relatively constant.
format Online
Article
Text
id pubmed-3303823
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-33038232012-03-19 Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids Casjens, Sherwood R. Mongodin, Emmanuel F. Qiu, Wei-Gang Luft, Benjamin J. Schutzer, Steven E. Gilcrease, Eddie B. Huang, Wai Mun Vujadinovic, Marija Aron, John K. Vargas, Levy C. Freeman, Sam Radune, Diana Weidman, Janice F. Dimitrov, George I. Khouri, Hoda M. Sosa, Julia E. Halpin, Rebecca A. Dunn, John J. Fraser, Claire M. PLoS One Research Article Lyme disease is the most common tick-borne human illness in North America. In order to understand the molecular pathogenesis, natural diversity, population structure and epizootic spread of the North American Lyme agent, Borrelia burgdorferi sensu stricto, a much better understanding of the natural diversity of its genome will be required. Towards this end we present a comparative analysis of the nucleotide sequences of the numerous plasmids of B. burgdorferi isolates B31, N40, JD1 and 297. These strains were chosen because they include the three most commonly studied laboratory strains, and because they represent different major genetic lineages and so are informative regarding the genetic diversity and evolution of this organism. A unique feature of Borrelia genomes is that they carry a large number of linear and circular plasmids, and this work shows that strains N40, JD1, 297 and B31 carry related but non-identical sets of 16, 20, 19 and 21 plasmids, respectively, that comprise 33–40% of their genomes. We deduce that there are at least 28 plasmid compatibility types among the four strains. The B. burgdorferi ∼900 Kbp linear chromosomes are evolutionarily exceptionally stable, except for a short ≤20 Kbp plasmid-like section at the right end. A few of the plasmids, including the linear lp54 and circular cp26, are also very stable. We show here that the other plasmids, especially the linear ones, are considerably more variable. Nearly all of the linear plasmids have undergone one or more substantial inter-plasmid rearrangements since their last common ancestor. In spite of these rearrangements and differences in plasmid contents, the overall gene complement of the different isolates has remained relatively constant. Public Library of Science 2012-03-14 /pmc/articles/PMC3303823/ /pubmed/22432010 http://dx.doi.org/10.1371/journal.pone.0033280 Text en Casjens et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Casjens, Sherwood R.
Mongodin, Emmanuel F.
Qiu, Wei-Gang
Luft, Benjamin J.
Schutzer, Steven E.
Gilcrease, Eddie B.
Huang, Wai Mun
Vujadinovic, Marija
Aron, John K.
Vargas, Levy C.
Freeman, Sam
Radune, Diana
Weidman, Janice F.
Dimitrov, George I.
Khouri, Hoda M.
Sosa, Julia E.
Halpin, Rebecca A.
Dunn, John J.
Fraser, Claire M.
Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title_full Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title_fullStr Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title_full_unstemmed Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title_short Genome Stability of Lyme Disease Spirochetes: Comparative Genomics of Borrelia burgdorferi Plasmids
title_sort genome stability of lyme disease spirochetes: comparative genomics of borrelia burgdorferi plasmids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3303823/
https://www.ncbi.nlm.nih.gov/pubmed/22432010
http://dx.doi.org/10.1371/journal.pone.0033280
work_keys_str_mv AT casjenssherwoodr genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT mongodinemmanuelf genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT qiuweigang genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT luftbenjaminj genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT schutzerstevene genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT gilcreaseeddieb genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT huangwaimun genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT vujadinovicmarija genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT aronjohnk genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT vargaslevyc genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT freemansam genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT radunediana genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT weidmanjanicef genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT dimitrovgeorgei genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT khourihodam genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT sosajuliae genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT halpinrebeccaa genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT dunnjohnj genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids
AT fraserclairem genomestabilityoflymediseasespirochetescomparativegenomicsofborreliaburgdorferiplasmids