Cargando…
High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis
BACKGROUND: Borrelia bavariensis is one of the agents of Lyme Borreliosis (or Lyme disease) in Eurasia. The genome of the Borrelia burgdorferi sensu lato species complex, that includes B. bavariensis, is known to be very complex and fragmented making the assembly of whole genomes with next-generatio...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542741/ https://www.ncbi.nlm.nih.gov/pubmed/33032522 http://dx.doi.org/10.1186/s12864-020-07054-3 |
_version_ | 1783591604819329024 |
---|---|
author | Becker, Noémie S. Rollins, Robert E. Nosenko, Kateryna Paulus, Alexander Martin, Samantha Krebs, Stefan Takano, Ai Sato, Kozue Kovalev, Sergey Y. Kawabata, Hiroki Fingerle, Volker Margos, Gabriele |
author_facet | Becker, Noémie S. Rollins, Robert E. Nosenko, Kateryna Paulus, Alexander Martin, Samantha Krebs, Stefan Takano, Ai Sato, Kozue Kovalev, Sergey Y. Kawabata, Hiroki Fingerle, Volker Margos, Gabriele |
author_sort | Becker, Noémie S. |
collection | PubMed |
description | BACKGROUND: Borrelia bavariensis is one of the agents of Lyme Borreliosis (or Lyme disease) in Eurasia. The genome of the Borrelia burgdorferi sensu lato species complex, that includes B. bavariensis, is known to be very complex and fragmented making the assembly of whole genomes with next-generation sequencing data a challenge. RESULTS: We present a genome reconstruction for 33 B. bavariensis isolates from Eurasia based on long-read (Pacific Bioscience, for three isolates) and short-read (Illumina) data. We show that the combination of both sequencing techniques allows proper genome reconstruction of all plasmids in most cases but use of a very close reference is necessary when only short-read sequencing data is available. B. bavariensis genomes combine a high degree of genetic conservation with high plasticity: all isolates share the main chromosome and five plasmids, but the repertoire of other plasmids is highly variable. In addition to plasmid losses and gains through horizontal transfer, we also observe several fusions between plasmids. Although European isolates of B. bavariensis have little diversity in genome content, there is some geographic structure to this variation. In contrast, each Asian isolate has a unique plasmid repertoire and we observe no geographically based differences between Japanese and Russian isolates. Comparing the genomes of Asian and European populations of B. bavariensis suggests that some genes which are markedly different between the two populations may be good candidates for adaptation to the tick vector, (Ixodes ricinus in Europe and I. persulcatus in Asia). CONCLUSIONS: We present the characterization of genomes of a large sample of B. bavariensis isolates and show that their plasmid content is highly variable. This study opens the way for genomic studies seeking to understand host and vector adaptation as well as human pathogenicity in Eurasian Lyme Borreliosis agents. |
format | Online Article Text |
id | pubmed-7542741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75427412020-10-08 High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis Becker, Noémie S. Rollins, Robert E. Nosenko, Kateryna Paulus, Alexander Martin, Samantha Krebs, Stefan Takano, Ai Sato, Kozue Kovalev, Sergey Y. Kawabata, Hiroki Fingerle, Volker Margos, Gabriele BMC Genomics Research Article BACKGROUND: Borrelia bavariensis is one of the agents of Lyme Borreliosis (or Lyme disease) in Eurasia. The genome of the Borrelia burgdorferi sensu lato species complex, that includes B. bavariensis, is known to be very complex and fragmented making the assembly of whole genomes with next-generation sequencing data a challenge. RESULTS: We present a genome reconstruction for 33 B. bavariensis isolates from Eurasia based on long-read (Pacific Bioscience, for three isolates) and short-read (Illumina) data. We show that the combination of both sequencing techniques allows proper genome reconstruction of all plasmids in most cases but use of a very close reference is necessary when only short-read sequencing data is available. B. bavariensis genomes combine a high degree of genetic conservation with high plasticity: all isolates share the main chromosome and five plasmids, but the repertoire of other plasmids is highly variable. In addition to plasmid losses and gains through horizontal transfer, we also observe several fusions between plasmids. Although European isolates of B. bavariensis have little diversity in genome content, there is some geographic structure to this variation. In contrast, each Asian isolate has a unique plasmid repertoire and we observe no geographically based differences between Japanese and Russian isolates. Comparing the genomes of Asian and European populations of B. bavariensis suggests that some genes which are markedly different between the two populations may be good candidates for adaptation to the tick vector, (Ixodes ricinus in Europe and I. persulcatus in Asia). CONCLUSIONS: We present the characterization of genomes of a large sample of B. bavariensis isolates and show that their plasmid content is highly variable. This study opens the way for genomic studies seeking to understand host and vector adaptation as well as human pathogenicity in Eurasian Lyme Borreliosis agents. BioMed Central 2020-10-08 /pmc/articles/PMC7542741/ /pubmed/33032522 http://dx.doi.org/10.1186/s12864-020-07054-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Becker, Noémie S. Rollins, Robert E. Nosenko, Kateryna Paulus, Alexander Martin, Samantha Krebs, Stefan Takano, Ai Sato, Kozue Kovalev, Sergey Y. Kawabata, Hiroki Fingerle, Volker Margos, Gabriele High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title | High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title_full | High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title_fullStr | High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title_full_unstemmed | High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title_short | High conservation combined with high plasticity: genomics and evolution of Borrelia bavariensis |
title_sort | high conservation combined with high plasticity: genomics and evolution of borrelia bavariensis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542741/ https://www.ncbi.nlm.nih.gov/pubmed/33032522 http://dx.doi.org/10.1186/s12864-020-07054-3 |
work_keys_str_mv | AT beckernoemies highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT rollinsroberte highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT nosenkokateryna highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT paulusalexander highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT martinsamantha highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT krebsstefan highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT takanoai highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT satokozue highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT kovalevsergeyy highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT kawabatahiroki highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT fingerlevolker highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis AT margosgabriele highconservationcombinedwithhighplasticitygenomicsandevolutionofborreliabavariensis |