Cargando…

Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms

Genetic diversity and genomic rearrangements are a driving force in bacterial evolution and niche adaptation. We sequenced and annotated the genome of Lactobacillus johnsonii DPC6026, a strain isolated from the porcine intestinal tract. Although the genome of DPC6026 is similar in size (1.97mbp) and...

Descripción completa

Detalles Bibliográficos
Autores principales: Guinane, Caitriona M., Kent, Robert M., Norberg, Sarah, Hill, Colin, Fitzgerald, Gerald F., Stanton, Catherine, Ross, R. Paul
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080392/
https://www.ncbi.nlm.nih.gov/pubmed/21533100
http://dx.doi.org/10.1371/journal.pone.0018740
_version_ 1782202114588540928
author Guinane, Caitriona M.
Kent, Robert M.
Norberg, Sarah
Hill, Colin
Fitzgerald, Gerald F.
Stanton, Catherine
Ross, R. Paul
author_facet Guinane, Caitriona M.
Kent, Robert M.
Norberg, Sarah
Hill, Colin
Fitzgerald, Gerald F.
Stanton, Catherine
Ross, R. Paul
author_sort Guinane, Caitriona M.
collection PubMed
description Genetic diversity and genomic rearrangements are a driving force in bacterial evolution and niche adaptation. We sequenced and annotated the genome of Lactobacillus johnsonii DPC6026, a strain isolated from the porcine intestinal tract. Although the genome of DPC6026 is similar in size (1.97mbp) and GC content (34.8%) to the sequenced human isolate L. johnsonii NCC 533, a large symmetrical inversion of approximately 750 kb differentiated the two strains. Comparative analysis among 12 other strains of L. johnsonii including 8 porcine, 3 human and 1 poultry isolate indicated that the genome architecture found in DPC6026 is more common within the species than that of NCC 533. Furthermore a number of unique features were annotated in DPC6026, some of which are likely to have been acquired by horizontal gene transfer (HGT) and contribute to protection against phage infection. A putative type III restriction-modification system was identified, as were novel Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) elements. Interestingly, these particular elements are not widely distributed among L. johnsonii strains. Taken together these data suggest intra-species genomic rearrangements and significant genetic diversity within the L. johnsonii species and indicate towards a host-specific divergence of L. johnsonii strains with respect to genome inversion and phage exposure.
format Text
id pubmed-3080392
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-30803922011-04-29 Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms Guinane, Caitriona M. Kent, Robert M. Norberg, Sarah Hill, Colin Fitzgerald, Gerald F. Stanton, Catherine Ross, R. Paul PLoS One Research Article Genetic diversity and genomic rearrangements are a driving force in bacterial evolution and niche adaptation. We sequenced and annotated the genome of Lactobacillus johnsonii DPC6026, a strain isolated from the porcine intestinal tract. Although the genome of DPC6026 is similar in size (1.97mbp) and GC content (34.8%) to the sequenced human isolate L. johnsonii NCC 533, a large symmetrical inversion of approximately 750 kb differentiated the two strains. Comparative analysis among 12 other strains of L. johnsonii including 8 porcine, 3 human and 1 poultry isolate indicated that the genome architecture found in DPC6026 is more common within the species than that of NCC 533. Furthermore a number of unique features were annotated in DPC6026, some of which are likely to have been acquired by horizontal gene transfer (HGT) and contribute to protection against phage infection. A putative type III restriction-modification system was identified, as were novel Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) elements. Interestingly, these particular elements are not widely distributed among L. johnsonii strains. Taken together these data suggest intra-species genomic rearrangements and significant genetic diversity within the L. johnsonii species and indicate towards a host-specific divergence of L. johnsonii strains with respect to genome inversion and phage exposure. Public Library of Science 2011-04-20 /pmc/articles/PMC3080392/ /pubmed/21533100 http://dx.doi.org/10.1371/journal.pone.0018740 Text en Guinane 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
Guinane, Caitriona M.
Kent, Robert M.
Norberg, Sarah
Hill, Colin
Fitzgerald, Gerald F.
Stanton, Catherine
Ross, R. Paul
Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title_full Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title_fullStr Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title_full_unstemmed Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title_short Host Specific Diversity in Lactobacillus johnsonii as Evidenced by a Major Chromosomal Inversion and Phage Resistance Mechanisms
title_sort host specific diversity in lactobacillus johnsonii as evidenced by a major chromosomal inversion and phage resistance mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080392/
https://www.ncbi.nlm.nih.gov/pubmed/21533100
http://dx.doi.org/10.1371/journal.pone.0018740
work_keys_str_mv AT guinanecaitrionam hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT kentrobertm hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT norbergsarah hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT hillcolin hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT fitzgeraldgeraldf hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT stantoncatherine hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms
AT rossrpaul hostspecificdiversityinlactobacillusjohnsoniiasevidencedbyamajorchromosomalinversionandphageresistancemechanisms