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CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium
Recently, a new Chlamydia-related organism, Protochlamydia naegleriophila KNic, was discovered within a Naegleria amoeba. To decipher the mechanisms at play in the modeling of genomes from the Protochlamydia genus, we sequenced the full genome of Pr. naegleriophila, which includes a 2,885,090 bp chr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010888/ https://www.ncbi.nlm.nih.gov/pubmed/27516530 http://dx.doi.org/10.1093/gbe/evw138 |
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author | Bertelli, Claire Cissé, Ousmane H. Rusconi, Brigida Kebbi-Beghdadi, Carole Croxatto, Antony Goesmann, Alexander Collyn, François Greub, Gilbert |
author_facet | Bertelli, Claire Cissé, Ousmane H. Rusconi, Brigida Kebbi-Beghdadi, Carole Croxatto, Antony Goesmann, Alexander Collyn, François Greub, Gilbert |
author_sort | Bertelli, Claire |
collection | PubMed |
description | Recently, a new Chlamydia-related organism, Protochlamydia naegleriophila KNic, was discovered within a Naegleria amoeba. To decipher the mechanisms at play in the modeling of genomes from the Protochlamydia genus, we sequenced the full genome of Pr. naegleriophila, which includes a 2,885,090 bp chromosome and a 145,285 bp megaplasmid. For the first time within the Chlamydiales order, we describe the presence of a clustered regularly interspaced short palindromic repeats (CRISPR) system, the immune system of bacteria, located on the chromosome. It is composed of a small CRISPR locus comprising eight repeats and associated cas-cse genes of the subtype I-E. A CRISPR locus is also present within Chlamydia sp. Diamant, another Pr. naegleriophila strain, suggesting that the CRISPR system was acquired by a common ancestor of Pr. naegleriophila, after its divergence from Pr. amoebophila. Both nucleotide bias and comparative genomics approaches identified probable horizontal gene acquisitions within two and four genomic islands in Pr. naegleriophila KNic and Diamant genomes, respectively. The plasmid encodes an F-type conjugative system highly similar to 1) that found in the Pam100G genomic island of Pr. amoebophila UWE25 chromosome, as well as on the plasmid of Rubidus massiliensis and 2) to the three genes remaining in the chromosome of Parachlamydia acanthamoebae strains. Therefore, this conjugative system was likely acquired on an ancestral plasmid before the divergence of Parachlamydiaceae. Overall, this new complete Pr. naegleriophila genome sequence enables further investigation of the dynamic processes shaping the genomes of the family Parachlamydiaceae and the genus Protochlamydia. |
format | Online Article Text |
id | pubmed-5010888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50108882016-09-06 CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium Bertelli, Claire Cissé, Ousmane H. Rusconi, Brigida Kebbi-Beghdadi, Carole Croxatto, Antony Goesmann, Alexander Collyn, François Greub, Gilbert Genome Biol Evol Research Article Recently, a new Chlamydia-related organism, Protochlamydia naegleriophila KNic, was discovered within a Naegleria amoeba. To decipher the mechanisms at play in the modeling of genomes from the Protochlamydia genus, we sequenced the full genome of Pr. naegleriophila, which includes a 2,885,090 bp chromosome and a 145,285 bp megaplasmid. For the first time within the Chlamydiales order, we describe the presence of a clustered regularly interspaced short palindromic repeats (CRISPR) system, the immune system of bacteria, located on the chromosome. It is composed of a small CRISPR locus comprising eight repeats and associated cas-cse genes of the subtype I-E. A CRISPR locus is also present within Chlamydia sp. Diamant, another Pr. naegleriophila strain, suggesting that the CRISPR system was acquired by a common ancestor of Pr. naegleriophila, after its divergence from Pr. amoebophila. Both nucleotide bias and comparative genomics approaches identified probable horizontal gene acquisitions within two and four genomic islands in Pr. naegleriophila KNic and Diamant genomes, respectively. The plasmid encodes an F-type conjugative system highly similar to 1) that found in the Pam100G genomic island of Pr. amoebophila UWE25 chromosome, as well as on the plasmid of Rubidus massiliensis and 2) to the three genes remaining in the chromosome of Parachlamydia acanthamoebae strains. Therefore, this conjugative system was likely acquired on an ancestral plasmid before the divergence of Parachlamydiaceae. Overall, this new complete Pr. naegleriophila genome sequence enables further investigation of the dynamic processes shaping the genomes of the family Parachlamydiaceae and the genus Protochlamydia. Oxford University Press 2016-08-11 /pmc/articles/PMC5010888/ /pubmed/27516530 http://dx.doi.org/10.1093/gbe/evw138 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Bertelli, Claire Cissé, Ousmane H. Rusconi, Brigida Kebbi-Beghdadi, Carole Croxatto, Antony Goesmann, Alexander Collyn, François Greub, Gilbert CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title | CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title_full | CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title_fullStr | CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title_full_unstemmed | CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title_short | CRISPR System Acquisition and Evolution of an Obligate Intracellular Chlamydia-Related Bacterium |
title_sort | crispr system acquisition and evolution of an obligate intracellular chlamydia-related bacterium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010888/ https://www.ncbi.nlm.nih.gov/pubmed/27516530 http://dx.doi.org/10.1093/gbe/evw138 |
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