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Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium

BACKGROUND: The genus Spiroplasma contains a group of helical, motile, and wall-less bacteria in the class Mollicutes. Similar to other members of this class, such as the animal-pathogenic Mycoplasma and the plant-pathogenic ‘Candidatus Phytoplasma’, all characterized Spiroplasma species were found...

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Autores principales: Lo, Wen-Sui, Chen, Ling-Ling, Chung, Wan-Chia, Gasparich, Gail E, Kuo, Chih-Horng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563533/
https://www.ncbi.nlm.nih.gov/pubmed/23324436
http://dx.doi.org/10.1186/1471-2164-14-22
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author Lo, Wen-Sui
Chen, Ling-Ling
Chung, Wan-Chia
Gasparich, Gail E
Kuo, Chih-Horng
author_facet Lo, Wen-Sui
Chen, Ling-Ling
Chung, Wan-Chia
Gasparich, Gail E
Kuo, Chih-Horng
author_sort Lo, Wen-Sui
collection PubMed
description BACKGROUND: The genus Spiroplasma contains a group of helical, motile, and wall-less bacteria in the class Mollicutes. Similar to other members of this class, such as the animal-pathogenic Mycoplasma and the plant-pathogenic ‘Candidatus Phytoplasma’, all characterized Spiroplasma species were found to be associated with eukaryotic hosts. While most of the Spiroplasma species appeared to be harmless commensals of insects, a small number of species have evolved pathogenicity toward various arthropods and plants. In this study, we isolated a novel strain of honeybee-associated S. melliferum and investigated its genetic composition and evolutionary history by whole-genome shotgun sequencing and comparative analysis with other Mollicutes genomes. RESULTS: The whole-genome shotgun sequencing of S. melliferum IPMB4A produced a draft assembly that was ~1.1 Mb in size and covered ~80% of the chromosome. Similar to other Spiroplasma genomes that have been studied to date, we found that this genome contains abundant repetitive sequences that originated from plectrovirus insertions. These phage fragments represented a major obstacle in obtaining a complete genome sequence of Spiroplasma with the current sequencing technology. Comparative analysis of S. melliferum IPMB4A with other Spiroplasma genomes revealed that these phages may have facilitated extensive genome rearrangements in these bacteria and contributed to horizontal gene transfers that led to species-specific adaptation to different eukaryotic hosts. In addition, comparison of gene content with other Mollicutes suggested that the common ancestor of the SEM (Spiroplasma, Entomoplasma, and Mycoplasma) clade may have had a relatively large genome and flexible metabolic capacity; the extremely reduced genomes of present day Mycoplasma and ‘Candidatus Phytoplasma’ species are likely to be the result of independent gene losses in these lineages. CONCLUSIONS: The findings in this study highlighted the significance of phage insertions and horizontal gene transfer in the evolution of bacterial genomes and acquisition of pathogenicity. Furthermore, the inclusion of Spiroplasma in comparative analysis has improved our understanding of genome evolution in Mollicutes. Future improvements in the taxon sampling of available genome sequences in this group are required to provide further insights into the evolution of these important pathogens of humans, animals, and plants.
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spelling pubmed-35635332013-02-08 Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium Lo, Wen-Sui Chen, Ling-Ling Chung, Wan-Chia Gasparich, Gail E Kuo, Chih-Horng BMC Genomics Research Article BACKGROUND: The genus Spiroplasma contains a group of helical, motile, and wall-less bacteria in the class Mollicutes. Similar to other members of this class, such as the animal-pathogenic Mycoplasma and the plant-pathogenic ‘Candidatus Phytoplasma’, all characterized Spiroplasma species were found to be associated with eukaryotic hosts. While most of the Spiroplasma species appeared to be harmless commensals of insects, a small number of species have evolved pathogenicity toward various arthropods and plants. In this study, we isolated a novel strain of honeybee-associated S. melliferum and investigated its genetic composition and evolutionary history by whole-genome shotgun sequencing and comparative analysis with other Mollicutes genomes. RESULTS: The whole-genome shotgun sequencing of S. melliferum IPMB4A produced a draft assembly that was ~1.1 Mb in size and covered ~80% of the chromosome. Similar to other Spiroplasma genomes that have been studied to date, we found that this genome contains abundant repetitive sequences that originated from plectrovirus insertions. These phage fragments represented a major obstacle in obtaining a complete genome sequence of Spiroplasma with the current sequencing technology. Comparative analysis of S. melliferum IPMB4A with other Spiroplasma genomes revealed that these phages may have facilitated extensive genome rearrangements in these bacteria and contributed to horizontal gene transfers that led to species-specific adaptation to different eukaryotic hosts. In addition, comparison of gene content with other Mollicutes suggested that the common ancestor of the SEM (Spiroplasma, Entomoplasma, and Mycoplasma) clade may have had a relatively large genome and flexible metabolic capacity; the extremely reduced genomes of present day Mycoplasma and ‘Candidatus Phytoplasma’ species are likely to be the result of independent gene losses in these lineages. CONCLUSIONS: The findings in this study highlighted the significance of phage insertions and horizontal gene transfer in the evolution of bacterial genomes and acquisition of pathogenicity. Furthermore, the inclusion of Spiroplasma in comparative analysis has improved our understanding of genome evolution in Mollicutes. Future improvements in the taxon sampling of available genome sequences in this group are required to provide further insights into the evolution of these important pathogens of humans, animals, and plants. BioMed Central 2013-01-16 /pmc/articles/PMC3563533/ /pubmed/23324436 http://dx.doi.org/10.1186/1471-2164-14-22 Text en Copyright ©2013 Lo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lo, Wen-Sui
Chen, Ling-Ling
Chung, Wan-Chia
Gasparich, Gail E
Kuo, Chih-Horng
Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title_full Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title_fullStr Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title_full_unstemmed Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title_short Comparative genome analysis of Spiroplasma melliferum IPMB4A, a honeybee-associated bacterium
title_sort comparative genome analysis of spiroplasma melliferum ipmb4a, a honeybee-associated bacterium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563533/
https://www.ncbi.nlm.nih.gov/pubmed/23324436
http://dx.doi.org/10.1186/1471-2164-14-22
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