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Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii

The Candidate Phyla Radiation (CPR) constitutes a large group of mostly uncultured bacterial lineages with small cell sizes and limited biosynthetic capabilities. They are thought to be symbionts of other organisms, but the nature of this symbiosis has been ascertained only for cultured Saccharibact...

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Autores principales: Moreira, David, Zivanovic, Yvan, López-Archilla, Ana I., Iniesto, Miguel, López-García, Purificación
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080830/
https://www.ncbi.nlm.nih.gov/pubmed/33911080
http://dx.doi.org/10.1038/s41467-021-22762-4
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author Moreira, David
Zivanovic, Yvan
López-Archilla, Ana I.
Iniesto, Miguel
López-García, Purificación
author_facet Moreira, David
Zivanovic, Yvan
López-Archilla, Ana I.
Iniesto, Miguel
López-García, Purificación
author_sort Moreira, David
collection PubMed
description The Candidate Phyla Radiation (CPR) constitutes a large group of mostly uncultured bacterial lineages with small cell sizes and limited biosynthetic capabilities. They are thought to be symbionts of other organisms, but the nature of this symbiosis has been ascertained only for cultured Saccharibacteria, which are epibiotic parasites of other bacteria. Here, we study the biology and the genome of Vampirococcus lugosii, which becomes the first described species of Vampirococcus, a genus of epibiotic bacteria morphologically identified decades ago. Vampirococcus belongs to the CPR phylum Absconditabacteria. It feeds on anoxygenic photosynthetic gammaproteobacteria, fully absorbing their cytoplasmic content. The cells divide epibiotically, forming multicellular stalks whose apical cells can reach new hosts. The genome is small (1.3 Mbp) and highly reduced in biosynthetic metabolism genes, but is enriched in genes possibly related to a fibrous cell surface likely involved in interactions with the host. Gene loss has been continuous during the evolution of Absconditabacteria, and generally most CPR bacteria, but this has been compensated by gene acquisition by horizontal gene transfer and de novo evolution. Our findings support parasitism as a widespread lifestyle of CPR bacteria, which probably contribute to the control of bacterial populations in diverse ecosystems.
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spelling pubmed-80808302021-05-11 Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii Moreira, David Zivanovic, Yvan López-Archilla, Ana I. Iniesto, Miguel López-García, Purificación Nat Commun Article The Candidate Phyla Radiation (CPR) constitutes a large group of mostly uncultured bacterial lineages with small cell sizes and limited biosynthetic capabilities. They are thought to be symbionts of other organisms, but the nature of this symbiosis has been ascertained only for cultured Saccharibacteria, which are epibiotic parasites of other bacteria. Here, we study the biology and the genome of Vampirococcus lugosii, which becomes the first described species of Vampirococcus, a genus of epibiotic bacteria morphologically identified decades ago. Vampirococcus belongs to the CPR phylum Absconditabacteria. It feeds on anoxygenic photosynthetic gammaproteobacteria, fully absorbing their cytoplasmic content. The cells divide epibiotically, forming multicellular stalks whose apical cells can reach new hosts. The genome is small (1.3 Mbp) and highly reduced in biosynthetic metabolism genes, but is enriched in genes possibly related to a fibrous cell surface likely involved in interactions with the host. Gene loss has been continuous during the evolution of Absconditabacteria, and generally most CPR bacteria, but this has been compensated by gene acquisition by horizontal gene transfer and de novo evolution. Our findings support parasitism as a widespread lifestyle of CPR bacteria, which probably contribute to the control of bacterial populations in diverse ecosystems. Nature Publishing Group UK 2021-04-28 /pmc/articles/PMC8080830/ /pubmed/33911080 http://dx.doi.org/10.1038/s41467-021-22762-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Moreira, David
Zivanovic, Yvan
López-Archilla, Ana I.
Iniesto, Miguel
López-García, Purificación
Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title_full Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title_fullStr Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title_full_unstemmed Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title_short Reductive evolution and unique predatory mode in the CPR bacterium Vampirococcus lugosii
title_sort reductive evolution and unique predatory mode in the cpr bacterium vampirococcus lugosii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080830/
https://www.ncbi.nlm.nih.gov/pubmed/33911080
http://dx.doi.org/10.1038/s41467-021-22762-4
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