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The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments

Spironucleus salmonicida causes systemic infections in salmonid fish. It belongs to the group diplomonads, binucleated heterotrophic flagellates adapted to micro-aerobic environments. Recently we identified energy-producing hydrogenosomes in S. salmonicida. Here we present a genome analysis of the f...

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Autores principales: Xu, Feifei, Jerlström-Hultqvist, Jon, Einarsson, Elin, Ástvaldsson, Ásgeir, Svärd, Staffan G., Andersson, Jan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916229/
https://www.ncbi.nlm.nih.gov/pubmed/24516394
http://dx.doi.org/10.1371/journal.pgen.1004053
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author Xu, Feifei
Jerlström-Hultqvist, Jon
Einarsson, Elin
Ástvaldsson, Ásgeir
Svärd, Staffan G.
Andersson, Jan O.
author_facet Xu, Feifei
Jerlström-Hultqvist, Jon
Einarsson, Elin
Ástvaldsson, Ásgeir
Svärd, Staffan G.
Andersson, Jan O.
author_sort Xu, Feifei
collection PubMed
description Spironucleus salmonicida causes systemic infections in salmonid fish. It belongs to the group diplomonads, binucleated heterotrophic flagellates adapted to micro-aerobic environments. Recently we identified energy-producing hydrogenosomes in S. salmonicida. Here we present a genome analysis of the fish parasite with a focus on the comparison to the more studied diplomonad Giardia intestinalis. We annotated 8067 protein coding genes in the ∼12.9 Mbp S. salmonicida genome. Unlike G. intestinalis, promoter-like motifs were found upstream of genes which are correlated with gene expression, suggesting a more elaborate transcriptional regulation. S. salmonicida can utilise more carbohydrates as energy sources, has an extended amino acid and sulfur metabolism, and more enzymes involved in scavenging of reactive oxygen species compared to G. intestinalis. Both genomes have large families of cysteine-rich membrane proteins. A cluster analysis indicated large divergence of these families in the two diplomonads. Nevertheless, one of S. salmonicida cysteine-rich proteins was localised to the plasma membrane similar to G. intestinalis variant-surface proteins. We identified S. salmonicida homologs to cyst wall proteins and showed that one of these is functional when expressed in Giardia. This suggests that the fish parasite is transmitted as a cyst between hosts. The extended metabolic repertoire and more extensive gene regulation compared to G. intestinalis suggest that the fish parasite is more adapted to cope with environmental fluctuations. Our genome analyses indicate that S. salmonicida is a well-adapted pathogen that can colonize different sites in the host.
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spelling pubmed-39162292014-02-10 The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments Xu, Feifei Jerlström-Hultqvist, Jon Einarsson, Elin Ástvaldsson, Ásgeir Svärd, Staffan G. Andersson, Jan O. PLoS Genet Research Article Spironucleus salmonicida causes systemic infections in salmonid fish. It belongs to the group diplomonads, binucleated heterotrophic flagellates adapted to micro-aerobic environments. Recently we identified energy-producing hydrogenosomes in S. salmonicida. Here we present a genome analysis of the fish parasite with a focus on the comparison to the more studied diplomonad Giardia intestinalis. We annotated 8067 protein coding genes in the ∼12.9 Mbp S. salmonicida genome. Unlike G. intestinalis, promoter-like motifs were found upstream of genes which are correlated with gene expression, suggesting a more elaborate transcriptional regulation. S. salmonicida can utilise more carbohydrates as energy sources, has an extended amino acid and sulfur metabolism, and more enzymes involved in scavenging of reactive oxygen species compared to G. intestinalis. Both genomes have large families of cysteine-rich membrane proteins. A cluster analysis indicated large divergence of these families in the two diplomonads. Nevertheless, one of S. salmonicida cysteine-rich proteins was localised to the plasma membrane similar to G. intestinalis variant-surface proteins. We identified S. salmonicida homologs to cyst wall proteins and showed that one of these is functional when expressed in Giardia. This suggests that the fish parasite is transmitted as a cyst between hosts. The extended metabolic repertoire and more extensive gene regulation compared to G. intestinalis suggest that the fish parasite is more adapted to cope with environmental fluctuations. Our genome analyses indicate that S. salmonicida is a well-adapted pathogen that can colonize different sites in the host. Public Library of Science 2014-02-06 /pmc/articles/PMC3916229/ /pubmed/24516394 http://dx.doi.org/10.1371/journal.pgen.1004053 Text en © 2014 Xu 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
Xu, Feifei
Jerlström-Hultqvist, Jon
Einarsson, Elin
Ástvaldsson, Ásgeir
Svärd, Staffan G.
Andersson, Jan O.
The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title_full The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title_fullStr The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title_full_unstemmed The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title_short The Genome of Spironucleus salmonicida Highlights a Fish Pathogen Adapted to Fluctuating Environments
title_sort genome of spironucleus salmonicida highlights a fish pathogen adapted to fluctuating environments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916229/
https://www.ncbi.nlm.nih.gov/pubmed/24516394
http://dx.doi.org/10.1371/journal.pgen.1004053
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