Cargando…

The complete mitochondrial genome of a parasite at the animal-fungal boundary

BACKGROUND: Sphaerothecum destruens is an obligate intracellular fish parasite which has been identified as a serious threat to freshwater fishes. Taxonomically, S. destruens belongs to the order Dermocystida within the class Ichthyosporea (formerly referred to as Mesomycetozoea), which sits at the...

Descripción completa

Detalles Bibliográficos
Autores principales: Sana, Salma, Hardouin, Emilie A., Paley, Richard, Zhang, Tiantian, Andreou, Demetra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027106/
https://www.ncbi.nlm.nih.gov/pubmed/32066491
http://dx.doi.org/10.1186/s13071-020-3926-5
_version_ 1783498801487544320
author Sana, Salma
Hardouin, Emilie A.
Paley, Richard
Zhang, Tiantian
Andreou, Demetra
author_facet Sana, Salma
Hardouin, Emilie A.
Paley, Richard
Zhang, Tiantian
Andreou, Demetra
author_sort Sana, Salma
collection PubMed
description BACKGROUND: Sphaerothecum destruens is an obligate intracellular fish parasite which has been identified as a serious threat to freshwater fishes. Taxonomically, S. destruens belongs to the order Dermocystida within the class Ichthyosporea (formerly referred to as Mesomycetozoea), which sits at the animal-fungal boundary. Mitochondrial DNA (mtDNA) sequences can be valuable genetic markers for species detection and are increasingly used in environmental DNA (eDNA) based species detection. Furthermore, mtDNA sequences can be used in epidemiological studies by informing detection, strain identification and geographical spread. METHODS: We amplified the entire mitochondrial (mt) genome of S. destruens in two overlapping long fragments using primers designed based on the cox1, cob and nad5 partial sequences. The mt-genome architecture of S. destruens was then compared to close relatives to gain insights into its evolution. RESULTS: The complete mt-genome of Sphaerothecum destruens is 23,939 bp in length and consists of 47 genes including 21 protein-coding genes, 2 rRNA, 22 tRNA and two unidentified open reading frames. The mitochondrial genome of S. destruens is intronless and compact with a few intergenic regions and includes genes that are often missing from animal and fungal mt-genomes, such as, the four ribosomal proteins (small subunit rps13 and 14; large subunit rpl2 and 16), tatC (twin-arginine translocase component C), and ccmC and ccmF (cytochrome c maturation protein ccmC and heme lyase). CONCLUSIONS: We present the first mt-genome of S. destruens which also represents the first mt-genome for the order Dermocystida. The availability of the mt-genome can assist the detection of S. destruens and closely related parasites in eukaryotic diversity surveys using eDNA and assist epidemiological studies by improving molecular detection and tracking the parasite’s spread. Furthermore, as the only representative of the order Dermocystida, its mt-genome can be used in the study of mitochondrial evolution of the unicellular relatives of animals. [Image: see text]
format Online
Article
Text
id pubmed-7027106
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-70271062020-02-24 The complete mitochondrial genome of a parasite at the animal-fungal boundary Sana, Salma Hardouin, Emilie A. Paley, Richard Zhang, Tiantian Andreou, Demetra Parasit Vectors Research BACKGROUND: Sphaerothecum destruens is an obligate intracellular fish parasite which has been identified as a serious threat to freshwater fishes. Taxonomically, S. destruens belongs to the order Dermocystida within the class Ichthyosporea (formerly referred to as Mesomycetozoea), which sits at the animal-fungal boundary. Mitochondrial DNA (mtDNA) sequences can be valuable genetic markers for species detection and are increasingly used in environmental DNA (eDNA) based species detection. Furthermore, mtDNA sequences can be used in epidemiological studies by informing detection, strain identification and geographical spread. METHODS: We amplified the entire mitochondrial (mt) genome of S. destruens in two overlapping long fragments using primers designed based on the cox1, cob and nad5 partial sequences. The mt-genome architecture of S. destruens was then compared to close relatives to gain insights into its evolution. RESULTS: The complete mt-genome of Sphaerothecum destruens is 23,939 bp in length and consists of 47 genes including 21 protein-coding genes, 2 rRNA, 22 tRNA and two unidentified open reading frames. The mitochondrial genome of S. destruens is intronless and compact with a few intergenic regions and includes genes that are often missing from animal and fungal mt-genomes, such as, the four ribosomal proteins (small subunit rps13 and 14; large subunit rpl2 and 16), tatC (twin-arginine translocase component C), and ccmC and ccmF (cytochrome c maturation protein ccmC and heme lyase). CONCLUSIONS: We present the first mt-genome of S. destruens which also represents the first mt-genome for the order Dermocystida. The availability of the mt-genome can assist the detection of S. destruens and closely related parasites in eukaryotic diversity surveys using eDNA and assist epidemiological studies by improving molecular detection and tracking the parasite’s spread. Furthermore, as the only representative of the order Dermocystida, its mt-genome can be used in the study of mitochondrial evolution of the unicellular relatives of animals. [Image: see text] BioMed Central 2020-02-17 /pmc/articles/PMC7027106/ /pubmed/32066491 http://dx.doi.org/10.1186/s13071-020-3926-5 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sana, Salma
Hardouin, Emilie A.
Paley, Richard
Zhang, Tiantian
Andreou, Demetra
The complete mitochondrial genome of a parasite at the animal-fungal boundary
title The complete mitochondrial genome of a parasite at the animal-fungal boundary
title_full The complete mitochondrial genome of a parasite at the animal-fungal boundary
title_fullStr The complete mitochondrial genome of a parasite at the animal-fungal boundary
title_full_unstemmed The complete mitochondrial genome of a parasite at the animal-fungal boundary
title_short The complete mitochondrial genome of a parasite at the animal-fungal boundary
title_sort complete mitochondrial genome of a parasite at the animal-fungal boundary
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027106/
https://www.ncbi.nlm.nih.gov/pubmed/32066491
http://dx.doi.org/10.1186/s13071-020-3926-5
work_keys_str_mv AT sanasalma thecompletemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT hardouinemiliea thecompletemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT paleyrichard thecompletemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT zhangtiantian thecompletemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT andreoudemetra thecompletemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT sanasalma completemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT hardouinemiliea completemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT paleyrichard completemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT zhangtiantian completemitochondrialgenomeofaparasiteattheanimalfungalboundary
AT andreoudemetra completemitochondrialgenomeofaparasiteattheanimalfungalboundary