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Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans

The ciliated protozoan Cryptocaryon irritans infects a wide range of marine fish and causes the highly lethal white spot disease. This parasite possesses three morphologically and physiologically distinct life stages: an infectious theront, a parasitic trophont, and an asexually reproductive tomont....

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Autores principales: Chi, Hongshu, Goldstein, Michael, Pichardo, Angel, Wei, Zung-Hang, Chang, Wei-Jen, Gong, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454944/
https://www.ncbi.nlm.nih.gov/pubmed/32857792
http://dx.doi.org/10.1371/journal.pone.0238167
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author Chi, Hongshu
Goldstein, Michael
Pichardo, Angel
Wei, Zung-Hang
Chang, Wei-Jen
Gong, Hui
author_facet Chi, Hongshu
Goldstein, Michael
Pichardo, Angel
Wei, Zung-Hang
Chang, Wei-Jen
Gong, Hui
author_sort Chi, Hongshu
collection PubMed
description The ciliated protozoan Cryptocaryon irritans infects a wide range of marine fish and causes the highly lethal white spot disease. This parasite possesses three morphologically and physiologically distinct life stages: an infectious theront, a parasitic trophont, and an asexually reproductive tomont. In the past few years, several attempts have been made to help elucidate how C. irritans transforms from one stage to another using transcriptomic or proteomic approaches. However, there has been no research studying changes in transcription profiles between different time points of a single C. irritans life stage—the development of this parasite. Here we use RNA-seq and compare gene expression profiles of theront cells collected by 1 and 10 hrs after they emerged from tomonts. It has been shown that infectivity of theront cells declines 6–8 hours post-emergence, and we used this characteristic as a physiological marker to confirm the aging of theront cells. We identified a total of 41 upregulated and 90 downregulated genes that were differentially expressed between young and aging theront cells. Using Blast2Go to further analyze functions of these genes, we show that genes related to energy production are downregulated, but quite surprisingly many genes involved in transcription/translation processes are upregulated. We also show that expression of all nine detectable agglutination/immobilization antigen genes, with great sequence divergence, is invariably downregulated. Functions of other differentially expressed genes and indications are also discussed in our study.
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spelling pubmed-74549442020-09-02 Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans Chi, Hongshu Goldstein, Michael Pichardo, Angel Wei, Zung-Hang Chang, Wei-Jen Gong, Hui PLoS One Research Article The ciliated protozoan Cryptocaryon irritans infects a wide range of marine fish and causes the highly lethal white spot disease. This parasite possesses three morphologically and physiologically distinct life stages: an infectious theront, a parasitic trophont, and an asexually reproductive tomont. In the past few years, several attempts have been made to help elucidate how C. irritans transforms from one stage to another using transcriptomic or proteomic approaches. However, there has been no research studying changes in transcription profiles between different time points of a single C. irritans life stage—the development of this parasite. Here we use RNA-seq and compare gene expression profiles of theront cells collected by 1 and 10 hrs after they emerged from tomonts. It has been shown that infectivity of theront cells declines 6–8 hours post-emergence, and we used this characteristic as a physiological marker to confirm the aging of theront cells. We identified a total of 41 upregulated and 90 downregulated genes that were differentially expressed between young and aging theront cells. Using Blast2Go to further analyze functions of these genes, we show that genes related to energy production are downregulated, but quite surprisingly many genes involved in transcription/translation processes are upregulated. We also show that expression of all nine detectable agglutination/immobilization antigen genes, with great sequence divergence, is invariably downregulated. Functions of other differentially expressed genes and indications are also discussed in our study. Public Library of Science 2020-08-28 /pmc/articles/PMC7454944/ /pubmed/32857792 http://dx.doi.org/10.1371/journal.pone.0238167 Text en © 2020 Chi 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chi, Hongshu
Goldstein, Michael
Pichardo, Angel
Wei, Zung-Hang
Chang, Wei-Jen
Gong, Hui
Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title_full Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title_fullStr Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title_full_unstemmed Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title_short Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
title_sort infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite cryptocaryon irritans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7454944/
https://www.ncbi.nlm.nih.gov/pubmed/32857792
http://dx.doi.org/10.1371/journal.pone.0238167
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