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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Veröffentlicht in:PloS one 2020-08, Vol.15 (8), p.e0238167-e0238167
Hauptverfasser: Chi, Hongshu, Goldstein, Michael, Pichardo, Angel, Wei, Zung-Hang, Chang, Wei-Jen, Gong, Hui
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creator Chi, Hongshu
Goldstein, Michael
Pichardo, Angel
Wei, Zung-Hang
Chang, Wei-Jen
Gong, Hui
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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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. 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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.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>32857792</pmid><doi>10.1371/journal.pone.0238167</doi><tpages>e0238167</tpages><orcidid>https://orcid.org/0000-0002-8065-2281</orcidid><oa>free_for_read</oa></addata></record>
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subjects Agglutination
Aging
Antigens
Biology
Biology and Life Sciences
Cell development (Biology)
Ciliates
Cryptocaryon irritans
Developmental stages
Diseases
Divergence
Earth Sciences
Fish
Fish diseases
Fish parasites
Gene expression
Genes
Genetic aspects
Immobilization
Infections
Infectivity
Marine fish
Marine fishes
Medicine and Health Sciences
Methods
Parasites
Parasitological research
Phylogenetics
Physiological aspects
Proteins
Proteomics
Protozoa
Ribonucleic acid
RNA
Transcription
Transcriptomics
title Infectivity and genes differentially expressed between young and aging theront cells of the marine fish parasite Cryptocaryon irritans
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