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The Cryptosporidium Parvum Transcriptome during In Vitro Development

Cryptosporidiosis is caused by an obligate intracellular parasite that has eluded global transcriptional or proteomic analysis of the intracellular developmental stages. The transcript abundance for 3,302 genes (87%) of the Cryptosporidium parvum protein coding genome was elucidated over a 72 hr inf...

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Autores principales: Mauzy, Mary J., Enomoto, Shinichiro, Lancto, Cheryl A., Abrahamsen, Mitchell S., Rutherford, Mark S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305300/
https://www.ncbi.nlm.nih.gov/pubmed/22438867
http://dx.doi.org/10.1371/journal.pone.0031715
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author Mauzy, Mary J.
Enomoto, Shinichiro
Lancto, Cheryl A.
Abrahamsen, Mitchell S.
Rutherford, Mark S.
author_facet Mauzy, Mary J.
Enomoto, Shinichiro
Lancto, Cheryl A.
Abrahamsen, Mitchell S.
Rutherford, Mark S.
author_sort Mauzy, Mary J.
collection PubMed
description Cryptosporidiosis is caused by an obligate intracellular parasite that has eluded global transcriptional or proteomic analysis of the intracellular developmental stages. The transcript abundance for 3,302 genes (87%) of the Cryptosporidium parvum protein coding genome was elucidated over a 72 hr infection within HCT8 cells using Real Time-PCR. The parasite had detectable transcription of all genes in vitro within at least one time point tested, and adjacent genes were not co-regulated. Five genes were not detected within the first 24 hr of infection, one containing two AP2 domains. The fewest genes detected were at 2 hr post infection, while 30% (985) of the genes have their highest expression at 48 and/or 72 hr. Nine expression clusters were formed over the entire 72 hr time course and indicate patterns of transcriptional increases at each of the 7 time points collected except 36 hr, including genes paralleling parasite 18S rRNA transcript levels. Clustering within only the first 24 hr of infection indicates spikes in expression at each of the 4 time points, a group paralleling 18S rRNA transcript levels, and a cluster with peaks at both 6 and 24 hr. All genes were classified into 18 functional categories, which were unequally distributed across clusters. Expression of metabolic, ribosomal and proteasome proteins did not parallel 18S rRNA levels indicating distinct biochemical profiles during developmental stage progression. Proteins involved in translation are over-represented at 6 hr, while structural proteins are over-represented at 12 hr. Standardization methods identified 107 genes with <80% at a single of its total expression at a single time point over 72 hr. This comprehensive transcriptome of the intracellular stages of C. parvum provides insight for understanding its complex development following parasitization of intestinal epithelial cells.
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spelling pubmed-33053002012-03-21 The Cryptosporidium Parvum Transcriptome during In Vitro Development Mauzy, Mary J. Enomoto, Shinichiro Lancto, Cheryl A. Abrahamsen, Mitchell S. Rutherford, Mark S. PLoS One Research Article Cryptosporidiosis is caused by an obligate intracellular parasite that has eluded global transcriptional or proteomic analysis of the intracellular developmental stages. The transcript abundance for 3,302 genes (87%) of the Cryptosporidium parvum protein coding genome was elucidated over a 72 hr infection within HCT8 cells using Real Time-PCR. The parasite had detectable transcription of all genes in vitro within at least one time point tested, and adjacent genes were not co-regulated. Five genes were not detected within the first 24 hr of infection, one containing two AP2 domains. The fewest genes detected were at 2 hr post infection, while 30% (985) of the genes have their highest expression at 48 and/or 72 hr. Nine expression clusters were formed over the entire 72 hr time course and indicate patterns of transcriptional increases at each of the 7 time points collected except 36 hr, including genes paralleling parasite 18S rRNA transcript levels. Clustering within only the first 24 hr of infection indicates spikes in expression at each of the 4 time points, a group paralleling 18S rRNA transcript levels, and a cluster with peaks at both 6 and 24 hr. All genes were classified into 18 functional categories, which were unequally distributed across clusters. Expression of metabolic, ribosomal and proteasome proteins did not parallel 18S rRNA levels indicating distinct biochemical profiles during developmental stage progression. Proteins involved in translation are over-represented at 6 hr, while structural proteins are over-represented at 12 hr. Standardization methods identified 107 genes with <80% at a single of its total expression at a single time point over 72 hr. This comprehensive transcriptome of the intracellular stages of C. parvum provides insight for understanding its complex development following parasitization of intestinal epithelial cells. Public Library of Science 2012-03-15 /pmc/articles/PMC3305300/ /pubmed/22438867 http://dx.doi.org/10.1371/journal.pone.0031715 Text en Mauzy 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
Mauzy, Mary J.
Enomoto, Shinichiro
Lancto, Cheryl A.
Abrahamsen, Mitchell S.
Rutherford, Mark S.
The Cryptosporidium Parvum Transcriptome during In Vitro Development
title The Cryptosporidium Parvum Transcriptome during In Vitro Development
title_full The Cryptosporidium Parvum Transcriptome during In Vitro Development
title_fullStr The Cryptosporidium Parvum Transcriptome during In Vitro Development
title_full_unstemmed The Cryptosporidium Parvum Transcriptome during In Vitro Development
title_short The Cryptosporidium Parvum Transcriptome during In Vitro Development
title_sort cryptosporidium parvum transcriptome during in vitro development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305300/
https://www.ncbi.nlm.nih.gov/pubmed/22438867
http://dx.doi.org/10.1371/journal.pone.0031715
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