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the cryptosporidium parvum transcriptome during in vitro development隐孢子虫的以及在体外转录组发展
The Cryptosporidium Parvum Transcriptome during In
Vitro Development
Mary J. Mauzy, Shinichiro Enomoto, Cheryl A. Lancto, Mitchell S. Abrahamsen, Mark S. Rutherford*
Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota, United States of America
Abstract
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-
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