Delivery of Parasite RNA Transcripts Into Infected Epithelial Cells During Cryptosporidium Infection and Its Potential Impact on Host Gene Transcription.

Cryptosporidium parvum is an important opportunistic parasite pathogen for immunocompromised individuals and a common cause of diarrhea in young children. Previous studies have identified a panel of RNA transcripts of very low protein-coding potential in C. parvum. Using an in vitro model of human i...

Descripción completa

Detalles Bibliográficos
Publicado en:Journal of Infectious Diseases Vol. 215; no. 4; pp. 636 - 644
Autores principales: Yang Wang, Ai-Yu Gong, Shibin Ma, Xiqiang Chen, Yan Li, Chun-Jen Su, Norall, Dana, Jing Chen, Strauss-Soukup, Juliane K., Xian-Ming Chen, Wang, Yang, Gong, Ai-Yu, Ma, Shibin, Chen, Xiqiang, Li, Yan, Su, Chun-Jen, Chen, Jing, Chen, Xian-Ming
Formato: pictorial research tables/charts Journal Article
Publicado: Oxford University Press / USA 2/15/2017
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Cryptosporidium parvum is an important opportunistic parasite pathogen for immunocompromised individuals and a common cause of diarrhea in young children. Previous studies have identified a panel of RNA transcripts of very low protein-coding potential in C. parvum. Using an in vitro model of human intestinal cryptosporidiosis, we report here that some of these C. parvum RNA transcripts were selectively delivered into the nuclei of host epithelial cells during C. parvum infection. Nuclear delivery of several such parasitic RNAs, including Cdg7_FLc_0990, involved heat-shock protein 70-mediated nuclear importing mechanism. Overexpression of Cdg7_FLc_0990 in intestinal epithelial cells resulted in significant changes in expression levels of specific genes, with significant overlapping with alterations in gene expression profile detected in host cells after C. parvum infection. Our data demonstrate that C. parvum transcripts of low protein-coding potential are selectively delivered into epithelial cells during infection and may modulate gene transcription in infected host cells.