Cryptosporidium parvum Genes Containing Thrombospondin Type 1 Domains

Author:

Deng Mingqi1,Templeton Thomas J.2,London Nicole R.1,Bauer Carrey1,Schroeder Alison A.1,Abrahamsen Mitchell S.1

Affiliation:

1. Department of Veterinary PathoBiology, University of Minnesota, St. Paul, Minnesota 55108

2. Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, New York 10021

Abstract

ABSTRACT Cryptosporidium parvum is recognized as an enteropathogen of great worldwide medical and veterinary importance, yet understanding of its pathogenesis has been hampered in part by limited knowledge of the invasion machinery of this parasite. Recently, genes containing thrombospondin type 1 (TSP1) domains have been identified in several genera of apicomplexans, including thrombospondin-related adhesive proteins (TRAPs) that have been implicated as key molecules for parasite motility and adhesion onto host cell surfaces. Previously, a large-scale random survey of the C. parvum genome conducted in our laboratory revealed the presence of multiple genomic DNA sequences with a high degree of similarity to known apicomplexan TRAP genes. In the present study, TBLASTN screening of available C. parvum genomic sequences by using TSP1 domains as queries identified a total of 12 genes possessing TSP1-like domains. All genes have putative signal peptide sequences, one or more TSP1-like domains, plus additional extracellular protein modules such as Kringle, epidermal growth factor, and Apple domains. Two genes, putative paralogs Cp TSP8 and Cp TSP9, contain predicted introns near their amino termini, which were verified by comparing PCR products from cDNA versus genomic DNA templates. Reverse transcription-PCR analysis of transcript levels reveals that C. parvum TSP genes were developmentally regulated with distinct patterns of expression during in vitro infection. TRAPC1, Cp TSP3, and Cp TSP11 were expressed at high levels during both early and late stages of infection, whereas Cp TSP2, Cp TSP5, Cp TSP6, Cp TSP8, and Cp TSP9 were maximally expressed during the late stages of infection. Only Cp TSP4 was highly expressed solely at an early stage of infection.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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