1. Identification of a gene cluster for cell-surface genes of the SRS superfamily in Neospora caninum and characterization of the novel SRS9 gene.
- Author
-
RISCO-CASTILLO, V., MARUGÁN-HERNÁNDEZ, V., FERNÁNDEZ-GARCÍA, A., AGUADO-MARTÍNEZ, A., JIMÉNEZ-RUIZ, E., RODRÍGUEZ-MARCO, S., ÁLVAREZ-GARCÍA, G., and ORTEGA-MORA, L. M.
- Subjects
- *
TOXOPLASMA gondii , *MOLECULAR cloning , *CYTOCHROME c , *GENE expression , *IMMUNOFLUORESCENCE , *IMMUNOHISTOCHEMISTRY , *POLYPEPTIDES - Abstract
Here we present the detection of a gene cluster for Neospora caninum surface genes, similar to the Toxoplasma gondii SRS9 locus, and the cloning and characterization of the NcSRS9 gene. PCR genome walking, using NcBSR4 gene as a framework, allows the identification, upstream NcBSR4, of 2 sequences homologous to the SRS5 and the Ubiquinol-cytochrome C reductase genes and, downstream NcBSR4, of an ORF of 1191 bp coding for a 396-amino acid polypeptide with 59% similarity to the TgSRS9 antigen. A putative 39-residue signal peptide was found at the NH2-terminus followed by a hydrophilic region, and a potential site for a glycosylphosphatidylinositol anchor at the COOH-terminus. A recombinant NcSRS9 protein was produced and was recognized on a Western blot by a low proportion of sera from a panel of naturally infected cows and calves. In addition, Western blot analysis using polyclonal anti-rNcSRS9 revealed stage-specific expression of NcSRS9 in bradyzoites but not in tachyzoites, and immunohistochemistry on brain from a congenitally infected calf showed NcSRS9 recognition in bradyzoites contained in tissue cysts. However, bradyzoite-specific expression of NcSRS9 could not be proven by immunofluorescence on bradyzoites obtained in vitro and RT-PCR analysis showed no significant variations of NcSRS9 transcripts during in vitro tachyzoite-bradyzoite switch, probably due to incomplete maturity of in vitro bradyzoites. Initial characterization of NcSRS9 in this study may lead to further studies for a better understanding of N. caninum persistence. [ABSTRACT FROM AUTHOR]
- Published
- 2011
- Full Text
- View/download PDF