parvum recombinant antigens, rCp23 and rCp15, have been cloned and sequenced, the antibody responses and the cellular immune responses to these antigens have been characterized, the immune efficiency against the fused Cp15–23 has not been determined. For reasons of the complexity of the life cycle of the parasite, an ideal effective vaccine would need to provide immunity to the multiple stages of the parasites. However, a multivalent vaccine might dilute SB203580 ic50 the specific immune response demonstrated for the single protein vaccine (12). To address this concern, we analysed the efficacy of the multiple recombinant protein in comparison with crude protein and single recombinant protein

in mouse model. The results showed that immunization with a multiple recombinant protein generated a substantially stronger protein-specific antibody response, proliferation of CD4+ and CD8+ T cells and secretion of the cytokines of gamma interferon (IFN-γ) and interleukin (IL)-12 compared with the single recombinant protein and crude extract of C. parvum. The C. parvum isolate used for this study was the Nanjing murine isolate.

Four-to-six-week-old female BALB/c mice were purchased from Shandong University Experimental Center (Jinan, China) and housed at Shandong www.selleckchem.com/products/LDE225(NVP-LDE225).html Institute of Parasitic Disease animal facility (China). Animals were fed sterile food and water and kept in a high-efficiency particulate air-filtered barrier-isolated facility. To obtain the parasites for the following experiments, the mice were fed in 15 μg/mL dexamethasone sodium phosphate water for 3 days, then 1 × 106 oocysts in 200 μL PBS were inoculated intragastrically. Faeces were collected at 3-day intervals and oocysts were purified through discontinuous sucrose gradients and stored as described previously (13). Genomic DNA of oocysts of C. parvum was extracted. The C. parvum 23 kDa antigen coding sequence (GenBank accession number U34390) was amplified by PCR, using Cp23 sense primer (5′-CGCGGATCCATGGGTTGTTCATCATCAAAGC-3′) (BamHI linker underlined) and Cp23 antisense primer (5′-GCGGAATTCATTAGGCATCAGCTGGCTTGTC-3′) (EcoRI

linker underlined). Bay 11-7085 The fragment was cloned into the BamHI and EcoRI restriction enzyme sites of the pET-30a(+) expression vector to generate plasmid pET23. The C. parvum 15 kDa antigen coding sequence (GenBank accession number U34390) was amplified by PCR, using Cp15 sense primer (5′-GCGCCATGGGTAACTTGAAATCCTG-3′) (NcoI linker underlined) and Cp15 antisense primer (5′-GCCGGATCCGTT-AAAGTTTGGTTTG-3′) (EcoRI linker underlined). The fragment was cloned into the NcoI and BamHI restriction enzyme sites of the pET-30a(+) expression vector to generate plasmid pET15. For construction of Cp15–23 fusion gene plasmid, a synthetic linker sequence encoding a peptide (G-S) was designed and the Cp23 gene fragment was subcloned behind plasmid pET15 by the sites of BamHI and EcoRI (Figure 1a, b, c).