Journal
PAKISTAN JOURNAL OF ZOOLOGY
Volume 54, Issue 1, Pages 87-97Publisher
ZOOLOGICAL SOC PAKISTAN
DOI: 10.17582/ournal.pjz/20200812070843
Keywords
Key Cryptosporidium parvum; Ct value comparison method; Cytokines; Relative expression
Categories
Funding
- Research and demonstration of key technologies for ecological dairy farming and disease prevention and control, Tangshan City's 2020 Science and Technology Research and Development Plan Project [20150203C]
- Dairy cow innovation team construction of Hebei modern agricultural industry technology system prevention and control of cow disease [HBCT2018120205]
- Key R&D project in Hebei Province Comprehensive prevention and treatment technology for multi-pathogenic infectious diarrhea of calves in dairy farms [20326603D]
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This study established a C. parvum infection model in mice and detected the expression levels of IFN-gamma, TNF-alpha, IL-2, IL-4, and IL-6 in the small intestine of infected mice. The results showed that the expression levels of these cytokines were up-regulated in the infected group, indicating their important role in controlling C. parvum infection. Therefore, the expression of these cytokines could serve as a reference for the diagnosis of C. parvum infection.
Cryptosporidium parvum (C. parvum) is a parasitic protozoan that causes cryptosporidiosis in mammalian intestinal tract. In this study, C. parvum infection model was established in Balb/c mice, followed by extraction of total RNA from small intestine of infected mice at 1, 3, 7 and 14 dpi, respectively. The relative expression of IFN-gamma, TNF-alpha, IL-2, IL-4 and IL-6 in the small intestine of Balb/cmice infected with C. parvum, were then detected using Ct value comparison method (RT-QPCR(2-Delta Delta Ct)). The primersj were designed according to the sequence of mouse cytokines in GenBank. The expression levels of the cytokines were normalized to GAPDH gene expression. Fluorescence threshold (Ct value) obtained from RT-QPCR(2-Delta Delta Ct) method with GAPDH standard curve (linearity R-2=1), followed by sequencing analysis showed that all tested cytokines were amplified. The PCR products exhibited consistent melting curves, suggesting reliable specificity of the cytokine primers. Compared with the control group, the expression levels of IFN-gamma, TNF-alpha, IL-2, IL-4, IL-6 of infected group were all up-regulated, demonstrating an important role of cytokines in controlling C. parvum infection. Hence, these findings suggest that expression of IFN-gamma, TNF-alpha, IL-2, IL-4 and IL-6cytokines could be used as reference for diagnosis of C.
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