Anti-Eimeria activity of berberine and identification of associated gene expression changes in the mouse jejunum infected with Eimeria papillata.

Plant-based natural products are promising sources for identifying novel agents with potential anti-Eimeria activity. This study explores possible effects of berberine on Eimeria papillata infections in the jejunum of male Swiss albino mice. Berberine chloride, when daily administered to mice during infection, impairs intracellular development and multiplication of E. papillata, evidenced as 60% reduction of maximal fecal output of oocysts on day 5 p.i. Concomitantly, berberine attenuates the inflammatory response, evidenced as decreased messenger RNA (mRNA) expression of IL-1ß, IL-6, TNFα, IFNγ, and iNOS, as well as the oxidative stress response, evidenced as impaired increase in malondialdehyde, nitrate, and H2O2 and as prevented decrease in glutathione and catalase activity. Berberine also alters gene expression in the infected jejunum. On day 5 p.i., mRNA expression of 29 genes with annotated functions is more than 10-fold upregulated and that of 14 genes downregulated. Berberine downregulates the genes Xaf1, Itgb3bp, and Faim3 involved in apoptotic processes and upregulates genes involved in innate immune responses, as e.g., Colec11, Saa2, Klra8, Clec1b, and Crtam, especially the genes Cpa3, Fcer1a, and Mcpt1, Mcpt2, and Mcpt4 involved in mast cell activity. Additionally, 18 noncoding lincRNA species are differentially expressed more than 10-fold under berberine. Our data suggest that berberine induces hosts to exert anti-Eimeria activity by attenuating the inflammatory and oxidative stress response, by impairing apoptotic processes, and by activating local innate immune responses and epigenetic mechanisms in the host jejunum. Berberine has the potential as an anti-Eimeria food additive in animal farming.

Biochemical fingerprints of salivary gland for some ticks species in Egypt by SDS-polyacrylamide gel electrophresis.

SDS-PAGE gel electrophoresis as a sensitive method is used for simultaneously comparing the total protein extracted from salivary glands in some ticks species (Argas percsicus, Hyalomm antolicum excavatum, H. an. antolicum, H. dromedarii, H. impeltatum and Rhipicephalus sanguineus). Results of A. persicus were characterized by 4 bands with molecular weights ranging from 82.76 to 16.076 KD. On the other hand, H. an. excavatum females were characterized by 6 bands with molecular weights ranging from 103.74 to 6.216 KD. H. an. antolicun males were characterized by 5 bands with molecular weights ranging from 79.183 to 2.092 KD. R. sanguineus was characterized by 4 and 8 bands with molecular weights ranging from 88.864 to 6.216 KD and 126.69 to 7.112 KD for male and female respectively. Female H. impeltatum was characterized by 8 bands with a range of molecular weights from 106.96 to 7.829 KD. H. dromedarii was characterized by 4 & 7 bands with ranges of molecular weights from 88.147 to 4.602 KD and 110.20 to 2.630 KD for male and female respectively.