Affiliation:
1. Medical Parasitology Department, Faculty of Medicine Tanta University Tanta Egypt
2. Histology Department Faculty of Medicine, Tanta University Tanta Egypt
3. Anatomy and Histology Department Mutah University Mutah Jordan
Abstract
ABSTRACTCryptosporidium is an opportunistic protozoan, with many species of cross‐human infectivity. It causes life‐threatening diarrhoea in children and CD4‐defective patients. Despite its limited efficacy, nitazoxanide remains the primary anti‐cryptosporidial drug. Cryptosporidium infects the intestinal brush border (intracellular–extracytoplasmic) and down‐regulates pyroptosis to prevent expulsion. Romidepsin is a natural histone deacetylase inhibitor that triggers pyroptosis. Romidepsin's effect on cryptosporidiosis was assessed in immunocompromised mice via gasdermin‐D (GSDM‐D) immunohistochemical expression, IFN‐γ, IL‐1β and IL‐18 blood levels by ELISA, and via parasite scanning by modified Ziehl–Neelsen staining and scanning electron microscopy (SEM). Oocyst deformity and local cytokines were also assessed in ex vivo ileal explants. Following intraperitoneal injection of romidepsin, oocyst shedding significantly reduced at the 9th, 12th and 15th d.p.i. compared with infected‐control and drug‐control (nitazoxanide‐treated) mice. H&E staining of intestinal sections from romidepsin‐treated mice showed significantly low intestinal scoring with marked reduction in epithelial hyperplasia, villous blunting and cellular infiltrate. SEM revealed marked oocyst blebbing and paucity (in vivo and ex vivo) after romidepsin compared with nitazoxanide. Regarding pyroptosis, romidepsin triggered significantly higher intestinal GSDM‐D expression in vivo, and higher serum/culture IFN‐γ, IL‐1β and IL‐18 levels in romidepsin‐treated mice than in the control groups. Collectively, in cryptosporidiosis, romidepsin succeeded in enhancing pyroptosis in the oocysts and infected epithelium, reducing infection and shifting the brush border towards normalisation.