Ibrahim, A., Ali, Y., Abd El-Aziz, A., El-Badry, A. (2022). Cryptosporidium spp. and Helicobacter pylori in a hospitalbased study of diarrheic immunocompromised Egyptian children: Insight into risk factors, and co-infection. Parasitologists United Journal, 15(2), 181-189. doi: 10.21608/PUJ.2022.140818.1170
Asmaa Ibrahim; Yasser Ali; Amal Abd El-Aziz; Ayman El-Badry. "Cryptosporidium spp. and Helicobacter pylori in a hospitalbased study of diarrheic immunocompromised Egyptian children: Insight into risk factors, and co-infection". Parasitologists United Journal, 15, 2, 2022, 181-189. doi: 10.21608/PUJ.2022.140818.1170
Ibrahim, A., Ali, Y., Abd El-Aziz, A., El-Badry, A. (2022). 'Cryptosporidium spp. and Helicobacter pylori in a hospitalbased study of diarrheic immunocompromised Egyptian children: Insight into risk factors, and co-infection', Parasitologists United Journal, 15(2), pp. 181-189. doi: 10.21608/PUJ.2022.140818.1170
Ibrahim, A., Ali, Y., Abd El-Aziz, A., El-Badry, A. Cryptosporidium spp. and Helicobacter pylori in a hospitalbased study of diarrheic immunocompromised Egyptian children: Insight into risk factors, and co-infection. Parasitologists United Journal, 2022; 15(2): 181-189. doi: 10.21608/PUJ.2022.140818.1170
Cryptosporidium spp. and Helicobacter pylori in a hospitalbased study of diarrheic immunocompromised Egyptian children: Insight into risk factors, and co-infection
1Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Egypt
2Department of Microbiology, Faculty of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia
Abstract
Background: Immunocompromised children are more susceptible to a diversity of pathogens including norovirus, rotavirus, diarrheagenic Escherichia coli, Cryptosporidium spp. and Helicobacter pylori. Objective: This study aimed to determine the detection rate of H. pylori and Cryptosporidium spp.; their co-infection in a hospital-based study of diarrheic immunocompromised children and their predictive risk factors; and to evaluate the diagnostic performance of the used assays. Subjects and Methods: Fecal specimens were collected from 102 immunocompromised diarrheic children, with ages ranging from few months old to 16 years. All fecal samples were examined microscopically for detection of parasites, as well as immunologically and molecularly for detection of H. pylori and Cryptosporidium spp. Copro-antigens of Cryptosporidium and H. pylori were detected immunologically using rapid chromatographic copro-immunoassay tests. Amplification of H. pylori and Cryptosporidium copro-DNA was performed using the nPCR assay targeting genes encoding H. pylori urease A and Cryptosporidium oocysts wall protein (COWP). Amplified Cryptosporidium PCR products were digested by a restrictive enzyme to detect genotype. Results: H. pylori copro-DNA and copro-antigen were detected in 56 (54.9%) and 18 (17.6%) patients, respectively. Cryptosporidium copro-DNA, and copro-antigen were detected in 22 (21.6%), and 16 (15.8%) patients, respectively, while microscopy detected Cryptosporidium oocysts in only 6 patients (5.9%), with a clear predominance of anthroponotic C. hominis (81%). Cryptosporidium spp. and H. pylori co-infection occurred in 15.8% of patients. None of the studied variables had a significant association with any of the tested pathogens, neither separately nor combined. Conclusion: There was a high detection rate of H. pylori and Cryptosporidium spp. and their co-existence in diarrheic immunocompromised children. Our study results highlight that PCR increased the sensitivity for the diagnosis of Cryptosporidium spp. and H. pylori. More research is needed to establish their relevance.
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