3 research outputs found

    Water pollution in the Middle Nile Delta, Egypt: An environmental study

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    Water-borne diseases have been estimated to cause more than two million deaths and four billion cases of diarrhea annually. Water-borne pathogenic organisms include bacteria, protozoa, and viruses. Heavy metal contamination of water is also a potential threat to human health. This study aimed to detect contamination of potable water with protozoal and bacterial pathogens as well as heavy metals in Gharbiya governorate in the middle of the Nile Delta, Egypt. Therefore, this study was conducted on water samples from 3 different localities in Gharbiya governorate throughout the year 2014. Water samples (108) were collected from source, plant and tap water at the four seasons. Parasitological, bacteriological, and toxicological evaluation was carried out for all samples. Parasitological evaluation was done to detect protozoal contamination by conventional diagnostic staining techniques, immunofluorescence assay, and flow cytometry. The study identified the protozoal contaminants in water, and showed that flow cytometry positive results were more than the conventional staining. Also, the study identified bacterial fecal contamination of source water as well as heavy metal pollution in source water. Since the integration of flow cytometry could facilitate detection of Giardia cysts and Cryptosporidium oocysts in water samples, we strongly recommend its use as a routine for the detection of these pathogenic protozoa. Finally, Ongoing evaluation of drinking water is needed as well as formulation and implementation of an integrated plan to limit the contamination by pathogens and heavy metals

    The interaction of Schistosoma mansoni infection with diabetes mellitus and obesity in mice

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    Abstract Human schistosomiasis is one of the most prevalent parasitic diseases worldwide. Various host factors can affect the host–parasite interactions. Therefore, the aim of the present work was to determine the parasitological, histopathological, biochemical, and immunological status of Schistosoma mansoni-infected hosts with metabolic disorders to identify the underlying possible mechanisms of these comorbidities. The study animals were divided into four groups. Group I represented the control groups, namely, the normal control group, the S. mansoni-infected control group, and the noninfected type 1 diabetes (T1DM), type 2 diabetes (T2DM), and obesity groups. The mice of the other three groups underwent induction of T1DM (Group II), T2DM (Group III) and obesity (Group IV) before being infected with S. mansoni. All mice were subjected to body weight measurement, blood glucose and insulin assessment, parasitological evaluation of adult worm count, tissue egg count and intestinal oogram. Histopathological and immunohistochemical study using anti-glial fibrillary acidic protein (GFAP) in hepatic stellate cells (HSCs) and image analysis of Masson’s trichrome-stained liver sections using ImageJ (Fiji) software were carried out. Additionally, immunological analysis of tumour necrosis factor (TNF) beta, interleukin-5 (IL-5), IL-10, Forkhead box P3 (FOXP3) and pentraxin 3 (PTX3) levels besides biochemical study of total lipid profile were evaluated. The present study revealed a significant increase in the adult worm count and tissue egg output in the obesity group compared to the infected control group. The oogram of counted eggs showed prevalence of immature eggs in T1DM group, while T2DM and obese groups showed prevalence of mature eggs. The fibrosis area percentage showed significant increase in T2DM and obese groups while it was decreased in T1DM group in comparison to infected control group. Our data also showed significant increase in the levels of TNF-β, IL-5, PTX3 in T1DM, T2DM and obesity groups in comparison to infected control group, whilst the levels of FOXP3 and IL-10 were increased in the infected groups in comparison to their noninfected controls. Moreover, infected T1DM, T2DM and obesity groups showed higher blood glucose and lipid profile in comparison to the infected control group. However, these parameters were improved in comparison to their noninfected controls. In sum, induction of T2DM and obesity increased tissue egg counts, mature egg percentage, and fibrosis density, while schistosome infection induced changes in the lipid profile and blood glucose levels in infected diabetic and obese groups and impacted favorably insulin levels in obese mice. By better understanding the complexities of host–parasite interactions, efforts to reduce the burden of these debilitating diseases can be improved
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