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Trophozoite of the G. duodenalis type of organism.

Trophozoite of the G. duodenalis type of organism.

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The intestinal protozoan Giardia duodenalis is a widespread opportunistic parasite of humans and animals. This parasite inhabits the upper part of the small intestine and has a direct life cycle. After ingestion of cysts, which are the infective stage, the trophozoites emerge from the cysts in the duodenum and attach to the small intestinal mucosa...

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... was credited with the dis- covery in 1859 of the flagellate Giardia. The name lamblia was given to the species by Blanchard in 1888 (121). Giardia, a flagellated protozoan, inhabits the upper part of the small intestine of its host and has a direct life cycle. After the host ingests cysts, which are the infective stage, the trophozoites ( Fig. 1) emerge from the cysts in the duodenum and attach to the small intestinal mucosa. They undergo mitotic division in the intracellular lumen; some will encyst to protect themselves and will be eliminated from the host in the feces. Cysts can survive for 3 months in water at 4°C (120,121). They are transmitted to a new host through ...
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... were isolated from mammal, bird, and amphibian hosts (105). Initially, assignment of a species name to Giardia was based on the animal host species from which the organism was isolated. Filice (66) rejected this concept of host specificity and proposed to use the morphology of the tropho- zoite microtubular organelles known as the median body ( Fig. 1) to classify species into three groups: (i) the amphibian group (G. agilis), which has a long teardrop-shaped median body; (ii) the rodent and bird group (G. muris), which has two small, rounded median bodies; and (iii) the human group (G. duo- denalis lamblia intestinalis), in which the single or double median bodies resemble the claw ...
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... species into three groups: (i) the amphibian group (G. agilis), which has a long teardrop-shaped median body; (ii) the rodent and bird group (G. muris), which has two small, rounded median bodies; and (iii) the human group (G. duo- denalis lamblia intestinalis), in which the single or double median bodies resemble the claw of a claw hammer (Fig. 1). Organisms of the duodenalis group have been described not only in humans but also in other mammals, birds, and ...
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... of caplike structures described by Erlandsen et al. (57). These large se- cretory vesicles form only during encystation, and they trans- port cyst antigens (Fig. 9) to the nascent wall (118). In contrast, only TSA 417 was found on the outer surface of the plasma- lemma of trophozoites, encysting cells, and underlying the walls of many cysts ( Fig. 9 and 10). As encystation progresses (Fig. 10), TSA 417 disappears from the plasmalemma and its level in the lysosome-like peripheral vesicles and other large cytoplasmic vesicles is increased ...
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... et al. (57). These large se- cretory vesicles form only during encystation, and they trans- port cyst antigens (Fig. 9) to the nascent wall (118). In contrast, only TSA 417 was found on the outer surface of the plasma- lemma of trophozoites, encysting cells, and underlying the walls of many cysts ( Fig. 9 and 10). As encystation progresses (Fig. 10), TSA 417 disappears from the plasmalemma and its level in the lysosome-like peripheral vesicles and other large cytoplasmic vesicles is increased ...

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Giardiasis is a neglected parasitic disease that affects primarily children, in whom it delays physical and mental development. The pathophysiology of giardiasis in not well understood, and most reports have identified Giardia intestinalis trophozoites only in the lumen and on the brush border of the small intestine. We identified Giardia trophozoi...

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... The main challenge with antibody-based detection methods for the diagnosis of giardiasis is that the antibody remains for a relatively long time after spontaneous recovery or drug treatment (4,(16)(17)(18). Therefore, the presence and detection of antibodies in the human serum do not indicate an active Giardia infection. ...
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... This observation was similar to studies recorded in Brazil (18) and Kenya (21). The probable explanation for the age-dependent decline rate seen has been attributed to the anti-Giardia immunity (22,23) developed during growing years. Furthermore, greater hygiene practices may have been developed, making it easier to avoid catching this infection (24). ...
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... As illustrated in table (2), serum zinc concentration mean±SE µg/dl of G. lamblia 79±15 and E. histolytica 78±13 and infected children were significantly lower than non-infected 96±7 at (p<0.05). See figure (3)(4)(5)(6). Serum copper concentration (mean±ES) µg/dl of G. lamblia infected group 110±19 µg/dl was not significantly different from non-infected 125±11 µg/dl, while E. hitolytica infected children 65±7 µg/dl were significantly lower than noninfected at (p<0.01). The serum iron levels decreased significantly (p<0.05) in children with giardiasis 54±6 µg/dl and amoebiasis 68±11 compared to the non-infected group 87±10 µg/dl. ...
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... An Indian study by Yadav et al. showed a total 9.8 % cases of refractory giardiasis [1]. The rise in giardiasis susceptibility and the rate of therapeutic failure have traditionally been attributed to B cell dysfunction [8], but more recent research suggests that T cells may also play a role in these outcomes. In an adult mouse model, T cells were required to control Giardia infections [9], and evidence suggests that T cell dysfunction occurs in patients with common variable hypogammaglobulinaemia [10][11][12]. ...
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... Although current knowledge regarding the mechanisms of immunity to Giardia is limited, several studies have produced significant advances in the understanding of innate and adaptive host responses against the parasite (Faubert, 2000). ...
... The mucus layer on the intestine surface and peristaltic movements constitute mechanical barriers to Giardia attachment. Antimicrobial peptides (AMP) released by paneth and other cells can kill trophozoites (Faubert, 2000). ...
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... The reason for the rise in these age groups may be attributed to the lack of effective immunity against various pathogenic microorganisms and because this age group is relatively less resistant to them. There are factors such as poor hygiene, low socioeconomic status and environmental conditions (Faubert, 2000) In addition, children are more in contact with the land, polluted and share things with each other, all of these factors may be responsible for the increased incidence at this age (Al Kahfaji et al., 2019) ...
... Infections usually associated with poor personal hygiene, poor water quality and over crowding. Disease variabilityis related with multiple factors such as host age and gender, level of host immunityand nutrition, strain genotype, infective dose and possibly co-infection [13,14]. ...
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... The main challenge with antibody-based detection methods for the diagnosis of giardiasis is that the antibody remains for a relatively long time after spontaneous recovery or drug treatment (4,(16)(17)(18). Therefore, the presence and detection of antibodies in the human serum do not indicate an active Giardia infection. ...
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... Even though Giardia infection is usually self-limiting in immunocompetent persons, probably due to the effective host immune response against infection, resistant or chronic giardiasis can develop despite a healthy immune system (Faubert 2000). Parasite clearance in giardiasis requires a complex interaction between innate and adaptive immune responses. ...
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Giardiasis, a parasitic infection of the gastrointestinal tract, is prevalent worldwide. The integrity of the intestinal epithelial barrier plays an important defensive role in giardiasis, and as Oral supplementation with prebiotics and probiotics is known to reinforce the intestinal barrier in many gastrointestinal diseases, this study assessed the effects of prebiotic and probiotic supplementation in giardiasis and compared the results with those obtained after nitazoxanide therapy. Swiss albino male lab-bred mice (n = 50) were divided into three major groups; Group I (control group), i.e., negative (noninfected nontreated) and positive controls (infected nontreated); Group II (preventive group), in which mice were provided prebiotic, probiotic, or a combination for 7 days before of infection, and Group III (therapy group), in which mice were administered prebiotic, probiotic, combined supplements and nitazoxanide from day 12 post-infection. The assessment was achieved through Giardia cyst count, histopathological examination and ultrastructure study. Also, Serological and immunohistochemical parameters were done to evaluate the modulation of IgA levels. Oral supplementation with prebiotic and probiotic, either before or after infection (in preventive or therapy groups respectively) resulted in a significant reduction in Giardia cyst shedding. Remarkable histological and ultrastructure improvement in the intestinal changes, along with a significant increase in the serological and immunohistochemical IgA levels, were seen in mice provided combined supplements and nitazoxanide (in therapy group). Thus, our results indicate that combined prebiotic and probiotic supplementation has promising anti-Giardia activity and that it can restore intestinal structures and modulate IgA response, apart from providing synergistic effects when added to nitazoxanide.