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Photomicrograph of F. gigantica miracidium showing epidermal plates (numbers referred to position and number of epidermal plates). 400×.

Photomicrograph of F. gigantica miracidium showing epidermal plates (numbers referred to position and number of epidermal plates). 400×.

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Both light microscopy and scanning electron microscopy were used in the description. There were variable measurements of eggs from the same fluke and there was no relationship between the size of the fluke and size of eggs. Light microscopy revealed that the operculum has different shapes in Fasciola gigantica and F. hepatica. Under normal laborato...

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... The developed miracidia exhibit some movements inside the egg shells before outside escaping from the eggs throughout repeated and strong pushing to the operculum, which became partially opened. The emergence of miracidia occurred within 4 days of their maturation. The miracidia of F. gigantica measured 98-119 (110 ± 0.1) · 63-77 (70 ± 0.04) lm (Fig. 2). The life span ranged between 9 and 12 ...
Context 2
... miracidium of F. gigantica was also chosen to detect the number and arrangement of the epidermal plates using di- luted neutral red (0.1%) which revealed 20 epidermal plates ar- ranged in four tiers of six, four, six, and four plates (Fig. ...

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Citations

... sediment was placed on a slide with a coverslip and viewed under the microscope. Eggs of Fasciola species were identified by their morphologic characteristics (operculated with thin shell, broadly ellipsoidal with the estimated measurements of 130-150 Mm in length and 63-90 Mm in breadth, and yellow color) (Hussein et al. 2010;Miller 1997 ;Roepstortf and Nansen 1998). The MacMaster counting technique was used to determine the egg burden of Fasciola species as indicated by Miller (1997). ...
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... Studying various parasite life cycle stages can open new ground for control and prevention programs to reduce the final host's infection risk [15]. Some reports have indicated the impact of environmental factors on the hatching Fasciola spp eggs [12,16]; however, the data on the host role in larva development and egg hatching is limited. Ashrafi et al. (2006) showed that the age of the host, helminth, and method of preparing the specimens affect the adult Fasciola eggs morphological characteristics [17]. ...
... In the current study, the hatching rates of F. gigantica and F. hepatica originated from cattle were higher than those from sheep, while there was no change in the percentage of developed eggs in the two hosts. Miracidia maturation occurs within 12-16 days in eggs of both F. hepatica and F. gigantica regardless of the host species [16]. Several reports showed that the chemical Downloaded from jommid.pasteur.ac.ir at 17:04 IRDT on Thursday April 1st 2021 composition of various plant extracts [19] could penetrate the eggshell and inhibit the egg hatching depending on the solubility in lipids [20]. ...
... In the current study, the hatching rates of F. gigantica and F. hepatica originated from cattle were higher than those from sheep, while there was no change in the percentage of developed eggs in the two hosts. Miracidia maturation occurs within 12-16 days in eggs of both F. hepatica and F. gigantica regardless of the host species [16]. Several reports showed that the chemical composition of various plant extracts [19] could penetrate the eggshell and inhibit the egg hatching depending on the solubility in lipids [20]. ...
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Introduction: Successful development of free-living stages of parasitic helminths depends on larva ability to survive, develop, and hatch. In this study, we aimed to study the host role in the hatching process of Fasciola species. Methods: Fasciola hepatica and Fasciola gigantica eggs were collected from adult worms that originated from naturally infected sheep and cattle livers and were incubated at 26±1°C for 15 days. The percentage of hatched and developed eggs were obtained for each isolate under a light microscope. A polymerase chain reaction followed by restriction fragment length polymorphism (PCR-RFLP) was applied to identify the F. hepatica and F. gigantica species. Results: Our findings showed no significant differences in the development rates of F. gigantica and F. hepatica eggs in sheep (69.32% and 72.71%) and cattle (73.56% and74.69%). However, the rates of hatched eggs of F. gigantica and F. hepatica originated from cattle (69.19% and 62.36%) were almost twice the rates in sheep (31.69% and 32.59%), indicating a significant difference. Conclusion: This study demonstrated that host species significantly affect the hatching of Fasciola eggs as the hatching rates of F. gigantica and F. hepatica originated from cattle were higher than those taken from sheep did not affect their larval development. Thus, in addition to environmental factors, the hatching phenomenon is influenced by host species.
... [2] Under room temperature, in distilled water, miracidium developed in 12-15 days in F. hepatica eggs. [7] OBSERVATION 4 ...
... Life span of the released F. hepatica miracidium was 10 h in the environment and might be similar for F. buski miracidium. [7] OBSERVATION 5 ...
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... According to our unpublished measurements and published data of other authors they vary in size from 10 µm (Microphallidae) to 40 µm (Heterophylidae); P. squamatum size (25 µm) falls within this range. Miracidia with active strategy of infection are generally larger: e.g. in Fasciola and Schistosoma they are between 100-200 µm in length (Southgate, Knowles, 1977;Hussein et al., 2010), and in Cyclocoelidae may be up to 340 µm (Ginetsinskaya, 1954). However, in several other groups "active" miracidia are as small as 50-70 µm (Allocreadiidae (Peters, LaBonte, 1965;Cannon, 1971), Zoogonidae (our unpublished data), Gorgoderidae (Goodchild, 1948)). ...
... The miracidia show positive photo tactic and negative geotropic behavior and enters the intermediate host in which it transforms into sporocyst, rediae and cercariae successively by asexual multiplication. Cercariae emerge out from snails into surrounding aquatic environment, attach to a substratum and start encystation process to transform into metacercarial cyst, preferably on the vegetation (FAO 2006;Raman et al., 2012;Dawes, 1960;Carmona, 2013;Hussein et al., 2010). The metacercariae are usually found encysted on the paddy crops (Prasad, 1989;Phalee et al., 2015). ...
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The parasitic disease, fasciolosis, in tropical and subtropical regions is caused by Fasciola gigantica, while in temperate regions the other species, Fasciola hepatica, is mainly responsible for this disease. It is one of the major food borne trematodiasis incurring huge economic losses to the livestock industry and exhibit significant threat to humans because of the zoonotic potential. Being the digenetic trematode, the life cycle of tropical liver fluke involves an intermediate host, Lymnaea auricularia, in Aligarh region. Due to the restricted access to the local private abattoirs and limited availability of the intermediate host from the field, it was decided to establish the life cycle of F. gigantica, involving experimental infection of the intermediate host with in vitro developed miracidia and collection of metacercariae following cercarial shedding from the snail host. Under optimal conditions the metacercarial cysts were successfully in vitro excysted. The newly emerged juvenile worms were assessed for the integrity of fine tegumental ultrastructures by scanning electron microscopy. The water temperature in the snail culture pots, which were kept under natural light and temperature conditions in different seasons, was found to be an important factor in the establishment of infection. The optimum temperature was found to be 25±2 °C for the successful establishment of infection in snails of about 8mm in size exposed to 10 miracidia per snail. Variation in the temperature significantly affected the 4 duration of cercarial shedding from the infected snails. The temperature changes negatively influence the cercarial output, thus affecting the metacercarial availability as well as the survival period of infected snails. Following in vitro excystation it was observed that 42 % metacercariae were viable as reflected by the emergence of juvenile worms (NEJs). Further, during the in vitro excystation the structural integrity of the tegumental surface of the NEJs remain intact as revealed by scanning electron microscopy. Thus, the invertebrate phase of the lifecycle of F. gigantica was successfully established to obtain an uninterrupted supply of normal and active larval stages of the tropical liver fluke for various studies.
... The eggs were stored in the refrigerator in distilled water till use after addition of penicillin G Sodium (100U) and dihydrostreptomycin (100 lg) (Sigma) per ml. Miracidia were developed in the eggs after their incubation as thin layer in Petri-dish in dark in the incubator at 28ºC (Hussein et al, 2010). ...
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With increasing the incidence of human Fasciola infection in Egypt, there had been speculations about an adoption of Schistosoma snail to transmit Fasciola infection, but the previous knowledge demonstrated more data about snail-trematode specification. For this reason the present study was designed to follow up the reaction of domestic and foreign snails for exposure to adapt or non-adapted miracidia on the tissue and cellular level. The data revealed failure of Fasciola gigantica and Schistosoma mansoni miracidia to complete their development in hosts other than Lymnaea natalensis (L. cailliaudi) or Biomphalaria alexandrina snails after exposure to low or high dose of miracidia. The foreign miracidia were able to penetrate the snail but the sporocysts were unable to migrate deeply in the sub-epithelial tissue of the foot. As marked specific tissue reaction was develop by the snail, trying to capsu-late them. The degree and thickness of tissue reaction was increased with the increase in time post exposure till complete disappearance of the invading sporocysts. Besides, no tissue reaction and successful infection was recorded when the miracidia penetrate their specific snail host. On the cellular level, B. alexandrina snail haemolymph contained two types of cells as hyalinocytes (H) which related mainly to humeral type of defense and phagocytic cell called granulocyte (G), The cells were in different forms and structures related to time elapsed post exposure to infection. G-3 was actively divided cell detected in infected snail only. L. na-talensis and Physa acuta contained granulocytes (amoebocyte) in HL and 3 connective tissue related cells as C.T. amebocytes, pore cell and granular cell. Amoebocyte is phagocytic cell showing morphological and numeral changes in relation to exposure of the snail for infection by different miracidia. Granulocytes in P. acuta were trapped close to foot epithelium and between C.T. matrix and playing a role in early destruction of the foreign invading miracidia.