Vol.1 No.2 -6 : Life cycle of Eimeria rhinopomi sp. nov. (Apicomplexa Eimeriidae) infecting lesser mouse-tailed bat, Rhinopoma hardwickii Gray, 1831 (Chiroptera Rhinopomatidae) in Egypt.

By : Fathy A. Abdel-Ghaffar1, Mohammed A. Shazly1,Ola H. El-Habit2 , Irene S. Gamil2,Reda M. Mansour2

Abstract

Developmental stages of the life cycle of E. rhinopomi sp. nov. were described for the first time from the lesser mouse-tailed bat, Rhinopoma hardwickii in Egypt. 152 bats were collected from October 2012 to December 2014 and examined for the presence of coccidian parasites. The infection rate was 26.32%. The collected unsporulated oocysts from the naturally infected bats were allowed to sporulate in 2.5% potassium dichromate solution. Events of sporulation and sporulation time were described. The sporulated oocysts were subspherical to ovoid measuring 29.1-36.2 x 27.3-30.2 μm and limited by a smooth double-layered wall; no micropyle but a polar granule and oocyst residuum were observed. The sporocyst measured 8.6-9.1 x 6.4-7.3 μm with a sporocyst residuum; Stieda and substieda bodies were also observed. Experimental inoculation of sporulated oocysts was carried out and the developmental endogenous stages (merogony and gamogony) were followed up and described. The prepatent period was 4 days while the patent period was 10-12 days. Endogenous stages took place in the lamina propria and epithelial cells of the upper third of the small intestine of the experimentally infected bats. Merogony occurred at 25-60 h p.i. and only one generation was observed. The mature meronts measured 10.3 x 6.2μm and yielded up to 50 merozoites. Gamogony occurred at 72-96 h p.i. The mature microgamonts measured 8.2 x 6 μm and contained up to 30 small nuclei while the mature macrogamonts measured 11.3 x 10.2 μm and contained 2 types of wall-forming bodies (types I&II). At 90-96 h p.i., newly-formed zygotes or young oocysts were observed.


Vol.1 No.2 -5 : Ultrastructural evidence of spermatogenesis in the rusty parrotfish, Scarus ferrugineus (Teleostei Scaridae).

By : T. El-Sayed Ali1*#, S. H. Abdel-Aziz1,

Abstract

This work analyses the spermatogenesis in the males of Scarus ferrugineus from histological and ultrastructural points of view. This study was carried out during the period of formation of spermatozoa thus being able to determine the pattern of spermiogenesis which is important for phylogenetic analysis. Histological examination revealed that the germ cells are classified into spermatogonia, spermatocytes, Sertoli cells, spermatids and spermatozoon based on morphology and size of the nucleus, organelles and centriolar morphology. Ultrastructural characteristics of primary spermatocytes show large nuclei with moderately compacted clusters of chromatin while secondary spermatocytes are comparatively smaller in size with central nuclei and scattered chromatin in either pole. The spermatozoon of this species is characterized by: the diplosome remains outside the nuclear fossa, the nucleus rotates at a slight degree and the flagellum is asymmetrically located, the two centrioles are arranged perpendicular to each other and no more than five spherical mitochondria are observed. Structural characteristics of Leydig cells and Sertoli cells were also described and discussed.


Vol.1 No.2 -4 : Microbiological and molecular studies on Salmonella spp. isolated from broilers in Kafr El-Sheikh governorate, Egypt.

By : Mohamed T. Shaaban 1, Hegazy , A.M 2,Sami I.Menisy 3

Abstract

Prevalence of Salmonella pathogen in poultry in Kafr El – Sheikh governorate, Egypt were analyzed in 100 pooled samples from poultry (liver, spleen , cloacal swab, gall bladder ), using culture and PCR based methods. The results showed that S. enteric was detected in 10 samples (10%), S. enterica serovar Enteritidis , S. enterica serovars Typhimurium and non-typable serovars were detected in 4(40%) , 2(20%) and 4(40%) respectively . All isolates were multi-drug resistant .Also, all isolates had drug resistant genes except for only one isolate was S. enterica serovar Enteritidis . No integrons were detected.


4. Microbiological and molecular studies on Salmonella spp. isolated from broilers in Kafr El-Sheikh governorate, Egypt.
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Vol.1 No.2 -3 : Environmental and physiological impacts of heavy metals on Nile tilapia (Oreochromis niloticus).

By : Bayomy, M. F. F1, Alne-na-ei, A. A.1, Gaber, H. S.2, Sayed, H. A3. Khairy D.M2

Abstract

The present study was conducted to investigate the distribution of selected metals (Fe, Zn, Cd, Pb, and Cu) in tissues of Nile Tilapia (Oreochromis niloticus) grown along El- Khadrawia drain – Mubark industrial Zone. The tissues analyzed included muscle and liver. Results showed metal concentrations in water followed a richness of: Fe> Zn> Cu> Pb >Cd mg/l (p < 0.05) while Fe> Cu > Zn > Pb > Cd mg/Kg dry wt. (p < 0.05) in muscles and liver tissues in winter season. Metal levels in muscles follow the level: Zn>Fe>Cu> Pb>Cd mg/Kg dry wt. (p < 0.05), while in liver they follow the level: Fe > Zn > Cu>Pb>Cd mg/Kg dry wt. (p < 0.05) in summer season. The presence of heavy metals led to significant decrease in nucleic acids (DNA & RNA) contents in liver tissue during summer season (p<0.05). So, the study showed that muscles of Nile Tilapia (Oreochromis niloticus) along El- Khadrawia drain are not safe from contamination with the metals investigated.


3. Environmental and physiological impacts of heavy metals on Nile tilapia (Oreochromis niloticus).
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Vol.1 No.2 -2 : Effect of starvation and drought on the activity of the freshwater crayfish, Procambarus clarkii.

By : Gamalat Y. Osman, Mansour A. Galal, Sherin K. Sheir* and Mona M. Soliman

Abstract

This study was designed to investigate the effect of starvation and drought on the adult Procumbarus clarkii. Samples were captured from the River Nile, Dakahleyia province, Egypt. Measurements were the animal weight and length and survival rate. The experiment was divided into four groups, control with food and water, starved with water only, drought with food only and starved – drought without any food or water groups. Crayfishes showed great tolerance for 14 weeks (P < 0.05). The body weight of the crayfish was more affected than the body and carapace lengths due to the loss of its chelae during starvation. In the starved groups, survival rate of the crayfish declined because its aggressive behavior such as killing each others (66.6%). Crayfishes could not tolerate drought for a long time (5 days). The body weight, length, and the carapace length were minimally influenced during drought, while the survival rate was dramatically affected within few days. The combined effect of both stressors affected the animal survival more drastically within four days (100, 50 and 0%). It can be concluded that starvation and drought caused serious changes in P. clarkii behavior, biometry and survival rate, which determine the ability of crayfish to adapt to one or more of the environmental changes.


2. Effect of starvation and drought on the activity of the freshwater crayfish, Procambarus clarkii.
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Vol.1 No.2 -1 : Clomiphene citrate induced kidney injury in female albino rat.

By : Hawazen A. Lamfon1 and Nahid A. Lamfon2

Abstract

Clomiphene citrate (clomid), a selective oestrogen-receptor modulator, is used in the treatment of polycystic ovary syndrome. On the other hand, it showed many adverse effects. The present work investigates the effects of clomiphene citrate (CC) on kidney of female albino rats. Many biochemical and histological changes were induced in these animals when treated with CC at doses of 50 and 100 mg/kg body weight. Treating animals with doses of 50 and 100 mg/kg body weight caused elevations in serum creatinine and urea. The histological changes in the kidney of treated animals included intertubular leucocytic infiltrations, congestion of blood vessels and degeneration of renal tubules. Moreover, atrophy of glomeruli was recorded. In conclusion, biochemical and histopathological alterations indicated that clomiphene citrate causes renal damage in female albino rats.


1. Clomiphene citrate induced kidney injury in female albino rat.
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