Phylogeny and ultrastructure of Henneguya fusiformis Kostoïngué, Fall, Faye and Toguebaye 1999, a newly recorded species infecting the ovaries of Clarias gariepinus in Egypt.

The genus Henneguya is the second largest within the class Myxosporea, which infects marine and freshwater fish. One hundred Clarias gariepinus specimens were collected alive from a branch of the Nile River in Kafrelsheikh, Egypt. Microscopic and molecular procedures were used to describe how Henneguya fusiformis infects the ovaries of C. gariepinus. The infected fish showed no pathogenic changes except for macroscopic creamy whitish nodules in their ovaries with the highest prevalence during the spring season. The mature spores are spindle-shaped. The total spore length, spore body length and width are 53.4 ± 0.8 (52.5-54.3) µm, 29.8 ± 0.5 (29.2-30.4) µm and 6.5 ± 0.3 (6.1-6.9) µm, respectively. The spore anterior end consisted of two equal polar capsules, located in a tandem position, each one measuring 4.2 × 2.1 µm. The polar filament formed a coil with 6-8 turns. The measurement of the spore end with two extended processes was 24.3 ± 0.4 (23.9-24.8) µm. Phylogenetic analyses of the 18S ribosomal RNA gene sequence revealed that H. fusiformis are clustered together with other myxobolids that are histozoic in channel catfish, Ictalurus punctatus, and Asian Redtail catfish, Hemibagrus nemurus" (Clariidae) in the United States and Malaysia, respectively. To the best of our knowledge, this is the first record of H. fusiformis in Egypt. Additionally, our study is the first record of H. fusiformis in the ovaries of C. gariepinus.

Molecular and phylogenetic study on Toxocara vitulorum from cattle in the mid-Delta of Egypt.

Toxocara vitulorum is an important intestinal nematode that commonly infects ruminants world-wide, notably in tropical and sub-tropical regions. In Egypt, T. vitulorum has a high prevalence rate in cattle and buffaloes calves. The current work aims to identify and verify T. vitulorum collected from cattle in El-Mahlla El-Kubra city in the mid-Delta of Egypt, using molecular and phylogenetic tools. The first internal transcribed spacer (ITS-1) and 18S genes of ribosomal DNA were amplified, sequenced, and compared with nucleotide sequences deposited in data bases, and also used to construct the phylogenetic trees. Our results confirm that T. vitulorum isolated from cattle in Egypt is genetically identical to those recorded in other countries. Moreover, the phylogenetic trees show a close relationship among different species of Toxocara, including the zoonotic species. Our results show that ITS genes can be targeted as genetic markers to diagnose and discriminate among different Toxocara spp. The data presented here may be helpful in the pursuit of further molecular and genetic studies of Toxocara species.

ELISA and some biochemical tests of heterophyidae infection in laboratory animals.

Heterophyiasis is an important food-borne parasitic zoonosis in Egypt, among the inhabitants living around brackish-water lakes especially fishermen, and it is a common human parasite in the Nile Delta. The experiment was done on two laboratory animals (rats and dogs), and the time of sample collection was done periodically at 6, 9, 15, 21, and 28 days post-infection to evaluate different tests required. Whole blood was collected with heparin or ethylenediamine tetra-acetic acid as anticoagulant to help in the hematological studies such as red blood cells count (RBCs), white blood cells count, packed cell volume (PCV), and hemoglobin (Hb). Only marked increase in the total leuckocytic count was recorded while RBCs, PCV, and Hb were decreased in most of the results obtained. Total protein and globulin decreased while albumin and A/G ratio increased. Liver enzymes showing marked increase in aspartate aminotransferase and increase in alanine aminotransferase in dogs and rats denoting that liver has a role in the response to that infection. Kidney-function tests, urea, and creatinine showed slight increase at 6 days post-infection (d.p.i.). After preparation of different Ag (antigen) from different collected helminthes, the protein content of each was determined. The sera of infected animals were collected to find antibodies in their blood against the parasite using enzyme-linked immunosorbent assay and using crude heterophyid antigen collected from their intestines after scarification. The worms washed, homogenized, and then centrifuged to collect supernatant fluid as antigens. The results indicated that antibody starts to appear at 9 d.p.i. and increases till 21 and 28 d.p.i. and detection depends on antigen concentration.