The use of new, highly sensitive diagnostic methods has revealed persistent infections to be a common feature of different tick-borne diseases, such as babesiosis, anaplasmosis and heartwater. Antigenic variation can contribute to disease persistence through the continual elaboration of new surface structures, and we know in several instances how this is achieved. Known or suspected mechanisms of persistence in babesial parasites include cytoadhesion and rapid variation of the adhesive ligand in Babesia bovis and genetic diversity in several merozoite stage proteins of different Babesia spp. In Anaplasma, extensive variation in the pfam01617 gene family accompanies cycling of organism levels in chronic infection. One result from the pioneering research at Onderstepoort is the definition of a related polymorphic gene family that is likely involved in immunity against heartwater disease. We are beginning to understand the sizes of the antigenic repertoires and full definition is close, with the possibility of applying simultaneous high-throughput sequencing to the order of 1 000 small genomes. We also, for the first time, can consider modifying these genomes and looking at effects on persistence and virulence. However, important biological questions remain unanswered; for example, why we are seeing a new emerging Anaplasma infection of humans and is infection of endothelial cells by Anaplasma significant to persistence in vivo.

Prevention, eradication and control of animal diseases, as well as public health assurance are major functions of veterinary authorities. The strategies to control animal diseases differ from disease to disease but are often similar on a disease basis from country to country depending on the main objective of the measure employed. These measures include among others movement control and quarantine, vaccination, treatment and mass slaughtering. However, not every country uses all these control measures at the same time. A combination of measures may be employed to avoid spreading of the disease from infected to clean animals and success is dependent on a variety of factors, including the strength and capacity of the veterinary services, cross border efforts for disease surveillance, political will, diagnostic facilities and financial support.

The present study was designed to investigate the sedative anaesthetic activity of a combination of Xylazine (X), Fentanyl (F) and Ketamine (K) in local domestic pigeons. Twelve pigeons of either sex were used. The combination of (X) and (K) were administered as pre-medication to induce sedation. Fiften minutes, after (X+F) administration, (K) was injected. All drugs were injected into the pectoral muscles. The anaesthetic effect of these drugs was reversed by injection of Yohambine (Y) and Naloxone (N) combination subcutaneously. The sedative and anesthetic activity of the (X+F-K) combination and, alterations in heart rate (RR), Respiratory rate (RR) and cloacal temperature (CT) were investigated at 10 minute before (X+F) injection, 10 and 15 minute after (X+F) administration, 5, 15, 25, 35, 45 and 55 minutes, after (K) injection and at 1, 5, 15, 25, 35, 45 and 60 minutes after (Y+N) injection. The HR, RR and CT of pigeon decreased within 10 minute after (X+F) injection and remained lower until its improvement after (Y-N) injection. The drugs combination used in this study produced a satisfactory general anaesthesia in ten of the twelve pigeons. The (Y-N) combination was an effective reverse that provide safe recovery from this anaesthetic protocol in pigeons.

The isolate of Alternaria alternata that isolated from soil produced extracellularsecondary metabolites (Mycotoxin) of carbohydrate with reducing nature which hadinhibitory effect against Gm positive & Gm negative standard and pathogenic bacteria insolid media. Three types of media Malt Extract Agar (MEA), Potato Dextrose Agar(PDA) and Potato Carrot Agar (PCA) can be using as solid or liquid media for productionthis mycotoxin. The mycotoxin extracted from free cell supernatant by simple extractionmethod using ethanol 90%. The cytotoxicity of extracted mycotoxin against human bloodcells (RBCs) was (25) ppm. The acute toxicity of extracted toxin as determined by LD50of laboratory mice was 150 mg/kg.

It was found that 0.1gm of para-aminophenyl mercuric acetate PAPMA dissolved in 10ml of distilled water added in to,Muller-Hinton agar, inhibited the growth of four standard strains bacteria [E.coli ATCC25922, S.aureus ATCC 25923, P.aeruginosa ATCC27853 and S.aureus NCTC6571] and four clinical strains bacteria positive and negative to gram stain [Klebsiella sp.,from blood isolate , E.coli, from stool isolate, Staphylococcus sp., from blood isolate, and Proteus sp.,from urine isolate]. Higher concentrations of PAPMA solution in to the medium inhibited growth of bacteria under study more strongly. The minimal inhibitory concentration (MIC) and cytotoxicity of PAPMA were studied against human blood and it was found that it has no hemolytic in RBCs for human in 1– 5µg/ml. The acute toxicity LD50 of PAPMA was studied and it was about 11.3mg/Kg.

A study was conducted during the autumn of 2000 with sheep fed on pasture from areas very near to the military operations yards in which bombs containing depleted uranium were used during 1991 war. These areas were:Safwan, Zubair, North Rumaila, tanks grave yards and Sanam Mountain. 18 samples were collected from sheep grazed in these areas Tow methods were used to measure the Radioactive nucleosides in the blood; Lyoluminescence and Track detectors methods, so that blood samples were divided into radiated and non radiated. Results of the hematological evaluation showed no significant difference between radiated and non radiated samples in Hb, PCY, and RBC. Insignificant increase was noticed in total and differential leukocytes of radiated blood samples-The biochemical parameters were also insignificantly changed in radiated blood samples as compared with those obtained from non radiated animals. These includes; total protein, cholesterol .Blood serum enzymes showed significant decreased in Aspartate aminotrasferase (AST) , while no such changes were observed in, Alaninaminotransferase (ALT), and Alkaline Phosphates (ALP)

The aim of this study is to investigate the effect of human chorionic gonadotophic (HCG), 17β-estradiol and hydrocortisone on some blood parameters and body weight in female rabbits. Twenty local rabbits were subdivided randomly and equally into four groups . The1st group used as control . The 2nd group was injected daily (30 IU /kg B.W) HCG intramuscularly . The 3rd group was injected subcutaneously daily with 0.1 mg /kg B.W s/c 17 β-estradiol and the 4th group was injected daily 0.1 mg /kg B.W intramuscularly hydrocortisone. After five weeks blood serum was tested for total Cholesterol, HDL(height density lipo-protein), LDL (low density lipo- protein),TG (triglycerides), total protein and pH. Body weight was taken dialy from first day . The results showed that the administration of HCG raised high significantly LDL(p>0.01) while total Cholesterol , TG, glucose failed to reach the significant level, .However HCG significantly lowered HDL (p>0.01) Total protein and body weight were decreased with no change in blood pH compared with the control group. The treatment with 17β-estradiol decreased the level of cholesterol , , TG and lowered significantly HDL(p 0.05 >and increased significantly LDL (p > ( 0.05. Glucose and total protein were increased with no significant effect on body weight and pH compared with the control group. While hydrocortisone increased ,HDL ,TG ,LDL and glucose and decreased cholesterol and total protein level moreover body weight and pH did n,t effected

Trocarization was used for diagnosis of sheep sarcocystosis for the first time with current study by using human biopsy needle. The obtained samples exposed to recommended sarcocystosis diagnosis techniques ( Trichinoscopy, Post trichinoscopy drop examination , Peptic digestion method and histopathlogical method ) . Out of eleven biopsy samples ( taken from the oblique muscles of the left flank )Trichinoscopy was the less sensitive ( 7/11 ) , Post trichinoscopy drop examination ( 9/11 and lately the most efficient methods which are Peptic digestion ( 11/11) and histopathological method (3/3 ). The biopsy technique showed to be suitable for sarcocystosis diagnosis in sheep without any effects on the live of the animals which make it the preferable method for advance researchs.

The present study was conducted on (40) white mice of approximately the same age (4-6 weeks) and body weight (23-25 gm) for the aim of observing the histopathological changes for male and female reproductive organs due to prolonged treatment (6 months) with anticancer chemotherapeutic agent namely methotrexate.Forty mice were divided into 4 groups (10 mice of each group 5 mice per sex). The first group (low or therapeutic dose group ) was received 0.15 mg/kg B.W. The second group ( intermediate dose group ) received 0.3 mg/kg B.W. The third group ( toxic dose group ) received 0.45 mg/kg B.W. the fourth group was a control group; it received 0.2 ml buffered physiological saline.All these groups injected intramuscularly, once weekly for 6 months. The results showed that methotrexate can cause suppression of spermatogenesis. In female, methotrexate can cause obvious pathological changes in uteri and ovaries such as reduced endometrial glands and ovarian follicles respectively