BACKGROUND: Aflatoxins are natural fungal toxins that weaken the immune system and damage the liver. OBJECTIVES: The effects of seeds and whole plant powder and extract of Milk thistle (MT) plant in reducing the negative effects of feeding aflatoxin (AF) on broiler chickens blood parameters and immune response were examined. METHODS: 192 one-day old chicks (Ross 308) for 35 days in a completely randomized design with six treatments, four replicates and eight birds per repetition were used. The experimental treatments included: 1) control, 2) contaminated control (CC), 3) CC + 0.5 percent of MT seed powder, 4) CC + 1 percent MT plant powder, 5) CC + 600mg/kg MT plant extract, 6) CC + 1000mg/kg MT plant extract. RESULTS: The treatments had no significant effect on plasma concentrations CHOL, HDL, LDL, ALP, LDH, AST, ImG and ImM. Feeding contaminated diet increased alanine aminotransferase enzyme compared with healthy control (P≤0.05). The addition of 0.5 percent MT seed powder, 1 percent MT plant powder and 1000mg/kg MT plant extract to the contaminated diets decreased alanine aminotransferase enzyme compared to the contaminated control (P≤0.05). Inclusion of 1 percent MT plant powder to AF infected diet significantly increased the antibody titer compared with healthy control and contaminated control (P≤0.05). CONCLUSIONS: It was concluded that compared to other treatments, 1 percent MT plant powder was more effective in reducing the negative effects of feeding AF in broiler chickens.

BACKGROUND: Honey is an excellent food product with health-giving characteristics. On the other hand, the honey quality can change based on various factors. OBJECTIVES: Physicochemical experiments intend to investigate the honey quality in four geographic directions of Kurdistan province shelf-life and the containers the honey is placed in. METHODS: In this research, totally 96 samples from 4 apiaries in various parts of the province were prepared and maintained in various dishes/containers and various (time) periods at 25.5±3.5 °C. After preparing the samples, some factors including moisture, reducing sugars, sucrose, pH, acidity, the ratio of fructose to glucose, ash, diastase, hydroxyl methyl furfural were evaluated. RESULTS: The result showed the moisture total average, reducing sugars, sucrose, pH, acidity, the ratio of fructose to glucose, and ash were 13.79%, 77.67%, 2.22%, 3.86, and 21.39 of meq/kg, 1.09% and 0.13%, respectively. Qualitative examinations showed, there was the distance in all samples but no HME. With the increase in shelf-life time, metabolites in the ratio of fructose to glucose and acidity increased significantly, but the factors, moisture, pH were reduced significantly (P<0.05). Various containers had no significant impact on physicochemical characteristics of honey. CONCLUSIONS: Generally, one can say that the comparison between the obtained amounts with the current standards, quality of the honey samples were standard and favorable. According to the results of this study, honey can remain at room temperature in different containers for 9 months and maintain anacceptable quality.

BACKGROUND: Ascites is a metabolic disease that has negative effects on broiler chickens. OBJECTIVES: This study was performed to investigate the effect of cold induced ascites on performance, meat quality and quantity indices and some blood indices of broiler chickens with cold induced ascites. METHODS: Three hundred one-day-old female chicks (Ross 308) were used in a completely randomized design with two treatments of control (under normal temperature) and ascitic (under cold stress) with five replicates and 30 birds per each replicate. RESULTS: The results showed that cold-induced ascites caused the lower performance, carcass weight and thigh and breast meat (P<0.05). Furthermore, ascites caused the increased anus temperature and thigh lightness (L) and redness (a) at day 42 of age (P<0.05). Cold induced ascites decreased the enzymes of glutathione peroxidase and superoxide dismutase, uric acid, albumen and malondihaldehyde in blood at day 42 of age (P<0.05). The higher blood hematocrit and hemoglobin were observed in ascetic birds (P<0.05). CONLUSIONS: In conclusion, cold induced ascites increase the meat lightness through the increased peroxidation and decreased antioxidants of the body. Moreover, ascites cause the higher anus temperature by increasing the body basal metabolism.

BACKGROUND: Neospora caninum is one of the most important pathogenic protozoan parasites causing bovine abortion around the world. Objectives: The aim of this study was to detect the presence of Neospora caninum in the brain, cerebellum and medulla oblongata of aborted fetuses in cattle in Arak by means of molecular method. Methods: 38 samples of brain, cerebellum and medulla oblongata from aborted fetuses in dairy cattle of Arak were tested for the presence of Neospora with nested-PCR. Results: Survey findings indicated the presence of DNA in 26.3 % of aborted fetal brains. In the cerebellum and medulla oblongata samples no Neospora caninum  DNA was detected. There was a significant relationship between neosporosis and maternal age (number of calvings), abortion history and the presence of dogs in the herd. Conclusions: The results showed a significant association between the infection and the number of abortions in the examined cows; As a result it seems that neosporosis could be an important factor in epidemic abortions in Arak city’s dairy farms which requires continuous monitoring and implementation of prevention programs in the dairy industry.

BACKGROUND: Peste des petits ruminants (PPR) is an acute and highly contagious viral disease of small ruminants that is characterized by high fever, ocular and nasal discharge, pneumonia, necrosis, ulceration of the mucous membranes and inflammation of the gastro-intestinal tract leading to severe diarrhea. OBJECTIVES: The aim of this study was to investigate the seroprevalence of peste des petits ruminants (PPR) virus infection in sheep and cattle in Ahvaz. METHODS: Blood samples were taken from 100 cattle and 100 sheep that were kept together from different parts of Ahvaz. Blood samples were also taken from 16 vaccinated sheep   against PPR for positive control. The sera were separated by centrifuge at 3000 ×g for 10 minutes and 3 mL of serum was harvested and stored at -20 °C until determination of antibody against PPR using VN method. RESULTS: The peste des petits ruminants (PPR) antibody seroprevalence was 23% in cattle and 58% in sheep and all the sheep samples collected for control were positive for PPR antibody. CONCLUSIONS: The present study indicates serological evidence for the natural transmission of PPRV from sheep to cattle under natural conditions and provides baseline information on prevalence of PPRV antibodies in cattle and sheep population in Ahvaz.

BACKGROUND: Leptin as a cytokine-like hormone is derived from ob gene (one of the major effect genes on birth weight and growth traits) and is secreted by adipose tissue. This hormone with binding to its receptors in the hypothalamus, inhibits food intake and increases energy consumption. OBJECTIVES: There is not any report about expression of leptin gene in response to oral administration of selenium in livestock. In the present study, the effects of selenium nanoparticle and sodium selenite on the transcription of leptin gene in placenta were studied. METHODS: Twenty, four-month pregnant ewes within the same age were selected randomly. During the 21 days leading up to birth, oral administration of selenium nanoparticles (Se NPs) with dosages of 0.05 and 0.10 mg/kg B.W. and sodium selenite with dosage of 0.1 mg/kg B.W. was carried out. At the same time the control group was fed distilled water in equal volume. With sampling of the placenta during childbirth, transcription amount of leptin gene was determined by RT PCR Real Time based on a comparison assay of 2-ΔΔCt. Results: The results of this study showed that leptin gene is expressed in placental tissue. The oral administration of selenium nanoparticle and sodium selenite caused a significant increment in terms of expression of mentioned gene in comparison to the control treatment. Also, there was a significant difference between the supplements, so that the highest leptin gene expression in placenta was observed in selenium nanoparticle treatment with dose of 0.1 mg and then supplement with selenium nanoparticles with dose of 0.05 mg. CONCLUSIONS: Selenium causes an increment of leptin gene expression in placental tissue.

BACKGROUND: Reproductive diseases are among the most important life threatening problems in captive female iguanas. Egg binding is a reproductive disorder in which female iguana cannot lay one or more of its eggs, mainly caused by improper husbandry. Physiological and pathological process of egg production such as egg binding in iguanas has to be assessed more. Objectives: In this study, diagnostic value of two modalities, radiography and ultrasonography, have been compared for evaluation of egg binding in green iguana. Methods: In this study ultrasonography and digital radiography were used as non-invasive methods to evaluate and describe dystocia in captive female green iguanas. Ultrasonography was performed in ventral aspect of abdomen in two sagittal and transverse planes. While radiographic images were taken in both dorso-ventral (DV) and lateral projections. Results: Ultrasonography provided more accurate and informative results than digital radiology. Radiography can be used to detect gravidity and presence of large eggs or follicles. Heterogeneous echogenic eggs or follicles, with different egg size, irregularity in egg borders and echogenic free fluid in celomic cavity were detected in egg-bound green iguanas. Among these ultrasongraphic evidences, the strongest sign was presence of echogenic free fluid in celomic cavity. However digital radiography is unable to delineate fluids in celomic cavity following egg binding in green female iguanas. Among two radiographic positioning, dorso-ventral view provides more information than lateral images. Conclusions: In conclusion, when we encounter a female green iguana with clinical signs of egg binding, ultrasonography has more advantages than radiography, however both modalities can be informative

BACKGROUND: Yersiniosis or enteric redmouth disease (ERM), caused by Yersinia ruckeri, is a serious bacterial disease in the farmed salmonids that causes economic problems in this industry. OBJECTIVES: This study was aimed to assess the experimental pathogenicity of Yersinia ruckeri in Rainbow trout (Oncorhynchus mykiss). METHODS: Two hundred Rainbow trout weighting 100-120 g, challenged with different strain of Yersinia ruckeri were obtained from affected trout farms using intra peritoneal injection route at a concentration of 108 cells/ml (0.1 mL per fish) to evaluate the virulence of these isolates. Each treatment group included 10 fish in two replicates and control fish received 0.1 mL sterile normal saline (0.9% NaCl). Following the intra peritoneal challenge, macroscopic and microscopic findings were determined. The most virulent strain was then used to determine the lethal concentration (LD50) using both intra peritoneal and bath method at dilutions of 103-1010 cells/mL. RESULTS: Macroscopically, anorexia, lethargy, circular swimming near the surface, blackening of skin, exophthalmia, hyperemia and hemorrhage in different parts of body, anal prolapse, enlarged liver and spleen were observed. Microscopically, hyperemia of hepatic sinusoids and vessels, necrosis and vacuolization of hepatocytes, increase in the abundance of macrophage centers in kidney, dilatation of Bowman’s space, degeneration and necrosis of kidney tubules, severe necrosis and detachment of intestinal villi, hyperplasia and clubbing of epithelial cells of secondary lamellae, spleen cell necrosis, goblet cell hyperplasia and thickening of epidermis layer in the tongue mucosa were observed.  The LD50 of intra peritoneal injection was calculated 1.2×106cells per fish 48 h post challenge. In bath route, LD50 was obtained 5×108 Cells/ml after 96 h. CONCLUSIONS: The results obtained from this study show virulence diversity of native strains.

Backgrounds: Avian Influenza is viruses from the Orthomyxovirida family. This disease, in poultry, turkey, and many other birds caused by different subtypes of type A influenza virus.Objectives: The aim of this study was to estimate probability infections of H5 and H7 subtypes of AI viruses in commercial and backyard poultry in Iran. Methods: This cross-sectional study was done in Iran’s commercial and domestic poultry from September to December in 2013. The samples were examined with the HI test to differentiate H5&amp; H7. A total of 1315 premises and 29058 birds were sampled. Results: All premises were negative for H7 subtype and five premises (3 broiler breeders and 2 villages) out of 1315 were positive in HI test. All the collected swab samples from H5 seropositive premises were PCR negative for detection of H5. The results of our study showed that existing live bird marketing with OR=19.68(CI 95% 2.18-177.38) and existing duck farm within up to a 3 km radius with OR=11.33 (CI 95% 1.30-96.68) were risk factors for H5 sub type. Conclusions: Based on live bird marketing role in transmission and spreading of Influenza viruses specially at the time of migration season in country and the probability of hunting and selling of them at these markets, continuous monitoring of these markets for early detection of probable infections and preventing the spread of infection to other poultry is recommended.

BACKGROUND: Aflatoxin B1 (AFB1) is a secondary toxic metabolite produced by some Aspergillus species, particularly Aspergillus flavus (A. flavus) and A. parasiticus that contaminate feedstuffs. OBJECTIVES: The aim of this study was to evaluate the contamination of the concentrate and corn silage samples to toxigenic fungi and aflatoxin B1 in cattle farms of Yazd province in Iran. METHODS: A total of 80 samples of concentrated feeds and 80 samples of silage feeds were collected from cattle breeding farms of 4 cities in Yazd province in winter and spring seasons (40 samples in each season and one sample from each cattle farm). The samples were cultured on mycological media in order to isolate and determine the amount of the toxigenic fungi. Concurrently, the content of AFB1 was measured in feedstuff samples using ELISA technique. RESULTS: The results indicated that the most frequent fungi isolated were Aspergillus spp. (49.3%), Penicillium spp. (23%), Mucor spp. (22.3%) and Fusarium spp. (4.8%) in winter and Aspergillus spp. (46.9%), Penicillium spp. (21.8%), Mucor spp. (28.5%) and Fusarium spp. (2.8%) in spring from all understudy feedstuffs. The mean of AFB1 in feedstuffs were 0.25 and 0.21 µg/kg in winter and spring, respectively. According to statistical analysis of the results, significant differences were observed between the frequency of Aspergillus isolates and other fungal species (p<0.05) and also between toxigenic fungi, such as Aspergillus, Fusarium and Penicillium, with other isolated fungi (p<0.05). Among toxigenic fungi, significant differences were observed between Aspergillus and Penicillium species, Aspergillus and Fusarium species and Penicillium and Fusarium species (p<0.05). Significant relationship was observed between the amount of toxigenic fungi and AFB1 in feedstuffs (p<0.05). CONCLUSIONS: The results obtained by this study show that rapid and specific detection of aflatoxigenic fungi is essential to ensure the mycological safety of animal feedstuffs.