BACKGROUND: It is necessary to potentiate the immune system of fishes against stresses in farms. OBJECTIVES: This study was carried out to address the potential effect of Levamisole on immune system of rainbow trout against density stress. METHODS: 1500 fish (average weight of 50 g) were divided into 5 test groups, in which each test group was repeated three times with average density of 33 kg/m3. They were fed with commercial diet supplemented with Levamisole at concentrations of 0 (control), 100, 250, 500 and 1000 mg / kg for a period of 45 days. The fishes of all groups were then fed with Levamisole free diet and exposed to 2 and 3-fold density stress for the following 15 days. Blood samples were collected on days 0, 15, 30, 45 and 60 to evaluate the serum compliment and lysozyme activity as well as total immunoglobulins. RESULTS: The results showed that all used concentrations of Levamisole just had significant effect on compliment activity after 45 days feeding period (p<0.05). Higher levels of lysozyme and complement activity as well as total immunoglobulin were observed in 1000 mg/kg Levamisole treated group when exposed to density stresses 2 and 3-fold at the end of trial (day 60) (p<0.05). The highest overall survival was found in group which was treated with 1000 mg/kg of Levamisole. CONCLUSIONS: Our results revealed that using 0/1% Levamisole as an immunostimulator in commercial diet could potentiate rainbow trout against outbreak of high density stresses and increase its overall survival.

BACKGROUND: Carnitine biosynthesis needs methionine and lysine amino acids, vitamins niacin and ascorbic acid. So the usage of both L-carnitine and vitamin C may  improve the effects of only L-carnitine. OBJECTIVES: This study was carried out to investigate the effects of different levels of L-carnitine and vitamin C on the growth performance‚ body composition; blood serum parameters in Rainbow trout (Oncorhynchus mykiss) were investigated. METHODS: For this purpose, 540 fingerlings with the average weight 40±2 g were arranged in treatments including 3 vitamin C levels: zero, 500, 1000 and 2 L-carnitine levels: zero, 800 (mg/kg diet), with 3 replicates. RESULTS: Results showed weight gain, special growth rate and feed conversion ratio in the level of 500/800 vitamin C/L-carnitine had a significant increase compared to control (p<0.05). The highest and the lowest lipid content were observed in control and 1000/800vitamin C/ L-carnitine, respectively (p<0.05). The highest protein content was observed in 500/800 vitamin C/L-carnitine (p<0.05). Cholesterol and glucose showed a significant decrease in 500/800 vitamin C/L-carnitine. It was observed that 1000/800 vitamin C/L-carnitine caused significant decrease in blood triglycerides (p<0.05). CONCLUSIONS: Finally, it was determined that using vitamin C 500 and L-carnitine 800 mg/kg diet caused some improvement in growth performance with no  negative effects on blood parameters.

Introduction and objective: Salmonella spp. are zoonotic pathogens have been infected a wide range of domestic and wild animals. Opportunistic wild carnivores such as Golden jackal (Canis aureus) which stray in high numbers around the rural areas can act as potential sources of salmonella spp in humans and wild &amp; domestic animals in North Iran.The object of this survey was to examine the Salmonella spp infection including the antibiotic-resistant pattern in golden jackals in Golestan and Mazandaran Province.Material and Methods: Between 2013 and 2015, fecal samples of 50 road-killed Golden jackals (Canis aureus), were collected and analyzed for Salmonella contamination by classical microbiological culture methods and PCR followed by serotyping and determining of antibiotic resistant pattern.Results: 5 Salmonella belonging to 2 serotypes: S typhymurium (3/5) and S arizona (2/5) were isolated by culturing and PCR. The rate of Salmonella contamination was similar between females and males and higher incidence detected in jackals under 2 years old.Conclusion: 10% Salmonella infection of sampled golden jackals highlights the neglected role of this species in zoonotic diseases dissemination and posing a great threat to human health in rural areas of Golestan and Mazandaran Provinces.The epidemiological study on role of wild animals in the spread of salmonella and developing strategy for salmonellosis prevention and control seems necessary.

Background: Anthrax is a widespread disease in Iran and its importance is not only restricted to the economic losses in livestock but also is significant in terms of public health. Objectives: The purpose of this study was to evaluate the anthrax combating program in livestock since 1989 to 2014. Methods: In this study, national strategy of anthrax disease in livestock was evaluated from the beginning to 2014. Data were analyzed using Pearson's correlation coefficients. Results: Vaccination against anthrax began from 1929. From1989 to 2014, vaccination had been done for 78621001 cattle and 1357680466 small ruminants. In these years, there were 452 and 761 epidemics of disease in cattle and small ruminants respectively. In addition, 666 cattle and 5775 small ruminants were dead due to anthrax. There was no statistically significant relationship between the number of epidemics and vaccination, as well as between the rate of mortality and vaccination in livestock population.Conclusion: Without planning based on epidemiological principles, vaccination alone will not actually be able to decrease the incidence of the disease, so vaccination should be targeted along with control and surveillance.

BACGROUNDS: Heat stress causes the lower performance in broiler chickens. OBJECTIVE: This research was conducted to investigate the effect of betaine supplementation in broiler chickens under heat stress condition. METHODS: Two hundred one-day-old male broiler chicks (Ross 308) were used in a completely randomized design with 4 treatments and 5 replicates per treatment and 10 birds per each replicate. The experimental treatments were the heat stressed birds fed the different levels of 0.0 (without any dietary supplement), 0.05, 0.1 and 0.2% betaine. The experimental diets were added to the diets during the finisher period (day 25 to 42 of age) and under heat stress condition (32±1º C from 9.00 AM to 5.00 PM). RESULTS: The results showed that feed consumption was not affected by betaine supplementation. Consumption of 0.2% betaine resulted in a higher weight gain during the whole period as compared to 0.05 betaine and control diet (P<0.05). The consumption of all betaine levels caused the decreased feed conversion ratio during the finisher period (P<0.05) and 0.2% betaine resulted in lowest feed conversion ratio between the experimental treatments. Dietary betaine supplementation had no effect on internal organ weights of heart, liver, abdominal fat, spleen and bursa at day 42 of age (P>0.05). Furthermore, consumption of different betaine levels had no effects on blood indices, the amounts of blood enzymes and antioxidant status at day 42 of age (P>0.05). CONCLUSIONS: Totally, the consumption of 0.2% betaine improves the performance without any effects on blood indices and internal organs under heat stress condition.

BACKGROUND: Aflatoxins are secondary metabolites due to the growth of molds in animal feed. Lactic acid bacteria are microorganisms that can absorb aflatoxins. Objectives: the effect of the yeast Lactobacillus rhamnosus (PTCC 1637) on Aflatoxin B1 detoxification and absorption of toxin in in vitro (the cow rumen) was investigated. METHODS: For this purpose, the bacteria used in various treatments (live-treated, autoclave, heat-treated, treated with acid 100ºC) was prepared and added to the rumen of cattle. Aflatoxin B1 in different doses (0, 5, 10, 20) ppb in the rumen were added and at times one and two hours were incubated at 37°C. The amount of toxin residues was measured by ELISA using Europroxima kits. RESULTS: The results showed that microorganisms have been treated in an autoclave have the largest amount toxin removal (90.5 percent) (p<0.05). Also with increases the incubation time, the amount of toxin absorbed significantly (78%) increased (p<0.05) and with increasing concentrations of toxin in vitro the bacteria’s ability to absorb toxin increases. Conclusions: As a solution to the livestock feed industry bacterial cell wall or its compounds can be helpful in reducing Aflatoxin B1 toxin.

BACKGROUND: Aflatoxin M1 (AFM1) is the main monohydroxylated derivative of aflatoxin B1 (AFB1) formed in liver and excreted into milk. AFM1  creates  certain hygienic risks for human health. OBJECTIVES: The aim of this study was to determine AFM1 level in raw milk samples in Yazd province. METHODS: This investigation was a descriptive-cross sectional study. Eighty raw milk samples were collected from four cities (Yazd, Taft, Mehriz and Sadogh) in Yazd province in winter and spring seasons. The concentration of AFM1 was determined by ELISA method. The analysis of the results was performed using ANOVA and Chi-square tests. RESULTS: All samples (100%) were contaminated with AFM1, with the concentrations ranging from 3.18 to 92.24 ng/l with a mean concentration of 22.07 ng/l. AFM1 level in 13.7% of raw milk samples was higher than the maximum tolerance limit of 50 ng/l accepted by the European Union (EU). The contamination level of AFM1 in winter samples (28.21 ng/l) was higher than spring samples (15.92 ng/l). Also, the highest and lowest contamination levels were observed in milk samples collected from Sadogh (mean 42.21 ng/l) and Yazd (12.79 ng/l) cities, respectively. CONCLUSIONS: Results demonstrated AFM1 was detected with a mean concentration of 22.07 ng/l in milk samples of Yazd province. Moreover, 13.7% of samples contained AFM1 at hazardous levels for human health.

BACKGROUND: Infectious bursal disease (IBD) is a highly contagious disease of young birds. Differentiation between classical virulent and very virulent IBDV (vvIBDV) isolate is very important for the poultry industry to choose the right vaccination program. Molecular and serological tests are time consuming and have variable sensitivity. However, the melting curve analysis is relatively fast method with high precision. OBJECTIVES: This study was designed to evaluate the efficacy of the melting curve analysis for differentiation of some Iranian IBDVs which their identity had been previously determined by RT-PCR/RFLP analysis. METHODS: In this study, after RNA extraction and reverse transcription and Real Time RT- PCR of IBDVs, high melting resolution at temperatures ranging from 81 to 92°C were performed. RESULTS: The findings of this study showed that in the high resolution melting curve analysis, the viruses were classified from A to D. Three vaccine strains of D78, Gumbokal, Bursa CE; IBD L; Bursine 2; and all field viruses were placed in groups A, B, C, and D, respectively. High resolution melting curve analysis after normalization also showed all viruses of this study were placed in 4 HRM genotypic group. Three strains, D78, Gumbokal, Bursa CE, produced similar and non-differentiable curve but were different from other vaccine and field strains. Two other vaccine strains, IBD L and Bursine 2, were different from each other and other viruses. CONCLUSIONS: We concluded that the real-time RT-PCR HRM technique is cost-effective and reliable among the currently used methods and can be used for differentiation of IBDV isolates.

BACKGROUND: PRP (Platelet-Rich Plasma) is a biological product that has shown significant therapeutic results compared to synthetic drugs and some traditional methods. The advantages of this method include: PRP, compared to other biological materials, is easily prepared in clinic and the safety is high as well. OBJECTIVES: We aimed to investigate the evaluation of histomorphometric properties after injection of plasma. METHODS: Thirty rats were divided randomly into three groups: control group (normal saline), PRP and PPP (Platelet-Poor Plasma) groups. In order to prepare PRP and PPP, blood samples (1cc) were collected through cardiac puncture and were centrifuged. The upper layer consisted of PPP and lower layer consisted of PRP. The 2% calcium gluconate solution (100 µl) was added to platelet-rich plasma (200 µl) layer to activate platelet. After seven days, the dorsal skin samples were collected. They are cut into 5 to 6 μm thickness sections using paraffin embedding method and were stained by hematoxylin, eosin and Masson’s trichrome. The epidermis, dermis and hypodermis layers of skin, the epithelial thickness of hair root sheath, maximum depth of hair follicles, the thickness of the whole skin, the number of sebaceous glands and hair follicles in the specified scale, finally the number of fibroblast cells and the percent distribution of connective tissue fibers were investigated in histometric structure of the skin and skin appendages. RESULTS: The results of this study indicated that systematic and controlled PRP may have beneficial effects on the reconstruction and rehabilitation of the skin and its appendages. CONCLUSIONS: The present study showed that growth factors in plasma especially PRP, could be stimulated connective tissue fibroblast of dermal layer in the skin.

BACKGROUND: The most common metal used in the body is iron and since it may produce ROS, it could potentially be a dangerous substance. OBJECTIVES: Regarding the side effects of nanomaterials such as nano iron particles and possibility of environmental contamination including air pollution with nanoscale iron particle, this study was designed to compare the effects of conventional iron oxide with iron oxide nanoparticles, on certain indexes of ovarian tissue in a rat experimental model. METHODS: This animal model was carried out in 5 groups of female rats, including control, iron oxide (15 mg) and iron oxide nanoparticles (5, 15 and 30 mg). The drugs were intraperitoneally injected daily for 16 days. On the seventeenth day the rats were euthanized by chloroform. Ovarian tissue was removed, and histological changes and iron accumulation were assessed by special staining and light microscopy. RESULTS: According to our findings, folliculogenesis was decreased in all groups receiving iron. The number of corpus luteum in the groups receiving different doses of nanoparticle was reduced and the number of atretic follicles was significantly increased in all groups compared to the control group. CONCLUSIONS: In conclusion, probably iron nanoparticles with impaired cellular oxidative pathways, reduces the number of follicles and corpus luteum and increase atretic follicles by producing oxygen free radicals and destructing microfilaments. This can cause a negative effect on the fertility of female rats.