BACKGROUND: There are different kinds of phytase from different sources used in poultry nutrition.OBJECTIVES: The present study aimed to evaluate the effects of addition of 2 sources of 6- phytase to the diet of male broilers in terms of growth performance, Tibia biometric, breacking straight, mineralization, blood biochemical parameters, and carcase yield.METHODS: Herein, we recruited 216 1-d-old male Ross broilers and divided them to three experimental groups and six replications for 42 D. The treatment (T) diets included: T1 (without phytase (control)), T2 (supplemented with 500 FTU/kg diet of Aspergillus niger phytase (fungi phytase)), T3 (supplemented with 500 FTU/kg diet of phytase produced by a genetically modified strain of Aspergillus oryzae by doner Citrobacter braakii gene (genetically modified phytase)).RESULTS: Serum P in the birds supplemented by genetically modified phytase was higher compared with that in the control birds (P<0.05). Additionally, Tibia P in this group was higher than that of birds supplemented by fungi phytase (P<0.05). However, Tibia breaking straight in birds supplemented by genetically modified phytase did not differ significantly with those fed with a diet with fungi phytase. Meanwhile, Tibia breaking straight in birds supplemented by genetically modified phytase was higher than control (P<0.05). Growth performance, Tibia length, diameter, ash, Ca, dry weight, average serum HDL, Triglyserid, Cholesterol, Ca, Alkalin phosphatase, Glucose, Total Protein, and Carcase yeild were not significantly different among any of the treatments.CONCLUSIONS: Supplementation of male broilers diet with genetically modified phytase (500 FTU/kg), without any differences in terms of performance, could increase P of serum, P of Tibia and breacking straight of Tibia compared to supplementation diet with Aspergillus niger phytase.

BACKGROUND: Over the recent years, Neospora caninum has been one of the most important causes of abortion in dairy cattle. OBJECTIVES: We conducted the present study in order to investigate the seroprevalence of N. caninum in dairy cattle in Semnan province and its effect on abortion. METHODS: 237 blood samples were obtained from various Semnan dairy farms and 104 bulk dairy samples from four milk collection centers in Semnan, Garmsar, Damghan, and Shahrood were tested for sera and milk utilizing ELISA (Svanova Biotech AB) test kits. RESULTS: The results revealed that 87.27 % of bovine serum was positive. The percentage of opacity density (OD) of positive sample (PP) ranged from 72.17 to 137.3 (114.21±24.65). In addition, the average rate of milk seroprevalence to the parasite was 95.23 % in Semnan province. CONCLUSIONS: The frequency of Neospora caninum infection in blood and milk was high in Semnan, yet no significant relationships were observed with abortion (p < /em>>0.05).

BACKGROUND: Trypanosomosis is a blood parasitic disease with veterinary and cosmopolitan importance due to Trypanosoma evansi (Kinetoplastida: Trypanosomatidae) type A in camels, cattle, buffaloes, and equine and type B in camels. OBJECTIVES: We conducted the present study to discriminate Trypanosoma evansi type A and B infection in one-humped camels (Camelus dromedarius) in Sistan-va-Baluchestan Province, south eastern Iran. METHODS: A total number of 369 blood samples were randomly taken from jugular vein of the examined one-humped camels from different parts of the region. Genomic DNA was extracted and polymerase chain reaction (PCR) was performed to amplify 205bp-fragment-length and 436bp-fragment-length of RoTat 1.2 VSG gene (T. evansi type A) and Minicircle gene (T. evansi type B), respectively. RESULTS: Molecular findings revealed that all the infected camels were affected by T. evansi type A. CONCLUSIONS: Based on the results of the current study, we could conclude that the cause of infection in the examined camels of the region, like other parts of the world, was T. evansi type A.

BACKGROUND: Yersiniosis is known as one of the most prevalent bacterial diseases in fish, which causes high mortality and economic losses in cultured fish farms every year. OBJECTIVES: The present study was conducted to investigate the changes in hematological indices and gut histopathology in Caspian roach (Rutilus caspicus) exposed to Yersinia ruckeri. METHODS: 60 Caspian roach broodstock with an average weight of 63.4 ± 2.1 g were divided into three groups (with two replicates for each group), including one treatment, one positive control, and one negative control groups. The treatment group was intraperitoneally injected with Yersinia ruckeri bacterium at a dosage of 3.8 × 107 cell/fish. The positive group just received normal saline (0.9 % NaCl) via intraperitoneal injection. No injection was performed in the negative control group. RESULTS: Symptoms appeared on the fourth day after exposure and 20 % of the fish in the treatment group died 5 days after the challenge. Cumulative mortality reached 53 % on day 9 after the challenge.  According to hematological analysis, the challenge with Yersinia ruckeri led to a significant increase in white blood cell counts (WBC) compared to the control groups. Moreover, 10 days following exposure, the treatment group experienced hypochromic macrocytic anemia. Gut histopathology was characterized with necrosis and detachment of intestinal epithelial cell and inflammatory cells infiltration in the treatment group. CONCLUSIONS: Based on the obtained results herein, Yersinia rackeri can cause acute disease in Caspian roach; therefore, preventing and controlling this disease is essential for these fish in infected regions.

BACKGROUND: Backyard poultry are at risk of exposure to various viral contagious diseases such as Newcastle (ND) and Avian Influenza (AI). These diseases, in addition to the backyard poultry infection have an influence on villagers’ livelihoods. Also, backyard poultry plays an important role in circulation and survival of these viruses in environment and are considered as a risk factor for the poultry industry. OBJECTIVES: Studying the prevalence level of ND and Influenza H9N2 diseases in backyard chickens in Iran, in 2014-2015. METHODS: A descriptive cross-sectional study was conducted for two years (2014-2015) in backyard chickens with mortalities suspected of infection with ND or AI H9N2 viruses. Each mortality report was considered as one outbreak. For detection of possible ND or influenza virus infection tracheal and lung tissue samples were investigated by RT-PCR reaction test. Results were analyzed statistically by SPSS software. RESULTS: Overall, 121 outbreaks of Newcastle or influenza (H9N2) disease with 25.936 cases of death from 17 provinces were reported in two years. of  these, 54 outbreaks (44/6 %) were caused by H9N2 influenza virus, 58 (47/9 %) by velogenic ND virus and 9 (7/4 %) outbreaks were caused by influenza and Newcastle concurrent infection. Hotspot ratio in 2015 was significantly higher than in 2014. In comparison with Newcastle disease alone or concurrent ND and influenza outbreaks, the highest mean mortality rate was observed in H9N2 outbreaks. Outbreaks were reported in all seasons but the rate of occurrence in the months of June and July was significantly higher than the rest of the year. CONCLUSIONS: According to our results ND and H9N2 influenza virus infections are widely distributed in backyard chickens of villages in Iran. So, for implementation of control strategies, education of villagers, vaccination and annual surveillance of backyard poultry seem necessary.

BACKGROUND: Plasma lipoprotein profile is one of the effective mechanisms in testicular tissue development and spermatogenesis process in roosters. OBJECTIVES: The present study was conducted to investigate the effect of dietary supplementation of l-carnitine during pre-pubertal period on testicular histology, spermatogenesis indexes and plasma lipoproteins of immature cockerels METHODS: A total of twelve Ross broiler breeder males (12 weeks) for 22 weeks in a completely randomized design with two treatments (0, and 250 mg/kg of L-carnitine in the diet) and six replications were used. Feeding program, and photoperiod regimen was performed based on ROSS 308 management handbook. To achieve the objectives of the study, at the age of 34 weeks, four birds were randomly selected from each treatment and after collecting blood samples from the veins under the wings, the birds were slaughtered. Finally, plasma cholesterol, LDL and HDL concentrations using a commercial kit and testicular parameters (number of seminiferous tubules, number of Sertoli cells, height of epithelium seminiferous tubules, seminiferous tubules diameter, spermatogenesis index, and tubular differentiation index) after preparation of 5-μm paraffin sections, were analyzed by SAS software. RESULTS: The results showed that the number of seminiferous tubules, and the number of Sertoli cells were significantly affected by l-carnitine (p < /em><0.05). L-carnitine supplementation in the diet of immature cockerels before sexual maturity significantly increased the spermatogenesis index (p < /em><0.003) and tubular differentiation index (p < /em><0.02). HDL levels were significantly affected by l-carnitine supplementation (p < /em><0.007). There was a significant tendency in LDL concentration (p < /em>=0.09) and LDL/HDL ratio (p < /em>=0.059) between treatments, but no significant differences were observed in cholesterol concentration between treatments. CONCLUSIONS: According to the results of this study, feeding immature cockerels before sexual maturity with 250 mg l-carnitine improves testicular tissue development and spermatogenesis process.

BACKGROUND: Due to the numerous biological effects of nanoparticles, nanotechnology can play a major role in future research areas in the poultry industry. OBJECTIVES: The SNP have antibacterial, antiviral and antifungal properties that are increasingly used in poultry farms. Therefore, the aim of this study was to investigate the effect of SNP on carcass and laying performance, qualitative and quantitative characteristics of eggs, fertility and hatchability in Japanese quail. METHODS: 96 quails including 24 male quails and 72 female quails were assigned to 4 experimental groups with 6 replications in a completely randomized design. The experimental groups consisted of 0 (control), 4, 8, and 12 ppm SNP, which were given to the birds in drinking water. Quantitative and qualitative parameters of eggs and determining the percentage of fertility and hatching were performed on a weekly basis. Also, at the end of the experiment, body weight and relative weight of internal organs were measured. RESULTS: The relative weight of liver and kidney organs increased in the SNP-receiving groups as compared to control (p < 0.05). There was a significant decrease in egg weight in SNP- receiving groups compared with the control group (p < 0.05). The effect of experimental groups on relative yolk weight was not significant. Albumin weight and yolk to albumin ratio increased in two groups of control and 8 ppm SNP, respectively (p < 0.05). Egg thickness and shape index decreased in groups 4, 8, and 12 ppm SNP as compared to control (p < 0.05). However, the effect of different experimental groups on quantitative and qualitative parameters of eggs including eggshell weight, eggshell membrane, and egg volume was not statistically significant. The SNP-receiving groups caused a dramatic increase in fertility rate as compared to control (p < 0.05); furthermore, the increase in hatchability rate in SNP groups was not significant (P>0.05). CONCLUSIONS: The results of the present study showed that the use of 4 and 8 ppm SNP can improve the laying performance, fertility and hatchability rates in Japanese quail.

BACKGROUND: Bovine tuberculosis caused by Mycobacterium bovis is an important disease that has negative effects on public health and entails economic loss. Traditional controlling programs for cattle  focus on test and slaughter strategy, and false positive is one of the disadvantages associated with tuberculin skin test. To overcome this limitation, proteins with high specificity have to be utilized. OBJECTIVES: The objective of this study was to clone and express virulent protein CFP-10 from Mycobacterium bovis AN5. METHODS: Full-length genes of cfp-10 were amplified by PCR technique. In parallel, pET23a(+) and PCR products were double digested by EcoRI and HindIII. Ligation was performed at 16˚C followed by transformation into competence E. coli DH5α. After being identified with sequencing, the cloned vector was transformed into E. coli BL21. Induction was performed by isopropyl-β-D-thiogalactopyranoside (IPTG). Urea 8M was used to dissolve the expressed protein in the inclusion body form. Recombinant protein was purified by Nickle-Resin, and urea was eliminated by decreasing the gradient. RESULTS: The CFP-10 gene clone was proved by sequencing method. The CFP-10, as a 10 KDa protein, was confirmed by Western blotting using monoclonal antibodies. Based on the results, the recombinant protein was successfully cloned and expressed. CONCLUSIONS: The results showed that cfp-10 gene was successfully cloned and expressed in prokaryotic system, indicating that this recombinant protein could be utilized in diagnostic kits against bovine tuberculosis in the future.

BACKGROUND: Cystic echinococosis (CE) is known to be one of the most important zoonotic diseases in different parts of Iran. Even though it causes major health problems, there is limited information regarding its transmission cycles and strain of this infection in eastern Iran. OBJECTIVES: The present study aimed to characterize the strain of Echinococcus granulosus cysts in the slaughtered sheep and goats in Birjand area using morphological and molecular criteria. METHODS: Isolates of E. granulosus were collected from sheep (30) and goats (30) from Birjand slaughterhouse and characterized employing both DNA (PCR-RFLP of ITS1) and morphological criteria (metacestode rostellar hook dimensions). In addition, the fragments of the genes coding for ITS-1 were sequenced. RESULTS: Among the two different identified strains/genotypes (sheep and camel), the sheep strain appeared to be the most common genotype of E. granulosus affecting sheep and goats. All of the 30 sheep samples and 20 out of 30 goat samples were infected with sheep strain. However, the camel genotype was only observed in the goats and 10 out of 30 goat isolates were infected with the camel genotype. The camel genotypes had RFLP patterns, which were different from the RFLP patterns of the rest of isolates (sheep strain). CONCLUSIONS: The results of this study revealed that the ‘sheep’ strain was the most prevalent strain in sheep and goats in this area. Moreover, the camel genotype (G6) was confirmed to trigger infection in the slaughtered goats of Birjand area.

BACKGROUND: Various flea species have already been reported from dogs, among which the most important ones include Ct. felis, Ct. canis, and P. irritans. Fleas can cause annoyance in dogs and human and transmit a variety of bacterial, fungal, and viral agents to the host. In addition, they could function as an intermediate host of Dipylidium caninum and Hymenolepis diminuta.  OBJECTIVES: Due to the lack of molecular species-associated identification data, we conducted the current study to differentiate Ct. felis and Ct. canis with molecular assay. METHODS: In the present study, 605 fleas were primarily collected from the dogs referred to Tehran Veterinary Faculty hospital. Subsequently, the flea species were identified under a microscope with morphological keys. Afterwards, COX1 genes of Ct. felis and Ct. canis were amplified via PCR and the locus was finally compared utilizing RFLP and sequencing. RESULTS: Totally, 605 fleas were isolated from 20 dogs. In morphological studies, three species were identified: Ctenocephalides felis, Ctenocephalides canis, Pulex irritans. Pulex irritans had the highest frequency (61.8 %). In molecular study, 552 bp fragment of COX1 gene in two species was amplified and seen on agarose gel. After sequencing, it was seen that two species sequences in COX1 locus had a similarity of 99 % and all of them depended on Ct. canis. In PCR-RFLP, in which Taq1 enzyme was used for differentiation of two species, the same result was obtained. CONCLUSIONS: Even though these two species of dog flea are distinct morphologically, their molecular differentiation using COX1 genes was not successful.