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.

BACKGROUND: Full supply of the nutritional requirements of C57BL/6 mice plays an important role in preventing ulcerative dermatitis syndrome. OBJECTIVES: We conducted this work to asses ulcerative dermatitis in C57BL/6 mice colony and reduce it through dietary modification. METHODS: During a two-years period, a C57BL/6 mice colony in a laboratory animal breeding center was monitored for the presence of ulcerative dermatitis syndrome. In the first year, the animals were fed with outbred laboratory mice pellet and in the second year, the modified diet was used based on the nutritional requirements of this inbred mouse. RESULTS: The average numbers of litters per parturition were 3 and 6 in the first year and the second year, respectively. The litter's mortality rate in the first year was 75 % and zero in the second year. The total number of mice remaining in the colony was 220 in the first year, which increased to 1100 in the next year. Syndrome symptoms were observed in the adult mice in the first year. Alopecia was observed mainly in the back and neck and the severity of the symptoms was mild to severe. No mortality was observed in the mice, even in severe cases, and their recovery was spontaneous, yet very slow. In the necropsy, axillary lymphadenopathy, splenomegaly, and hepatomegaly were observed. In histopathological samples taken from the skin lesions, the accumulation of inflammatory cells and the spongiosis of cornea cells were observed. In lymph nodes, spleen, and liver, pathological changes were observed from the accumulation of inflammatory cells to necrosis. In the second year, the number of cases reduced significantly to 2 %. The severity of the symptoms was mild and their recovery was faster than that in the previous year. CONCLUSIONS: By fully supplying the nutritional requirements of C57BL/6 mice, we could significantly prevent the occurrence of ulcerative dermatitis syndrome.

BACKGROUND: Microbial growth and unfavorable taste and aroma are the leading reasons of meat spoilage under refrigerated temperatures. Today, plant essential oils are good alternatives to synthetic preservatives. In the meantime, nanotechnology has been instrumental in helping to apply the most effective plant compounds on the target cell. OBJECTIVES: The present study aimed to identify the compounds of essential oil of Cuminum cyminum and to investigate the microbial counts (total count, psychrotrophs, lactic acid bacteria, mold and yeast) after preparation of nanoemulsions of cumin essential oil via ultrasonic method and its nanoemulsions. Moreover, herein, we intended to evaluate organoleptic in chicken fillet samples under temperature of 4 °C. METHODS: The essential oil components were analyzed with GC / MS and the effects of Cuminum cyminum essential oil nanoemulsion were examined on microbial count and organoleptic properties in terms of color, odor, and overall acceptance (with 9-point hedonic scale) on Cuminum cyminum EO nanoemulsions in chicken fillets under 4 °C. RESULTS: The major identified components of Cuminum cyminum by extraction time were: beta- pinene (8.90 %), benzene- methyl (16.51 %), gamma- terpene (13.39 %), propanal (29.43 %), 1 -Isopropylidene-3-N-butyl2-cyclobutene (6.52 %), and benzene methanol (8.36 %). The results of microbial count at the last day of storage showed that the treatment containing 20 % and 25 % nanoemulsions significantly delayed microbial spoilage compared to other treatments (p < /em><0.05). The control treatment also indicated the highest level of microbial spoilage; as represented in Log 6, the maximum bacterial count in chicken fillets and the shelf life of BHT at 0.02 % concentration continued until day 3. Furthermore, in organoleptic evaluation, 20 % and 25 % nanoemulsion treatment scored higher than other treatments. CONCLUSIONS: Nanoemulsions of Cuminum cyminum EO at concentrations of 20 % and 25 % were able to delay the microbial spoilage of chicken fillets and produced organoleptically favorable results.

BACKGROUND: Magnetic cell targeting is a novel non-invasive cellular delivery technique. It improves stem cell delivery to and retention in the injury site. Labeling cells with superparamagnetic iron oxide nanoparticle (SPION) is one of the most important steps of this technique. Appropriate SPIONs selection is believed to be of vital importance. OBJECTIVES: The current study aimed to produce SPIONs which are capable of attaching to Mesenchymal stem cells surface (MSCs). METHODS: Dextran coated SPIONs were produced following co-precipitation method under N2 atmosphere. Bone marrow derived MSCs were isolated and cultured from rabbit humerus bone. Anti-rabbit CD44 monoclonal antibody was attached to the surface of SPIONs and MSCs and were labeled with this final product. SPIONs coating process, particle size, and antibody conjugation efficacy were evaluated using FT-IR, SEM, and Bradford protein measurement assay, respectively. Attachment of antibody-linked dextran coated SPIONs to MSCs was accessed utilizing Prussian blue staining, immunofluorescence analysis, and SEM analysis. RESULTS: Peaks of FT-IR at 3200 cm-1 and 2922 cm-1 are representative of dextran. The average particle size was 56.13±6.67. The average antibody-SPION conjugation ratio was 77.78±6.35%. The average percentage of the labeled cells in Prussian blue and IF analysis were 71.57±2.53 and 95.04±0.95, respectively. MSCs-SPIONs conjugation was also confirmed via SEM analysis. CONCLUSIONS: In conclusion, it could be inferred that mesenchymal stem cells could successfully be labeled with dextran coated-anti CD44 antibody conjugated- superparamagnetic Iron oxide nanoparticles. This product could be used for further in-vitro and in-vivo evaluations.

BACKGROUND: Mastitis could be detected in various ways, including physical, on-farm, and laboratory tests. OBJECTIVES: The present research aimed to evaluate the accuracy of the diagnosis of mastitis using lactate dehydrogenase (LDH)-based dipsticks and to assess these dipsticks with regard to the effects of different lactation days, the amount of milk production, and parity. RESULTS: Considering bacteriologic culture as a gold standard method for the diagnosis of subclinical mastitis, the sensitivity and specificity of LDH test were 68.9 % and 54 %, respectively. The results revealed a high correlation between SCC and LDH. A statistically significant relationship was observed between the response of dipstick and CMT results; with the increase in the CMT score, the score of LDH dipstick increased. By investigating the effects of lactation days, the amount of milk production, and parity, it was determined that the chance of having subclinical mastitis in cows with positive dipstick result was 5.59 times greater than that in cows with negative dipstick result. There were no significant relationships among SCC, LDH, and CMT with lactation days and milk production; meanwhile, with the increase in parity, the three above-mentioned variables showed significant increase. CONCLUSIONS: The results of the present study indicated that the best methods for subclinical mastitis detection were SCC, CMT, and LDH based dipsticks, respectively.

BACKGROUND: Vitamin C and Carum copticum with antioxidant activity may eliminate the negative effects of heat stress on broiler performance and immunity.OBJECTIVES: This experiment was conducted to investigate the effect of feeding heat-stressed broilers with Carum copticum seed powder (CSP) and vitamin C (VC) on their growth performance, blood metabolites, carcass characteristics, and meat quality.METHODS: Herein, we carried out A 2*3 factorial arrangement in a completely randomized design with six treatments, including three levels of CSP (0, 0.75 and 1.5 % of diet), two levels of VC (0 and 250 mg/kg of DM of diet), and four replicates, on 240 one-day-old male Ross 308 broilers. The collected data were analyzed using PROC GLM of SAS. Treatment means were compared employing the Tukey test.RESULTS: The effect of CSP on their performance was not significant whereas VC treatment improved weight gain significantly (P<0.01). Interaction of CSP and VC on weight gain and feed conversion ratio was significant as broilers fed with 250 mg VC and those fed with 1.5 % CSP had the best WG and FCR (P<0.01). The addition of VC decreased the concentration of alkaline phosphatase in the blood (P<0.05). The heterophil to lymphocyte ratio was reduced through the use of VC and 1.5 % CSP (P<0.05). CSP supplementation at the rate of 1.5 % increased the relative weight of bursa of fabricius (P<0.05). Dripping loss percentage was reduced in birds fed with 1.5 % CP and VC (P<0.01). The effect of CSP and their interaction on water holding capacity was significant and the highest amount belonged to the birds fed with 1.5 % CSP (P<0.01). Additionally, VC increased meat ash percentage compared to the control group (P<0.01).CONCLUSIONS: The results of this study indicated that addition of 250 mg VC and 1.5 % CSP could be conducive to improving growth performance, blood metabolites, and meat quality of broilers under heat stress conditions.