BACKGROUND: Despite the availability of effective conjugate vaccines, Haemophilus influenza (HI) and Haemophilus somnus (HS) still result in enormous global morbidity in both human and cattle. Vaccines failure to protect against different strains can lead to the spread of Hemophilus infections. The absence of various epitopes from Haemophilus strains in existing vaccines is one of their weaknesses. Therefore, selection of a conserved and common set of proteins in the invasive strains of HI and HS is essential for predicting epitopes as potential vaccine candidate. OBJECTIVES: The aim of this study was to design an effective polyepitopic vaccine against invasive HI and HS strains using in silico approaches. METHODS: First, the protein sequences were retrieved from the databases and were aligned to determine the conserved areas with the Clustal omega software. Then, B and T cell epitopes identification was done for OapA, OMP6, PD, D15, IgA1 Protease and TbpA proteins using various immunoinformatic servers. The high ranked epitopes were selected from mentioned proteins. The selected epitopes were fused together by appropriate linkers. This designed construct was analyzed for physicochemical and structural characteristics using related servers. RESULTS: 6 TCD4+ and 3 B cell epitopes were selected to design the final construct from 6 common proteins. The immunoinformatics analysis revealed that the designed polyepitopic peptide is a safe, soluble, hydrophilic and thermostable antigen that could be a potential vaccine. CONCLUSIONS: The polyepitopic construct can be considered as a vaccine candidate against Haemophilus.

BACKGROUND: Medicinal plants have a long history in the treatment of parasitic diseases and are usually free of side effects. Removing and killing tomonts and theronts of this parasite can prevent the parasite pathogenicity in fish. OBJECTIVES: The present study aimed to investigate the inhibitory effect of ethanolic extract of Zataria multiflora on both free and parasitic life stages. METHODS: Three soluble forms of Zataria multiflora extract (80 ml/L) were prepared, which contained freshly prepared solution, stored solution at room temperature for one month and stored solution at refrigerator for one month. Afterwards, different dilutions were prepared for each of the solutions and the tomonts and Theronts were treated with different dilutions of the extract. RESULTS: Zataria multiflora extract can kill all theronts at concentrations of 20 ml/L during 6.04 to 6.37 min and concentration of 10 ml/L during 31/2 to 32.4 min, respectively. However, at these concentrations, only 3.46-6.11 % of tomonts were killed herein after 4 hours. CONCLUSIONS: Tomonts were found to be more resistant to the parasiticides than theronts. The use of Zataria multiflora extract significantly reduced tomont reproduction and decreased Ich infectivity prevalence and intensity. Zataria multiflora extract prevented Ich infestation in naive fish and effectively treated infected fish.

BACKGROUND: Oxidative stress is involved in pathogenesis of Polycystic Ovary Syndrome (PCOS). Lutein is a herbal compounds with antioxidant properties. OBJECTIVES: The current research aimed to evaluate the effect of lutein on body weight and histomorphometry of uterus in experimental PCOS induced with Dehydroepiandrosterone (DHEA) in mouse models. METHODS: Twenty-four female NMRI mice aged 20 days and weighing 14-17 g were randomly assigned to four equal groups: control, experimental PCOS, and PCOS treated groups with 125 and 250 mg/kg lutein. The induction period of PCOS with oral administration of DHEA (6 mg/100 g, daily) was 21 days and lutein treatment was followed by the induction period of 28 days. The mean body weight of the groups was evaluated on day 0, day 21 (at the end of DHEA treatment), and day 49 (at the end of treatment period) with lutein. The mean diameter of the uterine wall, the mean overall thickness of the uterine wall, the average thickness of the endometrium, myometrium and uterine epithelium, along with the number of endometrial gland branches were measured utilizing light microscope. RESULTS: The results revealed that body weight in the PCOS group was significantly higher than that in the control group on days 21 and 49. Treatment with 125 and 250 mg/kg of lutein reduced body weight in the lutein treated groups compared with PCOS (p < /em><0.01). The mean uterine wall diameter, mean total uterine wall thickness, mean thickness of endometrium, myometrium, and uterine epithelium with the number of uterine endometrial branching were significantly lower in the control and lutein treated groups compared to those in the PCOS group (p < /em><0.05). The use of both doses of lutein (125 and 250 mg / kg) significantly improved uterine histopathological indices, particularly the mean uterine wall diameter (p < /em>=0.0001) compared to the PCOS group. CONCLUSIONS: Lutein could improve the side effects of induced PCOS by DHEA on body weight and uterine parameters.

BACKGROUND: Several studies have reported the application of mesenchymal stem cells (MSCs) for the treatment of equine musculoskeletal disorders. Bone marrow (BM) and adipose tissue (AT) are the main sources for isolation of MSCs. Although the MSCs derived from various sources have similarities, certain differences have been reported in terms of biological, proliferative, immunological, and differentiative characteristics. They are also different concerning gene expression profiles. So, comparative gene expression analysis on mRNA level via quantitative real-time polymerase chain reaction (qRT-PCR) is believed to be of great value for better characterization of MSCs from different sources.

BACKGROUND: Mice are the most common laboratory animals used in research. Parasitic infections in laboratory animals affect both the research results and the health of researchers.OBJECTIVES: The present study aimed to investigate the infection status of intestinal parasites of mice in three main animal houses in Tehran.METHODS: In this study, 75 mice (25 from each animal house) were randomly purchased from an animal breeding house in Tehran and investigated. Mice were euthanized and autopsied. In order to study the gastrointestinal protozoa, wet smears were prepared from different parts of the intestine and feces and stained with Giemsa and Ziehl-Neelsen if necessary. Afterwards, the intestinal contents were examined and helminths were separated. If necessary, specific staining was used to diagnose helminths.RESULTS: Among the detected parasites, Aspiculuris tetraptera was the most prevalent (% 93.3). The mice were also infected with Syphacia obvelata (% 62.6), Hymenolepis nana (% 61.3), Tritrichomonas muris (% 22.6), Giardia muris (% 21.3), Spironucleus muris (% 18.6), Hymenolepis diminuta (% 17.3), and Cryptosporidium (% 6.6).CONCLUSIONS: Out of 75 adult mice studied, all had at least one parasite. This can affect the research results and jeopardize the health of researchers and related personnel.

BACKGROUND: Today, the fight against the bacteria causing foodborne diseases is of particular importance in the packaging of seafood. It is therefore vital to find new compounds with antibacterial properties.OBJECTIVES: In the present study, antibacterial properties of synthetic nanocomposite zinc chromite-zinc aluminate (ZnCr2O4-ZnAl2O4) on E. coli and Pseudomonas aeruginosa were studied.METHODS: After synthesis of nanocomposite, antibacterial activity of nanocomposite zinc chromite-zinc aluminate was evaluated via disk diffusion method, Minimum Inhibition Concentration (MIC), and Minimum Bactericidal Concentration (MBC) using the microdilution method.RESULTS: The results of this study revealed a higher sensitivity reaction of Pseudomonas aeruginosa (18.6±1.2 mm) compared to E. coli (12.7 ± 1.4 mm). No significant differences were observed between Gentamicin antibiotic and synthetic nanocomposite against Pseudomonas aeruginosa (P<0.05). The minimum MIC and MBC concentrations were seen in Pseudomonas aeruginosa (1.66 mg/ml) and the maximum concentration of MIC belonged to E. coli (5 mg/ml).CONCLUSIONS: In this study, the effects of nanoparticles on these gram-negative bacteria could be attributed to the small diameter of the ions, and hence the greater penetrability of these nanoparticles despite the wall's resistance. Based on the results, zinc chromite-zinc aluminate nanocomposite showed a better performance compared with gram-negative bacteria, specifically Pseudomonas aeruginosa resistant bacteria, and could be used for further studies in fisheries product packaging.

BACKGROUND: Fresh sausages are classified as one of the most perishable meat products due to the lack of using chemical preservatives.OBJECTIVES: The present study aimed to increase the refrigeration time of fresh sausages using Zataria multiflora Boiss. essential oil.METHODS: In this study, samples of fresh sausages, containing different concentrations of Zataria multiflora Boiss. essential oil (0, 0.05, 0.1, and 0.2 %), were prepared and stored under the refrigerated condition for 17 days. Subsequently, they were evaluated for microbial, chemical, and sensory properties at six time intervals (days 0, 2, 4, 6, 10, and 17).RESULTS: Based on the results of the study, by adding Zataria multiflora Boiss. essential oil to fresh sausages, the microbial count in the treatments containing high concentrations of essential oil (0.1 and 0.2 %) was significantly different from that in the control group (P<0.05). The amount of volatile nitrogen bases at the beginning of the study was 14 mg/ 100 g and after six days, in the control group, it reached 32.1 mg/ 100 g. Meanwhile, in the treated samples, it was less than 25 mg/ 100 g up to day 10. Moreover, at the end of the study, the level of TBARS in the control group reached 1.48 mg malondialdehyde /kg while this level was less than 0.78 mg malondialdehyde / kg for the groups treated with Zataria multiflora Boiss. essential oil. The results of this study also showed that the addition of essential oil has a non-significant effect (P>0.05) on sensory properties.CONCLUSIONS: Zataria multiflora Boiss. essential oil was found to have the potential to increase the shelf life of fresh sausages without adverse sensory effects.

BACKGROUND: Leucine is one of the subgroups of amino acids, which play an important role in the anabolism of muscles, adipose tissue, and the liver by stimulating insulin secretion.OBJECTIVES: Effects of different levels of leucine were investigated on carcass yield, characteristics, and quality, and expression of insulin-like growth factor (IGF-1) and insulin genes in male broilers.METHODS: Five levels of L-leucine (100, 110, 120, 130, and 140 % of Ross strain requirements) were tested with 250 male one-day-old chicks in a completely randomized design with five treatments and five replicates (containing 10 chicks each). On day 42 of their age, the blood samples of two birds from each replicate (10 birds per treatment) were taken to determine serum IGF-1 gene expression. Subsequently, these birds were slaughtered for analysis of carcass characteristics and quality, and collecting the samples of liver and breast for expression of IGF-1 and insulin genes.RESULTS: Body weight increased by consumption of 140 % of leucine as compared to 100 %. Reduction in feed conversion ratio was observed by feeding 140 % of leucine level. The IGF-1 gene expression of breast and liver increased by 110 % of leucine level. Moreover, feeding 110 % of leucine level caused a higher expression of insulin gene in breast and liver. Consumption of 130 % of leucine improved the meat protein, fat, and ash contents. Furthermore, consumption of 110 % of leucine increased the serum IGF-1 concentration.CONCLUSIONS: Consumption of leucine in broiler diets was found to increase the expression of IGF-1 and insulin genes and consequently, improve the performance and carcass quality. It also decreased the abdominal fat in broiler chickens.

BACKGROUND: The veterinary Rabies vaccine was produced using BHK-21 cells and PV strain. Although various protocols have been suggested for virus purification, they have an adverse effect on the final production and require further optimization.OBJECTIVES: The present study aimed to optimize the concentration and purification of the virus for rabies vaccine production.METHODS: First of all, the Pasteur virus strain (PV) was cultured by using BHK 21 cells with DMEM media contain bovine fetal serum (7 %) for five days. Subsequently, the virus purification was done via tangential flow filtration (TFF) system. The quality of purifying viruses was an assessment with titration and SDS-PAGE. Secondly, the virus inactivation was optimized using Minitab software based on three factors, namely time, temperature, and concentration. Afterwards, the inactivity of the samples was tested on mice. Finally, the virus potency was evaluated by the National Institute of Health (NIH) method.RESULTS: The viral titration test in TFF samples revealed that viral titer increased in comparison with the control group (P<0.05). The SDS-PAGE analysis of the purified and concentrated samples showed that the purified virus via TFF had a higher purity compared to the not-concentrated samples. Moreover, the NIH test indicated a 10-fold increase in potency result in the TFF group.CONCLUSIONS: The present study implied that the TFF method is highly suitable for condensation and purification of a high volume of viral fluid and could be applied on an industrial scale to increase the potency of the vaccine produced.

BACKGROUND: As the population grows, there is further need to food, and fish is not an exception. Several fish species are potential sources of common parasites between humans and fish. One of the important diseases common between human and fish is Anisakiasis. The parasitic agent of this disease is the larval stage of the Anisakid family nematodes, including Pseudoterranova and Anisakis.OBJECTIVES: In this study, Epinephelus fish, one of the edible and commercial valuable fishes of the Oman Sea, was examined for the presence of nematodes of the Anizakidae family.METHODS: Fifteen out of the 26 specimens were infected with Nematodes. Nematodes were isolated from fish abdominal area. For morphological study, each nematode sample was first clarified with lactophenol. Subsequently, it was examined using an optical microscope. After morphological examination of these nematodes, DNA extraction was performed. Using primers related to a part of cytochrome oxidase subunit 1 (Cox1), PCR products were 710 bp for PCR reaction. Finally, the amplified fragment was sequenced.RESULTS: The larvae were about 1 to 3 cm long, white, and often twisted. At the anterior end of the parasite, a button was seen, and in some larvae, a terminal spine was observed. In certain larvae, a small abdomen at the end of the esophagus can be seen. Out of the obtained 26 nematode specimens, eight Anisakis specimens were identified following morphological analysis. These specimens had terminal spines and three anterior lips. After sequencing, Pseudoterranova nematode was identified to belong to aniakidae family. Separate clad tree showed paraphylitic for isolated Pseudoterranova.CONCLUSIONS: Morphological examination categorized isolated larvae as the Anizakidae family. Other molecular results of this nematode showed Pseudoterranova krabbei. The results of sequencing this parasite were recorded in the gene bank under the Accession number: MK317965. This nematode was initially isolated from the Oman Sea Epinephelus fish.