Showing 9 results for Jorjani
Volume 2, Issue 2 (9-2013)
Abstract
: The effects of lidocaine on water quality and some hematological parameters in simulated transportation of the fingerling common carp, was investigated. Dissolved oxygen and ammonia of the control group and 0.01, 0.03 and 0.05 ml/lit lidocaine treated groups were tested at 0 h, 1, 2 h, 3 h, 4 h and 5 h simulated transportation. For the hematological assessment, blood samples were collected from the caudal peduncle of fish in all of the treatments at the beginning and termination of the experiment. The results showed decreased oxygen consumption and ammonia excretion by the fish treated with lidocaine during the experiment. No significant differences in the hematological parameters were found in the levels of RBC, Hb, HCT, MCV, MCH, MCHC and WBC in all the groups (p<0.05).
Volume 3, Issue 4 (12-2017)
Abstract
Background: Enterobious vermicularis (E. vermicularis) is one the most common parasitic infection among children.
Objectives: The present study aimed to determine the prevalence rate of enterobiasis among preschool children in Mazandaran province, northern Iran.
Materials and Methods: In this cross–sectional study, 653 preschool children were recruited via the cluster sampling method during April 2013 to Feb 2014. A questionnaire was administrated to parents by an interviewer and determined children’s socio-demographic characteristics, personal hygiene, and healthy behaviors. The Graham technique was applied for diagnosis. Data were analyzed using logistic regression model and chi-square test.
Results: In a total of 653 examined subjects, the prevalence rate of E. vermicularis was 19.4%, among which 40.9% were male, and 59.1% were female. The highest and lowest prevalence rates of E. vermicularis were found in Neka (61.4%) and Tonekabon (1.6%) districts, respectively. A significant association was found between infection and residency, parental occupations, parental education, number of family members, changing underwear, sterilization of linen clothing, taking daily bath, boiling or ironing clothes.
Conclusions: The high prevalence rate of E. vermicularis infection in this study proves the stability status of enterobiasis in this area, posing a risk for children there. Systematic control of infection in children is proposed.
Volume 4, Issue 4 (Fall 2018)
Abstract
Aims: The aim of this study was species identification and analysis of species of Leishmania isolated from clinical samples.
Materials & Methods: The samples were collected from patients that were infected from different parts of Iran. After microscopic examination, we used PCR method for the ITS1 (internal transcribed spacer 1) RFLP method (digestion with and for phylogenetic construction, DNA sequencing of
Findings: Two samples from Khorasan province (Mashhad) were Leishmania (L. ), while others were Leishmania major (L. ). L. more variable compared with L. . The molecular sequencing differences between L. to geographical distribution. Based on the results of PCR product in the gel electrophoresis and DNA sequencing for L. L. , the DNA sizes were between 350 and 369bp. The RFLP for L. L. and one respectively. The sequences all samples from central parts are the same, but there is difference with the samples isolated from of Iran.
Conclusion: The sequences of of Leishmania major separated from Damghan and Esfarayen are different from other samples. Similarity of DNA sequences of North-East part of Iran of L. from central parts was 99%. The similarity of two isolates of L. 96%. The most similarity of Leishmania isolated was 95% with Indian isolate and the most similarity for Leishmania major was 99% with Friedlin strain.
R. Daghaghelh, H. Sabouri , H. Hosseini Moghaddm, E. Jorjani , H.a. Fallahi ,
Volume 9, Issue 3 (Summer 2018)
Abstract
Aims: The important achievement of genetic analysis of Quantitative trait locus (QTLs) is to facilitate the investigation of the inheritance of simple Mendelian traits. The aim of this study was mapping genes controlling morphological traits in F3 Families caused by Becher×Kavir cross in barley.
Materials and Methods: In the present experimental research, in order to map QTLs, 103 F3 families caused by Becher×Kavir cross were cultivated in a randomized complete block design with 3 replications during 2014-2015. Number of germinated seeds, during the grain filling period, plant height, peduncle length, seed weight, and harvest index were evaluated. Linkage map was prepared, using SSR, iPBS, IRAP, and ISSR marker. QTLs were identified by QGENE 4.0 software and QTL analysis was performed by composite interval mapping.
Findings: The identified QTLs justified with load score of 2.007, 8.6% of variance of phenotype germinated seed number, score of 22.2, 9.5% variance of phenotype grain filling period, score of 2.74, 1.16% of variance of plant height, score of 2.19, 9.3% of the variance of the peduncle length, the score of 2.04, 8.7% of variance of the seed weight, and with the scores of 2.38, 2.38, and 2.16 justified 10.1, 10.1, and 9.2% of the variance of the harvest index, respectively.
Conclusion: There are one QTL on chromosome 6 and ISSR38-4 closely marker for number of germinated seeds, one QTL on chromosome 7 in iPBS2076-6-iPBS2085-1 distance of marker for during the grain filling period, one QTL on chromosome 2 in iPBS2083-3-HVBKASI distance of marker for plant height, one QTL on chromosome 6 and ISSR38-4 closely marker for peduncle length, one QTL on chromosome 3 in iPBS2075-5-ISSR38-7 distance of marker for seed weight, and 3 QTLs for harvest index, respectively.
M.s. Borhani , Z. Etemadifar , G. Emtiazi , E. Jorjani ,
Volume 9, Issue 4 (Fall 2018)
Abstract
Aims: Alkaline protease is one of the most important groups of industrial enzymes with many applications. The aim of this study was to determine the physicochemical parameters affecting the production of alkaline protease enzyme produced by Bacillus pseudofirmus MSB22 by one-factor-at-a-time (OFAT) method and optimize the production of this enzyme by the response surface methodology (RSM) in the form of a rotatable central composite design.
Materials and Methods: In the present experimental study, the isolation of microorganism producing alkaline protease from wastewater from sausage and lunch meat factories in Isfahan was carried out. The morphological and biochemical characteristics of the strain were performed according to the Bergey's book and amplification of 16S rRNA gene sequences. Detection of metalloproteinase gene and alkaline serine protease was done by polymerase chain reaction (PCR) reaction and enzyme activity measurement was performed by Folin reagent. Screening of variables effective in enzyme production was done, using one-factor-at-a-time method and optimization was performed by response surface methodology. MEGA 6 software was used for phylogenetic analyses. To analyze the data, the Design Expert 7 software and the one-way analysis of variance were used.
Findings: The maximum protease production, which was 1.85 times higher than that of OFAT method and 3.45 times higher than unoptimized conditions was obtained, using 1% w/v xylose, 3% w/v beef extract, 4% v/v inoculation size, pH 10, and 30°C. The established quadratic model had a great ability to predict responses to new observations due to a high value of the predicted determination coefficient.
Conclusion: OFAT and RSM strategies are useful screening and optimization methods, respectively and sub I and sub II genes (alkaline serine protease genes) are detected in Bacillus pseudofirmus MSB22.
M. Salehi, M.r. Aghamaali, R. Hasansajedi, S.m. Asghari, Eisa Jorjani,
Volume 10, Issue 1 (Winter 2019)
Abstract
The fruit of has a lot of acidic proteases and its extract has been used in cheese manufacturing. However, there are few studies about purification and characterization of this enzyme. must be satisfied for the enzyme to be used in industry: 1- stability of enzymes against metal ions and 2- Ability to sustain proper function and stability in the absence of metal ion. Accordingly, in this investigation, the effect of various ions different concentrations activity, stability and somewhat on structural properties of the purified protease were studied. Based on the results, it was shown that the enzyme was relatively stable against NaCl and CaCl2, but by increment of these salts, stability and activity of enzyme . Also, the enzyme was stable against low concentration of various metal ions and only Hg2+ reduces enzyme stability and activity. By studying the role of 2+ of , it was found that 2+ have any role in thermal stability of enzyme at 67˚C. Likewise, by observing the effect of metal ions on of it was that all tested ions increased intensity of emission and caused to shift toward lower wave length. In all, of these showed that the purified enzyme from bad is very stable against various metal heavy metals and it is favorable for industrial application.
Volume 11, Issue 0 (پاییز و زمستان 87- 2009)
Abstract
Objective: Leishmaniasis is caused by parasitic protozoa of the genus Leishmania which in the infected host is obligate intracellular parasite. LACK gene is conserved among related Leishmania species. LACK is the immuno-dominant antigen of L.major which is considered as the most promising molecule for a recombinant or DNA vaccine against leishmaniasis.
Materials and Methods: In this study the genomic DNA of an Iranian standard strain of Leishmania major (MRHO/IR/75/ER) was ertracted and the LACK gene was amplilified by PCR. Then the PCR product was cloned into pTZ57R/T cloning vector, The PT-LACK recombinant plasmid was extracted from transformed E.coli bacteria (TG1 strain) and sequenced.
Results: The LACK gene (Accession no LmjF28.2740) of MRHO/IR/75/ER & L. major was amplified using PCR method. LACK gene was cloned into pTZ57R/T coloning vector. Sequence analysis of the cloned LACK gene showed high homology 89% with LmjF28.2740 (LACK gene).
Conclusion: The LACK gene of L.major was cloned in pTZ57R/T vector successfully. Recombinant plasmid was confirmed and could be used for the production of recomiomort antigens is DNA vaccines, for further studies.
Volume 16, Issue 4 (2-2014)
Abstract
Objective: Inflammation and proinflammatory cytokines play an important role in the initiation and maintenance of central neuropathic pain. There are several reports that cytokine production is increased at the lesion site following spinal injury. A few studies have investigated the supraspinal levels of these cytokines. This study intended to determine TNF-α and IL-6 release in the ventroposterolateral nucleus of the thalamus in spinal cord injury-related neuropathic pain in rats. Methods: Male Sprague-Dawley rats that weighed 200-230 g were used. Following administration of anesthesia, spinothalamic tract injury was performed by a laminectomy at the T9-T10 level in male rats. Mechanical allodynia and motor performance were evaluated at 3, 7, 14, 21 and 28 days after spinal injury by Von Frey filament and the open field test, respectively, in the sham and lesion groups. Concentrations of TNF-α and IL-6 in the VPL microdialysate were detected by ELISA in both spinal cord injured and sham groups during four weeks after surgery. Results: Mechanical pain threshold reduced in both hind paws following lateral spinothalamic tract injury. Paw withdrawal threshold in the Spinothalamic tract-injured group was significantly (P<0.05) lower than in sham group at day 14 post-surgery. Motor performance did not show any significant change after surgery. In the microdialysate, TNF-α reduced significantly (P<0.05) at days 3 and 7 post-injury compared to the sham group which returned to a level close to the pre-surgery level. VPL concentration of IL-6 increased significantly (P<0.05) at day 21 post-injury compared to the sham group. Conclusion: Lesions in spinal pathways that contain afferent pain fibers appear to change the supraspinal levels of inflammatory mediators, including VPL, concentrations of TNF-α and IL-6 which are consistent with spinal injury related pain behavior. Cytokine production results in hyperexcitability of the thalamocortical neurons, a decrease in pain threshold, and persistent neuropathic pain after spinal injury.
Volume 20, Issue 142 (December 2023)
Abstract
The presence of methicillin-resistant (MRSA) and vancomycin-resistant (VRSA) Staphylococcus aureus in food raises a public health concern. This study aimed to investigate the antibacterial and anti-biofilm activity of some Lamiaceae essential oils including Melissa Officinalis, Salvia officinalis, and Mentha piperita against MRSA and for the first time on VRSA strains. For this purpose, the disk diffusion test, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), minimum biofilm inhibitory concentration (MBIC), and minimum biofilm eradication concentration (MBEC) were determined. Then, M. Officinalis essential oil compounds were investigated against PBP2a, agrA, and Bap proteins using AutoDocK Vina. Finally, pharmacokinetic properties were investigated using ADMETsar and SwissADME servers. Based on the obtained results, the MIC and MBC values of M. Officinalis essential oil against MRSA strain were equal to 0.05 and 0.112 mg/ml, and against VRSA strain were equal to 1.8 and 2.5 mg/ml, respectively. The MBIC and MBEC of M. Officinalis essential oil against MRSA strain were equal to 0.03 mg/ml and 0.112 mg/ml, and against VRSA strain were equal to 0.9 mg/ml and 3.2 mg/ml, respectively. The results of molecular docking showed that β-Caryophyllene had a greater binding affinity to PBP2a protein either in the active site or in the allosteric site (-6.6kcal/mol). On the other hand, the effective compounds of this essential oil, especially citronellol, thymol, and citral, were acceptable in terms of pharmacokinetic properties. Since natural antibiotics can be an alternative to conventional antibiotics in the treatment of Staphylococcus aureus food-borne diseases, the results of this study showed that Melissa Officinalis essential oil is effective on the growth and biofilm of MRSA and VRSA strains, and it can be used as a drug candidate in the prevention and treatment of infections caused by antibiotic-resistant strains of this bacterium.
