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Showing 3 results for Shapouri

Abbasali Imani Foolad , Zahra Rostami , Reza Shapouri,
Volume 10, Issue 3 (autumn 2010)
Abstract

  Background and Objectives: Detection of TEM and SHV genes in ESBL producing Pseudomonas aeruginosa and their antimicrobial resistance pattern can provide useful information about the epidemiology and risk factors of associated infections. In this study we determined the antimicrobial susceptibility pattern and prevalence of ESBLs in clinical isolates of Pseudomonas aeruginosa by phenotypic and genotypic methods.

  Methods: In this analytic-descriptive study, 110 Pseudomonas aeruginosa strains isolated from different clinical specimens were used. The pattern of antimicrobial resistance was determined by disk diffusion (Kirby-buer) method. The ESBL production was determined by combination disk method using disks containing ceftazidim and cefotaxim alone and in combination with Clavulanic acid. SHV and TEM types of ESBL producing genes was detected by PCR.

  Results: In this study Co-trimoxazole and Amoxicilin with 96.4% and 92.7% and Amikacin with 17.3% showed the highest and lowest resistance against isolates respectively. According to PCR results 37.5% and 12.5% of isolate were carried SHV and TEM genes respectively and 12.5% of isolate were carried both the SHV and TEM genes.

  Conclusion: According to the results most of the isolates are drug resistant and among the ESBL producing strains the frequency of SHV type is higher than TEM . The isolate ceftazidim resistance was contains SHV (37.5%) and TEM gene (12.5%), that showed SHV and TEM genes play more important role in create of ceftazidim resistance than cefotaxim resistance.


Peyman Abdolahzade, Reza Shapouri , Shahrzad Nasiri Semnani,
Volume 11, Issue 3 (autumn 2011)
Abstract

  Background & Objectives: Brucellosis is an infectious disease caused by intracellular pathogens of the genus Brucella that have their natural reservoir in domestic and wild animals. Many studies show that herbal medicines have been used safely and successfully to treat bacterial diseases without significant side effects and drug resistance problems.

  Methods: In this study aquatic, alcoholic and acetonic extracts of Eucalyptus globulus leaves were prepared, then MIC and MBC of extracts for B. melitensis 16M and B. abortus S99 were determined by broth macrodilution and agar well diffusion methods. In animal model study, 5 × 105 CFU/mL of Brucellae was injected intraperitoneally (i.p) to female BALB/c mice. After 24 hours, 0.5mL (equivalent MBC) of each Eucalyptus globulus extracts was injected (i.p) After 7 days, in spleen the colonies of brucellae were counted on Muller-Hinton agar as standard protocol. 

  Results: The MIC and MBC of Eucalyptus globulus for B. melitensis M16 and B. abortus S99 were 1:80 (10.81 mg/mL) and 1:40 (21.62 mg/mL) for aquatic extract, 1:1280 (0.64 mg/mL) and 1:640 (1.29 mg/mL) for acetonic extract, and 1:2560 (0.31 mg/mL) and 1:1280 (0.63 mg/mL), for ethanolic extract respectively. In culture of spleen supernatant (in vivo), after 48 hours, the average grown B. melitensis 16M colonies for aquatic, ethanolic and acetonic extracts were 5×103 CFU/ml, 2×102 CFU/ml and 6×102 CFU/ml, respectively in comparison with control group (4×1010 CFU/ml). These results for B.abortus S99 were 3×103 CFU/ml, 1×102 CFU/ml and 3×102 CFU/ml, respectively in comparison with control group (9×109 CFU/ml) The results showed that bacterial load was significantly decreased in all experimental groups (p<0.01). 

  Conclusion : The results of in vitro and in vivo indicate that ethanolic and acetonic extracts of Eucalyptus globulus have more effective antimicrobial activity on B.melitensis M16 and B.abortus S99 than aquatic extract. It seems that the extracts Eucalyptus globulus can be used in treatment of human and animal brucellosis.


Sm Rezavian, R Shapouri ,
Volume 15, Issue 2 (summer 2015)
Abstract

  Background & objectives: Yersiniosis is created by Yersinia enterocolitica O:8 and causes problems in the world especialy in cold and mild countries. The purpose of this study is to evaluate the immunogenicity of Yersinia enterocolitica O:8 oligopolysaccaride (OPS) conjugate to diphtheria toxoid (DT) as a vaccine candidate.

  Methods : After cultivation of bacteria, the LPS were isolated by modified hot phenol method. Then dialysis and concentration were done and the OPS were extracted by acetic acid 2%. To conjugate with diphtheria toxoid, ADH was used as a spacer molecule and EDAC as a linker. Conjugate was purified by gel filtration. Then 4 groups of female BALB/c mice were selected (15 mice in each group). Injection was performed intraperitoneally in three doses with two weeks interval. Then serum samples were collected and antibody response against OPS was measured by indirect ELISA method for detection of total IgG, IgA, IgM, IgG1, IgG2a, IgG2b and IgG3.

  Results: After second and third doses, OPS-DT recieved group showed significant increase in all types of antibodies titer in anti-OPS in comparison to group that recived nonconjugated OPS. The increase in titer of antibodies was as: OPS-DT>OPS>DT. A remarkable increase was shown in total IgG and IgM titers (with total amount of 3204 and 670, respectively). In IgG1 subclass the amount was 920 and in other subclasses of IgG (IgG3, IgG2a and IgG2b) the amounts were 910, 110, and 99, respectively.

  Conclusion: The results shows that OPS of Yersinia enterocolitica O:8 increases the anti-OPS antibodies in the form of conjugate with diphtheria toxoid and could be considered as an appropriate vaccine candidate.



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مجله دانشگاه علوم پزشکی اردبیل Journal of Ardabil University of Medical Sciences
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