en
jalali
1393
10
1
gregorian
2015
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1
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online
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fulltext
en
The Effect of Triclabendazole on ALT Enzyme activity in Fasciola hepatica helminths and parasitized sheep liver tissues
Introduction: To determine an indicator for Triclabendazole (TCBZ) efficacy, Alanine aminotransferase (ALT) activity in Fasciola hepatica (Iranian isolate) parasite in presence and absence of TCBZ was evaluated by an in vitro cultivation method. Also, ALT enzyme activity between none and parasitized-infected sheep liver tissues was assessed. Method: The sheep livers were collected and transferred immediately to the Department of Parasitology. Adult living parasites were recovered, washed and divided into two groups, treatment and control groups with 10 parasites in each. We added 15 μg TCBZ to the treatment group; then incubated both groups for 4 h at 37ºC. The parasites, infected and parasite free liver tissues were ground and homogenized by a Mortar and pestle, centrifuged, and supernatants were recovered. Protein concentration and ALT enzyme activity were measured in the supenatants. Results: The results of ALT enzyme activity assay showed 0.03 U/ml/mg protein for treated F. hepatica and 0.01 U/ml/mg protein for untreated samples, the mean values of difference was not significant (p>0.05). The difference between ALT activity in none and parasitized-infected liver was not significant (p>0.05). However, two-sample T-test analysis showed higher ALT activity in treated and untreated parasite in comparison with none and parasitized-infected liver specimens (p<0.05). In addition to ALT protein band for parasite and liver tissue, Cathepsin enzyme (proteases) was detected for parasite by SDS-PAGE analysis. Conclusion: ALT activity cannot be considered as a useful marker for TCBZ efficacy in F. hepatica treatment. However, ALT enzyme showed comparable activities in parasite and its host liver tissue.
Alanine Aminotransferase, Fasciola hepatica, Egaten®, Triclabendazole, Liver
1
5
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-80-1&slc_lang=en&sid=1
2015/12/27
1394/10/6
2016/08/9
1395/5/19
Ali
Farahnak
Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
farahnak@tums.ac.ir
0031947532846001135
0031947532846001135
Yes
Fariba
Amni
Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
hiva.hamidi63@yahoo.com
0031947532846001136
0031947532846001136
No
Taghi
Golmohammadi
Department of Biochemistry, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
Golmoham@tums.ac.ir
0031947532846001137
0031947532846001137
No
Mohammad Reza
Eshraghian
Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
eshraghianmr@tums.ac.ir
0031947532846001138
0031947532846001138
No
Mohammad Bagher
Molaei Rad
Department of Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
mb-molaeirad@farabi.tums.ac.ir
0031947532846001139
0031947532846001139
No
en
Antibacterial Effects of Aloe Vera Extracts on some Human and Animal Bacterial Pathogens
Introduction: Aloe Vera compounds have inhibitory activity on fungi, bacteria, and viruses. This study examines the antibacterial activity of A. Vera purified extracts including gel, boiled skin, boiled gel, and distilled extract against pathogenic bacteria, Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Klebsiella pneumonia and Pseudomonas aeruginosa were elucidated. Method: The bacterial strains were collected from veterinary hospital. Freshly collected A. vera leaves were used for the juice extraction of gel, skin and distilled extracts. Antibacterial effects of various A. Vera extracts were evaluated using broth microdilution method. The crude polysaccharides of boiled skin extract were purified by phenol method; and fractionated by anion exchange chromatography. For each bacterium, minimum inhibitory concentration of various A. Vera extracts was determined. The protein expression changes of treated bacteria were detected by SDS-PAGE electrophoresis. Results: The distillate extract exhibited more antibacterial effects than other extracts. Out of seven-carbohydrate fractions of the skin extract, the fractions 6 and 7 had antibacterial effects on S. aureus and MRSA at 0.089 and 0.134 mg/ml, respectively; also fraction 5 showed antibacterial effects on MRSA at 0.113 mg/ml concentration. The protein profiles of these strains before and after treatment with A. Vera showed significant differences at 175, 60, 200 and 70 kDa protein bands of S. aureus, MRSA, P. aeruginosa and K. pneumonia, respectively. Conclusion: This finding showed that the distillate extract despite the minimal amount of carbohydrate and protein was more efficient against both Gram-positive and Gram negative bacteria.
Aloe Vera, Extracts, Antibacterial
6
10
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-89-2&slc_lang=en&sid=1
2015/12/272016/03/15
1394/12/25
2016/08/92016/09/13
1395/6/23
Darioush
Gharibi
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
d.gharibi@scu.ac.ir
0031947532846001140
0031947532846001140
No
Mohammad
Khosravi
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
dr.khosravim@gmail.com
0031947532846001141
0031947532846001141
Yes
Zohreh
Hosseini
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
hossini895818@gmail.com
0031947532846001142
0031947532846001142
No
Fatemeh
Boroun
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
dr_mnemati58@yahoo.com
0031947532846001143
0031947532846001143
No
Seyedeh Kolsum
Barzgar
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
dvm_barzegar@yahoo.com
0031947532846001144
0031947532846001144
No
Ali
Forughi Far
Department of Pathobiology, Faculty of Veterinary Medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran
mamad_kh17@yahoo.com
0031947532846001145
0031947532846001145
No
en
An In Vitro Study on Impact of Environmental Stresses on Growth, Morphological and Biochemical Features of Listeria monocytogenes PTCC 1297
Introduction: Listeria monocytogenes is a serious concern for the food industry due to its high case fatality rate, widespread distribution, ability to survive a wide variety of food processing conditions, and the severity of the illness associated with this pathogen infection. The objective of this study was to determine the growth, cell morphology and biochemical characteristics of L. monocytogenes PTCC 1297 (Serotype 4a) under selected environmental stresses. Method: The environmental stresses were acid stress (HCl, pH 2.0-6.0), alkaline stress (NaOH, pH 8.0-12.0), ethanol stress (5.0%-25.0% vol/vol), oxidative stress (H2O2, 0.06%-6.0% vol/vol), osmotic stress (NaCl and sucrose, 2.0%-30.0% wt/vol) and heat stress (40-60°C). All stresses were applied to the exponential phase bacteria whereas non-stressed exponential phase cells served as a control and the cells were allowed to grow for 24 h. For evaluating the growth of L. monocytogenes PTCC 1297 after inoculation procedure and exposure of cells to selected stresses we used colony count method. Scanning electron microscopy (SEM) was implemented to visualize the external appearance of the bacteria. Results: According to the results, the bacteria at pH≤4 and pH≥10 achieved by HCl and, NaOH, respectively, died. Also, concentrations ethanol at ≥15% vol/vol, H2O2 ≥0.3% vol/vol, NaCl ≥14% wt/vol, and heat ≥50°C were lethal for the bacteria. Unlike other stresses, sucrose did not kill bacteria but decreased their growth. The phenotypical and biochemical characteristics of them changed when exposed to each stress. Conclusion: Different doses of various stresses were either lethal or sub-lethal for this bacterium and lead to various changes in its characteristics.
Listeria monocytogenes, Cell Biology, Environment, Stress Physiological
11
17
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-92-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/11
1395/1/23
2016/08/92016/09/132016/09/13
1395/6/23
Samaneh
Kazemi
Vice-chancellor of Research and Technology, Guilan University of Medical Sciences, Rasht, Iran
samaneh.kazemi@ymail.com
0031947532846001146
0031947532846001146
Yes
Mohammad
Faezi-Ghasemi
Department of Microbiology, Islamic Azad University, Lahijan Branch, Lahijan, Iran
0031947532846001147
0031947532846001147
No
en
Preparation of Proper Culture Medium for Saccharomyces cerevisiae var. boulardii with Molasses and Animal Serum
Introduction: The purpose of this study was formulation and preparation of a proper culture medium for Saccharomyces cerevisiae var. boulardii with molasses and animal serum. Methods: A fully-crossed factorial design contain 5%, 10% and 20% of molasses (M) with 0, 1% and 5% animal serum (S) was used in this study. The pH of all culture medias were adjusted to 5.6 with acetic acid. The seed was consisted of 106 yeast particles which was added to culture media. The inoculated medias were incubated at 37°C for 48 h and the mean yeast counts was recorded. Results: The mean of yeast counts for 5% M+0% S, 5% M+1% S, 5% M+5% S, 10% M+0% S, 10% M+1% S, 10% M+5% S, 20% M+0% S, 20% M+1% S, 20% M+5% S were 273333±20033, 228666±34428, 317333±170485, 499333±100425, 516000±38314, 514666±107057, 499333±100425, 516000±38314 and 514666±107057 particles in ml, respectively. In order to optimize culture medium, vitamins and vitamins in combination with minerals (at a concentration of 0.5%) were added to the optimal concentration of molasses and serum. Conclusion: Statistical analysis with ANOVA test showed that the growth rate of yeast in 10% molasses plus 1% serum had a significant difference with 5% and 10% molasses in solid medium or 5% molasses supplemented with 1% serum (p< 0.05). The addition of vitamins and minerals did not yield significant growth. Therefore, it can be concluded that the combination of molasses and serum may be able to provide basic requirements of the yeast S. cerevisiae var. boulardii.
Serum, Molasses, Saccharomyces cerevisiae var. boulardii.
18
22
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-95-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/112016/05/8
1395/2/19
2016/08/92016/09/132016/09/132016/10/17
1395/7/26
Mahdi
Salimi
sku.msalimi@yahoo.com
0031947532846001148
0031947532846001148
Yes
Mohamadreza
Mahzonieh
mehdisalimi69@yahoo.com
0031947532846001149
0031947532846001149
No
en
A Comparison between Culture and Multiplex PCR for Detection and Identification of Shigella Species in Patients with Shigellosis from Isfahan Province in 2014-2015
Introduction: Awareness of the species of Shigella has particular importance in the way of dealing with an outbreak, controlling it, and treating patients. The purpose of this study was to use the Multiplex PCR method and comparison with the culture method to detect Shigella species, as well as analysing the antibiotic resistance pattern in its different species. Methods: Simultaneously, the fecal samples of the patients with diarrhea and a sample from each patient in Cary-Blair medium were sent to the laboratory. Cultivation, serotyping, and antibiogram analysis were performed using the samples inoculated in the Cary-Blair medium. DNA extraction of the fecal samples and amplifying of invC, rfc, wbgZ, and rfpB genes were performed. Results: Totally, 300 samples from the patients were analyzed, out of which 240 Shigella isolated (80%) were detected using the culture method and serotyping, and 260 Shigella isolated (86.6%) using the PCR method (Shigella flexneri (77%), Shigella sonnei (19.2%), and Shigella dysenteriae (3.8%)). 20 samples suspicious of Shigella were observed in the culture method but were not identified by serotyping. However, in the PCR assay, they were identified as S. flexneri (n=16) and S. sonnei (n=4). The resistance of Shigella isolated to Co-trimoxazole was observed to be (78.3%), Ceftriaxone (42.5%), Cefixime (42%), Azithromycin (40.7%), Ofloxacin (34.5%), Nalidixic acid (25 %), and Ciprofloxacin (16%). Conclusion: Due to annual outbreaks of various Shigella species in the country, it is recommended that the Multiplex PCR method, be used along with culture method in laboratories to identify Shigella isolated. The antibiogram results showed increasing resistance of Shigella to the available antibiotics.
Shigella, Diarrhea, Antibiotics, Multiplex PCR.
23
28
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-101-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/112016/05/82016/06/21
1395/4/1
2016/08/92016/09/132016/09/132016/10/172016/11/23
1395/9/3
Azam
Fatahi
Food and water born diseses department ,isfahan provincial health center, isfahan university of medical sciences.
ne_fatahi@yahoo.com
0031947532846001150
0031947532846001150
Yes
Ali
Ajami
ali_ajami@yahoo.com
0031947532846001151
0031947532846001151
No
Mojgan
Bozorgzad
mojgan.bozorgzad@yahoo.com
0031947532846001152
0031947532846001152
No
Shahram
Nekoeian
nekoeian_sh@yahoo.com
0031947532846001153
0031947532846001153
No
Atefeh
Khazeni
khazeniat@yahoo.com
0031947532846001154
0031947532846001154
No
en
Genetic Characterization of Salmonella Typhimurium Isolates from Faeces of Children with Gastroenteritis Hospitalized in Baqiatollah-Azam Hospital, Tehran, Iran
Introduction: In Iran, invasive nontyphoidal Salmonella (iNTS) disease causes severe bacteremic illness among children <5 years old. The global yearly incidence of iNTS disease in children was reported to be in the 3.4 (range 2.1-6.5) million cases, (overall incidence 49 cases (range 30-94) per 100,000 population), the iNTS case-fatality ratio (CFR) of 20% yielded 681,316 deaths annually. Methods: The microarray analysis enables identification of the strains that have the 90kb Salmonella typhimurium virulence plasmid, presence or absence of the Salmonella pathogenicity islands (SPIs), adherence factors and other virulence determinants. Twelve isolates of S. typhimurium obtained from faeces of children with gastroenteritis were analyzed by microarray technique. Results: The virulence plasmid was present in 83.33% of isolates and all the isolates contained the SPI-4 and SPI-5. None of the strains had the cytolethal distending toxin, cdtB. All strains were positive for rck and mig-14. The adherence genes were present in all the strains in the range of 51.55% to 73.20% of the adherence genes interrogated in the microarray. Two strains were the least pathogenic S. typhimurium. Conclusion: Microarray analysis proved to be a valuable tool in confirmation of serotyping results and genetic characterization of S. Typhimurium.
Salmonella typhimurium, Gastroenteritis, Microarray Analysis
29
34
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-102-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/112016/05/82016/06/212016/07/1
1395/4/11
2016/08/92016/09/132016/09/132016/10/172016/11/232016/11/13
1395/8/23
Hamid
Staji
Department of Pathobiology, Faculty of Veterinary Medicine, Semnan University, Semnan, Iran.
hstaji@semnan.ac.ir
0031947532846001155
0031947532846001155
Yes
Alfreda
Tonelli
Istituto ‘‘G. Caporale’’, Campo Boario, 64100 Teramo, Italy.
a.tonelli@izs.it
0031947532846001156
0031947532846001156
No
Taghi
Zahraei Salehi
Department of Microbiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
tsalehi@ut.ac.ir
0031947532846001157
0031947532846001157
No
Mariangela
Iorio
Istituto ‘‘G. Caporale’’, Campo Boario, 64100 Teramo, Italy.
m.iorio@izs.it
0031947532846001158
0031947532846001158
No
Federica
Lopes
Istituto ‘‘G. Caporale’’, Campo Boario, 64100 Teramo, Italy.
f.lopes@izs.it
0031947532846001159
0031947532846001159
No
en
Antimicrobial Susceptibility of Stenotrophomonas maltophilia Clinical Isolates from Blood Samples in Iran
Introduction: Stenotrophomonas maltophilia is a nosocomial multi drug resistant opportunistic pathogen which causes infections in vulnerable patients with cancer, cystic fibrosis and indwelling catheters. Methods: 45 clinical S. maltophilia isolates were collected from blood samples and identified by biochemical tests. Susceptibility to different antibiotics including co-trimoxazole, levofloxacin, minocycline, ticarcillin/clavulanic acid, chloramphenicol and ceftazidime were determined by disk diffusion and E-test methods. Results: All isolates were resistant to ceftazidime and susceptible to co-trimoxazole and 11.1% were resistant to ticarcillin/clavulanic acid. Conclusion: Ceftazidime as one of the extended spectrum β-lactams was the least effective antibiotic. Ticarcillin/clavulanic acid is one of the choosen antibiotics for S. maltophilia infections treatment. Here, we report tcarcillin/clavulanic acid resistance in S. maltophilia isolates for the first time in Iran.
Stenotrophomonas maltophilia, Antimicrobial susceptibility, Iran
35
37
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-106-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/112016/05/82016/06/212016/07/12016/09/5
1395/6/15
2016/08/92016/09/132016/09/132016/10/172016/11/232016/11/132016/10/4
1395/7/13
Amir Hesam
Nemati
Bacteriology department, pasteur Institute of Iran, Tehran, Iran
Hesam.nemati@live.com
0031947532846001160
0031947532846001160
No
Hamid
Solgi
Bacteriology department, pasteur Institute of Iran, Tehran, Iran
0031947532846001161
0031947532846001161
No
Farzam
Vaziri
Tuberculosis and pulmonary research department, Pasteur institute of Iran, Tehran, Iran
farzam_vaziri@yahoo.com
0031947532846001162
0031947532846001162
No
Fereshteh
Shahcheraghi
Bacteriology department, pasteur Institute of Iran, Tehran, Iran
shahcheraghifereshteh@yahoo.com
0031947532846001163
0031947532846001163
Yes
en
Antimicrobial Activity of Lemon and Peppermint Essential oil in Edible Coating Containing Chitosan and Pectin on Rainbow Trout (Oncorhynchus mykiss) Fillets
Introduction: Essential oils are used as flavoring agents in various foods. Layer-by-Layer (LBL) technique is a method in which the material is dipped into a series of different solutions containing oppositely charged polyelectrolytes. The aim of this study is to investigate the effectiveness of a multilayered edible coating with an antimicrobial compound (Lemon and Peppermint) in enhancing the quality and shelf-life of rainbow trout (Oncorhynchus mykiss) during refrigerated storage (4 ± 1˚C) over a period of 16 days. Methods: In this study, multilayered coating was used with two concentrations of Lemon (LEO) and Peppermint (PEO) essential oils (0.5 and 1%). Antibacterial effect of these treatments was evaluated by enumeration of bacteria in special culture media. The control and the coated fish samples were analyzed periodically for pH and microbiological (total viable count, psychrotrophic count, lactic acid bacteria, Enterobacteriaceae, and coliform) characteristics. Results: The results obtained in this study demonstrate that multilayered coating in combination with Lemon and Peppermint essential oils can significantly decrease the number of bacteria and delay the spoilage of the samples (p<0.05). Conclusion: Multilayered edible coating with an antimicrobial compound can properly delay the growth of spoilage microorganisms and prolong the shelf life of meat products.
Lemon, Peppermint, Rainbow Trout, Essential Oil.
38
43
http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-108-1&slc_lang=en&sid=1
2015/12/272016/03/152016/04/112016/05/82016/06/212016/07/12016/09/52016/10/8
1395/7/17
2016/08/92016/09/132016/09/132016/10/172016/11/232016/11/132016/10/42016/12/20
1395/9/30
Leila
Tabatabaei Moradi
leila94132@yahoo.com
0031947532846001132
0031947532846001132
No
Anousheh
Sharifan
a_sharifan2000@yahoo.com
0031947532846001133
0031947532846001133
Yes
Kambiz
Larijani
klarijani@yahoo.com
0031947532846001134
0031947532846001134
No