Example of Jundishapur Journal of Microbiology format
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Example of Jundishapur Journal of Microbiology format Example of Jundishapur Journal of Microbiology format
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Example of Jundishapur Journal of Microbiology format Example of Jundishapur Journal of Microbiology format
Sample paper formatted on SciSpace - SciSpace
This content is only for preview purposes. The original open access content can be found here.

Jundishapur Journal of Microbiology — Template for authors

Categories Rank Trend in last 3 yrs
Infectious Diseases #211 of 288 down down by 65 ranks
Microbiology (medical) #87 of 116 down down by 27 ranks
Microbiology #130 of 150 down down by 32 ranks
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 352 Published Papers | 533 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 15/06/2020
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Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

0.593

38% from 2018

Impact factor for Jundishapur Journal of Microbiology from 2016 - 2019
Year Value
2019 0.593
2018 0.957
2017 1.233
2016 1.017
graph view Graph view
table view Table view

1.5

32% from 2019

CiteRatio for Jundishapur Journal of Microbiology from 2016 - 2020
Year Value
2020 1.5
2019 2.2
2018 2.9
2017 2.6
2016 1.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 38% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 32% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.281

13% from 2019

SJR for Jundishapur Journal of Microbiology from 2016 - 2020
Year Value
2020 0.281
2019 0.323
2018 0.471
2017 0.543
2016 0.463
graph view Graph view
table view Table view

0.517

17% from 2019

SNIP for Jundishapur Journal of Microbiology from 2016 - 2020
Year Value
2020 0.517
2019 0.62
2018 0.868
2017 0.86
2016 0.724
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 13% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 17% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Jundishapur Journal of Microbiology

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Kowsar Publishing Company

Jundishapur Journal of Microbiology

Approved by publishing and review experts on SciSpace, this template is built as per for Jundishapur Journal of Microbiology formatting guidelines as mentioned in Kowsar Publishing Company author instructions. The current version was created on 14 Jun 2020 and has been used by 738 authors to write and format their manuscripts to this journal.

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Last updated on
14 Jun 2020
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ISSN
2008-4161
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
Vancouver
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Citation Type
Numbered
(25)
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Bibliography Example
Blonder GE, Tinkham M, Klapwijk TM. Tran- sition from metallic to tunneling regimes in su- perconducting microconstrictions: Excess cur- rent, charge imbalance, and supercurrent con- version. Phys Rev B. 1982;25(7):4515–4532.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.5812/JJM.8720
Antibacterial effect of silver nanoparticles against four foodborne pathogens.
Mehdi Zarei1, Amirhesam Jamnejad1, Elahe Khajehali2

Abstract:

in the viable population of the tested pathogens was determined as the minimum exposure time for efficient bactericidal activity. Results: The MIC values of Ag NPs against tested pathogens were in the range of 3.12-6.25 µg/mL. While Listeria monocytogenes showed the MIC value of 6.25 µg/mL, Escherichia coli O157:H7, Salmonell... in the viable population of the tested pathogens was determined as the minimum exposure time for efficient bactericidal activity. Results: The MIC values of Ag NPs against tested pathogens were in the range of 3.12-6.25 µg/mL. While Listeria monocytogenes showed the MIC value of 6.25 µg/mL, Escherichia coli O157:H7, Salmonella typhimurium and Vibrio parahaemolyticus all showed the MIC values of 3.12 µg/ mL. However, all the pathogens showed the same MBC value of 6.25 µg/mL. To obtain an efficient bactericidal activity against E. coli O157:H7 and S. typhimurium, the exposure time should be at least ca. 6 hours., while this time was ca. 5 hours for V. parahaemolyticus and ca. 7 hours for L. monocytogenes. Conclusions: Silver nanoparticles showed great antibacterial effectiveness on four important foodborne pathogens. Therefore, Ag NPs could be a good alternative for cleaning and disinfection of equipment and surfaces in food-related environments. read more read less

Topics:

Vibrio parahaemolyticus (51%)51% related to the paper, Listeria monocytogenes (51%)51% related to the paper
View PDF
129 Citations
open accessOpen access Journal Article DOI: 10.5812/JJM.30682
Evaluation of Biofilm Formation Among Klebsiella pneumoniae Isolates and Molecular Characterization by ERIC-PCR.

Abstract:

Background: Klebsiella pneumoniae is among the most frequently recovered etiologic agents from nosocomial infections. This opportunistic pathogen can generate a thick layer of biofilm as one of its important virulence factors, enabling the bacteria to attach to living or abiotic surfaces, which contributes to drug resistance.... Background: Klebsiella pneumoniae is among the most frequently recovered etiologic agents from nosocomial infections. This opportunistic pathogen can generate a thick layer of biofilm as one of its important virulence factors, enabling the bacteria to attach to living or abiotic surfaces, which contributes to drug resistance. Objectives: The resistance of biofilm-mediated infections to effective chemotherapy has adverse effects on patient outcomes and survival. Therefore, the aim of the present study was to evaluate the biofilm-formation capacity of clinical K. pneumoniae isolates and to perform a molecular characterization using enterobacterial repetitive intergenic consensus-polymerase chain reaction (ERIC-PCR) to determine the dominant biofilm-producing genotype. Patients and Methods: In the present study, 94 K. pneumoniae isolates were obtained from two hospitals in Tehran, Iran. Biofilm formation was assayed by a modified procedure, then ERIC-PCR was carried out. Results: The distributions of the clinical specimens used in this study were 61.7% from urine, 18.1% from wounds, 11.7% from sputum, and 8.5% from blood. Among these isolates, 33% formed fully established biofilms, 52.1% were categorized as moderately biofilm-producing, 8.5% formed weak biofilms, and 6.4% were non-biofilm-producers. Genotyping of K. pneumoniae revealed 31 different ERIC types. Biofilmformation ability in a special ERIC type was not observed. Conclusions: Our results indicated that an enormous proportion of K. pneumoniae isolated from sputum and surgical-wound swabs produced fully established biofilms. It is reasonable to assume the existence of a relationship between the site of infection and the formation of biofilm. A high level of genetic diversity among the K. pneumoniae strains was observed. read more read less

Topics:

Klebsiella pneumoniae (55%)55% related to the paper, Klebsiella pneumonia (54%)54% related to the paper, Drug resistance (51%)51% related to the paper
View PDF
100 Citations
open accessOpen access Journal Article DOI: 10.5812/JJM.10741
Analysis of Virulence Genes Among Methicillin Resistant Staphylococcus aureus (MRSA) Strains

Abstract:

Background: Staphylococcus aureus is amongst major human pathogens both in hospitals and the community. This bacterium is an opportunistic pathogen responsible for a large number of self-limiting and even life-threatening diseases in humans. Methicillin resistant S. aureus (MRSA) strains are common causes of emerging nosocomi... Background: Staphylococcus aureus is amongst major human pathogens both in hospitals and the community. This bacterium is an opportunistic pathogen responsible for a large number of self-limiting and even life-threatening diseases in humans. Methicillin resistant S. aureus (MRSA) strains are common causes of emerging nosocomial infections and are considered as a major problem for public health. Objectives: We aimed to study the profile of some virulence genes including: sea, seb, sed, tst, eta, etb, LuKS/F-PV, hla and hld in methicillin- resistant S. aureus by the PCR technique. Materials and Methods: A total of 345 isolates of S. aureus were collected from clinical specimens of patients referred to teaching hospitals of Shiraz; identification was done by biochemical (catalase, coagulase and DNase) and molecular tests. One hundred and forty six isolates of methicillin-resistant S. aureus (MRSA) were obtained and the presence of some toxin genes in these isolates was investigated by the polymerase chain reaction (PCR) technique. Results: The results showed that among the 345 isolates of S. aureus, 148 were confirmed as MRSA by screening with the cefoxitin disc diffusion (30 µg) method. Also among the 148 MRSA isolates, 146 isolates were confirmed as methicillin-resistant by molecular methods. The results showed that the frequency of methicillin-resistant and methicillin-sensitive S. aureus isolates during 2012 to 2013 in Namazi and Faghihi hospitals were 146 (42.3%) and 199 (57.7%), respectively. Besides, among the 146 confirmed MRSA isolates, 36.98% (54 isolates) and 63.02% (92 isolates) were related to female and male, respectively. The largest number of cases belonged to sputum samples (58 out of 146). The frequency of the eta, etb, sed, LuKS/F-PV, seb, tst, sea, hld and hla genes were 0.68%, 2.05%, 2.05%, 5.47%, 10.95%, 11.64%, 27.39%, 84.24% and 93.15%, respectively. In addition, amongst all examined genes, hla (93.15%) and eta (0.68%) genes had the highest and lowest frequencies, respectively. The greatest coexistence of genes was observed for the hla + hld gene combination (48.83%). The results of our study indicate that 98.63% of the isolates were positive for at least one of the virulence genes. Conclusions: The relative higher frequency of some virulence genes in this study may reflect the emergence of isolates containing these genes in Shiraz medical centers. read more read less

Topics:

Coagulase (57%)57% related to the paper, Methicillin-resistant Staphylococcus aureus (55%)55% related to the paper, Staphylococcus aureus (53%)53% related to the paper
View PDF
96 Citations
open accessOpen access Journal Article DOI: 10.5812/JJM.17115
Effects of pH and Temperature on Antibacterial Activity of Zinc Oxide Nanofluid Against Escherichia coli O157: H7 and Staphylococcus aureus.
Mahsa Saliani1, Razieh Jalal1, Elaheh Kafshdare Goharshadi1

Abstract:

Background: Zinc oxide nanoparticles (ZnO NPs) are known as one of the important inorganic materials used in research and healthrelated applications with effective antibacterial activities. Although the toxic effects of ZnO NPs have already been evaluated, more information is required to understand the possible mechanisms. Ob... Background: Zinc oxide nanoparticles (ZnO NPs) are known as one of the important inorganic materials used in research and healthrelated applications with effective antibacterial activities. Although the toxic effects of ZnO NPs have already been evaluated, more information is required to understand the possible mechanisms. Objectives: The aim of the present study was to determine the influences of pH and temperature on antibacterial activity of ZnO NPs against some strains of pathogenic bacteria. Identifying the interrelationship between toxicity and cultural conditions helps us to have a better understanding of the optimum reaction conditions for maximum antimicrobial activity. Materials and Methods: ZnO NPs were prepared and characterized and then dispersed in glycerol with the help of ammonium citrate as the dispersant. The antibacterial tests were performed by measuring the growth of Escherichia coli O157:H7 and Staphylococcus aureus with different concentrations of ZnO NPs in glycerol. All the experiments were conducted at different incubation temperatures (25-42 ° C) and pH levels (4-10 for E. coli O157:H7 and 5-10 for S. aureus). Results: The results showed that ZnO nanofluid have antibacterial activity against E. coli O157:H7 and S. aureus and the inhibitory effect increases with increasing the nanofluid concentration. The experiments showed that the antibacterial activity of ZnO NPs was influenced by temperature and pH. Higher antibacterial activity was observed at acidic pH levels with the maximum toxicity at pH = 4 and pH = 5 for E. coli O157: H7 and S. aureus, respectively. By raising the temperature, the toxicity of ZnO nanofluid increased, with the highest antibacterial activity at 42°C for both bacterial types in comparison with positive controls under the same conditions. Conclusions: Analysis of the results demonstrated that exposure media of ZnO NPs and cultural factors play a role in their cytotoxic effects. It could be attributed to the principal mechanism at different reaction conditions. read more read less

Topics:

Antibacterial activity (53%)53% related to the paper
View PDF
90 Citations
open accessOpen access Journal Article DOI: 10.5812/JJM.26381
Antifungal Activity of Selenium Nanoparticles Synthesized by Bacillus species Msh-1 Against Aspergillus fumigatus and Candida albicans
Mojtaba Shakibaie1, Naser Salari Mohazab1, Seyyed Amin Ayatollahi Mousavi1

Abstract:

Background: Fungal infections affect various parts of the body and can be difficult to treat. Aspergillus infection causes a spectrum of diverse diseases particularly in lung according to host immunity. The two major entities are invasive pulmonary aspergillosis and chronic pulmonary aspergillosis. Candida infections can be s... Background: Fungal infections affect various parts of the body and can be difficult to treat. Aspergillus infection causes a spectrum of diverse diseases particularly in lung according to host immunity. The two major entities are invasive pulmonary aspergillosis and chronic pulmonary aspergillosis. Candida infections can be superficial or invasive. Superficial infections often affect the skin or mucous membranes. However, invasive fungal infections are often life-threatening. Advances in nanotechnology have opened new horizons in nanomedicine, allowing the synthesis of nanoparticles that can be assembled into complex architectures. Novel studies and technologies are devoted to understanding the mechanisms of disease for the design of new drugs. Objectives: In the present study, the antifungal activity of biogenic selenium nanoparticles (Se NPs) against Aspergillus fumigatus and Candida albicans was investigated. Materials and Methods: Se-reducing bacteria previously identified as Bacillus sp. MSh-1 were used for the intracellular biosynthesis of elemental Se NPs. The shape, size, and purity of the extracted NPs were determined with various instrumental techniques. The nanoparticles antifungal characterization mainly derives from the following pathways: (i) to generate sustained flux of nano-ions from the compounds that deposited on special substrates or imbedded in colloidal or semisolid matrices. (ii) To transport active those ions to sensitive targets on plasma membrane of fungi. Results: The results of energy-dispersive X-ray demonstrated that the purified NPs consisted of only Se. In addition, transmission electron micrographs showed that 120- to 140-nm spherical Se NPs were the most common. An antifungal assay was performed with a standard Clinical and Laboratory Standards Institute broth microdilution method. Minimum inhibitory concentration (MIC) measurements of the antifungal activity of the Se NPs against C. albicans (70 μg/mL) and A. fumigatus (100 μg/mL) showed that yeast cells were more sensitive than mold cells. Conclusions: The MICs against A. fumigatus (100 μg/mL) and C. albicans (70 μg/mL) showed that biogenic Se NPs are useful antifungal agents. read more read less

Topics:

Candida albicans (56%)56% related to the paper, Aspergillus fumigatus (55%)55% related to the paper
85 Citations
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Jundishapur Journal of Microbiology format uses Vancouver citation style.

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Frequently asked questions

1. Can I write Jundishapur Journal of Microbiology in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Jundishapur Journal of Microbiology guidelines and auto format it.

2. Do you follow the Jundishapur Journal of Microbiology guidelines?

Yes, the template is compliant with the Jundishapur Journal of Microbiology guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Jundishapur Journal of Microbiology?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Jundishapur Journal of Microbiology citation style.

4. Can I use the Jundishapur Journal of Microbiology templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Jundishapur Journal of Microbiology.

5. Can I use a manuscript in Jundishapur Journal of Microbiology that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Jundishapur Journal of Microbiology that you can download at the end.

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Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

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12. Is Jundishapur Journal of Microbiology's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Jundishapur Journal of Microbiology?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Jundishapur Journal of Microbiology. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Jundishapur Journal of Microbiology?

The 5 most common citation types in order of usage for Jundishapur Journal of Microbiology are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

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16. Can I download Jundishapur Journal of Microbiology in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Jundishapur Journal of Microbiology Endnote style according to Elsevier guidelines.

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