<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Microbiology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">World antimicrobial resistance (AMR) awareness week</title>
    <FirstPage>5167</FirstPage>
    <LastPage>5167</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mohammad Mehdi</FirstName>
        <LastName>Feizabadi</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>30</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>30</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">On the occasion of World Antimicrobial Resistance (AMR) Awareness Week, November 2024, we witnessed a lot of events throughout our country, Iran. Many different specialists throughout the country debated on the current situation, however, no one can predict the future outlook of this ongoing issue. The health policy makers try to find the right solutions for combating the drug-resistant superbugs but they should not ignore Microbiology principles. Carbapenem-resistant Klbesiella pneumoniae infections are definitely the main causes of morbidity and mortality in the Iranian Hospitals. In the current issue of this Journal, Dr. Solgi and his colleagues have raised an important and critical point: New Delhi metallo-beta-lactamase (NDM-MBL). Unfortunately, the number of cases infected with ceftazidime/avibactam-resistant Gram-negative bacteria has increased due to NDM-MBL production (Nearly 87% of K. pneumoniae clinical isolates in Isfahan). Therefore, our country resources are wasted with the current official protocol for administration of ceftazidime/avibactam, despite knowing that NDM-MBL producers are dominant. Physicians should be aware of the current situation of MBL strains in Iran, which is attainable through reviewing works published by Microbiologists in different provinces of Iran.
&#xD;

&#xA0;</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5167</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5167/1720</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Experimental prescription, rising resistance: the alarming misuse of ceftazidime-avibactam in healthcare systems</title>
    <FirstPage>720</FirstPage>
    <LastPage>721</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mojtaba</FirstName>
        <LastName>Akbari</LastName>
        <affiliation locale="en_US">Isfahan Endocrine and Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Christian</FirstName>
        <LastName>Giske</LastName>
        <affiliation locale="en_US">Division of Clinical Microbiology, Department of Laboratory Medicine, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden</affiliation>
      </Author>
      <Author>
        <FirstName>Hamid</FirstName>
        <LastName>Solgi</LastName>
        <affiliation locale="en_US">Isfahan Endocrine and Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, Iran; Amin Hospital, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>30</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">No Abstract No Abstract No Abstract</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5161</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5161/1721</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Systematic review and meta-analysis of colistin plus meropenem therapy for the treatment of nosocomial pneumonia</title>
    <FirstPage>722</FirstPage>
    <LastPage>731</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Hazhir</FirstName>
        <LastName>Moradi</LastName>
        <affiliation locale="en_US">Nosocomial Infection Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra Sadat</FirstName>
        <LastName>Sajadi-Javan</LastName>
        <affiliation locale="en_US">Nosocomial Infection Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sarah</FirstName>
        <LastName>Mousavi</LastName>
        <affiliation locale="en_US">Department of Clinical Pharmacy and Pharmacy Practice, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Soodabeh</FirstName>
        <LastName>Rostami</LastName>
        <affiliation locale="en_US">Nosocomial Infection Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Bita</FirstName>
        <LastName>Moradi Khaniabadi</LastName>
        <affiliation locale="en_US">Nosocomial Infection Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>03</Month>
        <Day>29</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Nosocomial pneumonia caused by multidrug-resistant gram-negative bacteria presents a significant challenge for healthcare systems, as there are limited effective treatments available. This systematic review and meta-analysis aim to investigate the outcomes of colistin plus meropenem combination therapy on nosocomial pneumonia.
Materials and Methods: An exhaustive search of PubMed, Scopus, Web of Science (WOS), and Embase databases was conducted, resulting in the extraction of 5 studies for qualitative assessment and meta-analysis. The study sample included 991 patients admitted with nosocomial pneumonia. The outcomes evaluated were clinical improvement, microbiological response, mortality, Sequential Organ Failure Assessment (SOFA) score, Acute Physiology and Chronic Health Evaluation (APACHE II) score, Charlson Comorbidity Index (CCI), Clinical Pulmonary Infection Score (CPIS), C-reactive protein (CRP) levels, procalcitonin (PCT) levels, and intensive care unit (ICU) duration.
Results: The results demonstrated that colistin plus meropenem combination therapy significantly improved clinical outcomes (OR = 1.37, 95% CI = 1.04-1.81, p = 0.027), reduced SOFA scores (OR = -0.28, 95% CI = -0.44 to -0.11, p = 0.001), and increased CCI scores (OR = 0.16, 95% CI = 0.02-0.29, p = 0.021) compared to other medications. However, other evaluated parameters did not show significant differences.
Conclusion: This meta-analysis indicates that colistin-meropenem combination therapy is superior to other colistin-based treatments for nosocomial pneumonia in terms of clinical improvement, SOFA score reduction, and CCI score increase. Nevertheless, other variables assessed did not exhibit remarkable differences between the treatment regimens.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/4673</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/4673/1722</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluating the in vitro activity of cefoperazone-sulbactam against Gram negative pathogens in blood stream infections using automated systems</title>
    <FirstPage>732</FirstPage>
    <LastPage>736</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Uksim</FirstName>
        <LastName>Qadri</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Sofiya</FirstName>
        <LastName>Zaffar</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Saleem</FirstName>
        <LastName>Wani</LastName>
        <affiliation locale="en_US">Department of General Medicine, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Shugufta</FirstName>
        <LastName>Roohi</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Munazah</FirstName>
        <LastName>Aman</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Sabah</FirstName>
        <LastName>Bhat</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
      <Author>
        <FirstName>Umaya</FirstName>
        <LastName>Majid</LastName>
        <affiliation locale="en_US">Department of Microbiology, Sher-i-Kashmir Institute of Medical Sciences, Jammu and Kashmir, India</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>07</Month>
        <Day>05</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: The incidence of multidrug-resistant, Gram-negative organisms, isolated as the etiological agents of infections is ascending. The advent of novel antibiotics poses significant challenges, necessitating the optimization and utilization of extant antimicrobial agents. Cefoperazone, a third-generation cephalosporin and &#x3B2;-lactam antimicrobial, when combined with sulbactam, an irreversible &#x3B2;-lactamase inhibitor, mitigates the vulnerability of cefoperazone to &#x3B2;-lactamase-producing organisms. Nonetheless, regional data on the susceptibility patterns for this pharmacological combination remains scarce. The primary objective of this investigation was to assess the efficacy of the cefoperazone-sulbactam combination against prevalent Gram-negative bacteria isolated from blood cultures.
Materials and Methods: A total of 700 Gram-negative isolates, comprising Escherichia coli, Klebsiella pneumoniae, Acinetobacter species, and Pseudomonas aeruginosa, were procured using the BacT/Alert 3D system. The identification and susceptibility testing for cefoperazone-sulbactam were performed using the VITEK Compact ID and AST system. Comparative analysis was conducted against other tested antibiotics.
Results: The study revealed that cefoperazone-sulbactam exhibited commendable in-vitro activity against Gram-negative pathogens isolated from blood, surpassed only by colistin and tigecycline.
Conclusion: Cefoperazone-sulbactam demonstrates robust activity against the most frequently encountered clinical pathogens, suggesting its potential as an efficacious therapeutic agent. The findings underscore the imperative for ongoing surveillance of resistance patterns and trends among commonly used antimicrobials.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/4891</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/4891/1723</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Lessons from an 11-year retrospective cohort study of Escherichi coli causing UTI in Imam Hospital Ardabil, Iran</title>
    <FirstPage>737</FirstPage>
    <LastPage>744</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Pegah</FirstName>
        <LastName>Shakib</LastName>
        <affiliation locale="en_US">Razi Herbal Medicines Research Center, Department of Microbiology, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Arzanlou</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Pouria</FirstName>
        <LastName>Sobhi</LastName>
        <affiliation locale="en_US">Student Research Committee, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>Mojebi</LastName>
        <affiliation locale="en_US">Student Research Committee, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Bahrami</LastName>
        <affiliation locale="en_US">Student Research Committee, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Faraz</FirstName>
        <LastName>Mahdizadeh</LastName>
        <affiliation locale="en_US">Student Research Committee, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Leyla</FirstName>
        <LastName>Asadi</LastName>
        <affiliation locale="en_US">Imam Hospital Laboratory, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoud</FirstName>
        <LastName>Amanzadeh</LastName>
        <affiliation locale="en_US">Department of Health Information Management, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Alireza</FirstName>
        <LastName>Mohammadnia</LastName>
        <affiliation locale="en_US">Department of Health Information Management, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Farzad</FirstName>
        <LastName>Khademi</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Rashid</FirstName>
        <LastName>Ramazanzadeh</LastName>
        <affiliation locale="en_US">Department of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>08</Month>
        <Day>03</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>11</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: The global problem of urinary tract infections (UTIs) caused by antibiotic-resistant bacteria is due to limited treatment options. This study aimed to examine the prevalence, etiology, and management implications of Escherichi coli causing UTI at Imam Hospital Ardabil, Iran.
Materials and Methods: 2340 samples of retrospective data on E. coli causing UTIs were collected at Imam Hospital in Ardabil, Iran, spanning from 2012 to 2022. The samples were cultured and isolated, and their antibiotic susceptibility was determined using standard laboratory methods and data were then organized and systematically categorized using Python.
Results: It was found that the lowest level of resistance was related to nitrofurantoin, followed by imipenem. In 2018, the number of E. coli patients resistant to trimethoprim was the highest. Cephalexin and ciprofloxacin trends indicate the reduction of the line during this retrospective period. There was a significant correlation between wards and some antibiotics like Cefepime, Cefotaxime, Ceftazidime, and Trimethoprim (P-Value &lt;0.05).
Conclusion: Significant correlations were identified between specific hospital wards and resistance to antibiotics. These findings underscore the need for continuous surveillance and tailored antibiotic stewardship programs to combat the rising trend of antibiotic resistance.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/4964</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/4964/1724</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>16</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="epublish">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>08</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">High prevalence of antimicrobial resistance genes in multidrug-resistant-ESBLs-producing Klebsiella pneumoniae post-COVID-19 pandemic</title>
    <FirstPage>745</FirstPage>
    <LastPage>754</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Golnar</FirstName>
        <LastName>Rahimzadeh</LastName>
        <affiliation locale="en_US">Pediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shaghayegh</FirstName>
        <LastName>Rezai</LastName>
        <affiliation locale="en_US">Department of Medical Microbiology and Virology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ghazal</FirstName>
        <LastName>Abbasi</LastName>
        <affiliation locale="en_US">Students Research Committee, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Saman</FirstName>
        <LastName>Soleimanpour</LastName>
        <affiliation locale="en_US">Department of Medical Microbiology and Virology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Valadan</LastName>
        <affiliation locale="en_US">Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Laleh</FirstName>
        <LastName>Vahedi</LastName>
        <affiliation locale="en_US">Department of Pathology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Somayeh</FirstName>
        <LastName>Sheidaei</LastName>
        <affiliation locale="en_US">Department of Pathology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Faezeh Sadat</FirstName>
        <LastName>Movahedi</LastName>
        <affiliation locale="en_US">Pediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Raha</FirstName>
        <LastName>Rezai</LastName>
        <affiliation locale="en_US">Pediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Sadegh</FirstName>
        <LastName>Rezai</LastName>
        <affiliation locale="en_US">Pediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>07</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>10</Month>
        <Day>31</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Klebsiella pneumoniae is a common pathogen associated with healthcare-related infections. It is particularly notable for its ability to develop resistance to multiple antibiotics, making treatment challenging. During the COVID-19 pandemic, increased antibiotic use to manage critically ill patients was contributed to the rise of multidrug-resistant Klebsiella pneumoniae. This study evaluated the antibiotic resistance patterns of multidrug-resistant, ESBL-producing Klebsiella pneumoniae in northern Iran after the COVID-19 pandemic.
Materials and Methods: This cross-sectional study was conducted between September 2022 and October 2023. Clinical samples were collected from patients with nosocomial infections at hospitals in Sari. This study included 114 multidrug-resistant ESBLs-producing Klebsiella pneumoniae isolates. Antimicrobial susceptibility was assessed using broth macro-dilution, and resistance genes were detected by multiplex PCR.
Results: Gentamicin, ampicillin-sulbactam, co-amoxiclav, and ceftazidime displayed the lowest activity against multidrug-resistant Klebsiella pneumoniae. In contrast, piperacillin-tazobactam showed the highest activity. The prevalence of resistance genes was as follows: blaTEM (99.12%), blaSHV (74.56%), blaCTX (88.60%), blaIMP (64.04%), acrA -B (92.98%), and OqXA -B (67.54%).
Conclusion: This study identified over 50% of antibiotic-resistance genes. Over half of multidrug-resistant Klebsiella pneumoniae isolates showed resistance to antibiotics except piperacillin-tazobactam, which is recommended for treating multidrug-resistant Klebsiella pneumoniae infections.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/4892</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index. of dogs and cats, their association with periodontal disease, and the possibility of a common source of infections between humans and companion animals is of great importance for the management of oral health in animals and humans.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5330</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5330/1817</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Incidence of drug resistance and expression of blaOXA-51 and adeA genes among Acinetobacter baumannii strains isolated from hospitalized patients at a government hospital in Irbid, Jordan</title>
    <FirstPage>725</FirstPage>
    <LastPage>733</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Aya</FirstName>
        <LastName>Maytah</LastName>
        <affiliation locale="en_US">Department of Basic Sciences, Ma&#x2032;an University College, Al-Balqa Applied University, Ma&#x2032;an, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Omar</FirstName>
        <LastName>AlKofahi</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Science, Faculty of Allied Medical Sciences, Zarqa University, Zarqa, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Rania</FirstName>
        <LastName>Al-Groom</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Science, Faculty of Allied Medical Sciences, Zarqa University, Zarqa, Jordan; Department of Allied Medical Sciences, Zarqa University College, Al-Balqa Applied University, Zarqa, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Mohd Sajjad</FirstName>
        <LastName>Ahmad Khan</LastName>
        <affiliation locale="en_US">Department of Basic Sciences, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia</affiliation>
      </Author>
      <Author>
        <FirstName>Basem Fouad</FirstName>
        <LastName>Dababneh</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Al-Ahliyya Amman University, Amman, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Anas</FirstName>
        <LastName>Da'meh</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Science, Faculty of Allied Medical Sciences, Zarqa University, Zarqa, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Rahaf</FirstName>
        <LastName>Alsarayereh</LastName>
        <affiliation locale="en_US">Department of Medical Laboratory Science, Faculty of Allied Medical Sciences, Zarqa University, Zarqa, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Fuad</FirstName>
        <LastName>Alhawarat</LastName>
        <affiliation locale="en_US">Department of Applied Medical Sciences, Al Hussein Bin Abdullah II Academy for Civil Protection, Al-Balqa Applied University, Salt, Jordan</affiliation>
      </Author>
      <Author>
        <FirstName>Heba</FirstName>
        <LastName>Ahmad Al Shqairat</LastName>
        <affiliation locale="en_US">Precision Medical Lab (PMLAB), AL-Karak, Jordan</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>08</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Acinetobacter baumannii (A. baumannii) is an opportunistic bacterial pathogen principally related with hospital-acquired infections. This study aimed to isolate and identify A. baumannii strains, investigate their resistance to various antibiotics, and characterize A. baumannii at the molecular level.
Materials and Methods: A total of 100 samples were obtained from various hospital departments, including the intensive care unit (ICU), emergency room, kidney dialysis and surgery units. The incidence of drug resistance was studied using the Vitek 2 Compact system and further using molecular techniques such as polymerase chain reaction to analyze the genes responsible for resistance.
Results: The study exhibited a high prevalence of multidrug-resistant (MDR) A. baumannii isolates, especially in ICU patients. The males were the predominant group, accounting for 60% whereas females were 40%. The most frequent samples were from urine (43%) and skin (24%). Majority of samples were from the ICU (42%) and emergency departments (20%). The tested isolates exhibited the highest resistance (66%) to oxacillin, whereas the maximum sensitivity (52%) was recorded for Erythromycin. Molecular analysis revealed the occurrence of resistance genes blaOXA-23, blaOXA-24, blaOXA-51, and blaOXA-58, which contribute to carbapenem resistance.
Conclusion: The findings emphasize that A. baumannii remains a formidable nosocomial pathogen, and there is pressing requirement for enhanced infection control procedures and antibiotic stewardship. Through improved molecular observation, judicious use of antibiotics and improved infection control practices, healthcare providers can alleviate the impact of MDR A. baumannii infections and improve the prognosis for affected patients in Jordan and beyond.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5606</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5606/1818</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Phenotypic and genotypic analysis of hypermucoviscous Klebsiella pneumoniae (hmkp) strain</title>
    <FirstPage>734</FirstPage>
    <LastPage>740</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Hayder</FirstName>
        <LastName>Ali</LastName>
        <affiliation locale="en_US">Department of Biology, College of Science, University of Al-Qadisiyah, Al Diwaniyah, Iraq</affiliation>
      </Author>
      <Author>
        <FirstName>Dhuha</FirstName>
        <LastName>Jabir</LastName>
        <affiliation locale="en_US">Department of Biology, College of Science, University of Al-Qadisiyah, Al Diwaniyah, Iraq</affiliation>
      </Author>
      <Author>
        <FirstName>Zainab</FirstName>
        <LastName>Falih</LastName>
        <affiliation locale="en_US">Department of Biology, College of Science, University of Al-Qadisiyah, Al Diwaniyah, Iraq</affiliation>
      </Author>
      <Author>
        <FirstName>Salam</FirstName>
        <LastName>Najm</LastName>
        <affiliation locale="en_US">Department Diwaniyah Health, Ministry of Health, Al Diwaniyah, Iraq</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>05</Month>
        <Day>01</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Hypermucoviscous Klebsiella pneumoniae exhibits distinct phenotypic and genetic characteristics that distinguish it from the classic K. pneumoniae pathogen. The aim of current study was to investigate some phenotypic and genetic markers used for hmKp identification.
Materials and Methods: Seventy-one K. pneumoniae isolates were obtained from the respiratory care unit in Al-Diwanyiah Teaching Hospital \Diwanyah, Iraq, from the first of November 2024 to the first of March 2025. The bacteria were identified, and antibiotic sensitivity testing was performed using VITEK 2 ID-GN and AST cards. Hypermucoviscosity was assessed using the string test, and an investigation into several adherence and virulence genes was conducted for all isolates. Then, multi-locus sequence typing was performed for hypermucoviscous K. pneumoniae isolates.
Results: 3 (4.22%) of 71 isolates were hypermucoviscous. The virulence and adherence genes were present in 100% of the isolates, whereas rmpA was only found in hypermucoviscous isolates. The results showed that the hmKp isolates were members of clonal group 147 (CG147) and were assigned to sequence type (ST) 293.
Conclusion: The string test is the primary phenotypical diagnosis for hmKp, while the genetically encoded rmpA gene is the most reliable genetic marker for hmKp identification. However, MLST is not beneficial for identification. The central positioning of ST392 within the MST highlights its potential role as an emerging high-risk clone.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5474</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5474/1819</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Phylogenetic analysis of blaNDM genes of carbapenem resistant uropathogens isolated from federal tertiary care hospital, Pakistan: insights into the evolution and dissemination of drug resistance</title>
    <FirstPage>741</FirstPage>
    <LastPage>750</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Shafiq</LastName>
        <affiliation locale="en_US">Department of Biosciences, Comsats University, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Amnah</FirstName>
        <LastName>Khan</LastName>
        <affiliation locale="en_US">Department of Biosciences, Comsats University, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Hyder</LastName>
        <affiliation locale="en_US">Department of Biosciences, Comsats University, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Umme</FirstName>
        <LastName>Farwa</LastName>
        <affiliation locale="en_US">Department of Pathology, Fazaia Medical College, Air University, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Farhan</FirstName>
        <LastName>Kursheed</LastName>
        <affiliation locale="en_US">Department of Microbiology, PMAS Arid Agriculture University, Rawalpindi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Sana</FirstName>
        <LastName>Khan</LastName>
        <affiliation locale="en_US">Department of Pathology, Pakistan Institute of Medical Sciences (PIMS), Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Ayesha</FirstName>
        <LastName>Siddiqa</LastName>
        <affiliation locale="en_US">Department of Pathology, Pakistan Institute of Medical Sciences (PIMS), Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Iftikhar</FirstName>
        <LastName>Ahmed</LastName>
        <affiliation locale="en_US">National Culture Collection of Pakistan (NCCP), Land Resources Research Institute (LRRI), National Agriculture Research Centre, Park Road, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Saeed</LastName>
        <affiliation locale="en_US">Department of Biosciences, Comsats University, Islamabad, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Muhammad</FirstName>
        <LastName>Fiaz</LastName>
        <affiliation locale="en_US">Department of Pathology, Pakistan Institute of Medical Sciences (PIMS), Islamabad, Pakistan</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>25</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Global health is seriously threatened by the rise of carbapenem-resistant Enterobacterales (CRE). The blaNDM gene, a key carbapenemase coding gene, causes global health concern due to its multidrug resistance and easy spread through mobile genetic elements. This study aimed to identify and genetically characterize the blaNDM genes from uropathogens, its antibiotic susceptibility, and its correlation with global sequences.
Materials and Methods: Urine samples were processed following microbiological guidelines. Isolates were identified using API-20E. Antibiotic susceptibility was tested using disc diffusion method, and bacterial DNAs were extracted for blaNDM gene sequencing for phylogenetic analysis.
Results: CREs were detected in 11.92% (n=51) of the 428 Enterobacterales. Among CRE isolates, 45% (n=23) were positive for blaNDM gene harbored by Klebsiella pneumoniae (57%), followed by Escherichia coli (26%). Uropathogenic CRE, harboring blaNDM, revealed susceptibility of 34.78%, 60.87%, and 65.22% to amikacin, nitrofurantoin, and fosfomycin respectively. The blaNDM-5 variant was most common (69.57%), followed by blaNDM-1 (26.09%) and blaNDM-7 (4.35%). Phylogenetic analysis revealed that blaNDM variants exhibit diverse relationships with Pakistani and worldwide sequences.
Conclusion: The significant presence of blaNDM in uropathogens, along with extensive antibiotic resistance, underscores the urgent need for continuous monitoring and antibiotic stewardship programs to manage the growing threat of CRE infections.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5216</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5216/1820</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Molecular characterization of multidrug-resistant Proteus mirabilis isolates from pregnant women with recurrent urinary tract infection in Erbil city, Iraq</title>
    <FirstPage>751</FirstPage>
    <LastPage>760</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Amer</FirstName>
        <LastName>Mustafa</LastName>
        <affiliation locale="en_US">Department of Microbiology, General Directorate of Health Erbil, Ministry of Health, Erbil, Iraq</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>03</Month>
        <Day>02</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>09</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Urinary tract infections (UTIs) are common in pregnancy and can cause maternal and fetal complications. Proteus mirabilis is a significant pathogen in recurrent UTIs due to its virulence factors. This study investigated the virulence genes and antibiotic resistance patterns of P. mirabilis isolates from pregnant women with UTIs in Erbil, Iraq.
Materials and Methods: This cross-sectional study (September 2024&#x2013;January 2025) included 120 urine specimens from pregnant women (15-44 years) with UTI symptoms. Bacterial identification was performed using culture, biochemical tests, as well as the Vitek 2 system. Virulence genes were detected by PCR, and antimicrobial susceptibility was assessed by standard methods.
Results: Of the 120 samples, 103 (85.8%) showed bacterial growth; 8 (6.7%) were positive for P. mirabilis, while 95 (79.1%) yielded other bacteria. The most affected age group was 25-34 years (52.5%), predominantly in the second trimester (42.5%) and urban residents (60.8%). Antimicrobial resistance was significant to ampicillin, trimethoprim-sulfamethoxazole, amoxicillin/clavulanic acid, and cephalosporins, although susceptibility was observed with several antibiotics. All P. mirabilis isolates harbored the UreC gene, and 75% possessed the MrpA virulence gene.
Conclusion: Multidrug-resistant P. mirabilis with key virulence genes was detected in pregnant women with UTIs. Regular screening and resistance monitoring are essential for effective management.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5325</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5325/1821</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Distribution of MBL and serine-&#x3B2;-lactamase-producing pathogens in ventilator-associated pneumonia: insights into MDR and XDR strains</title>
    <FirstPage>761</FirstPage>
    <LastPage>772</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Zeb</FirstName>
        <LastName>Hussain</LastName>
        <affiliation locale="en_US">Department of Microbiology, University of Karachi, Karachi, Pakistan; Department of Clinical Laboratory Sciences, Dow Institute of Medical Technology, Dow University of Health Sciences, Karachi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Asma</FirstName>
        <LastName>Naim</LastName>
        <affiliation locale="en_US">Department of Microbiology, University of Karachi, Karachi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Ambreen</FirstName>
        <LastName>Fatima</LastName>
        <affiliation locale="en_US">Department of Pathology, Dow International Medical College, Dow University of Health Sciences, Karachi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Asad</FirstName>
        <LastName>Karim</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Fakhur</FirstName>
        <LastName>Uddin</LastName>
        <affiliation locale="en_US">Department of Microbiology, Basic Medical Sciences Institute (BMSI), Jinnah Postgraduate Medical Centre (JPMC), Karachi, Pakistan</affiliation>
      </Author>
      <Author>
        <FirstName>Surraya</FirstName>
        <LastName>Shams</LastName>
        <affiliation locale="en_US">Department of Clinical Laboratory Sciences, Dow Institute of Medical Technology, Dow University of Health Sciences, Karachi, Pakistan</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>05</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Ventilator-associated pneumonia (VAP) caused by carbapenem-resistant Gram-negative bacteria is a serious ICU challenge. This study determined the prevalence, antimicrobial susceptibility profiles, and phenotypic carbapenemase resistance mechanisms of Gram-negative isolates from VAP patients in two tertiary hospitals in Karachi, Pakistan.
Materials and Methods: We included 104 consecutive cases of VAP (July 2021&#x2013;January 2023). A total of 67 carbapenem-resistant Gram-negative isolates were identified and tested. Antibiotic susceptibility was assessed by disk diffusion and broth micro dilution, according to CLSI and EUCAST guidelines. Modified and enhanced carbapenem inactivation methods (mCIM/eCIM) were used to distinguish metallo-&#x3B2;-lactamase (MBL) and serine carbapenemase production.
Results: The mean age was 44.6 &#xB1; 18.3 years; 52.2% were male. Early-onset VAP accounted for 37.3% and late-onset for 62.7%. The most frequent pathogens were Acinetobacter baumannii (49.3%, 33/67) and Klebsiella pneumoniae (20.9%, 14/67). Notably, 67% of isolates produced MBLs, and 33% produced serine carbapenemases (phenotypically). The prevalence of multidrug-resistant (MDR), extensively drug-resistant (XDR), and pan drug-resistant (PDR) phenotypes was 42.6%, 31.3%, and 19.4%, respectively.
Conclusion: VAP in our ICUs was dominated by A. baumannii and K. pneumoniae with high levels of MBL-mediated resistance. These findings highlight the urgent need for surveillance, stewardship, and new therapeutic options.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5505</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5505/1822</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Evaluation of the relationship between quorum sensing system genes and antibiotic resistance in isolated Pseudomonas aeruginosa from cystic fibrosis patients</title>
    <FirstPage>773</FirstPage>
    <LastPage>782</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Azadeh</FirstName>
        <LastName>Ehsani</LastName>
        <affiliation locale="en_US">Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Neda</FirstName>
        <LastName>Soleimani</LastName>
        <affiliation locale="en_US">Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammadreza</FirstName>
        <LastName>Modaresi Estehbanati</LastName>
        <affiliation locale="en_US">Department of Pediatric Pulmonary and Sleep Medicine, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>01</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Pseudomonas aeruginosa is a Gram-negative bacterium that causes respiratory infections in individuals with cystic fibrosis. Its level of virulence is primarily controlled through Quorum Sensing (QS), a communication mechanism that utilizes small signaling molecules. This study investigates P. aeruginosa antibiotic resistance in CF patients in Imam Khomeini Hospital and examines the presence of QS genes in resistant strains.
Materials and Methods: Sixty-five P. aeruginosa samples were identified in CF patients in Imam Khomeini Hospital in Tehran. Antibiotic resistance was assessed using the disk diffusion method, and QS genes (rhlI, rhlR, lasI, lasR) were evaluated by applying PCR.
Results: Approximately 61.5 % of P. aeruginosa strains were multiple-drug-resistant (MDR), with 30.7% classified as extensively drug-resistant (XDR). The highest resistance was observed against amoxicillin, amikacin, and cefepime. The most common QS gene in MDR and XDR strains was rhlR. Additionally, 78.9% of XDR isolates carried rhlI, rhlR, lasI, and lasR genes.
Conclusion: The study specified that more than half of the P. aeruginosa strains exhibited resistance to five antibiotic classes, and effective antibiotics against P. aeruginosa were colistin, meropenem, ciprofloxacin, piperacillin/tazobactam, and cefotaxime. A noteworthy correlation was identified between MDR and XDR strains and the existence of QS genes in the strains.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5169</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5169/1823</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Staphylococcus epidermidis modulates EMT-related gene expression and viability in MDA-MB-231 breast cancer cells</title>
    <FirstPage>783</FirstPage>
    <LastPage>790</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Farzaneh</FirstName>
        <LastName>Zarei Mahmoodabadi</LastName>
        <affiliation locale="en_US">Department of Biology, ET.C., Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Akram</FirstName>
        <LastName>Tabatabaee Bafroee</LastName>
        <affiliation locale="en_US">Department of Biology, ET.C., Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Arfa</FirstName>
        <LastName>Moshiri</LastName>
        <affiliation locale="en_US">Departments of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran; Laboratory of Molecular Medicine, IRCCS Instituto Giannina Gaslini, Genova, Italy</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Davar</FirstName>
        <LastName>Siadat</LastName>
        <affiliation locale="en_US">Departments of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran; Department of Biochemistry, Vanderbilt University Class of 2025, Microbiology Research Center (MRC), Pasteur Institute of Iran, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nayereh</FirstName>
        <LastName>Ebrahimzadeh</LastName>
        <affiliation locale="en_US">Departments of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>04</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>08</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Breast tissue microbiota differs between healthy and cancerous tissues, with some bacteria influencing tumor progression. Staphylococcus epidermidis, a common skin commensal found in breast tumors, may play a role in epithelial-mesenchymal transition (EMT), a key step in metastasis. This study evaluated the effects of S. epidermidis culture and cell-free supernatant (CFS) on MDA-MB-231 breast cancer cell survival and expression of EMT-related genes Snail1, fibronectin 1 (FN1), and N-cadherin (CDH2).
Materials and Methods: Different concentrations of S. epidermidis cultures and their CFS were applied to MDA-MB-231 cells. Cytotoxic effects were assessed by MTT assay at 2, 4, and 24 hours post-treatment. Real-time PCR analyzed gene expression after 24 hours of exposure to non-toxic concentrations (MOI 50 and 100 for cultures; 14% for CFS).
Results: Low concentrations did not affect viability, while higher doses (MOI 100 and 14% CFS) reduced viability by up to 60% and 90%, respectively, at 24 hours. MOI 50 did not significantly alter gene expression. At MOI 100, Snail1 and FN1 were significantly upregulated, but CDH2 was unchanged. Treatment with 5% and 7% CFS significantly increased all three EMT gene expressions, indicating EMT induction.
Conclusion: S. epidermidis affects EMT gene expression and cell viability, indicating potential involvement in breast cancer progression.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5468</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5468/1824</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Nano-based mouthwash containing white basil essential oil a potent alternative for oral hygiene</title>
    <FirstPage>791</FirstPage>
    <LastPage>803</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Nguyen</FirstName>
        <LastName>Vinh</LastName>
        <affiliation locale="en_US">Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, University of Health Sciences, Vietnam National University Ho Chi Minh City, Ho Chi Minh City, Vietnam; Department of Pharmaceutics, Research Center Of Discovery and Development Of Healthcare Products, Vietnam National University Ho Chi Minh City, Vietnam</affiliation>
      </Author>
      <Author>
        <FirstName>Nguyen</FirstName>
        <LastName>Bac</LastName>
        <affiliation locale="en_US">Department of Microbiology and Parasitology, School of Pharmacy, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City, Vietnam</affiliation>
      </Author>
      <Author>
        <FirstName>Nguyen</FirstName>
        <LastName>Thien</LastName>
        <affiliation locale="en_US">Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, University of Health Sciences, Vietnam National University Ho Chi Minh City, Ho Chi Minh City, Vietnam</affiliation>
      </Author>
      <Author>
        <FirstName>Do</FirstName>
        <LastName>Minh</LastName>
        <affiliation locale="en_US">Department of Science, John F. Kennedy Catholic High School, Washington, U.S.A</affiliation>
      </Author>
      <Author>
        <FirstName>Dao</FirstName>
        <LastName>Trung</LastName>
        <affiliation locale="en_US">Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, University of Health Sciences, Vietnam National University Ho Chi Minh City, Ho Chi Minh City, Vietnam</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>15</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>09</Month>
        <Day>14</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: White basil (Ocimum gratissimum L. Lamiaceae) essential oil exhibits potent antibacterial effects but its aqueous insolubility and high volatility restrict its applications. This study aimed to develop a nanodispersed mouthwash containing white basil essential oil, optimizing of surfactant/co-surfactant type and ratio, assess its physicochemical stability and antibacterial efficacy against Streptococcus mutans ATCC 25175.
Materials and Methods: Formulations combining white basil essential oil, Tween-80, isopropanol, Labrasol and water were prepared. Particle size, zeta potential, and pH were measured. Stability was evaluated under accelerated (40&#xB0;C, 75% RH) and stressed (60&#xB0;C, 75% RH) conditions over three months. Antimicrobial efficacy was assessed via minimum bactericidal concentration (MBC) after 30-second exposure.
Results: Characterization of the optimized formulation revealed an average particle size of 128 nm, neutral zeta potential, pH 3.42. Stability testing demonstrated thermodynamic resistance under all storage conditions for three months without phase separation or significant size change. The MBC against Streptococcus mutans was 0.4% w/v essential oil following 30 seconds of exposure. A corresponding mouthwash with 0.4% w/v essential oil demonstrated equivalent bactericidal activity.
Conclusion: Nanodispersion offers a promising strategy for white basil essential oil in mouthwash formulations. The developed formulation shows favorable stability and rapid bactericidal action, supporting further evaluation for clinical and commercial development.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5628</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5628/1825</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Assessing the beneficial effect of Lactobacillus plantarum MS1 and Lactobacillus delbrueckii YN1 on colitis in a rat model</title>
    <FirstPage>804</FirstPage>
    <LastPage>813</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Manizheh</FirstName>
        <LastName>Hajizadeh Varzeghan</LastName>
        <affiliation locale="en_US">Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Zarrini</LastName>
        <affiliation locale="en_US">Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Farzam</FirstName>
        <LastName>Sheikhzadeh Hesari</LastName>
        <affiliation locale="en_US">Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Hossein</FirstName>
        <LastName>Modarressi</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medicine Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>21</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>07</Month>
        <Day>17</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Probiotics are effective in improving inflammatory bowel disease (IBD). This study assessed the effect of mesalazine and two candidate probiotics on the improvement of acetic acid (AA)-induced colitis model.
Materials and Methods: Lactobacillus plantarum MS1and Lactobacillus delbrueckii YN1 were used for IBD model in rat. Twenty-five male Wistar rats weighing 250 &#xB1; 50 grams were used in 5 classified groups: Control (CO); Colitis (CL); Colitis, Probiotic (CLP); Colitis, Mesalazine (CLM); Colitis, Probiotic, Mesalazine (CLPM) and the treatment period was 3 weeks. The rats were treated with mesalazine 30 mg/kg and probiotic 109 CFU/ml after induction of colitis. Histopathological and immunological analyses were performed to evaluate the effects of probiotic bacteria on IBD.
Results: The results showed that the probiotic bacteria reduced inflammation (P&lt;0.05), extent (P&lt;0.01), crypt abscesses (P&lt;0.01), edema (P&lt;0.05), inflammatory cell infiltration (P&lt;0.5), and increased mucosa (P&lt;0.001) in rats. Mesalazine administration in animals with colitis did not have a significant effect. Administration of probiotics in both CLP and CLPM groups reduced extent, crypt abscesses, edema, and inflammatory cell infiltration and showed an important role in the down-regulation of consolidation of pro-inflammatory factors (TNF&#x3B1;, IL-6, and IL-17), as well as up-regulation of anti-inflammatory factors such as IL-10.
Conclusion: Lactobacillus plantarum MS1 and Lactobacillus delbrueckii YN1 have shown significant potential in alleviating AA-induced colitis symptoms. Their administration leads to a marked reduction in pro-inflammatory cytokines such as TNF-&#x3B1;, IL-17, and IL-6, while enhancing IL-10 levels, indicating their promise as therapeutic candidates for inflammatory bowel disease (IBD).</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/5210</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/5210/1826</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Investigation of the virulence, antibiotic resistance, and enterotoxin genes of methicillin-resistant Staphylococcus aureus (MRSA) isolated from nugget and salad samples</title>
    <FirstPage>814</FirstPage>
    <LastPage>825</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Najmeh</FirstName>
        <LastName>Vahed Dehkordi</LastName>
        <affiliation locale="en_US">Department of Food Hygiene, Faculty of Veterinary Medicine, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ebrahim</FirstName>
        <LastName>Rahimi</LastName>
        <affiliation locale="en_US">Research Center of Nutrition and Organic Products, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>05</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>12</Month>
        <Day>11</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: Methicillin-resistant Staphylococcus aureus (MRSA) is a significant cause of illness from consuming contaminated food. MRSA is mainly known for its ability to develop resistance to antibiotics including methicillin. This research examined the antimicrobial resistance pattern, enterotoxigenic dispensation, virulence factors, and biotyping for MRSA isolates.
Materials and Methods: Susceptibility of S. aureus isolates to 13 types of antibiotics were assessed, and the genes associated with the resistance were investigated. Disk diffusion was used to identify the phenotypic tenet of antibiotic resistance. PCR is instrumental in detecting genes that confer resistance to antibiotics, virulence and enterotoxin genes.
Results: S. aureus were found in 167 out of 363 nugget and salad samples, representing 46% of the total sample count. Seventy-eight isolates (46.71%) were identified as MRSA bacteria. Its prevalence in different sources was as follows: 10% in bovine, 0% in ovine, 30% in poultry, and 56% in humans. MRSA displays high prevalence of resistance to cefotaxime and tetracycline (100%). coa was the most prevalent virulence factor (100%) in MRSA.
Conclusion: Distribution of antibiotic resistance genes in MRSA, highlights a serious health issue, as the presence of different antibiotic resistance genes exacerbates multidrug resistance in MRSA isolates.</abstract>
    <web_url>https://ijm.tums.ac.ir/index.php/ijm/article/view/4807</web_url>
    <pdf_url>https://ijm.tums.ac.ir/index.php/ijm/article/download/4807/1827</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Microbiology</JournalTitle>
      <Issn>2008-3289</Issn>
      <Volume>17</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="epublish">
        <Year>2025</Year>
        <Month>10</Month>
        <Day>14</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">SARS-CoV-2 mRNA vaccine candidate encoding RBD chimera of Delta and Omicron variants: immunogenic potential and validation</title>
    <FirstPage>826</FirstPage>
    <LastPage>834</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Shahla</FirstName>
        <LastName>Shahsavandi</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sina</FirstName>
        <LastName>Soleimani</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>Tebyanian</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Amir Ali</FirstName>
        <LastName>Hariri</LastName>
        <affiliation locale="en_US">Biotechnology Department, Behyaar Sanaat Sepahan Company, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ashraf</FirstName>
        <LastName>Mohammadi</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abbas</FirstName>
        <LastName>Zare Mirakabadi</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mojtaba</FirstName>
        <LastName>Noofeli</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zarrin</FirstName>
        <LastName>Sharifnia</LastName>
        <affiliation locale="en_US">Biotechnology Department, Behyaar Sanaat Sepahan Company, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Mahdi</FirstName>
        <LastName>Ranjbar</LastName>
        <affiliation locale="en_US">Razi Vaccine and Serum Research Institute, Agricultural Research Education and Extension Organization, Karaj, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>02</Month>
        <Day>18</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>09</Month>
        <Day>06</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background and Objectives: The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants has presented a challenging issue for global health in the 21st century. Frequent mutations in viral genomes have diminished the effectiveness of current vaccines against new variants. Messenger RNA (mRNA) vaccine is a promising platform for eliciting a robust T cell