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2 "Reza Ranjbar"
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Original Articles
Profiling of Virulence-associated Factors in Shigella Species Isolated from Acute Pediatric Diarrheal Samples in Tehran, Iran
Sajad Yaghoubi, Reza Ranjbar, Mohammad Mehdi Soltan Dallal, Somayeh Yasliani Fard, Mohammad Hasan Shirazi, Mahmood Mahmoudi
Osong Public Health Res Perspect. 2017;8(3):220-226.   Published online June 30, 2017
DOI: https://doi.org/10.24171/j.phrp.2017.8.3.09
  • 4,535 View
  • 61 Download
  • 17 Crossref
AbstractAbstract PDF
Objectives

The genus Shigella comprises the most infectious and diarrheagenic bacteria causing severe diseases, mostly in children under five years of age. This study aimed to detect nine virulence genes (ipaBCD, VirA, sen, set1A, set1B, ial, ipaH, stx, and sat) in Shigella species (spp.) using multiplex polymerase chain reaction (MPCR) and to determine the relation of Shigella spp. from pediatric diarrheal samples with hospitalization and bloody diarrhea in Tehran, Iran.

Methods

Shigella spp. were isolated and identified using standard microbiological and serological methods. The virulence genes were detected using MPCR.

Results

Seventy-five Shigella spp. (40 S. sonnei, 33 S. flexneri, 1 S. dysenteriae, and 1 S. boydii) were isolated in this study. The prevalence of ial, sen, sat, set1A, and set1B was 74.7%, 45.4%, 28%, 24%, and 24%, respectively. All S. flexneri isolates, while no S. sonnei, S. dysenteriae, or S. boydii isolates, contained sat, set1A, and set1B. All isolates were positive for ipaH, ipaBCD, and virA, while one (1.4%) of the isolates contained stx. The highest prevalence of virulence determinants was found in S. flexneri serotype IIa. Nineteen (57.6%) of 33 S. flexneri isolates were positive for ipaBCD, ipaH, virA, ial, and sat. The sen determinants were found to be statistically significantly associated with hospitalization and bloody diarrhea (p = 0.001).

Conclusion

This study revealed a high prevalence of enterotoxin genes in S. flexneri, especially in serotype 2a, and has presented relations between a few clinical features of shigellosis and numerous virulence determinants of clinical isolates of Shigella spp.

Citations

Citations to this article as recorded by  
  • Epidemiological analysis and prevention strategies in response to a shigellosis cluster outbreak: a retrospective case series in an alternative school in the Republic of Korea, 2023
    Yeongseo Ahn, Sunmi Jin, Gemma Park, Hye Young Lee, Hyungyong Lee, Eunkyung Shin, Junyoung Kim, Jaeil Yoo, Yuna Kim
    Osong Public Health and Research Perspectives.2024; 15(1): 68.     CrossRef
  • Invasion of HeLa Cells by Shigella Species Clinical Isolates Recovered from Pediatric Diarrhea
    Zohreh Ghalavand, Marzieh Taheri, Gita Eslami, Mohammadmahdi Karimi-Yazdi, Mehrzad Sadredinamin
    Foodborne Pathogens and Disease.2023; 20(11): 509.     CrossRef
  • Plant-derived nanoparticles as alternative therapy against Diarrheal pathogens in the era of antimicrobial resistance: A review
    Tesleem Olatunde Abolarinwa, Daniel Jesuwenu Ajose, Bukola Opeyemi Oluwarinde, Justine Fri, Kotsoana Peter Montso, Omolola Esther Fayemi, Adeyemi Oladapo Aremu, Collins Njie Ateba
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Distribution of genes encoding virulence factors of Shigella strains isolated from children with diarrhea in southwest Iran
    Nabi Jomehzadeh, Khadijah Ahmadi, Hazhir Javaherizadeh, Maryam Afzali
    Molecular Biology Reports.2021; 48(2): 1645.     CrossRef
  • Evaluate the distribution of virulence genes and to investigate antibiotic resistance pattern among Shigella species isolated from children with shigellosis in Iran
    Samane Mohebi, Hossein Hosseini Nave, Kasra Javadi, Ali Amanati, Soudeh Kholdi, Mahtab Hadadi, Zahra Hashemizadeh, Mohammad Motamedifar
    Gene Reports.2021; 23: 101189.     CrossRef
  • Burden, Antibiotic Resistance, and Clonality of Shigella spp. Implicated in Community-Acquired Acute Diarrhoea in Lilongwe, Malawi
    Abel F.N.D. Phiri, Akebe Luther King Abia, Daniel Gyamfi Amoako, Rajab Mkakosya, Arnfinn Sundsfjord, Sabiha Y. Essack, Gunnar Skov Simonsen
    Tropical Medicine and Infectious Disease.2021; 6(2): 63.     CrossRef
  • Frequency and Antimicrobial Resistance of Shigella Species in Iran During 2000-2020
    Farhad Moradi, Nahal Hadi, Maryam Akbari, Zahra Hashemizadeh, Reyhaneh Rouhi Jahromi
    Jundishapur Journal of Health Sciences.2021;[Epub]     CrossRef
  • Virulence factors and molecular characteristics of Shigella flexneri isolated from calves with diarrhea
    Zhen Zhu, Weiwei Wang, Mingze Cao, Qiqi Zhu, Tenghe Ma, Yongying Zhang, Guanhui Liu, Xuzheng Zhou, Bing Li, Yuxiang Shi, Jiyu Zhang
    BMC Microbiology.2021;[Epub]     CrossRef
  • Development of quinolone resistance and prevalence of different virulence genes among Shigella flexneri and Shigella dysenteriae in environmental water samples
    B. Roy, S.K. Tousif Ahamed, B. Bandyopadhyay, N. Giri
    Letters in Applied Microbiology.2020; 71(1): 86.     CrossRef
  • High Rates of Antimicrobial Resistance and Virulence Gene Distribution Among Shigella spp. Isolated from Pediatric Patients in Tehran, Iran


    Mohammadmahdi Karimi-Yazdi, Zohreh Ghalavand, Mahdi Shabani, Hamidreza Houri, Mehrzad Sadredinamin, Marzieh Taheri, Gita Eslami
    Infection and Drug Resistance.2020; Volume 13: 485.     CrossRef
  • Molecular characterization of Shigella species isolated from diarrheal patients in Tehran, Iran: phylogenetic typing and its association with virulence gene profiles and a novel description of Shigella invasion associated locus
    Sina Arabshahi, Aytak Novinrooz, Reza Ranjbar, Abbas Ali Imani Fooladi
    European Journal of Clinical Microbiology & Infect.2020; 39(9): 1727.     CrossRef
  • Case report on a swift shift in uropathogens from Shigella flexneri to Escherichia coli: a thin line between bacterial persistence and reinfection
    Kukwah Anthony Tufon, Djike Puepi Yolande Fokam, Youmbi Sylvain Kouanou, Henry Dilonga Meriki
    Annals of Clinical Microbiology and Antimicrobials.2020;[Epub]     CrossRef
  • Virulence-related genes are associated with clinical and nutritional outcomes of Shigella/Enteroinvasive Escherichia coli pathotype infection in children from Brazilian semiarid region: A community case-control study
    Mariana Bona, Pedro Henrique Medeiros, Ana Karolina Santos, Thiago Freitas, Mara Prata, Herlice Veras, Marília Amaral, Daniel Oliveira, Alexandre Havt, Aldo Ângelo Lima
    International Journal of Medical Microbiology.2019; 309(2): 151.     CrossRef
  • Genotyping and diversity of virulence genes among Shigella sonnei isolated from children with diarrhoea
    Hamed Memariani, Mojtaba Memariani
    Reviews in Medical Microbiology.2019; 30(4): 217.     CrossRef
  • Virulence gene profiles of Shigella species isolated from stool specimens in India: its association with clinical manifestation and antimicrobial resistance
    Dhiviya Prabaa Muthuirulandi Sethuvel, Shalini Anandan, Joy Sarojini Michael, Dhivya Murugan, Ayyanraj Neeravi, Valsan Philip Verghese, Kamini Walia, Balaji Veeraraghavan
    Pathogens and Global Health.2019; 113(4): 173.     CrossRef
  • Prevalence of enterotoxin-encoding genes among diverse Shigella strains isolated from patients with diarrhea, southwest Iran
    Mojtaba Moosavian, Sakineh Seyed-Mohammadi, Ahmad Farajzadeh Sheikh, Saeed Khoshnood, Aram Asarehzadegan Dezfuli, Morteza Saki, Gholamreza Ghaderian, Fatemeh Shahi, Mahtab Abdi, Fariba Abbasi
    Acta Microbiologica et Immunologica Hungarica.2018; 66(1): 91.     CrossRef
  • Frequency of Mutations in Quinolone Resistance-Determining Regions and Plasmid-Mediated Quinolone Resistance in Shigella Isolates Recovered from Pediatric Patients in Tehran, Iran: An Overlooked Problem
    Sajad Yaghoubi, Reza Ranjbar, Mohammad Mehdi Soltan Dallal, Mohammad Hasan Shirazi, Mohammad Kazem Sharifi-Yazdi
    Microbial Drug Resistance.2018; 24(6): 699.     CrossRef
Rapid Molecular Approach for Simultaneous Detection of Salmonella spp., Shigella spp., and Vibrio cholera
Reza Ranjbar, Ali Naghoni, Davoud Afshar, Farhad Nikkhahi, Mohsen Mohammadi
Osong Public Health Res Perspect. 2016;7(6):373-377.   Published online December 31, 2016
DOI: https://doi.org/10.1016/j.phrp.2016.10.002
  • 3,346 View
  • 23 Download
  • 10 Crossref
AbstractAbstract PDF
Objectives
Gastrointestinal tract infection is still one of the serious public health problems in many geographic areas and is endemic in most countries including Iran. Early detection of the gastrointestinal tract pathogens can be extremely important. The aim of the current study was to apply a shortened time-multiplex polymerase chain reaction (PCR) for rapid and simultaneous detection of Salmonella spp., Shigella spp., and Vibrio cholera.
Methods
The standard and clinical strains of Salmonella spp., Shigella spp., and V. cholerae were used in the assay. Multiplex PCR was performed and optimized based on amplification of invA, putative integrase, and ompW genes for detecting Salmonella spp., Shigella spp., and V. cholerae, respectively. The specificity of the assay was evaluated by testing 12 different bacterial species.
Results
Only Salmonella spp., Shigella spp., and V. cholerae strains had positive results when subjected to the assay using multiplex PCR. The assay showed a high sensitivity, and no amplification products were observed in multiplex PCR with any of the other microorganisms.
Conclusion
Our study indicated that the invA, putative integrase, and ompW-based multiplex PCR assay appears to be an efficient method for rapid and simultaneous detection of Salmonella spp., Shigella spp., and V. cholerae.

Citations

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    Foodborne Pathogens and Disease.2023; 20(6): 222.     CrossRef
  • Rapid and multiplexed quantification of Salmonella, Escherichia coli O157:H7, and Shigella flexneri in ground beef using flow cytometry
    Ziquan Wang, Qian Xu, Siyuan Liu, Yingying Liu, Ying Gao, Meng Wang, Ling Zhang, Haiyan Chang, Qiang Wei, Zhiwei Sui
    Talanta.2022; 238: 123005.     CrossRef
  • Development of multiplex real-time quantitative PCR for simultaneous detection of Chlamydia trachomatis, Mycoplasma hominis, Ureaplasma urealyticum, and Mycoplasma genitalium in infertile women
    Sara Sadeqi, Farhad Nikkhahi, Amir Javadi, Sonia Eskandarion, Seyed Mahmoud Amin Marashi
    Indian Journal of Medical Microbiology.2022; 40(2): 231.     CrossRef
  • Multiple fluorescent saltatory rolling circle amplification (SRCA) for simultaneous and sensitive detection of Salmonella spp. and Shigella spp. in food
    Wei Guo, Qian Yang, Jie Liu, Xiuling Chen, Yunzhe Zhang, Wei Zhang
    LWT.2022; 168: 113875.     CrossRef
  • Campylobacter Species in the Middle East
    Daryoush Babazadeh, Reza Ranjbar
    Journal of Veterinary Physiology and Pathology.2022; 1(1): 1.     CrossRef
  • Development of rapid gold nanoparticles based lateral flow assays for simultaneous detection of Shigella and Salmonella genera
    Mohammad Lukman Yahaya, Nor Dyana Zakaria, Rahmah Noordin, Khairunisak Abdul Razak
    Biotechnology and Applied Biochemistry.2021; 68(5): 1095.     CrossRef
  • Ultrasensitive pathogen detection with a rolling circle amplification-empowered multiplex electrochemical DNA sensor
    Cheryl S.Y. Yeap, Thanyarat Chaibun, Su Yin Lee, Bin Zhao, Yuan Jan, Chan La-o-vorakiat, Werasak Surareungchai, Shiping Song, Benchaporn Lertanantawong
    Chemical Communications.2021; 57(91): 12155.     CrossRef
  • Taqman hydrolysis probe application for Escherichia coli, Salmonella enterica, and Vibrio cholerae detection in surface and drinking water
    Ahmed K. A. El-Sayed, Mohamed I. Abou-Dobara, Camelia A. Abdel-Malak, Amira A. E. El-Badaly
    Journal of Water, Sanitation and Hygiene for Devel.2019; 9(3): 492.     CrossRef
  • Pathways of healthcare and antibiotics use following reported gastrointestinal illness: a cross-sectional study in rural Anhui, China
    Xing Rong Shen, Maomao Xie, Jing Chai, Rui Feng, Jing Cheng, Rong Liu, Paul Kadetz, DeBin Wang
    BMJ Open.2019; 9(8): e030986.     CrossRef
  • DNA Microarray for Rapid Detection and Identification of Food and Water Borne Bacteria: From Dry to Wet Lab
    Reza Ranjbar, Payam Behzadi, Ali Najafi, Raheleh Roudi
    The Open Microbiology Journal.2017; 11(1): 330.     CrossRef

PHRP : Osong Public Health and Research Perspectives