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Pathogenicity Locus Determinants and Toxinotyping of Clostridioides Difficile Isolates Recovered From Iranian Patients Publisher



Aliramezani A1 ; Talebi M9 ; Baghani A1 ; Hajabdolbaghi M2 ; Salehi M2 ; Abdollahi A3 ; Afhami S4 ; Marjani M10 ; Golbabaei F11 ; Boroumand MA5 ; Sarrafnejad A6 ; Yaseri M7 ; Ghourchian S1 ; Douraghi M1, 8
Authors
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Authors Affiliations
  1. 1. Division of Microbiology, Department of Pathobiology, School of Public Health, Tehran, Iran
  2. 2. Department of Infectious Diseases and Tropical Medicine, Faculty of Medicine, Tehran, Iran
  3. 3. Department of Pathology, Imam Hospital Complex, Tehran, Iran
  4. 4. Department of Infectious Diseases, Shariati Hospital, Tehran, Iran
  5. 5. Department of Pathology, Tehran Heart Center, Tehran, Iran
  6. 6. Department of Immunology, School of Public Health, Tehran, Iran
  7. 7. Department of Epidemiology and Biostatistics, School of Public Health, Tehran, Iran
  8. 8. Food Microbiology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  10. 10. Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  11. 11. Department of Occupational Health, School of Public Health, Medical Sciences, University of Tehran, Tehran, Iran

Source: New Microbes and New Infections Published:2018


Abstract

Little is known about the toxin profiles, toxinotypes and variations of toxin Clostridioides difficile C (tcdC) in Iranian C. difficile isolates. A total of 818 stool specimens were obtained from outpatients (n = 45) and hospitalized patients (n = 773) in Tehran, Iran, from 2011 to 2017. The 44 C. difficile isolates were subjected to PCR of toxin C. difficile A (tcdA), toxin C. difficile B (tcdB), tcdA 3′-end deletion, toxinotyping and sequencing of the tcdC gene. Thirty-eight isolates (86.36%) were identified as tcdA and tcdB positive, and the remaining six isolates (13.63%) were nontoxigenic. All tcdA- and tcdB-positive isolates yielded an amplicon of 2535 bp by PCR for the tcdA 3′ end. Fourteen (36.84%), seventeen (44.73%) and seven (18.43%) isolates belonged to wild-type, toxin C. difficile C subclone3 (tcdC-sc3) and tcdC-A genotype of tcdC, respectively. Thirty-one isolates (81.57%) belonged to toxinotype 0, and seven isolates (18.42%) were classified as toxinotype V. This study provides evidence for the circulation of historical and hypervirulent isolates in the healthcare and community settings. Furthermore, it was also demonstrated that the tcdC-A genotype and toxinotype V are not uncommon among Iranian C. difficile isolates. © 2018