Title of article :
Evaluation of the genetic relatedness of Bacteroides fragilis isolates by TRs analysis
Author/Authors :
Khodaei, Niloofar Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran , Sadeghi Kalani, Behrooz Department of Medical Microbiology - Faculty of Medicine - Ilam University of Medical Sciences, Ilam , Zamani, Maryam Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran , Mohammadzadeh, Rokhsareh Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran , Talebi, Malihe Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran , Narimani, Tahmine Department of Microbiology - School of Medicine - Isfahan University of Medical Sciences, Tehran , Narimisa, Negar Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran , Masjedian Jazi, Faramarz Department of Microbiology - School of Medicine - Iran University of Medical Sciences, Tehran
Abstract :
Objective(s): Human gastrointestinal tract harbors a variety of bacteria with vital roles in human
health. Bacteroides fragilis is considered one of the dominant constituents of gut microflora which can
act as an opportunistic pathogen leading to various diseases, including colon cancer, diarrhea, uterine
and intrathecal abscesses, septicemia, and pelvic inflammation. In this study, multiple locus variable
number of tandem repeats analysis (MLVA) was performed to genetically differentiate 50 B. fragilis
isolates.
Materials and Methods: Eight suitable tandem repeats (TRs) were selected by bioinformatics tools and
were then subjected to PCR amplification using specific primers. Finally, MLVA profiles were clustered
using BioNumerics 7.6 software package.
Results: All VNTR loci were detected in all isolates using the PCR method. Overall, B. fragilis isolates
were differentiated into 27 distinct MLVA types. The highest diversity index was allocated to TR1,
TR2, TR5, TR6, and TR8; with this taken into account, strain type 14 was the most prevalent with 12
strains belonging to this type. Clustering revealed three major clusters of A, B, and C. With regards
to the pathogenicity of B. fragilis and the outcomes of infections related to this microorganism, it is
imperative to study this microorganism isolated from both patients and healthy individuals.
Conclusion: This study aimed at evaluating the efficiency of MLVA for the genetic differentiation of B.
fragilis. The results of this study indicate the promising efficiency of MLVA typing for cluster detection
of this bacterium.
Keywords :
Bacteroides fragilis , MLVA , PCR amplification , Tandem repeats , Typing
Journal title :
Iranian Journal of Basic Medical Sciences