Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens
Abstract Background Bacteroides fragilis is a part of the normal gastrointestinal flora, but it is also the most common anaerobic bacteria causing the infection. It is highly resistant to antibiotics and contains abundant antibiotic resistance mechanisms. Methods The antibiotic resistance pattern of...
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doaj-f05215252db64ef3a236183d990b48cb2021-04-25T11:05:27ZengBMCAnnals of Clinical Microbiology and Antimicrobials1476-07112021-04-012011810.1186/s12941-021-00435-wAntibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimensSeyedesomaye Jasemi0Mohammad Emaneini1Zahra Ahmadinejad2Mohammad Sadegh Fazeli3Leonardo A. Sechi4Fatemah Sadeghpour Heravi5Mohammad Mehdi Feizabadi6Department of Microbiology, School of Medicine, Tehran University of Medical SciencesDepartment of Microbiology, School of Medicine, Tehran University of Medical SciencesDepartment of Infectious Diseases, Imam Khomeini Hospital Complex, Tehran University of Medical SciencesDepartment of Surgery, Imam Khomeini Hospital Complex, Tehran University of Medical SciencesDepartment of Biomedical Sciences, University of SassariSurgical Infection Research Group, Faculty of Medicine and Health Sciences, Macquarie UniversityDepartment of Microbiology, School of Medicine, Tehran University of Medical SciencesAbstract Background Bacteroides fragilis is a part of the normal gastrointestinal flora, but it is also the most common anaerobic bacteria causing the infection. It is highly resistant to antibiotics and contains abundant antibiotic resistance mechanisms. Methods The antibiotic resistance pattern of 78 isolates of B. fragilis (22 strains from clinical samples and 56 strains from the colorectal tissue) was investigated using agar dilution method. The gene encoding Bacteroides fargilis toxin bft, and antibiotic resistance genes were targeted by PCR assay. Results The highest rate of resistance was observed for penicillin G (100%) followed by tetracycline (74.4%), clindamycin (41%) and cefoxitin (38.5%). Only a single isolate showed resistance to imipenem which contained cfiA and IS1186 genes. All isolates were susceptible to metronidazole. Accordingly, tetQ (87.2%), cepA (73.1%) and ermF (64.1%) were the most abundant antibiotic-resistant genes identified in this study. MIC values for penicillin, cefoxitin and clindamycin were significantly different among isolates with the cepA, cfxA and ermF in compare with those lacking such genes. In addition, 22.7 and 17.8% of clinical and GIT isolates had the bft gene, respectively. Conclusions The finding of this study shows that metronidazole is highly in vitro active agent against all of B. fragilis isolates and remain the first-line antimicrobial for empirical therapy.https://doi.org/10.1186/s12941-021-00435-wBacteroides fragilisAntibiotic resistanceResistance genebft gene |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Seyedesomaye Jasemi Mohammad Emaneini Zahra Ahmadinejad Mohammad Sadegh Fazeli Leonardo A. Sechi Fatemah Sadeghpour Heravi Mohammad Mehdi Feizabadi |
spellingShingle |
Seyedesomaye Jasemi Mohammad Emaneini Zahra Ahmadinejad Mohammad Sadegh Fazeli Leonardo A. Sechi Fatemah Sadeghpour Heravi Mohammad Mehdi Feizabadi Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens Annals of Clinical Microbiology and Antimicrobials Bacteroides fragilis Antibiotic resistance Resistance gene bft gene |
author_facet |
Seyedesomaye Jasemi Mohammad Emaneini Zahra Ahmadinejad Mohammad Sadegh Fazeli Leonardo A. Sechi Fatemah Sadeghpour Heravi Mohammad Mehdi Feizabadi |
author_sort |
Seyedesomaye Jasemi |
title |
Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens |
title_short |
Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens |
title_full |
Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens |
title_fullStr |
Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens |
title_full_unstemmed |
Antibiotic resistance pattern of Bacteroides fragilis isolated from clinical and colorectal specimens |
title_sort |
antibiotic resistance pattern of bacteroides fragilis isolated from clinical and colorectal specimens |
publisher |
BMC |
series |
Annals of Clinical Microbiology and Antimicrobials |
issn |
1476-0711 |
publishDate |
2021-04-01 |
description |
Abstract Background Bacteroides fragilis is a part of the normal gastrointestinal flora, but it is also the most common anaerobic bacteria causing the infection. It is highly resistant to antibiotics and contains abundant antibiotic resistance mechanisms. Methods The antibiotic resistance pattern of 78 isolates of B. fragilis (22 strains from clinical samples and 56 strains from the colorectal tissue) was investigated using agar dilution method. The gene encoding Bacteroides fargilis toxin bft, and antibiotic resistance genes were targeted by PCR assay. Results The highest rate of resistance was observed for penicillin G (100%) followed by tetracycline (74.4%), clindamycin (41%) and cefoxitin (38.5%). Only a single isolate showed resistance to imipenem which contained cfiA and IS1186 genes. All isolates were susceptible to metronidazole. Accordingly, tetQ (87.2%), cepA (73.1%) and ermF (64.1%) were the most abundant antibiotic-resistant genes identified in this study. MIC values for penicillin, cefoxitin and clindamycin were significantly different among isolates with the cepA, cfxA and ermF in compare with those lacking such genes. In addition, 22.7 and 17.8% of clinical and GIT isolates had the bft gene, respectively. Conclusions The finding of this study shows that metronidazole is highly in vitro active agent against all of B. fragilis isolates and remain the first-line antimicrobial for empirical therapy. |
topic |
Bacteroides fragilis Antibiotic resistance Resistance gene bft gene |
url |
https://doi.org/10.1186/s12941-021-00435-w |
work_keys_str_mv |
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