Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats
ne"> <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Background</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>:...
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Format: | Article |
Language: | English |
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Tehran University of Medical Sciences
2016-02-01
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Series: | Journal of Medical Bacteriology |
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Online Access: | http://jmb.tums.ac.ir/index.php/jmb/article/view/103 |
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DOAJ |
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English |
format |
Article |
sources |
DOAJ |
author |
Baharak Akhtardanesh Reza Ghanbarpour Elmira Yazdani |
spellingShingle |
Baharak Akhtardanesh Reza Ghanbarpour Elmira Yazdani Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats Journal of Medical Bacteriology Escherichia coli, Extendedspectrum β-lactamase, Phylogenetic group, cat |
author_facet |
Baharak Akhtardanesh Reza Ghanbarpour Elmira Yazdani |
author_sort |
Baharak Akhtardanesh |
title |
Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats |
title_short |
Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats |
title_full |
Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats |
title_fullStr |
Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats |
title_full_unstemmed |
Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy Cats |
title_sort |
determination of extended-spectrum beta-lactamases genes and antibiotic resistance patterns in escherichia coli isolates from healthy cats |
publisher |
Tehran University of Medical Sciences |
series |
Journal of Medical Bacteriology |
issn |
2251-8649 2322-2581 |
publishDate |
2016-02-01 |
description |
ne"> <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Background</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">This study was set to detect extended-spectrum beta-lactamases (ESBLs)<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">producing <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates and the genes underlying their resistance in relation to phylogenetic<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">background from fecal samples of healthy owned cats.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Methods</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">A total of 50 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates were confirmed by standard bacteriological tests. The<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">phylogenetic analyses of the isolates were carried out by combinations of three genetic markers<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>chuA</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>yjaA </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">and DNA fragment <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>TspE4.C2 </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">by a triplex PCR method. The ESBL (<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">CTXM<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">TEM<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">,<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">SHV<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;"><em>OXA</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">) encoding genes were detected. To identify ESBL producing phenotypes, all<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">selected isolates were screened with a double disk synergy test including cefotaxime, cefotaxime<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">with clavulanic acid, ceftazidime and ceftazidime with clavulanic acid.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Results</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">: Results showed that <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates fell into four phylogenetic groups (A, D, B1 and<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">B2) with prevalence of 78%, 4%, 8%, 10% and five phylogenetic subgroups including A0 (74<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">%), A1 (4 %), B1 (8 %), B2–2 (6 %), B2–3 (4 %) and D1 (4 %), respectively. Among all <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli</em><br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates, 4% were positive for <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;"><em>SHV</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">CTX-M-15 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">and <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">OXA-1 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">genes which distributed in B2-2,<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">B2-3, A0 subgroups, respectively. According to antibiotic susceptibility test, 20 isolates were<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">resistant which belonged to D (D1 phylogenetic subgroup) and A (A0 phylogenetic subgroup)<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">groups.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Conclusion</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">The results showed that healthy cats could be considered as potential source for the<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">dissemination of ESBL-encoding genes. Further investigations in companion animals and their<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">owners are needed to clarify the importance of spreading of these zoonotic strains.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><br style="font-style: normal; font-variant: normal; font-weight: normal; letter-spacing: normal; line-height: normal; orphans: 2; text-align: -webkit-auto; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px;" /></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span> |
topic |
Escherichia coli, Extendedspectrum β-lactamase, Phylogenetic group, cat |
url |
http://jmb.tums.ac.ir/index.php/jmb/article/view/103 |
work_keys_str_mv |
AT baharakakhtardanesh determinationofextendedspectrumbetalactamasesgenesandantibioticresistancepatternsinescherichiacoliisolatesfromhealthycats AT rezaghanbarpour determinationofextendedspectrumbetalactamasesgenesandantibioticresistancepatternsinescherichiacoliisolatesfromhealthycats AT elmirayazdani determinationofextendedspectrumbetalactamasesgenesandantibioticresistancepatternsinescherichiacoliisolatesfromhealthycats |
_version_ |
1725707336460271616 |
spelling |
doaj-d4830c1921c44021a3456d2a7c8871b52020-11-24T22:39:50ZengTehran University of Medical SciencesJournal of Medical Bacteriology2251-86492322-25812016-02-0145, 61689Determination of Extended-Spectrum Beta-lactamases Genes and Antibiotic Resistance Patterns in Escherichia coli Isolates from Healthy CatsBaharak Akhtardanesh0Reza Ghanbarpour1Elmira Yazdani2Department of Clinical Sciences, School of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran.Department of Pathobiology, School of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran.Department of Clinical Sciences, School of Veterinary Medicine, Shahid Bahonar University of Kerman, Kerman, Iran.ne"> <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Background</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">This study was set to detect extended-spectrum beta-lactamases (ESBLs)<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">producing <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates and the genes underlying their resistance in relation to phylogenetic<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">background from fecal samples of healthy owned cats.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Methods</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">A total of 50 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates were confirmed by standard bacteriological tests. The<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">phylogenetic analyses of the isolates were carried out by combinations of three genetic markers<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>chuA</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>yjaA </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">and DNA fragment <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>TspE4.C2 </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">by a triplex PCR method. The ESBL (<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">CTXM<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">TEM<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">,<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">SHV<span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;"><em>OXA</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">) encoding genes were detected. To identify ESBL producing phenotypes, all<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">selected isolates were screened with a double disk synergy test including cefotaxime, cefotaxime<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">with clavulanic acid, ceftazidime and ceftazidime with clavulanic acid.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Results</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">: Results showed that <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli </em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates fell into four phylogenetic groups (A, D, B1 and<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">B2) with prevalence of 78%, 4%, 8%, 10% and five phylogenetic subgroups including A0 (74<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">%), A1 (4 %), B1 (8 %), B2–2 (6 %), B2–3 (4 %) and D1 (4 %), respectively. Among all <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>E. coli</em><br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">isolates, 4% were positive for <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;"><em>SHV</em><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">, <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">CTX-M-15 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">and <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><em>bla</em><span style="font-size: 6pt; color: #000000; font-style: normal; font-variant: normal;">OXA-1 <span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">genes which distributed in B2-2,<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">B2-3, A0 subgroups, respectively. According to antibiotic susceptibility test, 20 isolates were<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">resistant which belonged to D (D1 phylogenetic subgroup) and A (A0 phylogenetic subgroup)<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">groups.<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong><em>Conclusion</em></strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;"><strong>: </strong><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">The results showed that healthy cats could be considered as potential source for the<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">dissemination of ESBL-encoding genes. Further investigations in companion animals and their<br /><span style="font-size: 9pt; color: #000000; font-style: normal; font-variant: normal;">owners are needed to clarify the importance of spreading of these zoonotic strains.</span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span><br style="font-style: normal; font-variant: normal; font-weight: normal; letter-spacing: normal; line-height: normal; orphans: 2; text-align: -webkit-auto; text-indent: 0px; text-transform: none; white-space: normal; widows: 2; word-spacing: 0px; -webkit-text-size-adjust: auto; -webkit-text-stroke-width: 0px;" /></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span></span>http://jmb.tums.ac.ir/index.php/jmb/article/view/103Escherichia coli, Extendedspectrum β-lactamase, Phylogenetic group, cat |