Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia

Background: The alarming rise in infections caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in animals and humans poses a serious threat due to its escalating antibiotic resistance. Unveiling this problematic bacteria's prevalence and resistance patterns in ani...

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Main Authors: Tati Ariyanti, Suhaemi Suhaemi, Sri Mulyati, Sukatma Sukatma, Sumirah Sumirah, Susan Maphilindawati Noor, Faidah Rachmawati, Prima Mei Widiyanti, Eddy Sukmawinata, Andriani Andriani, Eni Kusumaningtyas, Aswin Rafif Khairullah
Format: Article
Language:English
Published: Tripoli University 2025-03-01
Series:Open Veterinary Journal
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Online Access:http://www.ejmanager.com/fulltextpdf.php?mno=233841
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author Tati Ariyanti
Suhaemi Suhaemi
Sri Mulyati
Sukatma Sukatma
Sumirah Sumirah
Susan Maphilindawati Noor
Faidah Rachmawati
Prima Mei Widiyanti
Eddy Sukmawinata
Andriani Andriani
Eni Kusumaningtyas
Aswin Rafif Khairullah
author_facet Tati Ariyanti
Suhaemi Suhaemi
Sri Mulyati
Sukatma Sukatma
Sumirah Sumirah
Susan Maphilindawati Noor
Faidah Rachmawati
Prima Mei Widiyanti
Eddy Sukmawinata
Andriani Andriani
Eni Kusumaningtyas
Aswin Rafif Khairullah
author_sort Tati Ariyanti
collection DOAJ
description Background: The alarming rise in infections caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in animals and humans poses a serious threat due to its escalating antibiotic resistance. Unveiling this problematic bacteria's prevalence and resistance patterns in animals is crucial for formulating effective control strategies and safeguarding public health. Aim: The purpose of this study was to analyze the expression of three main genes: blaCTX-M, blaSHV, and blaTEM, in ESBL-producing E. coli isolates from The Research Center for Veterinary Science and the National Research and Innovation Agency. Moreover, their resistance profiles against various antibiotics should be systematically evaluated. Methods: Ninety-seven E. coli isolates from the bacteriology laboratory of The Research Center for Veterinary Science were identified on MacConkey medium supplemented with cefotaxime. The isolates were verified for the existence of the blaCTX-M, blaSHV, and blaTEM genes using PCR. Antimicrobial susceptibility testing was conducted using antibiotic discs following the CLSI standards. Results: The prevalence of ESBL-producing E. coli in chicken ceca, eggs, and fish intestines was 16.5% (16/97). The specific genes detected were blaCTX-M gene at 93.75% (15/16), followed by the blaTEM gene, at 81.25% (13/16), and blaSHV at 25% (4/16). The antimicrobial sensitivity test results revealed that all ESBL-producing E. coli isolates had multidrug resistance 81.25% to 1–5 antibiotics and 18.75% to 6–7 antibiotics. The isolate exhibited 100% resistance to ampicillin and sulfamethoxazole, with exclusive sensitivity to chloramphenicol. Conclusion: The dominant gene in the ESBL-producing isolates was blaCTX-M. This bacterium is completely resistant to ampicillin and sulfamethoxazole, whereas it displays multidrug resistance to 1–7 different types of antibiotics. [Open Vet J 2025; 15(3.000): 1340-1348]
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publishDate 2025-03-01
publisher Tripoli University
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series Open Veterinary Journal
spelling doaj-art-bf074e39e6964956bbf4c938e70719192025-08-20T02:28:05ZengTripoli UniversityOpen Veterinary Journal2226-44852218-60502025-03-011531340134810.5455/OVJ.2025.v15.i3.25233841Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in IndonesiaTati Ariyanti0Suhaemi Suhaemi1Sri Mulyati2Sukatma Sukatma3Sumirah Sumirah4Susan Maphilindawati Noor5Faidah Rachmawati6Prima Mei Widiyanti7Eddy Sukmawinata8Andriani Andriani9Eni Kusumaningtyas10Aswin Rafif Khairullah11Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, Indonesia Research Center for Veterinary Science, National Research and Innovation Agency (BRIN), Bogor, IndonesiaBackground: The alarming rise in infections caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in animals and humans poses a serious threat due to its escalating antibiotic resistance. Unveiling this problematic bacteria's prevalence and resistance patterns in animals is crucial for formulating effective control strategies and safeguarding public health. Aim: The purpose of this study was to analyze the expression of three main genes: blaCTX-M, blaSHV, and blaTEM, in ESBL-producing E. coli isolates from The Research Center for Veterinary Science and the National Research and Innovation Agency. Moreover, their resistance profiles against various antibiotics should be systematically evaluated. Methods: Ninety-seven E. coli isolates from the bacteriology laboratory of The Research Center for Veterinary Science were identified on MacConkey medium supplemented with cefotaxime. The isolates were verified for the existence of the blaCTX-M, blaSHV, and blaTEM genes using PCR. Antimicrobial susceptibility testing was conducted using antibiotic discs following the CLSI standards. Results: The prevalence of ESBL-producing E. coli in chicken ceca, eggs, and fish intestines was 16.5% (16/97). The specific genes detected were blaCTX-M gene at 93.75% (15/16), followed by the blaTEM gene, at 81.25% (13/16), and blaSHV at 25% (4/16). The antimicrobial sensitivity test results revealed that all ESBL-producing E. coli isolates had multidrug resistance 81.25% to 1–5 antibiotics and 18.75% to 6–7 antibiotics. The isolate exhibited 100% resistance to ampicillin and sulfamethoxazole, with exclusive sensitivity to chloramphenicol. Conclusion: The dominant gene in the ESBL-producing isolates was blaCTX-M. This bacterium is completely resistant to ampicillin and sulfamethoxazole, whereas it displays multidrug resistance to 1–7 different types of antibiotics. [Open Vet J 2025; 15(3.000): 1340-1348]http://www.ejmanager.com/fulltextpdf.php?mno=233841escherichia coliesblblactx-mblatemblashv
spellingShingle Tati Ariyanti
Suhaemi Suhaemi
Sri Mulyati
Sukatma Sukatma
Sumirah Sumirah
Susan Maphilindawati Noor
Faidah Rachmawati
Prima Mei Widiyanti
Eddy Sukmawinata
Andriani Andriani
Eni Kusumaningtyas
Aswin Rafif Khairullah
Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
Open Veterinary Journal
escherichia coli
esbl
blactx-m
blatem
blashv
title Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
title_full Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
title_fullStr Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
title_full_unstemmed Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
title_short Dissemination and phenotypic characterization of ESBL-producing Escherichia coli in Indonesia
title_sort dissemination and phenotypic characterization of esbl producing escherichia coli in indonesia
topic escherichia coli
esbl
blactx-m
blatem
blashv
url http://www.ejmanager.com/fulltextpdf.php?mno=233841
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