Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria

Avian colibacillosis caused by avian pathogenic <i>Escherichia coli</i> (APEC) strains is a bacterial disease responsible for enormous economic losses in the poultry industry, due to high mortality rates in farms, antibiotic therapy costs, and seizures at slaughterhouses. The aim of this...

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Main Authors: Nadia Safia Chenouf, Chafik Redha Messaï, Isabel Carvalho, Tamara Álvarez-Gómez, Vanessa Silva, Abdelghani Zitouni, Ahcene Hakem, Patricia Poeta, Carmen Torres
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Language:English
Published: MDPI AG 2025-03-01
Series:Antibiotics
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Online Access:https://www.mdpi.com/2079-6382/14/4/356
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author Nadia Safia Chenouf
Chafik Redha Messaï
Isabel Carvalho
Tamara Álvarez-Gómez
Vanessa Silva
Abdelghani Zitouni
Ahcene Hakem
Patricia Poeta
Carmen Torres
author_facet Nadia Safia Chenouf
Chafik Redha Messaï
Isabel Carvalho
Tamara Álvarez-Gómez
Vanessa Silva
Abdelghani Zitouni
Ahcene Hakem
Patricia Poeta
Carmen Torres
author_sort Nadia Safia Chenouf
collection DOAJ
description Avian colibacillosis caused by avian pathogenic <i>Escherichia coli</i> (APEC) strains is a bacterial disease responsible for enormous economic losses in the poultry industry, due to high mortality rates in farms, antibiotic therapy costs, and seizures at slaughterhouses. The aim of this study was to characterize the serogroups and molecular features of extended spectrum β-lactamase (ESBL)-producing APEC isolates recovered from 248 liver samples of 215 broilers and 33 turkeys with colibacillosis lesions in northeast Algeria. For this, microbiological tests were carried out, according to the recommended standards: <i>E. coli</i> isolates were recovered using standard microbiological protocols, and identification was carried out by MALDI-TOF MS. Serogrouping was performed using a rapid agglutination slide and the antisera of three O somatic groups (O1, O2, O78). Antimicrobial susceptibility was determined by the disk diffusion method. PCR assays and sequencing were used to detect antimicrobial resistance genes, integrons, phylogrouping, and MLST. Conjugation experiments were also conducted to determine the transferability of the retrieved ESBL-encoding genes. Overall, 211 (85.1%) APEC isolates were collected (one per positive sample), and 164 (77.7%) of them were typable. The O2 and O1 serogroups were the most detected (46.1% in broiler typable isolates and 61.5% in turkey typable isolates). Seventeen APEC isolates were ESBL-producers and harbored the following genes (number of isolates): <i>bla</i><sub>CTX-M-1</sub> (14), <i>bla</i><sub>CTX-M-15</sub> (2), and <i>bla</i><sub>SHV-12</sub> (1). They belonged to phylogroups D (10 isolates), B1 (6 isolates), and B2 (1 isolate). The MLST of 13 ESBL producers revealed seven STs: ST23, ST38, ST48, ST117, ST131, ST1146, and ST5087. The ESBL-encoding genes were transferred by conjugation among 15 ESBL-producing isolates, and transconjugants acquired either the IncK or IncI1 plasmids. Concerted efforts from all poultry actors are needed to establish surveillance monitoring strategies to mitigate the spread of ESBL-producing isolates implicated in avian colibacillosis.
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spelling doaj-art-e3f28a72b89e48049ba1d13333d84e572025-08-20T02:28:40ZengMDPI AGAntibiotics2079-63822025-03-0114435610.3390/antibiotics14040356Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in AlgeriaNadia Safia Chenouf0Chafik Redha Messaï1Isabel Carvalho2Tamara Álvarez-Gómez3Vanessa Silva4Abdelghani Zitouni5Ahcene Hakem6Patricia Poeta7Carmen Torres8Faculty of Natural and Life Sciences, Earth and Universe Sciences, University Mohamed El Bachir El Ibrahimi of Bordj Bou Arreridj, El Anasser, Bordj Bou Arreridj 34000, AlgeriaFaculty of Natural and Life Sciences, Earth and Universe Sciences, University Mohamed El Bachir El Ibrahimi of Bordj Bou Arreridj, El Anasser, Bordj Bou Arreridj 34000, AlgeriaMicrobiology and Antibiotic Resistance Team (MicroART), Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801 Vila Real, PortugalArea Biochemistry and Molecular Biology, OneHealth-UR Research Group, University of La Rioja, 26006 Logroño, SpainMicrobiology and Antibiotic Resistance Team (MicroART), Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801 Vila Real, PortugalLaboratoire de Biologie des Systèmes Microbiens (LBSM), Ecole Normale Supérieure Cheikh Mohamed El Bachir El Ibrahimi, BP 92, Kouba, Algiers 16000, AlgeriaAgropastoralism Research Center of Djelfa, Djelfa 17000, AlgeriaMicrobiology and Antibiotic Resistance Team (MicroART), Department of Veterinary Sciences, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801 Vila Real, PortugalArea Biochemistry and Molecular Biology, OneHealth-UR Research Group, University of La Rioja, 26006 Logroño, SpainAvian colibacillosis caused by avian pathogenic <i>Escherichia coli</i> (APEC) strains is a bacterial disease responsible for enormous economic losses in the poultry industry, due to high mortality rates in farms, antibiotic therapy costs, and seizures at slaughterhouses. The aim of this study was to characterize the serogroups and molecular features of extended spectrum β-lactamase (ESBL)-producing APEC isolates recovered from 248 liver samples of 215 broilers and 33 turkeys with colibacillosis lesions in northeast Algeria. For this, microbiological tests were carried out, according to the recommended standards: <i>E. coli</i> isolates were recovered using standard microbiological protocols, and identification was carried out by MALDI-TOF MS. Serogrouping was performed using a rapid agglutination slide and the antisera of three O somatic groups (O1, O2, O78). Antimicrobial susceptibility was determined by the disk diffusion method. PCR assays and sequencing were used to detect antimicrobial resistance genes, integrons, phylogrouping, and MLST. Conjugation experiments were also conducted to determine the transferability of the retrieved ESBL-encoding genes. Overall, 211 (85.1%) APEC isolates were collected (one per positive sample), and 164 (77.7%) of them were typable. The O2 and O1 serogroups were the most detected (46.1% in broiler typable isolates and 61.5% in turkey typable isolates). Seventeen APEC isolates were ESBL-producers and harbored the following genes (number of isolates): <i>bla</i><sub>CTX-M-1</sub> (14), <i>bla</i><sub>CTX-M-15</sub> (2), and <i>bla</i><sub>SHV-12</sub> (1). They belonged to phylogroups D (10 isolates), B1 (6 isolates), and B2 (1 isolate). The MLST of 13 ESBL producers revealed seven STs: ST23, ST38, ST48, ST117, ST131, ST1146, and ST5087. The ESBL-encoding genes were transferred by conjugation among 15 ESBL-producing isolates, and transconjugants acquired either the IncK or IncI1 plasmids. Concerted efforts from all poultry actors are needed to establish surveillance monitoring strategies to mitigate the spread of ESBL-producing isolates implicated in avian colibacillosis.https://www.mdpi.com/2079-6382/14/4/356Avian colibacillosisAPECSerogrouping<i>bla</i><sub>CTX-M</sub>ESBLAlgeria
spellingShingle Nadia Safia Chenouf
Chafik Redha Messaï
Isabel Carvalho
Tamara Álvarez-Gómez
Vanessa Silva
Abdelghani Zitouni
Ahcene Hakem
Patricia Poeta
Carmen Torres
Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
Antibiotics
Avian colibacillosis
APEC
Serogrouping
<i>bla</i><sub>CTX-M</sub>
ESBL
Algeria
title Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
title_full Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
title_fullStr Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
title_full_unstemmed Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
title_short Serogrouping and Molecular Characterization of ESBL-Producing Avian Pathogenic <i>Escherichia coli</i> from Broilers and Turkeys with Colibacillosis in Algeria
title_sort serogrouping and molecular characterization of esbl producing avian pathogenic i escherichia coli i from broilers and turkeys with colibacillosis in algeria
topic Avian colibacillosis
APEC
Serogrouping
<i>bla</i><sub>CTX-M</sub>
ESBL
Algeria
url https://www.mdpi.com/2079-6382/14/4/356
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