Genetic elements associated with antimicrobial resistance among avian pathogenic Escherichia coli
Annals of Clinical Microbiology and Antimicrobials volume 15, Article number: 59 (2016)
Avian-pathogenic Escherichia coli (APEC) are pathogenic strains of E. coli that are responsible for one of the most predominant bacterial disease affecting poultry worldwide called avian colibacillosis. This study describes the genetic determinants implicated in antimicrobial resistance among APEC isolated from different broiler farms in Egypt.
A total of 116 APEC were investigated by serotyping, antimicrobial resistance patterns to 10 antimicrobials, and the genetic mechanisms underlying the antimicrobial-resistant phenotypes.
Antibiogram results showed that the highest resistance was observed for ampicillin, tetracycline, nalidixic acid, and chloramphenicol. The detected carriage rate of integron was 29.3% (34/116). Further characterization of gene cassettes revealed the presence gene cassettes encoding resistance to trimethoprim (dfrA1, dfrA5, dfrA7, dfrA12), streptomycin/spectinomycin (aadA1, aadA2, aadA5, aadA23), and streptothricin (sat2). To our knowledge, this the first description of the presence of aadA23 in APEC isolates. Analysis of other antimicrobial resistance types not associated with integrons revealed the predominance of resistance genes encoding resistance to tetracycline (tetA and tetB), ampicillin (bla TEM), chloramphenicol (cat1), kanamycin (aphA1), and sulphonamide (sul1 and sul2). Among ciprofloxacin-resistant isolates, the S83L mutation was the most frequently substitution observed in the quinolone resistance-determining region of gyrA (56.3%). The bla TEM and bla CTX−M−1 genes were the most prevalent among APEC isolates producing extended-spectrum beta-lactamase (ESβL).
These findings provided important clues about the role of integron-mediated resistance genes together with other independent resistance genes and chromosomal mutations in shaping the epidemiology of antimicrobial resistance in E. coli isolates from poultry farms in Egypt.
Avian colibacillosis is an extraintestinal infection associated with upper respiratory tract infection typically air saculitis that can evolve into multiple lesions in different organs as polyserositis, cellulitis, salpingitis, perihepatitis, peritonitis, septicaemia, and death. These cause severe economic losses in the poultry industry due to the remarkable number of morbidities, mortalities, slaughter condemnation, and reduced productivity of the affected birds .
To reduce the high incidence and mortalities caused by avian colibacillosis in poultry farms, antimicrobials are considered as one of the gold choices among veterinarians in the poultry industry. However, in Egypt and other developing countries, antimicrobials are not only used for therapeutic reasons but also for prophylactic purposes in disease prevention and growth promotion. Such overuse and/or misuse contribute to the development and spread of antimicrobial resistance (AMR) among poultry flocks, leading to emergence of multiple drug resistance (MDR) pathogens . These MDR profiles can be transmitted to human through the food chain adding serious burden to human health. In addition, several studies supported the growing evidence that antimicrobial resistance can occur in the absence of selective pressure, highlighting the crucial role of antibiotic resistance genes in the development of MDR bacteria . The acquisition and dissemination of these antibiotic resistance genes is mainly mediated by horizontal gene transfer in which several mobile genetic elements facilitate this process, including plasmids, transposons, integrons, and bacteriophages . Integron is one of the major genetic elements by which bacteria can capture or excise one or more resistance gene cassettes by site-specific recombination. The mobilization of integron through transposons, plasmids, or other mobile genetic elements enables the spread of integrated resistance genes. This potentially facilitate the integration of almost all antimicrobial agents through the integron and increase the diversity of integrons in isolates from different sources, including human, avian, livestock, and environmental isolates [4–6].
The aim of this study was to determine the antibiotic susceptibility phenotypes of APEC isolated from different broiler farms in Egypt and to evaluate the association of observed phenotypes with the acquisition of integron mediated resistance gene cassettes or other resistance genes and chromosomal mutations located outside the integron.
In total, 116 APEC isolates recovered from 400 different samples were assayed. Samples were obtained from liver, lungs, air sacs and spleen from chicken with typical lesions of colisepticemia and were collected from 28 different broiler farms located in different geographic areas of Dakahlia Governorate in 2014 and 2015. Samples were cultured onto eosin methylene blue (EMB) agar (Oxoid, Basingstoke, UK) and incubated for 18–24 h at 37 °C. Typical colonies were subcultured onto MacConkey agar (Oxoid, Basingstoke, UK) and were biochemically confirmed using API 20E system (BioMérieux, Marcy-l’Étoile, France). Once identified, the isolates were preserved at −70 °C in brain heart infusion broth containing 20% glycerol (vol/vol) for further studies. Serotyping of E. coli isolates was performed using rapid diagnostic E. coli antisera sets (Denka Seiken Co., Japan) using 8 polyvalent, 43 monovalent somatic, and 22 flagellar antisera. Bacterial DNA for PCR analysis was prepared by boiling a bacterial culture in 300 µl of distilled water for 10 min, followed by centrifugation for 5 min at 10,000×g. A volume of 1 µl of the supernatant was used as a template for each 25 µl PCR mixture.
Antimicrobial susceptibility testing and detection of ESβL
The susceptibility of isolates to 10 different antimicrobial agents was determined by disc diffusion assay as described by Clinical and Laboratory Standards Institute (CLSI) . According to the measurement of inhibition zones, tested strains were evaluated as susceptible or resistant. The following antimicrobial discs (Oxoid, Basingstoke, UK) were used: gentamicin (GN, 10 μg), kanamycin (KAN, 30 μg), ampicillin (AMP, 10 μg), cefotaxime (CTX, 30 μg), nalidixic acid (NA, 30 μg), ciprofloxacin (CIP, 5 μg), tetracycline (TET, 30 μg), sulfamethoxazole-trimethoprim (STX, 25 μg), chloramphenicol (C, 30 μg), and streptomycin (S, 10 μg). The isolates were defined as multidrug-resistant APEC if they exhibited resistance to at least one agent in three or more antimicrobial categories . Escherichia coli strain ATCC 25922 was used as a reference strain for susceptibility test. All cefotaxime-resistant isolates were confirmed for the production of extended-spectrum beta-lactamase (ESβL) by using the double-disk synergy test (DDST) following recommendation and interpretations of CLSI standards .
Detection of integrons and characterization of associated gene cassettes
The presence of integrons among APEC isolates was assayed using primers hep35 and hep36 that amplify conserved regions of integron-encoded integrase genes intI1, intI2, and intI3 using published PCR protocols . Integron-positive isolates were characterized for the integron class using integron class-specific primers and PCR conditions previously described . Further characterization of gene cassette content within integron classes was determined using primers 5′CS/3′CS and hep74/hep51 for amplification of gene cassettes within integron classes 1 and 2, respectively as published [11, 12]. Samples with similar amplicon size were further subjected to restriction enzyme HinfI or RsaI  following manufacturer instructions (New England Biolabs, UK) and fragments obtained were separated on a 2.5% agarose gel. Isolates with similar polymorphism patterns were considered to harbor similar gene cassettes. Amplification products of samples with unique amplification products and one representative sample from samples with similar restriction patterns were purified from the agarose gel using QIA quick Gel Extraction Kit (Qiagen, USA) and sequenced using ABI Prism 377 automated sequencer (Applied Biosystems). All sequence results were compared with the available sequences in GenBank (http://www.ncbi.nlm.nih.gov/BLAST).
Detection of antimicrobial resistance genes outside the integron cassettes
Different PCR protocols were applied to detect specific genetic determinants corresponding to the resistance phenotype using Applied Biosystems 96-well thermal cycler and PCR conditions suggested by the referenced authors. These determinants included those encoding resistance to tetracycline (tetA, tetB, tetC, tetD, tetE, and tetG) , chloramphenicol (cat1, cat2, cat3, cmlA, and cmlB) , streptomycin (strA-strB) , Kanamycin (aphA1 and aphA2) , and sulfonamide including sul1, sul2 , and sul3 . The PCR amplification products were separated by agarose gel electrophoresis and visualized by ethidium bromide staining. Resistance to ciprofloxacin was assayed by determining mutations in DNA gyrase subunit A (gyrA) and topoisomerase IV subunit C (ParC) in the quinolone resistance determining region (QRDR) using protocol previously described . The resulting PCR amplicons were purified using QIA quick Gel Extraction Kit (Qiagen, USA) and bi-directionally sequenced using same primers. Strains that exhibited negative results for mutations in QRDR were screened for plasmid-mediated quinolone resistance (PMQR) including qnrA, qnrB, qnrS , qnrD , and aac (6′)-Ib-cr . Ampicillin-resistant isolates were screened for the β-Lactamases genes bla TEM and bla SHV, and bla OXA−1 using multiplex PCR protocol published . The later protocol was used to screen potential ESβL-producing E. coli isolates that initially exhibited resistance to cefotaxime. These isolates were further screened for bla CTX-M five phylogenetic groups (groups 1, 2, 8, 9, and 25) using multiplex PCR protocol previously described .
Pulsed-field gel electrophoresis (PFGE)
PFGE was performed to determine that isolates exhibiting similar antibiogram resistance profile and similar serotype are non-identical. PFGE for tested APEC isolates was performed using XbaI restriction enzyme according to the PulseNet protocol from the Centers for Disease Control and Prevention . At least one band difference was required to distinguish between pulsotypes.
Differences in the occurrence of integrons in resistant and susceptible APEC strains were tested using the Chi square (χ 2) test. Differences among means with P < 0.05 were considered as statistically significant. For the statistical analysis, intermediate resistant strains were considered as resistant.
A total of 116 E. coli isolates were recovered from 400 samples from diseased chicken. Serotyping recovered isolates identified 15 different E. coli serotypes (Table 1). All isolates exhibiting similar serotype and antimicrobial resistance patterns were confirmed to be non-duplicates as confirmed by PFGE. Among identified serotypes, O78 was found to be the most prevalent serotype (27.6%).
Antimicrobial resistance patterns and ESβL phenotype
Antibiotic susceptibility of 116 APEC isolates against 10 different antimicrobial drugs is presented in Table 2. The highest frequencies of resistance detected were those against ampicillin (100%), tetracycline (93.1%), nalidixic acid (84.5%), chloramphenicol (84.5%), kanamycin (69.0%), sulfamethoxazole-trimethoprim (58.6%), cefotaxime (58.6%), streptomycin (50.0%), gentamicin (48.3%), and ciprofloxacin (41.4%). A diversity of resistance patterns observed among tested E. coli isolates is shown in Table 1. Screening the potential ESβL producers confirmed that all cefotaxime-resistant isolates to be ESβL producers (68/68, 100%).
Distribution of integrons and associated gene cassettes
Of the 116 isolates tested, 34 isolates (29.3%) representing six serotypes were integron positive (Table 1). All integron-harboring E. coli isolates were multidrug resistant. Integron-positive isolates were significantly more resistant to streptomycin, kanamycin, gentamicin, and sulfamethoxazole-trimethoprim than integron-negative isolates (P < 0.05). Among integron-positive isolates, class 1 integrons were detected in 30 isolates (25.9%) and class 2 in four isolates (3.4%) (Table 1). None of the isolates possessed the combination of class 1 and class 2 integrons. Class 3 was absent in tested APEC isolates. Further characterization of gene cassettes by PCR, restriction digestion, and sequencing revealed eight different cassette arrangements within class 1 integron and a single cassette arrangement within class 2 integron. Among class 1 integron, the gene cassettes included those encoding resistance to trimethoprim (dfrA1, dfrA5, dfrA7, and dfrA12) and streptomycin (aadA1, aadA2, aadA5, and aadA23). A total of seven isolates harbored aadA1 + dfrA1 (20.6%); six isolates carried dfrA7 (17.6%); five isolates had aadA1 (14.7%); four isolates carried aadA5 (11.8%); three isolates (8.8%) contained dfrA5; two isolate (5.8%) carried aadA2 + dfrA12, two isolate (5.8%) carried aadA23, and one (2.9%) had dfrA1. All class 2 integron-carrying isolates possessed the gene cassette array dfrA1-sat2-aadA1 that encode resistance to trimethoprim, streptothricin, and streptomycin (Table 3).
Distribution of antimicrobial resistance genes outside the integron cassettes
Different frequencies of genes encoding resistance to tetracycline, chloramphenicol, ampicillin, streptomycin, kanamycin, ciprofloxacin, cefotaxime, sulfonamide, and ESβL production are reported in Table 2. Among tetracycline resistant isolates, 50 (46.3%) isolates carried tetA and 54 (50.0%) isolates were positive for tetB. Our results also showed that four isolates (3.7%) possessed both determinants. All isolates were negative for tetC, tetD, tetE, and tetG. Among the ampicillin-resistant isolates, 102 (87.9%) isolates possessed bla TEM, 14 (12.1%) isolates carried bla oxa1. None of these isolates carried bla SHV gene. The cat1 was the most common gene present among the chloramphenicol-resistant isolates (86/98; 87.8%). Isolates (n = 68) that were resistant for sulfamethoxazole were tested for amplification of the sul genes. The sul2 and sul1 genes were present in 39 (57.3%) and 23 (33.8%) isolates, respectively. All ciprofloxacin-resistant APEC isolates were screened for mutations in QRDR of gyrA and ParC by PCR and DNA sequencing. Our sequencing results showed that a total of 56.3% (27/48) of tested isolates possessed S83L mutation in gyrA. Four ciprofloxacin- resistant isolates harbored double mutations of gyrA at residues 83 and 87 (S83L + D87 N). One APEC isolate had a single mutation in parC encoding Ser80Ile. The PMQR were investigated in APEC isolates with no mutations in QRDR to explore further mechanisms of resistance. The qnrA, qnrB, and qnrS genes were found in these isolates (10, 4 and 2 isolates, respectively). None of the isolates were positive for qnrD or aac (6′)-Ib-cr genes. The strA-strB genes encoding streptomycin resistance were examined to investigate streptomycin resistance determinants other than aadA present in the integron cassette and both genes were detected in 34 (58.6%) isolates. The aphA1 and aphA2 gene markers, conferring kanamycin resistance were identified in a total of 65 (81.3%) and 11 (13.7%) isolates, respectively. The combined presence of both gene alleles was found in 4 (5%) isolates. Screening ESβL-producing E. coli isolates by multiplex PCR analysis revealed that 15 isolates were group in CTX-M-1 group. Group 9 enzymes were produced by two isolates. In addition, bla TEM and bla OXA−1 genes were present in 20 (29.4%) and 7 (10.3%) ESβL-producing E. coli isolates, respectively. A total of 24 isolates were observed to simultaneously carry bla TEM and contain alleles encoding group 1 CTX-M enzymes (Table 2).
The emerging antimicrobial resistance among different APEC isolates has stimulated our interest in exploring the mechanisms of resistance and the frequencies of genetic determinants. In this study, the majority of recovered isolates belonged to serogroups O1, O2, O78. A similar observation was reported by other studies supporting the previous postulation that these serotypes are the most common serotypes in E. coli of avian origin worldwide .
Similar to the findings of previous studies [2, 5], most (84–100%) APEC isolates were highly resistant to ampicillin, tetracycline, nalidixic acid, and chloramphenicol. Many (41–69%) APEC isolates were resistant to streptomycin, gentamycin, kanamycin, sulfamethoxazole combined with trimethoprim, ciprofloxacin, and cefotaxime. Most of these antimicrobial agents are regularly used as prophylactic agents or as growth promoters in the poultry industry in Egypt.
In the present study, the proportion of integron carriage among APEC isolates is consistent with previous studies worldwide [10, 27]. In a study conducted in Egypt on APEC isolated from septicemic broilers, higher prevalence was reported for class 1 and 2 (46.6 and 9.6%, respectively) . Our results revealed that the genes found in class 1 and class 2 integrons encode for adenyltransferase conferring resistance to streptomycin and spectinomycin (aadA) and for a dihydrofolate reductase conferring resistance to trimethoprim (dfr). These gene cassettes are the most frequently detectable genes from pathogenic and commensal E. coli from poultry farms and also from different animal, environmental, and human sources [4–6].
Among class 1 integron-harboring isolates, four different trimethoprim resistance genes (dfrA1, dfrA5, dfrA7, dfrA12) and four streptomycin/spectinomycin resistance genes (aadA1, aadA2, aadA5, aadA23) were detected as gene cassettes in class 1 integrons. The aadA23 gene cassette detected in this study was first reported in 2005 in Brazil from Salmonella Agona strains isolated from a pig carcass . In Egypt, this gene cassette was previously described among E. coli strains isolated from neonatal calf diarrhea . To our knowledge, the first description of aadA23 in E. coli of avian origin. All class 2 integron carrying isolates processed the gene cassette array dfrA1-sat2-aadA1 that is considered as the classical gene cassette found in class 2 integron among APEC strains [5, 30]. The absence of class 3 integron among our isolates corroborate previous studies [5, 30], suggesting the less significant role of this integron in dissemination of antimicrobial resistance among APEC.
We further assessed the presence of other genetic determinants located outside the integron that were previously proposed to be responsible for resistance to different antimicrobial agents. Among tetracycline-resistant isolates, tetA and tetB markers were the only tet genes reported in this study either in single or combined genes. These results supported the observation that these efflux genes are the most frequent tet genes found in Enterobacteriaceae . The high prevalence of these variants might be attributed to their higher association with plasmids, mainly the conjugative ones or transposons , suggesting that these genes are the major genes implicated in the efflux mechanism in APEC leading to the resistance phenotype. The high prevalence of cat1 among chloramphenicol-resistant isolates supports previous studies highlighting the crucial role of this allele in chloramphenicol resistance . The combined presence of strA-strB determinants encoding two enzymes required for high level of streptomycin resistance  was assayed in this study as aadA gene observed in the integron has been proposed to confer low level of streptomycin . In this study, the presence of the strA-strB gene pair among streptomycin-resistant was within the range reported among APEC strains isolated in Korea during the period 2000 to 2005 . The high prevalence of aphA1 among kanamycin-resistant isolates is consistent with other studies that proposed aphA1 to be the main neomycin/kanamycin resistance marker [16, 35]. The predominance of bla TEM gene (87.9%) among ampicillin-resistant isolates corroborates a previous study that suggested bla TEM gene to be the most common β-lactamase responsible for ampicillin resistance .
Resistance to quinolone in APEC is mainly mediated by spontaneous mutations in the QRDR of gyrA and parC genes [2, 34]. Nonetheless, in a previous study conducted among APEC isolates in Egypt, these substitutions in QRDR genes were not screened and only PMQR genes were investigated . Our results revealed that among ciprofloxacin-resistant isolates, the mutation in gyrA (S83L) involved in fluoroquinolone resistance was the most prevalent genetic determinant, an observation previously reported in a study conducted among quinolone-resistant APEC isolates in Korea .
One of the most striking findings from this study was the high prevalence of ESβL-producing isolates recovered from broilers (58.6%). This represents a serious public health threats attributed to the ability of these bacteria to hydrolyze third-generation cephalosporins that are commonly used to treat serious infections and the potential transfer and spread of these resistance genes to human through food chain, direct contact, or the environment [36–38]. The higher frequency of CTX-M-1-group in this study supports recent reports that postulated this group to the most predominant CTX-M group among ESβL-producing APEC in Egypt or worldwide [5, 39, 40].
Our results reported high rates of antibiotic resistance among APEC isolates recovered from different poultry farms in Egypt, including those drugs of broad-spectrum-activity such as β-lactams, third generation cephalosporins, and quinolones. Furthermore, our findings suggested diverse genetic makeup involved in antimicrobial resistance phenotype. Indeed, integron-mediated resistance could explain only a part of the resistance profile of the isolates as other independent genes were significantly observed. This diversity in distribution of resistance determinants could be responsible for the high resistance profiles recorded and the potential spread of antimicrobial resistance determinants among APEC. These advices more restriction in antimicrobials use in poultry farms among veterinarians to prevent and control the spread of antimicrobial-resistant bacteria and their genetic determinants. Consequently, our future studies will be directed to study the clonal link and compare the overlapping characteristics of recovered APEC isolates with human ExPEC (extra-intestinal pathogenic E. coli) to confirm the zoonotic potential of APEC, including their potential ability to transfer antimicrobial resistance to human.
avian-pathogenic Escherichia coli
Clinical and Laboratory Standards Institute
eosin methylene blue
extra-intestinal pathogenic E. coli
multiple drug resistance
pulsed-field gel electrophoresis
plasmid-mediated quinolone resistance
quinolone resistance determining region
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ME conceived and designed the study, performed the tests, analyzed and interpreted the data, and wrote the manuscript. AA and NA substantially contributed to collection of samples, isolation of strains and participated in data analysis, and revision of the manuscript. All authors read and approved the final manuscript.
The authors would like to thank Dr. Eman Abo Elfadl at the Department of Animal Husbandry and Development of Animal Wealth, Faculty of Veterinary Medicine, Mansoura University for her technical help during this study. Dr. Mohamed Elhadidy is currently a visiting research fellow at Scientific Institute of Public Health in Brussels funded by Federal Science Policy Office.
The authors declare that they have no competing interests.
The authors declare that they did not have any funding source or grant to support their research work.
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Awad, A., Arafat, N. & Elhadidy, M. Genetic elements associated with antimicrobial resistance among avian pathogenic Escherichia coli . Ann Clin Microbiol Antimicrob 15, 59 (2016). https://doi.org/10.1186/s12941-016-0174-9