- Research article
- Open Access
Distribution and characterization of ampicillin- and tetracycline-resistant Escherichia colifrom feedlot cattle fed subtherapeutic antimicrobials
© Mirzaagha et al; licensee BioMed Central Ltd. 2011
- Received: 16 September 2010
- Accepted: 19 April 2011
- Published: 19 April 2011
Feedlot cattle in North America are routinely fed subtherapeutic levels of antimicrobials to prevent disease and improve the efficiency of growth. This practice has been shown to promote antimicrobial resistance (AMR) in subpopulations of intestinal microflora including Escherichia coli. To date, studies of AMR in feedlot production settings have rarely employed selective isolation, therefore yielding too few AMR isolates to enable characterization of the emergence and nature of AMR in E. coli as an indicator bacterium. E. coli isolates (n = 531) were recovered from 140 cattle that were housed (10 animals/pen) in 14 pens and received no dietary antimicrobials (control - 5 pens, CON), or were intermittently administered subtherapeutic levels of chlortetracycline (5 pens-T), chlortetracycline + sulfamethazine (4 pens-TS), or virginiamycin (5 pens-V) for two separate periods over a 9-month feeding period. Phenotype and genotype of the isolates were determined by susceptibility testing and pulsed field gel electrophoresis and distribution of characterized isolates among housed cattle reported. It was hypothesized that the feeding of subtherapeutic antibiotics would increase the isolation of distinct genotypes of AMR E. coli from cattle.
Overall, patterns of antimicrobial resistance expressed by E. coli isolates did not change among diet groups (CON vs. antibiotic treatments), however; isolates obtained on selective plates (i.e., MA,MT), exhibited multi-resistance to sulfamethoxazole and chloramphenicol more frequently when obtained from TS-fed steers than from other treatments. Antibiograms and PFGE patterns suggested that AMR E. coli were readily transferred among steers within pens. Most MT isolates possessed the tet(B) efflux gene (58.2, 53.5, 40.8, and 50.6% of isolates from CON, T, TS, and V steers, respectively) whereas among the MA (ampicillin-resistant) isolates, the tem1-like determinant was predominant (occurring in 50, 66.7, 80.3, and 100% of isolates from CON, T, TS, and V steers, respectively).
Factors other than, or in addition to subtherapeutic administration of antibiotics influence the establishment and transmission of AMR E. coli among feedlot cattle.
- PFGE Pattern
- PFGE Type
In North America, antimicrobials are often fed to feedlot cattle at subtherapeutic levels for disease prevention and to improve feed efficiency . Although such a practice reduces production costs, it may also promote the development of antimicrobial resistance (AMR) both in pathogenic and in non-pathogenic bacteria . It has been hypothesized that continuous, low-dose administration of antimicrobials increases the risk of AMR development, in comparison with short term, high-dose therapeutic use [3, 4]. Concern also exists that subtherapeutic administration of antimicrobials promotes horizontal gene transfer between commensal and pathogenic bacteria .
In Canada, antimicrobials used for growth enhancement in livestock are approved through the guidelines established by the Food and Drugs Act and Regulations of Health Canada. Examples of antimicrobials presently approved for in-feed administration include tetracyclines, virginiamycin, penicillin, monensin, sulfonamides and tylosin. The potential risk to human health via promotion of AMR is perhaps greatest for those products used to treat both livestock and humans (i.e., tetracyclines and sulfonamides). There is also a concern that veterinary antimicrobials classed in the same antibiotic family as those used in human therapy may promote the development of cross-resistance. For example, the subtherapeutic use in livestock of virginiamycin, a streptogramin, may lead to resistance to Synercid®, an antibiotic of the same family, used as a last resort treatment of vancomycin-resistant Enterococcus faecium in humans .
Several studies (reviewed by ) have investigated the effect of administering subtherapeutic antimicrobials to swine and poultry on antibiotic resistance in commensal and pathogenic gut microflora, but comparatively few have examined the impact of this management practice on AMR in beef cattle [7, 8]. Comparisons of organic and conventional livestock production systems , dairies  and of ground beef originating from conventional vs. "natural" sources  have generally revealed a higher prevalence of AMR in conventional systems. The majority of the studies that have been conducted are of an epidemiological nature and detailed characterization of the limited number of AMR isolates collected has not been undertaken.
Our research team recently conducted a comprehensive study to document the prevalence of AMR Escherichia coli among feedlot cattle being fed various antibiotics at subtherapeutic levels, in two intermittent periods, over the course of their growing and fattening periods . From those data, we concluded that withdrawal of subtherapeutic antibiotics during the feeding period had little impact on the prevalence of tetracycline- or ampicillin-resistant E. coli in the cattle. In this paper, we present a more comprehensive assessment of 531 selected E. coli isolates collected from individual steers on four representative sampling days throughout the feeding period. Through phenotypic and genotypic characterization, the objective of this study was to explore the distribution of AMR E. coli among individual animals fed the different diets within the feedlot environment. It was hypothesized that the subtherapeutic administration of antibiotics would alter the occurrence of AMR E. coli phenotypes among animals.
The E. coli isolates investigated in the present work were a sub-set of those archived during a larger study  in which prevalence of AMR E. coli was assessed over the course of a backgrounding/finishing feeding trial in a research feedlot. Full methodological detail of their isolation has been described previously , and is described briefly below.
Animals, housing and diets
The study was conducted at the Lethbridge Research Centre feedlot (Lethbridge, Alberta, Canada) using crossbred steer calves penned in groups of 10. Cattle were housed in rows of parallel pens with the same antibiotic treatment administered to 5 adjacent pens. Pens were separated by porosity fencing and a pen-specific feed bunk lined the front of each pen. The bunk was of a sufficient length so that all individuals within a pen could feed at the same time. Cattle were retained in the pen throughout the feeding period and there was no need for equipment to enter any of the pens during the feeding period. Adjacent pens within each treatment shared a common water bowl, but the assignment of treatments to pens ensured that water bowls were shared only by steers in the same treatment group. Cattle were processed through a common handling area, but handled in the order of the control group first followed by the virginiamycin group, chlortetracycline group and finally the chlorotetracycline-sulfamethazine group (see below). The area was thoroughly cleaned after each group passed through the handling area. The calves used in the study received no antibiotics prior to or during shipment to the Lethbridge Research Centre feedlot. Furthermore, no subtherapeutic or therapeutic antibiotics were administered prior to this start of this study. Throughout the study, care of the steers was in accordance with guidelines set by the Canadian Council on Animal Care .
The larger trial  from which this study was drawn included six experimental treatments (control plus five different dietary antibiotics), each fed to five pens of 10 cattle with the exception of the Aureo S-700G treatment which only had four replicate pens. Limited resources for detailed characterization of E. coli isolates dictated that we reduce the number of treatments and sampling days examined. As a result, isolates from monesnin and tylosin treatments were not examined. The present analysis includes isolates from only the control group (CON; no antibiotics added to supplement) and three of the five antibiotic treatment groups: 1) chlortetracycline (T), provided as Aureomycin 100-G (Alpharma Inc., Vineland, NJ, USA) fed at 11 ppm; 2) chlortetracycline + sulfamethazine (TS), provided as Aureo S-700G (Alpharma Inc.) fed at 44 ppm; 3) virginiamycin (V), provided as V-Max (Pfizer Animal Health, New York, NY, USA) fed at 31 ppm. The antimicrobial agents were selected based on the commonality of their use in the Canadian feedlot industry and were fed at the concentrations recommended by the manufacturers. Virginiamycin was included in the study because it is not registered for use in Canada and, as a result, neither calves nor their dams would have had prior exposure to this antibiotic.
Fecal samples were obtained by rectal swab of each steer on 11 occasions  throughout the feeding period. This paper presents analysis of isolates collected on 5 of the 11 sampling days. The four samplings (Figure 1) were chosen to represent the five phases in the feeding trial: (i) during their first exposure (while being fed silage-based diet); (ii) during the first period of withdrawal of antibiotics (while being fed silage-based diet); (iii) during the second exposure to antibiotics (while fed grain-based diet); and (iv) following the second withdrawal (while fed grain-based diet). These sample days were designated B, C, D and E, respectively.
Screening for AMR E. coli
On each collection day, fecal swabs were transported to the laboratory in brain heart infusion broth (Becton Dickinson, Sparks, MD, USA) containing 20% glycerol (v/v). Fecal slurry from each steer was plated onto five media (one non-selective and four amended with antibiotics) as described by . Colonies selected from those plates were confirmed as E. coli using biochemical tests and fatty acid methyl ester (FAME) profiles , and isolates from each steer, sampling day and medium of isolation (when available) were selected for archiving. For the present study, isolates cultured on three media were considered: (i) MacConkey agar with no added antibiotics added (as a control, denoted MC); (ii) MacConkey agar amended with 4 μg/ml tetracycline hydrochloride (MT); and (iii) MacConkey agar amended with 50 μg/ml ampicillin (MA). The concentration of tetracycline was set below  standards to ensure isolation of tetracycline-resistant E. coli. Ampicillin concentration exceeded the CLSI standard, but was needed to curtail overgrowth that was interfering with isolation of distinct colonies. From the MC-, MT- and MA-selected colonies, a collection of 6354 isolates was established.
Distribution of isolates characterized in this study
Medium used for selectionb
Number of animals
Antimicrobial susceptibility testing
Using the agar dilution method according to National Clinical and Laboratory Standards Institute (CLSI) guidelines , each isolate was tested for susceptibility to 11 antimicrobials (concentrations, μg/ml): amikacin (AMI; 0.5, 1, 2, 4, 8, 16, 32, 64), ampicillin (AMP; 1, 2, 4, 8, 16, 32), ceftriaxone (AXO; 0.5, 1, 2, 4, 8, 16, 32, 64), cefoxitin (FOX; 0.5, 1, 2, 4, 8, 16, 32), cephalothin (CL; 2, 4, 8, 16, 32), chloramphenicol (CHL; 2, 4, 8, 16, 32), gentamicin (GEN; 0.25, 0.5, 1, 2, 4, 8, 16), nalidixic acid (NAL; 0.5, 1, 2, 4, 8, 16, 32), streptomycin (STR; 32, 64), sulfamethoxazole (SMX; 32, 64, 128, 256, 512), and tetracycline (TE; 1, 2, 4, 8, 16, 32). Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Enterococcus faecalis ATCC 29212 and Staphylococcus aureus ATCC 29213 were included in the panels as controls. Determination of antimicrobial resistance breakpoints for E. coli was in accordance with CLSI guidelines  except for streptomycin, for which a breakpoint of 64 μg/ml was used according to . These data were used to generate a resistance antibiogram (ABG) for each isolate.
Pulsed-field gel electrophoresis
Restriction (XbaI) digested DNA from each isolate was subjected to PFGE according to the PulseNet USA protocol developed for E. coli O157:H7  modified as described previously . PFGE banding patterns were analyzed using BioNumerics software program version 2.5 (Applied-Maths, Ghent, Belgium). DNA fragments on each gel were normalized using the Salmonella enterica serovar Braenderup "Universal Marker" as a molecular weight standard. Fingerprints were clustered into groups using Dice coefficient and evaluated by the unweighted-pair group method. All isolates in a single cluster (≥ 90% homology) were considered to be from a similar source and genetically related, as previously described  and Tenover et al., 1995 F.C. Tenover, R.D. Arbeit, R.V. Goering, P.A. Mickelsen, B.E. Murray, D.H. Persing and B. Swaminathan, Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing, Journal of Clinical Microbiology 33 (1995), pp. 2233-2239. View Record in Scopus | Cited By in Scopus (4225) and were assigned an arbitrary classification letter to enable temporal and phenotypic trends to be evaluated.
Multiplex PCR for tetracycline- and ampicillin-resistant isolates
Primers used in assay of isolates for resistance determinants
PCR primer sequence 5'-3' a
Amplicon size (bp)
Genbank accession no.
Source of plasmid and reference
GCT ACA TCC TGC TTG CCT TC
CAT AGA TCG CCG TGA AGA GG
TTG GTT AGG GGC AAG TTT TG
GTA ATG GGC CAA TAA CAC CG
CTT GAG AGC CTT CAA CCC AG
ATG GTC GTC ATC TAC CTG CC
AAA CCA TTA CGG CAT TCT GC
GAC CGG ATA CAC CAT CCA TC
AAA CCA CAT CCT CCA TAC GC
AAA TAG GCC ACA ACC GTC AG
GCT CGG TGG TAT CTC TGC TC
AGC AAC AGA ATC GGG AAC AC
TCG ATA GGA ACA GCA GTA
CAG CAG ATC CTA CTC CTT
TCG TTA GCG TGC TGT CAT TC
GTA TCC CAC CAA TGT AGC CG
GTG GAC AAA GGT ACA ACG AG
CGG TAA AGT TCG TCA CAC AC
AAC TTA GGC ATT CTG GCT CAC
TCC CAC TGT TCC ATA TCG TCA
CAT AGA CAA GCC GTT GAC C
ATG TTT TTG GAA CGC CAG AG
CTT GGA TTG CGG AAG AAG AG
ATA TGC CCA TTT AAC CAC GC
TTA TAC TTC CTC CGG CAT CG
ATC GGT TCG AGA ATG TCC AC
CAA TAA TTG GTG GTG GAC CC
TTC TTA CCT TGG ACA TCC CG
CGC TTC CCG TTA ACA AGT AC
CTG GTT CAT TTC AGA TAG CG
AGC AGC GCC AGT GCA TCA
ATT CGA CCC CAA GTT TCC
TTG GGT GCA CGA GTG GGT
TAA TTG TTG CCG GGA AGC
For PCR amplifications, bacterial cells from a single colony were collected using a sterile toothpick and resuspended in 25 μl of sterile deionized water. Amplifications were carried out in a Dyad PCR system (Bio-Rad Laboratories, Inc., Mississauga, ON, Canada) as described by . PCR mixture (total 25 μl) included 1 μl of DNA template, 1 × PCR buffer (Invitrogen), 2.5 U Platinum Taq polymerase (Invitrogen) 300 μM of dNTP (Invitrogen) and sterile deionized water. Primers and MgCl2 concentrations for the tetracycline group were optimized as described by ; for the ampicillin group, pse-1 (1.0 μM), oxa1-like (1.0 μM), tem1-like (1.0 μM), and 3.0 mM MgCl2 were used. For the tetracycline group, PCR conditions were: 5 min denaturing at 94°C; 28 cycles of 94°C for 1 min, 59.5°C for 1 min and 72°C for 1.5 min; final extension 5 min at 72°C. For the ampicillin group, denaturing was 5 min at 94°C, then 25 cycles of 94°C for 30 sec, 60°C for 30 sec and 72°C for 40 sec, and final extension 5 min at 72°C. PCR products were analyzed by gel electrophoresis on a 1.5% (w/v) agarose gel in 1× TAE buffer. DNA bands were stained with ethidium bromide and visualized by UV transillumination. Reference E. coli cultures and Salmonella typhimurium control plasmids and genomic DNA (gDNA) possessing tetracycline- and ampicillin-resistance genes (Table 2) were included, as well as a 100-bp DNA ladder (Invitrogen) for assessing size of PCR products.
The GENMOD procedure (SAS Institute Inc. 2008) was used to perform a log-linear analysis separately for each medium to evaluate differences among recovered isolates for antimicrobial resistance phenotypes, treatments and their interaction. P values ≤ 0.05 were interpreted as indicative of a significant difference.
PFGE patterns were either classified as unique or grouped into clusters based on ≥ 90% homology using Dice similarity coefficients using unweighted pair group methods with arithmetic average algorithms built into Bionumerics. The position tolerance and optimization were set at 1% and 0.5% respectively.
Resistance to AMI, FOX, AXO, GEN, or NAL was not observed in any of the 531 E. coli isolates examined (isolated on MC, MT or MA).
Populations selected on Mcplates
Forty-five of 55 isolates (81.8%) from non-selective medium MC were susceptible to all antimicrobials tested. Phenotypes observed in the MC isolates expressing AMR included resistance to SMX (7/10 isolates), STR (5/10), CHL (2/80), TE (2/10) and CL (1/10). Six of the 10 isolates obtained exhibited multi-drug resistance.
Populations selected on MTplates
Total number (n) and percentage of phenotype observed within isolates recovered from MacConkey agar amended with 4 μg/ml tetracycline hydrochloride after diet administration of control and three antimicrobial treatments.
CON % (n)
T % (n)
TS % (n)
V % (n)
Total ( n )
Population selected on MAplates
Total number (n) and percentage of phenotype observed within isolates recovered from MacConkey agar amended with 50 μg/ml ampicillin after diet administration of control and three antimicrobial treatments.
CON % (n)
T % (n)
TS % (n)
V % (n)
Total ( n )
Population selected on MT
The ABG patterns of MT isolates from steers in the CON and V treatments were similar (Figure 2). In both treatments, MT isolates with the STRSMXTE pattern were obtained primarily on sampling day D (in 22 CON isolates, and 12 from group V). In a similar fashion, the STRTE pattern was detected in MT isolates primarily on sampling day E (n = 18 and n = 17 in CON and V, respectively). The STRTE ABG pattern was not found in the CON isolates from pens 1 or 4, but STRTE isolates were recovered from all 5 pens in group V. From the V steers, 10 of 18 MT isolates from pen 2 exhibited the TE pattern. Four MT isolates with pattern AMPSMXTE were obtained from V steers in pen 1, whereas among isolates from CON steers, this pattern was identified only once (steer 48, day C). Antibiogram AMPSTRTE was identified in isolates from 5 CON steers in pen 3 on day C. The SMXTE phenotype was observed more commonly in CON isolates than in those from group V, notably in those collected in pen 1, where 8 of 18 isolates obtained exhibited SMXTE.
The TE phenotype accounted for 17 of 22 isolates collected from steers fed T during the growing phase (silage-based diet; days B and C), compared with only 15 of 52 isolates collected during grain feeding (days D and E). During that period, observation of SMXTE (12/52) and STRSMXTE (17/52) in MT isolates from group T was more frequent than it had been earlier (3 SMXTE and 2 STRSMXTE isolates from group T on days B and C). The SMXTE pattern was recovered mainly from pen 3, whereas MT isolates with pattern STRSMXTE were more widely distributed across pens, particularly on day D.
The ABG patterns of MT isolates from TS steers early in the feeding period (sampling days B and C) differed from isolates collected later (Figure 2). For example, the AMPCHLSMXTE pattern was observed on days B (n = 7) and C (n = 5), but not on days D or E. In contrast, few isolates with the SMXTE pattern were obtained from TS steers on sampling days B (n = 3) and C (n = 4). By sampling day D, however, this ABG was predominant among TS isolates (n = 17) in all pens except pen 1. Also in the TS group, MT isolates with ABG pattern STRTE were obtained more frequently on later (grain-based diet) sampling days (D; n = 4 (all in pen 1) and E; n = 7) as compared to isolates collected earlier, during feeding of silage-based diet (0 and 2 isolates from days B and C, respectively, exhibited STRTE). Isolates exhibiting the STRSMXTE antibiogram were widely distributed among MT isolates, as were those with the TE phenotype.
Population selected on MA
Two ABG types (AMPCL and AMPSTRTE) were observed in MA isolates collected from CON steers, and these tended to cluster with sampling day and pen of origin (Figure 2). On day C, AMPSTRTE was predominant, observed in 6 of 8 isolates expressing AMR, all in pen 3. On this sampling day, the two AMR isolates from pen 4 had AMPCL phenotype. On day E, AMPSTRTE isolates were also recovered from adjacent pens 2 and 4, but AMPCL pattern was predominant, both in pen 2 (4 of 5 AMR isolates) and particularly in pen 5 (10 of 10).
From steers in group T, MA E. coli isolates were relatively uncommon, with the majority (10/13) occurring only on day E (Figure 2). In this group, ABG patterns were distinctly associated with specific pens. Phenotypes AMPSTRTE, AMPCHLSMXTE, and AMPTE (each n = 3) were exclusive to pens 1, 2 and 3, respectively.
More MA isolates were associated with steers in group TS than with CON, T or V (Table 1; Figure 2), and the TS isolates were more routinely recovered across all sampling days, whereas in the other groups, isolation was more frequent later in the feeding period (days D, E) compared with the growing phase (days B, C). As with the CON isolates, sampling time and pen of origin influenced the likelihood with which MA isolates with a specific ABG were observed. The AMPCHLSMXTE phenotype was most common (23 of 51 isolates) in the TS group. It was observed primarily on the earlier sampling days (19/23 on days B and C), and exclusively in pens 2, 4 and 5 on day B. Late in the feeding period (grain-based diet; day E), phenotype AMPTE was prevalent (in 11 of 15 isolates from that day, clustered mainly in pens 3 and 5).
The ABG patterns characterized from the MA isolates from V steers was also dependent on the sampling time as well as the pen (Figure 3). For example, with the exception of steer 117 in treatment T, sampling B, MA isolates with ABG pattern AMP were obtained exclusively during sampling E from five V steers in pen 5 (Figure 3). Similarly, MA isolates with ABG pattern AMPCHL were isolated exclusively at sampling E from two V steers housed in pen 1, and 8 isolates with ABG pattern AMPSTRTE were isolated at sampling E from steers in adjacent pens 1 and 2. Finally from the V group, MA isolates with ABG pattern AMPSMXTE were obtained only from pen 1 during sampling B, C and D.
A large number of PFGE genotypes were detected from throughout the feedlot, in all treatments. Many of these genotypes were isolated only transiently during the feeding period. The MT-selected isolates in groups CON, T, TS and V presented 46, 37 35 and 34 PFGE genotypes. Among the MA isolates from CON, T, TS, V samples, 8, 7, 7, and 11 PFGE genotypes, respectively, were identified.
Population selected on MT
Unlike the MA isolates, many of the MT isolates with the same ABG exhibited two or more different PFGE profiles (Figure 2). For example, from CON, the TE isolates exhibited 19 different PFGE banding patterns, with two predominant patterns that were associated with pens 1 and 4. Isolates with ABG patterns STRSMXTE and STRTE obtained from CON steers also frequently exhibited different PFGE types. Of note, although the PFGE genotypes of STRSMXTE isolates in pens 3 and 4 clearly differed between pens, within pen, the majority of these isolates (9/11 in pen 3 and 6/7 in pen 4) were clones. All of the AMPSTRTE isolates from CON steers, with the exception of one isolate from pen 2, were associated with pen 3 and possessed indistinguishable PFGE patterns. Clonal isolates with the STRTE phenotype were also obtained from CON steers in pens 2, 3 and 5 during later samplings, but STRTE E. coli exhibiting different PFGE profiles were also present in pen 2 and pen 3.
In group T, MT isolates with the TE phenotype exhibited 16 different PFGE profiles (Figure 2), though within a pen, these isolates often exhibited the same PFGE profile (e.g., 7 of 12 TE isolates in pen 2 were indistinguishable, as were 4 of 7 in pen 4). The isolates with SMXTE phenotype also clustered by pen: 6 of 8 in pen 3 were indistinguishable, as were all three SMXTE isolates from pen 4. Throughout the feeding period, the TE isolates from diet group T tended to exhibit three predominant PFGE types. As the frequency of isolation of STRSMXTE isolates increased in the finishing feeding period, so too did the diversity of their PFGE types. The two isolates from days B and C (growing period) were indistinguishable, whereas 10 PFGE patterns were identified among the 17 STRSMXTE isolates from days D and E (finishing period).
In the TS group, the SMXTE ABG occurred frequently in all pens except pen 1 and was represented by 10 different PFGE profiles across pens (Figure 2) and all 10 were recovered on day D. Overall, the SMXTE isolates exhibited three main PFGE profiles. Similarly, the TS isolates with STRSMXTE phenotype were associated with 11 PFGE types, with diversity evident particularly in pen 1. A PFGE profile (J) that was also identified in TE isolates from diet group T, was the predominant PFGE type among the TE isolates from diet group TS, identified in 14 of the 25 isolates with that phenotype. These indistinguishable isolates were associated primarily with pens 2 and 5, and were not recovered from pen 3. The STRTE isolates from pens 1 and 3 (and the sole STRTE isolate in pen 2) were indistinguishable, whereas this phenotype was not observed in pen 5, and the four STRTE isolates in pen 4 exhibited different PFGE profiles. All 12 MT isolates with AMPCHLSMXTE phenotype, clustered in pens 2, 4 and 5, exhibited indistinguishable PFGE profiles.
Population selected on MA
Among the MA isolates, most that exhibited a given ABG pattern also presented indistinguishable PFGE profiles (Figure 3). In the CON group, 14 of the 16 AMPCL isolates, collected from pens 2 and 5, had indistinguishable PFGE profiles. Similarly, 6 of the 10 AMPSTRTE MA isolates from CON cattle were clones and associated only with pen 3.
As with the AMPCHLSMXTE isolates from MT, the MA isolates displaying this phenotype were all found to possess indistinguishable PFGE profiles, and were obtained primarily from steers on the TS treatment (Figure 3). Steer 99 (pen 5) was the only animal from which the same AMR clone was recovered on all four sampling days. The AMPTE isolates from group TS exhibited two distinct PFGE profiles - a predominant type recovered in pens 3, 4 and 5, and the second type from pen 1 with the exception of one isolate in pen 5. The phenotype AMPSTRTE was associated with only a single PFGE profile, and only in pens 3 and 4 on day C.
The PFGE profiles of AMPSTRTE and AMPCHLSMXTE isolates recovered from group T steers on day E were indistinguishable from those determined in the TS group, but the AMPTE isolates (3 clones in pen 3) exhibited a distinct PFGE to that of the AMPTE isolates from TS.
Similarly, associations of single PFGE profiles with specific ABG patterns were found among most of the MA isolates from diet group V, and mainly on day E. All of the AMP isolates obtained from steers in pen 5 were clones, as were 4 of the 5 AMPSTRTE isolates from pen 2, and 3 of 3 in pen 1. All five AMPSMXTE isolates from pen 1 (across three sampling days) exhibited indistinguishable PFGE profiles.
Tetracycline genes only from Group I [tet (B), tet (C), tet (D)] and Group II [tet (A), tet (E), tet (G)] were identified, with no genes from Group III [tet (K), tet (L), tet (M), tet (O), tet (S)] or Group IV [tet A (P), tet (Q), tet (X)] being detected in any of the isolates examined. The tet(B) gene was the most commonly observed of the tetracycline resistance determinants, present in 58.2%, 53.5%, 40.8% and 50.6% of MT isolates from CON, T, TS, and V steers, respectively. The tet(A) determinant was detected in 22.5%, 51.4% and 26.0% of the isolates from T, TS and V, respectively, but was present in only 12.2% of the isolates from CON. Determinant tet(C) was also present at low frequencies, detected in 7.1, 12.7, 2.1 and 13.0% of MT isolates from groups CON, T, TS and V, respectively. A small proportion of the isolates examined, 20.4, 5.6 and 2.6% from CON, T and V, respectively, did not possess any of the tetracycline determinants screened for. Few isolates possessed multiple tetracycline resistance determinants. The tet(A) and tet(B) genes were present together in only 0.7% of the isolates from the TS group, and 0.8% of the isolates from CON. Combinations of tet(B) and tet(C) were detected in 2.0, 5.6, 4.9 and 6.5% of the MT isolates from CON, T, TS and V. The tet(A) and tet (C) were detected in combination in only 1.3% of MT isolates from steers in group V.
Ampicillin-resistant isolates from all treatment groups were subjected to multiplex PCR to ascertain the presence of blaPSE-1, blaOXA1 and blaTEM-1 determinants. The blaTEM-1 determinant was present in 50.0, 66.7, 80.3 and 100% of MA isolates from the CON, T, TS and V groups, respectively. The other ampicillin resistance determinants that were screened were not detected in 54.4% of the other MA isolates.
Chlortetracycline alone and combined administration of chlortetracycline and sulfamethazine were selected as experimental treatments on the basis of their routine use in the Canadian feedlot industry. These antimicrobials are used to improve feed efficiency and prevent foot rot, liver abscesses and respiratory disease. Virginiamycin was included in the study as an antibiotic to which neither the steers nor their dams would have had prior exposure, given that it is not registered for use in cattle in Canada.
Resistance to amikacin, ceftriaxone (64 μg/ml), cefoxitin or nalidixic acid was not detected in any of the 531 E. coli isolates examined. Other researchers of E. coli from Canadian beef cattle have also reported the absence of resistance to these antibiotics  or, when resistance to nalidixic acid was found, it occurred in fewer than 2% of isolates studied . In the present study, the absence of resistance to these antibiotics in gut flora may be related to sole-source acquisition of the calves, and to the complete absence of antibiotic use prior to their arrival at the feedlot. Furthermore, our research feedlot had been constructed just prior to commencement of this experiment, thus there was no history of prior administration of subtherapeutic antibiotics at this site. Our results and those of others [30, 31] contrast with those of Hoyle et al. , who reported that all calves from a Scottish beef farm were found to shed nalidixic acid-resistant E. coli at least once during a 21-wk study.
Comparisons of AMR E. coli from steers in CON vs. T, TS and V groups suggests that subtherapeutic administration of these antimicrobials had only a limited impact on the nature of antimicrobial resistance in E. coli resident in these cattle. The resistances observed most commonly among these E. coli isolates were to tetracycline, sulfamethoxazole, ampicillin, chloramphenicol and streptomycin, which is consistent with the findings of other Canadian beef researchers [30, 31, 33].
In general, the antibiogram type and temporal point of isolation were more similar between isolates from CON and V groups than from those in T or TS. Virginiamycin, a streptogramin, that primarily targets Gram-positive bacteria , and appears to have had minimal influence on the nature of AMR in the non-target E. coli isolates obtained in this study. Similarly, dietary inclusion of monensin, another antibiotic that targets Gram-positive bacteria, also did not alter the nature of AMR E. coli isolated from beef cattle . These results suggest that antimicrobial suppression of Gram-positive bacteria does not give rise to unoccupied microbial niches that are filled via AMR E. coli.
Despite the fact that the E. coli characterized in this study were recovered from selective media, the fact that antibiotic resistance, particularly to tetracycline, streptomycin, sulfamethoxazole and ampicllin, was common in E. coli from cattle that were not administered tetracycline suggests that naturally occurring resistance determinants circulate in bovine gut microbial populations for reasons other than selection as a result of antimicrobial agents being included in the diet. Hoyle et al.  characterized bovine fecal E. coli from an organic farm and found that even with the restricted use of antimicrobials, ampicillin-resistant E. coli were readily isolated. In that study, age of the cattle and likely the diet they were provided, as opposed to subtherapeutic administration of antibiotics appeared to be an important factor for the acquisition and development of antibiotic-resistant commensal microflora. A higher prevalence of AMR E. coli in feces from younger than older animals within the same farm has been previously reported [37, 38]. A comprehensive longitudinal study of four feedlots in which antibiotics were only used therapeutically also found no difference in the nature of AMR among isolates collected from home pens compared with those from hospital pens in which antibiotics were administered . Our work as well as that of others has also observed that the presence and dissemination of AMR in E. coli during the feeding period may be a response to the diet rather than antimicrobial administration [12, 18, 40]. In the present study, short-term withdrawal of antibiotics appeared to have minimal impact on AMR in E. coli, given that AMR isolates were collected routinely on days C and E. Perhaps this is not surprising when one considers that even long term withdrawal of antimicrobials has in some cases had minimal impact on the nature of antimicrobial resistance . In the case of genetic determinants for tetracycline resistance, it has been proposed that these elements have established a steady state in E. coli populations, and that their presence is not necessarily related to antimicrobial usage .
Perhaps the most obvious impact of antimicrobial administration on the phenotype and genotype of E. coli was observed for isolates obtained from TS fed cattle, a response that may reflect the fact that two antimicrobials were administered to these animals. The MT isolates from the TS group exhibited a higher frequency of SMX resistance and as both sulfamethazine and sulfamethoxazole (SMX) are sulfonamides, this may reflect selection for strains resistant to SMX. Sharma et al.  recently reported similarities in the numbers of ampicillin-resistant and tetracycline-resistant isolates, as well as the types of resistance phenotypes observed, in E. coli collected from cattle fed chlortetracycline (44 ppm) alone or in combination with sulfamethazine at the same concentration. These results suggest that the administration of chlortetracycline, even in the absence of sulfamethazine, can lead to the emergence of resistance to SMX, as well as other antibiotics, including AMP and CHL.
E. coli exhibiting STRSMXTE and SMXTE resistance phenotypes have been frequently isolated from cattle . Enne et al.  documented that the prevalence of sulfonamide resistance among E. coli remained constant even with a 97% reduction in the clinical use of sulfonamides in the UK. Further work showed that a plasmid carrying the resistance determinants sul2, strA and strB enhanced host fitness even in the absence of antibiotic selective pressure . Linkages between CHL and TE phenotypes, sulphonamide resistance, and other resistance determinants have been described in plasmid profiling of human clinical isolates in Australia , but at this point it remains to be determined if similar linkages are responsible for the linked dissemination of these resistances in feedlot cattle. It is also possible that genes that confer fitness to environmental challenges (e.g., acid tolerance, nutrient limitations, metal concentration) other than those imposed by antibiotics are harboured on these plasmids and promote the acquisition of resistance determinants .
Detection of specific AMR E. coli frequently appeared to be transient over the duration of this study. Only in one steer (ID 99; group TS) was the same AMPCHLSMXTE E. coli clone obtained on all 4 sampling days. Others have also reported that the majority of E. coli O157:H7 subtypes occur intermittently within cattle and that few isolates persist for extended periods of time . Although isolates occurred transiently, there were instances where a particular isolate clearly occurred more frequently during specific phases of the feeding period. For example, E. coli isolates exhibiting STRTE phenotype were recovered almost exclusively on days D and E, particularly from CON, TS and V steers, and the majority of isolates were clones. This suggests that this particular isolate disseminated readily among pen mates within the feedlot or that this particular clone may have possessed fitness attributes that promoted its prevalence at these points during the feeding period.
In some instances, the occurrence of clones was clearly pen-associated. Some MT-isolated E. coli clones with specific PFGE profiles occurred exclusively or nearly exclusively within a single pen (e.g., STRSMXTE with PFGE type X in pen V-1). This same phenomenon was also observed for E. coli isolates with ampicillin resistance, i.e., cultured on MA (e.g., AMP with PFGE type F, pen V-5). The association of isolates with specific pens was not solely related to the administration of antibiotics, given that some pen associations were evident in the CON group as well (AMPSTRTE with PFGE type YY in pen CON-3; STRSMXTE with PFGE type W in pen CON-4). These findings suggest that the degree of transference of AMR E. coli in the feedlot depends on the subtype in question. A previous study in or laboratory used genotyping to document movement of E. coli strains from animal to animal within the feedlot environment . Others have reported that housing location can influence the nature of antimicrobial resistance in fecal coliforms from swine , but in that study, the pigs were housed in different barns as opposed to different pens within a common building. We determined previously that a rifampin-resistant strain of E. coli was transferred infrequently among feedlot cattle housed in adjacent pens even when it was inoculated (1010 CFU) into Trojan steers . In the present study, there was possible evidence of transmission of ampicllin-resistant E. coli among adjacent pens as identical AMPTE subtypes were recovered from TS steers in pens 3, 4, and 5 sampled on day E. Similarly, identical AMPSTRTE subtypes were obtained from V steers in adjacent pens 1 and 2 during this same sampling period. Our results suggest that the pen boundaries act as a significant impediment to the widespread dissemination of some AMR E. coli subtypes within the feedlot. At this point it is not known if a similar phenomenon would be observed in all feedlots as our feedlot only represented a single ecological unit.
Resource constraints limited our characterizations to only single isolate from each selective plate from each steer during later samplings. It further restricted our ability to study isolates from all steers on all treatments It is possible that this approach may not have given a complete picture of the genetic diversity of tetracycline- and ampicillin-resistant E. coli present in feedlot steers. Ensuring representative sampling is always a challenge considering the voluminous nature of digesta within the bovine intestinal tract and the number of cattle that are typically housed within a feedlot. Others have reported that examining single vs multiple isolates did not compromise interpretation of the temporal trends or the nature of diversity of E. coli within cohorts [50, 51]. In early samples, where we did select two isolates, PFGE frequently identified both isolates as clones. That finding is perhaps not surprising, given the frequency with which we isolated clones from individual pen mates. This pattern may have been amplified by the use of selective plates for establishing the isolate collections, a practice that obviously selects for less diverse subpopulations. In the present study, the degree of diversity was clearly related to the nature of the resistant phenotype. Some phenotypes such as TE, SMXTE and STRSMXTE exhibited a high degree of diversity whereas others, such as AMPCHLSMXTE were solely of a clonal nature suggesting the resistance genes may be chromosomally encoded while others may be plasmid mediated both of which could contribute to the varying degrees of diversity among isolates examined.
Screening for resistance determinants showed that the majority of tetracycline-resistant isolates harboured the tet(B) efflux gene, followed less frequently by tet(A) and tet(C). These findings are consistent with those of Walk et al.  who reported that 64.8%, 28.1 and 4.6 of tetracycline-resistant isolates from conventional and organic dairies possessed tet(B), tet(A) and tet(C) determinants. The prevalence of tet efflux genes in E. coli is likely related to their occurrence on mobile conjugative plasmids and transposons, although tet(B) has recently been reported also to integrate into chromosomal DNA . Tet(B) has been reported in a variety of other Gram-negative bacteria, including Enterobacter, Proteus, Salmonella, Actinobacillus, Haemophilus, Morazella and Treponema spp. This distribution is thought to reflect frequent gene transfer . In the present study, isolates from MT were screened for other efflux, ribosomal protection, and tetracycline catabolism determinants that included tet(K), tet(L), tet(M), tet(O), tet(S), tetA(P), tet(Q), and tet(X). This group of tet genes are normally present on mobile conjugative plasmids or chromosomally located in Gram-positive bacteria , but there has been reports of their transfer to phylogenetically distant bacteria, as tet(K) and tet(L) have been reported in Gram-negative bacteria . Our screening failed to detect these genes, and to our knowledge, there have been no reports of these determinants occurring in E. coli.
During screening of the ampicillin-resistant isolates for three β-lactamase genes the blaTEM1 determinant was detected in 50 to 100% of isolates from the four treatment groups. Amplicons for blaOXA1 or blaPSE1 were not produced in any of the remaining MA isolates. Other research teams have also failed to detect blaOXA1, blaSHV and blaPSE1 in ampicillin-resistant E. coli isolates recovered from cattle [20, 22]. We are presently in the process of screening for additional β-lactamase determinants in ampicillin-resistant E. coli isolates that were not equated with blaTEM1. A close association of blaTEM1 with class I integrons has been reported, which likely accounts for the wide dissemination of this determinant among Gram-negative bacteria . Others in Denmark and Spain also found blaTEM1 to be the most common determinant observed in ampicillin-resistant E. coli of animal origin, with blaOXA1 detected only occasionally [53, 54].
AMR bacteria are clearly able to persist in the bovine gut in the absence of antimicrobial selection pressure, evidenced by ready isolation of tetracycline- and ampicllin-resistant E. coli from steers that were not fed antibiotics. This study and previous reports suggest that the occurrence of AMR in commensal E. coli harboured by calves is complex, and dependent on multiple factors. Sampling time seemed to affect the presence of certain isolates, which is likely reflecting the transient nature of shedding of specific strains of E. coli by cattle. In addition, commonality was higher among isolates obtained from cattle within a pen than between pens, suggesting that animal-to-animal contact plays an important role in the dissemination of AMR bacteria within the feedlot. Feeding a mixture of subtherapeutic antibiotics, in this case tetracycline and sulfamethazine seemed to have a more pronounced impact on the occurrence and persistence of antimicrobial resistance than feeding a single or no antibiotics to cattle. Resistance to SMX and CHL was increased in isolates from the treatment group receiving chlortetracycline and sulfamethazine, which may have arisen from the inclusion of this sulfonamide in the diet. This treatment also appeared to be associated with increased isolation of ampicillin-resistant E. coli. Our findings suggest that a more comprehensive understanding of the development and emergence of AMR in feedlots requires that other factors in addition to administration of antimicrobials be taken into consideration.
This study was conducted with funding from the GAPS program of Agriculture and Agri-Food Canada and the Canada Alberta Beef Industry Development Fund. Steers were provided by the Canada/Alberta Livestock Research Trust. Thanks are extended to Dr. Linda Chui, Provincial Laboratory for Public Health, Edmonton, AB, for provision of Salmonella enterica serovar Braenderup "Universal Marker" for use as a molecular weight standard. The authors also thank Brant Baker, Hilma Busz, Zdenka Matic, Wendi Smart and Fred Van Herk for their technical assistance, and the staff of the Lethbridge Research Centre feedlot for their conscientious care of the cattle. Editorial assistance by Katherine Jakober and Krysty Munns is also gratefully appreciated.
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