Volume 18, Number 5—May 2012
Antimicrobial Drug Resistance in Escherichia coli from Humans and Food Animals, United States, 1950–2002
Highlight and copy the desired format.
|EID||Tadesse DA, Zhao S, Tong E, Ayers S, Singh A, Bartholomew MJ, et al. Antimicrobial Drug Resistance in Escherichia coli from Humans and Food Animals, United States, 1950–2002. Emerg Infect Dis. 2012;18(5):741-749. https://dx.doi.org/10.3201/eid1805.111153|
|AMA||Tadesse DA, Zhao S, Tong E, et al. Antimicrobial Drug Resistance in Escherichia coli from Humans and Food Animals, United States, 1950–2002. Emerging Infectious Diseases. 2012;18(5):741-749. doi:10.3201/eid1805.111153.|
|APA||Tadesse, D. A., Zhao, S., Tong, E., Ayers, S., Singh, A., Bartholomew, M. J....McDermott, P. F. (2012). Antimicrobial Drug Resistance in Escherichia coli from Humans and Food Animals, United States, 1950–2002. Emerging Infectious Diseases, 18(5), 741-749. https://dx.doi.org/10.3201/eid1805.111153.|
We conducted a retrospective study of Escherichia coli isolates recovered from human and food animal samples during 1950–2002 to assess historical changes in antimicrobial drug resistance. A total of 1,729 E. coli isolates (983 from humans, 323 from cattle, 138 from chickens, and 285 from pigs) were tested for susceptibility to 15 antimicrobial drugs. A significant upward trend in resistance was observed for ampicillin (p<0.001), sulfonamide (p<0.001), and tetracycline (p<0.001). Animal strains showed increased resistance to 11/15 antimicrobial agents, including ampicillin (p<0.001), sulfonamide (p<0.01), and gentamicin (p<0.001). Multidrug resistance (≥3 antimicrobial drug classes) in E. coli increased from 7.2% during the 1950s to 63.6% during the 2000s. The most frequent co-resistant phenotype observed was to tetracycline and streptomycin (29.7%), followed by tetracycline and sulfonamide (29.0%). These data describe the evolution of resistance after introduction of new antimicrobial agents into clinical medicine and help explain the range of resistance in modern E. coli isolates.
Antimicrobial drugs have played an indispensable role in decreasing illness and death associated with infectious diseases in animals and humans. However, selective pressure exerted by antimicrobial drug use also has been the major driving force behind the emergence and spread of drug-resistance traits among pathogenic and commensal bacteria (1). In addition, resistance has developed after advent of every major class of antimicrobial drugs, varying in time from as short as 1 year (penicillin) to >10 years (vancomycin) (2,3).
Escherichia coli is usually a commensal bacterium of humans and animals. Pathogenic variants cause intestinal and extraintestinal infections, including gastroenteritis, urinary tract infection, meningitis, peritonitis, and septicemia (4,5). Therapeutic options vary depending on the type of infection. For example, for urinary tract infections, trimethoprim/sulfamethoxazole and fluoroquinolones are treatments of choice (6), whereas for Shiga toxin–producing E. coli infections, antimicrobial drug therapy is not recommended (7). E. coli is sometimes used as a sentinel for monitoring antimicrobial drug resistance in fecal bacteria because it is found more frequently in a wide range of hosts, acquires resistance easily (8), and is a reliable indicator of resistance in salmonellae (9).
Surveillance data show that resistance in E. coli is consistently highest for antimicrobial agents that have been in use the longest time in human and veterinary medicine (10). The past 2 decades have witnessed major increases in emergence and spread of multidrug-resistant bacteria and increasing resistance to newer compounds, such as fluoroquinolones and certain cephalosporins (3). For example, a study of the susceptibility of E. coli isolates recovered from hospitals during a 12-year period (1971–1982) showed no major change in resistance to any of the antimicrobial drugs tested (11). In contrast, a retrospective analysis of E. coli from urine specimens collected from patients during 1997–2007 showed an increasing resistance trend for ciprofloxacin, trimethoprim/sulfamethoxazole, and amoxicillin/clavulanic acid (12). Similarly a 30-year (1979–2009) follow-up study on E. coli in Sweden showed an increasing resistance trend for ampicillin, sulfonamide, trimethoprim, and gentamicin (13). Although studies of farms have shown an association of multidrug-resistant E. coli with chronic antimicrobial drug exposure (14,15), there are few data on temporal trends of antimicrobial drug resistance in food animal E. coli isolates, particularly those recovered before 1980. Recent data are available in several countries that established resistance monitoring programs during the mid-1990s.
In the United States, the National Antimicrobial Resistance Monitoring System (NARMS) was established in 1996 to prospectively monitor changes in antimicrobial drug susceptibilities of zoonotic foodborne bacteria, including E. coli from retail meats (chicken breast, pork chops, ground beef, ground turkey), and chickens at slaughter. During 2000–2008, NARMS laboratories tested 13,521 E. coli isolates from chickens to determine the MIC to antimicrobial drugs essential in human and veterinary medicine. The resistance trend in chickens observed during this period varied on the basis of the antimicrobial agents. For example, resistance during 2000–2008 decreased slightly for kanamycin (16.1% to 10.2%), streptomycin (77.5% to 54.6%), trimethoprim/sulfamethoxazole (17.2% to 9.1%), and tetracycline (68.4% to 47.4%). Cefoxitin resistance increased from 7.4% in 2000 to 15% in 2006, and ceftriaxone resistance increased from 6.3% to 13.5%. Ciprofloxacin resistance remained low (<1%) during this period.
To better understand the historical emergence of resistance since the advent of the antimicrobial drug age, which led to baseline data in the first year of NARMS testing, we assayed E. coli collections from human and animal sources obtained during 1950–2002 for antimicrobial drug susceptibility. This information, when coupled with secular surveillance data, will provide a broader picture of evolution of resistance and lay the groundwork for understanding genetic mechanisms of resistance development and dissemination.
A total of 1,729 E. coli isolates from human and animal samples obtained from different US states were used in this study. Isolates were obtained by the American Type Culture Collection (ATCC) (Manassas, VA, USA) from the E. coli Reference Center (ECRC) at Pennsylvania State University (University Park, PA, USA) and the Centers for Disease Control and Prevention (CDC) (Atlanta, GA, USA) under contract with the US Food and Drug Administration Center for Veterinary Medicine (Rockville, MD, USA). These isolates were recovered from human and animal specimens (e.g., feces, blood, kidney, lymph nodes, urine, cerebrospinal fluid, peritoneal fluid, pleural fluid) submitted to ECRC and CDC from state public health and veterinary diagnostic laboratories. For human isolates obtained from CDC, most acquired during 1948 through the late 1980s were maintained on trypticase soy agar stabs sealed with paraffin and stored at room temperature. Starting in the late 1980s, strains were frozen in trypticase soy broth containing 30% glycerol at −70°C. Similarly, isolates were stored, according to the ECRC standard protocol at −70°C to −80°C in trypticase soy broth containing 30% glycerol until further processing.
Of 1,729 E. coli isolates, 983 (56.8%) were recovered from humans during 1950–2001, and the remaining 746 (43.2%) were recovered from animals during 1962–2002. Three hundred twenty-three (43.2%) E. coli isolates of animal origin were from cattle, 138 (18.5%) from chickens, and 285 (38.2%) from pigs. Fifty percent were from 10 states: Pennsylvania (183, 11.2%), California (100, 5.8%), Ohio (90, 5.2%), Maryland (83, 4.8%), Minnesota (82, 4.7%), Illinois (72, 4.2%), Texas (72, 4.2%), New York (70, 4.1%), North Carolina (61, 3.5%), and Virginia (58, 3.4%). Distribution of isolates by source and year are shown in Table 1.
Antimicrobial Drug Susceptibility Testing
Each isolate was streaked on trypticase soy agar supplemented with 5% defibrinated sheep blood (Becton Dickinson, Sparks, MD, USA) before antimicrobial drug susceptibility testing. MICs were determined by using the Sensititer automated antimicrobial susceptibility system (Trek Diagnostic Systems, Cleveland, OH, USA) according to the manufacturer’s instructions. Results were interpreted according to National Committee for Clinical and Laboratory Standards criteria (16) where available (Table 2). Antimicrobial drugs tested were ampicillin, amoxicillin/clavulanic acid, cefoxitin, ceftiofur, cephalothin, ceftriaxone, ciprofloxacin, nalidixic acid, streptomycin, gentamicin, kanamycin, chloramphenicol, tetracycline, sulfonamide, and trimethoprim/sulfamethoxazole. E. coli ATCC 25922 and ATCC 35218, Enterococcus faecalis ATCC 29212, Staphylococcus aureus ATCC 29213, and Pseudomonas aeruginosa ATCC 27853 were used as quality control organisms in MIC determinations. Multidrug resistance was defined as resistance to >3 classes of antimicrobial drugs.
The Mann-Kendall test, a nonparametric statistical test, was performed to detect a monotone increasing or decreasing resistance trend over time. Magnitude of annual change was estimated by using a slope parameter, Q, and the Sen nonparametric method (20). Calculations were performed by using the Excel (Microsoft, Redmond, WA, USA) template Mann-Kendall test for trend and Sen slope estimates (21). For time series <10 annual percentage resistance values, significance of the trend was determined from the exact distribution of the S test statistic, and a normal approximation (z statistic) was used when there were >10 values. Significance was assessed at 4 levels (α = 0.001, 0.01, 0.05, and 0.1); p values <0.05 were considered significant. Comparisons of drug resistance profiles between different sources (human, cattle, chicken, and pigs) were conducted by using the χ2 test; p values <0.05 was considered significant.
Antimicrobial Drug Susceptibility
Overall, 934 (54.0%) of 1,729 E. coli were resistant to >1 antimicrobial drug. As expected, the most common resistance phenotypes were to older drugs such as tetracycline (40.9%) (introduced in 1948), sulfonamide (36.2%) (introduced in 1936), streptomycin (34.2%) (introduced in 1943), and ampicillin (24.1%) (introduced in 1961). A much smaller number of isolates were resistant to antimicrobial drugs introduced for clinical use since 1980, such as amoxicillin/clavulanic acid (5.6%) (introduced in 1984), ceftriaxone (2.4%) (introduced in 1984), ceftiofur (2.3%) (introduced in 1988), and ciprofloxacin (0.4%) (introduced in 1987) (Table 2).
When analyzed by source, E. coli isolates of animal origin were more resistant than those of human origin. Among 983 human isolates, resistance was observed most often to sulfonamide (19.9%), followed by tetracycline (18%) and ampicillin (16.5%). No human E. coli isolates showed resistance to ciprofloxacin, and 1 isolate (0.1%) from 1997 showed resistance to ceftiofur, ceftriaxone, and gentamicin. Of 746 isolates recovered from animal sources, 531 (71.1%) were resistant to tetracycline, 441 (59%) to streptomycin, 431 (57.7%) to sulfonamide, 277 (37.1%) to kanamycin, and 255 (34.1%) to ampicillin. Among animal E. coli isolates, the rate of resistance was significantly higher in cattle isolates than in pig isolates for chloramphenicol (p = 0.039), amoxicillin/clavulanic acid (p = 0.03), sulfonamide (p = 0.038), and trimethoprim/sulfamethoxazole (p = 0.022). There was a significant difference in resistance rate between cattle and chicken isolates to ceftiofur (p = 0.008), ceftriaxone (p = 0.008), chloramphenicol (p = 0.011), and kanamycin (p = 0.037) (Table 2).
Antimicrobial drug resistance was observed for drugs tested at different frequencies (Table 2). Seven hundred ninety-six (46%) E. coli isolates analyzed were susceptible to all 15 drugs tested. Among these pan-susceptible isolates, 637 (80%) were from humans, 69 (8.7%) from cattle, 60 (7.5%) from pigs, and 29 (3.6%) from chickens. Approximately 65% of human isolates were pan susceptible, compared with ≈20% of cattle, chicken, and pig isolates (Table 3). The proportion of pan-susceptible E. coli isolates decreased from 73.9% in 1950–1959 to 18.5% in 2000–2002. Conversely, multidrug resistance increased from 7.2% in 1950–1959 to 63.6% in 2000–2002 (Figure 1). Five hundred seventy (32.9%) E. coli isolates showed multidrug-resistant phenotypes, and 176 (10.2%) showed resistance to >5 drug classes. A larger proportion of multidrug-resistant isolates was recovered from animals than humans (Figure 2). One hundred ninety-one (59.1%) isolates from cattle, 153 (53.7%) from pigs, and 76 (55.1%) from chickens were resistant to >3 drug classes (Table 3), compared with 15.3% from humans. Two strains showed resistance to all 15 drugs tested; both strains were recovered from cattle in 2001.
Concurrent resistance to tetracycline and streptomycin was the most common co-resistance phenotype (29.7%), followed by resistance to tetracycline and sulfonamide (29.0%); tetracycline, sulfonamide, and streptomycin (23.9%); tetracycline and ampicillin (18.8%); and tetracycline, ampicillin, streptomycin, and sulfonamide (12.9%). A total of 130 (92.9%) of 140 chloramphenicol-resistant E. coli isolates were also resistant to tetracycline. Resistance to ceftriaxone, ceftiofur, and ciprofloxacin was rare and found only in isolates resistant to ≥7 drugs. More than 80% of these isolates were resistant to ampicillin, amoxicillin/clavulanic acid, cephalothin, cefoxitin, streptomycin, tetracycline, and sulfonamide.
Antimicrobial Drug Resistance Trends
The major goal of this study was to document antimicrobial drug resistance among historical bacteria from humans and animals to associate emergence of resistance with approval of new antimicrobial classes. Animal E. coli isolates showed an increasing resistance trend to 11 antimicrobial agents (ampicillin, sulfonamide, tetracycline, cephalothin, trimethoprim/sulfamethoxazole, streptomycin, chloramphenicol, cefoxitin, gentamicin, amoxicillin/clavulanic acid, and kanamycin), and human E. coli isolates showed an increasing trend in resistance only to ampicillin, sulfonamide, and tetracycline (Figure 3, Table 4).
Human E. coli isolates showed an increased resistance trend for ampicillin (0.59%/year, 95% CI 0.38%–0.81%; p<0.001), sulfonamide (0.49%/year, 95% CI 0.23%–0.73%; p<0.001), and tetracycline (0.45%/year, 95% CI 0.22%–0.70%; p<0.001), and this trend ranged during the study period from 0% to 66.7% for ampicillin, 0% to 50% for sulfonamide, and 0% to 58% for tetracycline (Table 4). The resistance rate to ampicillin in animal E. coli isolates was similar to that in human isolates and ranged from 0% to 69.4%. In contrast, resistance rates for sulfonamide and tetracycline among animal E. coli isolates ranged from 0% to 73.7% and 0% to 85.5%, respectively, and were higher than those for human isolates. There was a linear increasing trend in resistance to ampicillin (0.97%/year, 95% CI 0.60%–1.33%; p<0.001), sulfonamide (1.11%/year, 95% CI 0.34%–1.85%; p<0.01), and tetracycline (0.7%/year, 95% CI 0.21%–1.21%; p<0.01) (Table 4).
Cephalothin resistance significantly increased over time (0.43%/year, 95% CI 0.08%–0.77%; p<0.05) among animal E. coli isolates. In contrast, a decreasing resistance trend to cephalothin (−0.2%/year, 95% CI −0.34% to 0%; p<0.05) was observed among human isolates (Table 4). Although animal E. coli isolates showed an increasing rate of streptomycin resistance over time (0.9%/year, 95% CI 0.14%–1.41%; p<0.05), there was no significant increase among human E. coli isolates during the study period (0.15%/year, 95% CI −0.10% to 0.39%; p>0.1) (Table 4). In our study isolates, gentamicin resistance was observed in the 1980s among animal E. coli isolates but not until the late 1990s in human isolates. In animal E. coli isolates, the prevalence of gentamicin resistance increased from 0% during the 1970s to 28.1% during 2000–2002, and an increasing trend for resistance to gentamicin (1.28%/year, 95% CI 0.90%–1.69%; p<0.001) was first observed in the 1980s and reached a prevalence of 40% in 2002. Chloramphenicol resistance varied widely between human and animal isolates (yearly range 0%–46.8% among animal isolates and 0%–20% among human isolates). A linear increase in chloramphenicol resistance was observed among animal isolates (p<0.01), which increased 0.30%/year. Ceftiofur-resistant and ceftriaxone-resistant strains were not detected until 1990–1999 among human and animal E. coli isolates. None of the human E. coli isolates showed resistance to ciprofloxacin.
There was no monotonic resistance trend for trimethoprim/sulfamethoxazole, chloramphenicol, cefoxitin, ceftiofur, ceftriaxone, gentamicin, amoxicillin/clavulanic acid, nalidixic acid, and kanamycin among human E. coli isolates. Similarly, animal E. coli isolates did not show a monotonic resistance trend for ceftiofur, ceftriaxone, ciprofloxacin, and nalidixic acid.
To help characterize evolution of drug resistance in E. coli since antimicrobial drugs were first widely used, we tested existing strain collections of E. coli for their susceptibility to a common panel of 15 antimicrobial agents. We tested 1,729 E. coli isolates from human and animal sources for susceptibility trends during the past 6 decades.
Resistance to sulfonamide was one of the most common resistance profiles identified among our study isolates and showed a monotone increasing resistance trend over time. Sulfonamide resistance has been observed in human E. coli isolates since 1950 and in animal isolates since 1964. Sulfonamides were introduced in the 1930s and have been in continuous use for >70 years. These drugs were administered alone from the 1930s through the 1960s in humans and were almost exclusively combined with diaminopyrimidines (e.g., trimethoprim) since the 1970s. In animal production systems, SUL is one of the most commonly used drugs as a single agent or in combination with diaminopyrimidines (e.g., ormetoprim) (14). A high prevalence of clinical resistance to sulfonamides was reported in enteric bacteria isolated from healthy food animals and humans (10,22,23) and is often associated with acquisition of the resistance genes sul1 and sul2 (23).
Sulfonamide resistance genes are commonly associated with mobile genetic elements, and these elements play a major role in dissemination of multiple antimicrobial drug resistance genes in E. coli isolates (24–26). In addition, despite a major reduction in the rate of sulfonamide use in the United Kingdom in 1995, resistance to sulfonamides persisted at high rates among clinical E. coli isolates (22,25). Similarly, a 30-year (1979–2009) follow-up study on antimicrobial drug resistance at the Karolinska Hospital in Stockholm, Sweden, reported an increase in sulfonamide resistance despite decreased use (13).
Linkage of sulfonamide resistance genes, particularly as a constituent of class I integrons, to determinants conferring resistance to antimicrobial drugs that are still commonly used might help explain persistence of sulfonamide resistance (22). In our study, 80% (502/627) and 74% (462/627) of sulfonamide-resistant E. coli isolates were also resistant to tetracycline and streptomycin, respectively. Wu et al. (27) demonstrated that streptomycin and ampicillin are the 2 most frequently co-transferred resistance phenotypes among sulfonamide-resistant E. coli isolates recovered from pigs, pig carcasses, and humans. In addition to co-selection by drugs still commonly used, Enne et al. (28) and Bean et al. (25) suggested that lack of selective disadvantage of sul2 (the most prevalent determinant of sulfonamide resistance) carriage and the genetic mobility of sul2 might account for persistence in the absence of clinical selection pressure.
Tetracycline resistance was the most common type of resistance observed and the most prevalent resistance phenotype in animal isolates (71.1%). This finding is not surprising because tetracycline has been widely used in therapy and to promote feed efficiency in animal production systems since its approval in 1948 (2,14). Persistence of tetracycline resistance was reported in animal coliforms a decade after it was no longer used in feed or for treatment (29). We commonly found co-resistance for tetracycline with streptomycin, sulfonamide, ampicillin, and chloramphenicol, as in other studies (23,30,31).
A small percentage of E. coli showed resistance to chloramphenicol, a drug approved in 1947 for human clinical use. Chloramphenicol is not approved for use in food animals in the United States. Persistence of chloramphenicol resistance in E. coli has been observed by other authors (10,32). Florfenicol, a closely related drug, was approved for treatment of respiratory diseases in cattle in the United States in 1996. Florfenicol resistance mediated by the flo gene confers nonenzymatic cross-resistance to chloramphenicol (33,34) and might select for nascent resistance in recent strains. Of known chloramphenicol-resistance genes, only a small number mediate resistance to florfenicol (34). For example, chloramphenicol-resistant strains in which resistance is exclusively based on activity of chloramphenicol acetyltransferases do not show resistance to florfenicol (35). Of 104 chloramphenicol-resistant animal E. coli isolates, 35.6% were isolated before approval of florfenicol. More than 90% of chloramphenicol-resistant E. coli isolates were concurrently resistant to tetracycline. In addition, our data showed not only persistence of chloramphenicol but an increasing tetracycline and SUL resistance trend over time among animal E. coli isolates. These observations could be explained by co-selection of mobile resistance elements or by unknown substrate(s) for the chloramphenicol-resistance determinants that serve as a selection pressure (23,36).
Gentamicin was approved for use in 1963 (2). Although gentamicin resistance was rare in human E. coli isolates, we found resistance rates <40% among animal E. coli in 2002. Since 1980, resistance to gentamicin has increased among animal E. coli isolates. The overall rate of gentamicin resistance was slightly higher in chicken (16.6%) and cattle (16%) isolates than in pig (14%) isolates. Gentamicin is widely used in the poultry industry. Aminoglycosides approved for use in food animals in the United States include dihydostreptomycin, efrotomycin, hygromycin B, neomycin, spectinomycin, streptomycin, and apramycin (37). A correlation between use of apramycin at the farm level and apramycin/gentamycin–resistant E. coli in diseased pigs and healthy finishers was reported (15). Yates et al. (38) reported apramycin-resistant E. coli isolates that were resistant to gentamicin and tobramycin, which are drugs used in human medicine. In our study, 93% of gentamicin-resistant E. coli isolates were multidrug resistant (>3 classes of drugs). Eighty-one percent (94/116) were resistant to >5 antimicrobial drugs, including 95.7% (111/116) to streptomycin, 93.1% (108/116) to sulfonamides, and 91.4% (106/116) to tetracycline.
Our data showed lack of a monotonic trend for extended-spectrum cephalosporins resistance. Ceftiofur, a third-generation cephalosporin, was first approved in 1988 for veterinary use in food animals to treat a variety of gram-negative bacterial infections, including acute bovine respiratory diseases (39). In our culture collection, ceftiofur resistance was not detected before 1993 in animal isolates and before 1997 in human isolates. In NARMS E. coli collections, ceftiofur resistance was detected in the first years of testing among chicken carcasses (6.3% in 2000) and retail chicken breast samples (7.1% in 2002) (10). Studies have shown ceftiofur use in animals can select for extended-spectrum cephalosporin resistance, including ceftriaxone resistance in bacteria isolated from animals and humans (40).
In the present study, 1 human E. coli isolate recovered in 1997 showed resistance to ceftiofur and ceftriaxone. This isolate was also resistant to 9 other antimicrobial drugs. Studies on E. coli isolates with decreased susceptibilities to ceftiofur and ceftriaxone showed carriage of a blaCMY allele that conferred resistance to cephalothin, ampicillin, and amoxicillin/clavulanic acid, as in salmonellae (24,40). Additional data that include more years are needed to determine the resistance trend over time because third-generation cephalosporins were introduced in the 1980s.
A recent NARMS report showed that resistance to ceftriaxone ranged from 6.3% to 13.5% among E. coli isolates from chickens during 2000–2008; resistance to ceftiofur ranged from 4.4% to 10.5% during the same period (10). Currently, the molecular mechanisms of antimicrobial drug resistance development and evolution of these resistance genes over time are being investigated.
Our study has limitations because of its retrospective nature and reliance on preexisting culture collections for analysis. These limitations resulted in an uneven distribution of isolates per year and decade, incomplete or absent patient/host information regarding prior treatment history, and potential for bias in selecting isolates that were ultimately tested in this study. ECRC and CDC accept clinical samples for diagnostic purposes. Thus, isolate sets cannot be considered truly random. Also, patient information was limited; we had no data for prior antimicrobial drug exposure, travel, and other epidemiologic information. Therefore, analyses of resistance as a function of time were confounded. We selected the nonparametric tests of Mann-Kendall and Sen for trend analysis because they are suitable for non-normally distributed data and data with small number of observations.
Despite these limitations, this analysis provides foundational information for resistance development over time, laying the groundwork for understanding evolution of multidrug resistance at the genetic level. In addition, these data show that multidrug resistance is not a congenital feature of E. coli, and that drug use and resistance are closely related temporally. Work is ongoing to analyze this isolate set for alleles underlying resistance and compare them with recent isolates. This work will provide more definitive data on how resistance gene clusters have evolved and the context in which genes are maintained in the absence of known selection pressures.
Dr Tadesse is a staff fellow in the Division of Animal and Food Microbiology, Office of Research, US Food and Drug Administration, Laurel, Maryland. His research interests include evolution of antimicrobial drug resistance genes and molecular epidemiology of foodborne pathogens.
Study isolates were collected by ATCC through contract agreement (***********) with Center for Veterinary Medicine, Office of Research, US Food and Drug Administration.
- Aarestrup FM, Wegener HC, Collignon P. Resistance in bacteria of the food chain: epidemiology and control strategies. Expert Rev Anti Infect Ther. 2008;6:733–50.
- Walsh CT. Antibiotics: actions, origins, resistance. Washington (DC): American Society for Microbiology Press; 2003.
- Levy SB, Marshall B. Antibacterial resistance worldwide: causes, challenges and responses. Nat Med. 2004;10(Suppl):S122–9.
- von Baum H, Marre R. Antimicrobial resistance of Escherichia coli and therapeutic implications. Int J Med Microbiol. 2005;295:503–11.
- Sodha SV, Lynch M, Wannemuehler K, Leeper M, Malavet M, Schaffzin J, Multistate outbreak of Escherichia coli O157:H7 infections associated with a national fast-food chain, 2006: a study incorporating epidemiological and food source traceback results. Epidemiol Infect. 2011;139:309–16.
- Taur Y, Smith MA. Adherence to the Infectious Diseases Society of America guidelines in the treatment of uncomplicated urinary tract infection. Clin Infect Dis. 2007;44:769–74.
- Igarashi T, Inatomi J, Wake A, Takamizawa M, Katayama H, Iwata T. Failure of prediarrheal antibiotics to prevent hemolytic uremic syndrome in serologically proven Escherichia coli O157:H7 gastrointestinal infection. J Pediatr. 1999;135:768–9.
- Erb A, Stürmer T, Marre R, Brenner H. Prevalence of antibiotic resistance in Escherichia coli: overview of geographical, temporal, and methodological variations. Eur J Clin Microbiol Infect Dis. 2007;26:83–90.
- Womack NA, Kabera CM, Tong EA, Jones S, Gaines S, Bartholomew M, ; The NARMS Working Group. The use of Escherichia coli as a sentinel for antimicrobial resistance in Salmonella. In: Abstracts of the National Foundation for Infectious Diseases Annual Conference on Antimicrobial Resistance, Bethesda, Maryland, February 1–3, 2010. Bethesda (MD): The Foundation; 2010. Abstract no. P12.
- US Food and Drug Administration. National antimicrobial resistance monitoring system –enteric bacteria (NARMS): 2008 executive report. Rockville (MD); 2010 [cited 2012 Feb 13]. http://www.fda.gov/AnimalVeterinary/SafetyHealth/AntimicrobialResistance/NationalAntimicrobialResistanceMonitoringSystem/default.htm.
- Atkinson BA, Lorian V. Antimicrobial agent susceptibility patterns of bacteria in hospitals from 1971 to 1982. J Clin Microbiol. 1984;20:791–6.
- Blaettler L, Mertz D, Frei R, Elzi L, Widmer AF, Battegay M, Secular trend and risk factors for antimicrobial resistance in Escherichia coli isolates in Switzerland 1997–2007. Infection. 2009;37:534–9.
- Kronvall G. Antimicrobial resistance 1979–2009 at Karolinska Hospital, Sweden: normalized resistance interpretation during a 30-year follow-up on Staphylococcus aureus and Escherichia coli resistance development. APMIS. 2010;118:621–39.
- McEwen SA, Fedorka-Cray P. Antimicrobial use and resistance in animals. Clin Infect Dis. 2002;34(Suppl 3):S93–106.
- Jensen VF, Jakobsen L, Emborg H, Seyfarth AM, Hammerum AM. Correlation between apramycin and gentamicin use in pigs and an increase reservoir of gentamicin-resistant Escherichia coli. J Antimicrob Chemother. 2006;58:101–7.
- National Committee for Clinical Laboratory Standards. Performance standards for antimicrobial susceptibility testing; 12th informational supplement. M100–S20. Wayne (PA): The Committee; 2010.
- Guilfoile P. 2006. Antibiotic resistant bacteria. Northborough (MA): Chelsea House Publishers; 2006.
- Kunin CM, Atuk N. Excretion of cephaloridine and cephalothin in patients with renal impairment. N Engl J Med. 1966;274:654–6.
- Bryskier A. Historical review of antibacterial chemotherapy. In: Bryskier A, editor. Antimicrobial agents: antibacterials and antifungals. Washington (DC): American Society for Microbiology Press; 2005. p. 1–11.
- Sen PK. Estimates of the regression coefficient based on Kendall’s tau. J Am Stat Assoc. 1968;63:1379–89.
- Salmi T, Määttä A, Anttila P, Ruoho-Airola T, Amnell T. Detecting trends of annual values of atmospheric pollutants by the Mann–Kendall test and Sen’s slope estimates: the Excel template application Helsinki: MAKESENS. Helsinki: Finnish Meteorological Institute; 2002.
- Enne VI, Livermore DM, Stephens P, Hall LM. Persistence of sulphonamide resistance in Escherichia coli in the UK despite national prescribing restriction. Lancet. 2001;357:1325–8.
- Kozak GK, Pearl DL, Parkman J, Reid-Smith RJ, Deckert A, Boerlin P. Distribution of sulfonamide resistance genes in Escherichia coli and Salmonella isolates from swine and chickens at abattoirs in Ontario and Québec, Canada. Appl Environ Microbiol. 2009;75:5999–6001.
- Zhao S, White DG, McDermott PF, Friedman S, English L, Ayers S, Identification and expression of cephamycinase bla (CMY) genes in Escherichia coli and Salmonella isolates from food animals and ground meat. Antimicrob Agents Chemother. 2001;45:3647–50.
- Bean DC, Livermore DM, Papa I, Hall LM. Resistance among Escherichia coli to sulphonamides and other antimicrobials now little used in man. J Antimicrob Chemother. 2005;56:962–4.
- Bean DC, Livermore DM, Hall LM. Plasmids imparting sulfonamide resistance in Escherichia coli: implications for persistence. Antimicrob Agents Chemother. 2009;53:1088–93.
- Wu S, Dalsgaard A, Hammerum AM, Porsbo LJ, Jensen LB. Prevalence and characterization of plasmids carrying sulfonamide resistance genes among Escherichia coli from pigs, pig carcasses and human. Acta Vet Scand. 2010;52:47.
- Enne VI, Bennett PM, Livermore DM, Hall LM. Enhancement of host fitness by the sul2-coding plasmid p9123 in the absence of selective pressure. J Antimicrob Chemother. 2004;53:958–63.
- Langlois BE, Cromwell GL, Stahly TS, Dawson KA, Hays VW. Antibiotic resistance of fecal coliforms after long-term withdrawal of therapeutic and subtherapeutic antibiotic use in a swine herd. Appl Environ Microbiol. 1983;46:1433–4.
- Roberts MC. Update on acquired tetracycline resistance genes. FEMS Microbiol Lett. 2005;245:195–203.
- Schroeder CM, Zhao C, DebRoy C, Torcolini J, Zhao S, White DG, Antimicrobial resistance of Escherichia coli O157 isolated from humans, cattle, swine, and food. Appl Environ Microbiol. 2002;68:576–81.
- Bischoff KM, White DG, Hume ME, Poole TL, Nisbet DJ. The chloramphenicol resistance gene cmlA is disseminated on transferable plasmids that confer multiple-drug resistance in swine Escherichia coli. FEMS Microbiol Lett. 2005;243:285–91.
- White DG, Hudson C, Maurer JJ, Ayers S, Zhao S, Lee MD, Characterization of chloramphenicol and florfenicol resistance in Escherichia coli associated with bovine diarrhea. J Clin Microbiol. 2000;38:4593–8.
- Schwarz S, Kehrenberg C, Doublet B, Cloeckaert A. Molecular basis of bacterial resistance to chloramphenicol and florfenicol. FEMS Microbiol Rev. 2004;28:519–42.
- Cannon M, Harford S, Davies J. A comparative study on the inhibitory actions of chloramphenicol, thiamphenicol and some fluorinated derivatives. J Antimicrob Chemother. 1990;26:307–17.
- Harada K, Asai T, Kojima A, Ishihara K, Takahashi T. Role of coresistance in the development of resistance to chloramphenicol in Escherichia coli isolated from sick cattle and pigs. Am J Vet Res. 2006;67:230–5.
- US Food and Drug Administration. 2009 summary report on antimicrobials sold or distributed for use in food-producing animals. December 9, 2010. Rockville, MD [cited 2011Feb 23]. http://www.fda.gov/AnimalVeterinary/NewsEvents/CVMUpdates/ucm236143.htm
- Yates CM, Pearce MC, Woolhouse ME, Amyes SG. High frequency transfer and horizontal spread of apramycin resistance in calf faecal Escherichia coli. J Antimicrob Chemother. 2004;54:534–7.
- Burton PJ, Thornsberry C, Cheung YY, Watts JL, Yancey RJ. Interpretive criteria for antimicrobial susceptibility testing of ceftiofur against bacteria associated with swine respiratory disease. J Vet Diagn Invest. 1996;8:464–8.
- Winokur PL, Vonstein DL, Hoffman LJ, Uhlenhopp EK, Doern GV. Evidence for transfer of CMY-2 AmpC beta-lactamase plasmids between Escherichia coli and Salmonella isolates from food animals and humans. Antimicrob Agents Chemother. 2001;45:2716–22.
- Figure 1. . . Change in antimicrobial drug resistance patterns among Escherichia coli isolates, United States, 1950–2002.
- Figure 2. . . Distribution of multidrug resistance patterns among Escherichia coli isolates recovered from different sources, United States, 1950–2002.
- Figure 3. . . Trend analysis of selected antimicrobial agents among Escherichia coli isolates from humans (A) and animals (B), United States, 1950–2002. AMP-R, ampicillin resistance; STR-R, streptomycin resistance; TET-R, tetracycline...
- Table 1. Period of isolation and source of Escherichia coli isolates tested, United States, 1950–2002
- Table 2. Antimicrobial drug resistance phenotypes of Escherichia coli isolates from different sources, United States, 1950–2002
- Table 3. Multiple antimicrobial drug resistance among Escherichia coli isolates analyzed by source, United States, 1950–2002
- Table 4. Mann-Kendall and Sen estimates for trend statistics of antimicrobial drug resistance among Escherichia coli isolates of human and animal origin, United States, 1950–2002
Please use the form below to submit correspondence to the authors or contact them at the following address:
Patrick F. McDermott, US Food and Drug Administration, 8401 Muirkirk Rd, Laurel, MD 20708, USA
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: April 12, 2012
- Page last updated: April 12, 2012
- Page last reviewed: April 12, 2012
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)