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Antimicrobial drug resistance in Escherichia coli from humans and food animals, United States, 1950-2002.

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.

Materials and Methods

Bacterial Strains

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[degrees]C. Similarly, isolates were stored, according to the ECRC standard protocol at -70[degrees]C to -80[degrees]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 [greater than or equal to] 3 classes of antimicrobial drugs.

Statistical Analysis

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 [greater than or equal to] 10 values. Significance was assessed at 4 levels ([alpha] = 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 [chi square] test; p values <0.05 was considered significant.


Antimicrobial Drug Susceptibility

Overall, 934 (54.0%) of 1,729 E. coli were resistant to [greater than or equal 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 [greater than or equal 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 [greater than or equal 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 [approximately equal 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 [less than or equal to] 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 ([greater than or equal to] 3 classes of drugs). Eighty-one percent (94/116) were resistant to [greater than or equal 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 [bla.sub.CMY] 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.

Study isolates were collected by ATCC through contract agreement (223-02-7010) with Center for Veterinary Medicine, Office of Research, US Food and Drug Administration.

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.


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Author affiliations: Food and Drug Administration, Laurel, Maryland, USA (D.A. Tadesse, S. Zhao, E. Tong, S. Ayers, A. Singh, P.F. McDermott); and Food and Drug Administration, Rockville, Maryland, USA (M.J. Bartholomew)


Address for correspondence: Patrick F. McDermott, US Food and Drug Administration, 8401 Muirkirk Rd, Laurel, MD 20708, USA; email:

Table 1. Period of isolation and source of Escherichia coli
isolates tested, United States, 1950-2002

                       Source, no. isolates

Period       Human    Cattle    Chickens    Pigs

1950-1959     180        0          0         0
1960-1969     112       17          0        15
1970-1979     292       32         11        25
1980-1989     211       86         65        96
1990-1999     182       108        44        81
2000-2002      6        81         18        68

Table 2. Antimicrobial drug resistance phenotypes of Escherichia coli
isolates from different sources, United States, 1950-2002 *

Drug class                 Drug               [micro]g/mL

Penicillins                 AMP       [less than or equal to] 32
[beta]-lactam/[beta]-       AUG       [less than or equal to] 32
  lactamase inhibitor
Cephems                     CEP       [less than or equal to] 32
                            FOX       [less than or equal to] 32
                            TIO       [less than or equal to] 8

                            AXO       [less than or equal to] 4

Phenicols                   CHL       [less than or equal to] 32
Aminoglycosides             GEN       [less than or equal to] 16
                            KAN       [less than or equal to] 64
                            STR       [less than or equal to] 64
Quinolones                  CIP       [less than or equal to] 4
                            NAL       [less than or equal to] 32
Tetracyclines               TET       [less than or equal to] 16
Folate pathway              SUL       [less than or equal to] 512
  inhibitors              TMP/SMX     [less than or equal to] 4

                                                  % Resistance

                                       Overall,     Human,    Cattle,
Drug class                 Drug       n = 1,729    n = 983    n = 323

Penicillins                 AMP          24.1        16.5        35
[beta]-lactam/[beta]-       AUG          5.6         2.4        12.7
  lactamase inhibitor
Cephems                     CEP          12.9        8.8        20.1
                            FOX          4.4         1.5        9.3
                            TIO          2.3         0.1        7.4

                            AXO          2.4         0.1        7.7

Phenicols                   CHL          8.1         3.7         18
Aminoglycosides             GEN          6.7         0.1        16.1
                            KAN          19.3        5.7        39.9
                            STR          34.2        15.3       61.3
Quinolones                  CIP          0.4          0         1.9
                            NAL          1.7          1         3.7
Tetracyclines               TET          40.9         18        71.2
Folate pathway              SUL          36.2        19.9        61
  inhibitors              TMP/SMX         7          2.2        16.1

                                            % Resistance

                                      Chickens,      Pigs,
Drug class                 Drug        n = 138      n = 285

Penicillins                 AMP          34.1        33.3
[beta]-lactam/[beta]-       AUG          7.3          7.4
  lactamase inhibitor
Cephems                     CEP          12.3        19.3
                            FOX          5.1          8.4
                            TIO          1.5          4.2

                            AXO          1.5          4.6

Phenicols                   CHL          8.7         11.9
Aminoglycosides             GEN          16.7         14
                            KAN          29.7        37.5
                            STR           58         57.2
Quinolones                  CIP          0.7           0
                            NAL          1.5          1.8
Tetracyclines               TET          68.8        72.3
Folate pathway              SUL          60.9        52.6
  inhibitors              TMP/SMX        13.8         9.8

                                            Timeline for
                                            use of drugs
Drug class                 Drug             (reference)

Penicillins                 AMP              1961 (17)
[beta]-lactam/[beta]-       AUG              1984 (17)
  lactamase inhibitor
Cephems                     CEP              1964 (18)
                            FOX              1977 (19)
                            TIO           1988 (FDA Green
                                          Book) ([dagger])
                            AXO           1984 (FDA Orange
                                      Book) ([double dagger])
Phenicols                   CHL              1947 (17)
Aminoglycosides             GEN              1963 (17)
                            KAN              1957 (17)
                            STR              1943 (17)
Quinolones                  CIP              1987 (17)
                            NAL              1962 (19)
Tetracyclines               TET              1948 (17)
Folate pathway              SUL              1936 (19)
  inhibitors              TMP/SMX            1968 (19)

* AMP, ampicillin; AUG, amoxicillin/clavulanic acid; CEP, cephalothin;
FOX, cefoxitin; TIO, ceftiofur; FDA, Food and Drug Administration;
AXO, ceftriaxone; CHL, chloramphenicol; GEN, gentamicin; KAN,
kanamycin; STR, streptomycin; CIP, ciprofloxacin; NAL, nalidixic acid;
TET, tetracycline; SUL, sulfonamide; TMP/SMX, trimethoprim/


([double dagger])

([section]) No Clinical and Laboratory Standards Institute breakpoint.
The National Antimicrobials Resistance Monitoring System breakpoint
was used.

Table 3. Multiple antimicrobial drug resistance among Escherichia coli
isolates analyzed by source, United States, 1950-2002

                                        % Resistant


No. drug         Human,    Cattle,   Chickens,     Pigs,      Total,
classes to       n = 983   n = 323     n =138     n = 285   n = 1,729
which isolates
are resistant

0 *               64.8      21.4        21.0       21.1         46
1                 12.4        9         7.2         9.1        10.8
2                  7.5      10.5        16.7       16.1        10.2
3                  6.5      22.6        26.8       23.9         14
4                  4.5      15.5        14.5       13.3        8.8
5                  3.8       7.7        7.2         8.4        5.5
6                  0.4       6.2        4.3         2.8        2.2
7                  0.1       5.3        2.2         5.3        2.1
8                   0        1.9         0           0         0.3

* Susceptible to all drug classes.

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

                                  Years of               trend test
Drug                  Source    time series    No. *       Z value

Ampicillin            Human      1950-2001       52         4.91
                      Animal     1962-2002       37         3.95
Cephalothrin          Human      1950-2001       52         -2.38
                      Animal     1962-2002       37         2.52
Sulfonamide           Human      1950-2001       52         3.41
                      Animal     1962-2002       37         3.24
Streptomycin          Human      1950-2001       52         1.16
                      Animal     1962-2002       37         2.24
Tetracycline          Human      1950-2001       52         3.84
                      Animal     1962-2002       37         2.78
Trimethoprim/         Animal     1982-2002       21         2.64
Chloramphenicol       Animal     1962-2002       37         2.75
Cefoxitin             Animal     1982-2002       21         3.72
Gentamicin            Animal     1978-2002       25         4.53
Amoxicillin/          Animal     1962-2002       37         3.09
  clavulanic acid
Kanamycin             Animal     1962-2002       7          4.38

                                      Sen's slope estimate

Drug                  Source    p value    Q ([dagger]) (95% CI)

Ampicillin            Human      <0.001      0.59 (0.38-0.81)
                      Animal     <0.001      0.97 (0.60-1.33)
Cephalothrin          Human      <0.05      -0.20 (-0.34 to 0)
                      Animal     <0.05       0.43 (0.08-0.77)
Sulfonamide           Human      <0.001      0.49 (0.23-0.73)
                      Animal     <0.01       1.11 (0.34-1.85)
Streptomycin          Human       >0.1     0.15 (-0.10 to 0.39)
                      Animal     <0.05       0.90 (0.14-1.41)
Tetracycline          Human      <0.001      0.45 (0.22-0.70)
                      Animal     <0.01       0.70 (0.21-1.21)
Trimethoprim/         Animal     <0.01       1.17 (0.32-2.15)
Chloramphenicol       Animal     <0.01         0.30 (0-0.59)
Cefoxitin             Animal     <0.001      0.88 (0.28-1.38)
Gentamicin            Animal     <0.001      1.28 (0.90-1.69)
Amoxicillin/          Animal     <0.01         0.14 (0-0.38)
  clavulanic acid
Kanamycin             Animal     <0.001      1.11 (0.59-1.50)

* Number of annual values for calculation of trend analysis.

([dagger]) Magnitude of annual percentage increase or decrease.
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Article Details
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Title Annotation:RESEARCH
Author:Tadesse, Daniel A.; Zhao, Shaohua; Tong, Emily; Ayers, Sherry; Singh, Aparna; Bartholomew, Mary J.;
Publication:Emerging Infectious Diseases
Article Type:Report
Geographic Code:1USA
Date:May 1, 2012
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