The Association of Virulence Determinants of Uropathogenic Escherichia coli With Antibiotic Resistance

Background: The emergence of antimicrobial resistant strains of Escherichia coli has raised considerable interest in understanding the diversity and epidemiology of E. coli infections in humans. Virulence factors of E. coli determine the specific infections caused by this microorganism. Objectives: This study aimed to determine the prevalence of eight E. coli virulence factors and their association with antimicrobial resistance in bacteria isolated from patients with urinary tract infections (UTI). Patients and Methods: One thousand patients with UTI were enrolled in this cross-sectional study. Antimicrobial susceptibility was examined by disc diffusion method according to CLSI guidelines. After DNA extraction, the materials were probed by PCR for eight virulence factors genes, namely fimH, hly, iucC, ibeA, sfa/foc, neuC, papC, and afa genes. Results: The frequency of virulence factors papC, afa, sfa/foc, fimH, hly, neuC, ibeA, and iucC were 53.3%, 51.7%, 53.3%, 56.7%, 23.3%, 31.7%, 20%, and 73.3%, respectively. In addition, there was a high degree resistance to cotrimoxazole and nalidixic acid while a high degree of susceptibility to nitrofurantoin was detected. There was a statistically significant association between fimH gene and resistance to ciprofloxacin (P = 0.006), nalidixic acid (P = 0.025), and cotrimoxazole (P = 0.02). Such associations were found between ibeA gene and amikacin (P = 0.02) and cotrimoxazole (P = 0.02) as well as between afa gene and gentamycin (P = 0.05). Conclusions: The results showed that E. coli isolated from patients with UTI had eight virulence factors with high frequencies. Moreover, these results alleged a direct connection between virulence factors and antimicrobial resistance in E. coli.


Background
The incidence of urinary tract infection (UTI) is estimated to be about 150-250 million cases worldwide. It also accounts for approximately 35% of all hospital acquired infections (1,2). Escherichia coli is one of the most common agent causing extra intestinal infections. These infections are an important cause of morbidity, mortality, and increased healthcare costs. In addition, they are common leading causes of UTI, pneumonia, meningitis, osteomyelitis, sepsis, and intra-abdominal as well as diverse soft tissue infections.
Non-complicated infections constitute the majority of UTIs. Patients recognized with acute non-complicated cystitis are treated as outpatients. The microbiological features of this infection are greatly predictable even in healthy subjects. Therefore, physicians have been informed that empirical antibiotic treatment without culture is convenient in such cases. The empirical therapy has been so widely used that only a few UTIs are routinely cultured (1). Worldwide data shows that there is an increasing resistance to conventional drugs among UTI pathogens. Resistance has emerged even to the newer and more potent antimicrobial agents. Antimicrobial re-sistance surveillance is necessary in order to determine the significance of the problem and to guide empirical selection of antimicrobial agents to treat infected patients (2).
During the last few decades, the frequency of antibiotic resistant infections have raised permanently around the world. This increase has been attributed to a combination of the selective pressure of antimicrobial use, microbial characteristics, social and technical changes that accelerate the transmission of resistance factors in microorganisms including misuse and increased use of antibiotics, a higher number of susceptible hosts, and mistakes in infection control programs leading to incremented transmission of resistant microorganisms (8).
However, several investigations have reported the opposite results. Their studies have shown that according to clinical feature, virulence factor, and antibiotic resistant profile, some E. coli strains tend to be less virulent than susceptible isolates. Furthermore, it remains unclear whether such trends are owing to causal relationships between virulence and resistance or result from co-associated factors (3).

Objectives
This study was conducted to assess the prevalence of VFs and their association with the antibiotics resistance in patients with UTI.

Sample Collection
In this cross-sectional study, 1000 urine samples from patients referred to Peimanieh Hospital Laboratory in Jahrom between 2010 and 2011 were examined. In addition, basic characteristics data such as age, sex, history of urinary infection, history of antibiotic usage, and history of any hospitalization during the past 28 days were recorded. Written informed consent was obtained from the patients or guardian of each child. Ethic Committee of Islamic Azad University approved all steps of this study.
Standard media, including blood agar and MacConkey agar (Merck, Germany) were used for pathogen isolation. Identification of all isolates was done on the basis of Gram staining and routine biochemical tests including fermentation of lactose, citrate utilization, motility of organism, ability to produce indole, reaction on triple sugar iron (TSI) medium, and hemolysis on blood agar. The organisms were stored at 4 °C on agar slants and at -20 °C in glycerol for further investigations. DNA was extracted from confirmed E. coli strains by using a DNA extraction kit (DNP TM kit, CinaGen Co., Iran) according to the manufacturer's instructions. The quality of extracted DNA was examined by 1% agarose gel electrophoresis and concentration of extracted DNA was analyzed by A260/A280 ratio in a biophotometer (Eppendorf, Germany).

PCR Method to Determine Virulence Factors
For identification of VFs, 2 µL of extracted DNA was amplified with 1.5 mM MgCl 2 , 0.2 mM deoxynucleoside triphosphates (dNTPs) mixture, 0.2 mM of each primer (Table 1), and 1 U of Taq DNA polymerase (CinaGen, Co., Tehran, Iran). The PCR was performed with a Perkin-Elmer Gene Amp 9600 thermal cycler under the following conditions: initial denaturation for 5 min at 94 °C followed by 30 cycles of 30 s at 94 °C, 30 s annealing at the specific melting temperature of each primer (Table 1), 30 s at 72 °C, and a final extension step of 7 min at 72 °C. The amplified products were visualized after electrophoresis on a 1.5% agarose gel stained with ethidium bromide ( Figure  1).

Statistical Analysis
Data were statistically analyzed using SPSS v.15 (SPSS Inc., Chicago, IL, USA). Descriptive analyses were done to the evaluation of parametric and non-parametric variables. In addition, caramer, fi, and logistic regression were performed to assess of variables correlation. P value < 0.05 was considered as statistically significant.

Discussion
E. coli is the leading causative agent of UTI and one of the most important bacterial infections. In most cases, uropathogenic clones originate from the fecal flora, and the pathogenic potential of E. coli isolates is thought to be dependent on the presence of various VFs (5). This study showed that there was a difference in rate of VFs in 60 examined UPEC.
The differences observed in the prevalence of E. coli VFs in this study and reports from some regions (7,11,12,14) could be explained by the sample type, source, size, type of VFs, and geographic location. Horcajada showed that nalidixic acid resistance was significantly associated with a decrease in prevalence of three VFs, namely sfa, hly, and cnf-1 (16). In another study, Arisoy et al. (17) showed an association between susceptibility to antibiotics and VFs of the E. coli isolates causing pyelonephritis. They reported that virulence genes pap, sfa, afaI, hly, and aer were increased in sensitive strains.
Zhao examined the prevalence of VFs and antibiotic resistance in UPEC. The feoB and fimH genes had the highest prevalence. in addition, among the 15 tested antibiotics for resistance, nalidixic acid, mezlocillin, and tetracycline had the most resistance (18). In this study, stronger associations were found between fimH gene and resistance to ciprofloxacin, nalidixic acid, and cotrimoxazole, between ibeA gene and amikacin and cotrimoxazole, and between afa gene and gentamycin. These findings were similar to those reported in other studies (16)(17)(18).
Antimicrobial susceptibility patterns varied in isolates from different categories of patients. it needs to be considered when developing guidelines for treatment of UTI and interpreting data from other published studies, which showed high prevalence of antimicrobial resistance among UPEC. From our data, older drugs like nitrofurantoin appeared to be useful and could be considered as a choice for treating uncomplicated lower UTI.
To sum up, E. coli causing UTI in different patient populations differ in their pathogenic potential and susceptibility to antimicrobial agents. It has to be considered when developing guidelines for management of UTI. Periodic reviews and formulation of antibiotic consumption policy are required to control the transmission and acquisition of antibiotic resistance. Further studies for better understanding of the interaction between different VFs at a molecular level are necessary as most UPEC isolates simultaneously express several VFs.