Characterization of Escherichia coli virulence genes, pathotypes and antibiotic resistance properties in diarrheic calves in Iran

Background Calf diarrhea is a major economic concern in bovine industry all around the world. This study was carried out in order to investigate distribution of virulence genes, pathotypes, serogroups and antibiotic resistance properties of Escherichia coli isolated from diarrheic calves. Results Totally, 76.45% of 824 diarrheic fecal samples collected from Isfahan, Chaharmahal, Fars and Khuzestan provinces, Iran were positive for E. coli and all of them were also positive for cnf2, hlyA, cdtIII, f17c, lt, st, stx1, eae, ehly, stx2 and cnf1 virulence genes. Chaharmahal had the highest prevalence of STEC (84.61%), while Isfahan had the lowest (71.95%). E. coli serogroups had the highest frequency in 1–7 days old calves and winter season. Distribution of ETEC, EHEC, AEEC and NTEC pathotypes among E. coli isolates were 28.41%, 5.07%, 29.52% and 3.49%, respectively. Statistical analyses were significant for presence of bacteria between various seasons and ages. All isolates had the high resistance to penicillin (100%), streptomycin (98.25%) and tetracycline (98.09%) antibiotics. The most commonly detected resistance genes were aadA1, sul1, aac[3]-IV, CITM, and dfrA1. The most prevalent serogroup among STEC was O26. Conclusions Our findings should raise awareness about antibiotic resistance in diarrheic calves in Iran. Clinicians should exercise caution when prescribing antibiotics.


Background
Calf diarrhea is one of the most economic and pervasive concern in veterinary industry all around the world. Infectious agents are the most commonly detected causes of calf diarrhea [1][2][3]. Several studies have been addressed the high distribution of Escherichia coli (E. coli) strains in infectious calf diarrhea [3][4][5][6]. Escherichia coli is a gram-negative, rod-shaped, flagellated, non-sporulating and facultative anaerobic bacterium of the family enterobacteriaceae that classically classified into enterohemorrhagic (EHEC), enterotoxigenic (ETEC), necrotoxigenic (NTEC), enteroinvasive (EIEC), enteropathogenic (EPEC) and attaching and effacing E. coli (AEEC) pathotypes [7]. Intimin genes are present in EPEC and some Shigatoxinproducing E. coli (STEC). EPEC strains are defined as eae harbouring diarrhoeagenic E. coli that possess the ability to form attaching-effacing (A/E) lesions on intestinal cells and that do not possess Shigatoxin encoding genes [8,9]. Diarrheagenic Escherichia coli are now broadly placed into 6 classes based on virulence mechanisms. One of these classes, enterotoxigenic E. coli, is the most common cause of diarrhea in beef and dairy calves in the first 4 days of life. Two other diarrheagenic classes, EHEC and EPEC, are important causes of disease in human beings, but less well substantiated causes of diarrhea in calves [8,9]. E. coli strains that cause hemorrhagic colitis and hemolytic uremic syndrome in humans, express high levels of Shiga toxin, cause A/E lesions in intestinal epithelial cells, and possess a specific 60-MDa EHEC plasmid are known as EHEC [8,9]. One feature EHEC and EPEC have in common is the causation of intestinal epithelial lesions known as A/E. AEEC is a designation for those E. coli strains known to cause A/E lesions or at least carry the genes for this trait, and therefore include organisms that fall into either the EHEC or EPEC classes. Because cattle are carriers of many different serotypes of EHEC, much emphasis has been placed on the public health and food safety concerns associated with the fecal shedding of these organisms. However, much less emphasis has been given to their roles as diarrheagenic pathogens of cattle [8,9]. In fact, several pathotypes of E. coli have been known by presence of certain genes. EAF and bfp are predominant in EPEC and typical genes of EAEC (pAA), cdt and cnf are the major genes of NTEC and finally sta, stb, lt, f4, f5, f18, stx1 and szx2 are the genes of the EHEC pathotype [8,9].
Heat-labile enterotoxins (LT) and heat-stable enterotoxins (STa or STb) are two of the most important bacterial virulence factors are able to causes severe diarrhea in calves [3,10]. Also, there are some another virulence factors including phage-encoded cytotoxins, called Shiga toxin 1 (stx1) and Shiga toxin 2 (stx2), the protein intimin (eae) and the plasmid-encoded enterohaemolysin or enterohaemorrhagic E. coli haemolysin (ehly) which are related to the pathogenesis of STEC strains [16]. The NTEC are able to elaborate two types of cytotoxic necrotizing factors (CNF1 and CNF2). CNF factors are heat-labile proteins which can cause diarrhea. Cytolethal distending toxin (CDT) induces enlargement and death of some cultured eukaryotic cell lines and causing diarrhea. Totally, five different cdt alleles (cdt-I, cdt-II, cdt-III, cdt-IV and cdt-V) have been reported in E. coli strains [17][18][19][20][21]. The 31A produces F17c fimbria (formerly called 20 K), which is responsible for N-acetyl-D-glucosaminedependent adhesion of bacteria to calves border villi [5,22]. The F17c includes fimbriae expressed by calf diarrheic [23,24]. Studies in France, Scotland and Belgium showed that pathogenic F17-producing E. coli strains represent a significant part of the bacterial strains isolated from diarrheic calves [25].
Diseases caused by E. coli often require antimicrobial therapy; however, antibiotic-resistant strains of this bacterium cause longer and more severe illnesses than their antibiotic-susceptible counterparts. Several studies have shown that antibiotic resistance in E. coli has increased over time [26][27][28]. Data on the distribution of serogroups, pathotypes, virulence genes and the antimicrobial resistance properties of E. coli strains isolated from diarrheic calves is scarce in Iran. Therefore, the aim of the present study was to characterize E. coli strains isolated from Iranian diarrheic calves at the molecule level and investigate their susceptibility to 13 commonly used antibiotics, as well as investigating seasonal variation in the prevalence and serogroup distribution of E. coli.

Results and discussion
We found that 630 out of 824 samples (76.45%) were positive for E. coli. Chaharmahal province had the highest incidence of E. coli in diarrhea specimens (84.61%), while Isfahan province had the lowest incidence (71.95%).
The high importance of geographical area and season on the incidence of E. coli strains in diarrheic calves were addressed in the present study. Similar results have been reported by Mohamed Ou Said et al. [29]. Season and geography are also known to influence passive transfer of colostral immunoglobulins in calves [30]. Season has a significant effect on the calf mortality [31] as well as on the absorption of immunoglobulins in neonatal calves. One possible explanation for the high prevalence of E. coli strains in calves in winter is that climatic variables such as heat, rain and thunderstorms, together with variable barometric pressure may have affected the autonomic nervous systems. These variables could affect immunity, thus making calves more susceptible to infections. Alternatively, the higher prevalence of E. coli strains in winter in our study may be related to the fact that the mean serum IgG1 concentrations were low in winter born calves and increased during the spring and summer [32]. The higher mortality rates of 69.6% and 15.36% were observed in winter born calves than 39.4% and 5.97% in summer born calves of Afzal et al. [33] and Sharma et al. [34] investigations. Similar results have been reported previously [35,36].
Herrera-Luna et al. [40] revealed that 17% of all diarrheic and healthy calves of Australian herds were infected by E. coli. They showed that 15.2% of E. coli strains harbored the shiga toxin genes including stx1, stx2 and ehly and eae genes. Low incidence of VTEC phenotype and O157:H7 serotypes of E. coli strains of diarrheic calves of Najaf, Iraq were reported by Al-Charrakh and Al-Muhana [41]. Diarrheic calves of Bradford et al. [42] investigation hadn't any cnf1, cnf2, stx2, stB and lt genes, while the K99 fimbriae, stA enterotoxin, stx1 and eae genes were detected in 8, 8, 1 and 1 isolates, respectively which was  In the present study, 211 E. coli strains that were isolated from diarrheic samples hadn't any virulence factors. One possible explanation for this finding is the fact that maybe these strains were non-pathogenic E. coli and the animals have diarrhea caused by some other infectious agent. Achá et al. [43] reported that 76% of calves were infected with E. coli, while the prevalence of other causative agents including Salmonella species and Campylobacter species were 2% and 11%, respectively. They also reported that 22/55 (40%) strains from diarrheal calves and 14/88 (16%) strains from healthy calves carried the K99 adhesin (P = 0.001).
Our results showed that O26 and O157 were the most common serogroups of our study, while O113 and O121 were the less common. Saridakis et al. [44] showed that O26, O114 and O119 were the most prevalent serogroups in E. coli strains isolated from diarrheic calves. Mora et al. [38] showed that 52% of E. coli strains isolated from bovine herds were belonged to O26, O22, O77, O4, O105, O20, O157, O113, and O171 serogroups which was similar to our results.
Bloody diarrhea, non-bloody diarrhea, HUS and other clinical complications of infection with STEC strains are serious among calves, compelling clinicians to consider the provision of early, and empirical antibiotic therapy. However, current recommendations and the available data (although limited in scope and only formally studied for O157 and non-O157-related infections in calves) suggest that antibiotics should be withheld if STEC infection is suspected, given concerns that antibiotics may trigger release of stx and progression to diarrhea, resulting in worse clinical outcomes. Furthermore, because inappropriate prescriptions of antibiotics select antibiotic resistance, it was not surprising that our study found that resistance to some antibiotic agents was higher than 80%. The E. coli strains of our study were resistant to penicillin (100%), streptomycin (98.25%), tetracycline  Hly-R CCTGCTCCAGAATAAACCACA Eae-R CGGTCGCCGCACCAGGATTC Cdt3-R TTTGTGTCGGTGCAGCAGGGAAAA O128-R CCGACGGACTGATGCCGGTGATT aadA1-F TATCCAGCTAAGCGCGAACT 447 Streptomycin resistance [60] aadA1-R ATTTGCCGACTACCTTGGTC tetA-F GGTTCACTCGAACGACGTCA 577 Tetracycline resistance [60] tetA-R CTGTCCGACAAGTTGCATGA and ciprofloxacin (60.31%). In terms of antibiotic resistance genes, aadA1, sul1, aac[3]-IV, CITM and dfrA1 were the most commonly detected. Totally, 73.8% of the STEC strains of our study were resistance to chloramphenicol. Chloramphenicol is a banned antibiotic and the high antibiotic resistance to this drug detected in our study indicates that irregular and unauthorized use of it may have occurred in Iran. Unfortunately, veterinarians in many fields of veterinary such as large animal internal medicine, poultry and even aquaculture, use this antibiotic as a basic one. Therefore, in a short period of time, antibiotic resistance will appear. Previous study showed that in some countries 300,000 kg of antibiotics is used yearly on veterinary prescription in animals [45].
The above data highlight large differences in the prevalence of STEC strains in the different studies, as well as differences in virulence genes and antibiotic resistance properties in the clinical samples. This could be related to differences in the type of samples tested, number of samples, method of sampling, experimental methodology, geographical area, antibiotic prescription preference among clinicians, antibiotic availability, and climate differences in the areas where the samples were collected, which would have differed between each study.

Conclusion
In conclusion, we identified a large number of pathotypes, serogroups, virulence factors and antibiotic resistance genes and resistance to more than one antibiotic in the E. coli strains isolated from diarrheic calves in Iran. Our data indicate that O26 and O157 serogroups are predominant in Iranian diarrheic calves. Marked seasonal, senile and geographical variation was also found. Our data revealed that the O26 serogroup, the lt, f5, f41, stx1, stx2, eaeA and hlyA putative virulence genes, the aadA1, sul1, aac [3]-IV, CITM and dfrA1 antibiotic resistance genes, and resistance to penicillin, streptomycin, tetracycline, lincomycin,

DNA extraction
All E. coli isolates were cultured on Peptone Water (PW, Merck, Germany) (24 h at 37°C). One hundred and fifty microliter of cultured PW media was added to 400 μL sterile distilled water. All components were boiled for 12 min. The mentioned suspension was frozen and then centrifuged at at 14,000 rpm for 14 min [51].
Detection of virulence genes, antibiotic resistance genes and serogroups using Polymerase Chain Reaction (PCR) The method of Sabat et al. [52] was used in order to E. coli confirmation. Several PCR protocols were used to study the presence of virulence genes, serogroups and antibiotic resistance properties of STEC strains. List of primers used for this instance is shown in Table 7. PCR conditions including temperature and volume of each reaction is shown in Table 8. All reactions were performed using the PCR thermocycler (Eppendrof Mastercycler 5330; Eppendorf-Nethel-Hinz GmbH, Hamburg, Germany). Amplified PCR products were electrophoresed on 1.5% agarose gel stained with ethidium bromide. Final products were examined using the gen documentation system. Distilled water and E. coli CAPM 5933, CAPM 6006, O159:H20 and O157:K88ac:H19 were used as negative and positive controls, respectively.

Antibiotic susceptibility testing
The Kirby-Bauer disc diffusion method based on the laboratory protocol of the Clinical and Laboratory Standards Institute [64] was used for study the antibiotic susceptibility pattern of E. coli isolates. All isolates were cultured on Mueller-Hinton agar in an aerobic condition (Merck, Germany) (24 h at 37°C). Susceptibility of E. coli isolates to commonly used antibiotic agents was measured and interpreted based on the CLSI protocol. E. coli ATCC 25922 was used as quality control.

Statistical analysis
The SPSS (Statistical Package for the Social Sciences) software (Ver. 16) and Chi-square and Fisher's exact tests were used in order to study the statistical relationship between the incidence of bacterium in various age, season and geographical regions and also between the frequency of various virulence factors, pathotypes, antibiotic resistance genes and serogroups. A P value < 0.05 was considered statistically significant.