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Revista do Instituto de Medicina Tropical de São Paulo

On-line version ISSN 1678-9946

Rev. Inst. Med. trop. S. Paulo vol.48 no.4 São Paulo July/Aug. 2006

http://dx.doi.org/10.1590/S0036-46652006000400002 

MICROBIOLOGY

 

Virulence factors of uropathogenic Escherichia coli from a University Hospital in Ribeirão Preto, São Paulo, Brazil

 

Fatores de virulência de Escherichia coli uropatogênicas provenientes de um Hospital Universitário em Ribeirão Preto, São Paulo, Brasil

 

 

Edilene SantoI; Claudia MacedoII; José Moacir MarinIII

IDepartamento de Microbiologia, FCAV, Universidade Estadual Julio de Mesquita, UNESP, 14884-900 Jaboticabal, SP, Brasil
IIDepartamento de Genética, FMRP/Universidade de São Paulo, 14040-900 Ribeirão Preto, SP, Brasil
IIIDepartamento de Morfologia, Estomatologia e Fisiologia, FORP/USP, 14040-904 Ribeirão Preto, SP, Brasil

Correspondence to

 

 


SUMMARY

The aim of the study was to determine the occurrence of virulence genes expressing fimbriae, production of hemolysin, colicin and aerobactin among a hundred Escherichia coli isolates obtained from in-and outpatients of a tertiary-care teaching hospital, between July and August 2000, showing clinical and laboratory signs of urinary tract infection (UTI). The presence of genes (pap, afa, sfa) for fimbriae expression was assayed using specific primers in a polymerase chain reaction. Among the isolates studied, the prevalence of the virulence factors was 96.0%, 76.0%, 24.0%, for hemolysin, aerobactin and colicin, respectively; the prevalence of genes coding for fimbrial adhesive systems was 32.0%, 19.0% and 11.0% for pap, sfa and afa respectively. The strains isolated from the outpatients displayed a greater number of virulence factors compared to those from hospitalized subjects, emphasizing the difference between these two kinds of patients.

Keywords: Escherichia coli; Urinary infection; Virulence factors.


RESUMO

O objetivo do trabalho foi determinar a ocorrência de fatores de virulência, tais como, a expressão de fímbrias, produção de hemolisina, colicina e aerobactina em 100 cepas de Escherichia coli isoladas de pacientes ambulatoriais e hospitalizados de um hospital universitário de nível de atendimento terciário, entre os meses de julho e agosto de 2000, que apresentavam sinais clínicos e laboratoriais de infecção do trato urinário (ITU). Foram pesquisados os genes pap, afa e sfa responsáveis pela expressão de fímbrias através da técnica de PCR. A freqüência dos fatores de virulência entre as cepas estudadas foi de 96,0%, 76,0% e 24,0% para hemolisina, aerobactina e colicina respectivamente, e a prevalência dos genes para os sistemas de adesinas fimbriais foi de 32,0%, 19,0% e 11,0% para os genes pap, sfa e afa respectivamente. As cepas isoladas dos pacientes ambulatoriais exibiram um número maior de fatores de virulência quando comparadas com aquelas provenientes de indivíduos hospitalizados.


 

 

INTRODUCTION

Escherichia coli is one of the major causes of human infectious diseases and is also the most common cause of urinary tract infection (UTI)19. At least 10 to 20% of women experience an acute symptomatic UTI at some point during their lives7. The severity of the infection depends both on the virulence of the infecting bacteria and on the susceptibility of the host. Urinary infections most often occur in patients with anatomically and functionally normal urinary tracts, and involve spontaneous ascent of bacteria from the urethra to the bladder and in a few patients to the kidney8. Adhesion of E. coli to the uroepithelium may protect the bacteria from urinary lavage, increasing their ability to multiply and invade renal tissue12. The uropathogenic E. coli (UPEC) possess adherence factors called pili or fimbriae, which allow them to successfully initiate infections. The two main pili (type 1 and P) found in patients with UTIs, are morphologically similar but differ in their ability to mediate hemagglutination in the presence of mannose20. Specific adhesion is mediated by bacterial proteins termed adhesins which may or may not be associated with fimbriae. Pap (pyelonephritis-associated pili), sfa (S fimbrial adhesin) and afa (afimbrial adhesin) operons are most commonly found encoding respectively, P, S and Afa (also designated Dr hemagglutinin) adhesins3,15.

Besides bacterial adherence, several virulence factors may contribute to the pathogenicity of UPEC, including the production of a-hemolysin, colicin and aerobactin4,5.

In the present study, we analyzed urinary tract E. coli isolates to search for possible evidence of a correlation between biological characteristics that could represent pathogenicity traits of these strains.

 

MATERIAL AND METHODS

Study design and patients: Virulence factors of nosocomial and community-acquired infections data according to obtained from the Clinical Hospital of the School of Medicine of Ribeirão Preto (HCFMRP), concerning E. coli isolated from UTI in-and outpatients, were monitored and analyzed. The study was carried out from July to August 2000. HCFMRP is a university teaching tertiary care hospital.

Bacterial isolates: A total of 100 strains of E. coli isolated from 100 patients (only one isolate from each) distributed as: 13 subjects aged between 0 and 15 years (11women and two men), 18 aged between 16 and 39 years (16 women and two men), and 69 aged > 40 years (40 women and 29 men), were analyzed. Thirty-three of the subjects were hospitalized (inpatients) and 67 were outpatients. UTI diagnoses were established by the hospital medical staff based on clinical symptoms and laboratory investigation. Urinary frequency, internal dysuria and suprapubic or pelvic pain are the characteristic symptoms of cystitis, in general acute pyelonephritis presents fever, flank pain, nausea and vomiting. The laboratory criterion for acute E. coli UTI was the presence of a positive culture response with at least 105 CFU of E. coli per mL of clean-voided urine. Among the subjects there were 15 cases of pyelonephritis. Escherichia coli was identified with the use of standard methods6. The strains were stored and subcultured, for further analysis as previously described1,15.

Hemagglutination and expression of type 1 and P fimbriae: The hemagglutinins were detected by agglutination of erythrocytes from humans blood group O and from guinea pig, in presence or in the absence of D-mannose14.

Hemolysin production: Production of hemolysin was assayed by growing the isolates overnight (16 h), at 37 ºC in Luria-Bertani Broth (LB), 50 µL are spot inoculated onto sheep blood agar base. The culture was incubated at 37 ºC overnight (16 h) and hemolysin production was verified by the presence of a clear hemolytic halo around the spot.

Aerobactin production: Production of aerobactin was assayed by growing isolated strains in LB medium containing 200 µM of a-a dipyridyl at 37 ºC for 24 h, without shaking. The growth was spun for three min (12000 g), supernatants were filtered through a nitrocellulose membrane (0.22 µm) and aliquots of 50 µL were added to orifices made in LA medium previously seeded with strain LG 15222. The plates were incubated at 37 ºC for 48 h and the production of aerobactin was visualized by the growth of strain LG 1522 around the orifices.

Colicin production: Cultures were examined for colicin production by the overlay method, described previously22, with indicator strain MA335 of E. coli.

DNA extraction: E. coli strains were grown in LB broth at 37 ºC overnight (16 h). Bacteria were pelleted from 1.5 mL broth, suspended in 200 µL sterile distilled water, and boiled at 100 ºC for 15 min. Following centrifugation of the lysate, a 150 µL sample of the supernatant was stored at -20 ºC as a template DNA stock11.

PCR: Specific primers were used to amplify sequences of the pap, sfa and afa genes as indicated in Table 1. Primer sequences, predicted sizes of the amplified products, and specific conditions were described by LE BOUGUENEC et al.15.

 

 

RESULTS AND DISCUSSION

Non properly managed from their onset, urinary tract infection can in time, become a real threat, capable of leading to renal failure. A better knowledge of the virulence characteristics of the microorganism causing the infection allows the clinician to anticipate the evolution of infection in the host.

The occurrence of virulence factors in the present study ranged from 11.0% for sfa to 96.0% for hemolysin. Among the adhesins, the P fimbriae was the most prevalent (42 strains), followed by type 1 fimbriae (25 strains) (Table 2), these results not agree with published reports10,18,21, which emphasize the predominance of fimbriae type 1 among the UPEC strains.

 

 

The presence of hemolysin and colicin, was related to tissue damage, and the prevalence of aerobactin which confers the capacity to bind iron5 among our isolates, was higher than those reported by other investigators10,21. However, the high prevalence of these virulence factors among the isolates from pyelonephritis in the present report agrees with that reported by others16,17. In general the virulence factors from outpatient isolates were found in more than double amounts compared with those from the nosocomial isolates (Table 2).

Based on the distribution of the various target sequences, the strains studied exhibited 10 most common virulence patterns, referred to as Ec followed by an Arabic numeral (Table 3). The strains isolated from patients admitted in hospital exhibited a great diversity of gene patterns, showing the Ec 1, Ec 2, Ec 3 and Ec 7 patterns in common with outpatients patterns and 14 new patterns that appear once a time, it means 43.7% of diversity in virulence patterns (results not showed), in agreement with other report21. The presence of the afa operon together with aerobactin was detected in the same strain as the Ec 4 pattern (Table 3); this association had been previously reported21. A co-dependence of these virulence factors in a particular pathogenic pathway has been discussed13 but needs to be confirmed.

 

 

Out of the 100 uropathogenic E. coli isolates tested by PCR, 49 carried sequences related to the three adhesion-encoding operon families investigated. Twenty, 10 and six of the isolates respectively, exhibited pap, afa and sfa genotypes alone (Table 4). The distribution of the S fimbriae-encoding operons found among the isolates studied was lower than previously reported1,18,21 but agree with those reported by others3,15. Regarding P fimbriae, pooled results from other studies indicate that among E. coli isolates from patients with pyelonephritis and cystitis, approximately 80% and 30% respectively, possess P fimbriae4,10. Although the frequency of pap in a cystitis strain agrees with literature data, we found that only 26.6% of the pyelonephritis strains contain pap sequences (Table 4). It is noteworthy that most of the pyelonephritis strains studied were isolated from patients with chronic infections and other diseases that complicate their clinical pictures of. Additional epidemiological studies have to be carried out to confirm this observation. However, these data agree with those reported by USEIN et al.21 in Romania.

 

 

A total of 12 isolates carried both pap and sfa operons, and one isolate carried both sfa and afa operons what it is new from other reports1,3,15,18,21, while the simultaneous presence of pap-afa operons was not detected, differently from others3,15,18 . A small number of UTI strains possessing afa-afimbrial adhesions have been reported1,3,15. Growing importance is attributed to the afa operon, which has been implicated in the development of chronic interstitial nephritis9. We found a small increase in the percentage of afa PCR-positive strains in isolates from patients with pyelonephritis (13.3%), compared with those associated with cystitis (9.4%) (Table 4); however, this finding indicates the need for studies on the association.

In conclusion, the strains isolated from patients attended at the outpatient clinic exhibited a higher number of virulence factors per strain and seemed to be more aggressive than strains from hospitalized patients, emphasizing the importance of these infected patients that arrive at a tertiary care teaching hospital. This study of the E. coli strains isolated from UTI in this kind of hospital was meant as a step towards improving the knowledge regarding their virulence genetic determinants.

 

ACKNOWLEDGMENTS

The authors thank Tania Marques for technical assistance. This work is part of a thesis submitted by Edilene Santo to UNESP University in partial fulfillment of the requirements for the Master's degree.

 

REFERENCES

1. BLANCO, M.; BLANCO, J.E.; ALONSO, M.P. et al. - Detection of pap, sfa and afa adhesin-encoding operons in uropathogenic Escherichia coli strains: relationship with expression of adhesins and production of toxins. Res. Microbiol., 148: 745-755, 1997.         [ Links ]

2. CARBONETTI, N.H. & WILLIAMS, P.H. - Detection of synthesis of the hydroxamate siderophore aerobactin by pathogenic isolates of Escherichia coli. In: SUSSMAN, M. The virulence of Escherichia coli. Reviews and methods. Orlando, Academic Press, 1985. p. 419-424.         [ Links ]

3. DAIGLE, F.; HAREL, J.; FAIRBROTHER, J.M. & LEBEL, P. - Expression and detection of pap-, sfa-, and afa-encoded fimbrial adhesin systems among uropathogenic Escherichia coli. Canad. J. Microbiol., 40: 286-291, 1994.         [ Links ]

4. DONNENBERG, M.S. & WECH, R.A. - Virulence determinants of uropathogenic Escherichia coli. In: MOBLEY, H.L.T. & WARREN, J.W., ed. Urinary tract infections: molecular pathogenesis and clinical management. Washington, ASM Press, 1996. p. 135-174.         [ Links ]

5. EMODY, L.; KERÉNYI, M. & NAGY, G. - Virulence factors of uropathogenic Escherichia coli. Int. J. Antimicrob. Agents, 22 (suppl.): S29-S33, 2003.         [ Links ]

6. FARMER, J.J. - Enterobacteriaceae: introduction and identification. In: MURRAY, P.R.; BARON, E.J.; PHALER, M.A.; TENOVER, F.C. & YOLKEN, R.H. ed. Manual of clinical microbiology. 7. ed. Washington, ASM Press, 1999.         [ Links ]

7. FOXMAN, B. - Epidemiology of urinary tract infection: incidence, morbidity and economic costs. Amer. J. Med., 113 (suppl): 5S-13S, 2002.         [ Links ]

8. FOWLER Jr., J.E. & STAMEY, T.A. - Studies of introital colonization in women with recurrent urinary infections. VII. The role of bacterial adherence. J. Urol., 117: 472-476, 1977.         [ Links ]

9. GOLUSZKO, P.; MOSELEY, S.; TRUONG, L.D. et al. - Development of experimental model of chronic pyelonephritis with Escherichia coli O75: K5: H-bearing Dr fimbriae: mutation in the dra region prevented tubulointerstitial nephritis J. clin. Invest., 99: 1662-1672, 1997.         [ Links ]

10. JOHNSON, J.R. - Virulence factors in Escherichia coli urinary tract infection. Clin. Microbiol. Rev., 4: 80-128, 1991.         [ Links ]

11. KESKIMAKI, M.; EKLUND, M.; PESONEN, H. et al. - EPC, EAEC, and STEC in stool specimens: prevalence and molecular epidemiology of isolates. Diag. Microbiol. infect. Dis., 40: 151-156, 2001.         [ Links ]

12. KORHONEN, T.K.; VIRKOLA, R.; WESTERLUND, B. et al. - Tissue interactions of Escherichia coli adhesins. Antonie van Leeuwenhoek, 54: 411-420, 1988.         [ Links ]

13. LALIOUI, L. & LE BOUGUENEC, C. - afa-8 gene cluster is carried by a pathogenicity island inserted into the tRNAPhe of human and bovine pathogenic Escherichia coli isolates. Infect. Immun., 69: 937-948, 2001.         [ Links ]

14. LATHAM, R.H. & STAMM, W.E. - Role of fimbriated Escherichia coli in urinary tract infections in adult women: correlation with localization studies. J. infect. Dis., 149: 835-840, 1984.         [ Links ]

15. LE BOUGUENEC, C.; ARCHAMBAUD, M. & LABIGNE, A. - Rapid and specific detection of the pap, afa, and sfa adhesion-encoding operons in uropathogenic Escherichia coli strains by polymerase chain reaction. J. clin. Microbiol., 30: 1189-1193, 1992.         [ Links ]

16. O'HANLEY, P.; LOW, D.; ROMERO, I. et al. - Gal-Gal binding and hemolysin phenotypes and genotypes associated with uropathogenic Escherichia coli. New Engl. J. Med., 313: 414-420, 1985.         [ Links ]

17. SANDBERG, T.; KAIJSER, B.; LIDIN-JANSON, G. et al. - Virulence of Escherichia coli in relation to host factors in women with symptomatic urinary tract infection. J. clin. Microbiol., 26: 1471-1476, 1988.         [ Links ]

18. SILVEIRA, W.D.; BENETTI, F.; LANCELLOTTI, M. et al. - Biological and genetic characteristics of uropathogenic Escherichia coli strains. Rev. Inst. Med. trop. S. Paulo, 43: 303-310, 2001.         [ Links ]

19. STAMM, W.E. - Scientific and clinical challenges in the management of urinary tract infections. Amer. J. Med., 113 (suppl. 1 A): 1S-4S, 2002.         [ Links ]

20. SVANBORG, C. & GODALY, G. - Bacterial virulence in urinary tract infection. Infect. Dis. Clin. N. Amer., 11: 513-529, 1997.         [ Links ]

21. USEIN, C.R.; DAMIAN, M.; TATU-CHITOIU, D. et al. - Prevalence of virulence genes in Escherichia coli strains isolated from Romanian adult urinary tract infection cases. J. cell. molec. Med., 5: 303-310, 2001.         [ Links ]

22. VIDOTTO, M.C.; MULLER, E.E.; FREITAS, J.C. et al. - Virulence factors of avian Escherichia coli. Avian Dis., 34: 531-538, 1990.        [ Links ]

 

 

Received: 15 August 2005
Accepted: 26 April 2006

 

 

Correspondence to:
José Moacir Marin
Phone: +55.16.3602-4101
email: jmmarin@forp.usp.br

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