点击显示 收起
Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de So Paulo
Instituto Adolfo Lutz
Departamento de Patologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de So Paulo, So Paulo, Brazil
Department of Microbiology and Immunology, University of Maryland, Baltimore, Maryland
ABSTRACT
One hundred twelve diffusely adherent Escherichia coli strains isolated from children in a case control study were evaluated for virulence-associated characteristics, serotyping, antibiotic resistance, and plasmid profiles. Half of the strains hybridized with the probes for icuA (aerobactin) and fimH (type 1 pili); daaE (F1845 fimbriae), afa (afimbrial Dr adhesin), agg-3A (aggregative adhesion fimbria type III fimbriae), pap (P fimbriae), astA (EAST1 toxin), and shET1 (Shigella enterotoxin 1) sequences were present in <20% of the strains. The shET1 gene was noted most frequently in strains isolated from patients. A minority (7%) of the strains produced hemolysin or colicin or showed cytotoxic effects on Vero cells. Forty-five different serotypes were found. The majority (70%) of the strains presented multiple antibiotic resistance. Antibiotic resistance and diffuse adherence were located on the same conjugative plasmids. These results suggest that the transfer of these potential virulence markers could be important in the epidemiology of diffusely adherent E. coli.
TEXT
Diffusely adherent Escherichia coli strains that are identified by their diffuse adherence (DA) pattern on cultured epithelial cells in vitro (24) have been recognized as the sixth class of diarrheagenic E. coli (17).
Two putative adherence factors have been described for diffusely adherent E. coli strains. Bilge et al. (6) have characterized surface fimbriae (designated F1845) that are responsible for the DA phenotype in a prototype strain, C1845. The gene cluster that encodes this fimbriae can be found on either the bacterial chromosome or a plasmid. F1845 fimbriae are homologous at the nucleotide and amino acid levels with members of the Afa/Dr family of adhesins (Afa-I, Afa-III, Dr, Dr-II, and F1845) (18). Afa/Dr diffusely adherent E. coli strains are identified in epidemiological studies by hybridization to a specific probe, daaC, which is common to operons encoding Afa/Dr adhesins (6). A second putative adhesin associated with the DA phenotype, an outer membrane protein, designated AIDA-I, has been described by Benz and Schmidt (4).
In a number of epidemiological studies, diffusely adherent E. coli strains have been associated with diarrheal disease in different geographic areas (2, 11, 12, 13). However, the diffusely adherent E. coli virulence markers associated with diarrhea are yet to be clarified. In this paper, 112 diffusely adherent E. coli strains isolated in a case control study (61 from patients and 51 from healthy control subjects) (25) were tested for a number of phenotypic and genotypic characteristics associated with potential E. coli virulence factors. We further characterized these strains by determining their serotypes, antibiotic resistance patterns, and the role of plasmids in mediating the diffuse adherence.
Strains were screened for hemolytic activity on blood agar base plates containing 5% sheep erythrocytes washed with phosphate-buffered saline. The plates were observed for lysis of erythrocytes after 24 h of growth at 37°C. Strains were tested for enterotoxin production by the Y1 adrenal cell culture method of Donta et al. (10) and by the infant mouse assay of Dean et al. (9). Cytotoxin production was detected by the Vero cell culture assay (15). Colicin production was detected by using the agar overlay method of Azevedo and Costa (1).
DNA probes for virulence factors associated with other pathogenic E. coli strains were employed in hybridization experiments as described previously (25) (Table 1).
Serotyping was performed by the method of rskov and rskov (21) with antisera against E. coli O antigens 1 to 181 and H antigens 1 to 53.
Antibiotic susceptibility testing was performed by the standard disk diffusion method of Bauer and Kirby (3). The antibiotic disks used were ampicillin (10 μg), cephalothin (30 μg), ciprofloxacin (5 μg), chloramphenicol (30 μg), cotrimoxazole (10 μg), lomefloxacin (10 μg), ceftazidime (30 μg), ofloxacin (5 μg), streptomycin (10 μg), gentamicin (10 μg), nalidixic acid (30 μg), sulfonamide (300 μg), and tetracycline (30 μg).
To test for the presence of DA conjugative plasmids, diffusely adherent E. coli isolates that were resistant to ampicillin, streptomycin, and tetracycline were mated with the E. coli K-12 C600 strain (supE44 hsdR thr-1 leuB6 lacY1 tonA21 Nalr Fur), as described elsewhere (23). The donor and recipient strains were grown in Luria broth for 18 h, mixed on the surface of Mueller-Hinton agar plates, and incubated for 24 h at 37°C. Transconjugants were selected on plates containing nalidixic acid (100 μg/ml) with ampicillin (100 μg/ml), tetracycline (30 μg/ml), and streptomycin (100 μg/ml) and were tested for HEp-2 cell adherence using the assay of Scaletsky et al. (24).
Colicin production was found in eight strains isolated from six patients and two healthy control subjects. Six strains isolated from four patients and two controls were hemolysin producers and hybridized with the hly probe. No strains produced enterotoxins as tested by the Y1 adrenal cell culture method and by the infant mouse assay. Eight strains isolated from six patients and two controls showed a cytotoxic effect on Vero cells after 3-h incubation (data not shown). A similar cytotoxic effect on HEp-2 cells was observed by Jallat et al. (13) in 16 diffusely adherent E. coli strains, 14 from patients and 2 from controls, in France.
According to the hybridization studies, 48% of strains harbored the iucA gene that is involved in the synthesis of the aerobactin siderophore (Table 1). In a recent study, it has been reported that 50% of the diffusely adherent E. coli strains hybridize with the irp2 probe, which is part of the yersiniabactin operon, encoding a siderophore-dependent iron transport system (8). Therefore, it appears that the genes for aerobactin and yersiniabactin siderophore production are widely distributed among diffusely adherent E. coli strains, as they are for enteroaggregative E. coli (20).
In addition, some strains possessed genes encoding the EAST1 toxin (astA) and eight strains had the shET1 sequence, virulence factors found frequently in enteroaggregative E. coli strains (28). The astA gene was detected more frequently in strains from patients (18%) than in strains from control subjects (12%). Of the eight strains with the shET1 profile, seven (87.5%) were isolated from children with diarrhea who carried no other well-established enteropathogen. To our knowledge, this is the first report of the prevalence of shET1 in diffusely adherent E. coli strains. Further studies are necessary to determine whether other virulent factors play a role in the pathogenicity of the diffusely adherent E. coli strains.
The cnf1 gene encoding cytotoxic necrotizing factor 1 was found in two strains from both patients and healthy controls. This virulence factor has been found in cell-detaching E. coli strains from children with and without diarrhea (19). None of the 112 strains hybridized with the cdt, pet, pic, shET2, and espC probes.
Besides the F1845 fimbriae and AIDA-I, little is known about possible adhesins expressed by diffusely adherent E. coli strains. We investigated the presence of putative adhesins in an attempt to identify the factor responsible for the DA phenotype. As shown in Table 1, 15 (13%) strains carried the daaE (F1845 major fimbrial subunit), and 17 (15%) other strains carried the afa (afimbrial adhesin) sequence, an afimbrial adhesin of the Dr family. The fimH gene, which encodes adhesin subunit type 1 fimbriae, was the most frequently found (54 strains [48%]). This adhesin is present in nearly all E. coli strains, including commensal strains (14). Our results for afa, agg-3A, sfa, and pap extended the observations of previous reports that investigated the distribution of some of these adhesins in a limited number of strains (16). Indeed, 20 strains carried the agg-3A sequence that encodes the aggregative adhesion fimbria type III (AAF/III) fimbrial subunit, 6 strains hybridized with pap (P fimbria), 3 strains hybridized with sfa (S fimbria), and one strain hybridized with aggA (AAF/I fimbria) probes. Thus, at least half of the strains must have adhered by means of an adhesin different from those described so far. Further studies are necessary to characterize the adhesin(s) of diffusely adherent E. coli strains.
The serotypes of the 112 diffusely adherent E. coli strains are indicated in Table 2. In total, 45 different serotypes were found. Thirty-five strains were O nontypeable, and three were rough.
A variety of different combinations of the specific virulence DNA sequences and serotypes was observed in diffusely adherent E. coli isolates from both patients with diarrhea and healthy controls (Table 2). However, an interesting combination of virulence markers was found in some of the strains studied: three strains isolated from patients of serotypes O89:HNT, O99:H33, and O126:H16, for example, carried astA shET1 sequences, which suggests that these strains are potentially pathogenic E. coli strains.
Frequent antibiotic use could predispose or select for infection with antibiotic-resistant diffusely adherent E. coli strains. In addition, antibiotic resistance patterns could serve as markers for virulent strains whose virulence factors have not been identified. For these reasons, we sought to characterize antibiotic resistance rates in our diffusely adherent E. coli isolates. The frequencies of resistance to ampicillin, cephalothin, cotrimoxazole, streptomycin, sulfonamide, and tetracycline were each >50%. Resistance to chloramphenicol (20%) was less frequent. All the isolates were susceptible to ceftazidime, gentamicin, lomefloxacin, ofloxacin, and nalidixic acid, and two strains were susceptible to all antibiotics tested.
Since it is well-known that plasmids are responsible for the horizontal spread of antibiotic resistance between microorganisms, we wanted to know whether the DA phenotype could be cotransferred by conjugation into an E. coli K-12 recipient strain. It was not possible to examine all isolates for plasmids, but in conjugation experiments, the transfer of multiple drug resistance was observed in 10 isolates from 6 patients and 4 controls (Table 3). In these in vitro conjugation experiments, 6 of the 10 isolates transferred only drug resistance to the recipient strain. Four isolates, however, transferred drug resistance determinants and DA phenotype to E. coli recipient C600. By transforming E. coli K-12 DH5 (supE44 lacU169 hsdR17 recA1 endA1 gyrA96 thi-1 relA1 Nalr) (23) with plasmid DNA from two isolates (strains 67 and 79), we were able to demonstrate that genes encoding ampicillin, streptomycin, and tetracycline resistance and diffuse adherence were encoded on a 67- to 75-MDa conjugative plasmid. Curing an Apr Smr Tcr DA transconjugant with acridine orange showed that both resistance and adherence traits were lost simultaneously.
In conclusion, our results show that diffusely adherent E. coli strains isolated from patients and control subjects present very different profiles when virulence markers and serotypes are considered. Among the virulence factors, Shigella enterotoxin 1 was noted most frequently in strains isolated from patients. The present study also demonstrated the high rate of resistance to certain antimicrobial agents in diffusely adherent E. coli strains in which resistance is apparently associated with conjugative plasmids. We also found plasmids encoding multiple drug resistance along with adhesion genes. The transfer of these potential virulence markers could be important in the epidemiology of diffusely adherent E. coli strains.
ACKNOWLEDGMENTS
We thank Rosa M. Silva for critically reading the manuscript and helpful comments.
This work was funded by Conselho Nacional de Desenvolvimento Científico e Tecnologico (CNPq) and Fundao de Amparo a Pesquisa do Estado de So Paulo (FAPESP).
REFERENCES
Azevedo, J. L., and S. O. P. Costa. 1973. Exercícios práticos de genetica, cia ed. Nacional e EDUSP, So Paulo, Brazil.
Baqui, A. H., R. B. Sack, R. E. Black, K. Haider, A. Hossain, A. R. Alim, M. Yumus, H. R. Chowdhury, and A. K. Siddique. 1992. Enteropathogens associated with acute diarrhea and persistent diarrhea in Bangladeshi children <5 years of age. J. Infect. Dis. 166:792-796.
Bauer, A. W., and W. N. N. Kirby. 1996. Antibiotic susceptibility testing by a standardized single disc method. Am. J. Clin. Pathol. 45:493-496.
Benz, I., and M. A. Schmidt. 1989. Cloning and expression of an adhesin (AIDA-I) involved in diffuse adherence of enteropathogenic Escherichia coli. Infect. Immun. 57:1506-1511.
Bernier, C., P. Gounon, and C. Le Bouguenec. 2002. Identification of an aggregative adhesion fimbria (AAF) type III-encoding operon in enteroaggregative Escherichia coli as a sensitive probe for detecting the AAF-encoding operon family. Infect. Immun. 70:4302-4311.
Bilge, S. S., C. R. Clausen, W. Lau, and S. L. Moseley. 1989. Molecular characterization of a fimbrial adhesin, F1845, mediating diffuse adherence of diarrhea-associated Escherichia coli to HEp-2 cells. J. Bacteriol. 171:4281-4289.
Campos, L. C., M. A. M. Vieira, L. R. Trabulsi, L. A. Silva, V. Monteiro-Neto, and T. A. T. Gomes. 1999. Diffusely adhering Escherichia coli (DAEC) strains of fecal origin rarely express F1845 adhesin. Microbiol. Immunol. 43:167-170.
Czeczulin, J. R., T. S. Whittam, I. R. Henderson, F. Navarro-Garcia, and J. P. Nataro. 1999. Phylogenetic analysis of enteroaggregative and diffusely adherent Escherichia coli. Infect. Immun. 67:2692-2699.
Dean, A. G., Y. C. Ching, R. G. Williams, and L. B. Harden. 1972. Test for Escherichia coli enterotoxin using infant mice: application in a study of diarrhea in children in Honolulu. J. Infect. Dis. 125:407-411.
Donta, S. T., H. W. Moon, and S. C. Whipp. 1974. Detection of heat-labile Escherichia coli enterotoxin with the use of adrenal cells in tissue culture. Science 183:334-336.
Giron, J. A., T. Jones, F. Millán-Velasco, E. C. Munoz, L. Zarate, J. Fry, G. Frankel, S. L. Moseley, B. Baudry, J. B. Kaper, G. K. Schoolnik, and L. W. Riley. 1991. Diffuse-adhering Escherichia coli (DAEC) as a putative cause of diarrhea in Mayan children in Mexico. J. Infect. Dis. 163:507-513.
Gunzburg, S. T., B. J. Chang, S. J. Elliott, V. Burke, and M. Gracey. 1993. Diffuse and enteroaggregative patterns of adherence of enteric Escherichia coli isolated from aboriginal children from the Kimberley region of western Australia. J. Infect. Dis. 167:755-758.
Jallat, C., V. Livrelli, A. Darfeuille-Michaud, C. Rich, and B. Joly. 1993. Escherichia coli strains involved in diarrhea in France: high prevalence and heterogeneity of diffuse adhering strains. J. Clin. Microbiol. 31:2031-2037.
Johnson, J. R., and A. L. Stell. 2000. Extended virulence genotypes of Escherichia coli strains from patients with urosepsis in relation to phylogeny and host compromise. J. Infect. Dis. 181:261-272.
Konowalchuk, J., J. I. Speirs, and S. Stavric. 1977. Vero response to a cytotoxin of Escherichia coli. Infect. Immun. 18:775-779.
Le Bouguenec, C., M. Archambaud, and A. Labigne. 1992. Rapid and specific detection of the pap, afa, and sfa adhesin-encoding operons in uropathogenic Escherichia coli strains by polymerase chain reaction. J. Clin. Microbiol. 30:1189-1193.
Nataro, J. P., and J. B. Kaper. 1998. Diarrheagenic Escherichia coli. Clin. Microbiol. Rev. 11:142-201.
Nowicki, B., A. Labigne, S. Mosely, R. Hull, S. Hull, and J. Moulds. 1990. The Dr hemagglutinin, afimbrial adhesins AFA-I and AFA-III, and F1845 fimbriae of uropathogenic and diarrhea-associated Escherichia coli belong to a family of hemagglutinins with Dr receptor recognition. Infect. Immun. 58:279-281.
Okeke, I. N., H. Steinruck, K. J. Kanack, S. J. Elliott, L. Sundstrom, J. B. Kaper, and A. Lamikanra. 2002. Antibiotic-resistant cell-detaching Escherichia coli strains from Nigerian children. J. Clin. Microbiol. 40:301-305.
Okeke, I. N., I. C. A. Scaletsky, E. H. Soars, L. R. Macfarlane, and A. G. Torres. 2004. Molecular epidemiology of the iron utilization genes of enteroaggregative Escherichia coli. J. Clin. Microbiol. 42:36-44.
rskov, F., and I. rskov. 1984. Serotyping of Escherichia coli. Methods Microbiol. 14:43-112.
Oswald, E., P. Pohl, E. Jacquemin, P. Lintermans, K. van Muylen, A. D. O'Brien, and J. Mainil. 1994. Specific DNA probes to detect Escherichia coli strains producing cytotoxic necrotizing factor type 1 or 2. J. Med. Microbiol. 40:428-434.
Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
Scaletsky, I. C. A., M. L. M. Silva, and L. R. Trabulsi. 1984. Distinctive patterns of adherence of enteropathogenic Escherichia coli to HeLa cells. Infect. Immun. 45:534-536.
Scaletsky, I. C. A., S. H. Fabbricotti, K. R. Aranda, M. B. Morais, and U. Fagundes-Neto. 2002. Comparison of DNA hybridization and PCR assays for detection of putative pathogenic enteroadherent Escherichia coli. J. Clin. Microbiol. 40:1254-1258.
Scott, D. A., and J. P. Kaper. 1994. Cloning and sequencing of genes encoding Escherichia coli cytolethal distending toxin. Infect. Immun. 62:244-251.
Stein, M., B. Kenny, M. A. Stein, and B. B. Finlay. 1996. Characterization of EspC, a 110-kilodalton protein secreted by enteropathogenic Escherichia coli which is homologous to members of the immunoglobulin A protease-like family of secreted proteins. J. Bacteriol. 178:6546-6554.
Vila, J., M. Vargas, I. R. Henderson, J. Gascon, and J. P. Nataro. 2000. Enteroaggregative Escherichia coli virulence factors in traveler's diarrhea strains. J. Infect. Dis. 182:1780-1783.
Welch, R. A., R. Hell, and S. Falkow. 1983. Molecular cloning and physical characterization of a chromosomal hemolysin from Escherichia coli. Infect. Immun. 42:178-186.
Yamamoto, T., and P. Echeverria. 1996. Detection of enteroaggregative Escherichia coli heat-stable enterotoxin 1 gene sequences in enterotoxigenic E. coli strains pathogenic for humans. Infect. Immun. 64:1441-1445.