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Journal of Clinical Microbiology, December 2002, p. 4585-4593, Vol. 40, No. 12
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.12.4585-4593.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Clinical Escherichia coli Strains Carrying stx Genes: stx Variants and stx-Positive Virulence Profiles

Marjut Eklund, Kirsikka Leino, and Anja Siitonen^*

Laboratory of Enteric Pathogens, National Public Health Institute, FIN-00300 Helsinki, Finland

Received 21 May 2002/ Returned for modification 31 July 2002/ Accepted 20 September 2002

Top Abstract Introduction Materials and Methods Results Discussion References

 
Altogether, 173 Shiga toxin-producing Escherichia coli (STEC) serotype O157 (n = 111) and non-O157 (n = 62) isolates from 170 subjects were screened by PCR-restriction fragment length polymorphism for eight different stx genes. The results were compiled according to serotypes, phage types of O157, production of Stx toxin and enterohemolysin, and the presence of eae. The stx genes occurred in 11 combinations; the most common were stx₂ with stx_2c (42%), stx₂ alone (21%), and stx₁ alone (16%). Of the O157 strains, 64% carried stx₂ with stx_2c versus 2% of the non-O157 strains (P < 0.001). In the non-O157 strains, the prevailing gene was stx₁ (99% versus 1% in O157 strains; P < 0.001). In addition, one strain (O Rough:H4:stx_2c) which has not previously been described as associated with hemolytic-uremic syndrome (HUS) was found. Ten stx-positive virulence profiles were responsible for 71% of all STEC infections. Of these profiles, five accounted for 71% of the 21 strains isolated from 20 patients with HUS or thrombotic thrombocytopenic purpura (TTP). The strains having the virulence profile that caused mainly HUS or TTP or bloody diarrhea produced Stx with titers of 1:128 (90%) more commonly than did other strains (51%; P < 0.001). These strains were also more commonly enterohemolytic (98% versus 68% for other strains; P < 0.001) and possessed the eae gene (100%) more commonly than did other strains (74%; P < 0.001). A particular virulence profile, O157:H7:PT2:stx₂:stx_2c:eae:Ehly, was significantly more frequently associated with HUS and bloody diarrhea than were other profiles (P = 0.02) and also caused the deaths of two children. In this study, the risk factors for severe symptoms were an age of <5 years and infection by the strain of O157:H7:PT2 mentioned above.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Shiga toxin-producing Escherichia coli (STEC) cells have emerged as new food-borne pathogens of clinical and public health concern (35). The most epidemic STEC serogroup has been O157, but about 200 other STEC serogroups have beenidentified (http://www.microbionet.com.au/frames/feature/vtec/brief01.html). Shiga toxins (Stx1 and/or Stx2) have a prominent role in the pathogenesis of STEC bacteria (15, 20, 26). The clinical picture of a STEC infection may vary from an asymptomatic state to bloody diarrhea and severe life-threatening complications such as hemolytic-uremic syndrome (HUS) or thrombotic thrombocytopenic purpura (TTP) (35). Children and elderly people have been more susceptible to STEC infections than healthy adults (32). It is estimated that the incidence of HUS varies from 2.0 to 3.0 cases per 100,000 children under 5 years of age (15) and from 0.9 to 1.2 cases per 100,000 in children under 18 years of age (5, 43).

The pathogenesis of STEC infection in humans is not fully understood. It is considered to be multifactorial and dependent on several bacterial virulence factors such as enterohemolysin (Ehly) and the eae gene, in addition to host factors (6, 35). A recent discovery of a quorum-sensing system, mediated by self-produced extracellular factors, may play an important role in the control of the colonization of STEC O157 on human cells (17, 18, 44). The main bacterial properties in the pathogenesis of HUS, however, are considered to be the Stx toxins encoded by the stx genes. It is known that STEC strains frequently carry more than one stx gene, and several variants of these genes (e.g., stx_1c, stx_1vO111, stx_2vha, stx_2vhb, stx_2vOX392, stx_2vOX393, stx_2c, stx_2d-Ount, stx_2d-OX3a, stx_2e, stx_2ev, stx_2f) have been found (1, 16, 27, 30, 37, 41, 42, 46, 48). In the literature, different designations have been used for the same genes, causing confusion. However, recently, Scheutz et al. (40) compiled data on the designations of the stx genes. In the Stx2 toxin family, the amino acid homologies in the A subunit to the mature Stx2 are 93, 99, and 100% for Stx2e, Stx2d (also designated as Stx2vh [40]), and Stx2c, respectively (31). The corresponding percentages in the B subunit are 84, 97, and 97% (31).

Previously obtained data (13, 16, 37) have suggested that not only the main toxin type but also the toxin variant type could be important in determining the probability of developing HUS. For example, humans infected by strains producing Stx2 have developed HUS more frequently than those infected by strains producing Stx1 only (7, 34). Of the stx₂ variants, stx_2c has been associated with HUS but the risk of developing HUS after infection with STEC of the stx_2c genotype has been significantly lower than that after infection with STEC of the stx₂ genotype only (13, 16). The strains carrying the stx_2d genes encoding VT2d-Ount or VT2d-OX3a have been concluded to be less pathogenic for humans than other Stx2-class-toxin-producing strains (37). stx_2d has been associated with various forms of diarrhea but not with HUS (13). Of the other stx variants, stx_2e has been associated with edema disease in pigs (30, 46) though it has been detected rarely in human infections (13). stx_2f has been isolated in STEC isolates from pigeons, and only a single STEC human isolate harboring a similar stx gene has been found (41).

By combining PCR with restriction fragment length polymorphism (PCR-RFLP) (37), we investigated all the 173 human STEC strains isolated during the period from 1990 to 2000 from Finns with STEC infection to evaluate the prevalence of the stx_2d genes for VT2d-Ount (hereafter referred to as stx_2d-Ount) or VT2d-OX3a (hereafter stx_2d-OX3a) among these strains. We also subtyped all STEC isolates for the possession of the stx₁/stx_1vO111 (hereafter stx₁), stx₂, stx_2c/stx_2vha/stx_2vOX393 (hereafter stx_2c), stx_2vhb, stx_2vO111/stx_2vOX392 (hereafter stx_2vO111 and stx_2vOX392), stx_2e, and stx_2ev genes (1, 27). In addition, the association of these stx genes with the clinical pictures of the subjects and with several other bacterial characteristics (the serotype, the possession of the eae gene, the titers of the Stx toxins, the production of Ehly, and the phage types [PTs] of the serogroup O157 strains) was studied. We also searched for specific virulence profiles potentially associated with the clinical picture of STEC infection.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Subjects. The age data and the clinical pictures (HUS or TTP, bloody diarrhea, nonbloody diarrhea, or asymptomatic carriage) of the 170 subjects were indicated on a special form that always accompanied the isolate that was received from the clinical microbiology laboratory, or the diagnosis was inquired from the hospital over the telephone. Also, the relationship between asymptomatic carriers and STEC-infected patients was indicated. The subjects were divided into seven age groups: <1, 1 to 5, 6 to 15, 16 to 25, 26 to 55, 56 to 65, and >65 years old (38).

STEC strains. One hundred seventy-three STEC strains (O157 isolates, n = 111; non-O157 isolates, n = 62) were isolated from Finns (n = 170) during an 11-year period (1990 to 2000). The pure cultures of the isolates or fecal cultures of the STEC-infected patients were referred to the Finnish routine microbiological laboratories for microbiological verification and detection of the stx₁, stx₂, and eae genes by PCR. All STEC isolates were also serotyped and their enterohemolytic activity was investigated, and the STEC O157 isolates were phage typed as previously described (12, 25, 39). Certain single characteristics of 161 strains have been reported previously (12, 22, 23, 24, 25, 39). Of the 173 strains, 15 were derived from one major outbreak (36) caused by strains of serotype O157:H7:PT2:stx₂:stx_2c (39). In addition, 65 strains were associated with small family clusters in 24 families.

Shiga toxin production. The production of Stx1 and Stx2 by the isolates was determined by using a reversed-passive latex agglutination kit (VTEC-RPLA; Denka Seiken Co., Ltd., Tokyo, Japan) after having been grown and shaken in 5 ml of Casamino Acids-yeast extract broth overnight at 37°C. Of this suspension, 1 ml was shaken with 1 ml of polymyxin B (5,000 U) solution (2) for 1 h at 37°C and was then centrifuged for 30 min at 3,000 rpm (BiofugeA instrument Heraeus, Sepatech, West Germany). The titer of the supernatant was determined in the VTEC-RPLA test according to the manufacturer's instructions up to 1:128. All strains were tested for the production of Stx1 and Stx2. Titers lower than 1:4 were interpreted as negative.

Detection of stx genes by PCR-RFLP. PCRs for the stx₁, stx₂, and stx₂ variants (1, 27, 37) (Table 1) were executed with minor modifications: boiled bacterial supernatant (1.0 µl) was used as a template, and a final elongation step (10 min at 72°C) was added to each PCR run (39). Amplified DNA fragments of specific sizes were located in electrophoresis gels by UV fluorescence after staining with ethidium bromide. Strain ATCC 43895 (RH 4270) was used as a positive control in the run according to Lin et al. (27) and Bastian et al. (1). Strain LMG 18459 (RH 4872) (the Belgian Coordinated Collections of Microorganisms-Laboratorium voor Microbiologie Universiteit Gent bacterium collection, Universiteit Gent, Ghent, Belgium) was used as a positive control in the run according to Piérard et al. (37). In all runs, strain ATCC 25922 (RH 1484) was used as a negative control. The stx-positive PCR products were restricted with 20 U of four restriction enzymes (New England Biolabs Inc., Beverly, Mass.): a ca. 900-bp fragment with HincII and AccI (1, 27) and a 348-bp fragment with HaeIII and PvuII (37).

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TABLE 1. stx genes expected to be detected by PCR or PCR-RFLP methods used in this study

Statistical methods. Epi-Info 2000 version 1.1.2 was used for Fisher's exact two-tailed test. A P of <0.05 indicated statistical significance.

Top Abstract Introduction Materials and Methods Results Discussion References

 
stx genotypes. Of the 173 STEC strains studied, 168 (97%) gave stx-positive results in PCR for the HincII and AccI restriction enzymes. Three strains were repeatedly negative in PCR, and two showed very weak positive reactions. The 168 STEC strains that were clearly positive in PCR were divided into 11 groups after HincII and AccI endonuclease restriction (Table 2). Seventy-two (42%) of all 173 strains possessed stx₂ in combination with stx_2c. The stx₂ gene alone was found in 36 strains (21%); the stx₁ gene was found alone in 28 strains (16%) and in combination with either stx₂ or some stx₂ variants (stx_2c and stx_2vhb) in 10 strains (6%). Of the latter strains, one possessed three stx genes: stx₁, stx₂, and stx_2vhb. Nine strains (5%) were positive for stx_2c only, five strains were positive for stx_2vhb, and three strains were positive for both stx₂ and stx_2vhb. Five strains were positive in PCR but were undigestible by the HincII or AccI restriction enzymes (Table 2).

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TABLE 2. stx genes in 173 STEC isolates and toxin production of the strains

In PCR for screening stx_2d, only two strains of the 173 were positive (1%). Both of them were confirmed as the stx_2d-Ount variant type after HaeIII and PvuII restriction (Table 2). These strains were undigestible by the HincII or AccI restriction enzymes in the PCR according to Lin et al. (27) and Bastian et al. (1).

Stx production. Of the 173 strains, 169 (98%) produced Stx1 or Stx2 or both (Table 2). The majority of the strains (119 of 173 [69%]) produced Stx with high titers (1:128) not depending on their stx type. However, of the 168 PCR-positive strains, 98 (87%) of the 113 strains possessing the stx₂ gene with or without any other genes produced Stx with titers of 1:128 whereas the strains without the stx₂ gene did not (24 of 55 strains [44%]; P < 0.001). Lower titers (<1:128) were observed especially in the strains possessing stx_2c (7 of 9 [78%]) and in the strains possessing stx₁ with or without other genes (29 of 38 strains [76%]). Of the strains producing Stx1 only, 32% (9 of 28) produced the Stx toxin with high titers (1:128) compared with 78% (102 of 130) of the strains producing Stx2 only (P < 0.001). Four strains (2%), three positive and one negative for stx in PCR, did not produce Stx. Of the two strains carrying stx_2d, one did not produce detectable levels of Stx2 and the Stx titer of the other was low (1:4). However, both strains produced Stx1 with titers of 1:16 although stx₁ was not detected by the method used.

Serotypes, presence of eae, and Ehly production. Of all the strains, 111 (64%) belonged to the O157 serogroup. Within this O group, the most common stx gene combination was stx₂ with stx_2c (71 strains [64%]) whereas among the 62 non-O157 strains, this gene combination was found in only one strain (2%; P < 0.001) (Table 3). In contrast, among non-O157 strains, the most common stx gene was stx₁ (27 of 62 strains [44%]), which, among the 111 O157 strains, was found in one strain only (1%; P < 0.001). The stx₂ gene alone was equally common among the O157 (21 of 111 [19%]) and non-O157 (15 of 62 [24%]) strains. Almost all the strains carrying these stx genes also had the eae gene, and they produced Ehly (Table 3). On the other hand, of the nine strains carrying the stx_2c gene only, six (67%) strains of the non-O157 group were negative for both eae and Ehly. The two strains carrying stx_2d-Ount were both of serogroup non-O157 (O Rough:H^- and O76:H19); neither of them carried eae, but both produced Ehly.

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TABLE 3. stx genes in 173 STEC isolates and other characteristics of the strains

PTs. Distribution of the stx genes by PTs among the strains of the O157 serogroup showed that 55 of 59 (93%) of the PT2 strains and all 10 PT49 strains had the stx₂ and stx_2c genes (Table 4). The PT4 strains had stx₂ only (7 of 13 [54%]) almost as often as stx₂ with stx_2c (5 of 13 [38%]), whereas the PT8 strains had most commonly stx₁ (8 of 9 [89%]) with the stx₂ genes (stx_2c [five strains], stx_2vhb [two strains], and stx₂ with stx_2vhb [one strain]). The nine strains belonging to the reacts- but-does-not-conform phenotype group had a variable set of the stx genes.

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TABLE 4. stx genes among sorbitol-negative and sorbitol-positive STEC O157 strains belonging to different PTs

Association of stx with clinical symptoms. The clinical diagnosis was available for 160 (94%) of the 170 patients (Fig. 1). Of them, three patients were simultaneously infected by two different STEC strains (O157 and non-O157 strains). HUS or TTP was diagnosed in 20 (12%) patients, bloody diarrhea occurred in 77 (45%) patients, nonbloody diarrhea occurred in 37 (22%) patients, and asymptomatic carriage was determined in 26 (16%) subjects. Twenty-four subjects were family members of the children with HUS (11 subjects), bloody diarrhea (6 subjects), nonbloody diarrhea (6 subjects), or an unknown clinical picture (1 subject). However, of the 11 patients with HUS, a STEC strain could be isolated from four of the subjects. Among the asymptomatic subjects, two findings were connected to enhanced screening of travelers (22). Of the 20 patients with HUS, most were 1- to 5-year-old children (13 of 20 subjects [65%] versus 47 of 150 [31%] for other clinical groups; P = 0.007), and of the asymptomatic carriers, most were 26- to 55-year-old subjects (15 of 26 subjects [58%] versus 20 of 144 [14%] for other clinical groups; P < 0.001).

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FIG. 1. Percentage of STEC-infected subjects in different age groups according to the clinical picture of the infection (asymptomatic carriage [Asy], nonbloody diarrhea [Di], bloody diarrhea [BDi], HUS or TTP, or clinical picture not known).

In the strains found in subjects with HUS or TTP, bloody diarrhea, nonbloody diarrhea, or asymptomatic carriage, the most common stx genes were stx₂ with stx_2c (detected in 50, 53, 30, and 35% of patients, respectively) and stx₂ only (detected in 25, 14, 22, and 31% of patients, respectively) (Table 5). Of the nine asymptomatic persons infected by STEC harboring stx₂ and stx_2c, all were associated with a patient with HUS, bloody diarrhea, or nonbloody diarrhea (two, three, and four subjects, respectively). Five were 16- to 55-year-old family members of the STEC-infected patients and four were <1- to 15 year-old siblings. Of the eight asymptomatic carriers from whom a STEC strain possessing stx₂ was isolated, six were connected to patients with HUS or to a patient with nonbloody diarrhea (one subject). One infection was sporadic. Of these eight subjects, five were 16- to 55-year-old adults and three were siblings under 10 years old.

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TABLE 5. Distribution of different stx genes in STEC strains according to the clinical pictures of the 160 patients for whom clinical data were available

In addition, among the strains associated with HUS or TTP, there were three (15%) strains possessing stx_2c alone, an undigestible strain, and a PCR-negative strain. None of the 38 stx₁-positive strains (28 stx₁ only, 10 with stx₂ or the stx₂ variant) were associated with HUS or TTP, although they were the third most common genes of all the STEC strains and were equally common in all other clinical groups. The only strain possessing three distinct stx genes (stx₁, stx₂, and stx_2vhb) was isolated from a patient with bloody diarrhea.

The strains of 10 different stx-positive virulence profiles (P1 through P10) were responsible for the majority (120 of 170 [71%]) of all STEC infections (Table 6). The strains belonging to five virulence profiles (P1 through P5) accounted for 71% (15 of 21) of all the strains found in patients with HUS or TTP but only 4% (6 of 152) of all remaining strains associated with HUS or TTP (P = 0.03). Of the strains associated with HUS or TTP, nine (43%) were of the non-O157 serogroup: three strains of O145:H28/H^-:stx₂ and one strain each of OX174:H21:stx_2c, O Rough:H4:stx_2c, O101:H^-:stx₂, O Rough:H49:stx_2c, O107:H27 lacking stx, and O2:H29:undigestible. P1 was the most prevalent virulence profile, with 55 strains, and these strains more often caused HUS and bloody diarrhea (39 of 55 [71%]) than other clinical symptoms (16 of 55 [29%]). This association with HUS and bloody diarrhea (71%) was statistically significant compared with that for all other strains (60 of 118 strains [51%]; P = 0.02). The P1 virulence profile also caused the deaths of two children under 5 years of age. The strains belonging to profiles P1 through P10 (95 of 120 strains [79%]) produced Stx toxin with titers of 1:128 more commonly than did other strains (24 of 53 strains [45%]; P < 0.001). These strains were also enterohemolytic (112 of 120 [93%] versus 32 of 53 [60%]; P < 0.001) and possessed the eae gene more often (119 of 120 [99%] versus 32 of 53 [60%]; P < 0.001) than the other strains. Three patients, one with HUS, one with bloody diarrhea, and one who was an asymptomatic carrier, had infections caused simultaneously by two strains belonging to the different virulence profiles (of P2 and P3, of P2 and other O157 groups, or of other non-O157 groups, correspondingly).

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TABLE 6. Most common virulence profiles of STEC strains and their distribution by the clinical pictures of 170 subjects

Top Abstract Introduction Materials and Methods Results Discussion References

 
To date, only a few studies have described the stx genes and their variants in STEC strains in relation to the symptoms of STEC-infected patients and the relative contributions of the various forms of Stx toxin to pathogenesis are not fully known (13, 14, 37). In a study concerning Stx production as a single microbial factor, the most pathogenic strains for humans have been found to produce Stx2 only (9, 34). The Stx2 toxin has been described as being 1,000 times more cytotoxic than Stx1 towards human renal microvascular endothelial cells, the putative target of Shiga toxins in the development of HUS (28). The STEC strains isolated from HUS patients have produced mostly Stx2 and/or Stx2c (19), but the risk of developing HUS after infection with STEC harboring stx₂ alone has been higher than that after infection with any of the strains harboring stx_2c alone (13). However, there are numerous variants of Stx2, differing by only 1 or 2 amino acids in either the A or B subunit (35) and the similarity of the sequences of different Stx2 toxins may vary from 80 to 99% (16). This may affect their catalytic activity or receptor binding, and pathogenicity. The ability of STEC bacteria to produce the Stx toxin only, however, is suspected to be insufficient for an organism to cause disease without appropriate complementary virulence factors (26, 45). The present situation has created a need for studies concerning the simultaneous data of several microbial characteristics combined with the data of the clinical pictures of the patients.

In our study, 111 STEC O157 and 62 non-O157 isolates from 170 Finns with STEC infection were investigated for the possession of various genes by PCR-RFLP. Also, data on other bacterial characteristics, namely, serotype, PT of O157, eae, and Ehly and Stx production, were included. In order to search for the virulence profiles among the strains, the bacterial data were combined and their potential correlation with the clinical diagnosis (HUS, bloody diarrhea, nonbloody diarrhea, or asymptomatic infection) of the subjects in different age groups was investigated. In the strains studied, stx genes occurred in 11 different combinations. In addition, 10 virulence profiles accounted for 71% of all 173 STEC strains isolated in Finland from humans since 1990. Moreover, a STEC serotype (O Rough:H4:stx_2c) which had never before been described as being associated with HUS was found.

In PCR-RFLP according to Lin et al. and Bastian et al. (1, 27), the HincII and AccI enzymes were expected to produce fragments of variant-specific size for the stx genes. However, some of our strains were negative, showed weak positive results, or were undigestible. The PCR products which the HincII and AccI enzymes were unable to cut possibly lacked the required specific site for the restriction enzymes to cut the DNA. Either these undigestible stx genes may have been rare stx variants which remained undetectable by the HincII and AccI enzymes or the strains may have changed during storage and cultivation.

A considerable share (21 or 42%) of the strains carried stx₂ only or stx₂ with stx_2c. Also, in Belgium and Germany, stx₂ alone and stx₂ with either stx_2vha or stx_2c have been prevalent (7, 13, 37). In our strains, the third most common gene was stx₁, which was present alone in 28 strains and in combination with stx₂, stx_2c, or stx_2vhb in 10 strains. In Germany, of the 212 human isolates harboring stx₁, almost half also carried stx₂, stx_2c, or stx_2d (48). Of our strains, only two (1%) were of the stx_2d-Ount variant type. In Belgium and Germany, the stx_2d gene has been more prevalent and has been found in 7% of 359 human or animal isolates (37) and in 4% of 626 human isolates (13). These data indicate similar distributions of the stx genes in different European countries.

By the VTEC-RPLA assay, the strains carrying the stx₂ gene with or without any other genes produced Stx significantly more than did the strains without the stx₂ gene. Lower titers were observed especially within the strains possessing stx₁, stx_2c, or stx_2d. The VTEC -RPLA assay has previously been found to be a reliable method for the detection of Stx1, Stx2, and Stx2c but not for the Stx2e porcine or Stx2d-Ount variant toxins (2, 3, 21). Our results might indicate a weak capability of the gene to express the Stx1 toxin or a putative carriage of the stx_1c gene and thus a possible weak ability to detect the Stx1c toxin by the VTEC-RPLA, as suggested by Zhang et al. (48). Of our two strains carrying stx_2d-Ount, both produced Stx1. However, these strains were negative for stx₁ although they were positive in PCR (12) with primers described by Olsvik and Strockbine (33). Similarly, four strains (O107:H27 lacking stx, O157:H- lacking stx, O157:H7:stx₁, and O43:H2:stx₁) negative for any stx₂ gene on the basis of the method of Lin et al. (27) and Bastian et al. (1) had previously been positive for stx₂ either as a sole gene (O107:H27 lacking stx and O157:H^- lacking stx) or in combination with stx₁ (O157:H7:stx₁ and O43:H2:stx₁) (12, 25, 39). In addition, one strain (O91:H40) possessed stx₁ with stx_2c in this study, although previously it has been shown to possess only stx₂ and to produce Stx2 toxin only (12, 25). These results clearly demonstrate the differences among different protocols in the detection of the stx genes.

The comparison of the distribution of the stx genes in strains of the O157 and non-O157 serogroups showed that stx₂ with stx_2c was statistically significantly associated with strains of the O157 serogroup. Also in Belgium, stx₂ with stx_2vha was prevalent among the human STEC O157 isolates, unlike stx₁, which was more prevalent in other O serogroups (37). Also among our non-O157 strains, the significant association with stx₁ was seen. This gene was most common in strains of serotypes O26:H11/H^- and O103:H2/H^-. In France, the serotype O103:H2 has commonly possessed stx₁ (29).

stx₂ with the stx_2c gene was found in strains associated with all symptoms but mostly in strains associated with bloody diarrhea or HUS. In contrast, none of the strains carrying stx₁ alone or in combination with another gene were associated with HUS or TTP. However, in France, strains of the serotype O103:H2 carrying stx₁ have been found in HUS patients (29). Also, in Germany, a child infected by STEC O118:H^- positive for stx₁ suffered from HUS (47). Neither of our stx_2d-Ount-infected patients had HUS or TTP; this supports other studies describing the presence of the stx_2d gene in isolates from patients with symptoms milder than HUS or TTP (13, 35, 47, 48).

One of our strains isolated from a patient with bloody diarrhea carried three distinct genes simultaneously. This finding is an example that the infection caused by STEC bacteria possessing several stx genes does not always cause a severe clinical picture, such as HUS, as observed previously also by others (14).

Most of the patients with HUS were 1- to 5-year-old children, and most of the asymptomatic carriers were 26- to 55-year-old adults. Thus, our data are in accordance with other studies concerning the age as a risk factor for STEC infection (8, 11, 13, 32).

Three of the 170 subjects, one with HUS, one with bloody diarrhea, and one an asymptomatic carrier, had infections caused by two STEC strains of different serotypes: correspondingly, O157:H^-:PT88:stx₂ and O145:H28:stx₂, O157:H^-:PT88 lacking stx and O145:H28:stx₂, or O102:H7:undigestible and O Rough:H18:undigestible. Similarly, in the Czech Republic, some HUS patients were infected with two different STEC serotypes: O157:H7 and O5:H^-, O157:H7 and O55H?, O157:H7 and O111:H^-, O26:H11 and O5:H^-, or O111:H^- and O1:H^- (4). These findings support the possibility of people being infected by several STEC strains simultaneously.

The strains belonging to five virulence profiles (from P1 to P5) accounted for 71% of all strains found in patients with HUS. In addition, of all the strains studied, those carrying stx₂ with stx_2c mainly belonged to the virulence profile P1 (O157:H7:PT2:stx₂:stx_2c) and, among them, the majority (71%) were associated with HUS or bloody diarrhea. All these strains possessed eae, were enterohemolytic, and produced Stx2 with high titers. Strains of the virulence profile P1 also caused the deaths of two children under 5 years of age. Our results are also supported by other studies concerning the carriage of stx₂ with stx_2c (7, 13). Friedrich et al. (13) found that 68 (25%) of 268 STEC isolates from HUS patients harbored stx₂ with stx_2c, and among all the 626 STEC isolates investigated, these 68 HUS-associated strains accounted for 11% of the cases of HUS infection. Also, in a study by Cornu et al. (7), nine STEC isolates of serogroup O157 and four STEC non-O157 isolates carrying stx₂ only or stx₂ with stx_2vha were identified in 13 cases of HUS.

In our study, seven virulence profiles of STEC non-O157 were associated with HUS or TTP (O145:H28/H^-:stx₂, OX174:H21:stx_2c, O Rough:H4:stx_2c, O101:H^-:stx₂, O Rough:H49:stx_2c, O107:H27 lacking stx, and O2:H29:undigestable). In the liter-ature (10; http://www.microbionet.com.au/frames/feature/vtec/brief01.html; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi), serotype O Rough:H4 has never been published as being associated with patients suffering from HUS.

In this study, the risk factor for HUS in STEC-infected subjects was young age (1 to 5 years) and an infection especially by STEC O157:H7:PT2:stx₂:stx_2c:eae:Ehly but also by O145:H28/H^-:stx₂:eae:Ehly. Of the 21 strains causing HUS or TTP, almost half (43%) belonged to the non-O157 serogroup. This high prevalence of the non-O157 STEC strains indicates the importance of the detection of all STEC serogroups in clinical diagnostics. PCR and Stx toxin detection assays have proven to be essential methods worldwide (10), and they should be used routinely in all hospital laboratories. However, the development of molecular methods of high capacity for detecting all stx genes should be considered in future studies. In addition, the further characterization of the stx genes can be exploited for predicting the clinical outcome of STEC infection, especially in young children.

 
We thank Sirkku Waarala and Tarja Heiskanen for their excellent technical assistance and Susanna Lukinmaa for her helpful advice on PCR-RFLP methodology.

This study was financially supported by the Finnish Association of Academic Agronomists, the ABS Graduate School (the Finnish Graduate School on Applied Bioscience Bioengineering, Food & Nutrition, Environment), and the Finnish Cultural Foundation.

 
* Corresponding author. Mailing address: National Public Health Institute, Laboratory of Enteric Pathogens, Mannerheimintie 166, FIN-00300 Helsinki, Finland. Phone: 358-9-47448245. Fax: 358-9-47448238. E-mail: anja.siitonen{at}KTL.fi.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Journal of Clinical Microbiology, December 2002, p. 4585-4593, Vol. 40, No. 12
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.12.4585-4593.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

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