RESUMEN

BACKGROUND/PURPOSE: Shiga-like toxin (Stx) is an important factor in the pathogenesis of Escherichia coli O157:H7 infection and is responsible for some severe complications. Stx2 is usually associated with hemolytic uremic syndrome in humans. Its expression is regulated by elements located upstream of the stx2 gene, including stx2-promoter sequence, ribosome binding site, and the antiterminator q gene. The present study aimed to find the correlation between regulatory elements and the expression level of Stx2 in two local isolates of E. coli O157:H7. METHODS: Two local E. coli O157:H7 strains SM-25(1) and KL-48(2), originating from human and cattle feces, respectively, and an E. coli reference strain, ATCC 43894, were investigated. The complete stx2 gene covering the sequences of promoter, ribosome binding site, and open reading frame and q gene of each strain was analyzed. The magnitude of Stx2 production was detected with a reverse passive latex agglutination method and Stx mediated cellular damage was determined with the Vero cell assay. RESULTS: A comparison of the complete stx2 gene contained stx2-promoter, ribosome binding site, and q genes of two local strains KL-48(2) and SM25(1), and the E. coli ATCC 43894 showed that the amino acid sequences were identical. Both local isolates were Stx negative in the reverse passive latex agglutination test and nontoxic in the Vero cell assay. CONCLUSION: The expression level of Shiga-like toxin of the two local isolates of E. coli O157:H7 did not only depend on the regulatory elements of the stx2 gene.

Asunto(s)

Escherichia coli O157/genética , Escherichia coli O157/metabolismo , Regulación Bacteriana de la Expresión Génica/genética , Toxina Shiga II/genética , Animales , Secuencia de Bases , Sitios de Unión , Bovinos , Adhesión Celular , Supervivencia Celular , Chlorocebus aethiops , ADN Bacteriano/química , ADN Bacteriano/genética , Infecciones por Escherichia coli/microbiología , Escherichia coli O157/patogenicidad , Heces/microbiología , Genes vif/genética , Humanos , Filogenia , Regiones Promotoras Genéticas , Alineación de Secuencia , Análisis de Secuencia , Toxina Shiga II/biosíntesis , Toxina Shiga II/clasificación , Células Vero

RESUMEN

The aim of this study was to investigate the virulence potential of the isolated bovine STEC for humans in Iran. In this study a collection of STEC strains (n = 50) had been provided via four stages, including sampling from feces of cattle, E. coli isolation, molecular screening of Shiga toxin (stx) genes, and saving the STEC strains from various geographical areas in Iran. The STEC isolates were subjected to stx-subtyping, O-serogrouping, and phylo-grouping by conventional polymerase chain reaction (PCR). Occurrence of stx1 (52%) and stx2 (64%) was not significantly different (p = 0.1), and 16% of isolates carried both stx1 and stx2, simultaneously. In addition, 36% and 80% of the isolates were positive for eae and ehxA, respectively. Molecular subtyping showed that stx1a (52%), stx2a (44%), stx2c (44%), and stx2d (30%) were the most prevalent subtypes; two combinations stx2a/stx2c and stx2c/stx2d coexisted in 18% and 10% of STEC strains, respectively. Three important non-O157 serogroups, including O113 (20%), O26 (12%), and O111 (10%), were predominant, and none of the isolates belonged to O157. Importantly, one O26 isolate carried stx1, stx2, eae and ehxA and revealed highly virulent stx subtypes. Moreover, all the 21 serogrouped strains belonged to the B1 phylo-type. Our study highlights the significance of non-O157 STEC strains carrying highly pathogenic virulence genes in cattle population as the source of this pathogen in Iran. Since non-O157 STEC strains are not routinely tried in most diagnostic laboratories, majority of the STEC-associated human infections appear to be overlooked in the clinical settings.

Asunto(s)

Infecciones por Escherichia coli/veterinaria , Filogenia , Serogrupo , Toxina Shiga/clasificación , Toxina Shiga/genética , Escherichia coli Shiga-Toxigénica/genética , Virulencia/genética , Adhesinas Bacterianas/genética , Animales , Bovinos , Infecciones por Escherichia coli/microbiología , Escherichia coli O157/genética , Proteínas de Escherichia coli/genética , Heces/microbiología , Genes Bacterianos/genética , Genotipo , Proteínas Hemolisinas/genética , Irán , Reacción en Cadena de la Polimerasa , Toxina Shiga I/clasificación , Toxina Shiga I/genética , Toxina Shiga II/clasificación , Toxina Shiga II/genética , Escherichia coli Shiga-Toxigénica/clasificación , Escherichia coli Shiga-Toxigénica/aislamiento & purificación

RESUMEN

Enterohemorrhagic E. coli (EHEC) causes diarrhea and hemorrhagic colitis with life-threatening complications, such as hemolytic uremic syndrome. Their major virulence factor is Shiga toxin (Stx), which is encoded by bacteriophages. Of the two types of Stx, the production of Stx2, particularly that of Stx2a (a subtype of Stx2), is a major risk factor for severe EHEC infections, but the Stx2 production level is highly variable between strains. Here, we define four major and two minor subtypes of Stx2a-encoding phages according to their replication proteins. The subtypes are correlated with Stx2a titers produced by the host O157 strains, suggesting a critical role of the phage subtype in determining the Stx2a production level. We further show that one of the two subclades in the clade 8, a proposed hyper-virulent lineage of O157, carries the Stx2 phage subtype that confers the highest Stx2 production to the host strain. The presence of this subclade may explain the proposed high virulence potential of clade 8. These results provide novel insights into the variation in virulence among O157 strains and highlight the role of phage variation in determining the production level of the virulence factors that phages encode.

Asunto(s)

Bacteriófagos/genética , Escherichia coli O157/metabolismo , Escherichia coli O157/virología , Toxina Shiga II/metabolismo , Factores de Virulencia/genética , Tipificación de Bacteriófagos , Bacteriófagos/clasificación , Bacteriófagos/metabolismo , Variación Genética , Genoma Viral , Recombinación Homóloga/genética , Filogenia , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN , Toxina Shiga II/clasificación , Toxina Shiga II/genética , Factores de Virulencia/clasificación , Factores de Virulencia/metabolismo

RESUMEN

The Shiga toxins of Shiga toxin-producing Escherichia coli (STEC) can be divided into Shiga toxin 1 (Stx1) and Shiga toxin 2 (Stx2) with several sub-variants. Variant Stx2f is one of the latest described, but has been rarely associated with symptomatic human infections. In the enhanced STEC surveillance in the Netherlands, 198 STEC O157 cases and 351 STEC non-O157 cases, including 87 stx2f STEC isolates, were reported between 2008 and 2011. Most stx2f strains belonged to the serogroups O63:H6 (n=47, 54%), O113:H6 (n=12, 14%) and O125:H6 (n=12, 14%). Of the 87 stx2f isolates, 84 (97%) harboured the E. coli attaching and effacing (eae) gene, but not the enterohaemorrhagic E. coli haemolysin (hly) gene. stx2f STEC infections show milder symptoms and a less severe clinical course than STEC O157 infections. Almost all infections with stx2f (n=83, 95%) occurred between June and December, compared to 170/198 (86%) of STEC O157 and 173/264 (66%) of other STEC non-O157. stx2f STEC infections in the Netherlands are more common than anticipated, and form a distinct group within STEC with regard to virulence genes and the relatively mild disease.

Asunto(s)

Infecciones por Escherichia coli/diagnóstico , Escherichia coli O157/genética , Toxina Shiga II/genética , Escherichia coli Shiga-Toxigénica/aislamiento & purificación , Adhesinas Bacterianas/biosíntesis , Adhesinas Bacterianas/genética , Infecciones por Escherichia coli/epidemiología , Infecciones por Escherichia coli/microbiología , Escherichia coli O157/patogenicidad , Proteínas de Escherichia coli/biosíntesis , Proteínas de Escherichia coli/genética , Proteínas Hemolisinas/biosíntesis , Proteínas Hemolisinas/genética , Humanos , Datos de Secuencia Molecular , Países Bajos/epidemiología , Reacción en Cadena de la Polimerasa/métodos , Prevalencia , Serotipificación , Toxina Shiga I/genética , Toxina Shiga II/clasificación , Escherichia coli Shiga-Toxigénica/genética , Especificidad de la Especie

RESUMEN

BACKGROUND: Shiga toxin-producing Escherichia coli (STEC) are frequent causes of severe human diseases ranging from diarrhea to hemolytic uremic syndrome. The existing strategy for detection of STEC relies on the unique sorbitol-negative fermentation property of the O157 strains, the most commonly identified serotype has been E. coli O157. It is becoming increasingly evident, however, that numerous non-O157 STEC serotypes also cause outbreaks and severe illnesses. It is necessary to have new methods that are capable of detecting all STEC strains. METHODS AND FINDINGS: Here we describe the development of a sandwich ELISA assay for detecting both O157 and non-O157 STECs by incorporating a novel polyclonal antibody (pAb) against Stx2. The newly established immunoassay was capable of detecting Stx2a spiked in environmental samples with a limit of detection between 10 and 100 pg/mL in soil and between 100 and 500 pg/mL in feces. When applied to 36 bacterial strains isolated from human and environmental samples, this assay detected Stx2 in all strains that were confirmed to be stx2-positive by real-time PCR, demonstrating a 100% sensitivity and specificity. CONCLUSIONS: The sandwich ELISA developed in this study will enable any competent laboratory to identify and characterize Stx2-producing O157 and non-O157 strains in human and environmental samples, resulting in rapid diagnosis and patient care. The results of epitope mapping from this study will be useful for further development of a peptide-based antibody and vaccine.

Asunto(s)

Anticuerpos Antibacterianos/inmunología , Microbiología Ambiental , Inmunoensayo/métodos , Toxina Shiga II/biosíntesis , Toxina Shiga II/clasificación , Escherichia coli Shiga-Toxigénica/inmunología , Animales , Especificidad de Anticuerpos/inmunología , Antígenos Bacterianos/inmunología , Chlorocebus aethiops , Ensayo de Inmunoadsorción Enzimática , Mapeo Epitopo , Humanos , Sueros Inmunes/inmunología , Inmunización , Inmunoglobulina G/inmunología , Pruebas de Neutralización , Toxina Shiga II/inmunología , Toxina Shiga II/aislamiento & purificación , Células Vero , Microbiología del Agua

RESUMEN

Shiga toxin (Stx)-producing Escherichia coli (STEC) are associated with potentially serious illness in humans. STEC detection is often based on the presence of Stxs, Stx(1) and/or Stx(2), and intimin, encoded by the eae gene. A 2-year collection of stool broth cultures was tested for variants of stx(1), stx(2), and eae. Approximately 80% (138 of 174) were positive for stx(1) and/or stx(2), with stx(1) as the most prevalent (66%). Of the stx(1) variants, stx(1) was the most common (76%) followed by stx(1c) (22%). Analysis of stx(2)-positive isolates found 20 (53%) stx(2), 13 (34%) stx(2)/stx(2v-ha), 3 (8%) stx(2v-ha), 1 (3%) stx(2v-hb), and 1 (3%) stx(2d-activatable). Findings of stx(2)/stx(2v-ha) and stx(2d-activatable) are noteworthy given associations with hemolytic uremic syndrome and increased cytotoxicity, respectively. Of the Stx positive, 94 (68%) were eae positive with 31 (33%) eae(varepsilon1), 19 (20%) eae(gamma1), and 18 (19%) eae(beta1). A predominance of eae(varepsilon1) may suggest a new pathogenic significance because, reportedly, eae(beta1) is one of the most widespread variants.

Asunto(s)

Adhesinas Bacterianas/genética , ADN Bacteriano/genética , ADN Bacteriano/aislamiento & purificación , Proteínas de Escherichia coli/genética , Heces/microbiología , Toxina Shiga I/genética , Toxina Shiga II/genética , Escherichia coli Shiga-Toxigénica/genética , Adhesinas Bacterianas/clasificación , Proteínas de Escherichia coli/clasificación , Humanos , Reacción en Cadena de la Polimerasa/métodos , Toxina Shiga I/clasificación , Toxina Shiga II/clasificación

RESUMEN

Shiga toxins (Stx) are believed to play a key role in the pathogenesis of diseases caused by Stx-producing Escherichia coli (STEC), including the potentially life-threatening hemolytic uremic syndrome (HUS). In this study, 201 STEC strains collected from patients and environmental sources were investigated with regard to the stx genotypes and pathogenicity. The stx(2) and stx(2c) alleles were associated with high virulence and the ability to cause HUS, whereas stx(2d), stx(2e,)stx(1), and stx(1c) occurred in milder or asymptomatic infections. Quantification of Stx using an enzyme immunoassay and the Vero cell cytotoxicity assay showed no significant differences between the strains associated with HUS and those causing milder diseases. We hypothesize that the stx genotype and perhaps other yet unknown virulence factors rather than the amount of Stx or the in vitro cytotoxicity correlate with the development of HUS.

Asunto(s)

Síndrome Hemolítico-Urémico/microbiología , Toxina Shiga I/genética , Toxina Shiga II/genética , Escherichia coli Shiga-Toxigénica/genética , Adhesinas Bacterianas/metabolismo , Animales , Chlorocebus aethiops , Proteínas de Escherichia coli/metabolismo , Microbiología de Alimentos , Enfermedades Transmitidas por los Alimentos , Genotipo , Humanos , Técnicas para Inmunoenzimas , Toxina Shiga I/clasificación , Toxina Shiga II/clasificación , Escherichia coli Shiga-Toxigénica/clasificación , Escherichia coli Shiga-Toxigénica/patogenicidad , Células Vero/microbiología , Virulencia/genética

RESUMEN

We examined 219 Shiga toxin-producing Escherichia coli (STEC) strains from meat, milk, and cheese samples collected in Germany between 2005 and 2006. All strains were investigated for their serotypes and for genetic variants of Shiga toxins 1 and 2 (Stx1 and Stx2). stx(1) or variant genes were detected in 88 (40.2%) strains and stx(2) and variants in 177 (80.8%) strains. Typing of stx genes was performed by stx-specific PCRs and by analysis of restriction fragment length polymorphisms (RFLP) of PCR products. Major genotypes of the Stx1 (stx(1), stx(1c), and stx(1d)) and the Stx2 (stx(2), stx(2d), stx(2-O118), stx(2e), and stx(2g)) families were detected, and multiple types of stx genes coexisted frequently in STEC strains. Only 1.8% of the STEC strains from food belonged to the classical enterohemorrhagic E. coli (EHEC) types O26:H11, O103:H2, and O157:H7, and only 5.0% of the STEC strains from food were positive for the eae gene, which is a virulence trait of classical EHEC. In contrast, 95 (43.4%) of the food-borne STEC strains carried stx(2) and/or mucus-activatable stx(2d) genes, an indicator for potential high virulence of STEC for humans. Most of these strains belonged to serotypes associated with severe illness in humans, such as O22:H8, O91:H21, O113:H21, O174:H2, and O174:H21. stx(2) and stx(2d) STEC strains were found frequently in milk and beef products. Other stx types were associated more frequently with pork (stx(2e)), lamb, and wildlife meat (stx(1c)). The combination of serotyping and stx genotyping was found useful for identification and for assignment of food-borne STEC to groups with potential lower and higher levels of virulence for humans.

Asunto(s)

Técnicas de Tipificación Bacteriana , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Microbiología de Alimentos , Toxina Shiga I , Toxina Shiga II , Animales , Bovinos , Queso/microbiología , Escherichia coli/genética , Escherichia coli/aislamiento & purificación , Proteínas de Escherichia coli/clasificación , Proteínas de Escherichia coli/genética , Contaminación de Alimentos/análisis , Humanos , Carne/microbiología , Leche/microbiología , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción , Análisis de Secuencia de ADN , Serotipificación , Toxina Shiga I/biosíntesis , Toxina Shiga I/clasificación , Toxina Shiga I/genética , Toxina Shiga II/biosíntesis , Toxina Shiga II/clasificación , Toxina Shiga II/genética

RESUMEN

Shiga toxin 2 (Stx2) from Shiga toxin-producing Escherichia coli (STEC) was subtyped by a method involving partial sequencing of the stxAB2 operon. Of 255 strains from the Danish STEC cohort, all 20 cases of hemolytic-uremic syndrome were associated with subtype Stx2 (11 cases), subtype Stx2c (1 case), or the two combined (8 cases).

Asunto(s)

Diarrea/fisiopatología , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Variación Genética , Síndrome Hemolítico-Urémico/fisiopatología , Toxina Shiga II/clasificación , Secuencia de Aminoácidos , Niño , Dinamarca , Diarrea/microbiología , Escherichia coli/genética , Infecciones por Escherichia coli/microbiología , Infecciones por Escherichia coli/fisiopatología , Síndrome Hemolítico-Urémico/microbiología , Humanos , Datos de Secuencia Molecular , Operón , Filogenia , Análisis de Secuencia de ADN , Toxina Shiga II/química , Toxina Shiga II/genética , Toxina Shiga II/metabolismo

RESUMEN

Shiga toxin-producing Escherichia coli (STEC) are a public health concern. Bacterial culture techniques commonly used to detect E. coli O157:H7 will not detect other STEC serotypes. Feces from cattle and other animals are a source of O157:H7 and other pathogenic serotypes of STEC. The objective of this study was to estimate the pen-level prevalence of Shiga toxins and selected STEC serotypes in pre-slaughter feedlot cattle. Composite fecal samples were cultured and a polymerase chain reaction (PCR) was used to detect genes for Shiga toxins (stx1 and stx2) and genes for O157:H7, O111:H8, and O26:H11 serotypes. Evidence of Shiga toxins was found in 23 pens (92%), O157:H7 in 2 (8%), O111:H8 in 5 (20%), and O26:H11 in 20 (80%) of the 25 pens investigated. Although pen-level prevalence estimates for Shiga toxins and non-O157 serotypes seem high relative to O157:H7, further effort is required to determine the human health significance of non-O157 serotypes of STEC in feedlot cattle.

Asunto(s)

Enfermedades de los Bovinos/microbiología , Infecciones por Escherichia coli/veterinaria , Escherichia coli O157/metabolismo , Escherichia coli/metabolismo , Heces/microbiología , Toxinas Shiga/análisis , Alberta/epidemiología , Animales , Bovinos , Enfermedades de los Bovinos/epidemiología , Escherichia coli/genética , Escherichia coli/aislamiento & purificación , Infecciones por Escherichia coli/epidemiología , Infecciones por Escherichia coli/microbiología , Escherichia coli O157/genética , Escherichia coli O157/aislamiento & purificación , Heces/química , Humanos , Reacción en Cadena de la Polimerasa/veterinaria , Prevalencia , Salud Pública , Serotipificación/veterinaria , Toxina Shiga I/análisis , Toxina Shiga I/clasificación , Toxina Shiga II/análisis , Toxina Shiga II/clasificación , Toxinas Shiga/biosíntesis , Toxinas Shiga/clasificación

RESUMEN

OBJECTIVE: To monitor the changes of predominant Shiga toxin types of Escherichia coli O157:H7 in Xuzhou City, Jiangsu Province. METHODS: PCR typing with slt2-specific primer pairs (slt2cslt2, slt2v1slt2v2), hybridization of chromosome DNA digested by PstI, and DNA sequencing of PCR products. with slt2-specific primer pairs (slt2cslt2d; slt2eslt2f) were conducted on 14 strains of E. coli isolated from diarrhea patients and dung beetles in 1999 and 2000. RESULTS: The 5 strains of E. coli isolated from diarrhea patients in 1999 carried slt1 and slt2. The 1 strains of E. coli O157:H7 isolated from diarrhea patients and the 5 strains isolated from dung beetles in 2000 only carried slt2vha, a variance of Shiga toxin 2. CONCLUSION: The predominant Shiga toxin types of E. coli O157:H7 in Xuzhou changed 1999 - 2000, which may be related to the changes of epidemiological features of E. coli O157:H7 infection in Xuzhou. A genotyping method based on restriction fragment length polymorphism (RFLP) analysis of a B-subunit-encoding DNA fragment obtained by PCR described in this study is a useful tool to identify slt2 gene and slt2 variant gene in epidemiological studies with O157:H7 strains.

Asunto(s)

Escherichia coli O157/patogenicidad , Toxina Shiga II/clasificación , Southern Blotting , Genotipo , Reacción en Cadena de la Polimerasa , Toxina Shiga II/genética

RESUMEN

stx(2) genes from 138 Shiga toxin-producing Escherichia coli (STEC) isolates, of which 127 were of bovine origin (58 serotypes) and 11 of human origin (one serotype; O113:H21), were subtyped. The bovine STEC isolates from Australian cattle carried ehxA and/or eaeA and predominantly possessed stx(2-EDL933) (103 of 127; 81.1%) either in combination with stx(2vhb) (32 of 127; 25.2%) or on its own (52 of 127; 40.4%). Of 22 (90.9%) bovine isolates of serotype O113:H21, a serotype increasingly recovered from patients with hemolytic uremic syndrome (HUS) or hemorrhagic colitis, 20 contained both stx(2-EDL933) and stx(2vhb); 2 isolates contained stx(2vhb) only. Although 7 of 11 (63.6%) human O113:H21 isolates associated with diarrhea possessed stx(2-EDL933), the remaining 4 isolates possessed a combination of stx(2-EDL933) and stx(2vhb). Three of the four were from separate sporadic cases of HUS, and one was from an unknown source.

Asunto(s)

Enfermedades de los Bovinos/microbiología , Infecciones por Escherichia coli/veterinaria , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Toxina Shiga II/clasificación , Adhesinas Bacterianas/genética , Adhesinas Bacterianas/metabolismo , Animales , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Bovinos , Escherichia coli/genética , Escherichia coli/metabolismo , Infecciones por Escherichia coli/microbiología , Proteínas de Escherichia coli/genética , Proteínas de Escherichia coli/metabolismo , Proteínas Hemolisinas/genética , Proteínas Hemolisinas/metabolismo , Humanos , Serotipificación , Toxina Shiga I/genética , Toxina Shiga I/metabolismo , Toxina Shiga II/genética , Toxina Shiga II/metabolismo , Factores de Virulencia/genética , Factores de Virulencia/metabolismo

RESUMEN

Shiga toxin 2 (Stx2) variants have been found to exhibit not only antigenic divergence, but also differences in toxicity for tissue culture cells and animals. To clarify whether all or just a subset of Stx2 variants are important for the virulence of Shiga toxin-producing Escherichia coli, we designed PCR primers to detect and type all reported variants. We classified them into four groups according to the nucleotide sequences of the Stx2 family; for example, group 1 (G1) contains VT2vha and group 2 (G2) contains VT2d-Ount. The 120 strains of Shiga toxin-producing E. coli used in this study were isolated from humans in Japan between 1986 and 1999. Among the four variant groups, the G1 gene only was detected in 23 of the 120 clinical strains (19.2%) and all belonged to the O157 serotype. G1 is considered the most important Stx2 variant group in terms of human pathogenicity. A multiplex PCR that can detect the stx1, stx2, and G1 genes was developed as a means of rapid and easy typing to better understand the roles of the different types of Stx.

Asunto(s)

Infecciones por Escherichia coli/microbiología , Escherichia coli/clasificación , Variación Genética , Reacción en Cadena de la Polimerasa/métodos , Toxina Shiga II/clasificación , Toxina Shiga II/genética , Técnicas de Tipificación Bacteriana , Secuencia de Bases , Cartilla de ADN , Escherichia coli/genética , Escherichia coli/metabolismo , Escherichia coli O157/clasificación , Escherichia coli O157/metabolismo , Humanos , Japón , Datos de Secuencia Molecular , Subunidades de Proteína/química , Subunidades de Proteína/genética , Subunidades de Proteína/metabolismo , Alineación de Secuencia , Análisis de Secuencia de ADN , Toxina Shiga I/química , Toxina Shiga I/genética , Toxina Shiga I/metabolismo , Toxina Shiga II/química , Toxina Shiga II/metabolismo

RESUMEN

At least 11 Stx2 variants produced by Shiga toxin-producing Escherichia coli (STEC) isolated from patients and animals have been described. The Stx2 subtyping of STEC isolated from healthy cows positive for stx(2) (n = 104) or stx(2) and stx(1) (n = 63) was investigated. Stx2vh-b, Stx2 (renamed Stx2-EDL933), and Stx2vh-a were the subtypes mostly detected among the bovine isolates (39.5, 39, and 25.5%, respectively). Stx2e was not present, and subtypes included in the Stx2d group (Stx2d-OX3a, Stx2d-O111, and Stx2d-Ount) were found infrequently among the isolates examined (8.5%). A combination of two distinct Stx2 subtypes was observed among 23.5% of the strains. For the first time, a combination of three subtypes (Stx2-EDL933/Stx2vh-b/Stx2d and Stx2vh-a/Stx2vh-b/Stx2d) was detected (3.5% of the isolates). In addition, bovine STEC harboring stx(1) and one or two stx(2) genes appeared highly cytotoxic toward Vero cells. A new Stx2 subtype (Stx2-NV206), present among 14.5% of the isolates, showed high cytotoxicity for Vero cells. Two amino acid residues (Ser-291 and Glu-297) important for the activation of Stx2 by human intestinal mucus were conserved on the Stx2-NV206 A subunit. The gene encoding Ehx enterohemolysin was prominent among STEC harboring stx(2)-EDL933 alone (78%) or a combination of stx(2)-EDL933 and stx(2)vh-b (85%). In addition, Stx2-EDL933 and/or Stx2vh-b subtypes were highly associated with other putative virulence factors such as Stx1 and EspP extracellular serine protease, but not with EAST1 enterotoxin.

Asunto(s)

Enfermedades de los Bovinos/microbiología , Infecciones por Escherichia coli/veterinaria , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Toxina Shiga II/clasificación , Animales , Bovinos , Chlorocebus aethiops , ADN Bacteriano/análisis , ADN Bacteriano/genética , Escherichia coli/metabolismo , Infecciones por Escherichia coli/microbiología , Francia , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción , Análisis de Secuencia de ADN , Toxina Shiga II/genética , Toxina Shiga II/metabolismo , Toxina Shiga II/toxicidad , Células Vero , Virulencia

RESUMEN

Shiga toxin 2 (Stx2) has been reported as the main Shiga toxin associated with human disease. In addition, the Stx2 toxin type can have a profound impact on the degree of tissue damage in animal models. We have characterized the stx(2) subtype of 168 Shiga toxin-producing Escherichia coli (STEC) isolates of which 146 were derived from ovine sources (principally feces and meat) and 22 were isolated from humans. The ovine STEC isolates were of serotypes that have been shown to occur commonly in the gastrointestinal tract of healthy sheep. The major stx(2) subtype in the ovine isolates was shown to be stx(2d-Ount) (119 of 146 [81.5%]) and was predominantly associated with serotypes O75:H(-)/H8/H40, O91:H(-), O123:H(-), O128:H2, and OR:H2. However, 17 of 18 (94.4%) ovine isolates of serotype O5:H(-) possessed a stx(2d-O111/OX3a) subtype. Furthermore, STEC isolates of serotypes commonly found in sheep and recovered from both clinical and nonclinical human infections also contained a stx(2d) (stx(2d-Ount/O111/OX3a)) subtype. These studies suggest that a specific stx(2) subtype(s) associates with serotype and may have important epidemiological implications for tracing sources of E. coli during outbreaks of STEC-associated diseases in humans.

Asunto(s)

Infecciones por Escherichia coli/microbiología , Escherichia coli/clasificación , Enfermedades de las Ovejas/microbiología , Toxina Shiga II/genética , Toxina Shiga II/metabolismo , Animales , Escherichia coli/metabolismo , Infecciones por Escherichia coli/veterinaria , Humanos , Datos de Secuencia Molecular , Reacción en Cadena de la Polimerasa , Análisis de Secuencia de ADN , Serotipificación , Ovinos , Toxina Shiga II/clasificación

RESUMEN

Subtyping of shiga toxin type 2 variant B-subunit in 35 non-O157 and two O157 strains isolated from 37 asymptomatic human carriers yielded two strains with stx2, 10 strains with stx2c and 24 strains with stx2d genes. One isolate harboured stx2 and stx2c. The high Stx2d prevalence in asymptomatic carriers was conspicuous and may indicate a reduced pathogenicity of these toxin variants. Therefore, in order to appraise a positive STEC laboratory result, the strain must be isolated in every case. Shiga toxin types and further virulence-associated factors have to be investigated.

Asunto(s)

Portador Sano/microbiología , Infecciones por Escherichia coli/microbiología , Escherichia coli O157/metabolismo , Escherichia coli/metabolismo , Toxina Shiga II/clasificación , Escherichia coli/clasificación , Escherichia coli/patogenicidad , Escherichia coli O157/clasificación , Escherichia coli O157/patogenicidad , Humanos , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción , Toxina Shiga II/genética , Toxina Shiga II/aislamiento & purificación , Virulencia