Therapeutic use of a receptor mimic probiotic reduces intestinal Shiga toxin levels in a piglet model of hemolytic uremic syndrome
© Hostetter et al.; licensee BioMed Central Ltd. 2014
Received: 1 November 2013
Accepted: 26 May 2014
Published: 2 June 2014
Hemolytic uremic syndrome (HUS) is a systemic and potentially fatal complication of gastroenteritis secondary to Shiga toxin-producing enterohemorrhagic Escherichia coli (EHEC) infection characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute renal damage. Shiga toxin (Stx), the toxin principle in HUS, is produced locally within the gut following EHEC colonization and is disseminated via the vasculature. Clinical development of HUS currently has no effective treatment and is a leading cause of renal failure in children. Novel post-exposure therapies are currently needed for HUS; therefore, the purpose of this study was to investigate the efficacy of a Stx receptor mimic probiotic in a porcine model of HUS. Edema disease, an infection of swine caused by host adapted Shiga toxin-producing Escherichia coli (STEC) and mediated by Shiga toxin 2e (Stx2e), shares many pathogenic similarities to HUS. In this study, three-week old piglets were inoculated with STEC and 24 hours later treated twice daily with a probiotic expressing an oligosaccharide receptor mimic for Stx2e to determine if the probiotic could reduce intestinal toxin levels.
Piglets were orally inoculated with 1010 CFU of STEC strain S1191 eight days after weaning. Beginning day 1 post-inoculation, piglets were treated orally twice daily with 5 × 1011 CFU of either the receptor mimic probiotic or a sham probiotic for 10 days. Intestinal Stx2e levels were assessed daily via Vero cell assay. The efficacy of the probiotic at reducing intestinal Stx2e, vascular lesions, and clinical disease was evaluated with repeated measures ANOVA and Fisher’s exact test as appropriate.
The probiotic significantly reduced intestinal Stx2e, as reflected by decreased fecal toxin titers on days 3–8 post-inoculation (p < 0.01). Despite this reduction in intestinal toxin levels, however, the probiotic failed to reduce the incidence of vascular necrosis in target organs and had no effect on clinical disease.
The data suggest that post-exposure treatment with a Stx-binding probiotic is effective in reducing intestinal toxin burden. Future studies could target this approach for possible development of post-exposure interventions.
Enterohemorrhagic Escherichia coli (EHEC), classically of serotype O157:H7, cause sporadic cases as well as outbreaks of food borne illness characterized by hemorrhagic colitis . Ruminants are the primary reservoir for EHEC, and contamination of either produce or meat with fecal matter from carriers serve as the primary source of infection . A small percentage of patients (typically 5-15%) with diarrhea secondary to EHEC infection develop a systemic and potentially fatal complication known as hemolytic uremic syndrome (HUS), characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute renal damage. Historically, HUS has been more prevalent in children under the age of 10 and the elderly, and it remains the leading cause of renal failure in children in the United States [1, 3–5]. More recently, a large outbreak of gastroenteritis and HUS in Germany caused by an atypical enteroaggregative E. coli that produced Shiga toxin (serotype O104:H4), was characterized by a higher prevalence of HUS in adults versus children. In this particular outbreak, 88% of the patients who developed HUS were adults [6–8]. At present, there is no known method to predict which patients with diarrhea caused by EHEC will develop HUS, and no single effective treatment for the disorder once it is diagnosed. Currently, HUS treatment involves fluid therapy, dialysis, and management of coagulation disorders; antimicrobial therapy, however, remains controversial [9–11].
Although the pathogenesis is multifactorial, Shiga toxin (Stx) produced by EHEC is the principal mediator of HUS. EHEC that produce Stx1, Stx2, or both toxins have been associated with HUS development. Epidemiologic evidence and data from animal models show that strains producing Stx2 only are more likely to cause severe disease [12, 13]. The preferred receptor for Stx1, Stx2, and most of its variants is globotriaosylceramide (Gb3); globotetraosylceramide (Gb4) is the preferred receptor of Stx2e, the Stx2 variant which is primarily associated with edema disease of swine . Following EHEC colonization, Stx is produced locally within the intestine, and then crosses the intestinal mucosa and vascular endothelium to gain access to the bloodstream. Although the exact mechanism for systemic absorption of Stx is unknown, recent evidence suggests absorption across the epithelium occurs via a transcellular pathway and is increased under microaerobic conditions . Once the toxin reaches the blood, it binds the receptor on the surface of vascular endothelial cells in key target organs (kidney, brain) and is internalized . Toxin internalization within endothelial cells results in inhibition of protein synthesis, leading to cell death .
Many experimental approaches to the treatment of EHEC infection and/or HUS have been explored. One potential therapeutic approach for HUS is to neutralize the activity of Stx and several compounds have been developed for that purpose, including oral synthetic receptor mimics and specific anti-Stx antibody [17–20]. In this fashion, a probiotic that expresses Stx receptor mimics on its surface was developed for treatment of active EHEC infection . The advantage of this particular probiotic is its ability to bind and absorb Stx within the intestinal lumen, therefore potentially increasing its utility as a post-exposure therapeutic agent. The probiotic is a recombinant E. coli R1 strain (CWG308) that contains a plasmid (pJCP-Gb3) encoding two Neisseria sp. galactosyltransferase genes that when expressed, create a cell surface mimic of the Stx receptor. The binding capacity of this recombinant strain for either Stx1 or Stx2 is approximately 10,000× greater than that of SYNSORB Pk (a synthetic carbohydrate receptor mimic previously developed for treatment of STEC infection), and this efficacy has been demonstrated by several in vivo protection studies in mice [19, 21–23]. This particular construct was effective at neutralizing most of the Stx2 variants; however, it was less efficacious against Stx2e, which binds preferentially to Gb4. As a result, a new recombinant strain that expressed surface Gb4 was created as a potential probiotic strain for use in the prevention of edema disease of swine .
Edema disease, an infection of weaned swine caused by host-adapted strains of E. coli, has been adapted by our laboratory as an animal model of systemic EHEC disease in human beings [24, 25]. The edema disease model has several advantages over other models of HUS, the most outstanding of which is that it is a naturally occurring disease. Edema disease and HUS share similar early events in their pathogeneses, including localized production of toxin in the gut, toxin translocation across gut epithelium, and dissemination to target organs via the bloodstream [24, 25]. Additionally, as in human EHEC infections, not all Shiga-toxin producing Escherichia coli (STEC) inoculated swine develop systemic disease; the majority of pigs undergo an uncomplicated recovery from the diarrhea phase. Other advantages include a similar time course of pathogenic events manifested by a prodromal diarrhea phase with delayed development of systemic complications . In this model, approximately 30% of STEC challenged swine succumb to clinical disease secondary to Shiga toxemia, characterized by subcutaneous edema, neurological signs and/or sudden death.
We hypothesized that treatment with the probiotic expressing surface globotetraose would bind and trap Stx2e within the intestinal lumen, thereby reducing systemic toxin absorption and preventing clinical edema disease. The primary purpose of this study was to assess the ability of this Stx receptor–mimic probiotic to reduce fecal Shiga toxin in a naturally occurring STEC infection when administered during active infection. A secondary goal was to test the efficacy of the probiotic at preventing clinical disease.
S1191 is an STEC strain isolated from a pig with edema disease. This strain belongs to serotype O139, is resistant to chloramphenicol, and produces Stx2e, hemolysin, F18ab fimbriae and heat-stable enterotoxin B. Strain 123 is a non-pathogenic E. coli, serogroup O143, isolated from a healthy pig. Inocula were prepared as described previously .
Creation of the probiotic strain, an E. coli R1 derivative expressing surface GalN Acβ(1 → 3)Galα(1 → 4)Galβ(1 → 4)Glc (globotetraose), has been described in detail previously . Briefly, three Neisseria sp. glycosyltransferase genes (lgtC, lgtE, and lgtD) and a UDP-GalN Ac-4-epimerase gene (gne) were cloned into the plasmid vector pK184 to create plasmid pGb4 and inserted into a derivative of E. coli R1 (CWG308). This strain has a waaO mutation in the outer core lipopolysaccharide (LPS) biosynthesis locus that results in production of a truncated LPS core terminating in glucose. Expression of the plasmid-encoded glycosyltransferase genes results in linkage of GalN Acβ(1 → 3)Galα(1 → 4)Galβ(1 → 4) onto the terminal glucose. The sham strain is the E. coli derivative R1 (CWG308) with the plasmid vector pK184 only. The treatment and sham strains were grown overnight in tryptic soy broth (TSB) plus kanamycin (30 μg/ml) and IPTG (20 μg/ml), concentrated 100× and re-suspended in TSB containing 10% NaCO3, 20% sucrose and 21% glycerol. Treatments were stored at -80C and thawed just prior to use.
Reproduction of clinical edema disease
Experimental design to assess the effect of a probiotic expressing a Shiga toxin receptor mimic on the incidence of edema disease
Number of pigsa
Pig age at inoculation
Treatment with the probiotic
Pigs inoculated with STEC strain S1191 were treated with either E. coli CWG308 containing the plasmid pGb4 (probiotic) or CWG308 containing the vector pK184 only (sham). Individual pigs were orally dosed with 5 × 1011 CFU of either strain twice daily for 10 days beginning day 1 post-inoculation.
Determination of Stx2e in feces
Feces were collected daily from control and STEC-inoculated pigs on days 1–10 post-inoculation, and stored at 4°C until processing. Stx2e concentrations were assessed using a Vero cell assay as described previously . Briefly, samples were diluted two-fold in PBS and added to monolayers of Vero cells in microtiter plates. Toxin titers were expressed as the log of the reciprocal of the greatest dilution that resulted in ≥ 50% Vero cell death. Specificity of the titers for Stx2e was confirmed by neutralization with anti-Stx2e antibody.
Comparison of fecal toxin titers was performed using a two way repeated measures ANOVA with an unweighted means analysis (Prism, Graphpad software, Inc, La Jolla, CA). Bonferroni post hoc test was used to compare group differences on specific days. For all analyses, a P value < 0.05 was considered statistically significant. Incidences of vascular lesions and clinical disease between probiotic and sham groups were compared using Fisher’s exact test.
STEC strain 1191 was recovered from feces of all challenged pigs (probiotic and sham groups) at both 2 and 5 days post inoculation. None of the negative control pigs were positive for STEC at either time-point. The probiotic E. coli strain CWG308 (pJCPGb4) was recovered from all pigs in the probiotic treated group at both 2 and 5 days post inoculation.
Fecal toxin titers
Incidences of clinical disease and vascular lesions in pigs inoculated with Shiga toxin-producing Escherichia coli and treated with a probiotic strain expressing a Shiga toxin receptor mimic vs. a sham strain lacking the receptor mimic
Number of pigsd
Incidence of clinical disease
Incidence of vascular lesions in brainstem
Incidence of vascular lesions in ileum
Comparison of fecal toxin titers between clinical and non-clinical pigs
Fecal toxin titers in clinical pigs were compared with titers in non-clinical pigs in both the sham and probiotic treatment groups (Figure 1B). Since all pigs that developed edema disease fell ill prior to day 8 post inoculation, fecal titers are not available for these pigs beyond day 7 post inoculation. Although treatment with the probiotic reduced fecal toxin titers overall, those pigs treated with the probiotic that developed clinical disease had, on average, toxin titers similar to the sham treated group.
The probiotic strain expressing globotetraose used in this study was designed specifically to bind and neutralize Stx2e, the toxic principal of piglet edema disease. This construct was effective at neutralizing 98.4% of Stx2e cytotoxicity in vitro . The dose of probiotic and frequency of administration used here were extrapolated from previous studies with a similar probiotic expressing a surface Gb3 mimic in a mouse model of STEC infection . Here we show that post-exposure treatment twice daily with the probiotic was effective at reducing the fecal Stx2e in STEC inoculated piglets. Fecal toxin titers were significantly reduced by day three of probiotic administration, and remained lower for several days. Reduction of intestinal Stx may be a first line of defense in HUS prevention for EHEC infected patients. Despite the favorable reduction in intestinal Stx, treatment with the receptor mimic probiotic failed to reduce the incidence of both vascular lesions in target organs and clinical disease in STEC inoculated swine, indicating systemic absorption of Shiga toxin still occurred. While not statistically significant, the incidence of vascular lesions in brainstems of probiotic treated pigs was less than that of sham treated pigs. This subtle trend towards lower disease incidence may warrant further studies to increase the power to experimentally detect lesion differences. Interestingly, those pigs that developed clinical disease within the probiotic group had, on average, higher fecal toxin titers than subclinical pigs within this group, with the average toxin titers of clinical pigs approaching those of the sham treated groups on days 2–6 post inoculation. This could indicate a failure of the probiotic to reduce toxin titers in those pigs that broke with clinical disease, despite an overall reduction in toxin titers within this treatment group.
In contrast to our findings here, several studies in mouse models have shown the efficacy of various probiotic strains at preventing disease caused by EHEC. Importantly, however, the probiotics used in these studies were administered prior to colonization. For example, Leatham et al. showed that certain commensal E. coli strains were efficacious at preventing growth of an E. coli O157:H7 strain in the streptomycin-treated mouse model of EHEC infection . Similarly, certain bifidobacterial strains were able to prevent mortality in a gnotobiotic mouse model of EHEC infection when administered seven days prior to inoculation with the EHEC strain . While these probiotics ameliorated disease caused by EHEC via inhibition of colonization, other probiotics are thought to confer protection via other mechanisms, such as suppression of virulence factor production or alteration of the host immune response [30, 31]. For example, in a recent study by Eaton et al., treatment with the probiotic Lactobacillus reuteri suppressed disease in a mouse model of EHEC infection, but had only a minimal effect on colonization. The authors propose that the probiotic may have affected production of Stx2, but that further investigation was required to confirm the mechanism . Based on these studies, we anticipated that the receptor mimic probiotic would be efficacious at preventing systemic disease in our pig model. However, one important difference between our study and those described above is the timing of probiotic administration. The probiotics used in the previous studies were most efficacious when administered prior to colonization with EHEC, and would therefore have limited therapeutic utility in the treatment of existing infections. The probiotic strain used in our study was given 1 day post STEC inoculation to investigate its efficacy in a post-exposure setting - similar to that which might be experienced during outbreaks of foodborne illness secondary to EHEC. Preemptive treatment of individuals during EHEC outbreaks may not be practical, given their sporadic nature. Our receptor mimic probiotic was designed specifically to bind Stx within the gut; therefore, we hypothesized that it would be useful as a post-exposure therapy and our experimental design reflected this. We speculate that the receptor mimic probiotic would likely have been more effective at preventing systemic disease had it been administered prior to STEC inoculation, similar to previous studies.
In mice, treatment with a similar probiotic expressing a Gb3 mimic was protective against fatal systemic complications of infection with human-derived EHEC . There are several differences between the mouse studies and the current study that may have influenced treatment outcome. The affinity of the Gb4 mimic bacterium for Stx2e is not quite as high as that of the previously described Gb3 mimic for other members of the Stx family that was used in the mouse studies . This reduced affinity may have resulted in sub-optimal retention of Stx2e in the gut lumen. A further disparity between these studies is the timing of probiotic treatment. In mice, treatment with the probiotic strain was initiated at the time of EHEC challenge. Our experimental design delayed treatment for 24 hours in an attempt to more closely mimic post-exposure therapy. As a result, pigs in this study were exposed to intestinal Stx2e prior to treatment with the probiotic. Pigs are known to be extremely susceptible to intravenous Shiga toxin (LD50 3 ng/kg) . It is likely that the early and continuous exposure to systemic toxin absorbed from the gut initiates an irreversible cascade of events leading to clinical disease development in some animals. This may represent an obstacle for post-exposure therapy in human beings because of the delay between the onset of diarrhea and diagnosis in EHEC infections . Similarly, when probiotic treatment was delayed in the mouse model for 24 or 48 hrs, mice were not protected from death when challenged with the most virulent EHEC strain .
In conclusion, the results of this study show that post-exposure treatment with a Stx2e-receptor mimic probiotic is effective at reducing Stx within the gut of a porcine model of STEC infection. Despite its efficacy at reducing gut Stx, the probiotic failed to prevent vascular necrosis in target organs and clinical disease, indicating systemic toxin absorption still occurred. Further investigation is warranted to determine if adjusting the time of treatment would have been more effective at ameliorating clinical STEC disease.
We thank Rich Evans for advice regarding statistical analyses, and Erin Brown, Tricia Beasley, Jiquan Gao, Carisa Ralph, Dianna Jordan and Sheri Booher for help with the animal experiments. This work was supported in part by a grant from the Iowa Pork Producers (03–163), although they had no direct role in study design.
- Melton-Celsa A, Mohawk K, Teel L, O’Brien A: Pathogenesis of Shiga-toxin producing Escherichia coli. Curr Top Microbiol Immunol. 2012, 357: 67-103.PubMedGoogle Scholar
- Moxley RA: Escherichia coli O157:H7: an update on intestinal colonization and virulence mechanisms. Anim Health Res Rev. 2004, 5 (1): 15-33. 10.1079/AHR200463.PubMedView ArticleGoogle Scholar
- Siegler R, Oakes R: Hemolytic uremic syndrome; pathogenesis, treatment, and outcome. Curr Opin Pediatr. 2005, 17 (2): 200-4. 10.1097/01.mop.0000152997.66070.e9.PubMedView ArticleGoogle Scholar
- Paton JC, Paton AW: Pathogenesis and diagnosis of Shiga toxin-producing Escherichia coli infections. Clin Microbiol Rev. 1998, 11 (3): 450-79.PubMedPubMed CentralGoogle Scholar
- Tarr PI, Gordon CA, Chandler WL: Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome. Lancet. 2005, 365 (9464): 1073-86.PubMedGoogle Scholar
- Muniesa M, Hammerl JA, Hertwig S, Appel B, Brussow H: Shiga toxin-producing Escherichia coli O104:H4: a new challenge for microbiology. Appl Environ Microbiol. 2012, 78 (12): 4065-73. 10.1128/AEM.00217-12.PubMedPubMed CentralView ArticleGoogle Scholar
- Frank C, Werber D, Cramer JP, Askar M, Faber M, an der Heiden M, Bernard H, Fruth A, Prager R, Spode A, Wadl M, Zoufaly A, Jordan S, Kemper MJ, Follin P, Müller L, King LA, Rosner B, Buchholz U, Stark K, Krause G, HUS Investigation Team: Epidemic profile of Shiga-toxin producing Escherichia coli O104:H4 outbreak in Germany. N Engl J Med. 2011, 365 (19): 1171-80.View ArticleGoogle Scholar
- Werber D, King LA, Müller L, Follin P, Buchholz U, Bernard H, Rosner B, Ethelberg S, De Valk H, Höhle M: Associations of age and sex with the clinical outcome and incubation period of Shiga toxin-producing Escherichia coli O104:H4 infections, 2011. Am J Epidemiol. 2013, 178 (6): 984-92. 10.1093/aje/kwt069.PubMedView ArticleGoogle Scholar
- Goldwater PN, Bettelheim KA: Treatment of enterohemorrhagic Escherichia coli (EHEC) infection and hemolytic uremic syndrome. BMC Med. 2012, 10: 12-10.1186/1741-7015-10-12.PubMedPubMed CentralView ArticleGoogle Scholar
- Loirat C, Saland J, Bitzan M: Management of hemolytic uremic syndrome. Presse Med. 2012, 41 (3 Pt 2): 115-35.View ArticleGoogle Scholar
- Bitzan M: Treatment options for HUS secondary to Escherichia coli O157:H7. Kidney Int Suppl. 2009, 112: S62-6.PubMedView ArticleGoogle Scholar
- Werber D, Fruth A, Buchholz U, Prager R, Kramer MH, Ammon A, Tschäpe H: Strong association between shiga toxin-producing Escherichia coli O157 and virulence genes stx2 and eae as possible explanation for predominance of serogroup O157 in patients with haemolytic uraemic syndrome. Eur J Clin Microbiol Infect Dis. 2003, 22 (12): 726-30. 10.1007/s10096-003-1025-0.PubMedView ArticleGoogle Scholar
- Tesh VL, Burris JA, Owens JW, Gordon VM, Wadolkowski EA, O'Brien AD, Samuel JE: Comparison of the relative toxicities of Shiga-like toxins type I and type II for mice. Infect Immun. 1993, 61 (8): 3392-402.PubMedPubMed CentralGoogle Scholar
- Boyd B, Tyrrell G, Maloney M, Gyles C, Brunton J, Lingwood C: Alteration of the glycolipid binding specificity of the pig edema toxin from globotetraosyl to globotriaosyl ceramide alters in vivo tissue targeting and results in a verotoxin 1-like disease in pigs. J Exp Med. 1993, 177 (6): 1745-53. 10.1084/jem.177.6.1745.PubMedView ArticleGoogle Scholar
- Tran SL, Billoud L, Lewis SB, Phillips AD, Schüller S: Shiga toxin production and translocation during microaerobic human colonic infection with Shiga toxin-producing E. coli O157:H7 and O104:H4. Cell Microbiol. 2014, Epub ahead of printGoogle Scholar
- Jacewicz M, Clausen H, Nudelman E, Donohue-Rolfe A, Keusch GT: Pathogenesis of shigella diarrhea. XI. Isolation of a shigella toxin-binding glycolipid from rabbit jejunum and HeLa cells and its identification as globotriaosylceramide. J Exp Med. 1986, 163 (6): 1391-404. 10.1084/jem.163.6.1391.PubMedView ArticleGoogle Scholar
- Matise I, Cornick NA, Booher SL, Samuel JE, Bosworth BT, Moon HW: Intervention with Shiga toxin (Stx) antibody after infection by Stx-producing Escherichia coli. J Infect Dis. 2001, 183 (2): 347-50. 10.1086/317930.PubMedView ArticleGoogle Scholar
- Sheoran AS, Chapman-Bonofiglio S, Harvey BR, Mukherjee J, Georgiou G, Donohue-Rolfe A, Tzipori S: Human antibody against shiga toxin 2 administered to piglets after the onset of diarrhea due to Escherichia coli O157: H7 prevents fatal systemic complications. Infect Immun. 2005, 73 (8): 4607-13. 10.1128/IAI.73.8.4607-4613.2005.PubMedPubMed CentralView ArticleGoogle Scholar
- Takeda T, Yoshino K, Adachi E, Sato Y, Yamagata K: In vitro assessment of a chemically synthesized Shiga toxin receptor analog attached to chromosorb P (Synsorb Pk) as a specific absorbing agent of Shiga toxin 1 and 2. Microbiol Immunol. 1999, 43 (4): 331-7. 10.1111/j.1348-0421.1999.tb02413.x.PubMedView ArticleGoogle Scholar
- Menne J, Nitschke M, Stingele R, Abu-Tair M, Beneke J, Bramstedt J, Bremer JP, Brunkhorst R, Busch V, Dengler R, Deuschl G, Fellermann K, Fickenscher H, Gerigk C, Goettsche A, Greeve J, Hafer C, Hagenmüller F, Haller H, Herget-Rosenthal S, Hertenstein B, Hofmann C, Lang M, Kielstein JT, Klostermeier UC, Knobloch J, Kuehbacher M, Kunzendorf U, Lehnert H, Manns MP: Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case–control study. BMJ. 2012, 345: e4565-10.1136/bmj.e4565.PubMedPubMed CentralView ArticleGoogle Scholar
- Paton AW, Morona R, Paton JC: A new biological agent for treatment of Shiga toxigenic Escherichia coli infections and dysentery in humans. Nat Med. 2000, 6 (3): 265-70. 10.1038/73111.PubMedView ArticleGoogle Scholar
- Paton AW, Morona R, Paton JC: Neutralization of Shiga toxins Stx1, Stx2c, and Stx2e by recombinant bacteria expressing mimics of globotriose and globotetraose. Infect Immun. 2001, 69 (3): 1967-70. 10.1128/IAI.69.3.1967-1970.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Paton JC, Rogers TJ, Morona R, Paton AW: Oral administration of formaldehyde-killed recombinant bacteria expressing a mimic of the Shiga toxin receptor protects mice from fatal challenge with Shiga-toxigenic Escherichia coli. Infect Immun. 2001, 69 (3): 1389-93. 10.1128/IAI.69.3.1389-1393.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Cornick NA, Matise I, Samuel JE, Bosworth BT, Moon HW: Shiga toxin-producing Escherichia coli infection: temporal and quantitative relationships among colonization, toxin production, and systemic disease. J Infect Dis. 2000, 181 (1): 242-51. 10.1086/315172.PubMedView ArticleGoogle Scholar
- Cornick NA, Matise I, Samuel JE, Bosworth BT, Moon HW: Edema disease as a model for systemic disease induced by Shiga toxin-producing E. coli. Adv Exp Med Biol. 1999, 473: 155-61. 10.1007/978-1-4615-4143-1_14.PubMedView ArticleGoogle Scholar
- Casey TA, Bosworth BT: Design and evaluation of a multiplex polymerase chain reaction assay for the simultaneous identification of genes for nine different virulence factors associated with Escherichia coli that cause diarrhea and edema disease in swine. J Vet Diagn Invest. 2009, 21 (1): 25-30. 10.1177/104063870902100104.PubMedView ArticleGoogle Scholar
- Matise I, Sirinarumitr T, Bosworth BT, Moon HW: Vascular ultrastructure and DNA fragmentation in swine infected with Shiga toxin-producing Escherichia coli. Vet Pathol. 2000, 37 (4): 318-27. 10.1354/vp.37-4-318.PubMedView ArticleGoogle Scholar
- Leatham MP, Banerjee S, Autieri SM, Mercado-Lubo R, Conway T, Cohen PS: Precolonized human commensal Escherichia coli strains serve as a barrier to E. coli O157:H7 growth in the streptomycin-treated mouse intestine. Infect Immun. 2009, 77 (7): 2876-86. 10.1128/IAI.00059-09.PubMedPubMed CentralView ArticleGoogle Scholar
- Yoshimura K, Matsui T, Itoh K: Prevention of Escherichia coli O157:H7 infection in gnotobiotic mice associated with Bifidobacterium strains. Antonie Van Leeuwenhoek. 2010, 97 (2): 107-17. 10.1007/s10482-009-9391-y.PubMedView ArticleGoogle Scholar
- Tsai YT, Cheng PC, Pan TM: Immunomodulating activity of lactobacillus paracasei subsp. paracasei NTU 101 in Enterohemorrhagic Escherichia coli O157:H7-Infected Mice. J Agric Food Chem. 2010, 58 (21): 11265-11272. 10.1021/jf103011z.PubMedView ArticleGoogle Scholar
- Eaton KA, Honkala A, Auchtung TA, Britton RA: Probiotic Lactobacillus reuteri ameliorates disease due to enterohemorrhagic Escherichia coli in germfree mice. Infect Immun. 2011, 79 (1): 185-91. 10.1128/IAI.00880-10.PubMedPubMed CentralView ArticleGoogle Scholar
- MacLeod DL, Gyles CL, Wilcock BP: Reproduction of edema disease of swine with purified Shiga-like toxin-II variant. Vet Pathol. 1991, 28 (1): 66-73. 10.1177/030098589102800109.PubMedView ArticleGoogle Scholar
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