It has been only thirty years since Shiga toxin-producing Escherichia coli was recognized as a human pathogen after the first outbreak investigated as hemorrhagic colitis in 47 patients in Oregon and Michigan [1]. This E. coli O157:H7 strain was then considered to be rare, but the 1993 multistate outbreak from undercooked hamburgers at a fast-food chain gained national attention for this newly emerging pathogen [2]. By 2002 there were 350 outbreaks (≥2 cases with same exposure source) reported to the CDC in 49 states, sickening 8598 people with a 17.4% hospitalization rate [3]. Contaminated ground beef and fresh produce account for about 75% of the infections, with the remainder being person-to-person, waterborne or animal contact sources and the vast majority (92%) occurring seasonally from May to November [3].

Enterohemorrhagic E. coli (EHEC) are not invasive, so bacteremia is rare, but they secrete ribosome inactivating Shiga-like toxins (Stx1 and Stx2 with variants) which are responsible for much of the organ damage [4,5], and Stx2 is more frequently associated with severe disease. Several recent reviews discuss the molecular basis for bacterial success and toxin biochemistry [6,7,8]. Bacterial colonization of the intestine with attaching and effacing lesions support type III secretion of toxins into the vasculature [6]. Micropinocytosis may contribute as toxin antigen is observed in patient gut epithelial cells in the absence of A/E lesions [9].

The very young and the elderly are most susceptible to complications and death from EHEC infection. This bacterial infection is the leading cause of acute kidney failure in otherwise healthy children in the US with an average infection rate of 1/100,000. Children less than five years of age are more likely to develop complications requiring hospitalization and kidney dialysis, and the elderly >60 years are more likely to die regardless of the clinical complications [10]. This emerging pathogen has become a global problem as well. The 1996 O157:H7 outbreak in thousands in Sakai City, Japan was purportedly from contaminated bean sprouts distributed in elementary school lunches [11]. The summer 2011 outbreak sourced to bean sprouts in Germany left over 4000 infected [12] and sent a clear warning through the EHEC research and clinical infectious disease communities that more virulent strains are emerging. This O104:H4 strain was a combination of an enteroaggregative E. coli strain, normally characterized by intestinal mucosa adherence to cause self-limiting diarrhea [13], that picked up the stx2 gene, thereby acquiring high virulence and causing severe clinical consequences, particularly acute kidney injury from hemolytic uremic syndrome and severe neurological abnormalities [14,15]. Karmali et al. was the first to make the association between Stx, diarrheal E. coli infection and the idiopathic hemolytic uremic syndrome of infancy and childhood [16,17]. This critical link provided the first molecular explanation for the clinical observations, thereby opening new routes for differential diagnosis and pathogen-specific treatment modalities.

Hemolytic uremic syndrome (HUS) is a serious clinical complication of EHEC infection and the severity of a public outbreak is often discussed in terms of the HUS rate. HUS is a clinical composite of thrombocytopenia, hemolytic anemia and thrombotic microangiopathy that contributes to acute kidney injury, often requiring dialysis and can progress to acute renal failure and death. Epidemiology studies have shown that HUS typically develops in about 5%–15% of patients, but this varies between bacterial strains and geographic location. Treatment is supportive, no toxin-specific therapies are available and antibiotics are usually contraindicated, depending on serotype. Recently, a large multi-state prospective study of 259 US children with HUS as a complication of EHEC O157:H7 infection demonstrated unequivocally that exposure to antibiotics of any class in the first week of illness was independently associated with development of HUS and tripled the risk [18]. For the O157:H7 strain, antibiotics increase toxin production due to location of stx genes within antibiotic-inducible resident lambdoid prophages [19]. The recent outbreak in Germany with the Stx2-producing O104:H4 strain was notable for its high HUS rate at 22%, occurring overwhelmingly in adults (88%) and most of these being young women [12,15,20]. In this outbreak, use of antibiotics at one hospital center was beneficial, significantly reducing intestinal bacterial colonization duration and improving clinical outcome [21]. Unlike the more common O157:H7 strain, antibiotics reduced Stx secretion from this strain in vitro [22]. Argentina has the dubious distinction of having the highest incidence of pediatric diarrhea-associated HUS (13.9/100,000 population) and ~20% of Argentina’s pediatric kidney transplants are the result of EHEC infections [23]. Relative to other infectious disease outbreaks, the death rate from EHEC infection is fairly low at around 3%–5%, but morbidity associated with kidney injury is significant. About 12% of patients with diarrhea-associated HUS progress to end stage renal failure within 4 years and about 25% have long term renal impairment [24,25], putting them at high risk for other clinical complications as eventually encounter pregnancy, high blood pressure, diabetes, cardiovascular disease and other complications of aging.

Because of the importance of HUS complications, considerable clinical and basic research has focused on this aspect of EHEC infections to define the onset of HUS and to identify cellular dysfunctions that contribute to the pathology. The intent is to identify clinical patterns and molecular biomarkers that identify those at highest risk in order to prevent or mitigate HUS. Not all cases of HUS are due to EHEC infections, and the similarities and distinctions between EHEC-induced HUS and related syndromes of atypical HUS and thrombotic thrombocytopenic purpura can delay diagnosis and complicate clinical management of patients. Identifying effective non-antibiotic adjunctive therapeutics depends on understanding the molecular and pathophysiological mechanisms that contribute to organ injury, and in this respect, development of appropriate and representative animal models is critical. Both of these aspects are discussed below.

Hemolytic uremic syndrome (HUS) is a clinical syndrome comprising the triad of thrombocytopenia, thrombotic microangiopathy, and hemolytic anemia, and is frequently associated with acute kidney injury. Pathogenic challenge that results in endothelial injury or dysfunction shifts the hemostatic balance toward a pro-thrombotic environment, resulting in thrombotic microangiopathy with inappropriate deposition of clots in microvascular beds causing tissue ischemia. The kidney is a particular target during EHEC infection in part because the toxin receptors are expressed at higher density on glomerular endothelial cells [26] and toxin activities induce endothelial expression of adhesion molecules that support interactions with activated platelets and leukocytes [27] which contribute significantly to clot formation [28].

Development of a thrombotic microangiopathy can arise as a complication of bacterial infections like EHEC, from genetic mutations in complement regulatory pathways (atypical HUS, aHUS), from deficiencies of regulatory ADAMTS13 enzyme (thrombotic thrombocytopenic purpura, TTP) or even secondarily as a consequence of autoimmune diseases such as systemic lupus erythematosus. These pathways to HUS have different etiologies but frequently overlapping clinical presentation (Figure 1).

Thrombotic microangiopathy is a shared consequence and is related to, but distinct from, disseminated intravascular coagulation (DIC), a consumptive coagulopathy. The coagulopathy of HUS is distinguished from DIC by several parameters, including a normal or elevated fibrinogen level and normal or slightly elevated clotting times because coagulation factors are not consumed (Figure 2). Markers of fibrinolysis (fibrin degradation products, D-dimer) are only modestly increased in HUS relative to DIC, but measures of microangiopathic hemolytic anemia (MAHA) such as schistocytes are markedly increased. Additionally, the renal failure of DIC is attributable to acute tubular necrosis, whereas that associated with HUS is predominately a thrombotic microangiopathy of glomerular vasculature, with or without tubular necrosis.

Murine models of EHEC toxemia do not develop thrombocytopenia and, therefore, do not present with HUS. Recently these Stx models have included bacterial endotoxin (Gram negative lipopolysaccharide, LPS), tumor necrosis factor-α (TNFα), adenosine diphosphate (ADP) or similar along with the toxin to induce platelet loss in an effort to replicate full-spectrum HUS [29]. While thrombocytopenia is observed in the mice after LPS + Stx, it is a consequence of pro-inflammatory priming, resulting in endotoxin-induced DIC [30], not Stx-induced HUS, with different coagulation mechanisms.

Over 90% of HUS cases are associated with EHEC infection, also referred to as D + HUS, to indicate that there was diarrhea before the development of HUS. HUS from infection with other pathogens, usually Streptococcus pneumoniae (SP-HUS) which exposes the Thomsen-Freidenreich antigen with autoimmune consequences, results in longer hospitalization and long-term kidney injury [31,32]. A diarrheal prodrome can be observed in non-EHEC HUS cases, albeit rarely [33]. Patients usually develop a prodromal hemorrhagic colitis after EHEC contaminated food or water has been ingested [34], with HUS developing after approximately 7–10 days [35].

It is widely acknowledged that the Shiga-like toxins produced by the enterohemorrhagic E. coli are the main virulence factors driving the organ damage in patients and animal models. EHEC secrete Shiga-like toxin-1 (Stx1) and/or Shiga-like toxin 2 (Stx2), and there are multiple Stx2 variants [36]. The two major toxins are structurally similar with a shared AB₅ domain structure, but only 56% amino acid homology. Stx are ribosome-inactivating toxins, similar to Shiga toxin from Shigella dysenteriae serotype-1 [37] and ricin from castor beans. The enzymatic A subunit and a cell binding B subunit that organizes into pentamers recognize a globotriaosylceramide (Gb₃) membrane receptor on cells, particularly glomerular endothelial cells [38]. Internalized toxin-receptor complexes undergo retrograde transport to the endoplasmic reticulum via the Golgi apparatus where the A subunit N-glycosidase activity removes an adenine from 28S ribosomal RNA to inhibit protein synthesis [39]. A recent study shows Stx1 intracellular trafficking is mediated by Golgi protein GPP130 and disruption of this interaction leads to lysosomal degradation of Stx1 and protection of mice from lethal toxemia [40]. The toxins also induce inflammation in patients [41] and animal models [42], and endoplasmic reticulum stress-induced transcriptional events are stimulated in susceptible cells [43,44].

The Shiga toxins target Gb₃-rich tubular epithelium, as well as the glomerular endothelial cells, with cellular apoptosis, necrosis and thrombotic microangiopathy contributing to the acute kidney failure seen in patients [45]. In patients, the renal pathology as a consequence of EHEC infection includes cortical necrosis, glomerular thromboses and congestion with widened subendothelial space, endothelial cell swelling, neutrophilia, and occasional mesangiolysis [46,47]. In the baboon model of Stx challenge which presents with all manifestations of HUS [48], glomerular injury after Stx1 and Stx2 challenge featured prominent HUS-like capillary wall changes, including thickening of the glomerular basement membrane and double contouring with prominent thrombus formation, and severe endothelial injury with diffuse cell swelling and focal endothelial denudation (Figure 3). Because this is an animal model allowing comparisons between toxins, some differences emerged with glomerular endothelial injury predominating after Stx1, whereas mesangiolysis and eosinophilic infiltration accompanied the glomerular injury in the Stx2-challenged animals [49].

Endothelial activation by the Shiga-like toxins induces an inflammatory milieu that is a strong contributor to the thrombi formation in the microvasculature during development of HUS. Stx2 upregulates chemokines monocyte chemotactic protein-1 (MCP-1, CCL2) and IL-8 (CCL8) [27,42] and Stx1 increases expression of cellular adhesion molecules ICAM-1, VCAM-1, and E-selectin on endothelial cells [50]. In human monocytes, EHEC infection and Shiga toxins induces inflammatory cytokines and chemokines including IL-1β, IL-6, IL-8, and TNFα [51]. In the GI of patients, the colon is severely affected, showing edema and hemorrhage, consistent with the hemorrhagic colitis that is often seen preceding HUS [52]. Intestinal leukocytosis is more prominent with D + HUS compared to non-EHEC HUS [53], and with Stx in the intestinal epithelial cells [9], there is likely production of pro-inflammatory and chemotactic mediators (IL-1, IL-6, IL-8, TNFα) from epithelial cells and resident macrophages [54,55,56]. Together, this group of chemokines and adhesion molecules serves to recruit and activate neutrophils, contributing to increased tissue damage.

Normally endothelial cells present non-thrombogenic surfaces, and both Shiga toxins and inflammatory mediators can shift the endothelium to a pro-thrombotic state, contributing to thrombus formation [57]. For example, Stx2 causes about a 15% decrease in thrombomodulin surface antigen expression of human glomerular endothelial cells in vitro, which is further potentiated by TNFα [58], although whether this amount of antigen loss significantly impacted function was not determined. Thrombomodulin is an essential cofactor of the protein C anticoagulant pathway, an assembly of molecules on the endothelium that maintains blood fluidity [59,60]. Loss of thrombomodulin expression, or other members of this pathway, correlates with a pro-coagulant environment [61] and circulating soluble thrombomodulin levels are accepted measures of endothelial injury [62].

However, endothelial and leukocyte activation are probably only part of what induces the formation of microthrombi during D + HUS. Studies have also looked at whether platelet activation might contribute to microthrombi genesis. Plasma from patients with D + HUS has shown evidence of platelet activation and degranulation [63]. Stx1 can activate endothelial cells, especially ones that express more Gb₃ receptor due to TNFα or LPS priming, to cause increased adhesion of platelets [64] and inhibition of platelet cluster degradation by the inhibition of ADAMTS13 [65]. Collectively, endothelial, platelet and neutrophil activation all contribute to the formation of microthrombi that then becomes a major driving force of D + HUS pathophysiology.

Cytokines can disrupt the anti-thrombotic properties of the microvascular endothelial cells and increase cell-surface Gb₃ receptor expression [53]. Obrig et al. hypothesized previously that the sensitivity of endothelial cells to Shiga toxins depended greatly on their source and levels of Gb₃ expression, and found that while TNFα and lipopolysaccharide (LPS) could increase sensitivity of human umbilical vein endothelial cells to Shiga toxins, they had no effect on renal microvascular endothelial cell Gb₃ expression or Stx sensitivity [26]. It has been shown that the numbers of polymorphonuclear leukocytes present at the beginning of D + HUS is predictive of outcome, but not in cases of atypical HUS [66], a related but distinct syndrome (see below). Stx induces an inflammatory and chemotactic environment, and recruited neutrophils may transport the toxins in the blood [67], which could explain how the toxin passes from the gut to the kidney without bacteremia or invasion by the EHEC. Whether this occurs in patients is debated [68] because Stx antigen is sometimes [67,69,70], but not always [71] detected on the surface of circulating neutrophils. Close proximity of neutrophils and their enzymes to renal endothelial cells can also alter the surface availability of some proteins, changing the functionality of the endothelium. It is well known that neutrophil elastase cleaves endothelial-expressed thrombomodulin [72], a necessary cofactor of the protein C anticoagulant pathway [59]. If this proteolysis is incomplete, and removes only the amino-terminal lectin domain of thrombomodulin, this may contribute to organ injury and thrombotic microangiopathy, as suggested in murine models of Stx2 challenge with endotoxin priming [73].

It is interesting to note that while this information helps to explain the forces driving disease in the kidney and other organs, they do not go as far in explaining the neurological signs that are often seen accompanying HUS. In the recent 2011 German outbreak of EHEC infection, the rate of HUS was unusually high and the neurologic complications were severe, from aphasia to epileptic seizures. Notably, there were no histologically observed brain microthrombi, vessel occlusions or evidence of ischemia [74]. How then did the patients develop neurological symptoms, and was Stx to blame? One study in rats has shown that Stx1 effect on astrocytes could indirectly affect the blood-brain barrier [75]. During the German outbreak, immunoadsorption of IgG helped attenuate the neurological complications of Stx2-producing E. coli O104:H4 [76]. They did not find evidence that the antibodies were directed against ADAMTS13, loss of which contributes to a related thrombotic microangiopathy (see below), and instead hypothesized that the antibodies were against Stx itself and were crosslinking receptors, causing the release of larger von Willebrand Factor multimers [77] to indirectly inhibit ADAMTS13 [65] and increasing risk of thrombus formation. Further investigation will show whether this interesting hypothesis is true.

A potential role for the complement pathway during development of Stx-induced HUS has recently gained renewed interest. Complement is an ancient non-specific opsonic defense mechanism dating to pre-Cambrian ancestors [78], and is now a highly regulated mammalian innate immune strategy contributing to host defense or tissue injury depending on the context [79]. There is some evidence that complement is activated during EHEC infection. During acute phase EHEC-HUS, complement factor C3 or C9 is detected on platelet-leukocyte complexes from patients, and Stx can induce ex vivo release of complement-bearing microparticles from platelets or monocytes [80]. Using purified components, Stx2 was shown to activate complement via the alternative pathway and slow complement factor H (CFH) regulatory activity [81]. A recent study showed Stx-induced C3b interactions with P-selectin to promote a pro-thrombotic surface on dermal microvascular endothelial cells activated with human serum and/or blood under shear stress [82]. These observations, along with C3 deposition on glomeruli from mice challenged with Stx2 + LPS [82], suggest a role for complement in the pathophysiology of endothelial dysfunction during HUS. However, patient data has less apparent clarity. In a small patient study, increased levels of alternative pathway members Bb and SC5b-9 were observed early in D + HUS patients, but there was no correlation with clinical parameters or outcome [83]. There also was no comparison with non-EHEC renal patients so it is difficult to evaluate a specific relationship to Stx-HUS as opposed to a generalized host defense response. In addition, despite apparent success in three severely ill infants [84], treatment of 67 patients with Eculizumab (Soliris^®, Alexion Pharmaceuticals), the anti-C5 inhibitor antibody treatment for atypical HUS [85], during the 2011 outbreak of Stx2-producing EHEC 0104:H4 in Germany was not effective and likely worsened patient outcome [21]. This was a severely ill cohort with other co-treatments so efficacy interpretation is debated [86,87], but this is likely the patient population that such a treatment would target. Given the fundamental contribution of the complement pathway to pathogenesis of many diseases, it could potentially contribute to disease severity, but whether it actually initiates HUS during this bacterial infection remains to be determined.

HUS not due to enteropathogenic bacterial infection is known as atypical HUS (aHUS) and there are many triggers besides infection, with the underlying cause being genetic deficiencies in regulators of the alternative pathway of complement [88]. In this case, the alternative pathway of complement is a fundamental initiator of disease. aHUS leads to recurring bouts of HUS, and can lead to stroke, heart complications and end-stage renal failure, although how quickly this progresses depends on the nature of mutation in the complement pathway members [89]. Histologically, aHUS is indistinguishable from D + HUS in the kidney. A majority (60%–70%) of patients with cofactor H (CFH) mutations progressed to end-stage renal failure within a year of aHUS symptoms [90]. Many children experience their first bout of aHUS before age 6 months, which can help lead a differential diagnosis towards aHUS instead of D + HUS [91]. Treatment with Eculizumab (Soliris^®), a humanized monoclonal antibody against complement C5, has had success in aHUS patients because it blocks the rampant, dysregulated activation of C5 thereby preventing formation of inflammatory C5a and the cytotoxic terminal attack complex C5b-9 [85,92].

Atypical HUS can be sporadic or familial, and is associated with dysregulation of complement typically characterized either by over-activation or compromised regulators of the alternative pathway of complement. Ordinarily, complement factor H (CFH), along with complement factor I (CFI) and membrane cofactor protein (MCP) accelerates the decay of C3 convertase, inhibiting complement activation. Thrombomodulin, an endothelial cell surface membrane protein usually associated with anti-coagulant function [62], aids this enzymatic complex in its activity. Mutations in thrombomodulin [93] as well as CFH [94], CFI [90], and MCP [95] are all implicated as risk factors for development of aHUS, along with mutations in complement factor B [96] and C3 [97]. In addition, autoantibodies against CFH have also been demonstrated [89]. While infection can be a possible trigger for the manifestation of aHUS, in general there is much less evidence of leukocytosis and inflammation in patients with aHUS than in those with D + HUS [53]. Yet, there may be overlap and at least one patient with EHEC-HUS has been shown to also have a mutation in MCP that would confer risk of developing aHUS [98], emphasizing how the lines between these syndromes can be blurred.

A third syndrome closely related to aHUS is thrombotic thrombocytopenic purpura (TTP), a thrombotic microangiopathy defined by a “pentad” consisting of the triad of HUS with accompanying fever and neurological manifestations [99]. Many HUS patients develop neurological symptoms and TTP patients can have kidney failure, so in many cases the diagnosis is given as HUS/TTP. A major risk factor for the development of TTP is a deficiency in the plasma von Willebrand factor-cleaving protease ADAMTS13, due to either a genetic etiology or autoimmune antibodies against the protease [99]. The resultant high levels of ultra-large vWF multimers in the circulation lead to increased platelet-containing thrombi. Although HUS, aHUS, and TTP are closely related diseases and often difficult to distinguish in the clinic, they do have separate causes as well as distinct outcomes. Because aHUS and TTP are due to autoantibodies, deficiencies or mutations of plasma factors, plasma exchange can be used to treat both. In addition, for aHUS, kidney or combined kidney-liver transplants have also shown to be beneficial when supplemented with plasma exchanges [100].

Recent studies have shown that the distinctions between TTP and D + HUS with respect to clinical signs and pathophysiology may be less defined based on the report by Motto et al. that Stx can trigger TTP in ADAMTS13-deficient mice although absence of ADAMTX13 alone is insufficient [77]. In addition, Stx1 or Stx2 causes the release of large vWF multimers from human endothelial cells, while also impairing ADAMTS13 activity, and LPS was shown to have minimal contribution [65]. Huang et al. later showed that the Stx B subunit was sufficient to induce vWF secretion and thrombotic microangiopathy in ADAMTS13^−/− mice back-bred for toxin susceptibility [77], something which had been shown for Shiga toxins earlier [101].

Though the first recorded US outbreak of enterohemorrhagic Escherichia coli occurred in 1982, a complete picture of how EHEC elicits disease in humans remains to be elucidated. EHEC infections are typically unpredictable common source outbreaks, so there are no endemic patient populations for systemic study of disease pathogenesis. The development of animal models has thus been necessary in order to study toxin-specific mechanisms that govern the observed disease process in humans. Animals may receive purified toxin(s) or bacteria, but despite the numerous animal models tried, none of them completely replicate the EHEC infection and HUS observed in patients. However, they do fulfill an important role in that they allow for the investigation of one or more aspects of pathogenesis of EHEC disease and HUS [102]. A brief summary of animal model features and limitations are shown in Table 1 with representative references.

One of the earliest animal models of EHEC-mediated HUS was the gnotobiotic piglet. This animal had previously been used to study other human enteric infections [115]. Piglets were infected with ~1 × 10¹⁰ CFU E. coli O157:H7 twenty-four hours after delivery and were euthanized and necropsied on either day three or day five. Ulcers and mononuclear cell infiltration were observed in the cecums of the animals euthanized on day five. Only minor focal lesions associated with bacterial antigen were observed in the kidney, and no hematological symptoms of hemolytic uremic syndrome were described [116].

Gnotobiotic piglets were again used as an animal model for EHEC infection by Gunzer et al. in 2002, and in these experiments the course of disease resembled that of human EHEC infection in the GI tract as well as other organs. Renal histopathology changes included surface petechiae and diffuse glomerular endothelial swelling with mild to moderate tubular damage. Notably, renal thrombotic microangiopathy was observed in most animals. Limitations to the model can be found in the clinical chemistry and hematologic findings. Though individual animals had elevated serum creatinine levels, the averages were not statistically significant between the experimental groups and the control animals. Furthermore, thrombocytopenia was not observed, nor were schistocytes in peripheral blood smears [103]. Use of gnotobiotic piglets as a model for EHEC is thus useful in studies that focus on neurological or renal changes, but does not accurately mimic the full spectrum of HUS symptoms observed in humans.

Relative to humans, mice are fairly resistant to EHEC infection, so murine models include stressors intended to increase susceptibility to intestinal bacterial colonization and infection. These approaches include pre-treatment with antibiotics, germ-free environments, and protein calorie malnutrition diets [117]. Antibiotics added to the animals’ drinking water reduces or alters the normal intestinal facultative bacteria, increasing the likelihood of EHEC intestinal colonization by decreasing bacterial competition. An early study used streptomycin to study the colonization abilities of several E. coli isolates [104] and Wadolkowski et al. adopted streptomycin pre-treatment to develop a murine model of EHEC infection [105]. Streptomycin-treated male CD-1 mice were infected with either wild-type E. coli O157:H7, a mutant strain that did not contain the plasmid encoding fimbriae, or both. Animals demonstrated colonization of the bacteria in all three conditions, though disease symptoms were not observed. However, mice inoculated with the mutant strain that had been previously recovered from the feces of one of the co-infection animals demonstrated symptoms of infection including loose stools, anorexia and lethargy between days 4–10 post-inoculation, with lethality following within a few days. Colonization without infection was the outcome unless the bacteria strain was host-adapted. The colons of these mice did not show gross or histological lesions, indicating that the animals did not die of hemorrhagic colitis. Rather, death appeared to be due to acute necrosis of proximal convoluted tubules, a lesion which is characteristic of toxin exposure in mice. However, the mice did not show evidence of glomerular damage, thrombotic microangiopathy, or thrombocytopenia [105].

It had been demonstrated previously that addition of mitomycin C to in vitro EHEC cultures resulted in induction of phage expression and increased toxin production [118,119]. Young male ICR mice were pre-treated with streptomycin and mitomycin, then infected with EHEC strain E32511/HSC (Stx2c variant) pre-selected to be resistant to both antibiotics. The animals developed weakness and weight loss, but not diarrhea [106]. Microhemorrhages were observed in the brain and spinal cord, as were slight degeneration of tubules in the kidney. Blood urea nitrogen was significantly higher in experimental mice than in controls, suggesting renal injury, but serum creatinine levels did not change and light microscopy kidney pathology examinations were unremarkable. Acute encephalopathy with loss of blood brain barrier function, brain endothelial cell edema, and demyelination were predominant histologic features. Toxin antigen was detected in affected neurons, but it was not clear whether the neurologic symptoms were from primary neuronal lesions or secondary to hypoxia from thrombotic microangiopathy.

The rationale behind antibiotic pretreatment of mice can be extended to include germ-free mouse models of EHEC infection. Isogai et al. showed that infection with a high dose (2 × 10⁹ CFU) of E. coli O157:H7 was lethal within 7 days of inoculation for germ-free IQI mice. The mice became anorexic and urine retention was associated with renal tubular necrosis [107]. Interestingly, thrombocytopenia and leukocytosis were observed in infected animals. In order to elucidate a role for pro-inflammatory TNFα in EHEC pathogenesis, the authors included a group of mice pretreated with the cytokine. The addition of TNFα nearly doubled the lethality from 60% to 100% with the addition of neurologic symptoms. Furthermore, cytokine-treated mice demonstrated histopathologic changes in the kidney including proliferation of glomerular mesangial cells and microthrombosis, and increased cytokine responses in serum, kidney and brains. Based on these experiments, the authors concluded that the toxins produced by EHEC and/or bacterial endotoxin, induce production of TNFα to have an additive effect EHEC pathogenesis [107]. Priming of cells with pro-inflammatory mediators, especially TNFα, is well known to enhance subsequent cellular responses to pathogenic challenge, and this occurs both in vitro and in vivo [120]. Similarly, TNFα induced by bacterial endotoxin enhances subsequent Stx cytotoxicity in rat astrocytes and releases chemokines that may attract PMNs to contribute to neurological injury and loss of endothelial barrier function [121,122].

Though pre-treatment with antibiotics or the use of germ-free animals increases the likelihood of gut EHEC colonization and infection, it does not accurately depict the circumstance when normal gut flora is present as is the case with patients. To address this, alternative models were developed. C3H/HeJ mice have a TLR4 mutation, rendering them moderately immunocompromised and thus more susceptible to infection. These mice were fasted for 24 h prior to infection, and challenged with 1 × 10⁹ CFU/mL EHEC expressing Stx2 by oral gavage [108]. They developed gastrointestinal symptoms including loose, watery stools, neurological symptoms including ataxia and convulsions, and systemic symptoms including lethargy, anorexia and shivering with ~40% mortality. Histologic examination of colon tissue demonstrated inflammatory infiltrates and necrotic foci. In the kidneys, they observed proliferation of glomerular mesangial cells, diffuse interstitial inflammation and necrosis of tubular cells. In addition, the authors noted fragmented red blood cells in the sick mice. Blood samples were not analyzed for markers of kidney function or for platelet numbers, so a full description of HUS pathology was not available [108].

Newly weaned BALB/c mice showed increased susceptibility to EHEC infection and Stx-mediated renal damage without pretreatment to alter commensal flora [109]. Between 22% and 27% of infected young animals developed high urea concentrations in the serum and all of these mice died. Mortality was associated with increased circulating neutrophils, followed by a significant decrease in all circulating leukocytes shortly before death. Colon pathology included leukocyte infiltration, and the kidney showed focal cortical necrosis with tubular epithelial swelling, although thrombotic microangiopathy was not evaluated.

To initiate EHEC colonization and infection, murine models require much higher bacteria doses compared to humans (murine ~10⁹ CFU versus 10–100 organisms for humans). The observation that a subset of children infected with EHEC had an unbalanced diet prior to infection inspired Kurioka et al. to hypothesize that protein calorie malnourished (PCM) mice would contract disease from lower doses of EHEC than conventional mice. Indeed, the minimal infectious dose of E. coli in the PCM mice was lower at 2 × 10⁶ CFU. [110]. The infected PCM mice developed systemic and neurologic symptoms, no gastrointestinal symptoms were observed. BUN levels, but not creatinine, increased and acute kidney injury was minimal with mild renal tubular degeneration and normal glomeruli. Significant platelet changes were not observed [110]. The advantage of the PCM murine model is the lower inoculum dose with neurologic complications, but the animals do not appear to develop HUS.

Dutch Belted rabbits orally infected with 5–9 × 10⁸ CFU of host-adapted EHEC O103 (Stx1+ Stx2-) or patient-derived O157:H7 (Stx1+ Stx2+) developed renal vascular lesions and glomerular lesions containing erythrocyte fragments [111]. These animals also demonstrated diarrhea, lethargy, anorexia, dehydration and weight loss with a low hematocrit observed in five of six infected animals. Similar to that seen in humans, glomerular, perivascular and tubular injury was observed in all animals after challenge with either strain, as was glomerular endothelial edema, mesangial deposits and fibrin thrombi occluding capillary lumens. Lack of changes in creatinine suggests renal injury rather than renal insufficiency, and although mild to moderate thrombocytopenia was observed in only 3 of 30 experimental animals, glomerular thrombi and renal congestion suggest the presence of coagulopathy if not a full thrombotic microangiopathy. Intestinal edema and vascular lesions with colonic inflammation with leukocyte infiltration was observed, as was surface-adherent E. coli in the cecal mucosa and crypt lumens. This animal model is a reasonable mimic of the human renal and intestinal lesions induced by EHEC and its toxins, although lack of consistent thrombocytopenia limits this model with respect to recapitulating human HUS.

Several animal models examine the effects of purified Shiga toxin, in the absence of bacteria, with variable success in mimicking human HUS symptoms. A descriptive study of a baboon model of Shiga toxin 1 responses observed renal failure with death in 57 h or less, and the animals presented, for the first time, with all the classic clinical symptoms of HUS [48]. Animals in the low-dose Shiga toxin 1 group (50–200 ng/kg i.v.; n = 8) demonstrated thrombocytopenia, schistocytosis and hemolytic anemia, renal injury with glomerular endothelial injury and an inflammatory profile, renal failure, and injury to the GI tract. Lesions in the central nervous system were observed by electron microscopy. Stearns-Kurosawa et al. expanded the baboon model to include dose-response studies of both toxins for comparative purposes [42]. Stx2-induced renal injury and mortality was delayed 2–3 days compared to Stx1 challenge, and animals were ultimately more sensitive to Stx2, succumbing at lower doses (50 ng/kg for Stx2 versus 100 ng/kg Stx1). Both toxins elicited a systemic inflammatory response, but levels of cytokines and chemokines were elevated earlier and to higher levels after Stx1 challenge. Care was taken to ensure low endotoxin contamination of the toxins, and TNFα was not detectable in either plasma or urine from any of the animals. If pro-inflammatory priming is a necessary event for Stx toxicity, then it may be more complicated than production of TNFα. Unlike other animal models, the development of thrombocytopenia was consistently observed and was toxin dose-dependent. Loss of platelets was more gradual in Stx2-challenged animals as compared to Stx1, however anemia development was comparable and long-lasting [112]. Challenge with either toxin resulted in renal failure, increased plasma blood urea nitrogen (BUN) and creatinine, and deteriorating urinalysis profiles. The baboons could be rescued from lethal Stx2 challenge with a custom synthetic peptide designed to counter Stx2 activity within cells [112]. Renal function and urine output was preserved even when the peptide was administered 24 h after the otherwise lethal Stx2 challenge. Thus, both Stx1 and Stx2 are capable of eliciting HUS in baboons, but the timing and magnitude of the responses differ.

Although the pathology of human HUS can be mimicked in nonhuman primates through the administration of Stx alone, a small animal model of HUS would provide many benefits and be accessible to more investigators.

C67BL/6J mice, when given only multiple sub-lethal doses of Stx2 and no pre-treatments, develop some but not all aspects of human HUS [113]. Significantly increased plasma BUN and creatinine levels and proteinuria reflect glomerular renal injury. Hemolysis, neutrophilia and lymphocytopenia were observed. Histologically, the kidneys showed fibrin (ogen) deposition in the glomerular capillary loops and swollen subendothelial zones containing flocculent material [113]. Thrombocytopenia, however, was not observed and lack of this HUS symptom appears to be common to all Stx murine models unless co-treated with an accessory pro-inflammatory mediator.

Modeling HUS using mice challenged with EHEC toxins has been described using co-administration of Gram negative endotoxin (a.k.a., lipopolysaccharide, LPS) and Stx2 [123], a model that has been used recently by multiple investigators. This approach was based on the hypothesis that LPS from the commensal flora of the gut could potentially contribute to the pathogenesis of HUS. However, LPS had either a synergistic or protective effect, depending on the timing of administration. Keepers et al. found that when C57BL/6 mice were given low sublethal doses of both LPS and Stx2 concurrently, they exhibited all signs of clinical HUS [29]. Neutrophilia, thrombocytopenia, red cell hemolysis and increases in serum creatinine and BUN were all observed. In the kidney, glomerular fibrin deposition, microthrombi formation and glomerular ultrastructure changes were demonstrated by histology and electron microscopy [29].

Priming of the Stx system in this way with LPS, TNFα, ADP or similar potentiates toxin chemotactic and inflammatory responses in vitro and in vivo [29,117], but the relevance to disease pathogenesis in patients is not clear. In experimental settings, addition of LPS priming to Stx2 challenge in mice will induce thrombocytopenia, but this etiology is a consumptive disseminated intravascular coagulation [124,125] rather than HUS and they have different coagulation profiles. This differentiation was discussed by Karmali et al. decades ago [17]. Additionally, the notion that compromised intestinal barrier function allows bacterial translocation or LPS leakage from commensal or pathogenic bacteria is far from established. This theory has been discussed with variable levels of support since the 1940s with respect to bacterial sepsis mechanisms and is proven to be poorly related to the patient condition, particularly for endotoxemia [126]. Some patients with EHEC O157:H7 infection have antibodies (usually IgM or IgA) against the bacterial LPS serotype [127,128] but detection in healthy control sera as well as cross-reactivity with other LPS serotypes adds complexity [129], and there is no prospective evidence showing these antibodies are protective or prognostic. In non-EHEC bacterial sepsis, circulating E. coli LPS is detectable in patients, but targeted neutralization of Gram negative LPS has consistently failed to improve 28 day all-cause mortality [130,131]. The current thinking is that the primary contribution of the intestine during these infections comes from host cellular injury with resultant host-derived mediators to propagate local and systemic inflammation effects [132,133].

Rats were studied as a Shiga toxemia model by Zotta et al. in 2008 to evaluate their ability to mimic development of HUS. Adult male Sprague-Dawley rats were challenged intraperitoneally with increasing volumes of filtered EHEC culture supernatant containing Stx2, but low endotoxin, and disease progression was monitored for 48 h. At an estimated toxin dose of 20 μg Stx2/kg body weight, all animals developed increased BUN and creatinine, thrombocytopenia (decreased from 84 × 10⁶/μL to 33 × 10⁶/μL), hemolytic anemia and leukocytosis [114], clinical markers that correlate with disease progression in patients [2,18]. Histological observations included necrotic glomerular areas, tubular injury, and thrombotic microangiopathy. Watery diarrhea due to colonic mucosa damage was also observed, but hemorrhagic colitis was not a feature. This methodology provides a small animal model of HUS that effectively reproduces the pathology of human HUS. However, this model has not been used frequently, likely because it used crude bacterial supernatants rather than purified toxin. Bacterial virulence factors other than Stx may contribute to disease pathophysiology [134] and the observation that crude bacterial supernatants, but not purified Stx, can induce HUS in rodents is consistent with this. These presumed non-Stx virulence factors bear further investigation.

In the pursuit of effective translational medicine for EHEC infection, animal models that accurately mimic the pathogenesis of EHEC-induced human HUS are crucial if we are to fully elucidate the mechanisms involved. A plethora of such models have been spurned by this need, however none encapsulate the pathogenesis of EHEC infection and Shiga toxins-induced human HUS in its entirety. Nonetheless, each model provides certain insights, and may ultimately help the scientific community progress in its understanding of this disease. From these models and patient studies, identification of biomarkers that discriminate related clinical syndromes, quantify the early onset or risk of HUS, and report patient physiological responses to clinical intervention will ultimately prove to be of greatest value.