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Shiga toxin-producing Escherichia coli is a principal source of regional outbreaks of bloody diarrhea and hemolytic-uremic syndrome in the United States and worldwide. Primary bacterial virulence factors are Shiga toxin types 1 and 2 (Stx1 and Stx2), and we performed parallel analyses of the pathophysiologies elicited by the toxins in nonhuman primate models to identify shared and unique consequences of the toxemias. After a single intravenous challenge with purified Stx1 or Stx2, baboons (Papio) developed thrombocytopenia, anemia, and acute renal failure with loss of glomerular function, in a dose-dependent manner. Differences in the timing and magnitude of physiologic responses were observed between the toxins. The animals were more sensitive to Stx2, with mortality at lower doses, but Stx2-induced renal injury and mortality were delayed 2 to 3 days compared to those after Stx1 challenge. Multiplex analyses of plasma inflammatory cytokines revealed similarities (macrophage chemoattractant protein 1 [MCP-1] and tumor necrosis factor alpha [TNF-α]) and differences (interleukin-6 [IL-6] and granulocyte colony-stimulating factor [G-CSF]) elicited by the toxins with respect to the mediator induced and timing of the responses. Neither toxin induced detectable levels of plasma TNF-α. To our knowledge, this is the first time that the in vivo consequences of the toxins have been compared in a parallel and reproducible manner in nonhuman primates, and the data show similarities to patient observations. The availability of experimental nonhuman primate models for Stx toxemias provides a reproducible platform for testing antitoxin compounds and immunotherapeutics with outcome criteria that have clinical meaning.
Infection with Shiga toxin-producing Escherichia coli (STEC) results in intestinal cramps and bloody diarrhea, followed 5 to 12 days later in some patients by the development of hemolytic-uremic syndrome (HUS) (16, 18). HUS is characterized clinically by the triad of thrombocytopenia, hemolytic microangiopathy, and renal injury and is the leading cause of acute renal failure in otherwise healthy children in the United States. An antibiotic regimen is not recommended, and treatment options are limited to critical care support (47). Patients with diarrhea-associated HUS can have long-term renal impairment of varying severity, and approximately one-fourth of patients have neurologic sequelae, including seizures, coma/stupor, cortical blindness, ataxia, and paraplegia (10, 14).
The natural infection route is gastrointestinal, via contaminated food or water. The bacteria colonize the intestinal lumen, with most strains forming characteristic attaching-and-effacing lesions, and the organisms may synthesize and release one or more toxins that are primary virulence factors contributing to the clinical manifestations of HUS (19). The toxins are AB5 holotoxins, referred to as Shiga toxins due to their functional and structural similarities to Shiga toxin expressed by Shigella dysenteriae serotype 1 (4). Shiga toxin type 1 (Stx1) is essentially identical to the Shigella toxin (4), differing by one amino acid, but shares only 58% amino acid identity with Shiga toxin type 2 (Stx2). Stx1 and Stx2 have distinct spatial conformations (8) and dissociation rates from receptor-lipid surfaces (24). STEC strains may secrete one or both toxins and several toxin variants, and clinical studies have demonstrated that HUS is most often associated with the expression of Stx2 (3), particularly following infection with E. coli O157:H7 strains (12, 20). All Shiga toxins share a cellular intoxication mechanism in which B subunits oligomerize into pentamers for interaction with a cell surface globotriaosylceramide Gb3 (CD77) receptor. Following binding, holotoxins are internalized via clathrin-dependent or clathrin-independent mechanisms and undergo retrograde transport through the trans-Golgi network and Golgi apparatus to reach the endoplasmic reticulum (33, 46). During transport, the A subunit undergoes limited proteolysis, and once in the endoplasmic reticulum, a fragment of the A subunit translocates into the cytoplasm, where its N-glycosidase activity inactivates the 28S rRNA component of eukaryotic ribosomes to inhibit protein synthesis and cause cell death (25, 43).
While Stx1 and Stx2 share many characteristics, they are not identical and there is evidence that toxin-specific activities may be clinically relevant. Both toxins are internalized after binding to Gb3, but the mechanisms of their intracellular trafficking through polarized intestinal epithelial cells to reach the intestinal endothelium are very different (15). Also, endothelial sensitivities to Stx1 and Stx2 differ depending on the vascular bed, with intestinal endothelium being more sensitive to the Shiga toxins than saphenous vein endothelium (12), and glomerular endothelial cells are about 1,000 times more sensitive to Stx2 than human umbilical vein endothelial cells (17). The mechanisms for these differences are not completely understood but may be related to receptor density, toxin effects on endoplasmic reticulum stress responses and apoptosis (22, 41), or local availability of sensitizing cytokines (5, 7, 11).
Most animal models show greater sensitivity to Stx2, including murine, rabbit, and gnotobiotic piglet models, although renal and neurologic micropathologies differ from those in humans and between animal species (6, 9, 45). Earlier studies with the baboon (Papio) model showed that a bolus infusion of purified Stx1 induced intestinal injury, kidney glomerular injury, microangiopathic anemia, thrombocytopenia, and neurologic abnormalities similar to those in humans, suggesting that the baboon represents a promising preclinical animal model (44). A systemic inflammatory response was minimal after Stx1 challenge, but urinary tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) levels were consistent with local kidney inflammatory responses. Baboons were also more sensitive to Stx2 (38), but a direct comparison of the pathophysiologies elicited by the two toxins was difficult because of differing experimental designs. We sought to expand these earlier studies of baboons to identify similarities and differences elicited by Stx1 and Stx2 under reproducible experimental conditions. Given the clinical relevance of Stx2 production during STEC infection in patients, we were particularly interested in responses after Stx2 challenge, for which few data are available from the baboon model. We present the metabolic, physiologic, and inflammatory responses in baboons after intravenous challenge with Stx1 or Stx2. The observed differences in pathophysiology elicited by the two toxins may contribute to a better understanding of the differences in clinical manifestations produced by the toxins.
Recombinant Stx2 was obtained from BEI Resources (Manassas, VA). Purified recombinant Stx1 was prepared from cell lysates obtained from E. coli DH5α harboring plasmid pCKS112, which contains the stx1 operon under the control of a thermoinducible promoter (45). Stx1 was purified from cell lysates by sequential ion-exchange and chromatofocusing chromatography. The purity of toxins was assessed by SDS-PAGE with silver staining and by Western blot analysis. Prepared toxins contained <0.1 ng endotoxin per ml, as determined by Limulus amoebocyte lysate assay (Associates of Cape Cod, Inc., East Falmouth, MA).
Papio cynocephalus cynocephalus or P. c. anubis baboons were purchased from the Oklahoma Baboon Research Resource at the University of Oklahoma Health Sciences Center. All baboons were juvenile (1.5 to 3 years; 6 to 8 kg), before sexual maturation, were outbred and free of tuberculosis, and had leukocyte concentrations of <15,000/mm3. The animals were housed and used in accordance with the guidelines and approved protocols of the institutional animal care and use committees and the institutional biosafety committees of Boston University School of Medicine and the University of Oklahoma Health Sciences Center.
The animal studies were performed at the University of Oklahoma Health Sciences Center animal annex, using previously published procedures (42, 44). Briefly, baboons were fasted overnight before the study, with free access to water. They were sedated the morning of the experiment by use of ketamine (10 mg/kg of body weight, given intramuscularly [i.m.]) and were orally intubated. Anesthesia was maintained using sodium pentobarbital (5 to 10 mg/kg for maintenance) as deemed necessary by monitoring the eyelid reflex. An indwelling catheter was placed in the forearm cephalic vein for bolus infusion of toxin (1 to 2 ml). A second catheter was inserted into the femoral vein by venous cutdown and secured subcutaneously by an internal injection cap (Braun), where it remained for the rest of the study period and was used for blood draws, infusion of saline to replace insensible loss, central venous pressure (CVP) monitoring, and anesthesia. Death is not an end point for these studies, and baboons were euthanized according to established criteria if deemed necessary before the end of the 7-day experimental period. At necropsy, the gross pathology of the organs was examined and tissues were harvested for archiving. All animals received enrofloxacin (Baytril; 10 mg/kg i.m.) prior to cutdown and catheter placement on day 0. Baboons then received either prophylactic levofloxacin (Levaquin; 3.5 mg/kg as an intravenous [i.v.] bolus) or enrofloxacin (10 mg/kg i.m.) each day over the experimental period.
Animals were weighed daily, and toxin-induced hypovolemia was controlled based on criteria developed in previous studies (44). Replacement of fluids with saline (no more than three bolus infusions of 10 ml/kg) was done according to the following criteria: (i) if weight is less than that at time zero (T0), then infuse sufficient normal saline to return animal to initial weight (1 g = 1 ml) at 1 ml/kg/min; (ii) if mean arterial pressure is <70 mm Hg, then infuse normal saline (10 ml/kg at 1 ml/kg/min), repeating as needed, while following CVP and mean systemic arterial pressure (MSAP) and stopping when MSAP is >70 mm Hg, or sooner if the CVP is >10 cm H2O; (iii) if CVP is <3 cm H2O, then infuse normal saline and repeat as needed to raise the CVP to >3 cm H2O; and (iv) if urine output is <2 ml/kg/h, but weight, MSAP, and CVP are not low, then infuse saline and repeat as needed or until the CVP is >10 cm H2O.
Blood samples were obtained at T0 (before toxin challenge), eight times during the first 24 h, and daily thereafter. Complete blood counts (CBCs) were determined with a Horiba ABX Micros 60 hematology analyzer (Horiba, Irvine, CA). Blood smears were stained with Wright's stain, and schistocyte counts were determined as percentages of 200 red blood cells. A Foley catheter (6 French units, 30 cm, 1.5-ml balloon; Rusch, Research Triangle Park, NC) was inserted for urine collection. The animals were all similar in size (body surface area); urine was collected on day 0 before toxin challenge for 60 min and on subsequent days for 20 min. Urinalysis was obtained using dipsticks (Multistix 10SG) on samples collected before saline infusion if indicated to correct for hypovolemia. Blood urea nitrogen (BUN) and creatinine levels were determined on citrated plasma by standard clinical chemistry analyses (Veterinary Associates Laboratory, Edmond, OK). Activated partial thromboplastin times (APTT) were determined on citrated plasma by use of a KC4 coagulation analyzer (Trinity Biotech, Wickland, Ireland) and TriniCLOT automated APTT reagent (Trinity Biotech). The APTT tests for all factors in the intrinsic coagulation pathway, including factors II, V, VIII, IX, X, XI, and XII, and is independent of platelet counts. Fibrinogen levels were determined by reference to a standard curve, using a KC4 coagulation analyzer. For the standard curve, bovine thrombin was added to a reference plasma of known fibrinogen content, and the clotting time was inversely proportional to the fibrinogen content. The fibrinogen level at T0 for the 21 animals in this study was 141.8 ± 40.6 mg/dl (mean ± standard deviation [SD]).
Cytokine protein levels were quantified by xMAP multiplex fluorescent bead-based assays, using a Luminex 200 IS system (Millipore, Billerica, MA), Luminex xPONENT software (Luminex, Austin, TX), and nonhuman primate cytokine panel kits (Millipore), which provide the beads, buffers, and detection reagents. Samples were thawed, diluted as appropriate, and incubated with beads for 2 h at room temperature with vigorous mixing. Samples were washed twice with vacuum filtration and incubated with biotin-conjugated antibodies selective for each biomarker for 1 h at room temperature. Phycoerythrin-conjugated streptavidin was added, and samples were incubated for 30 min at room temperature, followed by washing. Beads were resuspended in 150 μl sheath fluid, and samples were assayed on a Luminex 200 system. Standard curves for each biomarker ranged from 0 to 10,000 pg/ml. Samples with values of >9,000 pg/ml were diluted appropriately and reanalyzed. For each sample, the median fluorescence intensity was analyzed with a weighted 5-parameter logistic (Milliplex Analyst; Millipore) and quantified relative to the standard curve for that cytokine. Differences from baseline values were analyzed by paired Student's t test, and P values of <0.05 were considered significant.
Anesthetized baboons were challenged with a single intravenous bolus injection of recombinant, purified Stx1 or Stx2 at different doses. Blood was taken just before toxin challenge (T0), followed by sampling at defined periods thereafter. Survival after challenge with 10, 50, or 100 ng/kg Stx1 was dose dependent (Fig. (Fig.1A),1A), with the highest dose lethal for all animals, with mortality by day 2 or 3. All animals challenged with 10 ng/kg Stx1 (n = 3) survived. The 50-ng/kg Stx1 dose (n = 5) was more severe, but one animal eventually recovered, and the 100-ng/kg Stx1 dose (n = 5) was lethal. Baboons were more sensitive to Stx2, in that 3 of 4 animals challenged with 10 ng/kg Stx2 were survivors, but challenge with 50 ng/kg Stx2 (n = 4) was lethal, though mortality was delayed until day 4 or 5 (Fig. (Fig.1B).1B). Median survival times at the lethal dose were different (57.5 h for Stx1 and 121.3 h for Stx2; log rank [Mantel-Cox] test). The animals died at a much lower dose of Stx2, but the time to death was longer. For survivors, there were no changes in symptoms or mortality after this 7-day period. Several surviving baboons were monitored for 28 days, with no persistent or emerging clinical signs, and appeared to be fully recovered.
Complete blood counts performed on blood samples at each time point showed a progressive loss of circulating platelets after challenge with Stx1 or Stx2 (Fig. (Fig.2).2). The extent of thrombocytopenia was dose dependent, with recovery of cell counts if the animal received a low dose or was recovering. Compared to Stx1 challenge, a more gradual development of thrombocytopenia with time was observed after Stx2 challenge (Fig. 2A and B). Animals developed anemia after challenge with either toxin, with a gradual decline in red blood cell counts (Fig. 2C and D) that was reflected in significant declines in hematocrit (Table (Table1).1). In general, white blood cell counts did not change (Table (Table1),1), with the exception of low-dose Stx1-challenged animals, who had elevated white cell counts at 24 and 48 h, probably reflecting an acute-phase response. Examination of blood smears obtained at euthanasia or on day 6 or 7 revealed schistocytes (fragmented red blood cells) in toxin-challenged animals (Table (Table1).1). Although platelet levels declined, consumptive coagulopathy or disseminated intravascular coagulation was not evident because APTT were prolonged modestly only after 24 to 48 h and fibrinogen levels remained steady for several days, actually increasing during the acute-phase response (Fig. (Fig.33).
Renal damage was a consequence of challenge with either Stx1 or Stx2. Urine output decreased in both toxin-challenged groups in the first 24 h, essentially ceasing at the high doses (Fig. 4A and B). Proteinuria, indicative of glomerular damage and a loss of filtration function, was dose dependent for both toxins but more sensitive to Stx2 (Fig. 4C and D). Increases in plasma BUN and creatinine by 24 to 48 h paralleled the onset of kidney damage after challenge with either toxin (Fig. (Fig.5).5). The levels returned to baseline after low-dose toxin challenge or if the responses were compensated and the animal was recovering. Most animals showed physical signs of edema by 24 to 48 h, with swelling of the face and abdomen, which resolved within a day or two in the low-dose-challenged animals. However, despite frequent monitoring and fluid support to maintain central venous pressure, animals who received the higher toxin doses had progressive loss of kidney function and thrombocytopenia leading to death. Gross pathology observations of the kidneys at necropsy on day 2 (48 h) after challenge with a 100-ng/kg Stx1 lethal dose revealed mild to moderate congestion at the cortico-medullary junction (Fig. (Fig.6B).6B). In contrast, the 50-ng/kg Stx2 lethal dose resulted in severe medullary congestion and marked cortical ischemia at necropsy on day 5 (121.6 h) postchallenge (Fig. (Fig.6C6C).
Quantification of circulating proinflammatory biomarkers revealed a systemic inflammatory response with shared and unique features depending on the toxin challenge. Interleukin-6 (IL-6) and monocyte chemoattractant protein 1 (MCP-1) are global markers of systemic inflammation that predict outcomes in patients and animal models of bacterial sepsis (21, 28, 31), and increases were observed in baboons after challenge with the toxins (Fig. 7A to D). Notably, different response patterns could be observed between the two toxins. The early and sustained rise in IL-6 after Stx1 challenge, from 4 to 24 h, was not observed in the Stx2-challenged baboons, although the sharp rise in IL-6 levels in the high-dose groups (100 ng/kg Stx1 and 50 ng/kg Stx2) just before death was a shared response. A significant difference from baseline IL-6 levels was observed by 30 min after challenge with 50 or 100 ng/kg Stx1 (P < 0.01). At the high Stx1 dose, elevated IL-6 levels persisted, with differences from baseline at 6 to 8 h (P < 0.01) and 10 h (P < 0.001). Increases in MCP-1 levels occurred similarly 24 to 48 h after Stx1 or Stx2 challenge, in a dose-dependent fashion (Fig. 7C and D), although the rise was more gradual after Stx2 challenge. Granulocyte colony-stimulating factor (G-CSF) increased within 1 h (P = 0.05; P < 0.05 after 4 h) after challenge with 100 ng/kg Stx1, with sustained rises over several days with the 50- and 100-ng/kg Stx1 doses. In contrast, little G-CSF was induced after Stx2 challenge, even with the 50-ng/kg dose that otherwise elicited severe responses in the baboons (Fig. 7E and F). Baboon tumor necrosis factor alpha (TNF-α) was not detected in plasma after challenge with either toxin (Fig. 7G and H), consistent with previous observations in the baboon Stx1 model obtained with a different antibody-based assay (44). There were either no changes or no detectable levels of granulocyte-macrophage colony-stimulating factor (GM-CSF), IL-1β, IL-2, IL-4, IL-12/23, IL-13, IL-17, IL-18, gamma interferon (IFN-γ), and macrophage inflammatory protein 1β (MIP-1β).
The availability of the baboon Stx1 and Stx2 toxemia models permits parallel analyses of shared and unique responses elicited by the toxins in a near-human setting. The major observations from this study are that a single bolus injection of Stx1 or Stx2 induced shared responses of thrombocytopenia, anemia, and acute renal failure in baboons, but there were distinct differences in the timing and magnitude of responses elicited by the two toxins. Furthermore, although both toxins induced a systemic inflammatory response, the cytokine patterns induced were distinct between the toxins, with differences in the mediators induced as well as in the timing and magnitude of the responses.
We showed that both toxins alter hematologic parameters and target the kidneys, with resulting thrombocytopenia, anemia, red blood cell fragmentation, progressive anuria, proteinuria, and reduced glomerular function. In patients, complete HUS has been defined as having platelet counts of <150,000/μl, a hematocrit of <30% with evidence of intravascular hemolysis, and a BUN level of >20 mg/dl, and incomplete HUS is defined as having two of these criteria (2). The hematologic and renal function changes observed in the baboons after a single-dose challenge with Stx1 or Stx2 were similar to those observed in patients.
Differences in the physiologic responses elicited by the toxins in the baboons were largely in their timing. While the absolute losses of platelet counts were similar, a high dose of Stx1 resulted in fairly abrupt thrombocytopenia by 24 to 48 h, whereas the loss of platelets after Stx2 challenge was through a gradual daily decrease until either euthanasia at day 4 or 5 or resolution and recovery. Differences in renal gross pathology may also be attributable to the timing of organ injury. In the kidney, the cortico-medullary congestion noted on day 2 after high-dose Stx1 challenge may progress to the severe medullary congestion seen on day 5 after Stx2 challenge. While it is possible that the far more severe renal lesions after high-dose Stx2 challenge represent toxin specificity, it is also possible that the additional 2 to 3 days to euthanasia and necropsy allowed more time for the pathology to develop. It is notable that anemia developed after exposure to either toxin, and red cell counts continued to decrease and remained low even when markers of renal function and inflammation were resolving after low-dose toxin challenge and the animal appeared to be recovering. Patients with STEC-induced HUS can become profoundly anemic and require transfusions (16).
The shorter, 2- to 3-day survival time with a lethal dose of Stx1 (100 ng/kg; median time to death, 57.5 h) than the 4- to 5-day survival time after a lethal dose of Stx2 (50 ng/kg; median time to death, 121.3 h) demonstrated a higher sensitivity to Stx2 but a longer time to severe organ injury and death. More-rapid kidney injury by Stx1 is supported by the observations that BUN and creatinine levels increased more acutely and urine output dropped more rapidly and to a greater degree in the Stx1-challenged animals. We do not interpret this to mean that Stx1 preferentially targets the kidney, but rather that there may be differences in toxin dissemination or processing in vivo that could contribute to delayed Stx2 renal injury. The molecular basis for delayed organ damage and mortality after Stx2 remains enigmatic, because both toxins require the Gb3 (CD77) receptor for cell intoxication (27), although they bind with slightly different kinetics and affinities (17, 24). Using the gnotobiotic piglet model and isogenic E. coli strains with similar toxin production capabilities, Donohue-Rolfe et al. showed that oral challenge with strains expressing Stx2 alone induced more neurologic symptoms than did challenge with strains that express only Stx1 (6, 37). This also supports the notion that the toxins can induce different systemic pathophysiologies. With respect to timing differences, the current experimental baboon observations are reminiscent of clinical observations in which renal injury in young children correlates with Stx2 production from STEC and the development of hemolytic-uremic syndrome is delayed by an average of 6 days after infection (2).
Measurement of circulating biomarkers by bead-based multiplex assays revealed unexpected differences in the proinflammatory cytokines induced by Stx1 and Stx2, with differences in the mediator induced as well as in the timing and magnitude of the response. From a broad perspective, Stx1 appeared to induce a stronger systemic inflammatory response in the baboons, as judged by more cytokines being induced, and at higher levels. Though they are present in the circulation, a role for these mediators in disease severity, outcome, or prognosis cannot be inferred from the current study. An inflammatory response is well documented for pediatric patients with STEC infection, who have elevated IL-6, IL-10, IL-1Ra, G-CSF, and chemokine levels (29, 30) and may (23) or may not (30) have elevated plasma TNF-α levels. In the baboons, IL-6 and MCP-1 levels were induced to similar levels after either toxin and were dose dependent, but Stx2-induced responses were more gradual and were delayed by several days. In contrast, changes in G-CSF were very different between the toxins. Stx1 challenge increased circulating G-CSF levels, particularly at the 50- and 100-ng/kg doses, whereas G-CSF was only minimally increased early after Stx2 challenge, regardless of the toxin dose. To our knowledge, Stx toxin-specific changes in plasma cytokines have not been studied in parallel in other animal models, and the baboon data suggest that the toxins may exert independent influences on cytokine mRNA stability and/or gene transcription in susceptible cells. Increased G-CSF levels would be expected to result in increased white cell counts, but this did not occur, nor did differential cell counts change (not shown). In fact, the animals challenged with 10 ng/kg Stx1 paradoxically had the highest white cell counts and the lowest plasma G-CSF levels. G-CSF production is tightly regulated at both the translational and posttranslational levels, and stabilization of mRNA is observed as a result of multiple mediators, including IL-4, TNF-α, and IFN-γ (1). However, these mediators were not observed in the baboons, at least not systemically. In mice, Stx1 localizes to the bone marrow of the spine, long bones, and ribs (34), and it is possible that even though peripheral cells may produce G-CSF, its biological activity at the bone marrow may be inefficient or blocked. The distribution of toxins in patients or nonhuman primates is not known, and studies are in progress to understand the molecular basis and biologic significance of the cytokine responses unique to each toxin.
We did not detect plasma TNF-α in any of the baboons after challenge with either toxin, even at high doses, consistent with previous Stx1 studies of the baboon model (40, 44). TNF-α is a well-known early proinflammatory mediator of bacterial sepsis in patients and most animal models, including baboons (13, 26, 42). In contrast, mice have elevated plasma TNF-α and kidney TNF-α mRNA after multiple Stx2 injections that induce thrombocytopenia and renal injury (36), and cultured cells will undergo TNF-α transcription and protein release after Stx1 intoxication under lipopolysaccharide (LPS)-free conditions (35). These differences may be species dependent, or TNF-α production may rely on a balance of gene transcription induced by other local mediators despite toxin-induced pressures to undergo cellular apoptosis (22, 41).
While there are parallels between the current baboon results and patient observations, the current study models are most accurately viewed as nonhuman primate models of toxemia, not STEC infection, where the pathogen is bacterial and the infection route is gastrointestinal. Furthermore, the toxins were administered as a bolus challenge rather than as repeated or intermittent toxin exposures, as would be expected during an intestinal bacterial infection. We observed increased white cell counts only after low-dose Stx1 challenge, whereas in patients with STEC infection, a white cell count of >10,500/μl is associated with a 5-fold-increased risk of HUS (2). It is reasonable to expect that patients infected with STEC will be exposed to a variety of bacterial factors and that possible breaching of the gut epithelial barrier due to injury will exacerbate the insult, providing exposure to LPS from commensal flora. In an earlier baboon Stx1 study, LPS and Stx1 coadministration resulted in more-severe kidney damage in response to an otherwise subtoxic challenge (39). This is underscored by studies which demonstrated the importance of other bacterial molecules necessary for epithelial attachment in the gut and the interplay between the toxins, bacterial colonization, and inflammation that give rise to systemic disease (3, 32).
Ongoing studies in our laboratory continue to characterize the baboon toxemia models with respect to inflammation, pathology, and neurologic abnormalities to further advance our understanding of how the toxins exert their influence at the organ and cellular levels. The current nonhuman primate models of Stx1 and Stx2 toxemia provide a platform for reproducible testing of immunotherapeutics and antitoxin compounds in a near-human setting, with definable outcomes that have clinical meaning. With the baboon models, it should be possible to test therapeutics tailored to one or both toxins and to independently judge effects on toxin-specific responses. In this way, it may be possible to more rapidly develop and advance therapeutics for STEC infection for a clinical setting in which patients may present with STEC strains that secrete different ratios of toxins.
This work was supported by NIH NIAID grant U01 AI075386 (S.K.) and NIH NIAID grant RO1 AI034530 (V.L.T.). Baboons were purchased from the Oklahoma Baboon Research Resource at the University of Oklahoma Health Sciences Center, supported by NIH grant P40RR012317 (to G. White).
We are indebted to Gary White, Roman Wolf (Comparative Medicine), and Gary Kinasewitz (Pulmonary and Critical Care Medicine) at the University of Oklahoma Health Sciences Center and to Fletcher B. Taylor, Jr., at the Oklahoma Medical Research Foundation for veterinary support, advice, and discussions. We thank Ram Cherla for toxin purification, Lyndianne Joseph for administrative support, and Diana Weiner for technical assistance.
Editor: B. A. McCormick
Published ahead of print on 22 March 2010.