Abstract

Shiga toxin-producing E. coli (STEC) produces Stx1 and/or Stx2, and Subtilase cytotoxin (SubAB). Since these toxins may be present simultaneously during STEC infections, the purpose of this work was to study the co-action of Stx2 and SubAB. Stx2 + SubAB was assayed in vitro on monocultures and cocultures of human glomerular endothelial cells (HGEC) with a human proximal tubular epithelial cell line (HK-2) and in vivo in mice after weaning. The effects in vitro of both toxins, co-incubated and individually, were similar, showing that Stx2 and SubAB contribute similarly to renal cell damage. However, in vivo, co-injection of toxins lethal doses reduced the survival time of mice by 24 h and mice also suffered a strong decrease in the body weight associated with a lowered food intake. Co-injected mice also exhibited more severe histological renal alterations and a worsening in renal function that was not as evident in mice treated with each toxin separately. Furthermore, co-treatment induced numerous erythrocyte morphological alterations and an increase of free hemoglobin. This work shows, for the first time, the in vivo effects of Stx2 and SubAB acting together and provides valuable information about their contribution to the damage caused in STEC infections.

Highlights

  • Shiga-toxigenic Escherichia coli (STEC) is a food-borne pathogen responsible for different clinical conditions, including bloody diarrhea, hemorrhagic colitis, and hemolytic uremic syndrome (HUS) [1]

  • One of the most intriguing aspects of the pathophysiology of HUS is the possible contribution of Stx2 and SubAB together during STEC infections

  • Further studies are necessary to delineate the role of SubAB in the pathogenesis of HUS

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Summary

Introduction

Shiga-toxigenic Escherichia coli (STEC) is a food-borne pathogen responsible for different clinical conditions, including bloody diarrhea, hemorrhagic colitis, and hemolytic uremic syndrome (HUS) [1]. HUS is clinically characterized by microangiopathic hemolytic anemia, thrombocytopenia, and variable degrees of kidney injury [4]. Argentina has the highest worldwide incidence of HUS caused by STEC infections. From 2014 to 2018, a median of 314 new cases per year were notified by the National Health Surveillance System and the annual incidence was 6.52 cases per 100,000 children under five years of age [6]. In Argentina, HUS associated with STEC infections is the principal cause of acute renal injury in pediatric age groups and the second most recurrent cause of chronic renal disease [1,7]

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