Serum Shiga toxin 2 values in patients during acute phase of diarrhoea‐associated haemolytic uraemic syndrome. (2nd November 2015)

• Record Type: Journal Article
• Authors: He, Xiaohua; Quiñones, Beatriz; Loo, Maroeska Te; Loos, Sebastian; Scavia, Gaia; Brigotti, Maurizio; Levtchenko, Elena; Monnens, Leo
• Is Part Of: Acta pædiatrica. Volume 104:Number 12(2015:Dec.)
• Page Start: e564
• Page End: e568
• Publication Date: 2015-11-02
• Subjects: Foodborne pathogen -- Functional assay of Stx‐2 -- Haemolytic uraemic syndrome -- Shiga toxin; Pediatrics -- Periodicals; Pediatrics; 618.92
• DOI: 10.1111/apa.13211
• Languages: English
• ISSNs: 0803-5253

Abstract

Abstract: Aim: Shiga toxins are delivered via systemic circulation and are considered to be the cause of diarrhoea‐associated haemolytic uraemic syndrome (HUS), as they injure endothelial cells, particularly in the glomeruli. This study measured Shiga toxin 2 (Stx2) in the serum of children affected in by HUS due to Stx2 producing Escherichia coli . Methods: The concentration of free Stx2 was measured in the serum of 16 children, collected immediately after admission to the clinic in the acute phase of HUS, using a sandwich enzyme‐linked immunosorbent assay. The family members of two children were also investigated, with the relative toxicity of Stx2 assessed by a Vero cell‐based fluorescent assay. Results: Stx2 was found in the serum of eight of the 16 children who were investigated. It was also detected in four of the six family members not showing symptomatic HUS, with an extremely high level in two. Conclusion: An absent or rather low concentration of Stx2 was found in the serum of children admitted to the clinic with diarrhoea‐associated HUS. The high concentration of Stx2 in family members without HUS, but mostly with watery diarrhoea and raised functional activity, was in line with the concept of early injury by Stx2.