Detection of Cleaved Stx2a in the Blood of STEC-Infected Patients

Author:

Varrone Elisa1,Carnicelli Domenica1ORCID,He Xiaohua2ORCID,Grasse Marco3,Stampfer Karin3,Huber Silke3ORCID,Kellnerová Sára3,Tazzari Pier Luigi4,Ricci Francesca4ORCID,Paterini Paola15,Ardissino Gianluigi6,Morabito Stefano7,Orth-Höller Dorothea8,Würzner Reinhard3ORCID,Brigotti Maurizio1

Affiliation:

1. Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Via San Giacomo 14, 40126 Bologna, Italy

2. Western Regional Research Center, U.S. Department of Agriculture, Agricultural Research Service, 800 Buchanan Street, Albany, CA 94710, USA

3. Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck, 6020 Innsbruck, Austria

4. Immunohematology and Transfusion Center, S. Orsola-Malpighi Hospital, Via Massarenti 9, 40138 Bologna, Italy

5. Center for Applied Biomedical Research-CRBA, University of Bologna, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy

6. Center for HUS Control, Prevention and Management, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Via Commenda 9, 20122 Milano, Italy

7. European Reference Laboratory for Escherichia coli, Istituto Superiore di Sanità, 00161 Rome, Italy

8. MB-LAB—Clinical Microbiology Laboratory, 6020 Innsbruck, Austria

Abstract

Typical hemolytic uremic syndrome (HUS) is mainly caused by Shiga toxin-producing Escherichia coli (STEC) releasing Shiga toxin 2 (Stx2). Two different structures of this AB5 toxin have been described: uncleaved, with intact B and A chains, and cleaved, with intact B and a nicked A chain consisting of two fragments, A1 and A2, connected by a disulfide bond. Despite having the same toxic effect on sensitive cells, the two forms differ in their binding properties for circulating cells, serum components and complement factors, thus contributing to the pathogenesis of HUS differently. The outcome of STEC infections and the development of HUS could be influenced by the relative amounts of uncleaved or cleaved Stx2 circulating in patients’ blood. Cleaved Stx2 was identified and quantified for the first time in four out of eight STEC-infected patients’ sera by a method based on the inhibition of cell-free translation. Cleaved Stx2 was present in the sera of patients with toxins bound to neutrophils and in two out of three patients developing HUS, suggesting its involvement in HUS pathogenesis, although in association with other bacterial or host factors.

Funder

University of Bologna

Progetto ALICE ONLUS—Associazione per la lotta alla SEU

Austrian Science Fund FWF

Publisher

MDPI AG

Subject

Health, Toxicology and Mutagenesis,Toxicology

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