The EuroBioTox Project: Progress Towards the Detection and Identification of Biotoxins via Standardization, Training, and Method Evaluation

A special issue of Toxins (ISSN 2072-6651).

Deadline for manuscript submissions: 31 October 2026 | Viewed by 4158

Special Issue Editors


E-Mail Website
Guest Editor
Institut für Toxikologie, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, 30625 Hannover, Germany
Interests: botulinum neurotoxin; ricin; tetanus neurotoxin; Clostridium perfringens; Clostridium botulinum; Staphylococcus aureus enterotoxin (SE)
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Centre for Biological Threats and Special Pathogens, Biological Toxins, Robert Koch-Institute, Seestr. 10, 13353 Berlin, Germany
Interests: botulinum neurotoxins, ricin, abrin and other protein biotoxins; variability and functionality of biotoxins; (multiplex-) detection of biotoxins; antibodies for research and therapy
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Recent incidents in Europe have highlighted that terrorists take an interest in the production of biotoxins, and that they have even succeeded in the production of toxic material. Previous studies have shown that there is a lack of robustness in Europe’s preparedness for biotoxin incidents. Therefore, the EuroBioTox project—funded under the EU’s Horizon 2020 program—consolidated an expert network comprising 63 institutions from 23 countries to strengthen Europe’s capabilities to cope with the intentional release of biotoxins, namely, saxitoxin, ricin, abrin, Staphylococcus aureus enterotoxin B (SEB), and botulinum neurotoxins (BoNTs).

EuroBioTox produced the world’s first ISO 17034:2016 certified reference materials (CRMs) for protein biotoxins relevant in the security field. This Special Issue describes the comprehensive characterization of CRMs for ricin, abrin, BoNT/A, BoNT/B, and SEB, which are now available to authorised expert laboratories worldwide. The CRMs significantly increase quality assurance measures in the field of biotoxin detection and allow for the development and comparative validation of novel methods, particularly animal replacement methods, which are still in place for some of the mentioned biotoxins. The CRMs also serve as analytes in a series of large international proficiency tests (PTs) organized by the EuroBioTox consortium to demonstrate the technical progress in biotoxin detection, identification, and quantification. First, previously recommended detection methods were trained and subsequently employed in the PTs. This approach resulted in a clear improvement in the analytical results obtained in a two-stage PT scheme. In the absence of regular self-assessment, the PT scheme offered participants an opportunity to self-evaluate their analytical capabilities and to obtain or maintain an accreditation.

With respect to animal replacement methods for the detection of BoNTs, a comprehensive study evaluated the performance of in vitro and ex vivo methods on a wide panel of samples comprising C. botulinum neurotoxin sero- and subtypes spiked into representative clinical, food, and environmental matrices. The results highlighted superior animal replacement methods, which will help reduce animal experiments in the field of botulism diagnostics, directly supporting Directive 2010/63/EU on the protection of animals.

A review article in this Special Issue summarizes the major achievements of the EuroBioTox project, putting them into context, and sheds light on the future avenues for biotoxin detection.

Dr. Andreas Rummel
Dr. Brigitte G. Dorner
Guest Editors

Publisher’s notice:

As stated above, the central purpose of this Special Issue is to present research from the EuroBioTox Project. Given this purpose, the Guest Editors’ contribution to this Special Issue may be greater than outlined in MDPI’s Special Issue guidelines (https://www.mdpi.com/special_issues_guidelines). The Editorial Office and Editor-in-Chief of Toxins has approved this Topic and MDPI’s standard manuscript editorial processing procedure (https://www.mdpi.com/editorial_process) will be applied to all submissions. As per our standard procedure, Guest Editors are excluded from participating in the editorial process for their submission and/or for submissions from persons with whom a potential conflict of interest may exist. More details on MDPI’s Conflict of Interest policy for reviewers and editors can be found here: https://www.mdpi.com/ethics#_bookmark22.

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a double-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Toxins is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (3 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

17 pages, 7243 KiB  
Article
N-Glycosylation Profile of Abrin Certified EU Reference Material
by Roland Josuran, Andreas Wenger, Sylvia Worbs, Bettina Kampa, Andreas Rummel, Brigitte G. Dorner and Sabina Gerber
Toxins 2025, 17(3), 108; https://doi.org/10.3390/toxins17030108 - 26 Feb 2025
Viewed by 538
Abstract
Abrin is a highly toxic plant protein encompassing four isoforms, abrin-a, -b, -c and -d. An abrin reference material was isolated from Abrus precatorius and certified (EURM-113) by the EuroBioTox consortium. Here, we present a detailed characterisation of the N-glycosylation profile of [...] Read more.
Abrin is a highly toxic plant protein encompassing four isoforms, abrin-a, -b, -c and -d. An abrin reference material was isolated from Abrus precatorius and certified (EURM-113) by the EuroBioTox consortium. Here, we present a detailed characterisation of the N-glycosylation profile of EURM-113. The monosaccharide composition of the N-glycans was determined and quantified. Release of the N-glycans yielded 13 different partially xylosylated, oligomannosidic and paucimannosidic glycan structures. Two N-glycans were found at N82 and N110 of the abrin-b A-chain and another two at N100 and N140 of the B-chains. The N-glycosylation sites N200 in the A-chain and N141 in the B-chain were non-glycosylated. Whereas N82 and N110 of abrin-b comprised paucimannosidic glycans, N100 and N140 of the B-chains revealed oligomannosidic N-glycans. Xylose was absent in the glycans at N100 but was present in about half of the glycans at N140. Hence, this study revealed substantially different types of glycan structures within the B-chains compared to the abrin-b A-chain. Furthermore, the most C-terminal N-glycosylation site in the A-chain was found to be non-glycosylated in all abrin isoforms detected. Additionally, the establishment of the N-glycosylation profile of the abrin reference material led to the identification of the abrin isoforms -a, -b and -c. In conclusion, the abrin N-glycosylation profile is highly similar to the one of ricin and yields high analytical value to be further exploited as a fingerprint in forensic investigations to uncover toxin production or toxin provenance. Full article
Show Figures

Figure 1

19 pages, 1790 KiB  
Article
International Proficiency Test Targeting a Large Panel of Botulinum Neurotoxin Sero- and Subtypes in Different Matrices
by Christine Rasetti-Escargueil, Michel Robert Popoff, Bettina Kampa, Sylvia Worbs, Maud Marechal, Daniel Guerin, Eléa Paillares, Werner Luginbühl and Emmanuel Lemichez
Toxins 2024, 16(11), 485; https://doi.org/10.3390/toxins16110485 - 8 Nov 2024
Viewed by 1180
Abstract
Detection of botulinum neurotoxins (BoNTs) involves a combination of technical challenges that call for the execution of inter-laboratory proficiency tests (PTs) to define the performance and ease of implementation of existing diagnostic methods regarding representative BoNT toxin-types spiked in clinical, food, or environmental [...] Read more.
Detection of botulinum neurotoxins (BoNTs) involves a combination of technical challenges that call for the execution of inter-laboratory proficiency tests (PTs) to define the performance and ease of implementation of existing diagnostic methods regarding representative BoNT toxin-types spiked in clinical, food, or environmental matrices. In the framework of the EU project EuroBioTox, we organized an international proficiency test for the detection and quantification of the clinically relevant BoNT/A, B, E, and F sero- and subtypes including concentrations as low as 0.5 ng/mL. BoNTs were spiked in serum, milk, and soil matrices. Here, we evaluate the results of 18 laboratories participating in this PT. Participants have implemented a wide array of detection methods based on functional, immunological, and mass spectrometric principles. Methods implemented in this proficiency test notably included endopeptidase assays either coupled to mass spectrometry (Endopep-MS) or enzyme-linked immunosorbent assays (Endopep-ELISA). This interlaboratory exercise pinpoints the most effective and complementary methods shared by the greatest number of participants, also highlighting the importance of combining the training of selected methods and of distributing toxin reference material to reduce the variability of quantitative data. Full article
Show Figures

Figure 1

28 pages, 8762 KiB  
Article
Glycan Profile and Sequence Variants of Certified Ricin Reference Material and Other Ricin Samples Yield Unique Molecular Signature Features
by Roland Josuran, Andreas Wenger, Christian Müller, Bettina Kampa, Sylvia Worbs, Brigitte G. Dorner and Sabina Gerber
Toxins 2024, 16(6), 243; https://doi.org/10.3390/toxins16060243 - 26 May 2024
Cited by 2 | Viewed by 1613
Abstract
A certified reference material of ricin (CRM-LS-1) was produced by the EuroBioTox consortium to standardise the analysis of this biotoxin. This study established the N-glycan structures and proportions including their loci and occupancy of ricin CRM-LS-1. The glycan profile was compared with [...] Read more.
A certified reference material of ricin (CRM-LS-1) was produced by the EuroBioTox consortium to standardise the analysis of this biotoxin. This study established the N-glycan structures and proportions including their loci and occupancy of ricin CRM-LS-1. The glycan profile was compared with ricin from different preparations and other cultivars and isoforms. A total of 15 different oligomannosidic or paucimannosidic structures were identified in CRM-LS-1. Paucimannose was mainly found within the A-chain and oligomannose constituted the major glycan type of the B-chain. Furthermore, the novel primary structure variants E138 and D138 and four different C-termini of the A-chain as well as two B-chain variants V250 and F250 were elucidated. While the glycan proportions and loci were similar among all variants in CRM-LS-1 and ricin isoforms D and E of all cultivars analysed, a different stoichiometry for isoforms D and E and the amino acid variants were found. This detailed physicochemical characterization of ricin regarding the glycan profile and amino acid sequence variations yields unprecedented insight into the molecular features of this protein toxin. The variable attributes discovered within different cultivars present signature motifs and may allow discrimination of the biotoxin’s origin that are important in molecular forensic profiling. In conclusion, our data of in-depth CRM-LS-1 characterization combined with the analysis of other cultivars is representative for known ricin variants. Full article
Show Figures

Figure 1

Back to TopTop