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Identification of a novel botulinum neurotoxin gene cluster in Enterococcus

The deadly neurotoxins of Clostridium botulinum (BoNTs) comprise eight serotypes (A–G; X). The neurotoxin gene cluster encoding BoNT and its accessory proteins includes an operon containing an ntnh gene upstream of the boNT gene. Another operon contains either ha (haemagglutinin) or orfX genes (of u...

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Autores principales: Brunt, Jason, Carter, Andrew T., Stringer, Sandra C., Peck, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838542/
https://www.ncbi.nlm.nih.gov/pubmed/29323697
http://dx.doi.org/10.1002/1873-3468.12969
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author Brunt, Jason
Carter, Andrew T.
Stringer, Sandra C.
Peck, Michael W.
author_facet Brunt, Jason
Carter, Andrew T.
Stringer, Sandra C.
Peck, Michael W.
author_sort Brunt, Jason
collection PubMed
description The deadly neurotoxins of Clostridium botulinum (BoNTs) comprise eight serotypes (A–G; X). The neurotoxin gene cluster encoding BoNT and its accessory proteins includes an operon containing an ntnh gene upstream of the boNT gene. Another operon contains either ha (haemagglutinin) or orfX genes (of unknown function). Here we describe a novel boNT gene cluster from Enterococcus sp. 3G1_DIV0629, with a typical ntnh gene and an uncommon orfX arrangement. The neurotoxin (designated putative eBoNT/J) contains a metallopeptidase zinc‐binding site, a translocation domain and a target cell attachment domain. Structural properties of the latter suggest a novel targeting mechanism with consequent implications for application by the pharmaceutical industry. This is the first complete boNT gene cluster identified in a non‐clostridial genome.
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spelling pubmed-58385422018-03-12 Identification of a novel botulinum neurotoxin gene cluster in Enterococcus Brunt, Jason Carter, Andrew T. Stringer, Sandra C. Peck, Michael W. FEBS Lett Research Letters The deadly neurotoxins of Clostridium botulinum (BoNTs) comprise eight serotypes (A–G; X). The neurotoxin gene cluster encoding BoNT and its accessory proteins includes an operon containing an ntnh gene upstream of the boNT gene. Another operon contains either ha (haemagglutinin) or orfX genes (of unknown function). Here we describe a novel boNT gene cluster from Enterococcus sp. 3G1_DIV0629, with a typical ntnh gene and an uncommon orfX arrangement. The neurotoxin (designated putative eBoNT/J) contains a metallopeptidase zinc‐binding site, a translocation domain and a target cell attachment domain. Structural properties of the latter suggest a novel targeting mechanism with consequent implications for application by the pharmaceutical industry. This is the first complete boNT gene cluster identified in a non‐clostridial genome. John Wiley and Sons Inc. 2018-01-23 2018-02 /pmc/articles/PMC5838542/ /pubmed/29323697 http://dx.doi.org/10.1002/1873-3468.12969 Text en © 2018 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Letters
Brunt, Jason
Carter, Andrew T.
Stringer, Sandra C.
Peck, Michael W.
Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title_full Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title_fullStr Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title_full_unstemmed Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title_short Identification of a novel botulinum neurotoxin gene cluster in Enterococcus
title_sort identification of a novel botulinum neurotoxin gene cluster in enterococcus
topic Research Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838542/
https://www.ncbi.nlm.nih.gov/pubmed/29323697
http://dx.doi.org/10.1002/1873-3468.12969
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