Cargando…
Phage lysin that specifically eliminates Clostridium botulinum Group I cells
Clostridium botulinum poses a serious threat to food safety and public health by producing potent neurotoxin during its vegetative growth and causing life-threatening neuroparalysis, botulism. While high temperature can be utilized to eliminate C. botulinum spores and the neurotoxin, non-thermal eli...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725837/ https://www.ncbi.nlm.nih.gov/pubmed/33299101 http://dx.doi.org/10.1038/s41598-020-78622-6 |
_version_ | 1783620786379030528 |
---|---|
author | Zhang, Zhen Lahti, Meeri Douillard, François P. Korkeala, Hannu Lindström, Miia |
author_facet | Zhang, Zhen Lahti, Meeri Douillard, François P. Korkeala, Hannu Lindström, Miia |
author_sort | Zhang, Zhen |
collection | PubMed |
description | Clostridium botulinum poses a serious threat to food safety and public health by producing potent neurotoxin during its vegetative growth and causing life-threatening neuroparalysis, botulism. While high temperature can be utilized to eliminate C. botulinum spores and the neurotoxin, non-thermal elimination of newly germinated C. botulinum cells before onset of toxin production could provide an alternative or additional factor controlling the risk of botulism in some applications. Here we introduce a putative phage lysin that specifically lyses vegetative C. botulinum Group I cells. This lysin, called CBO1751, efficiently kills cells of C. botulinum Group I strains at the concentration of 5 µM, but shows little or no lytic activity against C. botulinum Group II or III or other Firmicutes strains. CBO1751 is active at pH from 6.5 to 10.5. The lytic activity of CBO1751 is tolerant to NaCl (200 mM), but highly susceptible to divalent cations Ca(2+) and Mg(2+) (50 mM). CBO1751 readily and effectively eliminates C. botulinum during spore germination, an early stage preceding vegetative growth and neurotoxin production. This is the first report of an antimicrobial lysin against C. botulinum, presenting high potential for developing a novel antibotulinal agent for non-thermal applications in food and agricultural industries. |
format | Online Article Text |
id | pubmed-7725837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77258372020-12-14 Phage lysin that specifically eliminates Clostridium botulinum Group I cells Zhang, Zhen Lahti, Meeri Douillard, François P. Korkeala, Hannu Lindström, Miia Sci Rep Article Clostridium botulinum poses a serious threat to food safety and public health by producing potent neurotoxin during its vegetative growth and causing life-threatening neuroparalysis, botulism. While high temperature can be utilized to eliminate C. botulinum spores and the neurotoxin, non-thermal elimination of newly germinated C. botulinum cells before onset of toxin production could provide an alternative or additional factor controlling the risk of botulism in some applications. Here we introduce a putative phage lysin that specifically lyses vegetative C. botulinum Group I cells. This lysin, called CBO1751, efficiently kills cells of C. botulinum Group I strains at the concentration of 5 µM, but shows little or no lytic activity against C. botulinum Group II or III or other Firmicutes strains. CBO1751 is active at pH from 6.5 to 10.5. The lytic activity of CBO1751 is tolerant to NaCl (200 mM), but highly susceptible to divalent cations Ca(2+) and Mg(2+) (50 mM). CBO1751 readily and effectively eliminates C. botulinum during spore germination, an early stage preceding vegetative growth and neurotoxin production. This is the first report of an antimicrobial lysin against C. botulinum, presenting high potential for developing a novel antibotulinal agent for non-thermal applications in food and agricultural industries. Nature Publishing Group UK 2020-12-09 /pmc/articles/PMC7725837/ /pubmed/33299101 http://dx.doi.org/10.1038/s41598-020-78622-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Zhen Lahti, Meeri Douillard, François P. Korkeala, Hannu Lindström, Miia Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title | Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title_full | Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title_fullStr | Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title_full_unstemmed | Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title_short | Phage lysin that specifically eliminates Clostridium botulinum Group I cells |
title_sort | phage lysin that specifically eliminates clostridium botulinum group i cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725837/ https://www.ncbi.nlm.nih.gov/pubmed/33299101 http://dx.doi.org/10.1038/s41598-020-78622-6 |
work_keys_str_mv | AT zhangzhen phagelysinthatspecificallyeliminatesclostridiumbotulinumgroupicells AT lahtimeeri phagelysinthatspecificallyeliminatesclostridiumbotulinumgroupicells AT douillardfrancoisp phagelysinthatspecificallyeliminatesclostridiumbotulinumgroupicells AT korkealahannu phagelysinthatspecificallyeliminatesclostridiumbotulinumgroupicells AT lindstrommiia phagelysinthatspecificallyeliminatesclostridiumbotulinumgroupicells |