Two-component signal transduction system CBO0787/CBO0786 represses transcription from botulinum neurotoxin promoters in Clostridium botulinum ATCC 3502
Autor: | Nigel P. Minton, Hannu Korkeala, Zhen Zhang, Miia Lindström, John T. Heap, Elina Sahala, Elias Dahlsten |
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Jazyk: | angličtina |
Rok vydání: | 2013 |
Předmět: |
Bacterial Diseases
Transcription Genetic medicine.disease_cause Sigma factor Genes Regulator Neurotoxin Botulinum Toxins Type A lcsh:QH301-705.5 2. Zero hunger Regulation of gene expression 0303 health sciences Recombinant Proteins 3. Good health Cell biology Bacterial Pathogens RNA Bacterial Infectious Diseases Medicine Research Article Signal Transduction lcsh:Immunologic diseases. Allergy Clostridium botulinum type A Immunology Neurotoxins Biology Muscle disorder Microbiology 03 medical and health sciences Bacterial Proteins Virology Genetics medicine Gene Silencing Molecular Biology Microbial Pathogens 030304 developmental biology Gram Positive 030306 microbiology Promoter Botulism Gene Expression Regulation Bacterial Repressor Proteins Response regulator Mutagenesis Insertional lcsh:Biology (General) Trans-Activators Clostridium botulinum Parasitology lcsh:RC581-607 |
Zdroj: | e1003252 PLoS Pathogens PLoS Pathogens, Vol 9, Iss 3, p e1003252 (2013) |
Popis: | Blocking neurotransmission, botulinum neurotoxin is the most poisonous biological substance known to mankind. Despite its infamy as the scourge of the food industry, the neurotoxin is increasingly used as a pharmaceutical to treat an expanding range of muscle disorders. Whilst neurotoxin expression by the spore-forming bacterium Clostridium botulinum appears tightly regulated, to date only positive regulatory elements, such as the alternative sigma factor BotR, have been implicated in this control. The identification of negative regulators has proven to be elusive. Here, we show that the two-component signal transduction system CBO0787/CBO0786 negatively regulates botulinum neurotoxin expression. Single insertional inactivation of cbo0787 encoding a sensor histidine kinase, or of cbo0786 encoding a response regulator, resulted in significantly elevated neurotoxin gene expression levels and increased neurotoxin production. Recombinant CBO0786 regulator was shown to bind to the conserved −10 site of the core promoters of the ha and ntnh-botA operons, which encode the toxin structural and accessory proteins. Increasing concentration of CBO0786 inhibited BotR-directed transcription from the ha and ntnh-botA promoters, demonstrating direct transcriptional repression of the ha and ntnh-botA operons by CBO0786. Thus, we propose that CBO0786 represses neurotoxin gene expression by blocking BotR-directed transcription from the neurotoxin promoters. This is the first evidence of a negative regulator controlling botulinum neurotoxin production. Understanding the neurotoxin regulatory mechanisms is a major target of the food and pharmaceutical industries alike. Author Summary Botulinum neurotoxin produced by the spore-forming bacterium Clostridium botulinum is the most poisonous biological substance known to mankind. By blocking neurotransmission, the neurotoxin causes a flaccid paralysis called botulism which may to lead to death upon respiratory muscle collapse. Despite its infamy as the scourge of the food industry, the neurotoxin is attracting increasing interest as a pharmaceutical to treat an expanding range of muscle disorders. Whilst neurotoxin production by C. botulinum appears tightly regulated, to date only positive regulatory elements, thus enhancing the neurotoxin production, have been implicated in this control. The identification of negative regulators, responsible for down-tuning the neurotoxin synthesis, has proven to be elusive, but would offer novel approaches both for the production of safe foods and for the development of therapeutic neurotoxins. Here, we report a two-component signal transduction system that negatively regulates botulinum neurotoxin production. Understanding the neurotoxin regulatory mechanisms is a major target of the food and pharmaceutical industries alike. |
Databáze: | OpenAIRE |
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