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Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT
The genus Yersinia comprises 19 species of which three are known as human and animal pathogens. Some species display toxicity toward invertebrates using the so-called toxin complex (TC) and/or determinants that are not yet known. Recent studies showed a remarkable variability of insecticidal activit...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246891/ https://www.ncbi.nlm.nih.gov/pubmed/30488025 http://dx.doi.org/10.3389/fcimb.2018.00392 |
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author | Springer, Katharina Sänger, Philipp-Albert Moritz, Christian Felsl, Angela Rattei, Thomas Fuchs, Thilo M. |
author_facet | Springer, Katharina Sänger, Philipp-Albert Moritz, Christian Felsl, Angela Rattei, Thomas Fuchs, Thilo M. |
author_sort | Springer, Katharina |
collection | PubMed |
description | The genus Yersinia comprises 19 species of which three are known as human and animal pathogens. Some species display toxicity toward invertebrates using the so-called toxin complex (TC) and/or determinants that are not yet known. Recent studies showed a remarkable variability of insecticidal activities when representatives of different Yersinia species (spp.) were subcutaneously injected into the greater wax moth, Galleria mellonella. Here, we demonstrate that Y. intermedia and Y. frederiksenii are highly toxic to this insect. A member of Y. Enterocolitica phylogroup 1B killed G. mellonella larvae with injection doses of approximately 38 cells only, thus resembling the insecticidal activity of Photorhabdus luminescens. The pathogenicity Yersinia spp. displays toward the larvae was higher at 15°C than at 30°C and independent of the TC. However, upon subtraction of all genes of the low-pathogenic Y. enterocolitica strain W22703 from the genomes of Y. intermedia and Y. frederiksenii, we identified a set of genes that may be responsible for the toxicity of these two species. Indeed, a mutant of Y. frederiksenii lacking yacT, a gene that encodes a protein similar to the heat-stable cytotonic enterotoxin (Ast) of Aeromonas hydrophila, exhibited a reduced pathogenicity toward G. mellonella larvae and altered the morphology of hemocytes. The data suggests that the repertoire of virulence determinants present in environmental Yersinia species remains to be elucidated. |
format | Online Article Text |
id | pubmed-6246891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62468912018-11-28 Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT Springer, Katharina Sänger, Philipp-Albert Moritz, Christian Felsl, Angela Rattei, Thomas Fuchs, Thilo M. Front Cell Infect Microbiol Cellular and Infection Microbiology The genus Yersinia comprises 19 species of which three are known as human and animal pathogens. Some species display toxicity toward invertebrates using the so-called toxin complex (TC) and/or determinants that are not yet known. Recent studies showed a remarkable variability of insecticidal activities when representatives of different Yersinia species (spp.) were subcutaneously injected into the greater wax moth, Galleria mellonella. Here, we demonstrate that Y. intermedia and Y. frederiksenii are highly toxic to this insect. A member of Y. Enterocolitica phylogroup 1B killed G. mellonella larvae with injection doses of approximately 38 cells only, thus resembling the insecticidal activity of Photorhabdus luminescens. The pathogenicity Yersinia spp. displays toward the larvae was higher at 15°C than at 30°C and independent of the TC. However, upon subtraction of all genes of the low-pathogenic Y. enterocolitica strain W22703 from the genomes of Y. intermedia and Y. frederiksenii, we identified a set of genes that may be responsible for the toxicity of these two species. Indeed, a mutant of Y. frederiksenii lacking yacT, a gene that encodes a protein similar to the heat-stable cytotonic enterotoxin (Ast) of Aeromonas hydrophila, exhibited a reduced pathogenicity toward G. mellonella larvae and altered the morphology of hemocytes. The data suggests that the repertoire of virulence determinants present in environmental Yersinia species remains to be elucidated. Frontiers Media S.A. 2018-11-14 /pmc/articles/PMC6246891/ /pubmed/30488025 http://dx.doi.org/10.3389/fcimb.2018.00392 Text en Copyright © 2018 Springer, Sänger, Moritz, Felsl, Rattei and Fuchs. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Springer, Katharina Sänger, Philipp-Albert Moritz, Christian Felsl, Angela Rattei, Thomas Fuchs, Thilo M. Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title | Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title_full | Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title_fullStr | Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title_full_unstemmed | Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title_short | Insecticidal Toxicity of Yersinia frederiksenii Involves the Novel Enterotoxin YacT |
title_sort | insecticidal toxicity of yersinia frederiksenii involves the novel enterotoxin yact |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6246891/ https://www.ncbi.nlm.nih.gov/pubmed/30488025 http://dx.doi.org/10.3389/fcimb.2018.00392 |
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