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Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects
Pseudomonas taiwanensis is a broad-host-range entomopathogenic bacterium that exhibits insecticidal activity toward agricultural pests Plutella xylostella, Spodoptera exigua, Spodoptera litura, Trichoplusia ni and Drosophila melanogaster. Oral infection with different concentrations (OD = 0.5 to 2)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140846/ https://www.ncbi.nlm.nih.gov/pubmed/25144637 http://dx.doi.org/10.1371/journal.ppat.1004288 |
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author | Chen, Wen-Jen Hsieh, Feng-Chia Hsu, Fu-Chiun Tasy, Yi-Fang Liu, Je-Ruei Shih, Ming-Che |
author_facet | Chen, Wen-Jen Hsieh, Feng-Chia Hsu, Fu-Chiun Tasy, Yi-Fang Liu, Je-Ruei Shih, Ming-Che |
author_sort | Chen, Wen-Jen |
collection | PubMed |
description | Pseudomonas taiwanensis is a broad-host-range entomopathogenic bacterium that exhibits insecticidal activity toward agricultural pests Plutella xylostella, Spodoptera exigua, Spodoptera litura, Trichoplusia ni and Drosophila melanogaster. Oral infection with different concentrations (OD = 0.5 to 2) of wild-type P. taiwanensis resulted in insect mortality rates that were not significantly different (92.7%, 96.4% and 94.5%). The TccC protein, a component of the toxin complex (Tc), plays an essential role in the insecticidal activity of P. taiwanensis. The ΔtccC mutant strain of P. taiwanensis, which has a knockout mutation in the tccC gene, only induced 42.2% mortality in P. xylostella, even at a high bacterial dose (OD = 2.0). TccC protein was cleaved into two fragments, an N-terminal fragment containing an Rhs-like domain and a C-terminal fragment containing a Glt symporter domain and a TraT domain, which might contribute to antioxidative stress activity and defense against macrophagosis, respectively. Interestingly, the primary structure of the C-terminal region of TccC in P. taiwanensis is unique among pathogens. Membrane localization of the C-terminal fragment of TccC was proven by flow cytometry. Sonicated pellets of P. taiwanensis ΔtccC strain had lower toxicity against the Sf9 insect cell line and P. xylostella larvae than the wild type. We also found that infection of Sf9 and LD652Y-5d cell lines with P. taiwanensis induced apoptotic cell death. Further, natural oral infection by P. taiwanensis triggered expression of host programmed cell death-related genes JNK-2 and caspase-3. |
format | Online Article Text |
id | pubmed-4140846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41408462014-08-25 Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects Chen, Wen-Jen Hsieh, Feng-Chia Hsu, Fu-Chiun Tasy, Yi-Fang Liu, Je-Ruei Shih, Ming-Che PLoS Pathog Research Article Pseudomonas taiwanensis is a broad-host-range entomopathogenic bacterium that exhibits insecticidal activity toward agricultural pests Plutella xylostella, Spodoptera exigua, Spodoptera litura, Trichoplusia ni and Drosophila melanogaster. Oral infection with different concentrations (OD = 0.5 to 2) of wild-type P. taiwanensis resulted in insect mortality rates that were not significantly different (92.7%, 96.4% and 94.5%). The TccC protein, a component of the toxin complex (Tc), plays an essential role in the insecticidal activity of P. taiwanensis. The ΔtccC mutant strain of P. taiwanensis, which has a knockout mutation in the tccC gene, only induced 42.2% mortality in P. xylostella, even at a high bacterial dose (OD = 2.0). TccC protein was cleaved into two fragments, an N-terminal fragment containing an Rhs-like domain and a C-terminal fragment containing a Glt symporter domain and a TraT domain, which might contribute to antioxidative stress activity and defense against macrophagosis, respectively. Interestingly, the primary structure of the C-terminal region of TccC in P. taiwanensis is unique among pathogens. Membrane localization of the C-terminal fragment of TccC was proven by flow cytometry. Sonicated pellets of P. taiwanensis ΔtccC strain had lower toxicity against the Sf9 insect cell line and P. xylostella larvae than the wild type. We also found that infection of Sf9 and LD652Y-5d cell lines with P. taiwanensis induced apoptotic cell death. Further, natural oral infection by P. taiwanensis triggered expression of host programmed cell death-related genes JNK-2 and caspase-3. Public Library of Science 2014-08-21 /pmc/articles/PMC4140846/ /pubmed/25144637 http://dx.doi.org/10.1371/journal.ppat.1004288 Text en © 2014 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Wen-Jen Hsieh, Feng-Chia Hsu, Fu-Chiun Tasy, Yi-Fang Liu, Je-Ruei Shih, Ming-Che Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title | Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title_full | Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title_fullStr | Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title_full_unstemmed | Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title_short | Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects |
title_sort | characterization of an insecticidal toxin and pathogenicity of pseudomonas taiwanensis against insects |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140846/ https://www.ncbi.nlm.nih.gov/pubmed/25144637 http://dx.doi.org/10.1371/journal.ppat.1004288 |
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