Characterization of an Insecticidal Toxin and Pathogenicity of Pseudomonas taiwanensis against Insects
Author(s) -
WenJen Chen,
Feng-Chia Hsieh,
FuChiun Hsu,
Yi-Fang Tasy,
JeRuei Liu,
MingChe Shih
Publication year - 2014
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1004288
Subject(s) - sf9 , biology , spodoptera litura , microbiology and biotechnology , spodoptera , spodoptera littoralis , plutella , toxin , biochemistry , gene , botany , recombinant dna , larva , noctuidae
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 Δ tccC 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 Δ tccC 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.
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