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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2011-7-4
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pubmed:abstractText |
Phenoloxidase (PO) and its activation system are implicated in several defense responses of insects. Upon wounding or infection, inactive prophenoloxidase (proPO) is converted to active PO through a cascade of serine proteases and their homologs. PO generates reactive compounds such as 5,6-dihydroxyindole (DHI), which have a broad-spectrum antibacterial and antifungal activity. Here we report that DHI and its spontaneous oxidation products are also active against viruses and parasitic wasps. Preincubation of a baculovirus stock with 1.25 mM DHI for 3 h near fully disabled recombinant protein production. The LC?? for lambda bacteriophage and eggs of the wasp Microplitis demolitor were 5.6 ± 2.2 and 111.0 ± 1.6 ?M, respectively. The toxicity of DHI and related compounds also extended to cells derived from insects that serve as hosts for several of the aforementioned pathogens. Pretreatment of Sf9 cells with 1.0 mM DHI for 4 h resulted in 97% mortality, and LC?? values of 20.3 ± 1.2 ?M in buffer and 131.8 ± 1.1 ?M in a culture medium. Symptoms of DHI toxicity in Sf9 cells included DNA polymerization, protein crosslinking, and lysis. Taken together, these data showed that proPO activation and DHI production is strongly toxic against various pathogens but can also damage host tissues and cells if not properly controlled.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-10704476,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-11134313,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-11268040,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-11837452,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-12075074,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-12197117,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-1450450,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-15110869,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-15804578,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-16061795,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-16332211,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-17879234,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-18032603,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-18395222,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-18457993,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-18474557,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-18519564,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-19597539,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-19773068,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-19808037,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-20417280,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-3532325,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/21554953-9017902
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1879-0240
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2011 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
41
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
645-52
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pubmed:meshHeading |
pubmed-meshheading:21554953-Animals,
pubmed-meshheading:21554953-Bacteriophage lambda,
pubmed-meshheading:21554953-Cell Line,
pubmed-meshheading:21554953-Cytotoxicity, Immunologic,
pubmed-meshheading:21554953-DNA,
pubmed-meshheading:21554953-Enzyme Activation,
pubmed-meshheading:21554953-Indoles,
pubmed-meshheading:21554953-Insect Proteins,
pubmed-meshheading:21554953-Kinetics,
pubmed-meshheading:21554953-Monophenol Monooxygenase,
pubmed-meshheading:21554953-Nucleopolyhedrovirus,
pubmed-meshheading:21554953-Oxidation-Reduction,
pubmed-meshheading:21554953-Polymerization,
pubmed-meshheading:21554953-Recombinant Proteins,
pubmed-meshheading:21554953-Spodoptera,
pubmed-meshheading:21554953-Substrate Specificity,
pubmed-meshheading:21554953-Wasps
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pubmed:year |
2011
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pubmed:articleTitle |
Antiviral, anti-parasitic, and cytotoxic effects of 5,6-dihydroxyindole (DHI), a reactive compound generated by phenoloxidase during insect immune response.
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pubmed:affiliation |
Department of Entomology and Plant Pathology, Oklahoma State University, 127 NRC, Stillwater, OK 74078, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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