pubmed-article:21569540 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0041234 | lld:lifeskim |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0012656 | lld:lifeskim |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0699819 | lld:lifeskim |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0887912 | lld:lifeskim |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0870071 | lld:lifeskim |
pubmed-article:21569540 | lifeskim:mentions | umls-concept:C0322616 | lld:lifeskim |
pubmed-article:21569540 | pubmed:dateCreated | 2011-6-20 | lld:pubmed |
pubmed-article:21569540 | pubmed:abstractText | Paratransgenesis is an approach to reducing arthropod vector competence using genetically modified symbionts. When applied to control of Chagas disease, the symbiont bacterium Rhodococcus rhodnii, resident in the gut lumen of the triatomine vector Rhodnius prolixus (Hemiptera: Reduviidae), is transformed to export cecropin A, an insect immune peptide. Cecropin A is active against Trypanosoma cruzi, the causative agent of Chagas disease. While proof of concept has been achieved in laboratory studies, a rigorous and comprehensive risk assessment is required prior to consideration of field release. An important part of this assessment involves estimating probability of transgene horizontal transfer to environmental organisms (HGT). This article presents a two-part risk assessment methodology: a theoretical model predicting HGT in the gut of R. prolixus from the genetically transformed symbiont R. rhodnii to a closely related non-target bacterium, Gordona rubropertinctus, in the absence of selection pressure, and a series of laboratory trials designed to test the model. | lld:pubmed |
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pubmed-article:21569540 | pubmed:language | eng | lld:pubmed |
pubmed-article:21569540 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21569540 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21569540 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21569540 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21569540 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21569540 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21569540 | pubmed:issn | 1756-3305 | lld:pubmed |
pubmed-article:21569540 | pubmed:author | pubmed-author:DurvasulaRavi... | lld:pubmed |
pubmed-article:21569540 | pubmed:author | pubmed-author:MatthewsScott... | lld:pubmed |
pubmed-article:21569540 | pubmed:author | pubmed-author:RaoVadrevu... | lld:pubmed |
pubmed-article:21569540 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21569540 | pubmed:volume | 4 | lld:pubmed |
pubmed-article:21569540 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21569540 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21569540 | pubmed:pagination | 77 | lld:pubmed |
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pubmed-article:21569540 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21569540 | pubmed:articleTitle | Modeling horizontal gene transfer (HGT) in the gut of the Chagas disease vector Rhodnius prolixus. | lld:pubmed |
pubmed-article:21569540 | pubmed:affiliation | Department of Internal Medicine, University of New Mexico, Albuquerque, NM 87108, USA. | lld:pubmed |
pubmed-article:21569540 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21569540 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |