Please use this identifier to cite or link to this item: https://hdl.handle.net/10137/256
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dc.contributor.authorBeebe NWen
dc.contributor.authorCooper RDen
dc.contributor.authorCorcoran Sen
dc.contributor.authorRitchie SAen
dc.contributor.authorvan den Hurk Aen
dc.contributor.authorWhelan PIen
dc.date.accessioned2009-04-08T04:57:12Zen
dc.date.available2009-04-08T04:57:12Zen
dc.date.issued2007-03en
dc.identifier.issn0022-2585en
dc.identifier.urihttp://hdl.handle.net/10137/256en
dc.description.abstractDengue outbreaks occur regularly in parts of northern Queensland, Australia, and there is concern that these outbreaks may spread with the introduction and range expansion of the two main vectors Aedes aegypti and Aedes albopictus (Skuse). Problems encountered in separating larvae of endemic and exotic container mosquito species resulted in the development of a polymerase chain reaction diagnostic procedure that uses a restriction enzyme to cut the internal transcribed spacer region 1 of the ribosomal DNA to separate Ae. aegypti and Ae. albopictus from a number of common local container mosquito species which can be used at any stage of the life cycle, including eggs up to 8 wk of age. Identification was possible using desiccated or alcohol-preserved specimens with a response time of <24 h after receipt of the specimens.en
dc.language.isoenen
dc.publisherEntomological Society of Americaen
dc.relation.ispartofseriesJournal of Medical Entomologyen
dc.relation.ispartofseriesVol. 44, No. 2en
dc.subjectInsectsen
dc.subjectMosquitoesen
dc.subjectDengueen
dc.subjectDiagnostic testsen
dc.subjectGenetic techniquesen
dc.titlePolymerase chain reaction based diagnostic to identify larvae and eggs of container mosquito species from the Australian regionen
dc.typeJournal Articleen
dc.identifier.sourceHealth Protection Divisionen
dc.kohastatus.transfertokohayesen
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