2010
DOI: 10.1111/j.1755-0998.2010.02835.x
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Multiplex assay to identify Korean vectors of malaria

Abstract: Following the recent emergence of malaria in South Korea, vector control has been an important task. For this, vector identification is very important. Earlier, two PCR-based assays have been described. But, poor species resolution and their ability to include only 4-5 species limit their use. Thus, it has now become important to revise the assay identifying these members. In this study, a new assay based on internal transcribed spacer 2 and 28S of ribosomal DNA has been described. The assay successfully ident… Show more

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Cited by 42 publications
(39 citation statements)
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(18 reference statements)
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“…Molecular identifications of An. sinensis species were done by using species-specific primers and amplification of the ITS2 and 28S rDNA regions (D1 and D2) [38]. A total of 100 mosquitoes per site were randomly selected and tested molecularly, and all of them identified as An.…”
Section: Methodsmentioning
confidence: 99%
“…Molecular identifications of An. sinensis species were done by using species-specific primers and amplification of the ITS2 and 28S rDNA regions (D1 and D2) [38]. A total of 100 mosquitoes per site were randomly selected and tested molecularly, and all of them identified as An.…”
Section: Methodsmentioning
confidence: 99%
“…Molecular identifications of An. sinensis species were conducted by using species-specific primers targeting amplification of the ITS2 and 28S rDNA regions (D1 and D2) [30]. To determine point mutations of the kdr gene at position 1014, we amplified a 325 bp fragment, using the primer pair: kdr -F TGCCACTCCGTGTGTTTAGA, and kdr -R GAGCGATGATGATCCGAAAT.…”
Section: Methodsmentioning
confidence: 99%
“…kleini were established successfully using the methods of [28]. An F 1 -progeny of each iso-female line was used for species identification following the keys of [29] as well as a molecular assay [30]. Then, one iso-female line of each species, with molecular identification of both nuclear (ITS2) and mitochondrial (COI) genes, were well matched with those in the GenBank nucleotide sequence database, and selected, i.e., An.…”
Section: Methodsmentioning
confidence: 99%
“…Primers for the amplification of ITS2 and COI regions followed a previous report by [30]. The ITS2 region of the rDNA was amplified using the ITS2 Forward and ANO 28S-20 primers [30,32].…”
Section: Methodsmentioning
confidence: 99%
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