2012
DOI: 10.1603/me11113
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Single-Nucleotide Polymorphisms for High-Throughput Genotyping of Anopheles arabiensis in East and Southern Africa

Abstract: Anopheles arabiensis Patton is one of the principal vectors of malaria in sub-Saharan Africa, occupying a wide variety of ecological zones. This species is increasingly responsible for malaria transmission in Africa and is becoming the dominant vector species in some localities. Despite its growing importance, little is known about genetic polymorphisms in this species. Multiple sequences of various gene fragments from An. arabiensis isolates from Cameroon were obtained from GenBank. In total, 20 gene fragment… Show more

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Cited by 11 publications
(9 citation statements)
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“…The average frequency of nucleotide variation was reported to be 7 and 12 SNPs per kb for A nopheles funestus and A.aegypti (29,30), respectively. An SNP frequency of ∼17 per kb was recently reported for selected gene fragments of field-captured An opheles arabiensis (31). …”
Section: Resultsmentioning
confidence: 96%
“…The average frequency of nucleotide variation was reported to be 7 and 12 SNPs per kb for A nopheles funestus and A.aegypti (29,30), respectively. An SNP frequency of ∼17 per kb was recently reported for selected gene fragments of field-captured An opheles arabiensis (31). …”
Section: Resultsmentioning
confidence: 96%
“…gambiae and An. arabiensis populations in Africa, and other pairs of sibling species of Anopheles [ 20 , 32 , 36 , 64 ]. Moreover, intraspecific estimates of genetic differentiation (F ST ) within An.…”
Section: Discussionmentioning
confidence: 99%
“…arabiensis from the island of Reunion and the African continent, which was attributed to the low effective population size (Ne) on the island [ 32 ]. Lee et al [ 36 ] reported a fixed nucleotide on the X chromosome between populations in East-southern Africa and those in Central Africa .…”
Section: Introductionmentioning
confidence: 99%
“…For a further comparison of the two different assay platforms see Lee et al. (). We designed the multiplex SNP genotyping assay using the Assay Designer module of the MassARRAY Typer 4.0 software package (Sequenom, San Diego, CA, USA), and conducted PCR reactions using Sequenom iPLEX Gold reagent kits following standard procedures at the Veterinary Genetics Laboratory, University of California‐Davis.…”
Section: Methodsmentioning
confidence: 99%