Translator Disclaimer
1 June 2010 Universal Primers for the Amplification and Sequence Analysis of Actin-1 from Diverse Mosquito Species
Author Affiliations +

We report the development of universal primers for the reverse-transcription polymerase chain reaction (RT-PCR) amplification and nucleotide sequence analysis of actin cDNAs from taxonomically diverse mosquito species. Primers specific to conserved regions of the invertebrate actin-1 gene were designed after actin cDNA sequences of Anopheles gambiae, Bombyx mori, Drosophila melanogaster, and Caenorhabditis elegans. The efficacy of these primers was determined by RT-PCR with the use of total RNA from mosquitoes belonging to 30 species and 8 genera (Aedes, Anopheles, Culex, Deinocerites, Mansonia, Psorophora, Toxorhynchites, and Wyeomyia). The RT-PCR products were sequenced, and sequence data were used to design additional primers. One primer pair, denoted as Act-2F (5′-ATGGTCGGYATGGGNCAGAAGGACTC-3′) and Act-8R (5′-GATTCCATACCCAGGAAGGADGG-3′), successfully amplified an RT-PCR product of the expected size (683-nt) in all mosquito spp. tested. We propose that this primer pair can be used as an internal control to test the quality of RNA from mosquitoes collected in vector surveillance studies. These primers can also be used in molecular experiments in which the detection, amplification or silencing of a ubiquitously expressed mosquito housekeeping gene is necessary. Sequence and phylogenetic data are also presented in this report.

Molly Staley, Karin S. Dorman, Lyric C. Bartholomay, Ildefonso Fernández-Salas, Jose A. Farfan-Ale, Maria A. Loroño-Pino, Julian E. Garcia-Rejon, Luis Ibarra-Juarez, and Bradley J. Blitvich "Universal Primers for the Amplification and Sequence Analysis of Actin-1 from Diverse Mosquito Species," Journal of the American Mosquito Control Association 26(2), (1 June 2010).
Published: 1 June 2010

This article is only available to subscribers.
It is not available for individual sale.

Get copyright permission
Back to Top