| Literature DB >> 20939366 |
A M Manonmani1, A Mathivanan, R Srinivasan, P Jambulingam.
Abstract
Species-specific differences encountered in the nucleotide sequences of a highly variable region of the 18S rRNA gene were used to design a multiplex polymerase chain reaction (PCR) assay for the identification of Phlebotomus papatasi Scopoli and Phlebotomus argentipes An-nandale & Brunetti, vectors of Leishmania. This multiplex PCR assay uses a common forward primer and two reverse primers, which are specific for the two species. Amplification of a PCR product of size 788 bp indicates the presence of P. papatasi, whereas a product of size 677 bp indicates the presence of P. argentipes. The assay was found to be highly specific and sensitive.Entities:
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Year: 2010 PMID: 20939366 DOI: 10.1603/me09195
Source DB: PubMed Journal: J Med Entomol ISSN: 0022-2585 Impact factor: 2.278