Accession Number:

ADA605529

Title:

The Characterization of the Phlebotomus papatasi Transcriptome

Descriptive Note:

Journal article

Corporate Author:

NOTRE DAME UNIV IN DEPT OF BIOLOGICAL SCIENCES

Report Date:

2013-04-01

Pagination or Media Count:

37.0

Abstract:

As important vectors of human disease, phlebotomine sand flies are of global significance to human health, transmitting several emerging and re-emerging infectious diseases. The most devastating of the sand fly transmitted infections are the leishmaniases, causing significant mortality and morbidity in both the Old and New World. Here we present the first global transcriptome analysis of the Old World vector of cutaneous leishmaniasis, Phlebotomus papatasi Scopoli and compare this transcriptome to that of the New World vector of visceral leishmaniasis, Lutzomyia longipalpis. A normalized cDNA library was constructed using pooled mRNA from Phlebotomus papatasi larvae, pupae, adult males and females sugar fed, adult females blood fed and fed blood infected with Leishmania major. A total of 47,615 generated sequences were cleaned and assembled into 17,120 unique transcripts. Of the assembled sequences, 50 8,837 sequences were classified using Gene Ontology GO terms. This collection of transcripts is comprehensive, as demonstrated by the high number of different GO categories. An in depth analysis has revealed 245 sequences with putative homology to proteins involved in blood and sugar digestion, immune response and peritrophic matrix formation. Twelve of the novel genes, including one trypsin, two peptidoglycan recognition proteins PGRP and nine chymotrypsins have a higher expression level during larval stages. Two novel chymotrypsins and one novel PGRP are abundantly expressed upon blood feeding. This study will greatly improve the available genomic resources for Ph. papatasi and will provide essential information for annotation of the full genome.

Subject Categories:

  • Medicine and Medical Research
  • Ecology
  • Microbiology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE