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TRANSCRIPTOME EXPLORATION OF THE SEX PHEROMONE GLAND OF LUTZOMYIA LONGIPALPIS (DIPTERA: PSYCHODIDAE: PHLEBOTOMINAE)
Author
Affilliation
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica e Fisiologia de Insetos. Rio de Janeiro, RJ, Brasil.
NIH. NIAID. Laboratory of Malaria and Vector Research. Rockville, MD, USA.
NIH. NIAID. Laboratory of Malaria and Vector Research. Rockville, MD, USA
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Pesquisa em Leishmaniose. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica e Fisiologia de Insetos. Rio de Janeiro, RJ, Brasil.
NIH. NIAID. Laboratory of Malaria and Vector Research. Rockville, MD, USA.
NIH. NIAID. Laboratory of Malaria and Vector Research. Rockville, MD, USA
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Pesquisa em Leishmaniose. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica e Fisiologia de Insetos. Rio de Janeiro, RJ, Brasil.
Abstract
Background: Molecules involved in pheromone biosynthesis may represent alternative targets for insect
population control. This may be particularly useful in managing the reproduction of Lutzomyia longipalpis, the main
vector of the protozoan parasite Leishmania infantum in Latin America. Besides the chemical identity of the major
components of the L. longipalpis sex pheromone, there is no information regarding the molecular biology behind
its production. To understand this process, obtaining information on which genes are expressed in the pheromone
gland is essential.
Methods: In this study we used a transcriptomic approach to explore the pheromone gland and adjacent
abdominal tergites in order to obtain substantial general sequence information. We used a laboratory-reared L.
longipalpis (one spot, 9-Methyl GermacreneB) population, captured in Lapinha Cave, state of Minas Gerais, Brazil for
this analysis.
Results: From a total of 3,547 cDNA clones, 2,502 high quality sequences from the pheromone gland and adjacent
tissues were obtained and assembled into 1,387 contigs. Through blast searches of public databases, a group of
transcripts encoding proteins potentially involved in the production of terpenoid precursors were identified in the
4th abdominal tergite, the segment containing the pheromone gland. Among them, protein-coding transcripts for
four enzymes of the mevalonate pathway such as 3-hydroxyl-3-methyl glutaryl CoA reductase, phosphomevalonate
kinase, diphosphomevalonate descarboxylase, and isopentenyl pyrophosphate isomerase were identified. Moreover,
transcripts coding for farnesyl diphosphate synthase and NADP+ dependent farnesol dehydrogenase were also
found in the same tergite. Additionally, genes potentially involved in pheromone transportation were identified
from the three abdominal tergites analyzed.
Conclusion: This study constitutes the first transcriptomic analysis exploring the repertoire of genes expressed in
the tissue containing the L. longipalpis pheromone gland as well as the flanking tissues. Using a comparative
approach, a set of molecules potentially present in the mevalonate pathway emerge as interesting subjects for
further study regarding their association to pheromone biosynthesis. The sequences presented here may be used
as a reference set for future research on pheromone production or other characteristics of pheromone
communication in this insect. Moreover, some matches for transcripts of unknown function may provide fertile
ground of an in-depth study of pheromone-gland specific molecules.
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