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Open Access Highly Accessed Research article

Comparative salivary gland transcriptomics of sandfly vectors of visceral leishmaniasis

Jennifer M Anderson1, Fabiano Oliveira12, Shaden Kamhawi3, Ben J Mans4, David Reynoso1, Amy E Seitz1, Phillip Lawyer3, Mark Garfield5, MyVan Pham1 and Jesus G Valenzuela1*

Author Affiliations

1 Vector Molecular Biology Unit, Laboratory of Malaria and Vector Research, NIAID, NIH

2 Centro de pesquisa Goncalo Moniz, Fundacao OswaldoCruz, and Faculdade de Medicina, Universidade Federal da Bahia, Salvador, Bahia, Brazil

3 Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, MD, USA

4 Vector Biology Section, LMVR, NIAID, NIH, Rockville, MD, USA

5 Research Technologies Branch, NIAID, Rockville, MD, USA

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BMC Genomics 2006, 7:52  doi:10.1186/1471-2164-7-52

Published: 15 March 2006

Abstract

Background

Immune responses to sandfly saliva have been shown to protect animals against Leishmania infection. Yet very little is known about the molecular characteristics of salivary proteins from different sandflies, particularly from vectors transmitting visceral leishmaniasis, the fatal form of the disease. Further knowledge of the repertoire of these salivary proteins will give us insights into the molecular evolution of these proteins and will help us select relevant antigens for the development of a vector based anti-Leishmania vaccine.

Results

Two salivary gland cDNA libraries from female sandflies Phlebotomus argentipes and P. perniciosus were constructed, sequenced and proteomic analysis of the salivary proteins was performed. The majority of the sequenced transcripts from the two cDNA libraries coded for secreted proteins. In this analysis we identified transcripts coding for protein families not previously described in sandflies. A comparative sandfly salivary transcriptome analysis was performed by using these two cDNA libraries and two other sandfly salivary gland cDNA libraries from P. ariasi and Lutzomyia longipalpis, also vectors of visceral leishmaniasis. Full-length secreted proteins from each sandfly library were compared using a stand-alone version of BLAST, creating formatted protein databases of each sandfly library. Related groups of proteins from each sandfly species were combined into defined families of proteins. With this comparison, we identified families of salivary proteins common among all of the sandflies studied, proteins to be genus specific and proteins that appear to be species specific. The common proteins included apyrase, yellow-related protein, antigen-5, PpSP15 and PpSP32-related protein, a 33-kDa protein, D7-related protein, a 39- and a 16.1- kDa protein and an endonuclease-like protein. Some of these families contained multiple members, including PPSP15-like, yellow proteins and D7-related proteins suggesting gene expansion in these proteins.

Conclusion

This comprehensive analysis allows us the identification of genus- specific proteins, species-specific proteins and, more importantly, proteins common among these different sandflies. These results give us insights into the repertoire of salivary proteins that are potential candidates for a vector-based vaccine.