Molecular cloning and sequencing of salivary gland-specific cDNAs of the blood-sucking bug Triatoma brasiliensis (Hemiptera: Reduviidae)

Haematophagous insects produce pharmacological substances in their saliva to counteract vertebrate host haemostasis events such as coagulation, vasoconstriction and platelet aggregation. To investigate the bioactive salivary molecules of the triatomine bug Triatoma brasiliensis, we produced subtract...

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Bibliographic Details
Published in:Insect molecular biology Vol. 11; no. 6; pp. 585 - 593
Main Authors: Sant Anna, M. R. V., Araújo, J. G. V. C., Pereira, M. H., Pesquero, J. L., Diotaiuti, L., Lehane, S. M., Lehane, M. J.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Science Ltd 01-12-2002
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Summary:Haematophagous insects produce pharmacological substances in their saliva to counteract vertebrate host haemostasis events such as coagulation, vasoconstriction and platelet aggregation. To investigate the bioactive salivary molecules of the triatomine bug Triatoma brasiliensis, we produced subtraction‐enriched cDNAs of salivary‐gland specific genes using suppression subtractive hybridization. Six full‐length differentially expressed cDNAs (Tb113, Tb125, Tb152, Tb169, Tb180 and Tb198) were selected, cloned and sequenced. Sequence similarity searches of the databases using the putative amino acid sequence of our clones gave the following results: Tb152 – Triabin, an antithrombin induced platelet aggregation factor found in salivary gland extracts of T. pallidipennis. Tb169 – Pallidipin, an anticollagen induced platelet aggregation factor also found in T. pallidipennis salivary homogenates. Tb180 – Procalin, the major allergen of T. protracta saliva. The other three salivary‐gland specific cDNAs produced no obvious homologies. Comparison of these salivary gland‐specific cDNAs of with those of other triatomines combined with functional studies using recombinant proteins will allow a better understanding of the co‐evolutionary process occurring between these insects and their vertebrate hosts, and may also lead to the discovery of novel antihaemostatic agents.
Bibliography:ark:/67375/WNG-CHFGKHD3-5
istex:A7B683DC4EC6730362C3DFFA88203F907E56F564
ArticleID:IMB369
ObjectType-Article-2
SourceType-Scholarly Journals-1
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ISSN:0962-1075
1365-2583
DOI:10.1046/j.1365-2583.2002.00369.x