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Research Project: MOLECULAR BIOLOGY OF BOOPHILUS MICROPLUS

Location: Tick and Biting Fly Research

Title: 454 pyrosequencing project identifying expressed genes from the horn fly, Haematobia irritans

Authors
item Saldivar, Leonel
item Guerrero, Felix
item Dowd, S -
item Djikeng, G -
item Wiley, G -
item Macmil, S -
item Najar, F -
item Roe, B -

Submitted to: National Center for Biotechnology Information (NCBI)
Publication Type: Other
Publication Acceptance Date: September 9, 2008
Publication Date: September 9, 2008
Repository URL: http://www.ncbi.nlm.nih.gov
Citation: Saldivar, L., Guerrero, F., Dowd, S.E., Djikeng, G., Wiley, G., Macmil, S., Najar, F., Roe, B.A. 2008. 454 pyrosequencing project identifying expressed genes from the horn fly, Haematobia irritans. National Center for Biotechnology Information (NCBI). Available: http://www.ncbi.nlm.nih.gov. Assession number SRA001542

Interpretive Summary: The horn fly, Haematobia irritans, is a blood-feeding parasite of cattle which is a controlled with good animal husbandry practices and the application of pesticides. Pesticide resistance is a developing problem for producers and has a negative economic impact upon production. We established a large sequencing project to identify genes from the horn fly. We hope to identify genes which are involved in the development of pesticide resistance and also identify genes which might prove candidate targets for the design of novel control technologies. In this project, we used 454 pyrosequencing techniques to sequence 73,512, 100,603, 71,550, and 85,769 expressed genes from the egg, first instar larvae, adult male, and adult female lifestages of the horn fly. These sequences have been submitted and published under accession number SRA001542 in the National Center for Biotechnology Information Public Database.

Technical Abstract: We used an EST approach to initiate a study of the genome of the horn fly, Haematobia irritans and have used 454 pyrosequencing techniques to sequence 73,512, 100,603, 71,550, and 85,769 expressed genes from the egg, first instar larvae, adult male, and adult female lifestages of the horn fly. cDNA was synthesized from eggs, first instar larvae, adult males, and adult females from a field population of horn flies. These sequences were used to search publicly accessible databases to identify sequence similarity to known genes and assign putative function to the horn fly genes. The unassembled sequences have been submitted and published under accession number SRA001542 in the National Center for Biotechnology Information Public Database.

   

 
Project Team
Pruett, John
Olafson, Pia
Perez De Leon, Adalberto - Beto
Li, Andrew
Guerrero, Felix
Temeyer, Kevin
Pound, Joe - Mat
 
Publications
   Publications
 
Related National Programs
  Veterinary, Medical and Urban Entomology (104)
 
 
Last Modified: 05/22/2013
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