Gene expression profiling of odorant binding proteins in the tsetse fly Glossina brevipalpis

Show simple item record

dc.contributor.author Murithi, Mary Kanyiri
dc.date.accessioned 2016-06-20T09:17:24Z
dc.date.available 2016-06-20T09:17:24Z
dc.date.issued 2016-06-20
dc.identifier.uri http://hdl.handle.net/123456789/2123
dc.description MASTER OF SCIENCE (Biochemistry) en_US
dc.description.abstract Glossina brevipalpis is a vector of trypanosomes that cause Animal African Trypanosomiasis. Chemoreception in tsetse flies is critical for identifying larvipositioning sites, hosts and mates. Odorant binding proteins (OBPs) are thought to mediate insect chemoreception by shuttling odours to receptors on olfactory sensory neurons. Little is known about the roles of OBPs in tsetse fly chemoreception. The genome of G. brevipalpis has been sequenced and 28 OBPs identified. This study aimed at profiling the expression levels of G. brevipalpis OBP genes at different starvation periods and developmental stages. Glossina morsitans morsitans OBP genes retrieved from VectorBase were queried against G. brevipalpis proteome. Putative G. brevipalpis OBP genes were then searched against Drosophila melanogaster proteome in FlyBase. Multiple sequence alignment of G. brevipalpis OBPs identified six conserved cysteines for most of the OBPs. Phylogenetic analysis of G. brevipalpis, G. m. morsitans and D. melanogaster OBPs showed that Glossina OBPs clustered closely. Wild G. brevipalpis collected from Shimba Hills National Park in Kwale County were fed on rabbits and starved for 2, 24, 48, 72 and 96 hours. Larvae, pupae and tenerals (newly emerged unfed flies) were also obtained. From the adults and tenerals, a pool of ten pairs of antennae plus one head were used for RNA extraction. Subsequently, one larva and one pupa were also used for RNA extraction. The RNA extracted was used for cDNA synthesis. Conventional PCR was used to screen the 28 putative G. brevipalpis OBP genes and the amplified genes were quantified by qRT- PCR. Glossina brevipalpis OBP8 was highly expressed in the differentially starved adults while two (GbrOBP2 and GbrOBP7) were found to be significantly expressed in the larval and pupal stages. Expression of OBPs in the adult flies confirmed their involvement in olfaction while expression in larva and pupa may suggest their involvement in non-olfactory processes. This study is the first to show the expression levels of OBPs at the starvation and developmental stages of G. brevipalpis. The findings suggest their roles in tsetse chemoreception and give insights on development of specific and environmentally friendly control strategies. en_US
dc.description.sponsorship Dr. Steven Ger Nyanjom JKUAT, Kenya Prof. Esther Magiri JKUAT, Kenya Dr. Daniel Masiga Icipe, Kenya en_US
dc.language.iso en en_US
dc.publisher Jomo Kenyatta University of en_US
dc.subject Gene expression profiling of odorant binding proteins in the tsetse fly Glossina brevipalpis en_US
dc.subject Odorant binding proteins en_US
dc.subject Biochemistry en_US
dc.title Gene expression profiling of odorant binding proteins in the tsetse fly Glossina brevipalpis en_US
dc.type Thesis en_US


Files in this item

This item appears in the following Collection(s)

  • College of Health Sciences (COHES) [755]
    Medical Laboratory; Agriculture & environmental Biotecthology; Biochemistry; Molecular Medicine, Applied Epidemiology; Medicinal PhytochemistryPublic Health;

Show simple item record

Search DSpace


Browse

My Account