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dc.contributor.authorAwuoche, Erick O
dc.contributor.authorWeiss, Brian L
dc.contributor.authorVigneron, Aurélien
dc.contributor.authorMireji, Paul O
dc.contributor.authorAksoy, Emre
dc.contributor.authorNyambega, Benson
dc.contributor.authorAttardo, Geoffrey M
dc.contributor.authorWu, Yineng
dc.contributor.authorO’Neill, Michelle
dc.contributor.authorMurilla, Grace
dc.contributor.authorAksoy, Serap
dc.date.accessioned2018-05-08T08:39:52Z
dc.date.available2018-05-08T08:39:52Z
dc.date.issued2017
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/500
dc.description.abstractTsetse flies (Glossina spp.) transmit parasitic African trypanosomes (Trypanosoma spp.), including Trypanosoma congolense, which causes animal African trypanosomiasis (AAT). AAT detrimentally affects agricultural activities in sub-Saharan Africa and has negative impacts on the livelihood and nutrient availability for the affected communities. After tsetse ingests an infectious blood meal, T. congolense sequentially colonizes the fly’s gut and proboscis (PB) organs before being transmitted to new mammalian hosts during subsequent feedings. Despite the importance of PB in blood feeding and disease transmission, little is known about its molecular composition, function and response to trypanosome infection. To bridge this gap, we used RNA-seq analysis to determine its molecular characteristics and responses to trypanosome infection. By comparing the PB transcriptome to whole head and midgut transcriptomes, we identified 668 PB-enriched transcripts that encoded proteins associated with muscle tissue, organ development, chemosensation and chitin-cuticle structure development. Moreover, transcripts encoding putative mechanoreceptors that monitor blood flow during tsetse feeding and interact with trypanosomes were also expressed in the PB. Microscopic analysis of the PB revealed cellular structures associated with muscles and cells. Infection with T. congolense resulted in increased and decreased expression of 38 and 88 transcripts, respectively. Twelve of these differentially expressed transcripts were PB-enriched. Among the transcripts induced upon infection were those encoding putative proteins associated with cell division function(s), suggesting enhanced tissue renewal, while those suppressed were associated with metabolic processes, extracellular matrix and ATP-binding as well as immunity. These results suggest that PB is a PLOS Neglected Tropical Diseases | https://doi.org/10.1371/journal.pntd.0006057 November 20, 2017 1 / 25 a1111111111 a1111111111 a1111111111 a1111111111 a1111111111 OPEN ACCESS Citation: Awuoche EO, Weiss BL, Vigneron A, Mireji PO, Aksoy E, Nyambega B, et al. (2017) Molecular characterization of tsetse’s proboscis and its response to Trypanosoma congolense infection. PLoS Negl Trop Dis 11(11): e0006057. https://doi.org/10.1371/journal.pntd.0006057 Editor: Alvaro Acosta-Serrano, Liverpool School of Tropical Medicine, UNITED KINGDOM Received: December 14, 2016 Accepted: October 20, 2017 Published: November 20, 2017 Copyright: © 2017 Awuoche et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability Statement: All relevant data are within the paper and its Supporting Information files. All Proboscis and Whole head data files are available from the NCBI database (accession number(s) PB = SRP093552, Whole Head = SRP090041) and Midgut data from (BioProject ID: PRJNA314786). Funding: This work was supported by National Institutes of Health (http://www.nih.gov) Fogarty Center grant D43TW007391, RO3TW009444, and a National Institute of Allergy an Infectious muscular organ with chemosensory and mechanosensory capabilities. The mechanoreceptors may be point of PB-trypanosomes interactions. T. congolense infection resulted in reduced metabolic and immune capacity of the PB. The molecular knowledge on the composition and putative functions of PB forms the foundation to identify new targets to disrupt tsetse’s ability to feed and parasite transmission.en_US
dc.publisherPublic Library of Scienceen_US
dc.titleMolecular characterization of tsetse’s proboscis and its response to Trypanosoma congolense infectionen_US
dc.typeArticleen_US


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