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          Enhancing Vector Refractoriness to Trypanosome Infection

          Closed for proposals

          Project Type

          Coordinated Research Project

          Project Code

          D42015

          CRP

          1764

          Approved Date

          14 December 2011

          Status

          Closed

          Start Date

          8 February 2013

          Expected End Date

          7 February 2018

          Completed Date

          20 April 2018

          Participating Countries

          Kenya
          Mali

          Description

          The success of the Agency supported project to eradicate Glossina austeni from the island of Unguja, Zanzibar, using SIT?has lead to considerable interest in utilizing this approach in other locations, and led to the African Union?initiative on PATTEC (Pan African Tsetse and Trypanosomosis Eradication Campaign). Projects are?underway in Ethiopia and Senegal with other projects in various African countries.?To date, IAEA supported SIT projects have been in areas without human sleeping sickness, and disease transmission has inthe past been minimized by adding trypanocidal drugs to the blood meal when feeding sterile males before release. Nevertheless for future projects that could include areas of actual or potential human disease transmission it would be desirable to develop strains refractory to the transmission of trypanosomes as a much simpler and more effective method of ensuring that released sterile flies do not transmit any disease. Therefore it is essential to understand the mechanisms that limit the development of infections in tsetse and how these may be enhanced.?CRP D42012 been studying the symbionts and pathogens of tsetse to understand their impact on the flies and therefore on colony management, sterile male performance and tsetse control. Recent research?has indicated that some of these pathogens have an impact on the tsetse-trypanosomosis interaction, and may perhaps be manipulated to induce refractoriness to infection.?This proposal is for a CRP to focus on a deeper and more focused understanding?of the three way interaction between the vectors, their symbionts and trypanosomes, with the objective of determining if and how refractoriness may be induced.

          Objectives

          To elucidate the molecular interactions between host-symbionts-pathogens to improve SIT and SIT-compatible interventions for the control of trypanosomosis by enhancing vector refractoriness to facilitate SIT expansion into areas of potential human disease transmission.
          and
          1. To decipher the molecular interplay between vector-symbiont-trypanosomes
          2. To characterize tsetse symbiome including gut microflora.
          3. To determine the effect of radiation on vector symbiome
          4. To develop innovative symbiont-based strategies, in conjunction with SIT, to control African trypanosomosis

          Specific objectives

          To characterize tsetse symbiome including gut micro-flora.

          To decipher the molecular interplay between vectors and trypanosomes.

          To determine the effect of radiation on vector symbionts and pathogens.

          To develop innovative symbiont-based strategies, in conjunction with SIT, to control African trypanosomosis.

          CRP Publications

          Country/Organization

          see attached file with a list of publications under Point 16.

          Stay in touch

          Newsletter

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