Schistosomes are parasitic flatworms that cause a chronic, debilitating disease afflicting over 200 million people in over 70 countries. The parasites live for years, sometimes decades, in what should be a very hostile environment - the blood of vertebrates - yet they appear to solicit little if any protective reaction from two of the host's major defensive systems: the hemostatic system and the immune system. We hypothesize that proteins at the host-interactive surface are central to the parasites ability to dampen host immunity and hemostasis while, at the same time, permitting metabolite exchange. In this competing renewal, we propose to use new molecular methods such as RNA interference that were first developed for use with schistosomes under our previous grant, RO1 AI056273, to test several key hypotheses concerning: 1) the role of tegumental ecto-enzymes in hemostasis and immunomodulation, 2) the ability of tegumental sphingomyelinase to alter permeability properties at the parasite surface, and 3) the molecular mechanisms of trans- tegumental metabolite exchange. The functional genomics approach we adopt here coupled with independent and direct, follow-up experiments employing more traditional cell biology and biochemistry techniques are designed to provide significant new information concerning the schistosome host interactive surface. In addition the work is designed to identify tegumental proteins critical for parasite survival in the host and subsequent screens will be undertaken to discover drugs that inhibit these molecules. In this way, our planned experiments have the potential to reveal novel and valid targets, as well as new treatments, for intervention in a parasite that remains a widespread and major cause of human disease.
Schistosomes are parasite worms that live in the blood streams of over 200 million people in more than 70 countries. These parasites are a major cause of death and disability worldwide. The worms have remarkable properties that allow them live inside people for many years. These properties include an ability to block our immune responses from targeting them, an ability to take in nutrients from our blood and an ability to detect environmental stresses and respond appropriately. By understanding more precisely how the parasites achieve these ends, we aim to block these capabilities and kill the worms.
|Wang, Qiang; Da'dara, Akram A; Skelly, Patrick J (2017) The human blood parasite Schistosoma mansoni expresses extracellular tegumental calpains that cleave the blood clotting protein fibronectin. Sci Rep 7:12912|
|Da'dara, Akram A; Siddons, Giles; Icaza, Melissa et al. (2017) How schistosomes alter the human serum proteome. Mol Biochem Parasitol 215:40-46|
|Da'dara, Akram A; de Laforcade, Armelle M; Skelly, Patrick J (2016) The impact of schistosomes and schistosomiasis on murine blood coagulation and fibrinolysis as determined by thromboelastography (TEG). J Thromb Thrombolysis 41:671-7|
|Figueiredo, Barbara C; Da'dara, Akram A; Oliveira, Sergio C et al. (2015) Schistosomes Enhance Plasminogen Activation: The Role of Tegumental Enolase. PLoS Pathog 11:e1005335|
|Da'dara, Akram A; Skelly, Patrick J (2015) Gene suppression in schistosomes using RNAi. Methods Mol Biol 1201:143-64|
|Da'dara, Akram A; Krautz-Peterson, Greice (2014) New insights into the reaction of Schistosoma mansoni cercaria to the human complement system. Parasitol Res 113:3685-96|
|Figueiredo, Barbara C; Assis, Natan R G; Morais, Suellen B et al. (2014) Schistosome syntenin partially protects vaccinated mice against Schistosoma mansoni infection. PLoS Negl Trop Dis 8:e3107|
|Skelly, Patrick J; Da'dara, Akram A; Li, Xiao-Hong et al. (2014) Schistosome feeding and regurgitation. PLoS Pathog 10:e1004246|
|Da'dara, Akram A; Skelly, Patrick J (2014) Schistosomes versus platelets. Thromb Res 134:1176-81|
|Da'dara, Akram A; Bhardwaj, Rita; Skelly, Patrick J (2014) Schistosome apyrase SmATPDase1, but not SmATPDase2, hydrolyses exogenous ATP and ADP. Purinergic Signal 10:573-80|
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