Difference between revisions of "Team:Uppsala"

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        <div class="under-heading"><h1>Uppsala iGEM 2018</h1></div>
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            <div class="under-heading"><h1>Uppsala iGEM 2018</h1></div>
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                     <!-- The Targets -->
 
                     <!-- The Targets -->
 
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                    <h1>The Targets</h1>
 
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                            <h1>The Targets</h1>
 
 
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                         <h1>The Worm Buster</h1>
 
                         <h1>The Worm Buster</h1>
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                         <p>The first thing the team did was to define the desired characteristics of the worm buster and outline the project strategy </p>
 
                         <p>The first thing the team did was to define the desired characteristics of the worm buster and outline the project strategy </p>
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                        <h3><b> 3. </b><a href="https://2018.igem.org/Team:Uppsala/Reporter_System" >Reporter System</a></h3>
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                            <h3><b> 3. </b><a href="https://2018.igem.org/Team:Uppsala/Reporter_System" >Reporter System</a></h3>
  
  
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                                <!-- Here you put your paragraphs -->  
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                                <p>After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
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                                    <p>After receiving the results from either the transcriptomics or the phage display, they need to be combined with a reported to get a functioning diagnostic tool (Worm Buster).  We have adapted and troubleshot the expression of a fluorescent chromoprotein, UnaG, to be able to detect our worms in both the intestines and in feces. This would enable a relatively simple and quantitative way for ranchers to detect the worms of interest, using a cheap UV lamp, a dark room, and a camera!<br><br>
  
                                In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies.<br><br><b>Figure 5: </b>We would be able to detect the wormd in feces with this method.</p>
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                                    In order to make this a viable reporter system, we wanted to make sure the original biobrick part was functional.  We show how we tweaked this part in order to study if it works properly so that it could be potentially used in future studies.<br><br><b>Figure 5: </b>We would be able to detect the wormd in feces with this method.</p>
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                         <h3><b>4. </b><a href="https://2018.igem.org/Team:Uppsala/Model" >Modeling</a></h3>
 
                         <h3><b>4. </b><a href="https://2018.igem.org/Team:Uppsala/Model" >Modeling</a></h3>
 
                             <h4>Optimization of the Time Between Treatments</h4>
 
                             <h4>Optimization of the Time Between Treatments</h4>
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                         <p>To make sure the unnecessary use of anthelmintics is minimized we have created a model that compares regular and optimized usage of anthelmintics. When referring to the optimized use of anthelmintics, this means that the horse only receives treatment when the amount of parasites exceeds a certain threshold. Our model calculates given the initial amount of worms on the pasture and in the horse. Ideally, the information could be used with the worm buster to get a better overall result of our project. Our solution will not only be able to tell how large the treatments should be but also when they should be administered. This would guarantee the lowest amount of anthelmintics usage, and hopefully help combat the issue of growing resistance. Due to this fact, our model constitutes a large improvement on the potential implementation of our project since it directly brings us closer to our ultimate goal, which is the decrease in resistance development and the improved physical health of horses. </p>
 
                         <p>To make sure the unnecessary use of anthelmintics is minimized we have created a model that compares regular and optimized usage of anthelmintics. When referring to the optimized use of anthelmintics, this means that the horse only receives treatment when the amount of parasites exceeds a certain threshold. Our model calculates given the initial amount of worms on the pasture and in the horse. Ideally, the information could be used with the worm buster to get a better overall result of our project. Our solution will not only be able to tell how large the treatments should be but also when they should be administered. This would guarantee the lowest amount of anthelmintics usage, and hopefully help combat the issue of growing resistance. Due to this fact, our model constitutes a large improvement on the potential implementation of our project since it directly brings us closer to our ultimate goal, which is the decrease in resistance development and the improved physical health of horses. </p>
  
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                    <!---- REFERENCES -->
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                        <h1>References</h1>
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                        <p><b>[1]</b> Karlsson J. Parasite detection in extensively hold Gotland ponies. 50. Source: https://stud.epsilon.slu.se/7939/7/karlsson_j_150622.pdf <br><br>
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                        <b>[2]</b> Molena RA, Peachey LE, Di Cesare A, Traversa D, Cantacessi C. 2018. Cyathostomine egg reappearance period following ivermectin treatment in a cohort of UK Thoroughbreds. Parasites & Vectors 11: 61. Source: https://parasitesandvectors.biomedcentral.com/articles/10.1186/s13071-018-2638-6 <br><br>
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                        <b>[3]</b> Andersson E. Hur påverkas prevalensen av selektiv avmaskning? 22.<br><br>
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                        <b>[4]</b> Traversa D, von Samson-Himmelstjerna G, Demeler J, Milillo P, Schürmann S, Barnes H, Otranto D, Perrucci S, di Regalbono AF, Beraldo P, Boeckh A, Cobb R. 2009. Anthelmintic resistance in cyathostomin populations from horse yards in Italy, United Kingdom and Germany. Parasites & Vectors 2: S2. Source :https://parasitesandvectors.biomedcentral.com/articles/10.1186/1756-3305-2-S2-S2 <br><br>
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                        <b>[5]</b> Matthews JB, Hodgkinson JE, Dowdall SMJ, Proudman CJ. 2004. Recent developments in research into the Cyathostominae and Anoplocephala perfoliata. Veterinary Research 35: 371–381. Source: https://www.ncbi.nlm.nih.gov/pubmed/15236671<br><br>
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                        <b>[6]</b> Jasovský D, Littmann J, Zorzet A, Cars O. 2016. Antimicrobial resistance—a threat to the world’s sustainable development. Upsala Journal of Medical Sciences 121: 159–164.<br><br>
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                        <b>[7]</b> K. Nielsen M, Andersson U, K. Howe D. 2015. Diagnosis of Strongylus Vulgaris. University of Kentucky<br><br>
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                        <b>[8]</b> C. Sellon D, T. Long M. Equine Infectious Diseases. Elsevier Health Sciences, 2007 Source: https://books.google.se/books?id=sZku4lppRfsC&pg=PA483&lpg=PA483&dq=Cyathostominae+horse&source=bl&ots=GtJJjXA5Kd&sig=9ktoAaiQnVSd6xTC_hhnvujvUBE&hl=sv&sa=X#v=onepage&q=Cyathostominae%20horse&f=false <br><br>
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                        <b>[9]</b> Colen MA, D. C. K van D, F. N. J. K. Anthelmintic resistance in Cyathostominae. Source: https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=20&ved=0ahUKEwj-xuHwxuDbAhXGFZoKHUsSBmM4ChAWCGQwCQ&url=https%3A%2F%2Fdspace.library.uu.nl%2Fbitstream%2Fhandle%2F1874%2F289404%2FOnderzoeksstage%2520anthelmintic%2520resistance%2520in%2520Cyathostominae%2520MAColen.doc%3Fsequence%3D2%26isAllowed%3Dy&usg=AOvVaw2PhKtv4XqGJTqJg86aFIFd <br><br>
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                        <b>[10]</b> Johnstone DC. 2000. S. vulgaris pathogenesis. WWW-dokument 2000-: http://cal.vet.upenn.edu/projects/merial/Strongls/strong_8d.htm. Retrieved 2018-06-20.
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                        <br><br>
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                        <b>[11]</b> Ling J. 2017. Strongylus vulgaris och Anoplocephela perfoliata. WWW-dokument 2017-07-14: https://stud.epsilon.slu.se/10486/.Retrieved 2018-06-20.<br><br>
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                        <b>[12]</b> Bracken MK, Wøhlk CBM, Petersen SL, Nielsen MK. 2012. Evaluation of conventional PCR for detection of Strongylus vulgaris on horse farms. Veterinary Parasitology 184: 387–391.<br><br>
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                        <b>[13]</b> 2013. New Method for Detecting Bloodworms. WWW-dokument 2013-07-27: https://thehorse.com/116401/new-method-for-detecting-bloodworms/. Retrieved 2018-06-21.<br><br>
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                        <b>[14]</b> Cobb R, Boeckh A. 2009. Moxidectin: a review of chemistry, pharmacokinetics and use in horses. Parasites & Vectors 2: S5.<br><br>
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                        <b>[15]</b> Corning S. 2009. Equine cyathostomins: a review of biology, clinical significance and therapy. Parasites & Vectors 2: S1.<br><br>
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                        <b>[16]</b> Nielsen MK, Scare J, Gravatte HS, Bellaw JL, Prado JC, Reinemeyer CR. 2015. Changes in Serum Strongylus Vulgaris-Specific Antibody Concentrations in Response to Anthelmintic Treatment of Experimentally Infected Foals. Frontiers in Veterinary Science, doi 10.3389/fvets.2015.00017.
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                        <b>[17]</b> The Swedish horse sector. WWW-dokument: https://hastnaringen.se/swedish-horse-sector/. Retrieved: 2018-06-23.
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                        <b>[18]</b> Häggblom M, Rantamäki-Lahtinen L, Vihinen H. Equine sector comparison between the Netherlands, Sweden and Finland. 36. Source: http://www.hippolis.fi/UserFiles/hippolis/File/EquineLife/equine_sector_comparison_between_the_netherlands_sweden_and_finland.pdf
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                        <b>[19]</b> Hästar och anläggningar med häst 2016 - JO24SM1701 - In English. WWW-dokument: http://www.jordbruksverket.se/webdav/files/SJV/Amnesomraden/Statistik,%20fakta/Husdjur/JO24/JO24SM1701/JO24SM1701_inEnglish.htm. Retrieved: 2018-06-24.
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Revision as of 22:16, 16 October 2018





Uppsala iGEM 2018