Difference between revisions of "Team:Uppsala"

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                  <p>Nematode parasites cost the agricultural industry lots of money and grief each year due to the many consequences they cause. The economic burden of these parasites is forecasted to increase, since these worms are rapidly gaining resistance to most drugs used to combat them. There are currently no easy methods for the diagnosis of these small strongyles. Our vision has been to apply synthetic biology to the untouched field of veterinary diagnostics to solve this problem. While working towards the goal of creating a reprogramed smart bacteria (nicknamed the worm buster) to detect and report the presence of the small strongyles, we discovered new useful applications of existing techniques along the way. This has made our vision about the worm buster more realistic, which in the future will provide the tools necessary to help farmers make a decisions whether to treat their animals or not.<br><br>
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                <p>Nematode parasites of the strongyle family cause the agricultural industry substantial losses and grief each year due to the detrimental effects they have on livestock. Common issues include severe health damage in the host animal as well as resistance development to anthelmintics in the most commonly occurring strongyles. There are currently no easy methods for diagnosing these parasites. By reprogramming a smart bacterium to detect and report the presence of the parasites, we aim to develop a simple diagnostic method. This will provide the tools necessary to help farmers both to make decisions on whether to treat their animals and to prevent infection to begin with. </p>
  
Our work has laid the foundation for our idea to someday potentially come to fruition. Our novel applications of cutting edge techniques such as <i>phage display</i> and <i>transcriptomics using third generation sequencing</i> provide groundwork for further expansions in the field of veterinary diagnostics.
 
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<h1>The Targets</h1><br><br>
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<p><strong>Figure 1:</strong>  Small Strongyles or <i>Cyathostominae</i> are among the most common equine parasites, with more than 52 species in their family [2]. The infectious stage of small strongyles is when they’ve developed into larvae while still lurking in the grass. While horses graze, they consume the worms and the small strongyles continue to develop in the horses’ intestines, forming cysts in the intestinal wall [1]. When further evolved, these small strongyles can burst out from their cysts during late winter or early spring, moving up towards the intestinal lumen where they become adult worms [1, 8].</p><br><br>
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                    <div class="content-card-heading"><h1>Our Targets:</h1></div>
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In a study of 461 horses in Sweden, 53,7 % of all horses were discovered to be infected [1].
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From July to September the prevalence was estimated to be 78,4% in the horse population, indicating a seasonal trend for infection rate [1].
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Similar trends are seen in Europe and North America showing reported cases with 100% of horses showing small strongyle infection [2].
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<br><h2>Symptoms</h2>
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<p>The release of larvae from cysts can lead to lesions, diarrhea, and potential weight loss. This condition is called cyathostominosis [1]. When untreated, the death tolI can reach up to 50%. During the seasonal rupture of cysts, millions of larvae can be released at the same time, which can result in severe and life-threatening consequences [5]. The infection of small strongyles is not one of presence, but one of quantity. They are not dangerous in small amounts and therefore it is difficult to tell whether a horse needs to be treated or not [9]. <br><br>
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If farmers had the possibility to know when to treat their horses, prevention of mass rupture and other severe consequences like increased resistance development could be achieved. To reach this goal we have developed a model that (based on multiple parameters) calculates the optimal amount of treatments in a specified period. This will avoid unnecessary use of anthelmintics by raising the awareness in farmers regarding when they actually need to treat their horses.<p>
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<br><h2>Current Methods of Detection</h2>
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<p>Currently the only method for detecting/counting how many worms there are in an animal is counting nematode eggs in fecal samples. This method is not reliable and also requires farmers and ranchers to send in fecal samples to a lab with trained personnel [4]. This technique is expensive, inconsistent, and requires time sensitive shipping of samples. Currently many horse owners are reluctant to conduct the testing; treating their horses regardless of need which contributes to the resistance problem [10]. </p>
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<br><h2>Resistance Development</h2>
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<p>Unfortunately, the extensive overuse of deworming drugs has now lead to the detection of worms that are resistant to the most commonly used drugs [2,4]. Since no new deworming drugs have been approved for use in horses the whole equine industry relies on macrocyclic lactones, currently the most common type of deworming drugs used. Unfortunately, cases of resistance among nematode adults have been spotted for macrocyclic lactones as well. So far, four studies with similar results spanning from Europe to North America have been published with concrete data, linking certain small strongyle species to reduced time until detection of eggs after deworming treatment, showing an increase in resistance[2]. <br><br>
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Moxidectin is a very common drug used. It is both hazardous for the environment and is also losing its effectiveness towards worm populations [14,15]. <br><br>
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Due to all of these facts, we have during our iGEM project developed a reporter that is suitable for the in vivo environment of horse intestines. Moreover, we have developed new applications on existing techniques to be able to find the promoter that would be coupled to the reporter which would at last create the worm buster. <br><br>
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By implementing the model described under Symptoms together with the worm buster, horse owners will not only know how large the treatments should be but also when the treatments should happen. Thus they complement each other to minimize the amount of anthelmintics used; thereby helping to prevent resistance development.</p>
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                             <h2>Small Strongyles</h2>
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                                <p>Small strongyles <i>(Cyathostominae)</i> are among the most common equine parasites with more than 52 species in their family. Horses are exposed when they graze on infested pastures, where they consume the worms in their larval stage. The strongyles move to the horses’ intestines, gathering into cysts in the intestinal wall and usually reach very large numbers.  These cysts eventually burst and the developed worms moves up towards the intestinal lumen where they become adult worms. The release of the larvae from the cysts can lead to lesions, diarrhea, and potential weight loss in the animal, a condition called cyathostominosis. When untreated, the mortality rate of a small strongyle infection can reach up to 50%. </p>
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<h1>Symptoms</h1>
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            <p><strong>The release of larvae from cysts can lead to lesions, diarrhea, and potential weight loss. This condition is called cyathostominosis [1]. When untreated, the death tolI can reach up to 50%. During the seasonal rupture of cysts, millions of larvae can be released at the same time, which can result in severe and life-threatening consequences [5]. The infection of small strongyles is not one of presence, but one of quantity. They are not dangerous in small amounts and therefore it is difficult to tell whether a horse needs to be treated or not [9]. <br><br>
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If farmers had the possibility to know when to treat their horses, prevention of mass rupture and other severe consequences like increased resistance development could be achieved. To reach this goal we have developed a model that (based on multiple parameters) calculates the optimal amount of treatments in a specified period. This will avoid unnecessary use of anthelmintics by raising the awareness in farmers regarding when they actually need to treat their horses.</strong><p>
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<h1>Current Methods of Detection</h1>
 
            <p><strong>Currently the only method for detecting/counting how many worms there are in an animal is counting nematode eggs in fecal samples. This method is not reliable and also requires farmers and ranchers to send in fecal samples to a lab with trained personnel [4]. This technique is expensive, inconsistent, and requires time sensitive shipping of samples. Currently many horse owners are reluctant to conduct the testing; treating their horses regardless of need which contributes to the resistance problem [10]. </strong><p>
 
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                                <p><i>Strongylus vulgaris</i> is the most pathogenic parasite in horses, posing a significant threat to the health of the animal. They, like small strongyles, live in the grass and infect the horse after being ingested. During the larval stages inside the animal, the parasite enters the intestinal blood vessels as a part of their life cycle. This causes them to commonly avoid deworming and detection measures. When the worms migrate in the arteries they cause inflammation in the arterial wall and induce the formation of blood clots. These blood clots may travel in the blood vessels and block smaller passages, inhibiting oxygen and nutrient supply to the surrounding tissues, and may result in colic or in the worst case, death. </p>
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<h1>Resistance Development</h1>
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            <p><strong>Unfortunately, the extensive overuse of deworming drugs has now lead to the detection of worms that are resistant to the most commonly used drugs [2,4]. Since no new deworming drugs have been approved for use in horses the whole equine industry relies on macrocyclic lactones, currently the most common type of deworming drugs used. Unfortunately, cases of resistance among nematode adults have been spotted for macrocyclic lactones as well. So far, four studies with similar results spanning from Europe to North America have been published with concrete data, linking certain small strongyle species to reduced time until detection of eggs after deworming treatment, showing an increase in resistance[2]. <br><br>
+
 
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Moxidectin is a very common drug used. It is both hazardous for the environment and is also losing its effectiveness towards worm populations [14,15]. <br><br>
+
 
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Due to all of these facts, we have during our iGEM project developed a reporter that is suitable for the in vivo environment of horse intestines. Moreover, we have developed new applications on existing techniques to be able to find the promoter that would be coupled to the reporter which would at last create the worm buster. <br><br>
+
 
+
By implementing the model described under Symptoms together with the worm buster, horse owners will not only know how large the treatments should be but also when the treatments should happen. Thus they complement each other to minimize the amount of anthelmintics used; thereby helping to prevent resistance development. </strong><p>
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  <h1>The Worm Busters</h1>
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                <p>One approach for designing a diagnostic system against the strongyles is to engineer a “smart” bacterium which will live in the intestinal tract and is capable of reacting to the presence of the parasite by emitting a quantifiable signal. This biosensor may, for instance, induce the production of a detectable fluorescent protein in the feces of the animal. Large strongyles, however, are more elusive and are less frequently present in the intestine during an infection. Here it would be suitable to instead try and detect the presence of the parasite on the pastures as to avoid infection altogether, by developing bacteria responding to the parasite outside of the animal body.  </p>
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<p> Our work is dependent on finding one or more genes in <i>E.coli</i> which will, exclusively, be highly expressed when the cell is exposed to the parasitic worms. This is done by co-culturing <i>E.coli</i> in liquid medium along with live strongyles, which are harvested from feces and sterilized. From here, the E.coli cells are separated from the solution and their entire transcriptomic suite is extracted and sequenced to detect genes of interest. Any found genes which display promise will have to be validated by qPCR (which is a similar method) in a second run to confirm that they are only expressed due to the strongyle presence. Another approach to tackle our challenge is to screen for interaction between the surface proteins on the strongyle and short peptides. Through affinity screening of a random peptide library displayed on the surface of phages, we can select a peptide with a high affinity to the nematodes surface.  </p>
  
  

Revision as of 10:06, 12 October 2018





Uppsala iGEM 2018