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        <strong><h1>Combating <em>N. ceranae</em> infections in honey bees with porphyrin</h1></strong>
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    <h1>Description</h1>
        <h2><em>Nosema ceranae</em>, the fungal freeloader</h2>
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    <h2><em>Nosema ceranae</em>: Fungal Freeloader</h2>  
        <p><em>Nosema ceranae</em>, a fungus which parasitizes bees, has recently been detected in the major commercial honey bee species, <em>Apis mellifera</em> (European honeybee). <em>N. ceranae</em> invades epithelial cells in the bee midgut, resulting in the debilitating nosemosis disease. Like all microsporidian fungi, <em>N. ceranae</em> lack mitochondria making them dependent on its honey bee host for its energy source. Thus, <em>Nosema</em> infections results in energetic stress and has been implicated in reduced longevity, immune function, and performance of commercial honey bees, causing decreased hive productivity. Due to the integral role that bees have in agriculture and in the environment, the adverse effects of <em>N. ceranae</em> to honey bees inspires much anxiety among the apiculture community.</p>
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         <h2>Fumagilin: Treatment to bees, or not to be?</h2>
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         <p>Team UAlberta was alerted of the <em>N. ceranae</em> threat by our discussions with local beekeepers and researchers, who expressed a desire for effective treatments against <em>Nosema</em> infections. Current methods of treating <em>N. ceranae</em> infections rely heavily on  an antifungal agent called Fumagilin-BHowever, Fumagilin-B is mutagenic, toxic to mammals, and has been shown to increase <em>N. ceranae</em> spore count at low doses. Moreover, the only North American supplier of Fumagilin-B has gone out of business and the remaining supply of Fumagilin-B is beginning to run low. Our discussions with the beekeeping community in Alberta, Canada revealed tremendous concern about the lack of an alternative safeguard against <em>N. ceranae</em>.</p>
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        <p>The honey industry's impact on the Canadian economy also drives much of the concern regarding <em>Nosema</em>. Between honey production and the contribution of their pollination to agriculture, honey bees contributed roughly $2 Billion to the Canadian economy in 2013. The economic impact of the bee industry in Canada is far-reaching and a lack of fumagillin alternatives poses a serious threat to industry and individual livelihoods. The developments regarding the supply of Fumagilin-B and the effects of nosemosis on hive productivity motivates Team UAlberta to develop an alternative treatment against <em>Nosema</em>.</p>
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        <p>
        <h2>Porphyrins</h2>
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    <em>Nosema ceranae</em> is a microsporidian parasite that infects the midgut of honeybees. <em>N. ceranae</em> invades the epithelial cells of the bee midgut and as it’s dependent on its honeybee host for its energy source, it causes debilitating energetic stress [1]. For individual honeybees, <em>Nosema</em> infections have symptoms which include shortened lifespans and weakened immune function. On the scale of a colony, the symptoms of <em>Nosema</em> infections greatly decrease hive productivity and contribute to colony failure[2][3][4].
        <p>Recent research has found that porphyrins, a class of organic compounds, are capable of deactivating <em>N. ceranae</em> spores. Porphyrin antifungal action is attributed to its disruption of spore cell walls (Figure 1). When bee diets were supplemented with chemically synthesized porphyrin species, spore count in the bee's midgut significantly decreased while no adverse effects on the bees were observed. Particularly, a porphyrin derivative, PP(Asp)2 was successful in reducing the spore load in treated bees. Therefore, using porphyrin-type molecules like PP(Asp)2 may be a feasible method of treating <em>N. ceranae</em> infections.</p>
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         <h2>Plan Bee</h2>
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        <p>Luckily, PP(Asp)2 is structurally similar to protoporphyrin IX, a porphyrin-type molecule produced endogenously in <em>E. coli</em>. Rather than feeding bees chemically synthesized PP(Asp)2, we aim to genetically engineer a strain of <em>E. coli</em> capable of living in the bee midgut to biosynthesize protoporphyrin IX. We will build off of the work of a previous iGEM team (BeeColi; NYMU-Taipei , 2013) that developed an alginate coat to allow <em>E. coli</em> to travel through the harsh environment of the bee stomach to colonize the bee midgut. Once in the midgut, our <em>E. coli</em> will secrete excess porphyrin IX using an endogenous efflux pump (TolC). Given that ingested porphyrin IX has been shown to damage <em>N. ceranae</em>, we hypothesize that porphyrin IX secreted directly into the midgut will also damage <em>N. ceranae</em>, allowing us to "bee" part of the <em>Nosema</em> solution.</p>
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        <h2>Objective One: <em>Engineer constructs exploiting C5 heme biosynthesis pathway to selectively express and secrete porphyrin intermediates</em></h2>
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              <img src="https://static.igem.org/mediawiki/2018/6/60/T--UAlberta--PolarFilaments.png" class="figure-img img-fluid rounded" alt="...">
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              <figcaption class="figure-caption text-left"><strong>Figure 1:</strong> <i>Nosema ceranae</i> spores imaged using phase contrast microscopy. The threadlike structures are polar filaments which spores use to penetrate honeybee epithelial cells. Pictured by Gisder S, et. al [5].
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              alt="Proposed porphyrin pathway">
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            <figcaption class="figure-caption text-center">Figure 1: Proposed process for the production of protoporphyrin IX by means of engineered E. coli through exploiting
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             the C5 pathway of heme synthesis.</figcaption>
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              <figcaption class="figure-caption text-left"><strong>Figure 2:</strong> A Western honeybee worker (<i>Apis mellifera</i>)—the new host of <i>N. ceranae</i>.</figcaption>
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            <p>
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        Unfortunately, <em>N. ceranae</em> has recently spread to the major commercial honeybee species—the Western honeybee, <em>Apis mellifera</em>—and is now regarded as the dominant <em>Nosema</em> species infecting honey bees globally. Through our conversations with Albertan beekeepers, we found that <em>N. ceranae</em> is a constant issue but when there is an outbreak it can lead to unsustainable rates of death. Some report over 80% hive loss due to <em>Nosema</em>. <em>Nosema</em> is also especially pervasive in cold climates, like the one found in Alberta, as colder temperatures contribute to increased hive losses in winter [6].</p>
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<h2>Previous <em>Nosema</em> Treatments</h2>
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        <p>
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Previous methods of treating <em>N. ceranae</em> infections rely heavily on fumagillin, a potent antifungal agent that is not only expensive but is mutagenic and toxic to mammals. At low doses, fumagillin has actually been shown to increase <em>N. ceranae</em> spore count in honeybees [7][8]. Moreover, Medivet Pharmaceuticals Ltd., the only company that produced fumagillin for the whole of North America’s supply, went out of business earlier this year. This development led to the collapse of the fumagillin supply chain and means that there is no longer any protection available against <em>Nosema</em>. Thus, the issues with using fumagillin and its recent discontinuation motivate the development of alternative treatments for combating <em>N. ceranae</em> as a replacement is imperative to Alberta’s honey industry and the survival of honeybees. Interestingly, Medivet was based in Alberta and we were able to interview their former CEO, Ursula De Runga.</p>
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              <img src="https://static.igem.org/mediawiki/2018/4/49/T--UAlberta--FumagillinStructure.svg" class="figure-img img-fluid rounded" alt="...">
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              <figcaption class="figure-caption text-left"><strong>Figure 3:</strong> The chemical structure of fumagillin [8].</figcaption>
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        <p>First, a liquid chromatography mass spectroscopy assay will be conducted to analyze the distribution of porphyrin-type species produced in wild-type <em>E. coli</em>, establishing a baseline for manipulation of heme biosynthesis. Next, strains of <em>E. coli</em> will be engineered to produce target porphyrin intermediates in the C5 pathway with high yield, by overexpressing genes encoding heme biosynthesis enzymes (Figure 4). To facilitate the activity of porphyrins in the bee midgut, and to avoid possible complications arising from negative feedback loops, we will engineer the <em>E. coli</em> to constitutively secrete the produced porphyrins.  Previous work has shown that the outer membrane channel-tunnel protein, TolC, functions with efflux pumps to export excess porphyrins and maintain homeostasis. Thus, with control over porphyrin intermediate accumulation, secretion of the compounds is achievable through existing cellular machinery. It should be noted that an introduction of a kill switch may be needed to prevent the unwanted proliferation of modified <em>E. coli</em>.</p>
 
        <h2>Objective Two: <em>Assay modified strains and associated porphyrin intermediates for their ability to inactivate N. ceranae spores in bees.</em></h2>
 
        <p>This assay will be performed using spores from an in vivo source, <em>A. mellifera</em> worker bees, and an in vitro source, Sf9 cells which are permissive to N. ceranae infection. Spores will be incubated with the engineered <em>E. coli</em> and infectivity will be quantified, using conventional PCR and fluorescent cell staining, which are consistent with established methods. A previous iGEM team (NYMU-Taipei 2013) has shown that modified <em>E. coli</em> are capable of persisting within the gut of bees. A similar protocol will be employed to introduce the <em>E. coli</em> into live bees and  the capability of the <em>E. coli</em> to confer extended resistance against <em>N. ceranae</em> will be measured by spore count. The total load of <em>E. coli</em> will be observed to evaluate the response of the microbiome to the modified strain.</p>
 
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<h2>Why <em>Nosema</em> and Honeybees?</h2>
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<p>Team UAlberta was made cognizant of the <em>Nosema</em> problem through contact with an Albertan beekeeper, Elisabeth Goldie. She made it very clear that <em>Nosema</em> was a massive concern to her and her fellow beekeepers. Honeybees and beekeepers are an integral part of everyday life as their ecological and economic impacts are far-reaching. This is particularly true in Alberta as our province contributed to almost half of all honey production in Canada in 2016, which is a $157.8 million CAD industry. The beekeeping industry also contributed 4 to 5.5 billions of dollars (CAD) in value through the pollination of agricultural crops [9].</p>
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              <figcaption class="figure-caption text-left"><strong>Figure 4:</strong> Percentage contribution of honey production of Canada’s provinces in 2016 [9].</figcaption>
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<h2>4 to 5.5 Billion CAD for Agroeconomy [9]
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<p>Having these different aspects of Alberta’s beekeeping industry come to light made it clear to our team just how important it was to tackle this issue. We were motivated by the hope that we could actually work towards a project that could positively impact our community.</p>
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<h3>Our  Plan</h3>
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<p>Once we identified the issue we wanted to combat, we conducted preliminary research which led us to recent findings that porphyrins, a class of organic compounds, are capable of inactivating <em>N. ceranae</em> spores. When bees’ diets were supplemented with porphyrin species, spore counts in their midgut decreased significantly with no observed adverse effects on the bees. In particular, the porphyrin PP(Asp)2, a chemically synthesized derivative of protoporphyrin IX (PPIX) harbouring aspartic amide moieties, was used to inactivate <em>N. ceranae</em>. The antifungal action observed was attributed to porphyrin disrupting the spores’ cell wall (Figure 5) [10].</p>
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              <img src="https://static.igem.org/mediawiki/2018/f/fd/T--UAlberta--DamagedNosema.png" class="figure-img img-fluid rounded" alt="...">
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              <figcaption class="figure-caption text-left"><strong>Figure 5:</strong> (A) shows <i>N. ceranae</i> spores without porphyrin treatment and (B) shows the damage done on the spore walls after incubation with the PP(Asp)2 [10].</figcaption>
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              <img src="https://static.igem.org/mediawiki/2018/c/c5/T--UAlberta--PP%28Asp%292vsPPIX.svg" class="figure-img img-fluid rounded" alt="...">
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              <figcaption class="figure-caption text-left"><strong>Figure 6:</strong> A comparison between the similar structures of (A) PP(Asp)2, used in [10] and (B) PPIX where the hydrophilic end of each molecule is highlighted.</figcaption>
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<p>This advancement was extremely interesting since porphyrins are ubiquitous in nature, such as PPIX, which is an intermediate in the endogenous heme biosynthesis pathway of <em>Escherichia coli</em> [11][12]. Given the structural similarities of PPIX to PP(Asp)2 (Figure 6), we hypothesized that biosynthesized PPIX may have similar antifungal effects on <em>N. ceranae</em> spores. What makes PPIX an attractive substitute to PP(Asp)2 is that PPIX is found in nature and can be biosynthetically produced by microbes instead of the inefficient chemical methods used for PP(Asp)2. Motivated by these results, Team UAlberta decided to focus on using porphyrins for treating <em>Nosema</em> infections in honeybees.</p>
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<p>To address the threat of <em>Nosema</em>, and provide an alternative to fumagillin, Team UAlberta presents our 2018 iGEM project:</p>
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<h4><strong>APIS:</strong> an Antifungal Porphyrin-based Intervention System for treating Nosema infections in honey bees!</h4>
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<p>APIS aims to augment the endogenous heme synthesis pathway in <em>E. coli</em> to produce an excess of protoporphyrin IX, a heme synthesis intermediate, to be used for inactivating <em>Nosema</em> spores.</p>
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<p>We planned to accomplish this by completing two objectives:</p>
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<ul>
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<li>Engineer genetic constructs exploiting the heme biosynthesis pathway to overproduce PPIX</li>
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<li>Test the engineered strains and PPIX for their ability to inactivate <em>N. ceranae</em> spores in honeybees.</li>
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</ul>
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<p>With continued input from beekeepers, we designed for two routes of implementation:</p>
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<ul>
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<li>Honeybee probiotic by introducing PPIX-producing microbes into the bee microbiome</li>
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<li>Large-scale PPIX-production to generate PPIX for conventional treatment application methods</li>
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              <figcaption class="figure-caption text-left"><strong>Figure 7:</strong> Overview of the intended outcomes of APIS: (1) generate a PPIX-producing honeybee probiotic to be fed directly to honeybees, or (2) producing porphyrin in traditional fermentation processes to be used in conventional applications methods</figcaption>
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<p>These project designs would allow us to develop a product that could address the issue of <em>Nosema ceranae</em> in a safer and potentially more effective way than fumagillin, while still keeping the feed form which beekeepers found preferable and were accustomed to as it was a common way to administer fumagillin.</p>
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<h2>References</h3>
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<p>[1] C. I. MacInnis, “<em>Nosema ceranae</em>: A sweet surprise? Investigating the viability and infectivity of the honey bee (<em>Apis mellifera</em> L.) parasite N. ceranae”, M.S. thesis, <em>University of Alberta</em>, Edmonton, 2017. [Online]. Available: <a href=“https://era.library.ualberta.ca/items/7b26607f-08fb-4e85-9f7a-0fbac0afee68”>https://era.library.ualberta.ca/items/7b26607f-08fb-4e85-9f7a-0fbac0afee68</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[2] D. M. Eiri, G. Suwannapong and N. J. C. Endler, "<em>Nosema ceranae</em> can infect honey bee larvae and reduces subsequent adult longevity," <em>PLoS ONE</em>, 10(5) e0126330. [Online serial]. Available: <a href=“https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0126330”>https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0126330</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[3] A. K., R. Hernandez-Martin and L. Prieto, "Immune suppression in the honey bee (<em>Apis mellifera</em>) following infection by <em>Nosema ceranae</em> (microsporidia)," <em>Environmental Microbiology</em>, vol. 11, no. 9, pp. 2284-2290, 2009. [Online serial]. Available: <a href=“https://www.ncbi.nlm.nih.gov/pubmed/19737304”>https://www.ncbi.nlm.nih.gov/pubmed/19737304</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[4]</a> S. L. Gage, C. Kramer, S. Calle, M. Carrol, M. Heien and G. DeGrandi-Hoffman, "<em>Nosema ceranae</em> parasitism impacts olfactory learning and memory and neurochemistry in honey bees (<em>Apis mellifera</em>)," <em>Journal of Experimental Biology</em>, vol. 221, no. 4, 2018. [Online serial]. Available: <a href=“http://jeb.biologists.org/content/early/2017/12/18/jeb.161489”>http://jeb.biologists.org/content/early/2017/12/18/jeb.161489</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[5] S. Gisder, N. Mockle, A. Linde and E. Genersch, "A cell culture model for Nosema ceranae and Nosema apis allows new insights into the life cycle of these important honey bee-pathogenic microsporidia," <em>Environmental Microbiology</em>, vol. 13, no. 2, pp. 404-413, 2011.</p>
 +
 +
<p>[6] M. L. Smith, "The Honey Bee Parasite <em>Nosema ceranae</em>: Transmissible via Food Exchange?," <em>PLoS ONE</em>, vol. 8, no. 8 , pp. 1-6, 2012.[Online serial]. Available: <a href=“https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0043319”>https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0043319</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
 +
<p>[7] W. Huang, L.F. Solter, P.M. Yau, B.S. Imai, “<em>Nosema ceranae</em> Escapes Fumagillin Control in Honey Bees,” <em>PLOS Pathogens</em>, vol. 9, no. 3:e1003185, 2013. [Online serial]. Available: <a href=“https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1003185”>https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1003185</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[8] v. d. Heever, "Fumagillin: An Overview of Recent Scientific Advances and their Significance for Apiculture," <em>Journal of Agricultural and Food Chemistry</em>, vol. 62, pp. 2728-2727, 2014. [Online serial]. Available: <a href=“https://www.ncbi.nlm.nih.gov/pubmed/24621007”>https://www.ncbi.nlm.nih.gov/pubmed/24621007</a> [Accessed: Oct. 15, 2018]</p>
 +
 +
<p>[9] Horticulture and Cross Sectoral Division Agriculture and Agri-Food Canada, "Statistical Overview of the Canadian Honey and Bee Industry and the Economic Contribution of Honey Bee Pollination 2013-2014," <em>Government of Canada</em>, 2016.</p>
 +
 +
<p>[10] A. A. Ptaszynska, M. Trytek, G. Borsuk, K. R.-J. K. Buczek and D. Gryko, "Porphyrins inactivate <em>Nosema</em> spp. microsporidia," <em>Scientific Reports</em>, vol. 8, no. 5523, pp. 1-11, 2018. [Online serial]. Available: <a href=“https://www.nature.com/articles/s41598-018-23678-8”>https://www.nature.com/articles/s41598-018-23678-8</a> [Accessed: Oct. 15, 2018]</p>
 +
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<p>[11] J. Zhang, K. Zhen, J. Chen and G. Du, "Optimization of the heme biosynthesis pathway for the production of 5-aminolevulinic acid in <em>Escherichia coli</em>," <em>Scientific Reports</em>, vol. 5, no. 8584, pp. 1-7, 2015.</p>
 +
 +
<p>[12] S. J. Kwon, A. L. de Boer, R. Petri and C. Schmidt-Dannert, "High-Level Production of Porphyrins in Metabolically Engineered Escherichia coli: System Extension of a Pathway Assembled from Overexpressed Genes Involved in Heme Biosynthesis," <em>Applied and Environmental Microbiology</em>, vol. 69, no. 8, pp. 4875-4883, 2003.</p>
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<!--<p> [13] E. Turlin, G. Heuck and M. I. S. Brandao, "Protoporphyrin (PPIX) efflux by the MacAB-TolC pump in Escherichia coli," Microbiology Open, vol. 3, no. 6, pp. 849-859, 2014.</p>
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<p>[14] R. Tatsumi and W. Masaaki, "TolC-Dependent Exclusion of Porphyrins in Escherichia coli," Journal of Bacteriology, vol. 190, no. 18, pp. 6228-6233, 2008.</p>
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<p> [15] NYMU-Taipei, "Entering of Bee. coli," 2013. [Online]. iGEM, 2013. [Online] Available: https://2013.igem.org/Team:NYMU-Taipei/Project/Enter. [Accessed 28 5 2018].</p>
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<p>[16] T. D. Mody, "Pharmaceutical development and medical applications of porphyrin-type macrocycles," <em>Journal of Porphyrins and Phthalocyanines</em>, vol. 4, pp. 362-367, 2000.</p>
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<p>[17]M. G. Walter, A. B. Rudine and C. C. Wamser, "Porphyrins and phthalocyanines in solar photovoltaic cells," <em>Journal of Porphyrins and Phthalocyanines</em>, vol. 14, no. 9, pp. 759-798, 2010.</p>-->
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Latest revision as of 04:51, 8 December 2018

...

Description

Nosema ceranae: Fungal Freeloader

Nosema ceranae is a microsporidian parasite that infects the midgut of honeybees. N. ceranae invades the epithelial cells of the bee midgut and as it’s dependent on its honeybee host for its energy source, it causes debilitating energetic stress [1]. For individual honeybees, Nosema infections have symptoms which include shortened lifespans and weakened immune function. On the scale of a colony, the symptoms of Nosema infections greatly decrease hive productivity and contribute to colony failure[2][3][4].

...
Figure 1: Nosema ceranae spores imaged using phase contrast microscopy. The threadlike structures are polar filaments which spores use to penetrate honeybee epithelial cells. Pictured by Gisder S, et. al [5].
...
Figure 2: A Western honeybee worker (Apis mellifera)—the new host of N. ceranae.

Unfortunately, N. ceranae has recently spread to the major commercial honeybee species—the Western honeybee, Apis mellifera—and is now regarded as the dominant Nosema species infecting honey bees globally. Through our conversations with Albertan beekeepers, we found that N. ceranae is a constant issue but when there is an outbreak it can lead to unsustainable rates of death. Some report over 80% hive loss due to Nosema. Nosema is also especially pervasive in cold climates, like the one found in Alberta, as colder temperatures contribute to increased hive losses in winter [6].

Previous Nosema Treatments

Previous methods of treating N. ceranae infections rely heavily on fumagillin, a potent antifungal agent that is not only expensive but is mutagenic and toxic to mammals. At low doses, fumagillin has actually been shown to increase N. ceranae spore count in honeybees [7][8]. Moreover, Medivet Pharmaceuticals Ltd., the only company that produced fumagillin for the whole of North America’s supply, went out of business earlier this year. This development led to the collapse of the fumagillin supply chain and means that there is no longer any protection available against Nosema. Thus, the issues with using fumagillin and its recent discontinuation motivate the development of alternative treatments for combating N. ceranae as a replacement is imperative to Alberta’s honey industry and the survival of honeybees. Interestingly, Medivet was based in Alberta and we were able to interview their former CEO, Ursula De Runga.

...
Figure 3: The chemical structure of fumagillin [8].

Why Nosema and Honeybees?

Team UAlberta was made cognizant of the Nosema problem through contact with an Albertan beekeeper, Elisabeth Goldie. She made it very clear that Nosema was a massive concern to her and her fellow beekeepers. Honeybees and beekeepers are an integral part of everyday life as their ecological and economic impacts are far-reaching. This is particularly true in Alberta as our province contributed to almost half of all honey production in Canada in 2016, which is a $157.8 million CAD industry. The beekeeping industry also contributed 4 to 5.5 billions of dollars (CAD) in value through the pollination of agricultural crops [9].

...
Figure 4: Percentage contribution of honey production of Canada’s provinces in 2016 [9].

4 to 5.5 Billion CAD for Agroeconomy [9]

Having these different aspects of Alberta’s beekeeping industry come to light made it clear to our team just how important it was to tackle this issue. We were motivated by the hope that we could actually work towards a project that could positively impact our community.

Our Plan

Once we identified the issue we wanted to combat, we conducted preliminary research which led us to recent findings that porphyrins, a class of organic compounds, are capable of inactivating N. ceranae spores. When bees’ diets were supplemented with porphyrin species, spore counts in their midgut decreased significantly with no observed adverse effects on the bees. In particular, the porphyrin PP(Asp)2, a chemically synthesized derivative of protoporphyrin IX (PPIX) harbouring aspartic amide moieties, was used to inactivate N. ceranae. The antifungal action observed was attributed to porphyrin disrupting the spores’ cell wall (Figure 5) [10].

...
Figure 5: (A) shows N. ceranae spores without porphyrin treatment and (B) shows the damage done on the spore walls after incubation with the PP(Asp)2 [10].
...
Figure 6: A comparison between the similar structures of (A) PP(Asp)2, used in [10] and (B) PPIX where the hydrophilic end of each molecule is highlighted.

This advancement was extremely interesting since porphyrins are ubiquitous in nature, such as PPIX, which is an intermediate in the endogenous heme biosynthesis pathway of Escherichia coli [11][12]. Given the structural similarities of PPIX to PP(Asp)2 (Figure 6), we hypothesized that biosynthesized PPIX may have similar antifungal effects on N. ceranae spores. What makes PPIX an attractive substitute to PP(Asp)2 is that PPIX is found in nature and can be biosynthetically produced by microbes instead of the inefficient chemical methods used for PP(Asp)2. Motivated by these results, Team UAlberta decided to focus on using porphyrins for treating Nosema infections in honeybees.

To address the threat of Nosema, and provide an alternative to fumagillin, Team UAlberta presents our 2018 iGEM project:

APIS: an Antifungal Porphyrin-based Intervention System for treating Nosema infections in honey bees!

APIS aims to augment the endogenous heme synthesis pathway in E. coli to produce an excess of protoporphyrin IX, a heme synthesis intermediate, to be used for inactivating Nosema spores.

We planned to accomplish this by completing two objectives:

  • Engineer genetic constructs exploiting the heme biosynthesis pathway to overproduce PPIX
  • Test the engineered strains and PPIX for their ability to inactivate N. ceranae spores in honeybees.

With continued input from beekeepers, we designed for two routes of implementation:

  • Honeybee probiotic by introducing PPIX-producing microbes into the bee microbiome
  • Large-scale PPIX-production to generate PPIX for conventional treatment application methods

...
Figure 7: Overview of the intended outcomes of APIS: (1) generate a PPIX-producing honeybee probiotic to be fed directly to honeybees, or (2) producing porphyrin in traditional fermentation processes to be used in conventional applications methods

These project designs would allow us to develop a product that could address the issue of Nosema ceranae in a safer and potentially more effective way than fumagillin, while still keeping the feed form which beekeepers found preferable and were accustomed to as it was a common way to administer fumagillin.

References

[1] C. I. MacInnis, “Nosema ceranae: A sweet surprise? Investigating the viability and infectivity of the honey bee (Apis mellifera L.) parasite N. ceranae”, M.S. thesis, University of Alberta, Edmonton, 2017. [Online]. Available: https://era.library.ualberta.ca/items/7b26607f-08fb-4e85-9f7a-0fbac0afee68 [Accessed: Oct. 15, 2018]

[2] D. M. Eiri, G. Suwannapong and N. J. C. Endler, "Nosema ceranae can infect honey bee larvae and reduces subsequent adult longevity," PLoS ONE, 10(5) e0126330. [Online serial]. Available: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0126330 [Accessed: Oct. 15, 2018]

[3] A. K., R. Hernandez-Martin and L. Prieto, "Immune suppression in the honey bee (Apis mellifera) following infection by Nosema ceranae (microsporidia)," Environmental Microbiology, vol. 11, no. 9, pp. 2284-2290, 2009. [Online serial]. Available: https://www.ncbi.nlm.nih.gov/pubmed/19737304 [Accessed: Oct. 15, 2018]

[4] S. L. Gage, C. Kramer, S. Calle, M. Carrol, M. Heien and G. DeGrandi-Hoffman, "Nosema ceranae parasitism impacts olfactory learning and memory and neurochemistry in honey bees (Apis mellifera)," Journal of Experimental Biology, vol. 221, no. 4, 2018. [Online serial]. Available: http://jeb.biologists.org/content/early/2017/12/18/jeb.161489 [Accessed: Oct. 15, 2018]

[5] S. Gisder, N. Mockle, A. Linde and E. Genersch, "A cell culture model for Nosema ceranae and Nosema apis allows new insights into the life cycle of these important honey bee-pathogenic microsporidia," Environmental Microbiology, vol. 13, no. 2, pp. 404-413, 2011.

[6] M. L. Smith, "The Honey Bee Parasite Nosema ceranae: Transmissible via Food Exchange?," PLoS ONE, vol. 8, no. 8 , pp. 1-6, 2012.[Online serial]. Available: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0043319 [Accessed: Oct. 15, 2018]

[7] W. Huang, L.F. Solter, P.M. Yau, B.S. Imai, “Nosema ceranae Escapes Fumagillin Control in Honey Bees,” PLOS Pathogens, vol. 9, no. 3:e1003185, 2013. [Online serial]. Available: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1003185 [Accessed: Oct. 15, 2018]

[8] v. d. Heever, "Fumagillin: An Overview of Recent Scientific Advances and their Significance for Apiculture," Journal of Agricultural and Food Chemistry, vol. 62, pp. 2728-2727, 2014. [Online serial]. Available: https://www.ncbi.nlm.nih.gov/pubmed/24621007 [Accessed: Oct. 15, 2018]

[9] Horticulture and Cross Sectoral Division Agriculture and Agri-Food Canada, "Statistical Overview of the Canadian Honey and Bee Industry and the Economic Contribution of Honey Bee Pollination 2013-2014," Government of Canada, 2016.

[10] A. A. Ptaszynska, M. Trytek, G. Borsuk, K. R.-J. K. Buczek and D. Gryko, "Porphyrins inactivate Nosema spp. microsporidia," Scientific Reports, vol. 8, no. 5523, pp. 1-11, 2018. [Online serial]. Available: https://www.nature.com/articles/s41598-018-23678-8 [Accessed: Oct. 15, 2018]

[11] J. Zhang, K. Zhen, J. Chen and G. Du, "Optimization of the heme biosynthesis pathway for the production of 5-aminolevulinic acid in Escherichia coli," Scientific Reports, vol. 5, no. 8584, pp. 1-7, 2015.

[12] S. J. Kwon, A. L. de Boer, R. Petri and C. Schmidt-Dannert, "High-Level Production of Porphyrins in Metabolically Engineered Escherichia coli: System Extension of a Pathway Assembled from Overexpressed Genes Involved in Heme Biosynthesis," Applied and Environmental Microbiology, vol. 69, no. 8, pp. 4875-4883, 2003.