16 research outputs found

    Bee survival: An applied network analytical strategy

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    In the interactive educational game, Pollinator Panic!, players learn crucial information about why pollinators are in peril, and ac tions to prevent community collapse. We will be presenting the many sophisticated threats to pollinator populations in the form of a game that will help players become more engaged and personally invested in existing conservation efforts. We hope to bridge the learning gap amongst differing learning styles through utilizing text, audio, and visual means of communicating these ideas in-game. The game will be publicly available online to promote ease of access and circulation via sharing on social media platforms. To accomplish this, we plan to utilize D3.js to build bipartite network models to most accurately illustrate how threats to a population can have severe ripple effects throughout a nested com- munity structure. Players will have to overcome various environmental challenges defined by empirical research to win the game and save the pollinators

    Plasmodium vivax populations revisited: mitochondrial genomes of temperate strains in Asia suggest ancient population expansion

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    <p>Abstract</p> <p>Background</p> <p><it>Plasmodium vivax </it>is the most widely distributed human malaria parasite outside of Africa, and its range extends well into the temperate zones. Previous studies provided evidence for vivax population differentiation, but temperate vivax parasites were not well represented in these analyses. Here we address this deficit by using complete mitochondrial (mt) genome sequences to elucidate the broad genetic diversity and population structure of <it>P. vivax </it>from temperate regions in East and Southeast Asia.</p> <p>Results</p> <p>From the complete mtDNA sequences of 99 clinical samples collected in China, Myanmar and Korea, a total of 30 different haplotypes were identified from 26 polymorphic sites. Significant differentiation between different East and Southeast Asian parasite populations was observed except for the comparison between populations from Korea and southern China. Haplotype patterns and structure diversity analysis showed coexistence of two different groups in East Asia, which were genetically related to the Southeast Asian population and Myanmar population, respectively. The demographic history of <it>P. vivax</it>, examined using neutrality tests and mismatch distribution analyses, revealed population expansion events across the entire <it>P. vivax </it>range and the Myanmar population. Bayesian skyline analysis further supported the occurrence of ancient <it>P. vivax </it>population expansion.</p> <p>Conclusions</p> <p>This study provided further resolution of the population structure and evolution of <it>P. vivax</it>, especially in temperate/warm-temperate endemic areas of Asia. The results revealed divergence of the <it>P. vivax </it>populations in temperate regions of China and Korea from other populations. Multiple analyses confirmed ancient population expansion of this parasite. The extensive genetic diversity of the <it>P. vivax </it>populations is consistent with phenotypic plasticity of the parasites, which has implications for malaria control.</p

    The transcription factor Krüppel homolog 1 is linked to hormone mediated social organization in bees

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    <p>Abstract</p> <p>Background</p> <p>Regulation of worker behavior by dominant queens or workers is a hallmark of insect societies, but the underlying molecular mechanisms and their evolutionary conservation are not well understood. Honey bee and bumble bee colonies consist of a single reproductive queen and facultatively sterile workers. The queens' influences on the workers are mediated largely via inhibition of juvenile hormone titers, which affect division of labor in honey bees and worker reproduction in bumble bees. Studies in honey bees identified a transcription factor, <it>Krüppel-homolog 1 </it>(<it>Kr-h1</it>), whose expression in worker brains is significantly downregulated in the presence of a queen or queen pheromone and higher in forager bees, making this gene an ideal candidate for examining the evolutionary conservation of socially regulated pathways in Hymenoptera.</p> <p>Results</p> <p>In contrast to honey bees, bumble bees foragers do not have higher <it>Kr-h1 </it>levels relative to nurses: in one of three colonies levels were similar in nurses and foragers, and in two colonies levels were higher in nurses. Similarly to honey bees, brain <it>Kr-h1 </it>levels were significantly downregulated in the presence versus absence of a queen. Furthermore, in small queenless groups, <it>Kr-h1 </it>levels were downregulated in subordinate workers with undeveloped ovaries relative to dominant individuals with active ovaries. Brain <it>Kr-h1 </it>levels were upregulated by juvenile hormone treatment relative to a vehicle control. Finally, phylogenetic analysis indicates that KR-H1 orthologs are presence across insect orders. Though this protein is highly conserved between honey bees and bumble bees, there are significant differences between orthologs of insects from different orders.</p> <p>Conclusions</p> <p>Our results suggest that <it>Kr-h1 </it>is associated with juvenile hormone mediated regulation of reproduction in bumble bees. The expression of this transcription factor is inhibited by the queen and associated with endocrine mediated regulation of social organization in two species of bees. Thus, KR-H1 may transcriptionally regulate a conserved genetic module that is part of a pathway that has been co-opted to function in social behavior, and adjusts the behavior of workers to their social environmental context.</p

    Chemoreceptors From the Hawk Moth Manduca Sexta L

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    121 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2005.In this study I cloned and characterized four M. sexta chemoreceptors. Differential screening of a male antennal cDNA library before the publication of the Drosophila melanogaster genome yielded one G coupled-protein receptor that had no matches in Genbank databases and the results of RT-PCR and quantitative real-time PCR experiments show MsOr1 is expressed only in male antennae suggesting a male-specific function for this receptor. In situ hybridization revealed MsOr1 was expressed exclusively in a single cell associated with male-specific type-I trichoid sensilla further suggesting this receptor is involved in pheromone detection. The second receptor, MsOr2, was discovered using fully degenerate inosine primers designed to conserved motifs of a unique group of highly conserved odorant receptors. Comparison of RT-PCR, quantitative real-time PCR and in situ hybridization results with those of previously described odorant receptors in the DmOr83b subfamily show a strong sequence and expression pattern similarity. The third receptor described in this paper, MsOr3, was found by 5'-end sequencing of a normalized and subtracted cDNA library from male M. sexta antennae. RT-PCR and quantitative real-time PCR show that this receptor is expressed only in male and female antennae. Moreover, it is expressed at much higher levels in females, suggesting it functions as a general Or, perhaps tuned to plant volatiles. A gustatory receptor was sequenced from the labial palp mRNA of M. sexta using degenerate inosine primers designed to the conserved motifs of two gustatory receptors found in the Anopheles gambiae and Drosophila melanogaster genomes. This gene fragment codes for the C-terminal region of a gustatory protein with 73% identity to DmGr21a. In D. melanogaster DmGr21a has been show to detect CO2; I propose a similar function for MsGr1 based on sequence similarity and the exclusive expression of this gustatory receptor in the labial palps of M. sexta as revealed by RT-PCR and quantitative real-time PCR. Higher expression levels of this gene in female labial palps suggest an enhanced sensitivity to the odorant that binds MsGr1, perhaps indicating a role for CO2 in oviposition.U of I OnlyRestricted to the U of I community idenfinitely during batch ingest of legacy ETD

    Primers used for molecular analysis for identification of bee populations, pathogens and parasites.

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    <p>Abbreviations: Israeli acute paralysis virus (IAPV), acute bee paralysis virus (ABPV), black queen cell virus, (BQCV), chronic bee paralysis virus (CBPV), deformed wing virus (DWV), kashmir bee virus (KBV), and sacbrood virus (SBV). References: Arias MC and WS Sheppard WS (1996) <i>Molecular Phylogenetics and Evolution</i> 5: 557–566; Benjeddou et al. (2001) <i>Applied and Environmental Microbiol</i>ogy 67:2384–2387; Chen et al. (2005) <i>Applied and Environmental Microbiol</i>ogy 71(1):436–441; Di Prisco et. al. (2011) <i>Journal of General Virology</i> 92: 151–15; Klee et al. (2007). Journal of Invertabrate Pathology 96: 1–10. Ribiere et al. (2002) <i>Apidologie</i> 33: 339–351; Stoltz et al. (1995) <i>Journal of Apicultural Research</i> 34: 153–160.</p

    Geographic location of surveyed apiaries.

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    <p>Twenty-four apiaries were surveyed throughout Kenya with an additional three apiaries (25–27), see supplemenatry material, surveyed for ecological effects on colony health. The location and numerical designation of the apiaries is indicated on the map.</p

    Association of <i>Varroa</i> infestation with elevation and colony size.

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    <p><b>A</b>. Levels of <i>Varroa</i> mites were positively correlated with elevation, with colonies at higher elevations having significantly higher average numbers of <i>Varroa</i> (r(53) = 0.44, p = 0.001). <b>B</b>. Levels were also positively correlated with colony size ((48) = 0.35, p = 0.013). <i>Varroa</i> counts were converted to logarithmic scale.</p
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