25 research outputs found

    PowerCells Payload on EuCROPIS - Measuring Synthetic Biology in Space

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    NASAs PowerCell payload on the DLR (Deutsches Zentrum fur Luft- und Raumfahrt, i.e. German Aerospace Center) Eu:CROPIS satellite will compare the effect of multiple simulated gravity regimes on basic processes required for synthetic biology in space including growth, protein production, and genetic transformation of the bacterium Bacillus subtilis. In addition, it will pioneer the use of a cyanobacterially-produced feedstock for microbial growth in space, a concept we call PowerCell. The PowerCell experiment system will be integrated using the Spaceflight Secondary Payload System with the German Space Agency's (DLR's) Euglena and Combined Regenerative Organic-food Production In Space (Eu:CROPIS) satellite, to be launched during the summer of 2017. In order to simulate the gravitational gradient of different celestial bodies, the Eu:CROPIS satellite will establish artificial microgravity, lunar, and Martian gravity levels prior to conducting each set of biological experiments, with experimental results compared to ground controls. Experiments will be carried out in microfluidics cards with experimental progress measured through absorbance as detected by the LED-based optical system. Here we describe the ground studies that led to these experiments, along with a description of the flight hardware and its performance. The results of this mission will provide foundational data for the use and production of genetically engineered organisms for extraterrestrial missions

    Origins of high latitude introductions of Aedes aegypti to Nebraska and Utah during 2019

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    Aedes aegypti (L.), the yellow fever mosquito, is also an important vector of dengue and Zika viruses, and an invasive species in North America. Aedes aegypti inhabits tropical and sub-tropical areas of the world and in North America is primarily distributed throughout the southern US states and Mexico. The northern range of Ae. aegypti is limited by cold winter months and establishment in these areas has been mostly unsuccessful. However, frequent introductions of Ae. aegypti to temperate, non-endemic areas during the warmer months can lead to seasonal activity and disease outbreaks. Two Ae. aegypti incursions were reported in the late summer of 2019 into York, Nebraska and Moab, Utah. These states had no history of established populations of this mosquito and no evidence of previous seasonal activity. We genotyped a subset of individuals from each location at 12 microsatellite loci and ~ 14,000 single nucleotide polymorphic markers to determine their genetic affinities to other populations worldwide and investigate their potential source of introduction. Our results support a single origin for each of the introductions from different sources. Aedes aegypti from Utah likely derived from Tucson, Arizona, or a nearby location. Nebraska specimen results were not as conclusive, but point to an origin from southcentral or southeastern US. In addition to an effective, efficient, and sustainable control of invasive mosquitoes, such as Ae. aegypti, identifying the potential routes of introduction will be key to prevent future incursions and assess their potential health threat based on the ability of the source population to transmit a particular virus and its insecticide resistance profile, which may complicate vector control

    Interactions Increase Forager Availability and Activity in Harvester Ants

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    Social insect colonies use interactions among workers to regulate collective behavior. Harvester ant foragers interact in a chamber just inside the nest entrance, here called the 'entrance chamber'. Previous studies of the activation of foragers in red harvester ants show that an outgoing forager inside the nest experiences an increase in brief antennal contacts before it leaves the nest to forage. Here we compare the interaction rate experienced by foragers that left the nest and ants that did not. We found that ants in the entrance chamber that leave the nest to forage experienced more interactions than ants that descend to the deeper nest without foraging. Additionally, we found that the availability of foragers in the entrance chamber is associated with the rate of forager return. An increase in the rate of forager return leads to an increase in the rate at which ants descend to the deeper nest, which then stimulates more ants to ascend into the entrance chamber. Thus a higher rate of forager return leads to more available foragers in the entrance chamber. The highest density of interactions occurs near the nest entrance and the entrances of the tunnels from the entrance chamber to the deeper nest. Local interactions with returning foragers regulate both the activation of waiting foragers and the number of foragers available to be activated

    The recombination landscape of the Khoe-San likely represents the upper limits of recombination divergence in humans.

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    BackgroundRecombination maps are  important resources for epidemiological and evolutionary analyses; however, there are currently no recombination maps representing any African population outside of those with West African ancestry. We infer the demographic history for the Nama, an indigenous Khoe-San population of southern Africa, and derive a novel, population-specific recombination map from the whole genome sequencing of 54 Nama individuals. We hypothesise that there are no publicly available recombination maps representative of the Nama, considering the deep population divergence and subsequent isolation of the Khoe-San from other African groups.ResultsWe show that the recombination landscape of the Nama does not cluster with any continental groups with publicly available representative recombination maps. Finally, we use selection scans as an example of how fine-scale differences between the Nama recombination map and the combined Phase II HapMap recombination map can impact the outcome of selection scans.ConclusionsFine-scale differences in recombination can meaningfully alter the results of a selection scan. The recombination map we infer likely represents an upper bound on the extent of divergence we expect to see for a recombination map in humans and would be of interest to any researcher that wants to test the sensitivity of population genetic or GWAS analysis to recombination map input

    Ae.aegypti_Ne_genepop_files

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    Aedes aegypti microsatellite alleles and SNP-chip genotypes from a worldwide sample of populations in "genepop" format, used in estimates of Ne for this paper. Details of the "genepop" format can be found at http://genepop.curtin.edu.au. For the microsatellite genotyping, we used the protocol described in (Brown et al, 2011) for 12 loci; A1, B2, B3, A9, AC2, CT2, AG2, AC4, AC1, AC5, AG1, and AG4. Briefly, amplifications were performed using standard PCR protocol (35 cycles at 54˚C) with fluorescently labeled M13 primers (6-FAM and HEX) in 10.0 μl reaction volumes using the Type-it Microsatellite PCR Master Mix (Qiagen), then diluted, multiplexed, and submitted for fragment analysis with GS 500 ROX internal size standard (Applied Biosystems, Foster City, CA, USA) on an Applied Biosystems 3730xl DNA Genetic Analyzer at the DNA Analysis Facility on Science Hill at Yale. Alleles were scored using GeneMapper v4.0 (Applied Biosystems). For the SNP-chip genotyping, 167 samples were analyzed on the Axiom_aegypti1 SNP-chip (Evans et al, 2015) at the Functional Genomics Core at University of North Carolina, Chapel Hill, using manufacturer protocols. Raw data were processed and converted into genotype calls following Evans et al. (2015) using Genotyping Console v4.2 (Affymetrix, Santa Clara, CA, USA) and SNPolisher v1.4 (Affymetrix) in the R environment with the call threshold set to 95%. SNPs were pruned to remove any linked SNPs in PLINK v1.7 (Purcell et al, 2007) with the command “--indep 100 10 2”, which recursively removed SNPs within a sliding window of 100 SNPs wide, shifting 10 SNPs per step, with a variance inflation factor (i.e. VIF) threshold of 2

    Multiple introductions of the dengue vector, <i>Aedes aegypti</i>, into California

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    <div><p>The yellow fever mosquito <i>Aedes aegypti</i> inhabits much of the tropical and subtropical world and is a primary vector of dengue, Zika, and chikungunya viruses. Breeding populations of <i>A</i>. <i>aegypti</i> were first reported in California (CA) in 2013. Initial genetic analyses using 12 microsatellites on collections from Northern CA in 2013 indicated the South Central US region as the likely source of the introduction. We expanded genetic analyses of CA <i>A</i>. <i>aegypti</i> by: (a) examining additional Northern CA samples and including samples from Southern CA, (b) including more southern US populations for comparison, and (c) genotyping a subset of samples at 15,698 SNPs. Major results are: (1) Northern and Southern CA populations are distinct. (2) Northern populations are more genetically diverse than Southern CA populations. (3) Northern and Southern CA groups were likely founded by two independent introductions which came from the South Central US and Southwest US/northern Mexico regions respectively. (4) Our genetic data suggest that the founding events giving rise to the Northern CA and Southern CA populations likely occurred before the populations were first recognized in 2013 and 2014, respectively. (5) A Northern CA population analyzed at multiple time-points (two years apart) is genetically stable, consistent with permanent <i>in situ</i> breeding. These results expand previous work on the origin of California <i>A</i>. <i>aegypti</i> with the novel finding that this species entered California on multiple occasions, likely some years before its initial detection. This work has implications for mosquito surveillance and vector control activities not only in California but also in other regions where the distribution of this invasive mosquito is expanding.</p></div
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