Transcriptional responses of Biomphalaria pfeifferi and Schistosoma mansoni following exposure to niclosamide, with evidence for a synergistic effect on snails following exposure to both stressors.

BackgroundSchistosomiasis is one of the world's most common NTDs. Successful control operations often target snail vectors with the molluscicide niclosamide. Little is known about how niclosamide affects snails, including for Biomphalaria pfeifferi, the most important vector for Schistosoma mansoni in Africa. We used Illumina technology to explore how field-derived B. pfeifferi, either uninfected or harboring cercariae-producing S. mansoni sporocysts, respond to a sublethal treatment of niclosamide. This study afforded the opportunity to determine if snails respond differently to biotic or abiotic stressors, and if they reserve unique responses for when presented with both stressors in combination. We also examined how sporocysts respond when their snail host is treated with niclosamide.Principal findingsCercariae-producing sporocysts within snails treated with niclosamide express ~68% of the genes in the S. mansoni genome, as compared to 66% expressed by intramolluscan stages of S. mansoni in snails not treated with niclosamide. Niclosamide does not disable sporocysts nor does it seem to provoke from them distinctive responses associated with detoxifying a xenobiotic. For uninfected B. pfeifferi, niclosamide treatment alone increases expression of several features not up-regulated in infected snails including particular cytochrome p450s and heat shock proteins, glutathione-S-transferases, antimicrobial factors like LBP/BPI and protease inhibitors, and also provokes strong down regulation of proteases. Exposure of infected snails to niclosamide resulted in numerous up-regulated responses associated with apoptosis along with down-regulated ribosomal and defense functions, indicative of a distinctive, compromised state not achieved with either stimulus alone.Conclusions/significanceThis study helps define the transcriptomic responses of an important and under-studied schistosome vector to S. mansoni sporocysts, to niclosamide, and to both in combination. It suggests the response of S. mansoni sporocysts to niclosamide is minimal and not reflective of a distinct repertoire of genes to handle xenobiotics while in the snail host. It also offers new insights for how niclosamide affects snails

Orbital Magnetization under an Electric Field and Orbital Magnetoelectric Polarizabilty for a Bilayer Chern System

In the the real space formalism of orbital magnetization (OM) for a Chern insulator without an external electric field, it is correct to average the local OM either over the bulk region or over the whole sample. However for a layered Chern insulator in an external electric field, which is directly related to the nontrivial nature of orbital magnetoelectric coupling, the role of boundaries remains ambiguous in this formalism. Based on a bilayer model with an adjustable Chern number at half filling, we numerically investigate the OM with the above two different average types under a nonzero perpendicular electric field. The result shows that in this case, the nonzero Chern number gives rise to a gauge shift of the OM with the bulk region average, while this gauge shift is absent for the OM with the whole sample average. This indicates that only the whole sample average is reliable to calculate the OM under a nonzero electric field for Chern insulators. On this basis, the orbital magnetoelectric polarizablity (OMP) and the Chern-Simons orbital magnetoelectric polarizablity (CSOMP) with the whole sample average are studied. We also present the relationship between the OMP (CSOMP) and the response of Berry curvature to the electric field. The stronger the response of Berry curvature to electric field, the stronger is the OMP (CSOMP). Besides clarify the calculation methods, our result also provides an effective method to enhance OMP and CSOMP of materials.Comment: 11 pages, 11 figure

Quantum Transports in Two-Dimensions with Long Range Hopping: Shielding, Localization and the Extended Isolated State

We investigate the effects of disorder and shielding on quantum transports in a two dimensional system with all-to-all long range hopping. In the weak disorder, cooperative shielding manifests itself as perfect conducting channels identical to those of the short range model, as if the long range hopping does not exist. With increasing disorder, the average and fluctuation of conductance are larger than those in the short range model, since the shielding is effectively broken and therefore long range hopping starts to take effect. Over several orders of disorder strength (until $\sim 10^4$ times of nearest hopping), although the wavefunctions are not fully extended, they are also robustly prevented from being completely localized into a single site. Each wavefunction has several localization centers around the whole sample, thus leading to a fractal dimension remarkably smaller than 2 and also remarkably larger than 0, exhibiting a hybrid feature of localization and delocalization. The size scaling shows that for sufficiently large size and disorder strength, the conductance tends to saturate to a fixed value with the scaling function $\beta\sim 0$, which is also a marginal phase between the typical metal ($\beta>0$) and insulating phase ($\beta<0$). The all-to-all coupling expels one isolated but extended state far out of the band, whose transport is extremely robust against disorder due to absence of backscattering. The bond current picture of this isolated state shows a quantum version of short circuit through long hopping.Comment: 15 pages, 8 figure

The in vivo transcriptome of Schistosoma mansoni in the prominent vector species Biomphalaria pfeifferi with supporting observations from Biomphalaria glabrata.

BackgroundThe full scope of the genes expressed by schistosomes during intramolluscan development has yet to be characterized. Understanding the gene products deployed by larval schistosomes in their snail hosts will provide insights into their establishment, maintenance, asexual reproduction, ability to castrate their hosts, and their prolific production of human-infective cercariae. Using the Illumina platform, the intramolluscan transcriptome of Schistosoma mansoni was investigated in field-derived specimens of the prominent vector species Biomphalaria pfeifferi at 1 and 3 days post infection (d) and from snails shedding cercariae. These S. mansoni samples were derived from the same snails used in our complementary B. pfeifferi transcriptomic study. We supplemented this view with microarray analyses of S. mansoni from B. glabrata at 2d, 4d, 8d, 16d, and 32d to highlight robust features of S. mansoni transcription, even when a different technique and vector species was used.Principal findingsTranscripts representing at least 7,740 (66%) of known S. mansoni genes were expressed during intramolluscan development, with the greatest number expressed in snails shedding cercariae. Many transcripts were constitutively expressed throughout development featuring membrane transporters, and metabolic enzymes involved in protein and nucleic acid synthesis and cell division. Several proteases and protease inhibitors were expressed at all stages, including some proteases usually associated with cercariae. Transcripts associated with G-protein coupled receptors, germ cell perpetuation, and stress responses and defense were well represented. We noted transcripts homologous to planarian anti-bacterial factors, several neural development or neuropeptide transcripts including neuropeptide Y, and receptors that may be associated with schistosome germinal cell maintenance that could also impact host reproduction. In at least one snail the presence of larvae of another digenean species (an amphistome) was associated with repressed S. mansoni transcriptional activity.Conclusions/significanceThis in vivo study, emphasizing field-derived snails and schistosomes, but supplemented with observations from a lab model, provides a distinct view from previous studies of development of cultured intramolluscan stages from lab-maintained organisms. We found many highly represented transcripts with suspected or unknown functions, with connection to intramolluscan development yet to be elucidated

Discriminating different scenarios to account for the cosmic e±e^\pm excess by synchrotron and inverse Compton radiation

The excesses of the cosmic positron fraction recently measured by PAMELA and the electron spectra by ATIC, PPB-BETS, Fermi and H.E.S.S. indicate the existence of primary electron and positron sources. The possible explanations include dark matter annihilation, decay, and astrophysical origin, like pulsars. In this work we show that these three scenarios can all explain the experimental results of the cosmic $e^\pm$ excess. However, it may be difficult to discriminate these different scenarios by the local measurements of electrons and positrons. We propose possible discriminations among these scenarios through the synchrotron and inverse Compton radiation of the primary electrons/positrons from the region close to the Galactic center. Taking typical configurations, we find the three scenarios predict quite different spectra and skymaps of the synchrotron and inverse Compton radiation, though there are relatively large uncertainties. The most prominent differences come from the energy band $10^4\sim 10^9$ MHz for synchrotron emission and $\gtrsim 10$ GeV for inverse Compton emission. It might be able to discriminate at least the annihilating dark matter scenario from the other two given the high precision synchrotron and diffuse $\gamma$-ray skymaps in the future.Comment: published in Pr