90 research outputs found

    Probing dark matter particles at CEPC

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    We investigate the capability of the future electron collider CEPC in probing the parameter space of several dark matter models, including millicharged dark matter models, Z′Z' portal dark matter models, and effective field theory dark matter models. In our analysis, the monophoton final state is used as the primary channel to detect dark matter models at CEPC. To maximize the signal to background significance, we study the energy and angular distributions of the monophoton channel arising from dark matter models and from the standard model to design a set of detector cuts. For the Z′Z' portal dark matter, we also analyze the Z′Z' boson visible decay channel which is found to be complementary to the monophoton channel in certain parameter space. The CEPC reach in the parameter space of dark matter models is also put in comparison with Xenon1T. We find that CEPC has the unprecedented sensitivity to certain parameter space for the dark matter models considered; for example, CEPC can improve the limits on millicharge by one order of magnitude than previous collider experiments for O(1)−100{\cal O}(1)-100 GeV dark matter.Comment: 21 pages, 31 figure

    Efficient postprocessing technique for fabricating surface nanoscale axial photonics microresonators with subangstrom precision by femtosecond laser

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    We demonstrated the subangstrom precise correction of surface nanoscale axial photonics (SNAP) micro-resonators by the femtosecond (fs) laser postprocessing technique for the first time. The internal stress can be induced by fs laser inscriptions in the fiber, causing nanoscale effective radius variation (ERV). However, the obtained ultraprecise fabrication usually undergoes multiple tries. Here, we propose a novel postprocessing technique based on the fs laser that significantly reduces the ERV errors and improves the fabrication precision without iterative corrections. The postexposure process is achieved at the original exposure locations using lower pulse energy than that in the initial fabrication process. The results show that the ERV is nearly proportional to the pulse energy of the postexposure process. The slope of the ERV versus the pulse energy is 0.07 Ã…/nJ. The maximum of the postprocessed ERV can reach 8.0 Ã…. The repeatability was experimentally verified by accomplishing the correction on three SNAP microresonators with the precision of 0.75 Ã…. The developed fabrication technique with fs laser enables SNAP microresonators with new breakthrough applications for optomechanics and filters

    The Rho-independent transcription terminator for the porA gene enhances expression of the major outer membrane protein and Campylobacter jejuni virulence in abortion induction

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    Campylobacter jejuni is a leading cause of foodborne illnesses worldwide. Its porA gene encodes the major outer membrane protein (MOMP) that is abundantly expressed and has important physiological functions including a key role in systemic infection and abortion induction in pregnant animals. Despite the importance of porA in C. jejuni pathogenesis, mechanisms modulating its expression levels remain elusive. At the 3′ end of the porA transcript, there is a Rho-independent transcription terminator (named TporA in this study). Whether TporA affects the expression and function of MOMP remains unknown and is investigated in this study. Green fluorescent protein (GFP) fusion constructs with the porA promoter at the 5′ end and an intact TporA or no TporA at the 3′ end of the gfp coding sequence revealed that both transcript level of gfp and its fluorescence signals were more than 2-fold higher in the construct with TporA than the one without TporA. qRT-PCR analysis of the porA mRNA and immunoblotting detection of the MOMP protein in C. jejuni showed that disruption of TporA significantly reduced the porA transcript level and expression of the MOMP protein. mRNA decay assay demonstrated that disruption of TporA resulted in shortened transcript half-life of the upstream gfp or porA genes, indicating TporA enhances mRNA stability. In the guinea pig model, the C. jejuni construct with an interrupted TporA was significantly attenuated in abortion induction. Together these results indicate that TporA enhances the expression level of MOMP by stabilizing its mRNA and influences the virulence of C. jejuni

    Transmissive fiber Bragg grating-based delay line interferometer for RZ-OOK to NRZ-OOK format conversion

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    We propose a return-to-zero on-off keying (RZ-OOK) to non-return-to-zero (NRZ) OOK conversion scheme based on a transmissive phase-modulated fiber Bragg grating (PM-FBG). The PM-FBG has a spectrum similar to the combination of a delay line interferometer and a narrow band optical filter, which is designed and synthesized using numerical optimization algorithm. The coupling strength of the PM-FBG is almost uniform and the grating period varies along the fiber length according to the optimization method. The designed PM-FBG has been fabricated using advanced ultraviolet laser inscription technique. Experimental results show that such a PM-FBG can perform RZ-OOK to NRZ-OOK format conversion successfully

    Yeast Probiotics Shape the Gut Microbiome and Improve the Health of Early-Weaned Piglets

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    Weaning is one of the most stressful challenges in the pig’s life, which contributes to dysfunctions of intestinal and immune system, disrupts the gut microbial ecosystem, and therefore compromises the growth performance and health of piglets. To mitigate the negative impact of the stress on early-weaned piglets, effective measures are needed to promote gut health. Toward this end, we tamed a Saccharomyces cerevisiae strain and developed a probiotic Duan-Nai-An, which is a yeast culture of the tamed S. cerevisiae on egg white. In this study, we tested the performance of Duan-Nai-An on growth and health of early-weaned piglets and analyzed its impact on fecal microbiota. The results showed that Duan-Nai-An significantly improved weight gain and feed intake, and reduced diarrhea and death of early-weaned piglets. Analysis of the gut microbiota showed that the bacterial community was shaped by Duan-Nai-An and maintained as a relatively stable structure, represented by a higher core OTU number and lower unweighted UniFrac distances across the early weaned period. However, fungal community was not significantly shaped by the yeast probiotics. Notably, 13 bacterial genera were found to be associated with Duan-Nai-An feeding, including Enterococcus, Succinivibrio, Ruminococcus, Sharpea, Desulfovibrio, RFN20, Sphaerochaeta, Peptococcus, Anaeroplasma, and four other undefined genera. These findings suggest that Duan-Nai-An has the potential to be used as a feed supplement in swine production

    Pharmacokinetics of tulathromycin in pregnant ewes (Ovis aries) challenged with Campylobacter jejuni

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    The purpose of this study was to evaluate the pharmacokinetics of tulathromycin in the plasma and maternal and fetal tissues of pregnant ewes when administered within 24 hours of a single, IV Campylobacter jejuni (C. jejuni) challenge. Twelve, pregnant ewes between 72–92 days of gestation were challenged IV with C. jejuni IA3902 and then treated with 1.1 ml/45.36 kg of tulathromycin subcutaneously 18 hours post-challenge. Ewes were bled at predetermined time points and euthanized either at a predetermined time point or following the observation of vaginal bleeding or abortion. Following euthanasia, tissues were collected for bacterial culture, pharmacokinetics and histologic examination. The maximum (geometric) mean tulathromycin plasma concentration was estimated at 0.302 μg/mL, with a peak level observed at around 1.2 hours. The apparent systemic clearance of tulathromycin was estimated at 16.6 L/h (or 0.28 L/kg/h) with an elimination half-life estimated at approximately 22 hours. The mean tissue concentrations were highest in the uterus (2.464 μg/g) and placentome (0.484 μg/g), and were lowest in fetal liver (0.11 μg/g) and fetal lung (0.03 μg/g). Compared to previous reports, results of this study demonstrate that prior IV administration of C. jejuni appeared to substantially alter the pharmacokinetics of tulathromycin, reducing both the peak plasma concentrations and elimination half-life. However, additional controlled trials are required to confirm those observations

    Effects of tumor necrosis factor-α polymorphism on the brain structural changes of the patients with major depressive disorder

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    Single Nucleotide Polymorphic (SNP) variations of proinflammatory cytokines such as Tumor Necrosis Factor-α (TNF-α) have been reported to be closely associated with the major depressive disorder (MDD). However, it is unclear if proinflammatory genetic burden adversely affects the regional gray matter volume in patients with MDD. The aim of this study was to test whether rs1799724, an SNP of TNF-α, contributes to the neuroanatomical changes in MDD. In this cross-sectional study, a total of 144 MDD patients and 111 healthy controls (HC) well matched for age, sex and education were recruited from Shanghai Mental Health Center. Voxel-based morphometry (VBM) followed by graph theory based structural covariance analysis was applied to locate diagnosis x genotype interactions. Irrespective of diagnosis, individuals with the high-risk genotype (T-carriers) had reduced volume in left angular gyrus (main effect of genotype). Diagnosis x genotype interaction was exclusively localized to the visual cortex (right superior occipital gyrus). The same region also showed reduced volume in patients with MDD than HC (main effect of diagnosis), with this effect being most pronounced in patients carrying the high-risk genotype. However, neither global nor regional network of structural covariance was found to have group difference. In conclusion, a genetic variation which can increase TNF-α expression selectively affects the anatomy of the visual cortex among the depressed subjects, with no effect on the topographical organization of multiple cortical regions. This supports the notion that anatomical changes in depression are in part influenced by the genetic determinants of inflammatory activity
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