381 research outputs found

    Genotyping of Salmonella enterica serovar Typhi strains isolated from 1959 to 2006 in China and analysis of genetic diversity by genomic microarray

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    Aim To determine the genotype of Salmonella enterica serovar Typhi (S. Typhi) strains in China and analyze their genetic diversity. Methods We collected S. Typhi strains from 1959 to 2006 in five highly endemic Chinese provinces and chose 40 representative strains. Multilocus sequence typing was used to determine the genotypes or sequence types (ST) and microarray-based comparative genomic hybridization (M-CGH) to investigate the differences in gene content among these strains. Results Forty representative S. Typhi strains belonged to 4 sequence types (ST1, ST2, ST890, and ST892). The predominant S. Typhi genotype (31/40) was ST2 and it had a diverse geographic distribution. We discovered two novel STs – ST890 and ST892. M-CGH showed that 69 genes in these two novel STs were divergent from S. Typhi Ty2, which belongs to ST1. In addition, 5 representative Typhi strains of ST2 isolated from Guizhou province showed differences in divergent genes. Conclusion We determined two novel sequence types, ST890 and ST892, and found that ST2 was the most prevalent genotype of S. Typhi in China. Genetic diversity was present even within a highly clonal bacterial population

    Fixation-induced cell blebbing on spread cells inversely correlates with phosphatidylinositol 4,5-bisphosphate level in the plasma membrane

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    AbstractWhile most attention has been focused on physiologically generated blebs, the molecular mechanisms for fixation-induced cell blebbing are less investigated. We show that protein-fixing (e.g. aldehydes and picric acid) but not lipid-stabilizing (e.g. OsO4 and KMnO4) fixatives induce blebbing on spread cells. We also show that aldehyde fixation may induce the loss or delocalization of phosphatidylinositol 4,5-bisphosphate (PIP2) in the plasma membrane and that the asymmetric distribution of fixation-induced blebs on spread/migrating cells coincides with that of PIP2 on the cells prefixed by lipid-stabilizing fixatives (e.g., OsO4). Moreover, fixation induces blebbing less readily on PIP2-elevated spread cells but more readily on PIP2-lowered or lipid raft-disrupted spread cells. Our data suggest that fixation-induced lowering of PIP2 level at cytoskeleton-attaching membrane sites causes bleb formation via local breakdown of the membrane–cytoskeleton coupling

    The Indoor Thermal Environment Simulation and Testing Validation of a Power Plant Turbine Room in Extreme Cold Area

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    AbstractThis paper conducts an analysis study on indoor thermal environment of a steam turbine room in power plant by CFD. Refer to a typical steam turbine room in an actual thermal power plant which has been conducted field test, the typical numerical simulation model is built including a reasonable indoor heat conditions, structural parameters and envelope architectural opening, flow boundary conditions. Indoor air temperature distribution and air velocity distribution of steam turbine room is obtained. Comparing the simulation results with the corresponding field measurement data on typical location show that two sets of results are very close. So accuracy and applicability of CFD simulations is proved. It is also proved that complete method for CFD simulations of the paper is appropriate for interior thermal environment study of typical steam turbine room and thus laid the foundation for the further studies of a large number of universal cases

    Circular RNAs in gynecologic cancers: mechanisms and implications for chemotherapy resistance

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    Chemotherapy resistance remains a major challenge in the treatment of gynecologic malignancies. Increasing evidence suggests that circular RNAs (circRNAs) play a significant role in conferring chemoresistance in these cancers. In this review, we summarize the current understanding of the mechanisms by which circRNAs regulate chemotherapy sensitivity and resistance in gynecologic malignancies. We also discuss the potential clinical implications of these findings and highlight areas for future research. CircRNAs are a novel class of RNA molecules that are characterized by their unique circular structure, which confers increased stability and resistance to degradation by exonucleases. Recent studies have shown that circRNAs can act as miRNA sponges, sequestering miRNAs and preventing them from binding to their target mRNAs. This can lead to upregulation of genes involved in drug resistance pathways, ultimately resulting in decreased sensitivity to chemotherapy. We discuss several specific examples of circRNAs that have been implicated in chemoresistance in gynecologic cancers, including cervical cancer, ovarian cancer, and endometrial cancer. We also highlight the potential clinical applications of circRNA-based biomarkers for predicting chemotherapy response and guiding treatment decisions. Overall, this review provides a comprehensive overview of the current state of knowledge regarding the role of circRNAs in chemotherapy resistance in gynecologic malignancies. By elucidating the underlying mechanisms by which circRNAs regulate drug sensitivity, this work has important implications for improving patient outcomes and developing more effective therapeutic strategies for these challenging cancers

    Application of diffusion kurtosis imaging in neonatal brain development

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    BackgroundDeviations from the regular pattern of growth and development could lead to early childhood diseases, suggesting the importance of evaluating early brain development. Through this study, we aimed to explore the changing patterns of white matter and gray matter during neonatal brain development using diffusion kurtosis imaging (DKI).Materials and methodsIn total, 42 full-term neonates (within 28 days of birth) underwent conventional brain magnetic resonance imaging (MRI) and DKI. The DKI metrics (including kurtosis parameters and diffusion parameters) of white matter and deep gray matter were measured. DKI metrics from the different regions of interest (ROIs) were evaluated using the Kruskal–Wallis test and Bonferroni method. Spearman rank correlation analysis of the DKI metrics was conducted, and the age at the time of brain MRI acquisition was calculated. The subjects were divided into three groups according to their age at the time of brain MRI acquisition: the first group, neonates aged ≤7 days; the second group, neonates aged 8–14 days; and the third group, neonates aged 15–28 days. The rate of change in DKI metrics relative to the first group was computed.ResultsThe mean kurtosis (MK), axial kurtosis (Ka), radial kurtosis (Kr), and fractional anisotropy (FA) values showed positive correlations, whereas mean diffusion (MD), axial diffusion (Da), and radial diffusion (Dr) values showed negative correlations with the age at the time of brain MRI acquisition. The absolute correlation coefficients between MK values of almost all ROIs (except genu of the corpus callosum and frontal white matter) and the age at the time of brain MRI acquisition were greater than other metrics. The kurtosis parameters and FA values of central white matter were significantly higher than that of peripheral white matter, whereas the MD and Dr values were significantly lower than that of peripheral white matter. The MK value of the posterior limb of the internal capsule was the highest among the white matter areas. The FA value of the splenium of the corpus callosum was significantly higher than that of the other white matter areas. The kurtosis parameters and FA values of globus pallidus and thalamus were significantly higher than those of the caudate nucleus and putamen, whereas the Da and Dr values of globus pallidus and thalamus were significantly lower than those of the caudate nucleus and putamen. The relative change rates of kurtosis parameters and FA values of all ROIs were greater than those of MD, Da, and Dr values. The amplitude of MK values of almost all ROIs (except for the genu of the corpus callosum and central white matter of the centrum semiovale level) was greater than that of other metrics. The relative change rates of the Kr values of most ROIs were greater than those of the Ka value, and the relative change rates of the Dr values of most ROIs were greater than those of the Da value.ConclusionDKI parameters showed potential advantages in detecting the changes in brain microstructure during neonatal brain development

    Pleiotropic effects of the twin-arginine translocation system on biofilm formation, colonization, and virulence in Vibrio cholerae

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    <p>Abstract</p> <p>Background</p> <p>The Twin-arginine translocation (Tat) system serves to translocate folded proteins, including periplasmic enzymes that bind redox cofactors in bacteria. The Tat system is also a determinant of virulence in some pathogenic bacteria, related to pleiotropic effects including growth, motility, and the secretion of some virulent factors. The contribution of the Tat pathway to <it>Vibrio cholerae </it>has not been explored. Here we investigated the functionality of the Tat system in <it>V. cholerae</it>, the etiologic agent of cholera.</p> <p>Results</p> <p>In <it>V. cholerae</it>, the <it>tatABC </it>genes function in the translocation of TMAO reductase. Deletion of the <it>tatABC </it>genes led to a significant decrease in biofilm formation, the ability to attach to HT-29 cells, and the ability to colonize suckling mouse intestines. In addition, we observed a reduction in the output of cholera toxin, which may be due to the decreased transcription level of the toxin gene in <it>tatABC </it>mutants, suggesting an indirect effect of the mutation on toxin production. No obvious differences in flagellum biosynthesis and motility were found between the <it>tatABC </it>mutant and the parental strain, showing a variable effect of Tat in different bacteria.</p> <p>Conclusion</p> <p>The Tat system contributes to the survival of <it>V. cholerae </it>in the environment and <it>in vivo</it>, and it may be associated with its virulence.</p

    Arranging Small Molecules with Subnanometer Precision on DNA Origami Substrates for the Single‐Molecule Investigation of Protein–Ligand Interactions

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    DNA origami nanostructures are versatile substrates for the single‐molecule investigation of biomolecular interactions as they enable the display of molecular species in complex arrangements. Herein, the fundamental limitations of this approach are explored by displaying pairs of small‐molecule ligands of the protein trypsin on DNA origami substrates and adjusting their ligand–ligand spacing with subnanometer precision. Bidentate binding of trypsin to the ligand pairs is investigated by atomic force microscopy (AFM), microscale thermophoresis (MST), and molecular dynamics simulations. Bidentate trypsin binding is strongly affected by the distance of the ligand pairs and the accessibility of the protein's binding pockets. MST cannot resolve the differences in bidentate trypsin binding because of the nonspecific binding of trypsin to the DNA origami substrates, rendering the AFM‐based single‐molecule detection of binding events superior to ensemble measurements. Finally, even monodentate binding to a single ligand may be affected by subnanometer variations in its position, highlighting the importance of local microenvironments that vary even over molecular distances. While this single‐molecule approach can provide viable information on the effects of ligand arrangements on bidentate protein binding, in‐depth investigations into the nature of local microenvironments will be required to exploit its full potential

    Evaluation of the CropSyst Model during Wheat-Maize Rotations on the North China Plain for Identifying Soil Evaporation Losses

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    The North China Plain (NCP) is a major grain production zone that plays a critical role in ensuring China's food supply. Irrigation is commonly used during grain production; however, the high annual water deficit [precipitation (P) minus evapotranspiration (ET)] in typical irrigated cropland does not support double cropping systems (such as maize and wheat) and this has resulted in the steep decline in the water table (~0.8 m year−1 at the Luancheng station) that has taken place since the 1970s. The current study aimed to adapt and check the ability of the CropSyst model (Suite-4) to simulate actual evapotranspiration (ETa), biomass, and grain yield, and to identify major evaporation (E) losses from winter wheat (WW) and summer maize (SM) rotations. Field experiments were conducted at the Luancheng Agro-ecosystem station, NCP, in 2010–2011 to 2012–2013. The CropSyst model was calibrated on wheat/maize (from weekly leaf area/biomass data available for 2012–2013) and validated onto measured ETa, biomass, and grain yield at the experimental station from 2010–2011 to 2011–2012, by using model calibration parameters. The revalidation was performed with the ETa, biomass, grain yield, and simulated ETa partition for 2008–2009 WW [ETa partition was measured by the Micro-lysimeter (MLM) and isotopes approach available for this year]. For the WW crop, E was 30% of total ETa; but from 2010–11 to 2013, the annual average E was ~40% of ETa for the WW and SM rotation. Furthermore, the WW and SM rotation from 2010–2011 to 2012–2013 was divided into three growth periods; (i) pre-sowing irrigation (PSI; sowing at field capacity) to emergence period (EP), (ii) EP to canopy cover period (CC) and (iii) CC to harvesting period (HP), and E from each growth period was ~10, 60, and 30%, respectively. In general, error statistics such as RMSE, Willmott's d, and NRMSE in the model evaluation for wheat ETa (maize ETa) were 38.3 mm, 0.81, and 9.24% (31.74 mm, 0.73, and 11.89%); for wheat biomass (maize biomass) they were 1.25 Mg ha−1, 0.83, and 9.64% (0.78 Mg ha−1, 0.96, and 7.96%); and for wheat grain yield (maize grain yield) they were 0.65 Mg ha−1, 0.82, and 9.87% (0.2 Mg ha−1, 0.99, and 3.79%). The results showed that CropSyst is a valid model that can be use with a reliable degree of accuracy for optimizing WW and SM grain yield production and water requirement on the NCP
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