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181.
Erin P. Price Derek S. Sarovich Emma J. Smith Barbara MacHunter Glenda Harrington Vanessa Theobald Carina M. Hall Heidie M. Hornstra Evan McRobb Yuwana Podin Mark Mayo Jason W. Sahl David M. Wagner Paul Keim Mirjam Kaestli Bart J. Currie 《Applied and environmental microbiology》2016,82(3):954-963
Melioidosis is a disease of humans and animals that is caused by the saprophytic bacterium Burkholderia pseudomallei. Once thought to be confined to certain locations, the known presence of B. pseudomallei is expanding as more regions of endemicity are uncovered. There is no vaccine for melioidosis, and even with antibiotic administration, the mortality rate is as high as 40% in some regions that are endemic for the infection. Despite high levels of recombination, phylogenetic reconstruction of B. pseudomallei populations using whole-genome sequencing (WGS) has revealed surprisingly robust biogeographic separation between isolates from Australia and Asia. To date, there have been no confirmed autochthonous melioidosis cases in Australia caused by an Asian isolate; likewise, no autochthonous cases in Asia have been identified as Australian in origin. Here, we used comparative genomic analysis of 455 B. pseudomallei genomes to confirm the unprecedented presence of an Asian clone, sequence type 562 (ST-562), in Darwin, northern Australia. First observed in Darwin in 2005, the incidence of melioidosis cases attributable to ST-562 infection has steadily risen, and it is now a common strain in Darwin. Intriguingly, the Australian ST-562 appears to be geographically restricted to a single locale and is genetically less diverse than other common STs from this region, indicating a recent introduction of this clone into northern Australia. Detailed genomic and epidemiological investigations of new clinical and environmental B. pseudomallei isolates in the Darwin region and ST-562 isolates from Asia will be critical for understanding the origin, distribution, and dissemination of this emerging clone in northern Australia. 相似文献
182.
Anisimov SV Christophersen NS Correia AS Hall VJ Sandelin I Li JY Brundin P 《Cellular & molecular biology letters》2011,16(1):79-88
The majority of human embryonic stem cell lines depend on a feeder cell layer for continuous growth in vitro, so that they can remain in an undifferentiated state. Limited knowledge is available concerning the molecular mechanisms
that underlie the capacity of feeder cells to support both the proliferation and pluripotency of these cells. Importantly,
feeder cells generally lose their capacity to support human embryonic stem cell proliferation in vitro following long-term culture. In this study, we performed large-scale gene expression profiles of human foreskin fibroblasts
during early, intermediate and late passages using a custom DNA microarray platform (NeuroStem 2.0 Chip). The microarray data
was validated using RT-PCR and virtual SAGE analysis. Our comparative gene expression study identified a limited number of
molecular targets potentially involved in the ability of human neonatal foreskin fibroblasts to serve as feeder cells for
human embryonic stem cell cultures. Among these, the C-KIT, leptin and pigment epithelium-derived factor (PEDF) genes were
the most interesting candidates. 相似文献
183.
Gomes CC Moreira LM Santos VJ Ramos AS Lyon JP Soares CP Santos FV 《Genetics and molecular biology》2011,34(1):116-121
The use of artificial implants provides a palliative or permanent solution for individuals who have lost some bodily function through disease, an accident or natural wear. This functional loss can be compensated for by the use of medical devices produced from special biomaterials. Titanium alloy (Ti-6Al-4V) is a well-established primary metallic biomaterial for orthopedic implants, but the toxicity of the chemical components of this alloy has become an issue of concern. In this work, we used the MTT assay and micronucleus assay to examine the cytotoxicity and genotoxicity, respectively, of an extract obtained from this alloy. The MTT assay indicated that the mitochondrial activity and cell viability of CHO-K1 cells were unaffected by exposure to the extract. However, the micronucleus assay revealed DNA damage and an increase in micronucleus frequency at all of the concentrations tested. These results show that ions released from Ti-6Al-4V alloy can cause DNA and nuclear damage and reinforce the importance of assessing the safety of metallic medical devices constructed from biomaterials. 相似文献
184.
Vanessa Zavatti Hector Budman Raymond Legge Melih Tamer 《Bioprocess and biosystems engineering》2016,39(6):855-869
Fluorescence spectroscopy in combination with multivariate statistical methods was employed as a tool for monitoring the manufacturing process of pertactin (PRN), one of the virulence factors of Bordetella pertussis utilized in whopping cough vaccines. Fluorophores such as amino acids and co-enzymes were detected throughout the process. The fluorescence data collected at different stages of the fermentation and purification process were treated employing principal component analysis (PCA). Through PCA, it was feasible to identify sources of variability in PRN production. Then, partial least square (PLS) was employed to correlate the fluorescence spectra obtained from pure PRN samples and the final protein content measured by a Kjeldahl test from these samples. In view that a statistically significant correlation was found between fluorescence and PRN levels, this approach could be further used as a method to predict the final protein content. 相似文献
185.
Nicolas Fossat Tania Radziewic Vanessa Jones Karin Tourle Patrick P. L. Tam 《Genesis (New York, N.Y. : 2000)》2016,54(3):115-122
Rbm47 encodes a RNA binding protein that is necessary for Cytidine to Uridine RNA editing. Rbm47gt/gt mutant mice that harbor inactivated Rbm47 display poor viability. Here it was determined that the loss of Rbm47gt/gt offspring is due to embryonic lethality at mid‐gestation. It was further showed that growth of the surviving Rbm47gt/gt mutants is impaired. Rbm47 is expressed in both the visceral endoderm and the definitive endoderm. Using the utility of the switchable FlEx gene‐trap cassette and the activity of Cre and FLP recombinases to generate mice that conditionally inactivate and restore Rbm47 function in tissue‐specific manner, it was demonstrated that Rbm47 function is required in the embryo proper, and not the visceral endoderm, for viability and growth. genesis 54:115–122, 2016. © 2016 Wiley Periodicals, Inc. 相似文献
186.
Vasopressin activates Akt/mTOR pathway in smooth muscle cells cultured in high glucose concentration
Daniela K. Montes Marianne Brenet Vanessa C. Muñoz Patricia V. Burgos Carolina I. Villanueva Carlos D. Figueroa Carlos B. González 《Biochemical and biophysical research communications》2013
Mammalian target of rapamycin (mTOR) complex is a key regulator of autophagy, cell growth and proliferation. Here, we studied the effects of arginine vasopressin (AVP) on mTOR activation in vascular smooth muscle cells cultured in high glucose concentration. 相似文献
187.
188.
Gabriel Capella Machado Daniela Vanessa Moris Thales Domingos Arantes Luciane Regina Franciscone Silva Raquel Cordeiro Theodoro Rinaldo P?ncio Mendes Adriana Pardini Vicentini Eduardo Bagagli 《Memórias do Instituto Oswaldo Cruz》2013,108(5):637-643
We aimed to evaluate whether the occurrence of cryptic species of
Paracoccidioides brasiliensis, S1, PS2, PS3 and
Paracoccidioides lutzii, has implications in the
immunodiagnosis of paracoccidioidomycosis (PCM). Small quantities of the antigen
gp43 were found in culture filtrates of P. lutzii strains and
this molecule appeared to be more variable within P. lutzii
because the synonymous-nonsynonymous mutation rate was lower, indicating an
evolutionary process different from that of the remaining genotypes. The
production of gp43 also varied between isolates belonging to the same species,
indicating that speciation events are important, but not sufficient to fully
explain the diversity in the production of this antigen. The culture filtrate
antigen AgEpm83, which was obtained from a PS3 isolate, showed large quantities
of gp43 and reactivity by immunodiffusion assays, similar to the standard
antigen (AgB-339) from an S1 isolate. Furthermore, AgEpm83 was capable of
serologically differentiating five serum samples from patients from the Botucatu
and Jundiaí regions. These patients had confirmed PCM but, were non-reactive to
the standard antigen, thus demonstrating an alternative for serological
diagnosis in regions in which S1 and PS2 occur. We also emphasise that it is not
advisable to use a single antigen preparation to diagnose PCM, a disease that is
caused by highly diverse pathogens. 相似文献
189.
Jamie Bryant Vanessa M McDonald Allison Boyes Rob Sanson-Fisher Christine Paul Jessica Melville 《Respiratory research》2013,14(1):109
Adherence to medication among individuals with chronic obstructive pulmonary disease (COPD) is suboptimal and has negative impacts on survival and health care costs. No systematic review has examined the effectiveness of interventions designed to improve medication adherence. Electronic databases Medline and Cochrane were searched using a combination of MeSH and keywords. Eligible studies were interventions with a primary or secondary aim to improve medication adherence among individuals with COPD published in English. Included studies were assessed for methodological quality using the Effective Practice and Organisation of Care (EPOC) criteria. Of the 1,186 papers identified, seven studies met inclusion criteria. Methodological quality of the studies was variable. Five studies identified effective interventions. Strategies included: brief counselling; monitoring and feedback about inhaler use through electronic medication delivery devices; and multi-component interventions consisting of self-management and care co-ordination delivered by pharmacists and primary care teams. Further research is needed to establish the most effective and cost effective interventions. Special attention should be given to increasing patient sample size and using a common measure of adherence to overcome methodological limitations. Interventions that involve caregivers and target the healthcare provider as well as the patient should be further explored. 相似文献
190.
Kristen L. Leslie Gyun Jee Song Stacey Barrick Vanessa L. Wehbi Jean-Pierre Vilardaga Philip M. Bauer Alessandro Bisello 《The Journal of biological chemistry》2013,288(51):36426-36436
The interaction between vascular cells and macrophages is critical during vascular remodeling. Here we report that the scaffolding protein, ezrin-binding phosphoprotein 50 (EBP50), is a central regulator of macrophage and vascular smooth muscle cells (VSMC) function. EBP50 is up-regulated in intimal VSMC following endoluminal injury and promotes neointima formation. However, the mechanisms underlying these effects are not fully understood. Because of the fundamental role that inflammation plays in vascular diseases, we hypothesized that EBP50 mediates macrophage activation and the response of vessels to inflammation. Indeed, EBP50 expression increased in primary macrophages and VSMC, and in the aorta of mice, upon treatment with LPS or TNFα. This increase was nuclear factor-κB (NF-κB)-dependent. Conversely, activation of NF-κB was impaired in EBP50-null VSMC and macrophages. We found that inflammatory stimuli promote the formation of an EBP50-PKCζ complex at the cell membrane that induces NF-κB signaling. Macrophage activation and vascular inflammation after acute LPS treatment were reduced in EBP50-null cells and mice as compared with WT. Furthermore, macrophage recruitment to vascular lesions was significantly reduced in EBP50 knock-out mice. Thus, EBP50 and NF-κB participate in a feed-forward loop leading to increased macrophage activation and enhanced response of vascular cells to inflammation. 相似文献