scholarly journals A novel universal nano-luciferase-involved reporter system for long-term probing food-borne probiotics and pathogenic bacteria in mice by in situ bioluminescence imaging

RSC Advances ◽  
2020 ◽  
Vol 10 (22) ◽  
pp. 13029-13036 ◽  
Author(s):  
Ning Zhao ◽  
Jing-Min Liu ◽  
Shuang Liu ◽  
Xue-Meng Ji ◽  
Huan Lv ◽  
...  
Keyword(s):  
Experimental Design ◽  
Pathogenic Bacteria ◽  
Bioluminescence Imaging ◽  
Reporter System ◽  
Bioluminescent Bacteria ◽  
Foodborne Bacteria ◽  
Food Borne

Schematic illustration of the preparation of bioluminescent bacteria and the experimental design of tracing of the foodborne bacteria in vivo.

scholarly journals Long-term evolution of antibiotic persistence in P. aeruginosa lung infections

2021 ◽  
Author(s):  
Melanie Ghoul ◽  
Sandra B Andersen ◽  
Helle Krogh Johansen ◽  
Lars Jelsbak ◽  
Søren Molin ◽  
...  
Keyword(s):  
Pathogenic Bacteria ◽  
Resistance Mechanisms ◽  
Term Evolution ◽  
Bacterial Clone ◽  
Evolution Of Resistance ◽  
Lung Infections

Pathogenic bacteria respond to antibiotic pressure with the evolution of resistance but survival can also depend on their ability to tolerate antibiotic treatment, known as persistence. While a variety of resistance mechanisms and underlying genetics are well characterised in vitro and in vivo, the evolution of persistence, and how it interacts with resistance in situ is less well understood. We assayed for persistence and resistance with three clinically relevant antibiotics: meropenem, ciprofloxacin and tobramycin, in isolates of Pseudomonas aeruginosa from chronic cystic fibrosis lung infections spanning up to forty years of evolution. We find evidence that persistence is under positive selection in the lung and that it can particularly act as an evolutionary stepping stone to resistance. However, this pattern is not universal and depends on the bacterial clone type and antibiotic used, indicating an important role for antibiotic mode of action.

scholarly journals The neutrophil-mobilizing cytokine interleukin-26 in the airways of long-term tobacco smokers

2018 ◽  
Vol 132 (9) ◽  
pp. 959-983 ◽  
Author(s):  
Karlhans Fru Che ◽  
Ellen Tufvesson ◽  
Sara Tengvall ◽  
Elisa Lappi-Blanco ◽  
Riitta Kaarteenaho ◽  
...  
Keyword(s):  
Gene Expression ◽  
Chronic Bronchitis ◽  
Pathogenic Bacteria ◽  
Cell Model ◽  
Water Soluble ◽  
Chronic Obstructive ◽  
Neutrophil Accumulation

Long-term tobacco smokers with chronic obstructive pulmonary disease (COPD) or chronic bronchitis display an excessive accumulation of neutrophils in the airways; an inflammation that responds poorly to established therapy. Thus, there is a need to identify new molecular targets for the development of effective therapy. Here, we hypothesized that the neutrophil-mobilizing cytokine interleukin (IL)-26 (IL-26) is involved in airway inflammation amongst long-term tobacco smokers with or without COPD, chronic bronchitis or colonization by pathogenic bacteria. By analyzing bronchoalveolar lavage (BAL), bronchail wash (BW) and induced sputum (IS) samples, we found increased extracellular IL-26 protein in the airways of long-term smokers in vivo without further increase amongst those with clinically stable COPD. In human alveolar macrophages (AM) in vitro, the exposure to water-soluble tobacco smoke components (WTC) enhanced IL-26 gene and protein. In this cell model, the same exposure increased gene expression of the IL-26 receptor complex (IL10R2 and IL20R1) and nuclear factor κ B (NF-κB); a proven regulator of IL-26 production. In the same cell model, recombinant human IL-26 in vitro caused a concentration-dependent increase in the gene expression of NF-κB and several pro-inflammatory cytokines. In the long-term smokers, we also observed that extracellular IL-26 protein in BAL samples correlates with measures of lung function, tobacco load, and several markers of neutrophil accumulation. Extracellular IL-26 was further increased in long-term smokers with exacerbations of COPD (IS samples), with chronic bronchitis (BAL samples ) or with colonization by pathogenic bacteria (IS and BW samples). Thus, IL-26 in the airways emerges as a promising target for improving the understanding of the pathogenic mechanisms behind several pulmonary morbidities in long-term tobacco smokers.

scholarly journals Mouse model of chronic post-arthroplasty infection: Noninvasive in vivo bioluminescence imaging to monitor bacterial burden for long-term study

2011 ◽  
Vol 30 (3) ◽  
pp. 335-340 ◽  
Author(s):  
Jonathan R. Pribaz ◽  
Nicholas M. Bernthal ◽  
Fabrizio Billi ◽  
John S. Cho ◽  
Romela Irene Ramos ◽  
...  
Keyword(s):  
Mouse Model ◽  
Bioluminescence Imaging ◽  
Bacterial Burden ◽  
Term Study ◽  
Long Term Study ◽  
In Vivo Bioluminescence Imaging

The Primary Investigation on Biological Effect of Mesoporous Bioactive Glass In Vivo

2013 ◽  
Vol 750-752 ◽  
pp. 1651-1655
Author(s):  
Bai Yan Sui ◽  
Cheng Tie Wu ◽  
Jiao Sun
Keyword(s):  
Bioactive Glass ◽  
Biological Effect ◽  
Degradation Products ◽  
Long Term Effect ◽  
Liver And Kidney ◽  
Mesoporous Bioactive Glass

Mesoporous bioactive glass (MBG) has superior bioactivity and degradation than non-mesoporous bioactive glass (BG) in vitro. But the biological effect of MBG in vivo is still unknown. In this study, MBG powders with 20μm were implanted into the femoral condyles in SD rats. BG powders with 20μm were used as a control. The local degradation and osteogenesis were observed at 1 week and 4 weeks after implantation, and the systemic toxicity of the degradation products were also evaluated simultaneously. The results revealed MBG powders had the faster rate of degradation and better osteogenesis effect than BG powders at 4 weeks, although the most of material still remained in situ. Histopathological analyses indicated the degradation products did not have any damage to major organs such as liver and kidney. In conclusion, this preliminary study demonstrated that MBG powders have more excellent biological effect at 4 weeks than that of BG in vivo. However the long-term effect needs to be confirmed.

scholarly journals Long‐term in vivo monitoring of transcription factor (TF) activation in cardiovascular (CV) control regions of mouse brain using bioluminescence imaging (BLI)

2007 ◽  
Vol 21 (6) ◽  
Author(s):  
David W Infanger ◽  
Jeffrey R Peterson ◽  
Ram V Sharma ◽  
Robin L Davisson
Keyword(s):  
Transcription Factor ◽  
Mouse Brain ◽  
Bioluminescence Imaging ◽  
In Vivo Monitoring ◽  
Control Regions

Visualization of in situ hydrogels by MRI in vivo

2016 ◽  
Vol 4 (7) ◽  
pp. 1343-1353 ◽  
Author(s):  
Jia Liu ◽  
Ke Wang ◽  
Jie Luan ◽  
Zhi Wen ◽  
Lei Wang ◽  
...  

Chitosan and PEG-based self-healable in situ hydrogel developed as a long-term MRI reporter.

scholarly journals A Liquid Hydrogel to Restore Long Term Corneal Integrity After Perforating and Non-Perforating Trauma in Feline Eyes

2021 ◽  
Vol 9 ◽  
Author(s):  
Alejandro Juarez ◽  
Mohamed Djallali ◽  
Marilyse Piché ◽  
Mathieu Thériault ◽  
Marc Groleau ◽  
...  
Keyword(s):  
Corneal Transplantation ◽  
Specular Microscopy ◽  
Slit Lamp ◽  
Cyanoacrylate Glue ◽  
Promising Alternative ◽  
A Cell ◽  
Feline Model

Purpose: To evaluate long-term in vivo functionality of corneas regenerated using a cell-free, liquid hydrogel filler (LiQD Cornea) after deep corneal trauma in the feline model.Methods: Two healthy cats underwent 4 mm diameter stepwise 250/450 µm deep surgical corneal ablation with and without needle perforation. The filler comprising 10% (w/w) collagen-like peptide conjugated to polyethylene glycol (CLP-PEG) and 1% fibrinogen and crosslinked with 2% (w/w) 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMTMM), was applied to the wound bed previously coated with thrombin (250 U/ml). In situ gelation occurred within 5 min, and a temporary tarsorrhaphy was performed. Eyes were examined weekly for 1 month, then monthly over 12 months. Outcome parameters included slit-lamp, Scheimpflug tomography, optical coherence tomography, confocal and specular microscopy, and immunohistochemistry studies.Results: The gelled filler was seamlessly incorporated, supporting smooth corneal re-epithelialization. Progressive in-growth of keratocytes and nerves into the filler corresponding to the mild haze observed faded with time. The regenerated neo-cornea remained stably integrated throughout the 12 months, without swelling, inflammation, infection, neovascularization, or rejection. The surrounding host stroma and endothelium remained normal at all times. Tomography confirmed restoration of a smooth surface curvature.Conclusion: Biointegration of this hydrogel filler allowed stable restoration of corneal shape and transparency in the feline model, with less inflammation and no neovascularization compared to previous reports in the minipig and rabbit models. It offers a promising alternative to cyanoacrylate glue and corneal transplantation for ulcerated and traumatized corneas in human patients.

scholarly journals Acellular Small-Diameter Tissue-Engineered Vascular Grafts

2019 ◽  
Vol 9 (14) ◽  
pp. 2864 ◽  
Author(s):  
Zhen Li ◽  
Xinda Li ◽  
Tao Xu ◽  
Lei Zhang
Keyword(s):  
Effective Means ◽  
Vascular Grafts ◽  
Small Diameter ◽  
Test Results ◽  
In Vivo Test ◽  
Current State

Tissue-engineered vascular grafts (TEVGs) are considered one of the most effective means of fabricating vascular grafts. However, for small-diameter TEVGs, there are ongoing issues regarding long-term patency and limitations related to long-term in vitro culture and immune reactions. The use of acellular TEVG is a more convincing method, which can achieve in situ blood vessel regeneration and better meet clinical needs. This review focuses on the current state of acellular TEVGs based on scaffolds and gives a summary of the methodologies and in vitro/in vivo test results related to acellular TEVGs obtained in recent years. Various strategies for improving the properties of acellular TEVGs are also discussed.

Kiwifruit-like Persistent Luminescent Nanoparticles with High-Performance and in Situ Activable Near-Infrared Persistent Luminescence for Long-Term in Vivo Bioimaging

2017 ◽  
Vol 9 (47) ◽  
pp. 41181-41187 ◽  
Author(s):  
Xia-Hui Lin ◽  
Liang Song ◽  
Shan Chen ◽  
Xiao-Feng Chen ◽  
Jing-Jing Wei ◽  
...  
Keyword(s):  
High Performance ◽  
Near Infrared ◽  
Persistent Luminescence ◽  
Luminescent Nanoparticles

scholarly journals Bioinspired Design of Sericin/Chitosan/Ag@MOF/GO Hydrogels for Efficiently Combating Resistant Bacteria, Rapid Hemostasis, and Wound Healing

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2812
Author(s):  
Meng Zhang ◽  
Dong Wang ◽  
Nana Ji ◽  
Shaoxiang Lee ◽  
Guohui Wang ◽  
...  
Keyword(s):  
Wound Healing ◽  
Pathogenic Bacteria ◽  
Antibacterial Properties ◽  
Resistant Bacteria ◽  
High Porosity ◽  
Drug Resistant ◽  
In Vivo Evaluation

Due to the spread of drug-resistant bacteria in hospitals, the development of antibacterial dressings has become a strategy to control wound infections caused by bacteria. Here, we reported a green strategy for in situ biomimetic syntheses of silver nanoparticles@organic frameworks/graphene oxide (Ag@MOF–GO) in sericin/chitosan/polyvinyl alcohol hydrogel. Ag@MOF–GO was synthesized in situ from the redox properties of tyrosine residues in silk sericin without additional chemicals, similar to a biomineralization process. The sericin/chitosan/Ag@MOF–GO dressing possessed a high porosity, good water retention, and a swelling ratio. The hemolysis rate of the composite was 3.9% and the cell viability rate was 131.2%, which indicated the hydrogel possessed good biocompatibility. The composite also showed excellent lasting antibacterial properties against drug-sensitive and drug-resistant pathogenic bacteria. The composite possessed excellent hemostatic activity. The coagulation effect of the composite may be related to its effect on the red blood cells and platelets, but it has nothing to do with the activation of coagulation factors. An in vitro cell migration assay confirmed and an in vivo evaluation of mice indicated that the composite could accelerate wound healing and re-epithelialization. In summary, the composite material is an ideal dressing for accelerating hemostasis, preventing bacterial infection, and promoting wound healing.

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