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Landsgaard, K.

Publications and source records attributed to Landsgaard, K..

2 recordsLinked to original sources

IN4MER Bioink: A Phosphorescent Biosensing Bio-ink for Multiple Analytes (Glucose, Lactate, Oxygen) Measurements and Temperature Sensing Applications

3D bioprinting has revolutionized tissue engineering by enabling researchers to create much more complex structures than was practical with earlier techniques. Bioprinting uses computer-controlled layer-by-layer deposition of a mixture of hydrogels and living cells and the resulting structures can mimic the complex geometries of many living tissues by incorporating multiple bioinks with varied material properties and cell populations, allowing researchers to design structures that vary not only in shape, but also in mechanical, chemical, and biological properties throughout the bioprinted construct. However, techniques for evaluating these living constructs and monitoring them over time have not yet caught up to these innovations. Here we describe a novel approach to reporting nutrient values in real-time throughout the scaffold itself, accomplished by dispersing oxygen, glucose, and lactate sensitive microspheres within bioinks. These can be noninvasively interrogated using low-cost phosphorescence lifetime readers to determine and track nutrient concentrations across our bioprinted constructs in real time. The wealth of information this technique produces suggests this may provide a powerful new tool for evaluating and designing future bioprinted constructs.

bioengineering↗

The duration of antibiotic treatment is associated with carriage of toxigenic and atoxigenic strains of Clostridioides difficile in dogs.

Clostridioides difficile is a leading cause of human antibiotic-associated diarrhoeal disease globally. Zoonotic reservoirs of infection are increasingly suspected to play a role in the emergence of this disease in the community and dogs are considered as one potential source. Here we use a canine case-control study at a referral veterinary hospital in Scotland to assess: i) the risk factors associated with carriage of C. difficile by dogs, ii) whether carriage of C. difficile is associated with clinical disease in dogs and iii) the similarity of strains isolated from dogs with local human clinical surveillance. The overall prevalence of C. difficile carriage in dogs was 18.7% (95% CI 14.8-23.2%, n=61/327) of which 36% (n=22/61) were toxigenic strains. We found risk factors related to prior antibiotic treatment were significantly associated with C. difficile carriage by dogs. However, the presence of toxigenic strains of C. difficile in a canine faecal sample was not associated with diarrhoeal disease in dogs. Active toxin was infrequently detected in canine faecal samples carrying toxigenic strains (2/11 samples). Both dogs in which active toxin was detected had no clinical evidence of gastrointestinal disease. Among the ten toxigenic ribotypes of C. difficile detected in dogs in this study, six of these (012, 014, 020, 026, 078, 106) were ribotypes commonly associated with human clinical disease in Scotland, while atoxigenic isolates largely belonged to 010 and 039 ribotypes. Whilst C. difficile does not appear commonly associated with diarrhoeal disease in dogs, antibiotic treatment increases carriage of this bacteria including toxigenic strains commonly found in human clinical disease.

microbiology↗