34 research outputs found
Upregulation of the Adhesin Gene EPA1 Mediated by PDR1 in Candida glabrata Leads to Enhanced Host Colonization.
Candida glabrata is the second most common Candida species causing disseminated infection, after C. albicans. C. glabrata is intrinsically less susceptible to the widely used azole antifungal drugs and quickly develops secondary resistance. Resistance typically relies on drug efflux with transporters regulated by the transcription factor Pdr1. Gain-of-function (GOF) mutations in PDR1 lead to a hyperactive state and thus efflux transporter upregulation. Our laboratory has characterized a collection of C. glabrata clinical isolates in which azole resistance was found to correlate with increased virulence in vivo. Contributing phenotypes were the evasion of adhesion and phagocytosis by macrophages and an increased adhesion to epithelial cells. These phenotypes were found to be dependent on PDR1 GOF mutation and/or C. glabrata strain background. In the search for the molecular effectors, we found that PDR1 hyperactivity leads to overexpression of specific cell wall adhesins of C. glabrata. Further study revealed that EPA1 regulation, in particular, explained the increase in adherence to epithelial cells. Deleting EPA1 eliminates the increase in adherence in an in vitro model of interaction with epithelial cells. In a murine model of urinary tract infection, PDR1 hyperactivity conferred increased ability to colonize the bladder and kidneys in an EPA1-dependent way. In conclusion, this study establishes a relationship between PDR1 and the regulation of cell wall adhesins, an important virulence attribute of C. glabrata. Furthermore, our data show that PDR1 hyperactivity mediates increased adherence to host epithelial tissues both in vitro and in vivo through upregulation of the adhesin gene EPA1. IMPORTANCE Candida glabrata is an important fungal pathogen in human diseases and is also rapidly acquiring drug resistance. Drug resistance can be mediated by the transcriptional activator PDR1, and this results in the upregulation of multidrug transporters. Intriguingly, this resistance mechanism is associated in C. glabrata with increased virulence in animal models and also with increased adherence to specific host cell types. The C. glabrata adhesin gene EPA1 is a major contributor of virulence and adherence to host cells. Here, we show that EPA1 expression is controlled by PDR1 independently of subtelomeric silencing, a known EPA1 regulation mechanism. Thus, a relationship exists between PDR1, EPA1 expression, and adherence to host cells, which is critical for efficient virulence. Our results demonstrate that acquisition of drug resistance is beneficial for C. glabrata in fungus-host relationships. These findings further highlight the challenges of the therapeutic management of C. glabrata infections in human patients
Global disparities in surgeonsâ workloads, academic engagement and rest periods: the on-calL shIft fOr geNEral SurgeonS (LIONESS) study
: The workload of general surgeons is multifaceted, encompassing not only surgical procedures but also a myriad of other responsibilities. From April to May 2023, we conducted a CHERRIES-compliant internet-based survey analyzing clinical practice, academic engagement, and post-on-call rest. The questionnaire featured six sections with 35 questions. Statistical analysis used Chi-square tests, ANOVA, and logistic regression (SPSSŸ v. 28). The survey received a total of 1.046 responses (65.4%). Over 78.0% of responders came from Europe, 65.1% came from a general surgery unit; 92.8% of European and 87.5% of North American respondents were involved in research, compared to 71.7% in Africa. Europe led in publishing research studies (6.6 ± 8.6 yearly). Teaching involvement was high in North America (100%) and Africa (91.7%). Surgeons reported an average of 6.7 ± 4.9 on-call shifts per month, with European and North American surgeons experiencing 6.5 ± 4.9 and 7.8 ± 4.1 on-calls monthly, respectively. African surgeons had the highest on-call frequency (8.7 ± 6.1). Post-on-call, only 35.1% of respondents received a day off. Europeans were most likely (40%) to have a day off, while African surgeons were least likely (6.7%). On the adjusted multivariable analysis HDI (Human Development Index) (aOR 1.993) hospital capacity > 400 beds (aOR 2.423), working in a specialty surgery unit (aOR 2.087), and making the on-call in-house (aOR 5.446), significantly predicted the likelihood of having a day off after an on-call shift. Our study revealed critical insights into the disparities in workload, access to research, and professional opportunities for surgeons across different continents, underscored by the HDI
Ăvaluation des greffons rĂ©naux avant la transplantation; une mise au point sur la situation actuelle et les mĂ©thodes Ă©mergentes
Le manque de greffons rĂ©naux adĂ©quats amĂšne Ă une augmentation du nombre de patients sur liste dâattente de transplantation. A ce jour, aucun processus dâĂ©valuation universel ne permet de prĂ©dire avec une fiabilitĂ© suffisante lâissue favorable de ces transplants. Les mĂ©thodes Ă©tablies comme lâĂ©valuation histologique, les scores cliniques et les techniques de perfusion offrent une prĂ©diction relativement fiable du retard du fonctionnement du greffon, mais ne sont pas systĂ©matiquement capables de prĂ©dire la survie dâun greffon. Les techniques Ă©mergentes comme les marqueurs molĂ©culaires, les nouvelles techniques dâimagerie et la perfusion des organes normothermique offrent des approches innovatrices tout en permettant dâidentifier des cibles dâinterventions thĂ©rapeutiques. Cependant, les Ă©tudes rigoureuses sur le sujet font dĂ©fauts et ces nouvelles mĂ©thodes nĂ©cessitent dâĂȘtre validĂ©es. Le but ultime Ă©tant que ces nouvelles approches permettent de diminuer le taux dâorganes non-utilisĂ©s tout en amĂ©liorant la finesse dans lâĂ©tablissement dâun pronostic pour les greffons rĂ©naux
Impact of maternal obesity on the gut microbiome, chronic liver disease and hepatocellular carcinoma in the offspring
LâĂ©pidĂ©mie dâobĂ©sitĂ© reprĂ©sente un enjeu de santĂ© majeur. Les femmes en Ăąge de procrĂ©er sont particuliĂšrement touchĂ©es. Lâobjectif de cette thĂšse est de comprendre lâimpact de lâobĂ©sitĂ© maternelle sur le risque de dĂ©velopper une maladie hĂ©patique. Nous avons dĂ©montrĂ© que lâobĂ©sitĂ© maternelle entraĂźnait de profonds changements de lâexpression des gĂšnes hĂ©patiques. Nous avons constatĂ© une association entre lâobĂ©sitĂ© maternelle et des taux plus Ă©levĂ©s de stĂ©atose, fibrose et dâinflammation. La descendance des mĂšres obĂšses prĂ©sente Ă©galement un risque plus Ă©levĂ© de dĂ©velopper des tumeurs hĂ©patiques. Les modifications du microbiome intestinal de la progĂ©niture des souris obĂšses sont conservĂ©es Ă lâĂąge adulte. En restaurant un microbiome normal, nous avons pu rĂ©duire le risque de dĂ©velopper un cancer du foie. Ces observations mettent en Ă©vidence le rĂŽle clĂ© du microbiome intestinal dans la transmission des maladies du foie de la mĂšre Ă lâenfant, et ouvrent la voie vers le dĂ©veloppement de thĂ©rapies.The obesity epidemic represents a major challenge to our health systems. Women of childbearing age are particularly affected. Overweight and obesity have a multitude of adverse health effects and can lead to chronic liver disease and liver cancer. In addition, maternal obesity is associated with metabolic disorders in children, and an increased rate of childhood cancers. Obesity alters the composition of the gut microbiome, which contributes to the progression of chronic liver disease and is passed on to the next generation. The objective of this thesis is to understand the impact of maternal obesity on the risk of developing chronic liver disease and liver cancer in children, and the role of the microbiome in this context. We have demonstrated, in a mouse model, that maternal obesity leads to profound changes in gene expression in their offspring. We observed that signaling pathways of the innate immune system and the cell cycle are altered, and that genes important for the development of chronic liver diseases are dysregulated. In addition, we found that maternal obesity leads to higher rates of steatosis, fibrosis and inflammation in adult offspring of obese mothers. The offspring of obese mothers also have a significantly higher risk of developing liver tumors. The gut microbiome of offspring of obese mouse mothers is altered and these alterations are retained into adulthood. By restoring a normal microbiome, we were able to normalize the next generation's risk of developing liver cancer. This highlights the key role of the gut microbiome and its alterations in the transmission of liver disease from mother to child, and paves the way for the development of a future therapy
Commentary: Insulin-Producing Organoids Engineered From Islet and Amniotic Epithelial Cells to Treat Diabetes
A Commentary on : "Insulin-Producing Organoids Engineered from Islet and Amniotic Epithelial Cells to Treat Diabetes" By Lebreton F, Lavallard V, Bellofatto K, Bonnet R, Wassmer CH, Perez L, Kalandadze V, Follenzi A, Boulvain M, Kerr-Conte J, Goodman DJ, Bosco D, Berney T, Berishvili E. Nat Commun. (2019). 10(1):4491. doi: 10.1038/s41467-019-12472-3
FGF21 negatively affects long-term female fertility in mice
AbstractIn this project we studied the impact of subcutaneously administered recombinant FGF21 on the female fertility in a murine model.
DOI:https://doi.org/10.1016/j.heliyon.2022.e1149
Impact of Maternal Obesity on Liver Disease in the Offspring - Biomedicines - 2022
AbstractSources data of the publication doi: 10.3390/biomedicines10020294
A Comprehensive Transcriptomic Analysis and Confirmation of Results in a Murine Mode
Evolution of the Surgical Residency System in Switzerland: An In-Depth Analysis Over 15Â Years
Background: The landscape of surgical training has been subject to many changes over the past 15 years. This study examines resident satisfaction, determinants of satisfaction, demographics, working hours and the teaching rate of common operations in a longitudinal fashion with the aim to identify trends, shortcomings and possible ways to improve the current training system.
Methods: The Swiss Medical Association administers an annual survey to all Swiss residents to evaluate the quality of postgraduate medical training (yearly respondents: 687-825, response rate: 68-72%). Teaching rates for general surgical procedures were obtained from the Swiss association for quality management in surgery.
Results: During the study period (2003-2018), the number of surgical residents (408-655 (+61%)) and graduates in general surgery per year (42-63 (+50%)) increased disproportionately to the Swiss population. While the 52 working hour restriction was introduced in 2005 reported average weekly working hours did not decline (59.9-58.4 h (-3%)). Workplace satisfaction (6 being highest) rose from 4.3 to 4.6 (+7%). Working climate and leadership culture were the main determinants for resident satisfaction. The proportion of taught basic surgical procedures fell from 24.6 to 18.9% (-23%).
Conclusions: The number of residents and graduates in general surgery has risen markedly. At the same time, the proportion of taught operations is diminishing. Despite the introduction of working hour restrictions, the self-reported hours never reached the limit. The low teaching rate combined with the increasing resident number represents a major challenge to the maintenance of the current training quality
Timing of surgical repair of bile duct injuries after laparoscopic cholecystectomy: A systematic review
Background: The surgical management of bile duct injuries (BDIs) after laparoscopic cholecystectomy (LC) is challenging and the optimal timing of surgery remains unclear. The primary aim of this study was to systematically evaluate the evidence behind the timing of BDI repair after LC in the literature. Aim: To assess timing of surgical repair of BDI and postoperative complications. Methods: The MEDLINE, EMBASE, and The Cochrane Library databases were systematically screened up to August 2021. Risk of bias was assessed via the Newcastle Ottawa scale. The primary outcomes of this review included the timing of BDI repair and postoperative complications. Results: A total of 439 abstracts were screened, and 24 studies were included with 15609 patients included in this review. Of the 5229 BDIs reported, 4934 (94%) were classified as major injury. Timing of bile duct repair was immediate (14%, n = 705), early (28%, n = 1367), delayed (28%, n = 1367), or late (26%, n = 1286). Standardization of definition for timing of repair was remarkably poor among studies. Definitions for immediate repair ranged from < 24 h to 6 wk after LC while early repair ranged from < 24 h to 12 wk. Likewise, delayed (> 24 h to > 12 wk after LC) and late repair (> 6 wk after LC) showed a broad overlap. Conclusion: The lack of standardization among studies precludes any conclusive recommendation on optimal timing of BDI repair after LC. This finding indicates an urgent need for a standardized reporting system of BDI repair