31 results on '"Dimopoulos, George"'
Search Results
2. Discovery of novel natural products for mosquito control
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Engdahl, Cecilia S., Tikhe, Chinmay V., and Dimopoulos, George
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- 2022
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3. Field-deployable molecular diagnostic platform for arbovirus detection in Aedes aegypti
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Rutkowski, Natalie, Dong, Yuemei, and Dimopoulos, George
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- 2020
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4. Understanding the nebulisation of antibiotics: the key role of lung microdialysis studies.
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Dhanani, Jayesh, Roberts, Jason A., Monsel, Antoine, Torres, Antoni, Kollef, Marin, Rouby, Jean-Jacques, Arvaniti, Kostoula, Assefi, Mona, Bassetti, Matteo, Blot, Stijn, Boisson, Matthieu, Bouglé, Adrien, Constantin, Jean-Michel, Dimopoulos, George, Dugernier, Jonathan, Dureau, Pauline, Felton, Timothy, Koutsoukou, Antonia, Kyriakoudi, Anna, and Laterre, Pierre-François
- Abstract
Background: Nebulisation of antibiotics is a promising treatment for ventilator-associated pneumonia (VAP) caused by multidrug-resistant organisms. Ensuring effective antibiotic concentrations at the site of infection in the interstitial space fluid is crucial for clinical outcomes. Current assessment methods, such as epithelial lining fluid and tissue homogenates, have limitations in providing longitudinal pharmacokinetic data. Main body: Lung microdialysis, an invasive research technique predominantly used in animals, involves inserting probes into lung parenchyma to measure antibiotic concentrations in interstitial space fluid. Lung microdialysis offers unique advantages, such as continuous sampling, regional assessment of antibiotic lung concentrations and avoidance of bronchial contamination. However, it also has inherent limitations including the cost of probes and assay development, the need for probe calibration and limited applicability to certain antibiotics. As a research tool in VAP, lung microdialysis necessitates specialist techniques and resource-intensive experimental designs involving large animals undergoing prolonged mechanical ventilation. However, its potential impact on advancing our understanding of nebulised antibiotics for VAP is substantial. The technique may enable the investigation of various factors influencing antibiotic lung pharmacokinetics, including drug types, delivery devices, ventilator settings, interfaces and disease conditions. Combining in vivo pharmacokinetics with in vitro pharmacodynamic simulations can become feasible, providing insights to inform nebulised antibiotic dose optimisation regimens. Specifically, it may aid in understanding and optimising the nebulisation of polymyxins, effective against multidrug-resistant Gram-negative bacteria. Furthermore, lung microdialysis holds promise in exploring novel nebulisation therapies, including repurposed antibiotic formulations, bacteriophages and immunomodulators. The technique's potential to monitor dynamic biochemical changes in pneumonia, such as cytokines, metabolites and inflammation/infection markers, opens avenues for developing theranostic tools tailored to critically ill patients with VAP. Conclusion: In summary, lung microdialysis can be a potential transformative tool, offering real-time insights into nebulised antibiotic pharmacokinetics. Its potential to inform optimal dosing regimen development based on precise target site concentrations and contribute to development of theranostic tools positions it as key player in advancing treatment strategies for VAP caused by multidrug-resistant organisms. The establishment of international research networks, exemplified by LUMINA (lung microdialysis applied to nebulised antibiotics), signifies a proactive step towards addressing complexities and promoting multicentre experimental studies in the future. [ABSTRACT FROM AUTHOR]
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- 2024
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5. Incidence and outcome of invasive candidiasis in intensive care units (ICUs) in Europe: results of the EUCANDICU project
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Bassetti, Matteo, Giacobbe, Daniele R., Vena, Antonio, Trucchi, Cecilia, Ansaldi, Filippo, Antonelli, Massimo, Adamkova, Vaclava, Alicino, Cristiano, Almyroudi, Maria-Panagiota, Atchade, Enora, Azzini, Anna M., Carannante, Novella, Carnelutti, Alessia, Corcione, Silvia, Cortegiani, Andrea, Dimopoulos, George, Dubler, Simon, García-Garmendia, José L., Girardis, Massimo, Cornely, Oliver A., Ianniruberto, Stefano, Kullberg, Bart Jan, Lagrou, Katrien, Le Bihan, Clement, Luzzati, Roberto, Malbrain, Manu L. N. G., Merelli, Maria, Marques, Ana J., Martin-Loeches, Ignacio, Mesini, Alessio, Paiva, José-Artur, Peghin, Maddalena, Raineri, Santi Maurizio, Rautemaa-Richardson, Riina, Schouten, Jeroen, Brugnaro, Pierluigi, Spapen, Herbert, Tasioudis, Polychronis, Timsit, Jean-François, Tisa, Valentino, Tumbarello, Mario, van den Berg, Charlotte H. S. B., Veber, Benoit, Venditti, Mario, Voiriot, Guillaume, Wauters, Joost, and Montravers, Philippe
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- 2019
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6. The mosquito adulticidal Chromobacterium sp. Panama causes transgenerational impacts on fitness parameters and elicits xenobiotic gene responses
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Short, Sarah M., van Tol, Sarah, Smith, Brendan, Dong, Yuemei, and Dimopoulos, George
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- 2018
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7. Colistin versus meropenem in the empirical treatment of ventilator-associated pneumonia (Magic Bullet study): An investigator-driven, open-label, randomized, noninferiority controlled trial
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Cisneros, José M, Rosso-Fernández, Clara María, Roca-Oporto, Cristina, De Pascale, Gennaro, Jiménez-Jorge, Silvia, Fernández-Hinojosa, Esteban, Matthaiou, Dimitrios K, Ramírez, Paula, Díaz-Miguel, Ramón Ortiz, Estella, Angel, Antonelli, Massimo, Dimopoulos, George, Garnacho-Montero, José, Magic Bullet Working Group WP1, and European Commission
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Male ,medicine.medical_specialty ,Multidrug-resistant bacteria ,Population ,Equivalence Trials as Topic ,Critical Care and Intensive Care Medicine ,Meropenem ,Loading dose ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Randomized controlled trial ,law ,Internal medicine ,polycyclic compounds ,Medicine ,Humans ,Ventilator-associated pneumonia ,Prospective Studies ,education ,Aged ,0303 health sciences ,education.field_of_study ,030306 microbiology ,business.industry ,Colistin ,Research ,lcsh:Medical emergencies. Critical care. Intensive care. First aid ,Pneumonia, Ventilator-Associated ,030208 emergency & critical care medicine ,lcsh:RC86-88.9 ,Middle Aged ,biochemical phenomena, metabolism, and nutrition ,medicine.disease ,Interim analysis ,bacterial infections and mycoses ,3. Good health ,Anti-Bacterial Agents ,Treatment Outcome ,bacteria ,Female ,Carbapenem-resistant gram-negative bacilli ,business ,Magic bullet ,medicine.drug - Abstract
© The Author(s)., [Background]: Colistin is recommended in the empirical treatment of ventilator-associated pneumonia (VAP) with a high prevalence of carbapenem-resistant gram-negative bacilli (CR-GNB). However, the efficacy and safety of colistin are not well defined. [Methods]: A multicenter prospective randomized trial conducted in 32 European centers compared the efficacy and safety of colistin (4.5 million unit loading dose followed by a maintenance dose of 3 million units every 8 h) versus meropenem (2 g every 8 h), both in combination with levofloxacin (500 mg every 12 h) for 7-14 days in patients with late VAP. Between May 2012 and October 2015, 232 patients were randomly assigned to the 2 treatment groups. The primary endpoint was mortality at 28 days after randomization in the microbiologically modified intention-to-treat (mMITT) population. Secondary outcomes included clinical and microbiological cure, renal function at the end of the treatment, and serious adverse events. The study was interrupted after the interim analysis due to excessive nephrotoxicity in the colistin group; therefore, the sample size was not achieved. [Results]: A total of 157 (67.7%) patients were included in the mMITT population, 36 of whom (22.9%) had VAP caused by CR-GNB. In the mMITT population, no significant difference in mortality between the colistin group (19/82, 23.2%) and the meropenem group (19/75, 25.3%) was observed, with a risk difference of - 2.16 (- 15.59 to 11.26, p = 0.377); the noninferiority of colistin was not demonstrated due to early termination and limited number of patients infected by carbapenem-resistant pathogens. Colistin plus levofloxacin increased the incidence of renal failure (40/120, 33.3%, versus 21/112, 18.8%; p = 0.012) and renal replacement therapy (11/120, 9.1%, versus 2/112, 1.8%; p = 0.015). [Conclusions]: This study did not demonstrate the noninferiority of colistin compared with meropenem, both combined with levofloxacin, in terms of efficacy in the empirical treatment of late VAP but demonstrated the greater nephrotoxicity of colistin. These findings do not support the empirical use of colistin for the treatment of late VAP due to early termination. Trial registration: ClinicalTrials.gov, NCT01292031. Registered 9 February 2011., Funded by the Seventh Framework Program of the European Commission. Magic Bullet grant agreement number 278232.
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- 2019
8. Colistin versus meropenem in the empirical treatment of ventilator-associated pneumonia (Magic Bullet study): An investigator-driven, open-label, randomized, noninferiority controlled trial
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European Commission, Cisneros, José Miguel, Rosso-Fernández, Clara, Roca-Oporto, Cristina, De Pascale, Gennaro, Jiménez-Jorge, Silvia, Fernández-Hinojosa, Esteban, Matthaiou, Dimitrios K., Ramírez, Paula, Ortiz Díaz-Miguel, Ramón, Estella, Á., Antonelli, Massimo, Dimopoulos, George, Garnacho-Montero, Carmen, European Commission, Cisneros, José Miguel, Rosso-Fernández, Clara, Roca-Oporto, Cristina, De Pascale, Gennaro, Jiménez-Jorge, Silvia, Fernández-Hinojosa, Esteban, Matthaiou, Dimitrios K., Ramírez, Paula, Ortiz Díaz-Miguel, Ramón, Estella, Á., Antonelli, Massimo, Dimopoulos, George, and Garnacho-Montero, Carmen
- Abstract
[Background]: Colistin is recommended in the empirical treatment of ventilator-associated pneumonia (VAP) with a high prevalence of carbapenem-resistant gram-negative bacilli (CR-GNB). However, the efficacy and safety of colistin are not well defined. [Methods]: A multicenter prospective randomized trial conducted in 32 European centers compared the efficacy and safety of colistin (4.5 million unit loading dose followed by a maintenance dose of 3 million units every 8 h) versus meropenem (2 g every 8 h), both in combination with levofloxacin (500 mg every 12 h) for 7-14 days in patients with late VAP. Between May 2012 and October 2015, 232 patients were randomly assigned to the 2 treatment groups. The primary endpoint was mortality at 28 days after randomization in the microbiologically modified intention-to-treat (mMITT) population. Secondary outcomes included clinical and microbiological cure, renal function at the end of the treatment, and serious adverse events. The study was interrupted after the interim analysis due to excessive nephrotoxicity in the colistin group; therefore, the sample size was not achieved. [Results]: A total of 157 (67.7%) patients were included in the mMITT population, 36 of whom (22.9%) had VAP caused by CR-GNB. In the mMITT population, no significant difference in mortality between the colistin group (19/82, 23.2%) and the meropenem group (19/75, 25.3%) was observed, with a risk difference of - 2.16 (- 15.59 to 11.26, p = 0.377); the noninferiority of colistin was not demonstrated due to early termination and limited number of patients infected by carbapenem-resistant pathogens. Colistin plus levofloxacin increased the incidence of renal failure (40/120, 33.3%, versus 21/112, 18.8%; p = 0.012) and renal replacement therapy (11/120, 9.1%, versus 2/112, 1.8%; p = 0.015). [Conclusions]: This study did not demonstrate the noninferiority of colistin compared with meropenem, both combined with levofloxacin, in terms of efficacy in the empiric
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- 2019
9. Transcriptomic and functional analysis of the Anopheles gambiae salivary gland in relation to blood feeding
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Das, Suchismita, Radtke, Andrea, Choi, Young-Jun, Mendes, Antonio M, Valenzuela, Jesus G, and Dimopoulos, George
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- 2010
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10. Functional genomic analyses of Enterobacter, Anopheles and Plasmodium reciprocal interactions that impact vector competence.
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Dennison, Nathan J., Saraiva, Raúl G., Cirimotich, Chris M., Mlambo, Godfree, Mongodin, Emmanuel F., and Dimopoulos, George
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FUNCTIONAL genomics ,MALARIA ,ENTEROBACTER ,ANOPHELES ,PLASMODIUM ,OXIDATIVE stress - Abstract
Background: Malaria exerts a tremendous socioeconomic impact worldwide despite current control efforts, and novel disease transmission-blocking strategies are urgently needed. The Enterobacter bacterium Esp_Z, which is naturally harboured in the mosquito midgut, can inhibit the development of Plasmodium parasites prior to their invasion of the midgut epithelium through a mechanism that involves oxidative stress. Here, a multifaceted approach is used to study the tripartite interactions between the mosquito, Esp_Z and Plasmodium, towards addressing the feasibility of using sugar-baited exposure of mosquitoes to the Esp_Z bacterium for interruption of malaria transmission. Methods: The ability of Esp_Z to colonize Anopheles gambiae midguts harbouring microbiota derived from wild mosquitoes was determined by qPCR. Upon introduction of Esp_Z via nectar feeding, the permissiveness of colonized mosquitoes to Plasmodium falciparum infection was determined, as well as the impact of Esp_Z on mosquito fitness parameters, such as longevity, number of eggs laid and number of larvae hatched. The genome of Esp_Z was sequenced, and transcriptome analyses were performed to identify bacterial genes that are important for colonization of the mosquito midgut, as well as for ROS-production. A gene expression analysis of members of the oxidative defence pathway of Plasmodium berghei was also conducted to assess the parasite's oxidative defence response to Esp_Z exposure. Results: Esp_Z persisted for up to 4 days in the An. gambiae midgut after introduction via nectar feeding, and was able to significantly inhibit Plasmodium sporogonic development. Introduction of this bacterium did not adversely affect mosquito fitness. Candidate genes involved in the selection of a better fit Esp_Z to the mosquito midgut environment and in its ability to condition oxidative status of its surroundings were identified, and parasite expression data indicated that Esp_Z is able to induce a partial and temporary shutdown of the ookinetes antioxidant response. Conclusions: Esp_Z is capable of inhibiting sporogonic development of Plasmodium in the presence of the mosquito's native microbiota without affecting mosquito fitness. Several candidate bacterial genes are likely mediating midgut colonization and ROS production, and inhibition of Plasmodium development appears to involve a shutdown of the parasite's oxidative defence system. A better understanding of the complex reciprocal tripartite interactions can facilitate the development and optimization of an Esp_Z-based malaria control strategy. [ABSTRACT FROM AUTHOR]
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- 2016
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11. Characteristics and risk factors for 28-day mortality of hospital acquired fungemias in ICUs: data from the EUROBACT study.
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Paiva, José-Artur, Pereira, José Manuel, Tabah, Alexis, Mikstacki, Adam, de Carvalho, Frederico Bruzzi, Koulenti, Despoina, Ruckly, Stéphane, Çakar, Nahit, Misset, Benoit, Dimopoulos, George, Antonelli, Massimo, Rello, Jordi, Xiaochun Ma, Tamowicz, Barbara, Timsit, Jean-François, and Ma, Xiaochun
- Abstract
Background: To characterize and identify prognostic factors for 28-day mortality among patients with hospital-acquired fungemia (HAF) in the Intensive Care Unit (ICU).Methods: A sub-analysis of a prospective, multicenter non-representative cohort study conducted in 162 ICUs in 24 countries.Results: Of the 1156 patients with hospital-acquired bloodstream infections (HA-BSI) included in the EUROBACT study, 96 patients had a HAF. Median time to its diagnosis was 20 days (IQR 10.5-30.5) and 9 days (IQR 3-15.5) after hospital and ICU admission, respectively. Median time to positivity of blood culture was longer in fungemia than in bacteremia (48.7 h vs. 38.1 h; p = 0.0004). Candida albicans was the most frequent fungus isolated (57.1%), followed by Candida glabrata (15.3%) and Candida parapsilosis (10.2%). No clear source of HAF was detected in 33.3% of the episodes and it was catheter-related in 21.9% of them. Compared to patients with bacteremia, HAF patients had a higher rate of septic shock (39.6% vs. 21.6%; p = 0.0003) and renal dysfunction (25% vs. 12.4%; p = 0.0023) on admission and a higher rate of renal failure (26% vs. 16.2%; p = 0.0273) at diagnosis. Adequate treatment started within 24 h after blood culture collection was less frequent in HAF patients (22.9% vs. 55.3%; p < 0.001). The 28-day all cause fatality was 40.6%. According to multivariate analysis, only liver failure (OR 14.35; 95% CI 1.17-175.6; p = 0.037), need for mechanical ventilation (OR 8.86; 95% CI 1.2-65.24; p = 0.032) and ICU admission for medical reason (OR 3.87; 95% CI 1.25-11.99; p = 0.020) were independent predictors of 28-day mortality in HAF patients.Conclusions: Fungi are an important cause of hospital-acquired BSI in the ICU. Patients with HAF present more frequently with septic shock and renal dysfunction on ICU admission and have a higher rate of renal failure at diagnosis. HAF are associated with a significant 28-day mortality rate (40%), but delayed adequate antifungal therapy was not an independent risk factor for death. Liver failure, need for mechanical ventilation and ICU admission for medical reason were the only independent predictors of 28-day mortality. [ABSTRACT FROM AUTHOR]- Published
- 2016
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12. How to treat fungal infections in ICU patients.
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Matthaiou, Dimitrios K., Christodoulopoulou, Theodora, and Dimopoulos, George
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MUCORMYCOSIS ,MEDICAL mycology ,INPATIENT care ,MEDICAL records ,ASPERGILLOSIS - Abstract
Fungal infections represent a major burden in the critical care setting with increasing morbidity and mortality. Candidiasis is the leading cause of such infections, with C. albicans being the most common causative agent, followed by Aspergillosis and Mucormycosis. The diagnosis of such infections is cumbersome requiring increased clinical vigilance and extensive laboratory testing, including radiology, cultures, biopsies and other indirect methods. However, it is not uncommon for definitive evidence to be unavailable. Risk and host factors indicating the probability of infections may greatly help in the diagnostic approach. Timely and adequate intervention is important for their successful treatment. The available therapeutic armamentarium, although not very extensive, is effective with low resistance rates for the newer antifungal agents. However, timely and prudent use is necessary to maximize favorable outcomes. [ABSTRACT FROM AUTHOR]
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- 2015
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13. Safety and efficacy of colistin versus meropenem in the empirical treatment of ventilator-associated pneumonia as part of a macro-project funded by the Seventh Framework Program of the European Commission studying off-patent antibiotics: study protocol for a randomized controlled trial
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Rosso-Fernández, Clara, Garnacho-Montero, José, Antonelli, Massimo, Dimopoulos, George, and Cisneros, José Miguel
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COLISTIN ,ETIOLOGY of diseases ,ANTI-infective agents ,ANTIBIOTICS ,BIOSYNTHESIS - Abstract
Background: Ventilator-associated pneumonia (VAP) is one of the most common and severe hospital-adquired infections, and multidrugresistant gram-negative bacilli (MDR-GNB) constitute the main etiology in many countries. Inappropriate empiric antimicrobial treatment is associated with increased mortality. In this context, the empirical treatment of choice for VAP is unknown. Colistin, is now the antimicrobial with greatest in vitro activity against MDR-GNB. Methods/Design: The MagicBullet clinical trial is an investigator-driven clinical study, funded by the Seventh Framework Program of the European Commission. This is designed as a phase IV, randomized, controlled, open label, non-inferiority and international trial to assess the safety and efficacy of colistin versus meropenem in late onset VAP. The study is conducted in a total of 32 centers in three European countries (Spain, Italy and Greece) with specific high incidences of infections caused by MDR-GNB. Patients older than 18 years who develop VAP with both clinical and radiological signs, and are on mechanical ventilation for more than 96 hours, or less than 96 hours but with previous antibiotic treatment plus one week of hospitalization, are candidates for inclusion in the study. A total sample size of 496 patients will be randomized according to a severity clinical score (at the time of VAP diagnosis in a 1:1 ratio to receive either colistin 4.5 MU as a loading dose, followed by 3 MU every eight hours (experimental arm), or meropenem 2 g every eight hours (control arm), both combined with levofloxacin. Mortality from any cause at 28 days will be considered as the main outcome. Clinical and microbiological cure will be evaluated at 72 hours, eight days, the finalization of antibiotic treatment, and 28 days of follow-up. The efficacy evaluation will be performed in every patient who receives at least one study treatment drug, and with etiologic diagnosis of VAP, intention-to-treat population and per protocol analysis will be performed.Discussion: Currently, there is no study being undertaken which analyzes empiric treatment of (VAP) with a suspicion of multi-resistance. Colistin, an off-patent antibiotic commercialized for more than 60 years, could widen the antibiotic alternatives for a high-mortality illness aggravated by antibiotic resistance. [ABSTRACT FROM AUTHOR]
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- 2015
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14. Pharmacokinetic variability and exposures of fluconazole, anidulafungin, and caspofungin in intensive care unit patients: Data from multinational Defining Antibiotic Levels in Intensive care unit (DALI) patients Study.
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Sinnollareddy, Mahipal G., Roberts, Jason A., Lipman, Jeffrey, Akova, Murat, Bassetti, Matteo, De Waele, Jan J., Kaukonen, Kirsi-Maija, Koulenti, Despoina, Martin, Claude, Montravers, Philippe, Rello, Jordi, Rhodes, Andrew, Starr, Therese, Wallis, Steven C., and Dimopoulos, George
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- 2015
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15. Epidemiology of invasive aspergillosis in critically ill patients: clinical presentation, underlying conditions, and outcomes.
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Taccone, Fabio Silvio, Van den Abeele, Anne-Marie, Bulpa, Pierre, Misset, Benoit, Meersseman, Wouter, Cardoso, Teresa, Paiva, José-Artur, Blasco-Navalpotro, Miguel, De Laere, Emmanuel, Dimopoulos, George, Rello, Jordi, Vogelaers, Dirk, and Blot, Stijn I.
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- 2015
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16. Epidemiology of invasive aspergillosis in critically ill patients: clinical presentation, underlying conditions, and outcome.
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Silvio Taccone, Fabio, Van Den Abeele, Anne-Marie, Bulpa, Pierre, Misset, Benoit, Meersseman, Wouter, Cardoso, Teresa, Paiva, José-Artur, Blasco-Navalpotro, Miguel, De Laere, Emmanuel, Dimopoulos, George, Rello, Jordi, Vogelaers, Dirk, and Blot, Stijn I.
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- 2015
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17. Does contemporary vancomycin dosing achieve therapeutic targets in a heterogeneous clinical cohort of critically ill patients? Data from the multinational DALI Study.
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Blot, Stijn, Koulenti, Despoina, Akova, Murat, Bassetti, Matteo, De Waele, Jan J., Dimopoulos, George, Kaukonen, Kirsi-Maija, Martin, Claude, Montravers, Philippe, Rello, Jordi, Rhodes, Andrew, Starr, Therese, Wallis, Steven C., Lipman, Jeffrey, and Roberts, Jason A.
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- 2014
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18. Diagnosis and Management of Temperature Abnormality in ICUs: A EUROBACT Investigators Survey.
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Niven, Daniel, Laupland, Kevin, Tabah, Alexis, Vesin, Aurélien, Rello, Jordi, Koulenti, Despoina, Dimopoulos, George, de Waele, Jan, and Timsit, Jean-Francois
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INTENSIVE care units ,HYPOTHERMIA ,FEVER ,ACETAMINOPHEN ,ACUTE coronary syndrome ,SEPTIC shock ,BACTEREMIA - Abstract
Introduction: Although fever and hypothermia are common abnormal physical signs observed in patients admitted to intensive care units (ICU), little data exists on their optimal management. The objective of this study was to describe contemporary practices and determinants of management of temperature abnormalities among patients admitted to ICUs. Methods: Site leaders of the multi-national EUROBACT study were surveyed regarding diagnosis and management of temperature abnormalities among patients admitted to their ICUs. Results: Of the 162 ICUs originally included in EUROBACT, responses were received from 139 (86%) centres in 23 countries in Europe (117), South America (8), Asia (5), North America (4), Australia (3), and Africa (2). 117 (84%) respondents reported use of a specific temperature threshold in their ICU to define fever. A total of 14 different discrete levels were reported with a median of 38.2 °C (inter-quartile range, IQR, 38.0°C-38.5°C). The use of thermometers was protocolized in 91 (65%) ICUs and a wide range of methods were reportedly used, with axillary, tympanic, and urinary bladder sites as the most common as primary modalities. Only 31 (22%) of respondents indicated that there was a formal written protocol for temperature control among febrile patients in their ICUs. In most or all cases practice was to control temperature, to use acetaminophen, and to perform a full septic workup in febrile patients and that this was usually directed by physician order. While reported practice was to treat nearly all patients with neurological impairment and most patients with acute coronary syndromes and infections, severe sepsis, and septic shock, this was not the case for most patients with liver failure and fever. Conclusions: A wide range of definitions and management practices were reported regarding temperature abnormalities in the critically ill. Documenting temperature abnormality management practices, including variability in clinical care, is important to inform planning of future studies designed to optimize infection and temperature management strategies in the critically ill. [ABSTRACT FROM AUTHOR]
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- 2013
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19. DALI: Defining Antibiotic Levels in Intensive care unit patients: a multi-centre point of prevalence study to determine whether contemporary antibiotic dosing for critically ill patients is therapeutic.
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Roberts, Jason A., De Waele, Jan J., Dimopoulos, George, Koulenti, Despoina, Martin, Claude, Montravers, Philippe, Rello, Jordi, Rhodes, Andrew, Starr, Therese, Wallis, Steven C., and Lipman, Jeffrey
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ANTIBIOTICS ,CRITICAL care medicine ,ANTI-infective agents ,INTENSIVE care units ,ANTIBACTERIAL agents ,MEDICAL personnel - Abstract
Background: The clinical effects of varying pharmacokinetic exposures of antibiotics (antibacterials and antifungals) on outcome in infected critically ill patients are poorly described. A large-scale multi-centre study (DALI Study) is currently underway describing the clinical outcomes of patients achieving pre-defined antibiotic exposures. This report describes the protocol. Methods: DALI will recruit over 500 patients administered a wide range of either beta-lactam or glycopeptide antibiotics or triazole or echinocandin antifungals in a pharmacokinetic point-prevalence study. It is anticipated that over 60 European intensive care units (ICUs) will participate. The primary aim will be to determine whether contemporary antibiotic dosing for critically ill patients achieves plasma concentrations associated with maximal activity. Secondary aims will compare antibiotic pharmacokinetic exposures with patient outcome and will describe the population pharmacokinetics of the antibiotics included. Various subgroup analyses will be conducted to determine patient groups that may be at risk of very low or very high concentrations of antibiotics. Discussion: The DALI study should inform clinicians of the potential clinical advantages of achieving certain antibiotic pharmacokinetic exposures in infected critically ill patients. [ABSTRACT FROM AUTHOR]
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- 2012
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20. Post-operative Aspergillus mediastinitis in a man who was immunocompetent: a case report.
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Dimopoulos, George, Tsangaris, Iraklis, Poulakou, Garyphalia, Panayiotides, John, Tsaknis, George, Orfanos, Stylianos, and Armaganides, Apostolos
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ASPERGILLOSIS , *MYCOSES , *IMMUNOCOMPETENT cells , *IMMUNE system , *HYPERTENSION - Abstract
Introduction: Aspergillus spp. infections mainly affect patients who are immunocompromised, and are extremely rare in immunocompetent individuals.Case Presentation: Aspergillus post-operative mediastinitis is considered to be a devastating infection, usually affecting patients undergoing cardiothoracic surgery with specific predisposing factors. We describe the case of an immunocompetent 68-year-old Caucasian man with severe chronic thromboembolic pulmonary hypertension, who underwent pulmonary thromboendarterectomy and developed post-operative mediastinitis due to Aspergillus flavus. The environmental control did not reveal the source of A. flavus infection and, despite combined antifungal therapy, our patient died as a result of septic shock and multiple organ failure.Conclusion: Aspergillus mediastinitis mainly affects patients after cardiosurgery operations with predisposing factors, and it is unusual in patients who are immunocompetent. The identification of the Aspergillus spp. source is often difficult, and there are no guidelines for the administration of pre-emptive therapy in this population of at-risk patients. [ABSTRACT FROM AUTHOR]- Published
- 2010
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21. Genome-wide transcriptomic profiling of Anopheles gambiaehemocytes reveals pathogen-specific signatures upon bacterialchallenge and Plasmodium berghei infection.
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Baton, Luke A., Robertson, Anne, Warr, Emma, Strand, Michael R., and Dimopoulos, George
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ANOPHELES gambiae ,MALARIA ,BLOOD cells ,IMMUNE response ,PARASITES - Abstract
Background: The mosquito Anopheles gambiae is a major vector of human malaria. Increasing evidence indicates that blood cells (hemocytes) comprise an essential arm of the mosquito innate immune response against both bacteria and malaria parasites. To further characterize the role of hemocytes in mosquito immunity, we undertook the first genome-wide transcriptomic analyses of adult female An. gambiae hemocytes following infection by two species of bacteria and a malaria parasite. Results: We identified 4047 genes expressed in hemocytes, using An. gambiae genome-wide microarrays. While 279 transcripts were significantly enriched in hemocytes relative to whole adult female mosquitoes, 959 transcripts exhibited immune challenge-related regulation. The global transcriptomic responses of hemocytes to challenge with different species of bacteria and/or different stages of malaria parasite infection revealed discrete, minimally overlapping, pathogenspecific signatures of infection-responsive gene expression; 105 of these represented putative immunity-related genes including anti-Plasmodium factors. Of particular interest was the specific coregulation of various members of the Imd and JNK immune signaling pathways during malaria parasite invasion of the mosquito midgut epithelium. Conclusion: Our genome-wide transcriptomic analysis of adult mosquito hemocytes reveals pathogen-specific signatures of gene regulation and identifies several novel candidate genes for future functional studies. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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22. Gene discovery in an invasive tephritid model pest species, the Mediterranean fruit fly, Ceratitis capitata.
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Gomulski, Ludvik M., Dimopoulos, George, Zhiyong Xi, Soares, Marcelo B., Bonaldo, Maria F., Malacrida, Anna R., and Gasperi, Giuliano
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CERATITIS , *MEDITERRANEAN fruit-fly , *TEPHRITIDAE , *BIOLOGICAL control of agricultural pests , *GENETIC transcription , *GENETIC code , *GENETIC sex determination - Abstract
Background: The medfly, Ceratitis capitata, is a highly invasive agricultural pest that has become a model insect for the development of biological control programs. Despite research into the behavior and classical and population genetics of this organism, the quantity of sequence data available is limited. We have utilized an expressed sequence tag (EST) approach to obtain detailed information on transcriptome signatures that relate to a variety of physiological systems in the medfly; this information emphasizes on reproduction, sex determination, and chemosensory perception, since the study was based on normalized cDNA libraries from embryos and adult heads. Results: A total of 21,253 high-quality ESTs were obtained from the embryo and head libraries. Clustering analyses performed separately for each library resulted in 5201 embryo and 6684 head transcripts. Considering an estimated 19% overlap in the transcriptomes of the two libraries, they represent about 9614 unique transcripts involved in a wide range of biological processes and molecular functions. Of particular interest are the sequences that share homology with Drosophila genes involved in sex determination, olfaction, and reproductive behavior. The medfly transformer2 (tra2) homolog was identified among the embryonic sequences, and its genomic organization and expression were characterized. Conclusion: The sequences obtained in this study represent the first major dataset of expressed genes in a tephritid species of agricultural importance. This resource provides essential information to support the investigation of numerous questions regarding the biology of the medfly and other related species and also constitutes an invaluable tool for the annotation of complete genome sequences. Our study has revealed intriguing findings regarding the transcript regulation of tra2 and other sex determination genes, as well as insights into the comparative genomics of genes implicated in chemosensory reception and reproduction. [ABSTRACT FROM AUTHOR]
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- 2008
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23. Spatial and sex-specific dissection of the Anopheles gambiae midgut transcriptome.
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Warr, Emma, Aguilar, Ruth, Yuemei Dong, Mahairaki, Vassiliki, and Dimopoulos, George
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ANOPHELES gambiae ,MALARIA ,PATHOGENIC microorganisms ,GENE expression ,IMMUNITY ,PROTEINS ,PEPTIDES - Abstract
Background: The midgut of hematophagous insects, such as disease transmitting mosquitoes, carries out a variety of essential functions that mostly relate to blood feeding. The midgut of the female malaria vector mosquito Anopheles gambiae is a major site of interactions between the parasite and the vector. Distinct compartments and cell types of the midgut tissue carry out specific functions and vector borne pathogens interact and infect different parts of the midgut. Results: A microarray based global gene expression approach was used to compare transcript abundance in the four major female midgut compartments (cardia, anterior, anterior part of posterior and posterior part of posterior midgut) and between the male and female Anopheles gambiae midgut. Major differences between the female and male midgut gene expression relate to digestive processes and immunity. Each compartment has a distinct gene function profile with the posterior midgut expressing digestive enzyme genes and the cardia and anterior midgut expressing high levels of antimicrobial peptide and other immune gene transcripts. Interestingly, the cardia expressed several known anti-Plasmodium factors. A parallel peptidomic analysis of the cardia identified known mosquito antimicrobial peptides as well as several putative short secreted peptides that are likely to represent novel antimicrobial factors. Conclusion: The A. gambiae sex specific midgut and female midgut compartment specific transcriptomes correlates with their known functions. The significantly greater functional diversity of the female midgut relate to hematophagy that is associated with digestion and nutrition uptake as well as exposes it to a variety of pathogens, and promotes growth of its endogenous microbial flora. The strikingly high proportion of immunity related factors in the cardia tissue most likely serves the function to increase sterility of ingested sugar and blood. A detailed characterization of the functional specificities of the female mosquito midgut and its various compartments can greatly contribute to our understanding of its role in disease transmission and generate the necessary tools for the development of malaria control strategies. [ABSTRACT FROM AUTHOR]
- Published
- 2007
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24. Colistin versus meropenem in the empirical treatment of ventilator-associated pneumonia (Magic Bullet study): an investigator-driven, open-label, randomized, noninferiority controlled trial.
- Author
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Cisneros, José M., Rosso-Fernández, Clara María, Roca-Oporto, Cristina, De Pascale, Gennaro, Jiménez-Jorge, Silvia, Fernández-Hinojosa, Esteban, Matthaiou, Dimitrios K., Ramírez, Paula, Díaz-Miguel, Ramón Ortiz, Estella, Angel, Antonelli, Massimo, Dimopoulos, George, Garnacho-Montero, José, on behalf of the Magic Bullet Working Group WP1, Di Gravio, V., Bello, G., González, V., Leal, R., Puppo, A., and Lepe, J. A.
- Abstract
Background: Colistin is recommended in the empirical treatment of ventilator-associated pneumonia (VAP) with a high prevalence of carbapenem-resistant gram-negative bacilli (CR-GNB). However, the efficacy and safety of colistin are not well defined.Methods: A multicenter prospective randomized trial conducted in 32 European centers compared the efficacy and safety of colistin (4.5 million unit loading dose followed by a maintenance dose of 3 million units every 8 h) versus meropenem (2 g every 8 h), both in combination with levofloxacin (500 mg every 12 h) for 7-14 days in patients with late VAP. Between May 2012 and October 2015, 232 patients were randomly assigned to the 2 treatment groups. The primary endpoint was mortality at 28 days after randomization in the microbiologically modified intention-to-treat (mMITT) population. Secondary outcomes included clinical and microbiological cure, renal function at the end of the treatment, and serious adverse events. The study was interrupted after the interim analysis due to excessive nephrotoxicity in the colistin group; therefore, the sample size was not achieved.Results: A total of 157 (67.7%) patients were included in the mMITT population, 36 of whom (22.9%) had VAP caused by CR-GNB. In the mMITT population, no significant difference in mortality between the colistin group (19/82, 23.2%) and the meropenem group (19/75, 25.3%) was observed, with a risk difference of - 2.16 (- 15.59 to 11.26, p = 0.377); the noninferiority of colistin was not demonstrated due to early termination and limited number of patients infected by carbapenem-resistant pathogens. Colistin plus levofloxacin increased the incidence of renal failure (40/120, 33.3%, versus 21/112, 18.8%; p = 0.012) and renal replacement therapy (11/120, 9.1%, versus 2/112, 1.8%; p = 0.015).Conclusions: This study did not demonstrate the noninferiority of colistin compared with meropenem, both combined with levofloxacin, in terms of efficacy in the empirical treatment of late VAP but demonstrated the greater nephrotoxicity of colistin. These findings do not support the empirical use of colistin for the treatment of late VAP due to early termination.Trial Registration: ClinicalTrials.gov, NCT01292031. Registered 9 February 2011. [ABSTRACT FROM AUTHOR]- Published
- 2019
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25. Past history of stage I/II solid tumor malignancy impacts considerably on sepsis mortality: a propensity score matching analysis from the hellenic sepsis study group.
- Author
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Dimοpoulos, George, Rovina, Nikoletta, Patrani, Maria, Antoniadou, Eleni, Konstantonis, Dimitrios, Vryza, Konstantina, Vlachogianni, Glykeria, Kyprianou, Miltiades, Routsi, Christina, Giamarellos-Bourboulis, Evangelos J., Hellenic Sepsis Study Group, and Dimopoulos, George
- Subjects
PROPENSITY score matching ,SEPSIS ,SEPTIC shock ,PLASMINOGEN activators ,MORTALITY - Abstract
Background: Whether past history of solid stage I/II inactive cancer has an impact on 28-day mortality of sepsis remains unclear. We aimed to determine the impact of history of stage I or II solid tumor malignancy in complete remission the last 3 years on sepsis outcome.Methods: Using the database of the Hellenic Sepsis Study Group from 1553 patients with sepsis admitted in the ICU, 83 patients with sepsis by Sepsis-3 definition with past-history of stage I/II inactive solid malignancy the last 3 years were depicted. A comparator group of 83 patients fully matched for age, severity, type of infection and comorbidities was selected by propensity score matching.Results: Mortality after 28 days was 37.3% in the comparator group and 54.2% in the solid tumor stage I/II group (odds ratio for death 1.98; p: 0.030). Following step-wise forward Cox regression analysis, septic shock (hazard ratio 1.80), acute renal injury (hazard ratio 2.06), history of coronary heart disease (hazard ratio 0.36) and history of stage I/II solid tumor malignancy (hazard ratio 1.79) were the only independent variables associated with 28-day mortality. Serum levels of procalcitonin and of soluble urokinase plasminogen activator receptor were similar between the two groups of comparisons.Conclusions: Past history of stage I/II solid malignancy is an independent risk factor for unfavorable outcome from sepsis the first 28 days. [ABSTRACT FROM AUTHOR]- Published
- 2019
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26. The mosquito adulticidal <italic>Chromobacterium</italic> sp. Panama causes transgenerational impacts on fitness parameters and elicits xenobiotic gene responses.
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Short, Sarah M., van Tol, Sarah, Smith, Brendan, Dong, Yuemei, and Dimopoulos, George
- Subjects
CHROMOBACTERIUM ,VECTOR control ,MOSQUITOES ,INSECTICIDES ,INSECT longevity - Abstract
Background: Vector control is critical in reducing the disease burden caused by mosquitoes, and insecticides are an effective tool to control vector populations. Resistance to common insecticides is now widespread, and novel classes of insecticides are needed. In previous work, we described the mosquitocidal activity of
Chromobacterium sp. Panama (C. sp_P), a bacterium found in association with mosquitoes in natural populations. In the current work, we further explored the effects of exposure to the bacterium on mosquito fitness and mosquito physiology. Results: We found thatC. sp_P has mosquitocidal activity against a broad range of mosquito taxa. When exposed toC. sp_P as adults, femaleAn. gambiae suffered reduced longevity, but experienced no change in fecundity. The offspring of these females, however, had higher mortality as larvae and were slower to develop compared to offspring of control females. We also found that the mosquitocidal activity ofC. sp_P was retained after removal of live cells from biofilm culture media, suggesting the bacteria secrete mosquitocidal compound(s) into the media during growth. Exposure to this cell-freeC. sp_P-conditioned media caused female midgut transcriptional changes comprising detoxification, xenobiotic response, and stress response genes, suggesting the physiological response toC. sp_P is similar to that of insecticide exposure. Finally, we found that multiple members of theChromobacterium genus had mosquitocidal activity, but this activity was highest in mosquitoes treated withC. sp_P. Conclusions: Our findings suggest thatC. sp_P produces factor(s) with strong effects on mosquito longevity and fitness, which may be of interest for mosquitocide development. More generally, they indicate that further exploration of mosquito-associated and environmental microbes for novel insecticidal compounds or biocontrol agents is warranted. [ABSTRACT FROM AUTHOR]- Published
- 2018
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27. Yeast central nervous system infection in a critically ill patient: a case report.
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Frantzeskaki, Frantzeska, Diakaki, Chryssi, Rizos, Michalis, Theodorakopoulou, Maria, Papadopoulos, Panagiotis, Antonopoulou, Anastasia, Nikitas, Nikitas, Lignos, Michail, Brountzos, Elias, Velegraki, Aristea, Paramythiotou, Elisabeth, Panagyotides, John, Armaganidis, Apostolos, and Dimopoulos, George
- Abstract
Introduction: Invasive fungal infections are alarmingly common in intensive care unit patients; invasive fungal infections are associated with increased morbidity and mortality. Risk factors are the increased use of indwelling central venous catheters, the use of broad spectrum antibiotics, parenteral nutrition, renal replacement therapy and immunosuppression. Diagnosis of these infections might be complicated, requiring tissue cultures. In addition, therapy of invasive fungal infections might be difficult, given the rising resistance of fungi to antifungal agents.Case Presentation: We describe the case of a 28-year-old Greek man with yeast central nervous system infection.Conclusions: Difficult-to-treat fungal infections may complicate the clinical course of critically ill patients and render their prognosis unfavorable. This report presents a case that was rare and difficult to treat, along with a thorough review of the investigation and treatment of these kinds of fungal infections in critically ill patients. [ABSTRACT FROM AUTHOR]- Published
- 2014
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28. Past history of stage I/II solid tumor malignancy impacts considerably on sepsis mortality: a propensity score matching analysis from the hellenic sepsis study group.
- Author
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Dimopoulos G, Rovina N, Patrani M, Antoniadou E, Konstantonis D, Vryza K, Vlachogianni G, Kyprianou M, Routsi C, and Giamarellos-Bourboulis EJ
- Subjects
- Acute Kidney Injury complications, Aged, Aged, 80 and over, Coronary Disease complications, Female, Humans, Intensive Care Units, Male, Middle Aged, Odds Ratio, Proportional Hazards Models, Risk Factors, Shock, Septic complications, Neoplasm Staging, Neoplasms complications, Neoplasms pathology, Propensity Score, Sepsis mortality
- Abstract
Background: Whether past history of solid stage I/II inactive cancer has an impact on 28-day mortality of sepsis remains unclear. We aimed to determine the impact of history of stage I or II solid tumor malignancy in complete remission the last 3 years on sepsis outcome., Methods: Using the database of the Hellenic Sepsis Study Group from 1553 patients with sepsis admitted in the ICU, 83 patients with sepsis by Sepsis-3 definition with past-history of stage I/II inactive solid malignancy the last 3 years were depicted. A comparator group of 83 patients fully matched for age, severity, type of infection and comorbidities was selected by propensity score matching., Results: Mortality after 28 days was 37.3% in the comparator group and 54.2% in the solid tumor stage I/II group (odds ratio for death 1.98; p: 0.030). Following step-wise forward Cox regression analysis, septic shock (hazard ratio 1.80), acute renal injury (hazard ratio 2.06), history of coronary heart disease (hazard ratio 0.36) and history of stage I/II solid tumor malignancy (hazard ratio 1.79) were the only independent variables associated with 28-day mortality. Serum levels of procalcitonin and of soluble urokinase plasminogen activator receptor were similar between the two groups of comparisons., Conclusions: Past history of stage I/II solid malignancy is an independent risk factor for unfavorable outcome from sepsis the first 28 days.
- Published
- 2019
- Full Text
- View/download PDF
29. Genome-wide transcriptomic profiling of Anopheles gambiae hemocytes reveals pathogen-specific signatures upon bacterial challenge and Plasmodium berghei infection.
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Baton LA, Robertson A, Warr E, Strand MR, and Dimopoulos G
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- Animals, Anopheles immunology, Anopheles microbiology, Anopheles parasitology, Female, Gene Expression Regulation, Genes, Insect, Hemocytes metabolism, Host-Parasite Interactions, Host-Pathogen Interactions, Insect Vectors genetics, Insect Vectors parasitology, Oligonucleotide Array Sequence Analysis, Anopheles genetics, Bacteria, Gene Expression Profiling, Plasmodium berghei
- Abstract
Background: The mosquito Anopheles gambiae is a major vector of human malaria. Increasing evidence indicates that blood cells (hemocytes) comprise an essential arm of the mosquito innate immune response against both bacteria and malaria parasites. To further characterize the role of hemocytes in mosquito immunity, we undertook the first genome-wide transcriptomic analyses of adult female An. gambiae hemocytes following infection by two species of bacteria and a malaria parasite., Results: We identified 4047 genes expressed in hemocytes, using An. gambiae genome-wide microarrays. While 279 transcripts were significantly enriched in hemocytes relative to whole adult female mosquitoes, 959 transcripts exhibited immune challenge-related regulation. The global transcriptomic responses of hemocytes to challenge with different species of bacteria and/or different stages of malaria parasite infection revealed discrete, minimally overlapping, pathogen-specific signatures of infection-responsive gene expression; 105 of these represented putative immunity-related genes including anti-Plasmodium factors. Of particular interest was the specific co-regulation of various members of the Imd and JNK immune signaling pathways during malaria parasite invasion of the mosquito midgut epithelium., Conclusion: Our genome-wide transcriptomic analysis of adult mosquito hemocytes reveals pathogen-specific signatures of gene regulation and identifies several novel candidate genes for future functional studies.
- Published
- 2009
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30. Molecular analysis of photic inhibition of blood-feeding in Anopheles gambiae.
- Author
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Das S and Dimopoulos G
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- Animals, Circadian Rhythm physiology, Darkness, Female, Lighting methods, Male, Anopheles physiology, Blood, Feeding Behavior physiology, Photic Stimulation methods
- Abstract
Background: Anopheles gambiae mosquitoes exhibit an endophilic, nocturnal blood feeding behavior. Despite the importance of light as a regulator of malaria transmission, our knowledge on the molecular interactions between environmental cues, the circadian oscillators and the host seeking and feeding systems of the Anopheles mosquitoes is limited., Results: In the present study, we show that the blood feeding behavior of mosquitoes is under circadian control and can be modulated by light pulses, both in a clock dependent and in an independent manner. Short light pulses (approximately 2-5 min) in the dark phase can inhibit the blood-feeding propensity of mosquitoes momentarily in a clock independent manner, while longer durations of light stimulation (approximately 1-2 h) can induce a phase advance in blood-feeding propensity in a clock dependent manner. The temporary feeding inhibition after short light pulses may reflect a masking effect of light, an unknown mechanism which is known to superimpose on the true circadian regulation. Nonetheless, the shorter light pulses resulted in the differential regulation of a variety of genes including those implicated in the circadian control, suggesting that light induced masking effects also involve clock components. Light pulses (both short and long) also regulated genes implicated in feeding as well as different physiological processes like metabolism, transport, immunity and protease digestions. RNAi-mediated gene silencing assays of the light pulse regulated circadian factors timeless, cryptochrome and three takeout homologues significantly up-regulated the mosquito's blood-feeding propensity. In contrast, gene silencing of light pulse regulated olfactory factors down-regulated the mosquito's propensity to feed on blood., Conclusion: Our study show that the mosquito's feeding behavior is under circadian control. Long and short light pulses can induce inhibition of blood-feeding through circadian and unknown mechanisms, respectively, that involve the chemosensory system.
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- 2008
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31. Continuous exposure to Plasmodium results in decreased susceptibility and transcriptomic divergence of the Anopheles gambiae immune system.
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Aguilar R, Das S, Dong Y, and Dimopoulos G
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- Animals, Anopheles genetics, Disease Susceptibility, Down-Regulation, Female, Gene Expression, Genes, Insect, Host-Parasite Interactions immunology, Insect Proteins immunology, Insect Vectors, Malaria immunology, Malaria parasitology, Mice, Oligonucleotide Array Sequence Analysis, Transcription, Genetic, Anopheles immunology, Anopheles parasitology, Gene Expression Profiling, Host-Parasite Interactions genetics, Plasmodium berghei physiology
- Abstract
Background: Plasmodium infection has been shown to compromise the fitness of the mosquito vector, reducing its fecundity and longevity. However, from an evolutionary perspective, the impact of Plasmodium infection as a selective pressure on the mosquito is largely unknown., Results: In the present study we have addressed the effect of a continuous Plasmodium berghei infection on the resistance to infection and global gene expression in Anopheles gambiae. Exposure of A. gambiae to P. berghei-infected blood and infection for 16 generations resulted in a decreased susceptibility to infection, altered constitutive expression levels for approximately 2.4% of the mosquito's total transcriptome and a lower basal level of immune genes expression, including several anti-Plasmodium factors. The infection-responsiveness for several defense genes was elevated in the P. berghei exposed mosquito colonies., Conclusion: Our study establishes the existence of a selective pressure exerted by the parasite P. berghei on the malaria vector A. gambiae that results in a decreased permissiveness to infection and changes in the mosquito transcriptome regulation that suggest a decreased constitutive immune gene activity but a more potent immune response upon Plasmodium challenge.
- Published
- 2007
- Full Text
- View/download PDF
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