Scedosporium apiospermum Complex: Diagnosis and Species Identification, Current Fungal Infection Reports, vol.147, issue.6, pp.211-219, 2014. ,
DOI : 10.1099/00221287-147-6-1499
Scedosporium and Lomentospora: an updated overview of underrated opportunists, Medical Mycology, vol.61, issue.suppl_1, pp.102-125, 2018. ,
DOI : 10.1093/mmy/myx113
URL : https://hal.archives-ouvertes.fr/hal-01789215
complex in French patients with cystic fibrosis, Medical Mycology, vol.60, issue.6, pp.603-613, 2013. ,
DOI : 10.1128/AAC.00981-06
Prevalence of Scedosporium species and Lomentospora prolificans in patients with cystic fibrosis in a multicenter trial by use of a selective medium, Journal of Cystic Fibrosis, vol.14, issue.2, pp.237-241, 2015. ,
DOI : 10.1016/j.jcf.2014.12.014
Species in Respiratory Tract Specimens from Patients with Cystic Fibrosis by Use of Selective Media, Journal of Clinical Microbiology, vol.48, issue.1, pp.314-316, 2010. ,
DOI : 10.1128/JCM.01470-09
URL : http://jcm.asm.org/content/48/1/314.full.pdf
Fungal colonization and immune response to fungi in cystic fibrosis, J Mycol Méd, vol.5, pp.211-216, 1995. ,
Clinical Significance of Scedosporium apiospermum in Patients with Cystic Fibrosis, European Journal of Clinical Microbiology & Infectious Diseases, vol.19, issue.1, pp.53-56, 2000. ,
DOI : 10.1007/s100960050011
Occurrence and relevance of filamentous fungi in respiratory secretions of patients with cystic fibrosis ??? a review, Medical Mycology, vol.40, issue.1, pp.387-397, 2008. ,
DOI : 10.1128/JCM.40.9.3544-3545.2002
Characteristics and consequences of airway colonization by filamentous fungi in 201 adult patients with cystic fibrosis in France, Medical Mycology, vol.21, issue.3, pp.32-36, 2010. ,
DOI : 10.1002/(SICI)1099-0496(199601)21:1<6::AID-PPUL1>3.0.CO;2-R
Lack of standardization in the procedures for mycological examination of sputum samples from CF patients: a possible cause for variations in the prevalence of filamentous fungi, Medical Mycology, vol.47, issue.O1, pp.88-97, 2010. ,
DOI : 10.1128/JCM.01685-08
URL : https://hal.archives-ouvertes.fr/hal-01118199
Developing collaborative works for faster progress on fungal respiratory infections in cystic fibrosis, Medical Mycology, vol.30, issue.1, pp.42-59, 2018. ,
DOI : 10.1093/mmy/myx106
URL : https://hal.archives-ouvertes.fr/hal-01789211
Genotyping Study of Scedosporium apiospermum Isolates from Patients with Cystic Fibrosis, Journal of Clinical Microbiology, vol.40, issue.6, pp.2108-2114, 2002. ,
DOI : 10.1128/JCM.40.6.2108-2114.2002
URL : http://jcm.asm.org/content/40/6/2108.full.pdf
Endobronquitis por Scedosporium apiospermum en una ni??a con fibrosis qu??stica, Revista Iberoamericana de Micolog??a, vol.23, issue.4, pp.245-248, 2006. ,
DOI : 10.1016/S1130-1406(06)70054-7
Pseudallescheria boydii (Anamorph Scedosporium apiospermum) Infection in Solid Organ Transplant Recipients in a Tertiary Medical Center and Review of the Literature, Medicine, vol.81, issue.5, pp.333-348, 2002. ,
DOI : 10.1097/00005792-200209000-00001
Infections Due to Scedosporium apiospermum and Scedosporium prolificans in Transplant Recipients: Clinical Characteristics and Impact of Antifungal Agent Therapy on Outcome, Clinical Infectious Diseases, vol.47, issue.1, pp.89-99, 2005. ,
DOI : 10.1128/AAC.47.1.106-117.2003
Disseminated Scedosporium apiospermum Infection in a Cystic Fibrosis Patient After Double-lung Transplantation, The Journal of Heart and Lung Transplantation, vol.25, issue.5, pp.603-607, 2006. ,
DOI : 10.1016/j.healun.2005.12.011
Scedosporium apiospermum (Pseudoallescheria boydii) Infection in Lung Transplant Recipients, The Journal of Heart and Lung Transplantation, vol.26, issue.4, pp.350-356, 2007. ,
DOI : 10.1016/j.healun.2007.01.011
Disseminated Scedosporium/Pseudallescheria Infection after Double-Lung Transplantation in Patients with Cystic Fibrosis, Journal of Clinical Microbiology, vol.48, issue.5, pp.1978-1982, 2010. ,
DOI : 10.1128/JCM.01840-09
URL : http://jcm.asm.org/content/48/5/1978.full.pdf
The respiratory burst of phagocytes., Journal of Clinical Investigation, vol.73, issue.3, pp.599-601, 1984. ,
DOI : 10.1172/JCI111249
Antimicrobial reactive oxygen and nitrogen species: concepts and controversies, Nature Reviews Microbiology, vol.115, issue.Suppl. 1, pp.820-832, 2004. ,
DOI : 10.1016/S0092-8674(03)00803-1
Reactive Nitrogen Species Contribute to Innate Host Defense against Campylobacter jejuni, Infection and Immunity, vol.76, issue.3, pp.986-993, 2008. ,
DOI : 10.1128/IAI.01063-07
URL : http://iai.asm.org/content/76/3/986.full.pdf
Neutrophils and inflammatory metabolism in antimicrobial functions of the mucosa, Journal of Leukocyte Biology, vol.98, issue.4, pp.517-522, 2015. ,
DOI : 10.1189/jlb.3MR1114-556R
Microbial antioxidant defense enzymes, Microbial Pathogenesis, vol.110, pp.56-65, 2017. ,
DOI : 10.1016/j.micpath.2017.06.015
Oxidative stress and lipid-derived inflammatory mediators during acute exacerbations of cystic fibrosis, Respirology, vol.7, issue.1, pp.63-69, 2007. ,
DOI : 10.1152/ajpcell.00188.2002
Oxidative stress and antioxidant therapy in cystic fibrosis, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, vol.1822, issue.5, pp.690-713, 2012. ,
DOI : 10.1016/j.bbadis.2011.12.012
Reactive oxygen species and the strategy of antioxidant defense in fungi: A review, Applied Biochemistry and Microbiology, vol.1067, issue.1, pp.506-515, 2007. ,
DOI : 10.1152/physrev.00018.2001
Protection from nitrosative stress: A central role for microbial flavohemoglobin, Free Radical Biology and Medicine, vol.52, issue.9, pp.1620-1633, 2012. ,
DOI : 10.1016/j.freeradbiomed.2012.01.028
Draft Genome Sequence of the Pathogenic Fungus Scedosporium apiospermum, Genome Announcements, vol.56, issue.5, pp.988-1002, 2014. ,
DOI : 10.1128/AAC.05910-11
URL : http://genomea.asm.org/content/2/5/e00988-14.full.pdf
, Biochemical Journal, vol.315, issue.1, pp.119-126, 1996.
DOI : 10.1042/bj3150119
Proteins and Peptidases from Conidia and Mycelia of Scedosporium apiospermum Strain HLPB, Mycopathologia, vol.44, issue.1, pp.25-30, 2009. ,
DOI : 10.1099/00221287-147-6-1499
Metallopeptidase inhibitors arrest vital biological processes in the fungal pathogen Scedosporium apiospermum, Mycoses, vol.17, issue.2, pp.105-112, 2011. ,
DOI : 10.1023/B:BIOM.0000029438.97990.c6
Molecular cloning and biochemical characterization of a Cu,Zn-superoxide dismutase from Scedosporium apiospermum, Microbes and Infection, vol.9, issue.5, pp.558-565, 2007. ,
DOI : 10.1016/j.micinf.2007.01.027
ABSTRACT, Clinical and Vaccine Immunology, vol.32, issue.1, pp.37-45, 2015. ,
DOI : 10.1007/BF01962169
Identification of Scedosporium boydii catalase A1 gene, a reactive oxygen species detoxification factor highly expressed in response to oxidative stress and phagocytic cells, Fungal Biology, vol.119, issue.12, pp.1322-1333, 2015. ,
DOI : 10.1016/j.funbio.2015.09.007
Enzymatic Mechanisms Involved in Evasion of Fungi to the Oxidative Stress: Focus on Scedosporium apiospermum, Mycopathologia, vol.119, issue.6, pp.227-239, 2018. ,
DOI : 10.1016/j.funbio.2015.09.007
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2???????CT Method, Methods, vol.25, issue.4, pp.402-408, 2001. ,
DOI : 10.1006/meth.2001.1262
Chronic granulomatous disease, British Medical Bulletin, vol.27, issue.1, pp.50-63, 2016. ,
DOI : 10.1038/ng1058
URL : https://hal.archives-ouvertes.fr/hal-00382226
Successful Treatment of Systemic Exophiala dermatitidis Infection in a Patient with Chronic Granulomatous Disease, Clinical Infectious Diseases, vol.14, issue.1, pp.235-242, 1992. ,
DOI : 10.1093/clinids/14.1.235
Fungal infections in paediatric patients with chronic granulomatous disease, Rev Iberoam Micol, vol.17, pp.6-9, 2000. ,
Scedosporium prolificans brain abscess in a patient with chronic granulomatous disease: Successful combination therapy with voriconazole and terbinafine, Scandinavian Journal of Infectious Diseases, vol.33, issue.1, pp.87-90, 2007. ,
DOI : 10.1111/j.1442-9071.2005.01045.x
Geosmithia argillacea: an Emerging Pathogen in Patients with Cystic Fibrosis, Journal of Clinical Microbiology, vol.48, issue.7, pp.2381-2386, 2010. ,
DOI : 10.1128/JCM.00047-10
URL : http://jcm.asm.org/content/48/7/2381.full.pdf
The oxidative stress response of the opportunistic fungal pathogen Candida glabrata, Revista Iberoamericana de Micolog??a, vol.31, issue.1, pp.67-71, 2014. ,
DOI : 10.1016/j.riam.2013.09.012
A Multifaceted Study of Scedosporium boydii Cell Wall Changes during Germination and Identification of GPI-Anchored Proteins, PLOS ONE, vol.280, issue.Suppl 1, p.128680, 2015. ,
DOI : 10.1371/journal.pone.0128680.s003
URL : https://hal.archives-ouvertes.fr/hal-01392256
, Molecular Microbiology, vol.178, issue.Suppl 1, pp.910-923, 2010.
DOI : 10.4049/jimmunol.178.10.6367
The bZip transcription factor Cap1p is involved in multidrug resistance and oxidative stress response in Candida albicans, J Bacteriol, vol.181, pp.700-708, 1999. ,
Granulocytes govern the transcriptional response, morphology and proliferation of Candida albicans in human blood, Molecular Microbiology, vol.97, issue.2, pp.397-415, 2005. ,
DOI : 10.1128/jb.179.7.2202-2209.1997
Contribution of Fdh3 and Glr1 to Glutathione Redox State, Stress Adaptation and Virulence in Candida albicans, PLOS ONE, vol.181, issue.6, p.126940, 2015. ,
DOI : 10.1371/journal.pone.0126940.s003
Posttranslational, Translational, and Transcriptional Responses to Nitric Oxide Stress in Cryptococcus neoformans: Implications for Virulence, Eukaryotic Cell, vol.5, issue.3, pp.518-529, 2006. ,
DOI : 10.1128/EC.5.3.518-529.2006
Catalases of Aspergillus fumigatus, Infection and Immunity, vol.71, issue.6, pp.3551-3562, 2003. ,
DOI : 10.1128/IAI.71.6.3551-3562.2003
The Cryptococcus neoformans Catalase Gene Family and Its Role in Antioxidant Defense, Eukaryotic Cell, vol.5, issue.9, pp.1447-1459, 2006. ,
DOI : 10.1128/EC.00098-06
Cloning and sequencing of a Candida albicans catalase gene and effects of disruption of this gene, Infect Immun, vol.66, pp.1953-1961, 1998. ,
The Crystal Structure of Peroxiredoxin Asp f3 Provides Mechanistic Insight into Oxidative Stress Resistance and Virulence of Aspergillus fumigatus, Scientific Reports, vol.93, issue.1, p.33396, 2016. ,
DOI : 10.1111/mmi.12679
Comparative genomics allowed the identification of drug targets against human fungal pathogens, BMC Genomics, vol.8, issue.1, p.75, 2011. ,
DOI : 10.1093/bioinformatics/btg180
URL : https://hal.archives-ouvertes.fr/inria-00610630
Essential gene discovery in the basidiomycete Cryptococcus neoformans for antifungal drug target prioritization, MBio, vol.6, pp.2334-2348, 2015. ,
: Absence of a General Stress Response, Molecular Biology of the Cell, vol.19, issue.4, pp.1460-1467, 2003. ,
DOI : 10.1002/yea.831
Proteomic analysis of the oxidative stress response inCandida albicans, PROTEOMICS, vol.198, issue.5, pp.686-697, 2007. ,
DOI : 10.1128/MCB.17.12.6982
Candida albicans TRR1 heterozygotes show increased sensitivity to oxidative stress and decreased pathogenicity, Afr J Microbiol Res, vol.6, pp.1796-1805, 2012. ,
Structural and functional characterization of the recombinant thioredoxin reductase from Candida albicans as a potential target for vaccine and drug design, Applied Microbiology and Biotechnology, vol.9, issue.13, pp.4015-4025, 2015. ,
DOI : 10.2174/138945011501140115112242
Auranofin: Repurposing an Old Drug for a Golden New Age, Drugs in R&D, vol.193, issue.7, pp.13-20, 2015. ,
DOI : 10.1128/JB.01063-10
Auranofin exerts broad-spectrum bactericidal activities by targeting thiol-redox homeostasis, Proceedings of the National Academy of Sciences, vol.63, issue.2, pp.4453-4458, 2015. ,
DOI : 10.1038/ja.2014.36
Inhibition of bacterial and fungal pathogens by the orphaned drug auranofin, Future Medicinal Chemistry, vol.254, issue.18, pp.117-132, 2016. ,
DOI : 10.3390/molecules15042203
Antibacterial activity and mechanism of action of auranofin against multi-drug resistant bacterial pathogens, Scientific Reports, vol.9, issue.1, p.22571, 2016. ,
DOI : 10.1371/journal.pone.0116259
Repurposing auranofin for the treatment of cutaneous staphylococcal infections, International Journal of Antimicrobial Agents, vol.47, issue.3, pp.195-201, 2016. ,
DOI : 10.1016/j.ijantimicag.2015.12.016
URL : http://europepmc.org/articles/pmc4792765?pdf=render
activity against a variety of medically important fungi, Virulence, vol.8, issue.2, pp.138-142, 2016. ,
DOI : 10.1080/13693780802510224
Characterization of the Aspergillus fumigatus detoxification systems for reactive nitrogen intermediates and their impact on virulence, Frontiers in Microbiology, vol.381, issue.e1000868, p.469, 2014. ,
DOI : 10.1016/j.bbrc.2009.01.112