دورية أكاديمية

Corrected and republished from: "Extracellular Vesicle Formation in Cryptococcus deuterogattii Impacts Fungal Virulence".

التفاصيل البيبلوغرافية
العنوان: Corrected and republished from: "Extracellular Vesicle Formation in Cryptococcus deuterogattii Impacts Fungal Virulence".
المؤلفون: Castelli RF; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil.; Programa de Pós-Graduação em Biologia Parasitária, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, Brazil., Pereira A; Instituto de Química, Universidade de Campinas, São Paulo, Brazil., Honorato L; Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil., Valdez A; Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil., de Oliveira HC; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil., Bazioli JM; Instituto de Química, Universidade de Campinas, São Paulo, Brazil.; Faculty of Pharmaceutical Sciences, State University of Campinas, Campinas, São Paulo, Brazil., Garcia AWA; Programa de Pós-graduação em Biologia Celular e Molecular, Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil., Klimeck TDF; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil., Reis FCG; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil.; Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Fundação Oswaldo Cruz, Rio de Janeiro, Brazil., Camillo-Andrade AC; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil., Santos MDM; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil.; Analytical Biochemistry and Proteomics Unit. IIBCE/Institut Pasteur de Montevideo, Montevideo, Uruguay., Carvalho PC; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil., Zaragoza O; Mycology Reference Laboratory. National Centre for Microbiology. Instituto de Salud Carlos III, Madrid, Spain.; Center for Biomedical Research in Network in Infectious Diseases, CB21/13/00105, Instituto de Salud Carlos III, Madrid, Spain., Staats CC; Programa de Pós-graduação em Biologia Celular e Molecular, Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil., Nimrichter L; Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil., Fill TP; Instituto de Química, Universidade de Campinas, São Paulo, Brazil., Rodrigues ML; Instituto Carlos Chagas, Fundação Oswaldo Cruz (Fiocruz), Curitiba, Brazil.; Instituto de Microbiologia Paulo de Góes (IMPG), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
المصدر: Infection and immunity [Infect Immun] 2024 Apr 09; Vol. 92 (4), pp. e0003724. Date of Electronic Publication: 2024 Mar 12.
نوع المنشور: Journal Article; Corrected and Republished Article
اللغة: English
بيانات الدورية: Publisher: American Society For Microbiology Country of Publication: United States NLM ID: 0246127 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-5522 (Electronic) Linking ISSN: 00199567 NLM ISO Abbreviation: Infect Immun Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Publication: Washington, DC : American Society For Microbiology
Original Publication: [Bethesda, Md.] American Society for Microbiology.
مستخلص: Small molecules are components of fungal extracellular vesicles (EVs), but their biological roles are only superficially known. NOP16 is a eukaryotic gene that is required for the activity of benzimidazoles against Cryptococcus deuterogattii . In this study, during the phenotypic characterization of C. deuterogattii mutants expected to lack NOP16 expression, we observed a reduced EV production. Whole-genome sequencing, RNA-Seq, and cellular proteomics revealed that, contrary to our initial findings, these mutants expressed Nop16 but exhibited altered expression of 14 genes potentially involved in sugar transport. Based on this observation, we designated these mutant strains as Past1 and Past2, representing p otentially a ltered s ugar t ransport. Analysis of the small molecule composition of EVs produced by wild-type cells and the Past1 and Past2 mutant strains revealed not only a reduced number of EVs but also an altered small molecule composition. In a Galleria mellonella model of infection, the Past1 and Past2 mutant strains were hypovirulent. The hypovirulent phenotype was reverted when EVs produced by wild-type cells, but not mutant EVs, were co-injected with the mutant cells in G. mellonella . These results connect EV biogenesis, cargo, and cryptococcal virulence.
Competing Interests: The authors declare no conflict of interest.
التعليقات: Republished from: Infect Immun. 2022 Aug 18;90(8):e0023222. (PMID: 35862719)
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معلومات مُعتمدة: 440015/2018-9 Ministério da Saúde (Ministry of Health); 405520/2018-2, 301304/2017-3 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq); PROEP-ICC 442186/2019-3, VPPCB-007-FIO-18, VPPIS-001-FIO18 Fundação Oswaldo Cruz (FIOCRUZ); 2021/00728-0 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP); Finance Code 001 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES); PID2020-114546RB Ministerio de Ciencia e Innovación (MCIN)
فهرسة مساهمة: Keywords: Cryptococcus; extracellular vesicles
تواريخ الأحداث: Date Created: 20240312 Date Completed: 20240410 Latest Revision: 20240411
رمز التحديث: 20240411
مُعرف محوري في PubMed: PMC11003230
DOI: 10.1128/iai.00037-24
PMID: 38470135
قاعدة البيانات: MEDLINE
الوصف
تدمد:1098-5522
DOI:10.1128/iai.00037-24