CHEMANI, Chanez, Anne IMBERTY, Sophie DE BENTZMANN, Maud PIERRE, Michaela WIMMEROVÁ, Benoit P. GUERY a Karine FAURE. Role of LecA and LecB Lectins in Pseudomonas aeruginosa-Induced Lung Injury and Effect of Carbohydrate Ligands. Online. INFECTION AND IMMUNITY. The American Society for Microbiology, 2009, roč. 77, č. 5, s. 2065-2075. ISSN 0019-9567. [citováno 2024-04-23]
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Základní údaje
Originální název Role of LecA and LecB Lectins in Pseudomonas aeruginosa-Induced Lung Injury and Effect of Carbohydrate Ligands
Název česky Uloha lektinu LecA a LecB v poskozeni plic vyvolanych Pseudomonas aeruginosa a efekt ligandu na bazi sacharidu
Název anglicky Role of LecA and LecB Lectins in Pseudomonas aeruginosa-Induced Lung Injury and Effect of Carbohydrate Ligands
Autoři CHEMANI, Chanez (250 Francie), Anne IMBERTY (250 Francie), Sophie DE BENTZMANN (250 Francie), Maud PIERRE (250 Francie), Michaela WIMMEROVÁ (203 Česká republika, garant), Benoit P. GUERY (250 Francie) a Karine FAURE (250 Francie)
Vydání INFECTION AND IMMUNITY, The American Society for Microbiology, 2009, 0019-9567.
Další údaje
Originální jazyk čeština
Typ výsledku Článek v odborném periodiku
Obor 10610 Biophysics
Stát vydavatele Norsko
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 4.205
Kód RIV RIV/00216224:14310/09:00029451
Organizační jednotka Přírodovědecká fakulta
UT WoS 000265279900037
Klíčová slova anglicky lectin; infection;preudomonas aeruginosa
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: prof. RNDr. Michaela Wimmerová, Ph.D., učo 854. Změněno: 24. 8. 2009 16:15.
Anotace
Pseudomonas aeruginosa is a frequently encountered pathogen that is involved in acute and chronic lung infections. Lectin-mediated bacterium-cell recognition and adhesion are critical steps in initiating P. aeruginosa pathogenesis. This study was designed to evaluate the contributions of LecA and LecB to the pathogenesis of P. aeruginosa-mediated acute lung injury. Using an in vitro model with A549 cells and an experimental in vivo murine model of acute lung injury, we compared the parental strain to lecA and lecB mutants. The effects of both LecA- and Lec B-specific lectin-inhibiting carbohydrates (a-methyl-galactoside and a-methyl-fucoside, respectively) were evaluated. In vitro, the parental strain was associated with increased cytotoxicity and adhesion on A549 cells compared to the lecA and lecB mutants. In vivo, the P. aeruginosa-induced increase in alveolar barrier permeability was reduced with both mutants. The bacterial burden and dissemination were decreased for both mutants compared with the parental strain. Coadministration of specific lectin inhibitors markedly reduced lung injury and mortality. Our results demonstrate that there is a relationship between lectins and the pathogenicity of P. aeruginosa
Anotace anglicky
Pseudomonas aeruginosa is a frequently encountered pathogen that is involved in acute and chronic lung infections. Lectin-mediated bacterium-cell recognition and adhesion are critical steps in initiating P. aeruginosa pathogenesis. This study was designed to evaluate the contributions of LecA and LecB to the pathogenesis of P. aeruginosa-mediated acute lung injury. Using an in vitro model with A549 cells and an experimental in vivo murine model of acute lung injury, we compared the parental strain to lecA and lecB mutants. The effects of both LecA- and Lec B-specific lectin-inhibiting carbohydrates (a-methyl-galactoside and a-methyl-fucoside, respectively) were evaluated. In vitro, the parental strain was associated with increased cytotoxicity and adhesion on A549 cells compared to the lecA and lecB mutants. In vivo, the P. aeruginosa-induced increase in alveolar barrier permeability was reduced with both mutants. The bacterial burden and dissemination were decreased for both mutants compared with the parental strain. Coadministration of specific lectin inhibitors markedly reduced lung injury and mortality. Our results demonstrate that there is a relationship between lectins and the pathogenicity of P. aeruginosa
Návaznosti
GA303/09/1168, projekt VaVNázev: Lektiny z lidských patogenů - struktura, funkce, inženýrství
Investor: Grantová agentura ČR, Lektidy z lidských patogenů - struktura, funkce, inženýrství
MSM0021622413, záměrNázev: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Proteiny v metabolismu a při interakci organismů s prostředím
VytisknoutZobrazeno: 23. 4. 2024 17:33