2012
DOI: 10.1128/ec.00016-12
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Molecular Characterization of the Putative Transcription Factor SebA Involved in Virulence in Aspergillus fumigatus

Abstract: ABSTRACTAspergillus fumigatusis a major opportunistic pathogen and allergen of mammals. Nutrient sensing and acquisition mechanisms, as well as the capability to cope with different stressing conditions, are essential forA. fumigatusvirulence and survival in the mammalian host. This study characterized the Show more

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Cited by 41 publications
(56 citation statements)
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“…In many systems, the transcriptional machinery that regulates gene expression in response to ROS is well characterized (12,13,(47)(48)(49)(50)(51)(52). In the pathogenic protist E. histolytica, increased virulence has been linked to the parasite's ability to survive exposure to ROS (21), and the transcriptional response to hydrogen peroxide stress has been characterized (2).…”
Section: Discussionmentioning
confidence: 99%
“…In many systems, the transcriptional machinery that regulates gene expression in response to ROS is well characterized (12,13,(47)(48)(49)(50)(51)(52). In the pathogenic protist E. histolytica, increased virulence has been linked to the parasite's ability to survive exposure to ROS (21), and the transcriptional response to hydrogen peroxide stress has been characterized (2).…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, SEB1 is involved in but not essential for glycerol dehydrogenase (gld1) gene expression and glycerol accumulation in T. atroviride during osmotic stress (1024). In A. fumigatus, SEB1 is involved in the response to oxidative stress and virulence, and the absence of seb1 results in the deregulation of Afatf1 and Afyap1, which have also been implicated in the response to stress (1025).…”
Section: C2h2 Zinc Finger Transcription Factorsmentioning
confidence: 99%
“…The murine model of pulmonary aspergillosis was performed according to the method of Dinamarco et al (44). Outbreed female mice (BALB/c strain; body weight, 20 to 22 g) were housed in vented cages containing 5 animals.…”
Section: Methodsmentioning
confidence: 99%
“…The AMs were counted in a hemocytometer. The phagocytic assay was performed according to the methods of Dinamarco et al and Mech et al (44,45), with some changes. Briefly, in a 24-well plate containing one 15-mm-diameter coverslip per well, about 2 ϫ 10 4 macrophages were incubated with 1 ml of RPMI-FBS at 37°C with 5% CO 2 for 1 h. Afterward, the wells were washed with 1 ml of assay medium to remove nonadherent cells.…”
Section: Methodsmentioning
confidence: 99%
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