Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractEnterococcus faecalis virulence regulator FsrA binding to target promoters    Next AbstractDeficient pheromone responses in mice lacking a cluster of vomeronasal receptor genes »

Infect Immun


Title:Cryptococcus neoformans differential gene expression detected in vitro and in vivo with green fluorescent protein
Author(s):del Poeta M; Toffaletti DL; Rude TH; Sparks SD; Heitman J; Perfect JR;
Address:"Departments of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA"
Journal Title:Infect Immun
Year:1999
Volume:67
Issue:4
Page Number:1812 - 1820
DOI: 10.1128/IAI.67.4.1812-1820.1999
ISSN/ISBN:0019-9567 (Print) 1098-5522 (Electronic) 0019-9567 (Linking)
Abstract:"Synthetic green fluorescent protein (GFP) was used as a reporter to detect differential gene expression in the pathogenic fungus Cryptococcus neoformans. Promoters from the C. neoformans actin, GAL7, or mating-type alpha pheromone (MFalpha1) genes were fused to GFP, and the resulting reporter genes were used to assess gene expression in serotype A C. neoformans. Yeast cells containing an integrated pACT::GFP construct demonstrated that the actin promoter was expressed during vegetative growth on yeast extract-peptone-dextrose medium. In contrast, yeast cells containing the inducible GAL7::GFP or MFalpha1::GFP reporter genes expressed significant GFP activity only during growth on galactose medium or V-8 agar, respectively. These findings demonstrated that the GAL7 and MFalpha1 promoters from a serotype D C. neoformans strain function when introduced into a serotype A strain. Because the MFalpha1 promoter is induced by nutrient deprivation and the MATalpha locus containing the MFalpha1 gene has been linked with virulence, yeast cells containing the pMFalpha1::GFP reporter gene were analyzed for GFP expression in the central nervous system (CNS) of immunosuppressed rabbits. In fact, significant GFP expression from the MFalpha1::GFP reporter gene was detected after the first week of a CNS infection. These findings suggest that there are temporal, host-specific cues that regulate gene expression during infection and that the MFalpha1 gene is induced during the proliferative stage of a CNS infection. In conclusion, GFP can be used as an effective and sensitive reporter to monitor specific C. neoformans gene expression in vitro, and GFP reporter constructs can be used as an approach to identify a novel gene(s) or to characterize known genes whose expression is regulated during infection"
Keywords:"Actins/genetics Animals Blotting, Southern Cryptococcus neoformans/*genetics *Gene Expression Regulation, Fungal *Genes, Reporter Green Fluorescent Proteins *Luminescent Proteins/genetics Mating Factor Peptides/genetics Rabbits Transformation, Genetic;"
Notes:"Medlinedel Poeta, M Toffaletti, D L Rude, T H Sparks, S D Heitman, J Perfect, J R eng R56 AI028388/AI/NIAID NIH HHS/ R01 AI028388/AI/NIAID NIH HHS/ AI41937/AI/NIAID NIH HHS/ AI28388/AI/NIAID NIH HHS/ AI-94-014/AI/NIAID NIH HHS/ Research Support, U.S. Gov't, P.H.S. 1999/03/20 Infect Immun. 1999 Apr; 67(4):1812-20. doi: 10.1128/IAI.67.4.1812-1820.1999"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 29-06-2024