Characterization of a secreted aspartyl protease of the fungal pathogen Paracoccidioides brasiliensis

2009 ◽  
pp. 1-11
Author(s):  
Bruno Aluisio Coutinho De Assis Tacco ◽  
Juliana Alves Parente ◽  
Monica Santiago Barbosa ◽  
Sonia Nair Bao ◽  
Tercio De Souza Goes ◽  
...  
1999 ◽  
Vol 274 (34) ◽  
pp. 24431-24437 ◽  
Author(s):  
Hiroto Komano ◽  
Nathan Rockwell ◽  
Gary T. Wang ◽  
Grant A. Krafft ◽  
Robert S. Fuller

2016 ◽  
Author(s):  
Nor’Aishah Hasan ◽  
Mohd Y. Rafii ◽  
Harun A. Rahim ◽  
Nusaibah Syd Ali ◽  
Norida Mazlan ◽  
...  

2009 ◽  
Vol 11 (10-11) ◽  
pp. 895-903 ◽  
Author(s):  
Sabrina Fonseca Ingênito Moreira Dantas ◽  
Tereza Cristina Vieira de Rezende ◽  
Alexandre Melo Bailão ◽  
Carlos Pelleschi Taborda ◽  
Rodrigo da Silva Santos ◽  
...  

Author(s):  
Guy Honée ◽  
Guido F. J. M. van den Ackerveken ◽  
Henk W. J. van den Broek ◽  
Ton J. Cozijnsen ◽  
Matthieu H. A. J. Joosten ◽  
...  

2020 ◽  
Vol 20 (3) ◽  
Author(s):  
Jiu Yi ◽  
Junjun Sang ◽  
Jingyu Zhao ◽  
Lei Gao ◽  
Yali Yang ◽  
...  

ABSTRACT Cryptococcus neoformans is an important invasive fungal pathogen that causes life-threatening meningoencephalitis in humans. Its biological and pathogenic regulatory mechanisms remain largely unknown, particularly due to the presence of those core transcription factors (TFs). Here, we conducted a detailed characterization of the TF Liv4 in the biology and virulence of C. neoformans. Deletion of TF Liv4 protein resulted in growth defect under both normal and stress conditions (such as high temperature and cell wall/membrane damaging agents), drastic morphological damage and also attenuated virulence in C. neoformans. These phenotypic changes might be contributed to transcriptional abnormality in the liv4Δ mutant, in which several cryptococcal genes involved in energy metabolism and cell wall integrity were downregulated. Furthermore, ChIP-seq and ChIP-qPCR assays suggested TF Liv4 might exert its regulatory function in transcription by its activation of RBP1 in C. neoformans. Taken together, our work highlights the importance of TF Liv4 in the growth and virulence of C. neoformans, and it facilitates a better understanding of cryptococcal pathogenesis mechanisms.


1988 ◽  
Vol 51 (3) ◽  
pp. 229-241 ◽  
Author(s):  
Richard S. Soper ◽  
Mitsuaki Shimazu ◽  
Richard A. Humber ◽  
Mark E. Ramos ◽  
Ann E. Hajek

2021 ◽  
Vol 10 (1) ◽  
pp. ACCEPTED
Author(s):  
Iqra Haider Khan ◽  
Arshad Javaid ◽  
Syeda Fakehha Naqvi

Penicillium expansum Link causes an economically important postharvest blue mold disease in a number of fruits and vegetables. In the present study, this fungus was isolated from rotted grapes and identified on morphological basis. Identification of the pathogen was further confirmed on molecular basis by using four different primer pairs namely ITS, β-tubulin, CMD and CF under accession numbers MN752155, MN787831, MN787832 and MN787833, respectively. Leaf extract of Chenopodium murale was assessed for its potential to control in vitro growth of P. expansum. For this purpose, leaves were extracted in methanol and after evaporation of the solvent, the resulting extract was successively partitioned with n-hexane, chloroform, ethyl acetate and n-butanol followed by antifungal bioassays with different concentrations (1.562 to 200 mg mL-1) each organic solvent fraction. Although all the fractions variably controlled the fungal pathogen, however, n-butanol fraction showed the highest antifungal activity causing 45–86% reduction in biomass of the pathogen. Ethyl acetate fraction was also highly antifungal and reduced fungal biomass by 44–81%. Chloroform and n-hexane fractions were comparatively less effective and reduced biomass of P. expansum by 30–72% and 11–44%, respectively. This study concludes that ethyl acetate and n-butanol fractions are highly antifungal in nature against P. expansum.


2021 ◽  
Author(s):  
Yi Song ◽  
Xue-Cheng Zhang ◽  
Yichun Qiu ◽  
Annika Briggs ◽  
Yves Millet ◽  
...  

Despite the importance of the root immune system in the interaction with rhizosphere microbes, the majority of genetic screens for immunity regulators have been performed in leaves. A previous screen identified 27 hsm (hormone-mediated suppression of MAMP-triggered immunity) mutants that are impaired in jasmonic acid (JA)-mediated suppression of pattern-triggered immunity (PTI) in roots. Here we characterized 16 of the hsm mutants that retain JA sensitivity and are potential negative regulators of root immunity. We found that the majority of hsm mutants show enhanced resistance to Fusarium, a root fungal pathogen; however, only a subset are more resistant to a foliar pathogen. Surprisingly, 12 of 16 hsm mutants are also impaired in abscisic acid (ABA)-mediated suppression of PTI, suggesting a largely shared pathway between JA- and ABA-mediated immune suppression in roots. Although all hsm mutants are insensitive to JA-mediated suppression of root immunity, hsm4 shows hypersensitivity to JA-mediated root growth inhibition and JA-induced gene expression. Consistently, hsm4 is more resistant to leaf pathogens, suggesting that HSM4 is a negative regulator of both root and leaf immunity. Hsm4 was mapped to a mutation in a conserved ARM-repeat protein homologous to yeast SDA1, which has been reported to regulate 60S ribosome biogenesis. As translational reprogramming is a critical layer of immune regulation, this work suggests that AtSDA1 is a novel negative translational regulator of immunity. Additionally, a comprehensive characterization of all 16 hsm mutants provides a genetic toolkit to identify novel mechanisms that regulate root immunity.


Sign in / Sign up

Export Citation Format

Share Document