The Fusarium oxysporum cell wall proteome under adhesion-inducing conditions

PROTEOMICS ◽  
2009 ◽  
Vol 9 (20) ◽  
pp. 4755-4769 ◽  
Author(s):  
Rafael Prados-Rosales ◽  
Jose L. Luque-Garcia ◽  
Raquel Martínez-López ◽  
Concha Gil ◽  
Antonio Di Pietro
BIO-PROTOCOL ◽  
2016 ◽  
Vol 6 (17) ◽  
Author(s):  
Elena Pérez-Nadales ◽  
Antonio Di Pietro

2008 ◽  
Vol 10 (6) ◽  
pp. 1339-1351 ◽  
Author(s):  
Ana Lilia Martínez-Rocha ◽  
M. Isabel G. Roncero ◽  
Adriana López-Ramirez ◽  
Marçal Mariné ◽  
Josep Guarro ◽  
...  

2015 ◽  
Vol 28 (1) ◽  
pp. 55-68 ◽  
Author(s):  
Carmen Ruiz-Roldán ◽  
Yolanda Pareja-Jaime ◽  
José Antonio González-Reyes ◽  
M. Isabel G. Roncero

Previous studies have demonstrated the essential role of morphogenetic regulation in Fusarium oxysporum pathogenesis, including processes such as cell-wall biogenesis, cell division, and differentiation of infection-like structures. We identified three F. oxysporum genes encoding predicted transcription factors showing significant identities to Magnaporthe oryzae Con7p, Con7-1, plus two identical copies of Con7-2. Targeted deletion of con7-1 produced nonpathogenic mutants with altered morphogenesis, including defects in cell wall structure, polar growth, hyphal branching, and conidiation. By contrast, simultaneous inactivation of both con7-2 copies caused no detectable defects in the resulting mutants. Comparative microarray-based gene expression analysis indicated that Con7-1 modulates the expression of a large number of genes involved in different biological functions, including host–pathogen interactions, morphogenesis and development, signal perception and transduction, transcriptional regulation, and primary and secondary metabolism. Taken together, our results point to Con7-1 as general regulator of morphogenesis and virulence in F. oxysporum.


2019 ◽  
Vol 209 ◽  
pp. 103506 ◽  
Author(s):  
Lu Xiao ◽  
Taotao Li ◽  
Guoxiang Jiang ◽  
Yueming Jiang ◽  
Xuewu Duan

Biology ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 60 ◽  
Author(s):  
Sergeant ◽  
Printz ◽  
Guerriero ◽  
Renaut ◽  
Lutts ◽  
...  

In this study, the cell-wall-enriched subproteomes at three different heights of alfalfa stems were compared. Since these three heights correspond to different states in stem development, a view on the dynamics of the cell wall proteome during cell maturation is obtained. This study of cell wall protein-enriched fractions forms the basis for a description of the development process of the cell wall and the linking cell wall localized proteins with the evolution of cell wall composition and structure. The sequential extraction of cell wall proteins with CaCl2, EGTA, and LiCl-complemented buffers was combined with a gel-based proteome approach and multivariate analysis. Although the highest similarities were observed between the apical and intermediate stem regions, the proteome patterns are characteristic for each region. Proteins that bind carbohydrates and have proteolytic activity, as well as enzymes involved in glycan remobilization, accumulate in the basal stem region. Beta-amylase and ferritin likewise accumulate more in the basal stem segment. Therefore, remobilization of nutrients appears to be an important process in the oldest stem segment. The intermediate and apical regions are sites of cell wall polymer remodeling, as suggested by the high abundance of proteins involved in the remodeling of the cell wall, such as xyloglucan endoglucosylase, beta-galactosidase, or the BURP-domain containing polygalacturonase non-catalytic subunit. However, the most striking change between the different stem parts is the strong accumulation of a DUF642-conserved domain containing protein in the apical region of the stem, which suggests a particular role of this protein during the early development of stem tissues.


PROTEOMICS ◽  
2006 ◽  
Vol 6 (1) ◽  
pp. 301-311 ◽  
Author(s):  
Emmanuelle M. Bayer ◽  
Andrew R. Bottrill ◽  
John Walshaw ◽  
Marielle Vigouroux ◽  
Mike J. Naldrett ◽  
...  

2017 ◽  
Vol 7 (7) ◽  
pp. 2125-2138 ◽  
Author(s):  
Shiwen Qin ◽  
Chunyan Ji ◽  
Yunfeng Li ◽  
Zhenzhong Wang

Abstract The fungal pathogen Fusarium oxysporum f. sp. cubense causes Fusarium wilt, one of the most destructive diseases in banana and plantain cultivars. Pathogenic race 1 attacks the “Gros Michel” banana cultivar, and race 4 is pathogenic to the Cavendish banana cultivar and those cultivars that are susceptible to Foc1. To understand the divergence in gene expression modules between the two races during degradation of the host cell wall, we performed RNA sequencing to compare the genome-wide transcriptional profiles of the two races grown in media containing banana cell wall, pectin, or glucose as the sole carbon source. Overall, the gene expression profiles of Foc1 and Foc4 in response to host cell wall or pectin appeared remarkably different. When grown with host cell wall, a much larger number of genes showed altered levels of expression in Foc4 in comparison with Foc1, including genes encoding carbohydrate-active enzymes (CAZymes) and other virulence-related genes. Additionally, the levels of gene expression were higher in Foc4 than in Foc1 when grown with host cell wall or pectin. Furthermore, a great majority of genes were differentially expressed in a variety-specific manner when induced by host cell wall or pectin. More specific CAZymes and other pathogenesis-related genes were expressed in Foc4 than in Foc1 when grown with host cell wall. The first transcriptome profiles obtained for Foc during degradation of the host cell wall may provide new insights into the mechanism of banana cell wall polysaccharide decomposition and the genetic basis of Foc host specificity.


Author(s):  
Yamily Y. Burgos-Canul ◽  
Blondy Canto-Canché ◽  
Maxim V. Berezovski ◽  
Gleb Mironov ◽  
Víctor M. Loyola-Vargas ◽  
...  

2021 ◽  
Vol 146 ◽  
pp. 103486
Author(s):  
Tânia R. Fernandes ◽  
Encarnación Sánchez Salvador ◽  
Ángela G. Tapia ◽  
Antonio Di Pietro

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