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Series GSE43648 Query DataSets for GSE43648
Status Public on Oct 01, 2013
Title Examining gene expression of the fungus Magnaporthe oryzae during challenge with the bacterium Lysobacter enzymogenes
Organism Pyricularia oryzae
Experiment type Expression profiling by high throughput sequencing
Summary Plants and animals have evolved a first line of defense response to pathogens called innate or basal immunity. While basal defenses in these organisms are well studied, there is almost a complete lack of understanding of such systems in fungal species, and more specifically, how they are able to detect and mount a defense response upon pathogen attack. Hence, the goal of the present study was to understand how fungi respond to biotic stress by assessing the transcriptional profile of the rice blast pathogen, Magnaporthe oryzae, when challenged with the bacterial antagonist Lysobacter enzymogenes. Based on microscopic observations of interactions between M. oryzae and wild-type L. enzymogenes strain C3, we selected early and intermediate stages represented by time-points of 3 and 9 hours post-inoculation, respectively, to evaluate the fungal transcriptome using RNA-seq. For comparative purposes, we also challenged the fungus with L. enzymogenes mutant strain DCA, previously demonstrated to be devoid of antifungal activity. A comparison of transcriptional data from fungal interactions with the wild-type bacterial strain C3 and the mutant strain DCA revealed 463 fungal genes that were down-regulated during attack by C3; of these genes, 100 were also found to be up-regulated during the interaction with DCA. Functional categorization of genes in this suite included those with roles in carbohydrate metabolism, cellular transport and stress response. One gene in this suite belongs to the CFEM-domain class of fungal proteins. Another CFEM class protein called PTH11 has been previously characterized, and we found that a deletion in this gene caused advanced lesion development by C3 compared to its growth on the wild-type fungus. We discuss the characterization of this suite of 100 genes with respect to their role in the fungal defense response.
 
Overall design Included in the analysis are two biological replicates each of the fungus in buffer alone (control), the fungus challenged with wild type bacterium at 3 and 9 hours post-inoculation (hpi) and the fungus challeged with the mutant bacterium (mutated for ability to secrete antibiotics and enzymes) at 3 and 9 hpi.
 
Contributor(s) Mathioni SM, Patel N, Riddick B, Sweigard JA, Czymmek KJ, Caplan JL, Kunjeti SG, Kunjeti S, Raman V, Kobayashi DY, Donofrio NM
Citation(s) 24098512
Submission date Jan 21, 2013
Last update date May 15, 2019
Contact name Sridhara G Kunjeti
E-mail(s) sridhara@udel.edu
Phone 3028317371
Organization name University of Delaware
Department Plant and Soil Sciences
Lab Donofrio
Street address 531, S. college Ave
City Newark
State/province DE
ZIP/Postal code 19711
Country USA
 
Platforms (1)
GPL16530 Illumina HiSeq 2000 (Magnaporthe oryzae)
Samples (12)
GSM1067597 CON_3hpi_rep1
GSM1067598 CON_3hpi_rep2
GSM1067599 CON_9hpi_rep1
Relations
BioProject PRJNA187047
SRA SRP018111

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE43648_Input_LOX_Lysobacter.txt.gz 401.0 Kb (ftp)(http) TXT
GSE43648_Output_LOX_Lysobacter.xlsx.gz 2.7 Mb (ftp)(http) XLSX
GSE43648_readme.txt.gz 654 b (ftp)(http) TXT
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Processed data are available on Series record
Raw data are available in SRA

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