2013
DOI: 10.1371/journal.pone.0067534
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Assessing Global Transcriptome Changes in Response to South African Cassava Mosaic Virus [ZA-99] Infection in Susceptible Arabidopsis thaliana

Abstract: In susceptible plant hosts, co-evolution has favoured viral strategies to evade host defenses and utilize resources to their own benefit. The degree of manipulation of host gene expression is dependent on host-virus specificity and certain abiotic factors. In order to gain insight into global transcriptome changes for a geminivirus pathosystem, South African cassava mosaic virus [ZA:99] and Arabidopsis thaliana, 4×44K Agilent microarrays were adopted. After normalization, a log2 fold change filtering of data (… Show more

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Cited by 50 publications
(44 citation statements)
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References 92 publications
(193 reference statements)
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“…Contrarily to what observed for CabLCV [19] and SACMV [20], we could not detect in our dataset any indication of cell cycle activation probably because of the very low number of infected cells. The inability of the approach to highlight such change underscores the difficulty to investigate cell-autonomous processes, particularly for phloem-limited viruses, and the need to study infected cells instead of cell tissues.…”
Section: Discussioncontrasting
confidence: 60%
“…Contrarily to what observed for CabLCV [19] and SACMV [20], we could not detect in our dataset any indication of cell cycle activation probably because of the very low number of infected cells. The inability of the approach to highlight such change underscores the difficulty to investigate cell-autonomous processes, particularly for phloem-limited viruses, and the need to study infected cells instead of cell tissues.…”
Section: Discussioncontrasting
confidence: 60%
“…The extent of these interactions is illustrated by host transcriptome studies that have identified thousands of plant genes that are differentially expressed in response to geminivirus infection (52,53). In contrast, less is known about posttranscriptional regulation in the infection process.…”
Section: Discussionmentioning
confidence: 99%
“…qRT-PCR was performed using the SsoFast EvaGreen Supermix (BioRad, Hercules, CA, USA) with the Bio-Rad iQ5 Real-Time PCR system with gene specific primers (Additional file 1), each reaction containing 10 μl SsoFast EvaGreen Supermix, 1 μl cDNA, 1 μl primers and 8 μl water. The expression levels of transcripts are presented relative to the corresponding control samples for each condition, EF1-a and actin2 were used as internal control gene [26, 27]. …”
Section: Methodsmentioning
confidence: 99%