Gene expression analysis of the biocontrol fungus Trichoderma harzianum in the presence of tomato plants, chitin, or glucose using a high-density oligonucleotide microarray

<p>Abstract</p> <p>Background</p> <p>It has recently been shown that the <it>Trichoderma </it>fungal species used for biocontrol of plant diseases are capable of interacting with plant roots directly, behaving as symbiotic microorganisms. With a view to providing further information at transcriptomic level about the early response of <it>Trichoderma </it>to a host plant, we developed a high-density oligonucleotide (HDO) microarray encompassing 14,081 Expressed Sequence Tag (EST)-based transcripts from eight <it>Trichoderma </it>spp. and 9,121 genome-derived transcripts of <it>T. reesei</it>, and we have used this microarray to examine the gene expression of <it>T. harzianum </it>either alone or in the presence of tomato plants, chitin, or glucose.</p> <p>Results</p> <p>Global microarray analysis revealed 1,617 probe sets showing differential expression in <it>T. harzianum </it>mycelia under at least one of the culture conditions tested as compared with one another. Hierarchical clustering and heat map representation showed that the expression patterns obtained in glucose medium clustered separately from the expression patterns observed in the presence of tomato plants and chitin. Annotations using the Blast2GO suite identified 85 of the 257 transcripts whose probe sets afforded up-regulated expression in response to tomato plants. Some of these transcripts were predicted to encode proteins related to <it>Trichoderma</it>-host (fungus or plant) associations, such as Sm1/Elp1 protein, proteases P6281 and PRA1, enchochitinase CHIT42, or QID74 protein, although previously uncharacterized genes were also identified, including those responsible for the possible biosynthesis of nitric oxide, xenobiotic detoxification, mycelium development, or those related to the formation of infection structures in plant tissues.</p> <p>Conclusion</p> <p>The effectiveness of the <it>Trichoderma </it>HDO microarray to detect different gene responses under different growth conditions in the fungus <it>T. harzianum </it>strongly indicates that this tool should be useful for further assays that include different stages of plant colonization, as well as for expression studies in other <it>Trichoderma </it>spp. represented on it. Using this microarray, we have been able to define a number of genes probably involved in the transcriptional response of <it>T. harzianum </it>within the first hours of contact with tomato plant roots, which may provide new insights into the mechanisms and roles of this fungus in the <it>Trichoderma</it>-plant interaction.</p