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This article is part of the supplement: IUFRO Tree Biotechnology Conference 2011: From Genomes to Integration and Delivery

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The effect of heterologous VHb expression to the functioning of stress-related genes in hybrid aspen lines exposured to biotic stress

Hely Häggman1*, Suvi Sutela1, Soile Jokipii-Lukkari1, Tiina Ylioja2, Risto Kasanen3, Anna-Kaisa Anttila1, Marko Suokas1, Estelle Dumont1 and Pauli T Kallio4

Author Affiliations

1 Department of Biology, University of Oulu, Finland

2 Finnish Forest Research Institute, Suonenjoki Research Unit, Finland

3 Department of Forest Sciences, University of Helsinki, Finland

4 Institute of Microbiology, ETH-Zürich, CH-8093 Zürich, Switzerland

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BMC Proceedings 2011, 5(Suppl 7):P88  doi:10.1186/1753-6561-5-S7-P88


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/5/S7/P88


Published:13 September 2011

© 2011 Häggman et al; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background

The hemoglobin produced by Vitreoscilla bacterium, VHb, is capable to promote the respiratory activity and ATP production under hypoxic conditions [1]. In micro-organisms grown under oxygen-limited conditions, the heterologous vhb expression improves the production of primary and secondary compounds, growth as well as stress tolerance [2,3]. VHb has also been shown to protect plants against deleterious effects of nitric oxide (NO), the important signalling molecule produced during pathogen challenges [4]. We have previously studied the vhb expressing hybrid aspen lines (Populus tremula L. x tremuloides Michx.) under elevated UV-B illumination and showed that the VHb lines had increased secondary metabolite production and also enhanced accumulation of starch in chloroplasts when grown in standard greenhouse conditions [5]. In order to reveal the effect of VHb on the expression of stress-related genes in hybrid aspen exposed to biotic stress, we conducted experiments with pathogenic fungus and larvae of insect herbivore.

Materials and methods

In the herbivory experiment, two-year-old VHb line and non-transgenic hybrid aspen line were exposed to the feeding of chestnut moths larvae (Conistra vaccinii L.) for 24 hours. Four VHb hybrid aspen lines and two non-transgenic hybrid aspen lines were infected with pathogenic fungus Venturiatremulae, in vitro. Samples for the RNA and protein extractions were collected after 10 and 21 days of the pathogen inoculation. In both experiments, the transcriptome changes were studied with microarrays and real-time RT-PCR. The cDNA slides contained 8256 stress-related oligos of Populus euphratica. The relative expression of selected genes were conducted with the LightCycler® 2.0 (Roche) and LightCycler® 480 instruments according to the manufacturer’s chemistry. The amount of VHb protein during pathogen fungus experiment was analysed by Western blots.

Results and conclusions

The consumption of the leaves by the chestnut moth larvae was comparable on the non-transgenic and the VHb line. The effect of herbivory to the gene expression levels of wounded and systemic leaves was similar in the VHb and non-transgenic hybrid aspen lines, but in the non-transgenic line, the detected changes were more severe than in the VHb hybrid aspen line. The genes encoding bark storage proteins (BSPs), copper chaperone (CCH), and nitrate transporter (NRT) were among the limited number of genes which showed different expression changes between the VHb and non-transgenic hybrid aspen line.

The hybrid aspen lines infected with V. tremulae showed symptoms of shoot blight i.e. blackened stems and leaves, but the amount of VHb protein did not correlate with the severity of the disease. At the transcriptome level, the studied lines responded to the pathogen treatment individually in the first sampling (10 days) whereas the expression profiles of the lines resembled each other in the second sampling (21 days). The functional grouping of the genes with known mode of action resulted most representatives in protein metabolism, photosynthesis, stress as well as RNA metabolism groups.

In general, the transcriptome profiling of fungus- and herbivory-induced responses did not reveal any biological or molecular process altered in all of the VHb lines due to the biotic interactions. Moreover, based on the real-time RT-PCR results, the vhb expression did not show induction after the 24-hour herbivore treatment or the inoculation with the V. tremulae.

References

  1. Kallio PT, Kim D-J, Tsai PS, Bailey JE: Intracellular expression of Vitreoscilla hemoglobin alters Escherichia coli energy metabolism under oxygen-limited conditions.

    Eur. J. Biochem 1994, 219:201-208. PubMed Abstract | Publisher Full Text OpenURL

  2. Frey AD, Kallio PT: Bacterial hemoglobins and flavohemoglobins: versatile proteins and their impact on microbiology and biotechnology.

    FEMS Microbiol. Rev 2003, 27:525-545.3. PubMed Abstract | Publisher Full Text OpenURL

  3. Jokipii-Lukkari S, Frey AD, Kallio PT, Häggman H: Intrinsic non-symbiotic and truncated haemoglobins and heterologous Vitreoscilla haemoglobin expression in plants.

    J. Exp. Bot 2009, 60:409-422. PubMed Abstract | Publisher Full Text OpenURL

  4. Mur LAJ, Carver TLW, Prats E: NO way to live; the various roles of nitric oxide in plant-pathogen interactions.

    J. Exp. Bot 2006, 57:489-505. PubMed Abstract | Publisher Full Text OpenURL

  5. Häggman H, Frey AD, Ryynänen L, Aronen T, Julkunen-Tiitto R, Tiimonen H, Pihakaski-Maunsbach K, Jokipii S, Chen X, Kallio PT: Expression of Vitreoscilla haemoglobin in hybrid aspen (Populus tremula x tremuloides).

    Plant Biotechnol. J 2003, 1:287-300. PubMed Abstract | Publisher Full Text OpenURL