23 research outputs found

    Impact of biological agents on postsurgical complications in inflammatory bowel disease: A multicentre study of Geteccu

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    Background: The impact of biologics on the risk of postoperative complications (PC) in inflammatory bowel disease (IBD) is still an ongoing debate. This lack of evidence is more relevant for ustekinumab and vedolizumab. Aims: To evaluate the impact of biologics on the risk of PC. Methods: A retrospective study was performed in 37 centres. Patients treated with biologics within 12 weeks before surgery were considered “exposed”. The impact of the exposure on the risk of 30-day PC and the risk of infections was assessed by logistic regression and propensity score-matched analysis. Results: A total of 1535 surgeries were performed on 1370 patients. Of them, 711 surgeries were conducted in the exposed cohort (584 anti-TNF, 58 vedolizumab and 69 ustekinumab). In the multivariate analysis, male gender (OR: 1.5; 95% CI: 1.2–2.0), urgent surgery (OR: 1.6; 95% CI: 1.2–2.2), laparotomy approach (OR: 1.5; 95% CI: 1.1–1.9) and severe anaemia (OR: 1.8; 95% CI: 1.3–2.6) had higher risk of PC, while academic hospitals had significantly lower risk. Exposure to biologics (either anti-TNF, vedolizumab or ustekinumab) did not increase the risk of PC (OR: 1.2; 95% CI: 0.97–1.58), although it could be a risk factor for postoperative infections (OR 1.5; 95% CI: 1.03–2.27). Conclusions: Preoperative administration of biologics does not seem to be a risk factor for overall PC, although it may be so for postoperative infections

    The transcriptomics of an experimentally evolved plant-virus interaction

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    [EN] Models of plant-virus interaction assume that the ability of a virus to infect a host genotype depends on the matching between virulence and resistance genes. Recently, we evolved tobacco etch potyvirus (TEV) lineages on different ecotypes of Arabidopsis thaliana, and found that some ecotypes selected for specialist viruses whereas others selected for generalists. Here we sought to evaluate the transcriptomic basis of such relationships. We have characterized the transcriptomic responses of five ecotypes infected with the ancestral and evolved viruses. Genes and functional categories differentially expressed by plants infected with local TEV isolates were identified, showing heterogeneous responses among ecotypes, although significant parallelism existed among lineages evolved in the same ecotype. Although genes involved in immune responses were altered upon infection, other functional groups were also pervasively over-represented, suggesting that plant resistance genes were not the only drivers of viral adaptation. Finally, the transcriptomic consequences of infection with the generalist and specialist lineages were compared. Whilst the generalist induced very similar perturbations in the transcriptomes of the different ecotypes, the perturbations induced by the specialist were divergent. Plant defense mechanisms were activated when the infecting virus was specialist but they were down-regulated when infecting with generalist.We thank Francisca de la Iglesia and Paula Agudo for excellent technical assistance and our labmates for useful discussions and suggestions. This work was supported by grants BFU2012-30805 from the Spanish Ministry of Economy and Competitiveness (MINECO), PROMETEOII/2014/021 from Generalitat Valenciana and EvoEvo (ICT610427) from the European Commission 7th Framework Program to SFE, and grant PROMETEOII/2014/025 to JD. JMC was supported by a JAE-doc postdoctoral contract from CSIC. JH was recipient of a predoctoral contract from MINECO.Hillung, J.; García-García, F.; Dopazo, J.; Cuevas Torrijos, JM.; Elena Fito, SF. (2016). The transcriptomics of an experimentally evolved plant-virus interaction. Scientific Reports. 6:1-19. https://doi.org/10.1038/srep24901S1196Duffy, S., Shackelton, L. A. & Holmes, E. C. Rates of evolutionary change in viruses: patterns and determinants. Nat. Rev. Genet. 9, 267–276 (2008).Parrish, C. R. et al. Cross-species virus transmission and the emergence of new epidemic diseases. Microbiol. Mol. Biol. Rev. 72, 457–470 (2008).Holmes, E. C. The comparative genomics of viral emergence. Proc. Natl. Acad. Sci. USA 107, 1742–1746 (2010).Sanjuán, R., Nebot, M. R., Chirico, N., Mansky, L. M. & Belshaw, R. Viral mutation rates. J. Virol. 84, 9733–9748 (2010).Elena, S. F. et al. The evolutionary genetics of emerging plant RNA viruses. Mol. Plant-Microbe Interact. 24, 287–293 (2011).Holmes, E. C. The evolutionary genetics of emerging viruses. Annu. Rev. Ecol. Evol. Syst. 40, 353–372 (2009).Domingo, E. Mechanisms of viral emergence. Vet. Res. 41, 38 (2010).King, K. C. & Lively, C. M. Does genetic diversity limit disease spread in natural host populations? Heredity 109, 199–203 (2012).Kearney, C. M., Thomson, M. J. & Roland, K. E. Genome evolution of Tobacco mosaic virus populations during long-term passaging in a diverse range of hosts. Arch. Virol. 144, 1513–1526 (1999).Tan, Z. et al. Mutations in Turnip mosaic virus genomes that have adapted to Raphanus sativus . J. Gen. Virol. 88, 501–510 (2005).Rico, P., Ivars, P., Elena, S. F. & Hernández, C. Insights into the selective pressures restricting Pelargonium flower break virus genome variability: evidence for host adaptation. J. Virol. 80, 8124–8132 (2006).Wallis, C. M. et al. Adaptation of Plum pox virus to a herbaceous host (Pisum sativum) following serial passages. J. Gen. Virol. 88, 2839–2845 (2007).Agudelo-Romero, P., de la Iglesia, F. & Elena, S. F. The pleiotropic cost of host-specialization in tobacco etch potyvirus. Infect. Genet. Evol. 8, 806–814 (2008).Bedhomme, S., Lafforgue, G. & Elena, S. F. Multihost experimental evolution of a plant RNA virus reveals local adaptation and host-specific mutations. Mol. Biol. Evol. 29, 1481–1492 (2012).García-Arenal, F. & Fraile A. Trade-offs in host range evolution of plant viruses. Plant Pathol. 62, S2–S9. (2013).Calvo, M., Malinowski, T. & García, J. A. Single amino acid changes in the 6K1-CI region can promote the alternative adaptation of Prunus- and Nicotiana- propagated Plum pox virus C isolates to either host. Mol. Plant-Microbe Interact. 27, 136–149 (2014).Cuevas, J. M., Willemsen, A., Hillung, J., Zwart, M. P. & Elena, S. F. Temporal dynamics of intra-host molecular evolution for a plant RNA virus. Mol. Biol. Evol. 32, 1132–1147 (2015).Minicka, J., Rymelska, N., Elena, S. F., Czerwoniec, A. & Hasiów-Jaroszewska, B. Molecular evolution of Pepino mosaic virus during long-term passaging in different hosts and its impact on virus virulence. Ann. Appl. Biol. 166, 389–401 (2015).Agudelo-Romero, P., Carbonell, P., Pérez-Amador, M. A. & Elena, S. F. Virus adaptation by manipulation of host's gene expression. PLos ONE 3, e2397 (2008).Weigel, D. Natural variation in arabidopsis: from molecular genetics to ecological genomics. Plant Physiol. 158, 2–22 (2012).Mahajan, S. K., Chisholm, S. T., Whitham, S. A. & Carrington, J. C. Identification and characterization of a locus (RTM1) that restricts long-distance movement of Tobacco etch virus in Arabidopsis thaliana . Plant J. 14, 177–186 (1998).Whitham, S. A., Yamamoto, M. L. & Carrington, J. C. Selectable viruses and altered susceptibility mutants in Arabidopsis thaliana . Proc. Natl. Acad. Sci. USA 96, 772–777 (1999).Whitham, S. A., Anderberg, R. J., Chisholm, S. T. & Carrington, J. C. Arabidopsis RTM2 gene is necessary for specific restriction of Tobacco etch virus and encodes an unusual small heat shock-like protein. Plant Cell 12, 569–582 (2000).Chisholm, S. T., Mahajan, S. K., Whitham, S. A., Yamamoto, M. L. & Carrington, J. C. Cloning of the Arabidopsis RTM1 gene, which controls restriction of long-distance movement of Tobacco etch virus . Proc. Natl. Acad. Sci. USA 97, 489–494 (2000).Chisholm, S. T., Parra, M. A., Anderberg, R. J. & Carrington, J. C. Arabidopsis RTM1 and RTM2 genes function in phloem to restrict long-distance movement of Tobacco etch virus . Plant Physiol. 127, 1667–1675 (2001).Cosson, P. et al. RTM3, which controls long-distance movement of potyviruses, is a member of a new plant gene family encoding a MEPRIN and TRAF homology domain-containing protein. Plant Physiol. 154, 222–232 (2010).Cosson, P., Sofer, L., Schurdi-Levraud, V. & Revers, F. A member of a new plant gene family encoding a MEPRIN and TRAF homology (MATH) domain-containing protein is involved in restriction of long distance movement of plant viruses. Plant Signal. Behav. 5, 1321–1323 (2010).Agudelo-Romero P. et al. Changes in gene expression profile of Arabidopsis thaliana after infection with Tobacco etch virus . Virol. J. 5, 92 (2008).Lalić, J., Agudelo-Romero, P., Carrasco, P. & Elena, S. F. Adaptation of tobacco etch potyvirus to a susceptible ecotype of Arabidopsis thaliana capacitates it for systemic infection of resistant ecotypes. Phil. Trans. R. Soc. B 65, 1997–2008 (2010).Hillung, J., Cuevas, J. M. & Elena, S. F. Transcript profiling of different Arabidopsis thaliana ecotypes in response to tobacco etch potyvirus infection. Front. Microbiol. 3, 229 (2012).Hillung, J., Cuevas, J. M. & Elena, S. F. Evaluating the within-host fitness effects of mutations fixed during virus adaptation to different ecotypes of a new host. Phil. Trans. R. Soc. B 370, 20140292 (2015).Hillung, J., Cuevas, J. M., Valverde, S. & Elena, S. F. Experimental evolution of an emerging plant virus in host genotypes that differ in their susceptibility to infection. Evolution 68, 2467–2480 (2014).Sartor, M. A., Leikauf, G. D. & Medvedovic, M. LRpath: a logistic regression approach for identifying enriched biological groups in gene expression data. Bioinformatics 25, 211–217 (2009).Montaner, D. & Dopazo, J. Multidimensional gene set analysis of genomic data. PLos ONE 5, e10348 (2010).Supek, F., Bosnjak, M., Skunca, N. & Smuc, T. REVIGO summarizes and visualizes long lists of gene ontology terms. PLos ONE 6, e21800 (2011).Grennan, A. K. Regulation of starch metabolism in Arabidopsis leaves. Plant Physiol. 142, 1343–1345 (2006).Johnson, P. R. & Ecker, J. R. The ethylene gas signal transduction pathway: a molecular perspective. Annu. Rev. Genet. 32, 227–254 (1998).Wang, K. L., Li, H. & Ecker, J. R. Ethylene biosynthesis and signaling networks. Plant Cell 14, S131–S151 (2002).Binns, D. et al. QuickGO: a web-based tool for gene ontology searching. Bioinformatics 25, 3045–3046 (2009).Stintzi, A., Weber, H., Reymond, P., Browse, J. & Farmer, E. E. Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proc. Natl. Acad. Sci. USA 98, 12837–12842 (2001).Luna, E. et al. Callose deposition: a multifaceted plant defense response. Mol. Plant-Microbe Interact. 24, 183–193 (2011).Ghoshroy, S., Freedman, K., Lartey, R. & Citovsky, V. Inhibition of plant viral systemic infection by non-toxic concentrations of cadmium. Plant J. 13, 591–602 (1998).Hayashi, N. et al. Nef of HIV-1 interacts directly with calcium-bound calmodulin. Protein Sci. 11, 529–537 (2002).Zacharias, D. A., Violin, J. D., Newton, A. C. & Tsien, R. Y. Partitioning of lipic-modified monomeric GFPs into membrane microdomains of live cells. Science 296, 913–916 (2002).Rojas, M. R. et al. Functional analysis of proteins involved in movement of the monopartite begomovirus, Tomato yellow leaf curl virus. Virology 291, 110–125 (2001).Padmanabhan, M. S., Goregaoker, S. P., Golem, S., Shiferaw, H. & Culver, J. N. Interaction of the Tobacco mosaic virus replicase protein with the Aux/IAA protein PAP1/IAA26 is associated with disease development. J. Virol. 79, 2549–2558 (2005).Lurin, C. et al. Genome-wide analysis of Arabidopsis pentatricopeptide repeat proteins reveals their essential role in organelle biogenesis. Plant Cell 16, 2089–2103 (2004).Takenaka, M., Verbitskiy, D., Zehrmann, A. & Brennicke, A. Reverse genetic screening identifies five E-class PPR proteins involved in RNA editing in mitochondria of Arabidopsis thaliana . J. Biol. Chem. 285, 27122–27129 (2010).Gillissen, B. et al. A new family of high-affinity transporters for adenine, cytosine, and purine derivatives in Arabidopsis . Plant Cell 12, 291–300 (2000).Li, S., Fu, Q., Chen, L., Huang, W. & Yu, D. Arabidopsis thaliana WRKY25, WRKY26, and WRKY33 coordinate induction of plant thermotolerance. Planta 233, 1237–1252 (2011).Divol, F. et al. Involvement of the xyloglucan endotransglycosylase/hydrolases encoded by celery XTH1 and Arabidopsis XTH33 in the phloem response to aphids. Plant Cell. Environ. 30, 187–201 (2007).Vissenberg, K., Fry, S. C., Pauly, M., Höfte, H. & Verbelen, J. P. XTH acts at the microfibril-matrix interface during cell elongation. J. Exp. Bot. 56, 673–683 (2005).Ham, B. K., Li, G., Kang, B. H., Zeng, F. & Lucas, W. J. Overexpression of Arabidopsis plasmodesmata germin-like proteins disrupts root growth and development. Plant Cell 24, 3630–3648 (2012).Bae, M. S., Cho, E. J., Choi, E. Y. & Park, O. K. Analysis of the Arabidopsis nuclear proteome and its response to cold stress. Plant J. 36, 652–663 (2003).Zargar, S. M. et al. Correlation analysis of proteins responsive to Zn, Mn, or Fe deficiency in Arabidopsis roots based on iTRAQ analysis. Plant Cell Rep. 34, 157–166 (2015).Kleffmann, T. et al. The Arabidopsis thaliana chloroplast proteome reveals pathway abundance and novel protein functions. Curr. Biol. 14, 354–362 (2004).Zybailov, B. et al. Sorting signals, N-terminal modifications and abundance of the chloroplast proteome. PLos ONE 3, e1994 (2008).Wu, P. et al. Phosphate starvation triggers distinct alterations of gene expression in Arabidopsis roots and leaves. Plant Physiol. 132, 1260–1271 (2003).Oh, S. A., Lee, S. Y., Chung, I. K., Lee, C. H. & Nam H. G. A senescence-associated gene of Arabidopsis thaliana is distinctively regulated during natural and artificially induced leaf senescence. Plant Mol. Biol. 30, 739–754 (1996).Schenk, P. M., Kazan, K., Rusu, A. G., Manners, J. M. & Maclean, D. J. The SEN1 gene of Arabidopsis is regulated by signals that link plant defence responses and senescence. Plant Physiol. Biochem. 43, 997–1005 (2005).Fernández-Calvino, L. et al. Activation of senescence-associated dark-inducible (DIN) genes during infection contributes to enhanced susceptibility to plant viruses. Mol. Plant Pathol. 17, 3–15 (2016).Vierstra, R. D. Proteolysis in plants: mechanisms and functions. Plant Mol. Biol. 32, 275–302 (1996).Bögre, L., Okrész, L., Henriques, R. & Anthony, R. G. Growth signalling pathways in Arabidopsis and the AGC protein kinases. Trends Plant Sci. 8, 424–431 (2003).An, L. et al. A zinc finger protein gene ZFP5 integrates phytohormone signalling to control root hair development in Arabidopsis . Plant J. 72, 474–490 (2012).Zhou, Z., An, L., Sun, L. & Gan, Y. ZFP5 encodes a functionally equivalent GIS protein to control trichome initiation. Plant Signal. Behav. 7, 28–30 (2012).Zhou, Z. et al. Zinc finger protein 5 is required for the control of trichome initiation by acting upstream of zinc finger protein 8 in Arabidopsis . Plant Physiol. 157, 673–682 (2011).Lee, D. J. et al. Genome-wide expression profiling of ARABIDOPSIS RESPONSE REGULATOR 7 (ARR7) overexpression in cytokinin response. Mol. Genet. Genomics 277, 115–137 (2007).Theologis, A. et al. Sequence and analysis of chromosome 1 of the plant Arabidopsis thaliana . Nature 408, 816–820 (2000).Heyndrickx, K. S. & Vandepoele, K. Systematic identification of functional plant modules through the integration of complementary data sources. Plant Physiol. 159, 884–901 (2012).Martinoia, E. et al. Multifunctionality of plant ABC transporter - more than just detoxifiers. Planta 214, 345–355 (2002).Kaneda, M. et al. ABC transporters coordinately expressed during lignification of Arabidopsis stems include a set of ABCBs associated with auxin transport. J. Exp. Bot. 62, 2063–2077 (2011).Alejandro, S. et al. AtABCG29 is a monolignol transporter involved in lignin biosynthesis. Curr. Biol. 22, 1207–1212 (2012).Riechmann, J. L. et al. Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes. Science 290, 2105–2110 (2000).Ohashi-Ito, K. & Bergmann, D. C. Regulation of the Arabidopsis root vascular initial population by LONESOME HIGHWAY . Development 134, 2959–2968 (2007).Averyanov, A. Oxidative burst and plant disease resistance. Front. Biosci. 1, 142–152 (2009).Flury, P., Klauser, D., Schulze, B., Boller, T. & Bartels, S. The anticipation of danger: microbe-associated molecular pattern perception enhances AtPep-triggered oxidative burst. Plant Physiol. 161, 2023–2035 (2013).Tanaka, K., Nguyen, C. T., Liang, Y., Cao, Y. & Stacey, G. Role of LysM receptors in chitin-triggered plant innate immunity. Plant Signal. Behav. 8, e22598 (2013).Nakamura, K. & Matsuoka, K. Protein targeting to the vacuole in plant cells. Plant Physiol. 101, 1–5 (1993).Elena, S. F., Agudelo-Romero, P. & Lalić, J. The evolution of viruses in multi-host fitness landscapes. Open Virol. J. 3, 1–6 (2009).Bolstad, B. M., Irizarry, R. A., Astrand, M. & Speed, T. P. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 19, 185–193 (2003).Smyth, G. K. Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat. Appl. Genet. Mol. Biol. 3, 3 (2004).Benjamini, Y. & Hochberg, Y. Controlling the false discovery rate: A practical and powerful approach to multiple testing. J. R. Stat. Soc. B 57, 289–300 (1995).Benjamini,Y. & Yekutieli, D. The control of the false discovery rate in multiple testing under dependency. Ann. Statist. 29, 1165–1188 (2001).Sneath, P. & Sokal, R. Numerical Taxonomy. ( W.H. Freeman, 1973).D'Haeseler, P. How does gene expression clustering work? Nat. Biotech. 23, 1499–1501 (2005).Suzuki, R. & Shimodaira, H. Pvclust: an R package for assessing the uncertainty in hierarchical clustering. Bioinformatics 22, 1540–1542 (2006)

    HOP3, a member of the HOP family in Arabidopsis, interacts with BiP and plays a major role in the ER stress response

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    HSP70-HSP90 organizing protein (HOP) is a well-studied family of cytosolic cochaperones. However, the possible role of HOP during the endoplasmic reticulum (ER) stress response and the identity of its interactors within the ER were not previously addressed in any eukaryote. We have demon_x0002_strated that Arabidopsis HOP3, whose function was not studied before, interacts in vivo with cytosolic HSP90 and HSP70, and, unexpectedly, with binding immunoglobulin pro_x0002_tein (BiP), a HSP70 ER-resident protein. Although BiP lacks the domain described in other eukaryotes for HOP-HSP70 binding, it interacts with HOP3 through a non-canonical asso_x0002_ciation to its nucleotide binding domain. Consistent with this interaction with BiP, HOP3 is partially localized at the ER. Moreover, HOP3 is induced both at transcript and protein levels by unfolded protein response (UPR) inducer agents by a mechanism dependent on inositol-requiring enzyme 1 (IRE1). Importantly, hop3 loss-of-function mutants show a reduction in pollen germination and a hypersensitive phenotype in the presence of ER stress inducer agents, a phenotype that is reverted by the addition of the chemical chaperone tauroursodeoxycholic acid (TUDCA). All these data demonstrate, for the first time in any eukaryote, a main role of HOP as an important regulator of the ER stress response, a process intimately linked in plants to important spe_x0002_cific developmental programs and to environmental stress sens_x0002_ing and response

    HOP3 a new regulator of the ER stress response in Arabidopsis with possible implications in plant development and response to biotic and abiotic stresses

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    HOPs (heat shock protein 70 (HSP70)-heat shock protein 90 (HSP90) organizing proteins) are a highly conserved family of cytosolic cochaperones. In a recent study we showed that HOP3, a member of the HOP family in Arabidopsis, plays an essential role during endoplasmic reticulum (ER) stress in plants. Interestingly, we also demonstrated that AtHOP3 interacts with binding immunoglobulin protein (BiP), a major ER-resident chaperone. All these data suggest that HOP3 could assist BiP in protein folding in the ER. These findings open the exciting possibility that HOP3, through its role in the alleviation of ER stress, could play an important function during different developmental processes and in response to different biotic and abiotic stresses. © 2017 The Author(s). Published with license by Taylor & Francis Group, LL

    Virus infection and primary metabolism

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    58 p.-8 fig.1 tab. Llave, César et al.During compatible virus infections, plants respond by reprogramming gene expression and metabolite content. While gene expression studies are profuse, our knowledge of the metabolic changes that occur in the presence of the virus is limited. Here, we combine gene expression and metabolite profiling in Arabidopsis (Arabidopsis thaliana) infected with Tobacco rattle virus (TRV) in order to investigate the influence of primary metabolism on virus infection. Our results revealed that primary metabolism is reconfigured in many ways during TRV infection, as reflected by significant changes in the levels of sugars and amino acids. Multivariate data analysis revealed that these alterations were particularly conspicuous at the time points of maximal accumulation of TRV, although infection time was the dominant source of variance during the process. Furthermore, TRV caused changes in lipid and fatty acid composition in infected leaves. We found that several Arabidopsis mutants deficient in branched-chain amino acid catabolism or fatty acid metabolism possessed altered susceptibility to TRV. Finally, we showed that increments in the putrescine content in TRV-infected plants correlated with enhanced tolerance to freezing stress in TRV-infected plants and that impairment of putrescine biosynthesis promoted virus multiplication. Our results thus provide an interesting overview for a better understanding of the relationship between primary metabolism and virus infection.This work was supported by grants BIO2006-13107 and BIO2009-12004 from the Spanish Ministry of Science and Innovation (MICINN), and P09-AGR-4516 from the Andalusian Government (Spain). F.J.T. and I.B.H. were supported by graduate fellowships from MICINN. L.F.-C. and M.L.H. were the recipients of JAE-Doc contracts from Consejo Superior de Investigaciones Científicas (CSIC). S.O. was supported in part by grant from Ministerio de Ciencia e Innovación, Spain (Ramón and Cajal contract).Peer reviewe

    Comparison of Potato virus Y and Plum Pox Virus transmission by two aphid species in relation to their probing behaviour

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    Two different aphid species,Myzus persicae (Sulzer) andHyalopterus pruni (Geoffroy) (Homoptera: Aphididae), were used to analyze their ability to transmit two different potyviruses,Potato virus Y (PVY) andPlum pox virus (PPV), to pepper (Capsicum annuum) andNicotiana benthamiana plants, respectively. In parallel experiments,M. persicae consistently transmitted both viruses with high efficiency, whereasH. pruni always failed to transmit either virus. This is in contrast to previous reports describingH. pruni as a vector of these potyviruses. Different aphid probing behavior among individual aphids of each species was obtained in electrical penetration graph (EPG) experiments performed on pepper plants. This suggested thatH. pruni did not transmit these potyviruses due to behavioral differences during probing that impeded virus acquisition and/or inoculation. It was found thatM. persicae usually makes its first probe within the first 2 min, whereasH. pruni individuals remained for more than 10 min on the plant before starting to probe. Furthermore,M. persicae individuals displayed their first intracellular puncture during the first minute of probing whereasH. pruni needed ∼ 15 min to penetrate the cell plasmalemma with their stylets. In addition, intracellular stylet punctures occurred very frequently forM. persicae but was a rare event, never exceeding a single one, forH. pruni. The relevance of these findings for the epidemiological spread of potyviruses by different aphid species is discussed.Peer reviewe

    HOP family plays a major role in long-term acquired thermotolerance in Arabidopsis

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    HSP70‐HSP90 organizing protein (HOP) is a family of cytosolic cochaperones whose molecular role in thermotolerance is quite unknown in eukaryotes and unexplored in plants. In this article, we describe that the three members of the AtHOP family display a different induction pattern under heat, being HOP3 highly regulated during the challenge and the attenuation period. Despite HOP3 is the most heat‐regulated member, the analysis of the hop1 hop2 hop3 triple mutant demonstrates that the three HOP proteins act redundantly to promote long‐term acquired thermotolerance in Arabidopsis. HOPs interact strongly with HSP90 and part of the bulk of HOPs shuttles from the cytoplasm to the nuclei and to cytoplasmic foci during the challenge. RNAseq analyses demonstrate that, although the expression of the Hsf targets is not generally affected, the transcriptional response to heat is drastically altered during the acclimation period in the hop1 hop2 hop3 triple mutant. This mutant also displays an unusual high accumulation of insoluble and ubiquitinated proteins under heat, which highlights the additional role of HOP in protein quality control. These data reveal that HOP family is involved in different aspects of the response to heat, affecting the plant capacity to acclimate to high temperatures for long periods.HSP70‐HSP90 organizing protein (HOP) is a family of cytosolic cochaperones whose molecular role in thermotolerance is quite unknown in eukaryotes and unexplored in plants. In this article, we describe that the three members of the AtHOP family display a different induction pattern under heat, being HOP3 highly regulated during the challenge and the attenuation period. Despite HOP3 is the most heat‐regulated member, the analysis of the hop1 hop2 hop3 triple mutant demonstrates that the three HOP proteins act redundantly to promote long‐term acquired thermotolerance in Arabidopsis. HOPs interact strongly with HSP90 and part of the bulk of HOPs shuttles from the cytoplasm to the nuclei and to cytoplasmic foci during the challenge. RNAseq analyses demonstrate that, although the expression of the Hsf targets is not generally affected, the transcriptional response to heat is drastically altered during the acclimation period in the hop1 hop2 hop3 triple mutant. This mutant also displays an unusual high accumulation of insoluble and ubiquitinated proteins under heat, which highlights the additional role of HOP in protein quality control. These data reveal that HOP family is involved in different aspects of the response to heat, affecting the plant capacity to acclimate to high temperatures for long periods.HSP70‐HSP90 organizing protein (HOP) is a family of cytosolic cochaperones whose molecular role in thermotolerance is quite unknown in eukaryotes and unexplored in plants. In this article, we describe that the three members of the AtHOP family display a different induction pattern under heat, being HOP3 highly regulated during the challenge and the attenuation period. Despite HOP3 is the most heat‐regulated member, the analysis of the hop1 hop2 hop3 triple mutant demonstrates that the three HOP proteins act redundantly to promote long‐term acquired thermotolerance in Arabidopsis. HOPs interact strongly with HSP90 and part of the bulk of HOPs shuttles from the cytoplasm to the nuclei and to cytoplasmic foci during the challenge. RNAseq analyses demonstrate that, although the expression of the Hsf targets is not generally affected, the transcriptional response to heat is drastically altered during the acclimation period in the hop1 hop2 hop3 triple mutant. This mutant also displays an unusual high accumulation of insoluble and ubiquitinated proteins under heat, which highlights the additional role of HOP in protein quality control. These data reveal that HOP family is involved in different aspects of the response to heat, affecting the plant capacity to acclimate to high temperatures for long periods

    Production of Plum pox virus HC-Pro functionally active for aphid transmission in a transient-expression system

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    Potyviruses are non-persistently transmitted by aphid vectors with the assistance of a viral accessory factor known as helper component (HC-Pro), a multifunctional protein that is also involved in many other essential processes during the virus infection cycle. A transient Agrobacterium-mediated expression system was used to produce Plum pox virus (PPV) HC-Pro in Nicotiana benthamiana leaves from constructs that incorporated the 5′ region of the genome, yielding high levels of HC-Pro in agroinfiltrated leaves. The expressed PPV HC-Pro was able to assist aphid transmission of purified virus particles in a sequential feeding assay, and to complement transmission-defective variants of the virus. Also, HC-Pro of a second potyvirus, Tobacco etch virus (TEV), was expressed and found to be functional for aphid transmission. These results show that this transient system can be useful for production of functionally active HC-Pro in potyviruses, and the possible uses of this approach to study the mechanism of transmission are discussed. © 2006 SGM.E. G. and L. F.-C. are recipients of Spanish Ministerio de Educación y Ciencia (MEC) FPI and FPU fellowships, respectively. The work was supported by grant AGL2004-00704 from MEC to J. J. L.-M. Financial support from the Centre de Referència en Biotecnologia (CeRBa) of the Generalitat de Catalunya is acknowledged.Peer Reviewe

    The helper-component protease transmission factor of tobacco etch potyvirus binds specifically to an aphid ribosomal protein homologous to the laminin receptor precursor

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    12 páginas, 3 figuras, 2 tablas -- PAGS nros. 2862-2873Potyviruses are plant pathogens transmitted by aphids in a non-persistent manner. During transmission, the virus-encoded factor helper-component protease (HCPro) is presumed to act as a molecular bridge, mediating the reversible retention of virions to uncharacterized binding sites in the vector mouthparts. Whilst the predicted interaction between HCPro and the coat protein (CP) of virions has been confirmed experimentally, the characterization of putative HCPro-specific receptors in aphids has remained elusive, with the exception of a report that described binding of HCPro of zucchini yellow mosaic virus to several cuticle proteins. To identify other aphid components that could play a role during transmission, this study used purified HCPro of tobacco etch virus (TEV) in far-Western blotting assays as bait to select interactors among proteins extracted from aphid heads. With this approach, new HCPro-interacting proteins were found, and several were identified after mass spectrometry analysis and searches in databases dedicated to aphid sequences. Among these interactors, a ribosomal protein S2 (RPS2) was chosen for further investigation due to its homology with the laminin receptor precursor, known to act as the receptor of several viruses. The specific interaction between RPS2 and TEV HCPro was confirmed after cloning and heterologous expression of the corresponding Myzus persicae gene. The possible involvement of RPS2 in the transmission process was further suggested by testing a variant of HCPro that was non-functional for transmission due to a mutation in the conserved KITC motif (EITC variant). This variant retained its ability to bind CP but failed to interact with RPS2Financial support was provided from Micinn (Spain) to J. J. L.-M. by grants AGL2004-00704 and AGL2007-60229, with additional aid from Xarxa de Referencia en Biotecnología (Generalitat de Catalunya) and CONSOLIDER Centre (Micinn). L. F.-C. was recipient of an FPU fellowship, and E. G., A. G. and M. U. were supported by the FPI programme (Micinn)Peer reviewe

    New concepts for process intensification in the conversion of glycerol carbonate to glycidol

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    Glycerol is a major by-product in biodiesel manufacturing, which surplus raises a critical need to transform it into high added-value products. In particular, glycerol carbonate is an important glycerol derivative being the most valuable intermediate for the production of glycidol, which is an added-value product of major industrial interest used, for example, as a precursor for the synthesis of a large number of polymers. Solvent-free conventional thermal activation, ultrasound-activation and microwave-activation in the liquid phase are able to selectively transform glycerol carbonate into glycidol under mild conditions using a ZSM-5 zeolite catalyst and a zinc oxide-supported nanoscaled cobalt oxide catalyst with short reaction times and in the absence of solvent. To the best of our knowledge, we report the highest selectivity to glycidol (>99%) from glycerol carbonate at high conversion values (71%).Dr. V. Calvino-Casilda is indebted to CSIC for a JAE-DOC fellowship. The Spanish Ministry of Science and Innovation (CTQ2011-13343-E and MAT2010-21088-C03-01) funded this work.Peer Reviewe
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