546 research outputs found

    Onset of virus systemic infection in plants is determined by speed of cell-to-cell movement and number of primary infection foci

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    The cornerstone of today's plant virology consists of deciphering the molecular and mechanistic basis of host-pathogen interactions. Among these interactions, the onset of systemic infection is a fundamental variable in studying both within-and between-host infection dynamics, with implications in epidemiology. Here, we developed a mechanistic model using probabilistic and spatio-temporal concepts to explain dynamic signatures of virus systemic infection. The model dealt with the inherent characteristic of plant viruses to use two different and sequential stages for their within-host propagation: cell-to-cell movement from the initial infected cell and systemic spread by reaching the vascular system. We identified the speed of cell-to-cell movement and the number of primary infection foci in the inoculated leaf as the key factors governing this dynamic process. Our results allowed us to quantitatively understand the timing of the onset of systemic infection, describing this global process as a consequence of local spread of viral populations. Finally, we considered the significance of our predictions for the evolution of plant RNA viruses.This work was supported by the grant no. BFU2012-30805 from Spain Ministerio de Economia y Competitividad (MINECO) to S. F. E. G. R. was supported by an EMBO long-term fellowship co-funded by Marie Curie actions (ALTF-1177-2011) and an AXA post-doctoral fellowship, and M.P.Z. by a Juan de la Cierva post-doctoral contract (JCI-2011-10379) from MINECO.Rodrigo Tarrega, G.; Zwart, MP.; Elena Fito, SF. (2014). Onset of virus systemic infection in plants is determined by speed of cell-to-cell movement and number of primary infection foci. Interface. 11(98):1-8. https://doi.org/10.1098/rsif.2014.0555S181198Waigmann, E., Ueki, S., Trutnyeva, K., & Citovsky, V. (2004). 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(2005). The implications of network structure for epidemic dynamics. Theoretical Population Biology, 67(1), 1-8. doi:10.1016/j.tpb.2004.08.002Dolja, V. V., McBride, H. J., & Carrington, J. C. (1992). Tagging of plant potyvirus replication and movement by insertion of beta-glucuronidase into the viral polyprotein. Proceedings of the National Academy of Sciences, 89(21), 10208-10212. doi:10.1073/pnas.89.21.10208Zwart, M. P., Daròs, J.-A., & Elena, S. F. (2011). One Is Enough: In Vivo Effective Population Size Is Dose-Dependent for a Plant RNA Virus. PLoS Pathogens, 7(7), e1002122. doi:10.1371/journal.ppat.1002122Bedoya, L. C., Martínez, F., Orzáez, D., & Daròs, J.-A. (2012). Visual Tracking of Plant Virus Infection and Movement Using a Reporter MYB Transcription Factor That Activates Anthocyanin Biosynthesis. Plant Physiology, 158(3), 1130-1138. doi:10.1104/pp.111.192922Lafforgue, G., Tromas, N., Elena, S. F., & Zwart, M. P. (2012). Dynamics of the Establishment of Systemic Potyvirus Infection: Independent yet Cumulative Action of Primary Infection Sites. Journal of Virology, 86(23), 12912-12922. doi:10.1128/jvi.02207-12Holmes, F. O. (1929). Local Lesions in Tobacco Mosaic. Botanical Gazette, 87(1), 39-55. doi:10.1086/333923BALD, J. G. (1937). THE USE OF NUMBERS OF INFECTIONS FOR COMPARING THE CONCENTRATION OF PLANT VIRUS SUSPENSIONS: DILUTION EXPERIMENTS WITH PURIFIED SUSPENSIONS. Annals of Applied Biology, 24(1), 33-55. doi:10.1111/j.1744-7348.1937.tb05019.xBaulcombe, D. (2004). RNA silencing in plants. Nature, 431(7006), 356-363. doi:10.1038/nature02874Kunkel, B. N., & Brooks, D. M. (2002). Cross talk between signaling pathways in pathogen defense. Current Opinion in Plant Biology, 5(4), 325-331. doi:10.1016/s1369-5266(02)00275-3Kørner, C. J., Klauser, D., Niehl, A., Domínguez-Ferreras, A., Chinchilla, D., Boller, T., … Hann, D. R. (2013). The Immunity Regulator BAK1 Contributes to Resistance Against Diverse RNA Viruses. Molecular Plant-Microbe Interactions, 26(11), 1271-1280. doi:10.1094/mpmi-06-13-0179-rRodrigo, G., Carrera, J., Jaramillo, A., & Elena, S. F. (2010). Optimal viral strategies for bypassing RNA silencing. Journal of The Royal Society Interface, 8(55), 257-268. doi:10.1098/rsif.2010.0264Kleczkowski, A. (1950). Interpreting Relationships between the Concentrations of Plant Viruses and Numbers of Local Lesions. Journal of General Microbiology, 4(1), 53-69. doi:10.1099/00221287-4-1-53Van der Plank, J. E. (1965). Dynamics of Epidemics of Plant Disease: Population bursts of fungi, bacteria, or viruses in field and forest make an interesting dynamical study. Science, 147(3654), 120-124. doi:10.1126/science.147.3654.120Zwart, M. P., Daròs, J.-A., & Elena, S. F. (2012). Effects of Potyvirus Effective Population Size in Inoculated Leaves on Viral Accumulation and the Onset of Symptoms. Journal of Virology, 86(18), 9737-9747. doi:10.1128/jvi.00909-12Carrington, J. C., Kasschau, K. D., Mahajan, S. K., & Schaad, M. C. (1996). Cell-to-Cell and Long-Distance Transport of Viruses in Plants. The Plant Cell, 1669-1681. doi:10.1105/tpc.8.10.1669Gibbs, A. (1976). Viruses and Plasmodesmata. Intercellular Communication in Plants: Studies on Plasmodesmata, 149-164. doi:10.1007/978-3-642-66294-2_8Hillung, J., Elena, S. F., & Cuevas, J. M. (2013). Intra-specific variability and biological relevance of P3N-PIPO protein length in potyviruses. BMC Evolutionary Biology, 13(1), 249. doi:10.1186/1471-2148-13-249Dengler, N., & Kang, J. (2001). Vascular patterning and leaf shape. Current Opinion in Plant Biology, 4(1), 50-56. doi:10.1016/s1369-5266(00)00135-7SAMUEL, G. (1934). The Movement of Tobacco Mosaic Virus Within the Plant. Annals of Applied Biology, 21(1), 90-111. doi:10.1111/j.1744-7348.1934.tb06891.xKawakami, S., Watanabe, Y., & Beachy, R. N. (2004). Tobacco mosaic virus infection spreads cell to cell as intact replication complexes. Proceedings of the National Academy of Sciences, 101(16), 6291-6296. doi:10.1073/pnas.0401221101Bedoya, L., Martínez, F., Rubio, L., & Daròs, J.-A. (2010). Simultaneous equimolar expression of multiple proteins in plants from a disarmed potyvirus vector. Journal of Biotechnology, 150(2), 268-275. doi:10.1016/j.jbiotec.2010.08.006Wei, T., Zhang, C., Hong, J., Xiong, R., Kasschau, K. D., Zhou, X., … Wang, A. (2010). Formation of Complexes at Plasmodesmata for Potyvirus Intercellular Movement Is Mediated by the Viral Protein P3N-PIPO. PLoS Pathogens, 6(6), e1000962. doi:10.1371/journal.ppat.1000962Bragard, C., Caciagli, P., Lemaire, O., Lopez-Moya, J. J., MacFarlane, S., Peters, D., … Torrance, L. (2013). Status and Prospects of Plant Virus Control Through Interference with Vector Transmission. Annual Review of Phytopathology, 51(1), 177-201. doi:10.1146/annurev-phyto-082712-102346Sacristan, S., Diaz, M., Fraile, A., & Garcia-Arenal, F. (2011). Contact Transmission of Tobacco Mosaic Virus: a Quantitative Analysis of Parameters Relevant for Virus Evolution. Journal of Virology, 85(10), 4974-4981. doi:10.1128/jvi.00057-11Sanchez-Navarro, J. A., Zwart, M. P., & Elena, S. F. (2013). Effects of the Number of Genome Segments on Primary and Systemic Infections with a Multipartite Plant RNA Virus. Journal of Virology, 87(19), 10805-10815. doi:10.1128/jvi.01402-1

    Possible chiral phase transition in two-dimensional solid 3^3He

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    We study a spin system with two- and four-spin exchange interactions on the triangular lattice, which is a possible model for the nuclear magnetism of solid 3^3He layers. It is found that a novel spin structure with scalar chiral order appears if the four-spin interaction is dominant. Ground-state properties are studied using the spin-wave approximation. A phase transition concerning the scalar chirality occurs at a finite temperature, even though the dimensionality of the system is two and the interaction has isotropic spin symmetry. Critical properties of this transition are studied with Monte Carlo simulations in the classical limit.Comment: 4 pages, Revtex, 4 figures, to appear in Phys.Rev.Let

    Environmental pressure from the 2014–15 eruption of Bárðarbunga volcano, Iceland

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    The effusive six months long 2014-2015 Bárðarbunga eruption (31 August-27 February) was the largest in Iceland for more than 200 years, producing 1.6 ± 0.3 km3 of lava. The total SO2 emission was 11 ± 5 Mt, more than the amount emitted from Europe in 2011. The ground level concentration of SO2 exceeded the 350 μg m−3 hourly average health limit over much of Iceland for days to weeks. Anomalously high SO2 concentrations were also measured at several locations in Europe in September. The lowest pH of fresh snowmelt at the eruption site was 3.3, and 3.2 in precipitation 105 km away from the source. Elevated dissolved H2SO4, HCl, HF, and metal concentrations were measured in snow and precipitation. Environmental pressures from the eruption and impacts on populated areas were reduced by its remoteness, timing, and the weather. The anticipated primary environmental pressure is on the surface waters, soils, and vegetation of Iceland

    Water in low-mass star-forming regions with Herschel: HIFI spectroscopy of NGC1333

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    'Water In Star-forming regions with Herschel' (WISH) is a key programme dedicated to studying the role of water and related species during the star-formation process and constraining the physical and chemical properties of young stellar objects. The Heterodyne Instrument for the Far-Infrared (HIFI) on the Herschel Space Observatory observed three deeply embedded protostars in the low-mass star-forming region NGC1333 in several H2-16O, H2-18O, and CO transitions. Line profiles are resolved for five H16O transitions in each source, revealing them to be surprisingly complex. The line profiles are decomposed into broad (>20 km/s), medium-broad (~5-10 km/s), and narrow (<5 km/s) components. The H2-18O emission is only detected in broad 1_10-1_01 lines (>20 km/s), indicating that its physical origin is the same as for the broad H2-16O component. In one of the sources, IRAS4A, an inverse P Cygni profile is observed, a clear sign of infall in the envelope. From the line profiles alone, it is clear that the bulk of emission arises from shocks, both on small (<1000 AU) and large scales along the outflow cavity walls (~10 000 AU). The H2O line profiles are compared to CO line profiles to constrain the H2O abundance as a function of velocity within these shocked regions. The H2O/CO abundance ratios are measured to be in the range of ~0.1-1, corresponding to H2O abundances of ~10-5-10-4 with respect to H2. Approximately 5-10% of the gas is hot enough for all oxygen to be driven into water in warm post-shock gas, mostly at high velocities.Comment: Accepted for publication in the A&A HIFI special issu

    HERSCHEL-HIFI spectroscopy of the intermediate mass protostar NGC7129 FIRS 2

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    HERSCHEL-HIFI observations of water from the intermediate mass protostar NGC7129 FIRS 2 provide a powerful diagnostic of the physical conditions in this star formation environment. Six spectral settings, covering four H216O and two H218O lines, were observed and all but one H218O line were detected. The four H2 16 O lines discussed here share a similar morphology: a narrower, \approx 6 km/s, component centered slightly redward of the systemic velocity of NGC7129 FIRS 2 and a much broader, \approx 25 km/s component centered blueward and likely associated with powerful outflows. The narrower components are consistent with emission from water arising in the envelope around the intermediate mass protostar, and the abundance of H2O is constrained to \approx 10-7 for the outer envelope. Additionally, the presence of a narrow self-absorption component for the lowest energy lines is likely due to self-absorption from colder water in the outer envelope. The broader component, where the H2O/CO relative abundance is found to be \approx 0.2, appears to be tracing the same energetic region that produces strong CO emission at high J.Comment: 6 pages, 4 figures, accepted by A&

    Sensitive limits on the abundance of cold water vapor in the DM Tau protoplanetary disk

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    We performed a sensitive search for the ground-state emission lines of ortho- and para-water vapor in the DM Tau protoplanetary disk using the Herschel/HIFI instrument. No strong lines are detected down to 3sigma levels in 0.5 km/s channels of 4.2 mK for the 1_{10}--1_{01} line and 12.6 mK for the 1_{11}--0_{00} line. We report a very tentative detection, however, of the 1_{10}--1_{01} line in the Wide Band Spectrometer, with a strength of T_{mb}=2.7 mK, a width of 5.6 km/s and an integrated intensity of 16.0 mK km/s. The latter constitutes a 6sigma detection. Regardless of the reality of this tentative detection, model calculations indicate that our sensitive limits on the line strengths preclude efficient desorption of water in the UV illuminated regions of the disk. We hypothesize that more than 95-99% of the water ice is locked up in coagulated grains that have settled to the midplane.Comment: 5 pages, 3 figures. Accepted for publication in the Herschel HIFI special issue of A&

    Hydrides in Young Stellar Objects: Radiation tracers in a protostar-disk-outflow system

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    Context: Hydrides of the most abundant heavier elements are fundamental molecules in cosmic chemistry. Some of them trace gas irradiated by UV or X-rays. Aims: We explore the abundances of major hydrides in W3 IRS5, a prototypical region of high-mass star formation. Methods: W3 IRS5 was observed by HIFI on the Herschel Space Observatory with deep integration (about 2500 s) in 8 spectral regions. Results: The target lines including CH, NH, H3O+, and the new molecules SH+, H2O+, and OH+ are detected. The H2O+ and OH+ J=1-0 lines are found mostly in absorption, but also appear to exhibit weak emission (P-Cyg-like). Emission requires high density, thus originates most likely near the protostar. This is corroborated by the absence of line shifts relative to the young stellar object (YSO). In addition, H2O+ and OH+ also contain strong absorption components at a velocity shifted relative to W3 IRS5, which are attributed to foreground clouds. Conclusions: The molecular column densities derived from observations correlate well with the predictions of a model that assumes the main emission region is in outflow walls, heated and irradiated by protostellar UV radiation.Comment: Astronomy and Astrophysics Letters, in pres

    Water in massive star-forming regions: HIFI observations of W3 IRS5

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    We present Herschel observations of the water molecule in the massive star-forming region W3 IRS5. The o-H17O 110-101, p-H18O 111-000, p-H2O 22 202-111, p-H2O 111-000, o-H2O 221-212, and o-H2O 212-101 lines, covering a frequency range from 552 up to 1669 GHz, have been detected at high spectral resolution with HIFI. The water lines in W3 IRS5 show well-defined high-velocity wings that indicate a clear contribution by outflows. Moreover, the systematically blue-shifted absorption in the H2O lines suggests expansion, presumably driven by the outflow. No infall signatures are detected. The p-H2O 111-000 and o-H2O 212-101 lines show absorption from the cold material (T ~ 10 K) in which the high-mass protostellar envelope is embedded. One-dimensional radiative transfer models are used to estimate water abundances and to further study the kinematics of the region. We show that the emission in the rare isotopologues comes directly from the inner parts of the envelope (T > 100 K) where water ices in the dust mantles evaporate and the gas-phase abundance increases. The resulting jump in the water abundance (with a constant inner abundance of 10^{-4}) is needed to reproduce the o-H17O 110-101 and p-H18O 111-000 spectra in our models. We estimate water abundances of 10^{-8} to 10^{-9} in the outer parts of the envelope (T < 100 K). The possibility of two protostellar objects contributing to the emission is discussed.Comment: Accepted for publication in the A&A HIFI special issu

    Water in Star-Forming Regions with the Herschel Space Observatory (WISH): Overview of key program and first results

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    `Water In Star-forming regions with Herschel' (WISH) is a key program on the Herschel Space Observatory designed to probe the physical and chemical structure of young stellar objects using water and related molecules and to follow the water abundance from collapsing clouds to planet-forming disks. About 80 sources are targeted covering a wide range of luminosities and evolutionary stages, from cold pre-stellar cores to warm protostellar envelopes and outflows to disks around young stars. Both the HIFI and PACS instruments are used to observe a variety of lines of H2O, H218O and chemically related species. An overview of the scientific motivation and observational strategy of the program is given together with the modeling approach and analysis tools that have been developed. Initial science results are presented. These include a lack of water in cold gas at abundances that are lower than most predictions, strong water emission from shocks in protostellar environments, the importance of UV radiation in heating the gas along outflow walls across the full range of luminosities, and surprisingly widespread detection of the chemically related hydrides OH+ and H2O+ in outflows and foreground gas. Quantitative estimates of the energy budget indicate that H2O is generally not the dominant coolant in the warm dense gas associated with protostars. Very deep limits on the cold gaseous water reservoir in the outer regions of protoplanetary disks are obtained which have profound implications for our understanding of grain growth and mixing in disks.Comment: 71 pages, 10 figures, PASP, in pres

    Herschel-HIFI detections of hydrides towards AFGL 2591 (Envelope emission versus tenuous cloud absorption)

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    The Heterodyne Instrument for the Far Infrared (HIFI) onboard the Herschel Space Observatory allows the first observations of light diatomic molecules at high spectral resolution and in multiple transitions. Here, we report deep integrations using HIFI in different lines of hydrides towards the high-mass star forming region AFGL 2591. Detected are CH, CH+, NH, OH+, H2O+, while NH+ and SH+ have not been detected. All molecules except for CH and CH+ are seen in absorption with low excitation temperatures and at velocities different from the systemic velocity of the protostellar envelope. Surprisingly, the CH(JF,P = 3/2_2,- - 1/2_1,+) and CH+(J = 1 - 0, J = 2 - 1) lines are detected in emission at the systemic velocity. We can assign the absorption features to a foreground cloud and an outflow lobe, while the CH and CH+ emission stems from the envelope. The observed abundance and excitation of CH and CH+ can be explained in the scenario of FUV irradiated outflow walls, where a cavity etched out by the outflow allows protostellar FUV photons to irradiate and heat the envelope at larger distances driving the chemical reactions that produce these molecules.Comment: Accepted for publication in Astronomy and Astrophysics (HIFI first results issue
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