606 research outputs found

    Postsurgical Prosthetic Rehabilitation after Mandibular Ameloblastoma Resection: A 7-Year Follow-Up Case Report

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    Ameloblastomas are benign but locally invasive odontogenic tumors most frequently located in the mandible. The gold standard of treatment is the surgical resection of the tumor with safety margins. Postsurgical defects generate a significant morbidity that needs reconstruction and oral rehabilitation to restore the oral functions. This case report describes the prosthetic rehabilitation of a 42-year-old male after resection of a mandibular ameloblastoma. Excision of the lesion by segmental mandibulectomy and mandibular reconstruction by microvascularized fibula flap was performed. After placement of 6 dental implants, the patient was rehabilitated with a lower hybrid prosthesis fabricated using computer-aided design-computer-aided manufacturing. During a 7-year and 5-month follow-up, some clinical complications were observed

    Interleukin-15 antagonizes muscle protein waste in tumour-bearing rats

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    Tissue protein hypercatabolism (TPH) is an important feature in cancer cachexia, particularly with regard to the skeletal muscle. The Yoshida AH-130 rat ascites hepatoma is a model system for studying the mechanisms involved in the processes that lead to tissue depletion, since it induces in the host a rapid and progressive muscle wasting, primarily due to TPH. The present study was aimed at investigating if IL-15, which is known to favour muscle fibre hypertrophy, could antagonize the enhanced muscle protein breakdown in this cancer cachexia model. Indeed, IL-15 treatment partly inhibited skeletal muscle wasting in AH-130-bearing rats by decreasing (8-fold) protein degradative rates (as measured by14C-bicarbonate pre-loading of muscle proteins) to values even lower than those observed in non-tumour-bearing animals. These alterations in protein breakdown rates were associated with an inhibition of the ATP-ubiquitin-dependent proteolytic pathway (35% and 41% for 2.4 and 1.2 kb ubiquitin mRNA, and 57% for the C8 proteasome subunit, respectively). The cytokine did not modify the plasma levels of corticosterone and insulin in the tumour hosts. The present data give new insights into the mechanisms by which IL-15 exerts its preventive effect on muscle protein wasting and seem to warrant the implementation of experimental protocols involving the use of the cytokine in the treatment of pathological states characterized by TPH, particularly in skeletal muscle, such as in the present model of cancer cachexia. © 2000 Cancer Research Campaig

    Evaluation of the efficiency of a conventional PCR protocol for the diagnosis of bacterial spot disease caused by Xanthomonas arboricola pv. pruni in stone fruits and almond

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    Xanthomonas arboricola pv. pruni (Xap), the causal agent of bacterial spot disease of stone fruits and almond, has a quarantine status for the European Union and the European and Mediterranean Plant Protection Organization. The symptoms in the diverse hosts show some differences and, although being quite typical, could be confused with those of some fungal diseases or other biotic or abiotic causes. Consequently, an accurate molecular diagnosis method is required for a rapid identification of the pathogen in samples of imported plants, from nurseries, orchards, etc. A protocol for conventional PCR designed by Pagani (2004) has been the only molecular analytic tool available for several years. It has been optimised for improving its specificity and sensitivity, and the results of its evaluation in 316 bacterial spot-like symptomatic samples of almond, apricot, cherry, Japanese plum and peach, compared with those of isolation and real-time PCR, are reported. The optimised PCR protocol showed specificity for a collection of Xap strains tested. Few non-desired reactions were obtained with some other xanthomonads which have not been reported from Prunus species. Sensitivity thresholds ranged from 102 to 105 CFU ml-1, depending on the hosts and type of plant material. This conventional PCR assay proved to be an excellent candidate for a rapid screening and presumptive diagnosis in cases where real-time PCR equipment is not available

    Reading-related Cognitive Deficits in Spanish Developmental Dyslexia

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    AbstractSpanish-speaking children learn to read words written in a relatively transparent orthography. Variations in orthographic transparency may shape the manifestation of reading difficulties. This study was intended to help clarify the nature of developmental dyslexia in Spanish. Developmentally Dyslexic children (DD) were compared to a chronological age-matched control group (CA). Measures included rapid automated naming, verbal working memory, phonological short-term memory, and phonemic awareness. Results demonstrated that developmental dyslexics show reading-related cognitive deficits in areas such as naming speed, verbal working memory, phonological short-term memory, and phonemic awareness. Our results are consistent with studies conducted in the Spanish language and in other transparent orthographies

    Lateral flow immunoassay for on-site detection of Xanthomonas arboricola pv. Pruni in symptomatic field samples

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    [EN] Xanthomonas arboricola pv. pruni is a quarantine pathogen and the causal agent of the bacterial spot disease of stone fruits and almond, a major threat to Prunus species. Rapid and specific detection methods are essential to improve disease management, and therefore a prototype of a lateral flow immunoassay (LFIA) was designed for the detection of X. arboricola pv. pruni in symptomatic field samples. It was developed by producing polyclonal antibodies which were then combined with carbon nanoparticles and assembled on nitrocellulose strips. The specificity of the LFIA was tested against 87 X. arboricola pv. pruni strains from different countries worldwide, 47 strains of other Xanthomonas species and 14 strains representing other bacterial genera. All X. arboricola pv. pruni strains were detected and cross-reactions were observed only with four strains of X. arboricola pv. corylina, a hazelnut pathogen that does not share habitat with X. arboricola pv. pruni. The sensitivity of the LFIA was assessed with suspensions from pure cultures of three X. arboricola pv. pruni strains and with spiked leaf extracts prepared from four hosts inoculated with this pathogen (almond, apricot, Japanese plum and peach). The limit of detection observed with both pure cultures and spiked samples was 10(4) CFU ml(-1). To demonstrate the accuracy of the test, 205 samples naturally infected with X. arboricola pv. pruni and 113 samples collected from healthy plants of several different Prunus species were analyzed with the LFIA. Results were compared with those obtained by plate isolation and real time PCR and a high correlation was found among techniques. Therefore, we propose this LFIA as a screening tool that allows a rapid and reliable diagnosis of X. arboricola pv. pruni in symptomatic plants.The work was supported by the following: Instituto Nacional de Tecnologia Agraria y Alimentaria, Project RTA-2011-00140-C03-01 (http://www.inia.es), PLS MTG EMN MML; Instituto Nacional de Tecnologia Agraria y Alimentaria, FPI-INIA grant (http://www.inia.es), PLS; Generalitat Valenciana (Prometeo II 2014/040) (http://www.gva.es), PN RP AM; Ministerio de Economia y Competitividad (MINECO) (CTQ2013-45875R) (http://www.mineco.gob.es), PN RP AM; European Social Fund, PLS MTG EMN MML; and European Regional Development Fund, PLS MTG EMN MML.López-Soriano, P.; Noguera Murray, PS.; Gorris, MT.; Puchades, R.; Maquieira Catala, A.; Marco-Noales, E.; López, M. (2017). Lateral flow immunoassay for on-site detection of Xanthomonas arboricola pv. Pruni in symptomatic field samples. PLoS ONE. 12(4):1-13. https://doi.org/10.1371/journal.pone.0176201113124Tjou-Tam-Sin, N. N. A., van de Bilt, J. L. J., Bergsma-Vlami, M., Koenraadt, H., Naktuinbouw, J. W., van Doorn, J., … Martin, W. S. (2012). First Report of Xanthomonas arboricola pv. pruni in Ornamental Prunus laurocerasus in the Netherlands. Plant Disease, 96(5), 759-759. doi:10.1094/pdis-04-11-0265-pdnPothier, J. F., Vorhölter, F.-J., Blom, J., Goesmann, A., Pühler, A., Smits, T. H. M., & Duffy, B. (2011). The ubiquitous plasmid pXap41 in the invasive phytopathogen Xanthomonas arboricola pv. pruni: complete sequence and comparative genomic analysis. FEMS Microbiology Letters, 323(1), 52-60. doi:10.1111/j.1574-6968.2011.02352.xPalacio-Bielsa, A., Cubero, J., Cambra, M. A., Collados, R., Berruete, I. M., & López, M. M. (2010). Development of an Efficient Real-Time Quantitative PCR Protocol for Detection ofXanthomonas arboricolapv. pruni inPrunusSpecies. Applied and Environmental Microbiology, 77(1), 89-97. doi:10.1128/aem.01593-10Xanthomonas arboricola pv. pruni. (2006). EPPO Bulletin, 36(1), 129-133. doi:10.1111/j.1365-2338.2006.00925.xPagani MC. An ABC transporter protein and molecular diagnoses of Xanthomonas arboricola pv. pruni causing bacterial spot of stone fruits. Raleigh, North Carolina, USA: North Carolina State University, PhD thesis. 2004; Online, http://repository.lib.ncsu.edu/ir/bitstream/1840.16/4540/1/etd.pdfPark, S. Y., Lee, Y. S., Koh, Y. J., Hur, J.-S., & Jung, J. S. (2010). Detection of Xanthomonas arboricola pv. pruni by PCR using primers based on DNA sequences related to the hrp genes. The Journal of Microbiology, 48(5), 554-558. doi:10.1007/s12275-010-0072-3Pothier, J. F., Pagani, M. C., Pelludat, C., Ritchie, D. F., & Duffy, B. (2011). A duplex-PCR method for species- and pathovar-level identification and detection of the quarantine plant pathogen Xanthomonas arboricola pv. pruni. Journal of Microbiological Methods, 86(1), 16-24. doi:10.1016/j.mimet.2011.03.019Ballard, E. L., Dietzgen, R. G., Sly, L. I., Gouk, C., Horlock, C., & Fegan, M. (2011). Development of a Bio-PCR Protocol for the Detection of Xanthomonas arboricola pv. pruni. Plant Disease, 95(9), 1109-1115. doi:10.1094/pdis-09-10-0650Boonham, N., Glover, R., Tomlinson, J., & Mumford, R. (2008). Exploiting generic platform technologies for the detection and identification of plant pathogens. European Journal of Plant Pathology, 121(3), 355-363. doi:10.1007/s10658-008-9284-3Posthuma-Trumpie, G. A., Korf, J., & van Amerongen, A. (2008). Lateral flow (immuno)assay: its strengths, weaknesses, opportunities and threats. A literature survey. Analytical and Bioanalytical Chemistry, 393(2), 569-582. doi:10.1007/s00216-008-2287-2De Boer, S. H., & López, M. M. (2012). New Grower-Friendly Methods for Plant Pathogen Monitoring. Annual Review of Phytopathology, 50(1), 197-218. doi:10.1146/annurev-phyto-081211-172942Thornton, C. R., Groenhof, A. C., Forrest, R., & Lamotte, R. (2004). A One-Step, Immunochromatographic Lateral Flow Device Specific to Rhizoctonia solani and Certain Related Species, and Its Use to Detect and Quantify R. solani in Soil. Phytopathology®, 94(3), 280-288. doi:10.1094/phyto.2004.94.3.280Lane, C. R., Hobden, E., Walker, L., Barton, V. C., Inman, A. J., Hughes, K. J. D., … Barker, I. (2007). Evaluation of a rapid diagnostic field test kit for identification of Phytophthora species, including P. ramorum and P. kernoviae at the point of inspection. Plant Pathology, 56(5), 828-835. doi:10.1111/j.1365-3059.2007.01615.xSafenkova, I., Zherdev, A., & Dzantiev, B. (2012). Factors influencing the detection limit of the lateral-flow sandwich immunoassay: a case study with potato virus X. Analytical and Bioanalytical Chemistry, 403(6), 1595-1605. doi:10.1007/s00216-012-5985-8Safenkova, I. V., Pankratova, G. K., Zaitsev, I. A., Varitsev, Y. A., Vengerov, Y. Y., Zherdev, A. V., & Dzantiev, B. B. (2016). Multiarray on a test strip (MATS): rapid multiplex immunodetection of priority potato pathogens. Analytical and Bioanalytical Chemistry, 408(22), 6009-6017. doi:10.1007/s00216-016-9463-6Braun-Kiewnick, A., Altenbach, D., Oberhänsli, T., Bitterlin, W., & Duffy, B. (2011). A rapid lateral-flow immunoassay for phytosanitary detection of Erwinia amylovora and on-site fire blight diagnosis. Journal of Microbiological Methods, 87(1), 1-9. doi:10.1016/j.mimet.2011.06.015Safenkova, I. V., Zaitsev, I. A., Pankratova, G. K., Varitsev, Y. A., Zherdev, A. V., & Dzantiev, B. B. (2014). Lateral flow immunoassay for rapid detection of potato ring rot caused by Clavibacter michiganensis subsp. sepedonicus. Applied Biochemistry and Microbiology, 50(6), 675-682. doi:10.1134/s0003683814120011Hodgetts, J., Karamura, G., Johnson, G., Hall, J., Perkins, K., Beed, F., … Smith, J. (2014). Development of a lateral flow device for in-field detection and evaluation of PCR-based diagnostic methods forXanthomonas campestrispv.musacearum, the causal agent of banana xanthomonas wilt. Plant Pathology, 64(3), 559-567. doi:10.1111/ppa.12289Noguera, P., Posthuma-Trumpie, G. A., van Tuil, M., van der Wal, F. J., de Boer, A., Moers, A. P. H. A., & van Amerongen, A. (2010). Carbon nanoparticles in lateral flow methods to detect genes encoding virulence factors of Shiga toxin-producing Escherichia coli. Analytical and Bioanalytical Chemistry, 399(2), 831-838. doi:10.1007/s00216-010-4334-zCambra M, López MM. Titration of Agrobacterium radiobacter var. tumefaciens antibodies by using enzyme labeled anti-rabbit γ-globulines (ELISA indirect method). In: Proceedings of the 4th International Conference on Plant Pathogenic Bacteria, ed. Station Pathologie Végétale, INRA Angers, 1978. pp: 327–331.O’Keeffe, M., Crabbe, P., Salden, M., Wichers, J., Van Peteghem, C., Kohen, F., … Moneti, G. (2003). Preliminary evaluation of a lateral flow immunoassay device for screening urine samples for the presence of sulphamethazine. Journal of Immunological Methods, 278(1-2), 117-126. doi:10.1016/s0022-1759(03)00207-2PM 7/98 (2) Specific requirements for laboratories preparing accreditation for a plant pest diagnostic activity. (2014). EPPO Bulletin, 44(2), 117-147. doi:10.1111/epp.12118Lamichhane, J. R., & Varvaro, L. (2013). Xanthomonas arboricoladisease of hazelnut: current status and future perspectives for its management. Plant Pathology, 63(2), 243-254. doi:10.1111/ppa.12152Fischer-Le Saux, M., Bonneau, S., Essakhi, S., Manceau, C., & Jacques, M.-A. (2015). Aggressive Emerging Pathovars of Xanthomonas arboricola Represent Widespread Epidemic Clones Distinct from Poorly Pathogenic Strains, as Revealed by Multilocus Sequence Typing. Applied and Environmental Microbiology, 81(14), 4651-4668. doi:10.1128/aem.00050-15Bühlmann, A., Pothier, J. F., Tomlinson, J. A., Frey, J. E., Boonham, N., Smits, T. H. M., & Duffy, B. (2012). Genomics-informed design of loop-mediated isothermal amplification for detection of phytopathogenicXanthomonas arboricolapv. pruniat the intraspecific level. Plant Pathology, 62(2), 475-484. doi:10.1111/j.1365-3059.2012.02654.xGarita-Cambronero, J., Palacio-Bielsa, A., López, M. M., & Cubero, J. (2017). Pan-Genomic Analysis Permits Differentiation of Virulent and Non-virulent Strains of Xanthomonas arboricola That Cohabit Prunus spp. and Elucidate Bacterial Virulence Factors. Frontiers in Microbiology, 8. doi:10.3389/fmicb.2017.00573Ghezzi, J. I., & Steck, T. R. (1999). Induction of the viable but non-culturable condition in Xanthomonas campestris pv. campestris in liquid microcosms and sterile soil. FEMS Microbiology Ecology, 30(3), 203-208. doi:10.1111/j.1574-6941.1999.tb00648.xDel Campo, R., Russi, P., Mara, P., Mara, Hã©., Peyrou, M., de León, I. P., & Gaggero, C. (2009). 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    Erythropoietin administration partially prevents adipose tissue loss in experimental cancer cachexia models

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    Cancer-associated cachexia is characterized, among other symptoms, by a dramatic loss of both muscle and fat. In addition, the cachectic syndrome is often associated with anemia. The object of the present investigation was to assess the effects of erythropoietin (EPO) treatment on experimental cancer cachexia models. The results clearly show that, in addition to the improvement of the hematocrit, EPO treatment promoted a partial preservation of adipose tissue while exerting negligible effects on muscle loss. Administration of EPO to tumor-bearing animals resulted in a significant increase of lipoprotein lipase (LPL) activity in adipose tissue, suggesting that the treatment favored triacylglycerol (TAG) accumulation in the adipose tissue. In vitro experiments using both adipose tissue slices and 3T3-L1 adipocytes suggests that EPO is able to increase the lipogenic rate through the activation of its specific receptor (EPOR). This metabolic pathway, in addition to TAG uptake by LPL, may contribute to the beneficial effects of EPO on fat preservation in cancer cachexia

    Xanthomonas prunicola sp. nov., a novel pathogen that affects nectarine (Prunus persica var. nectarina) trees

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    Three isolates obtained from symptomatic nectarine trees (Prunus persica var. nectarina) cultivated in Murcia, Spain, which showed yellow and mucoid colonies similar to Xanthomonas arboricola pv. pruni, were negative after serological and real-time PCR analyses for this pathogen. For that reason, these isolates were characterized following a polyphasic approach that included both phenotypic and genomic methods. By sequence analysis of the 16S rRNA gene, these novel strains were identified as members of the genus Xanthomonas, and by multilocus sequence analysis (MLSA) they were clustered together in a distinct group that showed similarity values below 95 % with the rest of the species of this genus. Whole-genome comparisons of the average nucleotide identity (ANI) of genomes of the strains showed less than 91 % average nucleotide identity with all other species of the genus Xanthomonas. Additionally, phenotypic characterization based on API 20 NE, API 50 CH and BIOLOG tests differentiated the strains from the species of the genus Xanthomonas described previously. Moreover, the three strains were confirmed to be pathogenic on peach (Prunus persica), causing necrotic lesions on leaves. On the basis of these results, the novel strains represent a novel species of the genus Xanthomonas, for which the name Xanthomonas prunicola is proposed. The type strain is CFBP 8353 (=CECT 9404=IVIA 3287.1)

    Experiments of Interfacial Roughening in Hele-Shaw Flows with Weak Quenched Disorder

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    We have studied the kinetic roughening of an oil--air interface in a forced imbibition experiment in a horizontal Hele--Shaw cell with quenched disorder. Different disorder configurations, characterized by their persistence length in the direction of growth, have been explored by varying the average interface velocity v and the gap spacing b. Through the analysis of the rms width as a function of time, we have measured a growth exponent beta ~= 0.5 that is almost independent of the experimental parameters. The analysis of the roughness exponent alpha through the power spectrum have shown different behaviors at short (alpha_1) and long (alpha_2) length scales, separated by a crossover wavenumber q_c. The values of the measured roughness exponents depend on experimental parameters, but at large velocities we obtain alpha_1 ~= 1.3 independently of the disorder configuration. The dependence of the crossover wavenumber with the experimental parameters has also been investigated, measuring q_c ~ v^{0.47} for the shortest persistence length, in agreement with theoretical predictions.Comment: 20 pages, 22 figure

    La interpretación geomorfológica en la cartografía de peligro de inundación

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    La interpretación geomorfológica de los procesos fluviales resulta fundamental para la elaboración de cartografía de peligro de inundación. Los ríos se comportan de una manera dinámica y pueden variar su topografía de una crecida a otra. Por ello, una cartografía de peligrosidad, excesivamente dependiente de modelos hidráulicos e hidrológicos, puede resultar ineficaz y quedarse obsoleta tras un suceso de alta energía. Conocer los elementos de geomorfología fluvial, así como sus procesos asociados permite una previsión a más largo plazo y una aproximación más realista al riesgo. En este trabajo se presentan ejemplos de interpretación geomorfológica de formas y procesos fluviales, en clave de peligro de inundación. Se han seleccionado tres cuencas de diferentes entornos morfoclimáticos que, a distintas escalas, permiten ilustrar algunos puntos donde la geomorfología propicia un determinado proceso y, en consecuencia, condiciona el tipo de peligro de la zona. La interpretación geomorfológica se ha llevado a cabo mediante trabajo de campo, de laboratorio y a partir de imágenes de satélite (RADARSAT e Ikonos)
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