Identification of superior reference genes for data normalisation of expression studies via quantitative PCR in hybrid roses (Rosa hybrida)

Background: Gene expression studies are a prerequisite for understanding the biological function of genes. Because of its high sensitivity and easy use, quantitative PCR (qPCR) has become the gold standard for gene expression quantification. To normalise qPCR measurements between samples, the most prominent technique is the use of stably expressed endogenous control genes, the so called reference genes. However, recent studies show there is no universal reference gene for all biological questions. Roses are important ornamental plants for which there has been no evaluation of useful reference genes for gene expression studies. Results: We used three different algorithms (BestKeeper, geNorm and NormFinder) to validate the expression stability of nine candidate reference genes in different rose tissues from three different genotypes of Rosa hybrida and in leaves treated with various stress factors. The candidate genes comprised the classical "housekeeping genes" (Actin, EF-1α, GAPDH, Tubulin and Ubiquitin), and genes showing stable expression in studies in Arabidopsis (PP2A, SAND, TIP and UBC). The programs identified no single gene that showed stable expression under all of the conditions tested, and the individual rankings of the genes differed between the algorithms. Nevertheless the new candidate genes, specifically, PP2A and UBC, were ranked higher as compared to the other traditional reference genes. In general, Tubulin showed the most variable expression and should be avoided as a reference gene. Conclusions: Reference genes evaluated as suitable in experiments with Arabidopsis thaliana were stably expressed in roses under various experimental conditions. In most cases, these genes outperformed conventional reference genes, such as EF1-α and Tubulin. We identified PP2A, SAND and UBC as suitable reference genes, which in different combinations may be used for normalisation in expression analyses via qPCR for different rose tissues and stress treatments. However, the vast genetic variation found within the genus Rosa, including differences in ploidy levels, might also influence expression stability of reference genes, so that future research should also consider different genotypes and ploidy levels.

Chilean IPNV isolates: Robustness analysis of PCR detection

Background: The genomes of several infectious pancreatic necrosis viruses (IPNVs) isolated in Chile were sequenced with a single amplification approach for both segments A and B. The resulting sequences were then used to determine the conservation of the primer-binding regions used in polymerase chain reaction (PCR)-based diagnostic methods proposed in the literature. Thus, the robustness of each technique was studied, particularly the eventual effect of further mutations within the primer-binding sites. Results: On analysis, most methods currently used to detect Chilean IPNV varieties were deemed adequate. However, the primers were designed to be genogroup specific, implying that most detection methods pose some risk of detecting all strains prevalent in the country, due to the coexistence of genogroups 1 and 5. Conclusions: Negative resultsmust be interpreted carefully given the high genomic variability of IPNVs. Detection techniques (quantitative reverse transcription (qRT)-PCR) based on degenerate primers can be used to minimize the possibilities of false-negative detections.

Qualification zoo-sanitaire du naissain de captage 2013 de l'huître creuse Crassostrea gigas (QUALIF) - Détection précoce des maladies en épreuve thermique de laboratoire

Depuis 2008, des mortalités massives d’huîtres creuses âgées de moins d’un an sont relevées sur le littoral français dès que la température de l’eau de mer atteint le seuil de 16°C. Ces mortalités de naissains sont associées à la détection du virus OsHV-1 μVar. Des travaux de qualification zoo-sanitaire menés depuis 2010 ont montré qu’un lot de naissains issus du captage naturel sur deux était infecté par le virus bien avant l’apparition des mortalités dans le milieu naturel, mais qu’a contrario les naissains d’écloserie expertisés présentaient une fréquence plus faible de portage latent. Dans ce contexte de crise zoo-sanitaire chronique, l’objectif de notre étude consistait à obtenir une information du statut zoo-sanitaire OsHV-1 μVar des populations de naissains du captage 2013 à l’échelle national. Ce travail avait pour finalité de permettre l’identification précoce des zones de captage associées à un risque de mortalité due à l’infection par OsHV-1 μVar. La méthodologie de l’épreuve thermique de laboratoire (ETL) correspond en une période de 1 mois d’isolement des naissains à évaluer en conditions contrôlées de laboratoire. Lors de cette période la température de l’eau de mer est maintenue constante à 21°C et la mortalité est relevée tous les 10 jours. La survie finale associée à des analyses qPCR permettent de qualifier le statut sanitaire en terme de portage OsHV-1 μVar de l’échantillon (statut infecté ou non infecté). Entre février et mars 2014, vingt et un échantillons de naissains âgés de 5 à 7 mois ont été échantillonnés dans six sites du littoral français (étang de Thau, bassin d’Arcachon, pertuis Charentais, baie de Bourgneuf, baie de Vilaine et rade de Brest) pour être qualifiés par ETL au site expérimental Ifremer d’Argenton. Les résultats de la campagne 2014 de qualification zoo-sanitaire confirment qu’en période hivernale, dans le milieu naturel, des naissains de captage peuvent être infectés par OsHV-1 μVar sans développement apparent de maladies ni mortalité. En revanche en ETL, ces lots de naissains infectés par OsHV-1 μVar présentent des taux de mortalité importants. Ainsi, sur les 20 échantillons de naissains de captage étudiés, onze ont révélé des maladies en ETL avec des mortalités cumulées variant de 16 % à 80 %. Ce ratio d’un échantillon sur deux de naissains infectés par OsHV-1 μVar demeure proche de celui observé de 2010 à 2013 lors des travaux précédents qui avaient permis de définir l’ETL. les six sites étudiés ont montré des résultats contrastés. En effet, les résultats se sont révélés favorables pour l’étang de Thau et la baie de Bourgneuf et défavorables dans le cas de la rade de Brest et la Baie de Vilaine. Pour ces deux derniers sites, tous les échantillons de naissains testés ont montré de fortes mortalités pendant l’ETL. Des différences s’observent également intra-site, notamment à Marennes Oléron avec 1 échantillon sur 3 infectés par OsHV-1 μVar ou dans pour Arcachon avec 3 échantillons sur 5. Dans le contexte préoccupant de l’épizootie actuelle, nos résultats confirment que certains lots de naissains de captage sont infectés par OsHV-1 μVar dès les mois de février-mars et pourrait être des acteurs actifs dans le déclenchement annuel du processus infectieux en milieu naturel quand la température de l’eau dépasse 16°C. Par ailleurs, notre étude démontre qu’il serait possible chaque année d’obtenir une qualification sanitaire précoce des zones de captage. Cela permettrait d’améliorer la gestion des risques liés aux transferts de naissains infectés par OsHV-1 μVar dans les différents bassins de production.

Qualification zoo-sanitaire du naissain de captage 2014 de l'huître creuse Crassostrea gigas (QUALIF) - Détection précoce des maladies en épreuve thermique de laboratoire

Depuis 2008, des mortalités massives d’huîtres creuses âgées de moins d’un an sont relevées sur le littoral français dès que la température de l’eau de mer atteint le seuil de 16°C. Ces mortalités de naissains sont associées à la détection du virus OsHV-1 μVar. Depuis 2010, des travaux de qualification zoo-sanitaire ont montré qu’environ un lot de naissains de captage sur deux était infecté par le virus avant l’apparition des mortalités dans le milieu naturel. En 2014, dans le cadre de la première action QUALIF, les résultats de la qualification zoo-sanitaire des naissains du captage de l’année 2013 à l’échelle nationale ont mis en évidence le caractère infectieux des maladies développées par ces naissains porteurs latents d’OsHV-1 μVar. L’objectif 2015 du second volet QUALIF consistait à reproduire le travail de qualification zoo-sanitaire OsHV-1 μVar pour les naissains du captage de l’année 2014. Les résultats (2014 et 2015) permettront d’aborder la variation interannuelle du statut zoo-sanitaire des naissains pour chacun des sites étudiés. La méthodologie de l’épreuve de qualification zoo-sanitaire consiste en une période de 1 mois d’isolement des naissains en conditions contrôlées de laboratoire. Lors de cette épreuve, la température de l’eau de mer est maintenue constante à 21°C et la mortalité est relevée tous les 10 jours. La survie finale et les analyses qPCR permettent de qualifier le statut sanitaire en terme de portage OsHV-1 μVar de l’échantillon (infecté ou non infecté). De début janvier à fin mars 2015, 39 échantillons de naissains âgés de 5 à 7 mois ont été prélevés dans 6 sites du littoral français (étang de Thau, bassin d’Arcachon, bassin de Marennes Oléron, baie de Bourgneuf, embouchure de La Vilaine et rade de Brest) pour être testés en épreuve thermique de laboratoire (ETL) dans l’outil expérimental Ifremer à Argenton. Les résultats montrent que 25 des 39 (soit 64 %) lots de naissains de captage testés ont développé des maladies en ETL associés à des mortalités cumulées variant de 6 à 72 %. Cette valeur de 64 % de lots détectés est plus élevée que celle précédemment observée en 2014 (55 %). Les résultats de cette seconde campagne de qualification zoo-sanitaire sont favorables pour les naissains de l’étang de Thau (absence de mortalité), moins favorables pour ceux d’Arcachon, Marennes Oléron, et ceux de la baie de Bourgneuf (réponses contrastées en terme de mortalité intra-site) et très défavorables pour les naissains de La Vilaine et de la rade de Brest (mortalités observées sur tous les échantillons testés). La principale conclusion de cette seconde étude de qualification zoo-sanitaire est identique à celle de 2014, à savoir qu’il est existe dans le milieu naturel en période hivernale des lots de naissains de captage infectés par OsHV-1 μVar sans développement apparent des maladies. Ces lots de naissains porteurs latents d’OsHV-1 μVar sont détectables en ETL et la présence d’OsHV-1 μVar peut alors être confirmée par qPCR. Dans le contexte actuel d’épizooties chroniques, nos résultats confirment à nouveau qu’il est possible d’identifier précocement les lots de naissains infectés ou non par OsHV-1 μVar. Ces animaux infectés sont un réservoir du virus en période hivernale. Dès que la température de l’eau de mer franchit le seuil de 16°C, ils participeront à la réémergence des maladies en milieu naturel. Par ailleurs, cette seconde étude de qualification zoo-sanitaire confirme la possibilité d’apprécier le risque sanitaire pour chaque zone de captage en fonction de la détection précoce des lots de naissains infectés par OsHV-1 μVar.

Caracterização transcricional dos genes CTR1 e ATP7B no peixe Poecilia vivipara: efeitos do cobre e da salinidade

Em peixes, o cobre (Cu) é absorvido a partir da água, via branquial, e pela ingestão de água e alimento, via gastrintestinal. Para evitar reações não específicas prejudiciais e suprir proteínas dependentes de Cu, existem transportadores específicos, como as proteínas de absorção de alta afinidade ao Cu (CTR1) e as Cu-ATPases (ATP7), que auxiliam na translocação intracelular do metal. No presente estudo, os genes CTR1 e ATP7B foram identificados em Poecilia vivipara e os seus transcritos foram quantificados por RT-qPCR nas brânquias, no fígado e no intestino de guarús expostos (96 h) ao Cu (0, 5, 9 e 20 µg/L) em água doce e salgada (salinidade 24). Foram identificadas novas sequências nucleotídicas dos genes CTR1 (1560 pb, completa) e ATP7B (617 pb, parcial), as quais tiveram altos valores de identidade com as descritas para Fundulus heteroclitus (CTR1=81%) e Sparus aurata (ATP7B=81%). A análise por RT-qPCR indicou níveis de transcrição para CTR1 e ATP7B em todos os tecidos analisados. Em guarús na água doce, a maior expressão da CTR1 e da ATP7B se deu no fígado. Em guarús na água salgada, a maior expressão da CTR1 ocorreu no intestino, enquanto a da ATP7B se deu no fígado e intestino. Na água doce, a exposição ao Cu aumentou o conteúdo branquial e hepático de Cu, diminuiu os transcritos de CTR1 e ATP7B nas brânquias e aumentou os transcritos destes genes no fígado, sem alterar o conteúdo corporal de Cu. Na água salgada, a exposição ao Cu aumentou o conteúdo de Cu e diminuiu o transcrito de ATP7B no intestino, sem alterar o conteúdo corporal de Cu nos P. vivipara. Estes resultados indicam que a homeostasia do Cu em P. vivipara envolve a redução da expressão do CTR1 e ATP7B nas brânquias (água doce) e intestino (água salgada) para limitar a absorção do Cu e o aumento da expressão destes genes no fígado (água doce) para facilitar o armazenamento e desintoxicação do Cu.

Perfil de memória e ativação de linfócitos T na leishmaniose visceral

Visceral leishmaniasis (VL) in Brazil is a disease caused by Leishmania infantum chagasi (L.i.chagasi). The clinical evolution post-infection depends on the vertebrate host immune response, which is genetically mediated. This study aimed to evaluate the immune response of individuals living in endemic area for VL in the state of the Rio Grande do Norte, considering individuals with VL under treatment (n = 9), recovered VL <1 year post treatment (n = 10), > 10 years posttreatment (n = 9), uninfected individuals living in endemic areas (n = 7), individuals that lost DTH response (n=6) and asymptomatic individuals for VL (n=9). Peripheral blood cells were evaluated in the presence and absence of soluble Leishmania antigens (SLA) and ex vivo, to determine activation, presence of regulatory cells and memory cells. The Leishmania parasitemia and anti-Leishmania antibodies were determined respectively by qPCR and ELISA. Cells from individuals with VL under treatment showed less cell activation after stimulation with SLA for the markers CD4/CD69, CD8/CD69 and CD8/CD25 compared with VL post treatment treatment (p <0.001). Apparently uninfected individuals have a higher cell activation than symptomatic VL (p <0.001), with the exception of CD8/CD25 marker (p = 0.6662). On the other hand, in the ex-vivo group, significant differences were observed for CD4/CD69, CD8/CD69 and CD8/CD25 between the 4 groups due to increased cell activation present in cells of individuals symptomatic LV (p <0.001). VL cells under treatment, ex vivo, have a lower percentage of memory cells (CD4/CD45RO and CD8/CD45RO) than individuals VL post-treatment or control group (p = <0.01). Likewise, individuals with symptomatic VL have fewer regulatory cells when stimulated by SLA [CD4/CD25 (p = 0.0022) and CD4/FOXP3 (p = 0.0016)] and in the ex-vivo group (p = 0.0017). Finally, DNA isolated from recovered VL contained Leishmania DNA, supporting the hypothesis of non-sterile clinical cure for Leishmania infection. Recovered VL, even 10 years after treatment have high levels of memory cells, which may be due to the presence of stimulation, either by reexposure to Leishmania or non-sterile cure

Caracterização funcional de dois cDNAs homólogos à ciclofilina e à proteína reprimida por auxina (ARP) identificados em bibliotecas subtrativas a para floração em tomateiro

Flowering is a fundamental process in the life cycle for plant. This process is marked by vegetative to reproductive apical meristem conversion, due to interactions between several factors, both internal and external to plant. Therefore, eight subtractive libraries were constructed using apical meristem induced or not induced for two contrasting species: Solanum lycopersicum cv. Micro-Tom and Solanum pimpinellifolium. Several cDNAs were identified and among these, were selected two cDNAs: one homologous cDNA to cyclophilin (LeCYP1) and the other to Auxin repressed protein (ARP). It has observed that LeCYP1 and ARP genes are important in the developmental process to plants. In silico analysis, were used several databases with the exclusion criterion E-value <1.0x10-15. As a result, conservation was observed for proteins analyzed by means of multiple alignments and the presence of functional domains. Then, overexpression cassettes were constructed for the ARP cDNA in sense and antisense orientations. For this step, it was used the CaMV35S promoter. The cDNA orientation (sense or antisense) in relation to the promoter was determined by restriction enzymes and sequencing. Then, this cassette was transferred to binary vector pZP211 and these cassettes were transferred into Agrobacterium tumefaciens LBA4404. S. lycopersicum cv. Micro-Tom (MT) and MT-Rg1 plants were transformed. In addition, seedlings were subjected to hormone treatments using a synthetic auxin (- naphthalene acetic acid) and cyclosporin A (cyclophilin inhibitor) treatments and it was found that the hormone treatment there were changes in development of lateral roots pattern, probably related to decreases in auxin signaling caused by reduction of LeCYP1 in MT-dgt plants while cyclosporin A treatments, there was a slight delay in flowering in cv. MT plants. Furthermore, assay with real-time PCR (RT-qPCR) were done for expression level analysis from LeCYP1 and ARP in order to functionally characterize these sequences in tomato plants.

Aspectos a considerar en una actualización de la normativa nacional en materia de legionelosis

Objetivo: En España, el vigente Real Decreto 865/2003 establece una serie de medidas destinadas a la prevención de la legionelosis que inciden especialmente en el mantenimiento de las instalaciones de riesgo relacionadas con la proliferación y transmisión de Legionella. Este trabajo pretende revisar determinados aspectos estructurales, de mantenimiento, operacionales y documentales que, desde el punto de vista del Control Oficial, podrían ser incluidos en una futura nueva norma que pudiera ser más efectiva, si cabe, en la prevención y control de la legionelosis en las instalaciones de riesgo. Materiales y Métodos: Se ha utilizado la normativa nacional vigente en materia de la legionelosis, documentación técnica de apoyo, otras normativas de aplicación en países de la Unión Europea, así como servicios en línea de información científica (ISI Web of Knowledge) y bases de datos de bibliografía médica (MEDLINE PubMed). Resultados y Discusión: Tras más de una década en vigor, es necesario que ciertos aspectos técnicos de las instalaciones de riesgo en la transmisión de la legionelosis sean revisados y adecuados al conocimiento actual y a la experiencia adquirida. Entre ellos se encuentran la clasificación de riesgo de las instalaciones, aspectos técnicos y operacionales de los sistemas de agua fría de consumo humano y caliente sanitaria, de los equipos de enfriamiento evaporativos, de los sistemas de agua climatizada y de los procedimientos de toma de muestras. Por último, se discute sobre la inclusión de técnicas analíticas basadas en la Biología Molecular (qPCR) como método oficial en la determinación de Legionella. Conclusiones: Una posible nueva normativa sobre prevención y control de la legionelosis debe contemplar una clasificación de las instalaciones en función del riesgo, que recoja las de reciente aparición que han sido asociadas a brotes. También deberá contar con anexos sobre las medidas preventivas para cada una de ellas, que desarrollen protocolos de toma de muestras específicos y modelos para la evaluación de riesgos adecuados que tengan en cuenta establecimientos especialmente sensibles, debería estudiarse la inclusión de las técnicas analíticas moleculares como métodos oficiales o complementarios a los oficiales. Esta actualización permitirá una actuación más rápida y eficaz ante la identificación de casos y la asociación de los mismos a las instalaciones de riesgo implicadas.

O papel modulatório do ferro sobre a resposta imune na Leishmaniose Visceral

Iron is an essential element for many cellular functions, including the immune response against intracellular pathogens. In this study, we aimed evaluate the effect of iron on IRP2, IFN-γ, TNF-α, IL-6, IL-10, MIG and IP10 expression in PBMC and assess the effect of the spleen parasite load on the expression of these genes in the spleen of L. infantum naturally infected dogs. Blood sample from 7 DTH+ donor was collected and PBMC was obtained. The cells were cultivated in absence (iron chelator desferroximane, DFO 10 μM supplemented media) or in presence of iron (hemin 6 mM) for 1 h, followed by stimulation with Leishmania infatum antigen for 4 h. 44 dog spleen samples were obtained and parasite load in this organ was determinate by qPCR. Gene expression was analyzed by qPCR and cytokine production quantified by flow cytometry. In antigen stimulated cells, genes involved in immune response are significantly more expressed in presence of iron. T CD4+ and TCD8+ lymphocytes produces IFN-γ, TNF-α and IL-10 possibly in iron dependent pathway. Monocytes antigen stimulated reduced TNF-α, IL-6 and IL-10 production in presence of iron. We found spleen of infected dogs IRP2 expression increases according to parasite load in that organ, while an inverse profile was found for IFN-γ, TNF-α e IL-10 expression. These results suggest that T lymphocytes depends on iron to produce IFN-γ, TNF-α and IL-10, while iron seems to inhibit cytokine production in monocytes. So, we propose an immunoregulatory mechanism carried out by iron during L. infantum infection in humans and dogs

Anticorpos anti-trypanosoma cruzi como preditivos de infecção por leishmania infantum

Leishmania infantum and Trypanosoma cruzi are trypanosomatids of medical importance and are, respectively, the etiologic agents of visceral leishmaniasis (VL) and Chagas disease (CD) in Brazil. People infected with L. infantum or T. cruzi may develop asymptomatically, enabling the transmission of pathogens through blood transfusion and / or organs. The assessment of the infection by T. cruzi is included among the tests performed for screening blood donors in Brazil, however, there is no availability of tests for Leishmania. Serological tests for T. cruzi are very sensitive, but not specific, and may have cross-reactions with other microorganisms. Thus, the aim of this study was to determine the prevalence of Leishmania infection in blood donors and assess whether the serological test for T. cruzi detect L. infantum. Among the 300 blood samples from donors, discarded in 2011, 61 were T. cruzi positive, 203 were from donors with other infections and 36 were from handbags with low blood volume, but without infection. We also assessed 144 samples from donors without infections and able to donate blood, totaling 444 subjects. DNA was extracted from blood samples of all to perform quantitative PCR (qPCR) to detect Leishmania DNA. The buffy coat obtained from all samples was grown in Schneider medium supplemented and NNN. All samples were evaluated for the presence of anti-Leishmania antibody. The serological results indicate a percentage of 22% of Leishmania infection in blood samples obtained from discarded bags. A total of 60% of samples positive in ELISA for T. cruzi were negative by IFI, used as confirmatory test, ie 60% false positive for Chagas. Among these samples false positive for Chagas, 72% were positive by ELISA for Leishmania characterizing the occurrence of cross reaction between serologic assays. Of the 300 cultures performed, 18 grew parasites that were typed by qPCR and specific isoenzymes, found the species Leishmania infantum crops. Among the 18 cultures, 4 were purged from scholarships for low volume and all negative serology blood bank, thus demonstrating that there is a real risk of Leishmania transmission via transfusion. It is concluded that in an area endemic for leishmaniasis in Brazil, serological diagnosis performed to detect infection by T. cruzi among blood donors can identify infection by L. infantum and although cause false positive for Chagas, this cross-reactivity reduces the risk of Leishmania infection via blood transfusion, since tests are not applied specific detection of the parasite. In this way, there remains the need to discuss the implementation of a specific serological screening test for Leishmania in endemic countries such as Brazil

Linfócitos T : uma análise do perfil diferencial da expressão gênica na imunorregulação

Tese (doutorado)—Universidade de Brasília, Faculdade de Medicina, Pós-Graduação em Patologia Molecular, 2016.

Nuevas perspectivas sobre la histopatología de la infección de Pinus Radiata por Fusarium Circinatum

223 p.

Evaluación de los perfiles de respuesta a interferón inducidos como respuesta a la infección con el virus del dengue

Introducción: El dengue es la principal enfermedad viral transmitida a humanos por artrópodos. Una de las características del cuadro clínico de la infección por el virus del dengue (DENV) es su alta variabilidad en la severidad, pronóstico y resolución de la enfermedad. Estudios recientes sugieren que diferentes cepas virales parecen inducir respuestas de interferón variables y que de ello pudiese depender la presentación clínica. No existen estudios previos que evalúen este fenómeno en cepas virales circulantes en México. Sumado a esto, se ha reportado que 80% de las infecciónes por DENV son asintomáticas: por lo tanto, los donadores de sangre virémicos son un riesgo para la seguridad en transfusiones. También nos propusimos estudiar si la seroprevalencia de anticuerpos anti-DENV permanecía constante en donadores de sangre con respecto al tiempo. Objetivo: Conocer la contribución epidemiológica e impacto del dengue en Nuevo León, así como establecer si existe una asociación entre la patogénesis y la variabilidad genética de los serotipos 1 y 2 del DENV, mediante la evaluación de los perfiles de expresión y respuesta a interferón, en cultivos celulares infectados con cepas virales aisladas a partir de sujetos mexicanos virémicos. Materiales y métodos: Se hizo un estudio retrospectivo de los registros semanales de CENAVECE para conocer el panorama actual oficial del dengue en Nuevo León. En colaboración con el banco de sangre HU y el Centro Estatal de la Transfusión se recolectaron 285000 donaciones de sangre en el periodo de enero 2010 a diciembre 2012, con carta de consentimiento informado. A 2061 donadores sanos se les realizó ELISA para buscar anticuerpos contra Brucella, VHC, VDRL, HBsAg, HIV1 y 2, WNV, DENV IgM-IgG. Los sueros positivos a DENV se confirmaron por detección de NS1-DENV y RT-qPCR. A la par en colaboración con LESP-NL se recolectaron 1079 sueros NS1-DENV positivos de Nuevo León los cuales se analizaron por PCR en tiempo real para identificar serotipos, y fueron sembrados en células C6/36 para aislar partículas virales. Los virus aislados se titularon en células BHK-21. Posteriormente, se infectaron células Huh-7 a una m.o.i. de 0.1 durante 36h. Se usaron como control virus prototipo inactivados con luz UV. Transcurrido el tiempo de infección, las células se trataron 1h con IFNα (1000UI/mL). Los RNAs totales se montaron sobre arreglos de PCR tiempo real (PAHS-016Z, QIAGEN) para evaluar la respuesta de interferón de las cepas aisladas de pacientes. Resultados: Se encontró que en el transcurso de 5 años, el estado de Nuevo León pasó del lugar 12 al 5º con mayor incidencia de dengue a nivel nacional, y que la seroprevalencia de anticuerpos anti-DENV en donadores asintomáticos fue del 2.6%. Se aislaron 13 virus a partir de cutivos celulares infectados con sueros NS1 positivos y los virus tuvieron la capacidad de infectar otras líneas celulares, generar partículas infecciosas funcionales y de generar enfermedad en un sistema In vivo. Al infectar células Huh-7 se observó que las cepar virales tenían una capacidad diferente para modular la respuesta de interferón, regulando con diferente intensidad diferentes genes involucrados en el establecimiento del estado antiviral intracelular. Los virus serotipo 2 indujeron niveles de expresión más altos que los virus serotipo 1.

Transcription of alternative oxidase (AOX) and plastid terminal oxidase (PTOX) during stress-regulated root tissue growth in Daucus carota L. - An approach to identify functional marker candidates for breeding on carrot yield stability

A presente tese explora a hipótese de utilização dos genes da oxidase alternativa (AOX) e da oxidase terminal da plastoquinona (PTOX) como genes-alvo para o desenvolvimento de marcadores funcionais (MF) para avaliar a performance do crescimento em cenoura, fator determinante da produtividade. Para avaliar se os referidos genes estão associados com o crescimento da cenoura procedeu—se ao seu isolamento e posterior análise dos seus perfis de transcrição em diversos sistemas biológicos. O sistema in vitro selecionado, denominado sistema de culturas primárias, permitiu avaliar alterações na quantidade de transcritos desses genes durante os processos de reprogramação celular e crescimento. Ao nível da planta foi também estudado o efeito do frio na expressão precoce dos genes AOX. Ambos os genes DcAOX1 e DcAOX2a revelaram uma resposta rápida e um padrão semelhante apos stresse (inoculação in vitro e resposta ao frio). Foi igualmente verificado um incremento na expressão do gene DcPTOX durante a fase inicial do processo de reprogramação celular. Estudos de expressão dos genes AOX durante o desenvolvimento da raiz da cenoura revelaram que o gene DcAOX2a será potencialmente o gene mais envolvido neste processo. De modo a avaliar a hipótese de envolvimento do gene DcPTOX no crescimento da raíz procederam—se a estudos de expressão ao nível do tecido meristemático. Todavia, para um mais completo entendimento da ligação entre DcPTOX e o crescimento secundário e/ou acumulação de carotenos, a expressão do gene DcPTOX foi também avaliada em raízes de cenoura durante o desenvolvimento, utilizando cultivares caracterizadas por distintos conteúdos de carotenos. Os resultados obtidos demonstraram a associação do gene DcPTOX a ambos os processos. O envolvimento da PTOX no crescimento adaptativo da raiz foi analisado com um ensaio que permitiu identificar, no tecido meristemático, uma resposta precoce do gene DcPTOX face a uma diminuição da temperatura. Adicionalmente, foi efetuada a seleção de genes de referência para uma analise precisa da expressão génica por RT-qPCR em diversos sistemas biológicos de cenoura, e a importância do seu estudo ao nível do sistema biológico foi realçada. Os resultados desta tese são encorajadores para prosseguir os estudos de utilização dos genes AOX e PTOX como MF no melhoramento da performance do crescimento adaptativo em cenoura, fator determinante para a produtividade; ABSTRACT: This thesis explores the hypothesis of using the alternative oxidase (AOX) and theplastid terminal oxidase (PTOX) as target genes for functional marker (FM) development for yield-determining growth performance in carrot. To understand if these genes are associated to growth, different AOX gene family members and the single PTOX gene were isolated, and their expression patterns evaluated in diverse carrot plant systems. An in-vitro primary culture system was selected to study AOX and PTOX transcript changes during cell reprogramming and growth performance. At plant level, a putative early response of AOX to chilling was also evaluated. In fact, both DcAOXl and DcAOXZa were early responsive and showed similar patterns under stress conditions (in vitro inoculation and chilling). A role for DcPTOX during earliest events of cell reprogramming was also suggested. Next, the expression profiles of AOX gene family members during carrot tap root development were investigated. DcAOXZa was identified as the most responsive gene to root development. In order to evaluate if DcPTOX is associated with carrot tap root growth performance, DcPTOX transcript levels were measured in the central root meristem. To further understand whether DcPTOX is associated with secondary growth and/or carotenoids accumulation, DcPTOX expression was also studied in deveIOping carrot tap roots in cultivars with different carotenoids contents. The results indicated that DcPTOX associates to both carotenoid biosynthesis and secondary growth during storage root development. To obtain further insights into the involvement of PTOX on adaptive growth, the early effects of temperature decrease were explored in the root meristem, where a short—term early response in DcPTOX was found, probably associated with adaptive growth. Furthermore, a selection of the most suitable reference genes for accurate RT—qPCR analysis in several carrot experimental systems was performed and discussed. The present research provides the necessary toolbox for continuing studies in carrot AOX and PTOX genes as promising resources for FM candidates in order to assist breeding on yield—determining adaptive growth performance.

Association between ferritin, high sensitivity c-reactive protein (hsCRP) and relative abundance of Hepcidin mRNA with the risk of type 2 diabetes in obese subjects

Obesity and Type 2 diabetes mellitus share a strong pro-inflammatory profile. It has been observed that iron is a risk factor in the development of type 2 diabetes. The aim of this study was to evaluate the relationship between iron nutritional status and inflammation with the risk of type 2 diabetes development in obese subjects. We studied 30 obese men with type 2 diabetes (OBDM); 30 obese subjects without diabetes (OB) and 30 healthy subjects (Cn). We isolated peripheral mononuclear cells (PMCs) and challenged them with high Fe concentrations. Total mRNA was isolated and relative abundance of TNF-αIL-6 and hepcidin were determined by qPCR. Iron status, biochemical, inflammatory and oxidative stress parameters were also characterized. OBDM and OB patients showed increased hsCRP levels compared to the Cn group. OBDM subjects showed higher levels of ferritin than the Cn group. TNF-α and IL-6 mRNA relative abundances were increased in OBDM PMCs treated with high/Fe. Hepcidin mRNA was increased with basal and high iron concentration. We found that the highest quartile of ferritin was associated with an increased risk of type 2 diabetes when it was adjusted to BMI and HOMA-IR; this association was independent of the inflammatory status. The highest level of hepcidin gene expression also showed a trend of increased risk of diabetes, however it was not significant. Levels of hsCRP over 2 mg/L showed a significant trend of increasing the risk of diabetes. In conclusion, iron may stimulate the expression of pro-inflammatory genes (TNF-α and IL-6), and both hepcidin and ferritin gene expression levels could be a risk factor for the development of type 2 diabetes. Subjects that have an increased cardiovascular risk also have a major risk to develop type 2 diabetes, which is independent of the BMI and insulin resistance state.