Detección molecular de Cucumber mosaic virus y Pepper severe mottle virus en arvenses asociadas al cultivo de ají (Capsicum spp.)

En los últimos años, el ají (Capsicum chinense, Capsicum frutescens y Capsicum annuum var. Acuminatum), cultivado en el Valle del Cauca, se ha visto afectado por enfermedades virales causadas por Cucumber mosaic virus (CMV-ají) y Pepper severe mottle virus (PepSMoV). Pese a que estos dos virus son limitantes para producción del cultivo de ají, en la actualidad, pocos estudios han identificado los hospederos alternos de CMV-ají y PepSMoV. En este trabajo, se evaluó la presencia de CMV-ají y PepSMoV, mediante RT-PCR, en muestras de tejido foliar, de 121 plantas arvenses, asociadas al cultivo de ají, en el Valle del Cauca, Colombia. El análisis molecular indicó la presencia de CMV-ají, en el 21,4 % de las plantas recolectadas y de PepSMoV, en el 20,6 %. Se identificaron las especies arvenses Amaranthus viridis, Parthenium hysterophorus, Hippobroma longiflora, Commelina diffusa, Clitoria ternatea, Crotalaria incana, Desmodium tortuosum, Desmodium intortum, Macroptilium lathyroides, Anoda acerifolia, Boerhavia erecta, Bougainvillea glabra, Rivina humilis, Browallia americana, Capsicum rhomboideum, Solanum americanum y Lantana camara, como hospederas de CMV-ají o PepSMoV. Se presentó infección mixta de CMV-ají y PepSMoV, en 57 % de las arvenses positivas a virus, las cuales, están distribuidas en zonas productores de ají, localizadas en seis municipios del Valle del Cauca. Estos resultados brindan información sobre la distribución de estos virus en el Valle del Cauca, contribuyen al conocimiento de la epidemiología viral y servirán para diseñar medidas de manejo, orientadas a prevenir las infecciones virales en los cultivos de ají.

In recent years, chili pepper (Capsicum chinense, Capsicum frutescens y Capsicum annuum var. Acuminatum) grown in Valle del Cauca has been affected by viral diseases caused by Cucumber mosaic virus (CMV-chili pepper) and Pepper severe mottle virus (PepSMoV). Although these two viruses are limiting to the production of the chili pepper crop, at present, few studies have identified the alternate hosts of CMV-chili pepper and PepSMoV. In this work, the presence of CMV-chili pepper and PepSMoV were evaluated by RT-PCR in leaf tissue samples from 121 weed plants associated with chili pepper cultivation in Valle del Cauca, Colombia. Molecular analysis indicated the presence of CMV-chili pepper in 21.4 % of the collected plants and PepSMoV in 20.6 %. Weed species Amaranthus viridis, Parthenium hysterophorus, Hippobroma longiflora, Commelina diffusa, Clitoria ternatea, Crotalaria incana, Desmodium tortuosum, Desmodium intortum, Macroptilium lathyroides, Anoda acerifolia, Boerhavia erecta, Bougainvillea glabra, Rivina humilis, Browallia americana, Capsicum rhomboideum, Solanum americanum and Lantana camara, as hosts of CMV-chili pepper or PepSMoV. Mixed infection of CMV-chili pepper and PepSMoV was present in 57 % of the weeds positive for viruses, which are distributed in chili pepper producing areas located in six municipalities of Valle del Cauca. These results provide information on the distribution of these viruses in Valle del Cauca. Contribute to the knowledge of viral epidemiology and will serve to design management measures aimed to prevent viral infections in chili pepper crops.

Ocurrence of pepper yellow mosaic virus and cucumber mosaic virus on Capsicum chinense in the state of Amazonas, Brazil

The habanero chilli pepper, Capsicum chinense is an important crop in the Amazon Basin, mainly grown by small-scale producers. Capsicum chinense plants in an experimental field in the northern Brazilian state of Amazonas were found exhibiting characteristic symptoms of viral infection. Leaf sap from symptomatic plants examined under a transmission electron microscope revealed the presence of elongated flexuous particles and isometric particles. Using molecular assays, the viruses were identified as pepper yellow mosaic virus (PepYMV) and cucumber mosaic virus (CMV). Aphids, identified as Aphis gossypii, were found colonizing the C. chinense plants in the field and may be the vector for both PepYMV and CMV. We report the first occurrence of these viruses infecting C. chinense in the state of Amazonas. (AU)

Ocurrence of pepper yellow mosaic virus and cucumber mosaic virus on Capsicum chinense in the state of Amazonas, Brazil / Ocorrência do pepper yellow mosaic virus e cucumber mosaic virus em Capsicum chinense no estado do Amazonas, Brasil

The habanero chilli pepper, Capsicum chinense is an important crop in the Amazon Basin, mainly grown by small-scale producers. Capsicum chinense plants in an experimental field in the northern Brazilian state of Amazonas were found exhibiting characteristic symptoms of viral infection. Leaf sap from symptomatic plants examined under a transmission electron microscope revealed the presence of elongated flexuous particles and isometric particles. Using molecular assays, the viruses were identified as pepper yellow mosaic virus (PepYMV) and cucumber mosaic virus (CMV). Aphids, identified as Aphis gossypii, were found colonizing the C. chinense plants in the field and may be the vector for both PepYMV and CMV. We report the first occurrence of these viruses infecting C. chinense in the state of Amazonas.

A pimenta-de-cheiro, Capsicum chinense é uma cultura importante na Bacia Amazônica, cultivada principalmente por pequenos produtores. Plantas de C. chinense em um campo experimental localizado no norte do estado brasileiro do Amazonas, foram encontradas apresentando sintomas característicos de infecção viral. Extratos de amostras de folhas sintomáticas examinados ao microscópio eletrônico de transmissão revelaram a presença de partículas alongadas e flexuosas e de partículas isométricas. Análises moleculares permitiram identificar a presença do pepper yellow mosaic virus (PepYMV) e do cucumber mosaic virus (CMV). Pulgões, identificados como Aphis gossypii foram encontrados colonizando pimenteiras-de-cheiro neste campo experimental e podem representar o provável vetor de PepYMV e CMV. Este trabalho relata a primeira ocorrência desses vírus infectando C. chinense no estado do Amazonas.

Characterization of Cowpea aphid-borne mosaic virus in Passiflora edulis 'Catarina' in the southern coast of Santa Catarina State, Brazil / Caracterização do Cowpea aphid-borne mosaic virus em Passiflora edulis cv. Catarina no litoral sul de Santa Catarina, Brasil

CABMV is a limiting virus for passion fruit crop in Brazil, its main producing country. This virus has been reported in all producing states of the country, with the state of Santa Catarina (SC) in 2017 standing as the third largest passion fruit producer. In 2017, it reached 8.4% of the national production. The southern coast is the main responsible for the increase in production, which has been supplying the domestic market. However, in that same year, this region recorded the first symptom expressions in plants and fruits. The evaluation of the samples collected in the municipalities of Sombrio, Praia Grande and São João do Sul, southern coast of SC, was performed by using a mechanical transmission to indicator plants, PTA-ELISA and RT-PCR, and by sequencing. The evaluation results were positive for CABMV and negative for CMV in PTA-ELISA. In RT-PCR, there was the formation of a 700bp ca band, expected size for Potyvirus, whose sequence comparison with those deposited in GenBank reveled 98% identity with the isolates from São Paulo State. The occurrence of the virus in the southern coast of SC did not reach a serious decrease in passion fruit production due to the union of producers, who adopted preventive management measures to control the virus, whose effect led to a consolidation of the passion fruit production chain in the region.(AU)

O CABMV é um vírus limitante para a cultura do maracujá no Brasil, principal país produtor mundial, cuja ocorrência já foi relatada em todos os estados produtores. Em 2017, o estado de Santa Catarina (SC) foi o terceiro maior produtor de maracujá no Brasil, responsável por 8,4% da produção nacional, sendo o litoral sul o principal responsável pelo aumento da produção, garantindo o abastecimento do mercado interno. Entretanto, nesse mesmo ano, essa região registrou as primeiras expressões de sintomas em plantas e frutos. Uma avaliação das amostras coletadas nos municípios de Sombrio, Praia Grande e São João do Sul, litoral sul de Santa Catarina, foi realizada por transmissão mecânica para plantas indicadoras, PTA-ELISA, RT-PCR e sequenciamento. Os resultados foram positivos para o CABMV e negativos para o CMV, tanto em PTA-ELISA quanto RT-PCR. Na RT-PCR, houve a amplificação de bandas com ca de 700pb, tamanho esperado para o Potyvirus cuja comparação de sequências com as depositadas no GenBank revelaram 98% de similaridade com os isolados do estado de São Paulo. A ocorrência do vírus na região do litoral sul de Santa Catarina não causou quebra na produção de maracujá devido à adoção conjunta de medidas preventivas de manejo pelos produtores, fato que consolidou a cadeia produtiva do maracujá na região.(AU)

Design of primers for specific detection of Potato Virus Y (PVY) by RT-PCR / Diseño de cebadores específicos para la detección por rt-pcr del potato virus y (pvy)

RESUMEN El Potato virus Y (PVY) es uno de los virus más limitantes para la producción de papa (Solanum tuberosum y S. phureja) en el mundo. Este virus es transmitido por tubérculo-semilla de papa y por diferentes especies de áfidos. Para su manejo es fundamental la siembra de tubérculos certificados por su sanidad viral, para lo que se requieren metodologías de detección altamente sensibles como ELISA y RT-PCR. Para éstas últimas pruebas, es necesario disponer de cebadores específicos que permitan el diagnóstico del virus en tejidos asintomáticos. En este estudio se reportan los cebadores PVY_Col para la detección del PVY en RT-PCR convencional y en tiempo real (RT-qPCR). Estos cebadores fueron diseñados con base en las secuencias de este virus que se han reportado en Colombia sobre diferentes hospedantes, así como de las diferentes variantes encontradas en el mundo. Una particularidad adicional de estos cebadores es que no presentan reacción cruzada con el genoma del Potato virus V (PVV), otro potyvirus que recientemente se ha encontrado afectando cultivos de papa en Colombia. Se espera que los cebadores PVY_Col sean utilizados para apoyar los programas de certificación de material de siembra de papa, así como para adelantar estudios epidemiológicos y de manejo fitosanitario de este virus.

ABSTRACT Potato virus Y (PVY) is one of the most limiting viruses in the production of potato (Solanum tuberosum and S. phureja) worldwide. This virus is transmitted by aphids and infected tuber-seeds, and for this reason, disease management of PVY requires, among others, using certified planting material through highly sensitive techniques such as ELISA and RT-PCR. However, RT-PCR-based methods require primers of high specificity to allow the unequivocal detection of viruses in asymptomatic tissues. In this work, we report a new set of primers (PVY_Col) for detection of PVY by RT-PCR and real-time RT-PCR (RT-qPCR). These primers were designed using sequences of PVY isolates from Colombia and the rest of the world. An essential feature of these primers is their specificity, since they don't amplify templates from Potato virus V (PVV), a close PVY relative that also infects potato crops in Colombia. It is expected that the PVY_Col primer set will be useful to support potato seed certification programs, epidemiological studies, and PVY disease management programs.

CARACTERIZACIÓN MOLECULAR DEL Potato virus V (PVV) INFECTANDO Solanum phureja MEDIANTE SECUENCIACIÓN DE NUEVA GENERACIÓN / Molecular Characterization of Potato virus V (PVV) Infecting Solanum phureja Using Next-Generation Sequencing

Las enfermedades virales son uno de los problemas más limitantes para la producción de papa en el mundo. Uno de los materiales de papa más susceptibles a los virus corresponde a Solanum phureja; sin embargo, en Colombia son pocos los estudios adelantados sobre los agentes causales que lo afectan. En este trabajo se realizó una caracterización molecular del Potato virus V (PVV) infectando plantas de S. phureja en Antioquia, utilizando métodos de secuenciación de nueva generación (NGS), pruebas de DAS-ELISA, RT-PCR en tiempo real (RT-qPCR) y RT-PCR convencional. Los resultados indican la ocurrencia de niveles muy variables de incidencia del virus entre lotes de cultivo (6,7 % a 86 %). El PVV tiene un genoma de 9828 nt que codifica para una poliproteína de 3066 aa y presenta dos variantes principales (Var_A y Var_B) en proporciones de 72 y 28 %. Estas variantes comparten altos niveles de identidad genética (99,7 % en todo el genoma) entre ellas y con respecto a la cepa PVV-Phureja reportada en Colombia, pero no con otras cepas del mundo (82-83 %). Con base en dichos genomas, se diseñaron y evaluaron en muestras foliares de S. phureja, dos pares de cebadores para la detección del virus en pruebas de RT-PCR (459 pb) y RT-qPCR (89 pb, Ct=12,08-21,86 y Tm= 78,7°C-80,2 °C), confirmándose la presencia de este virus en tejidos sintomáticos y asintomáticos de papa criolla. La ocurrencia generalizada de PVV en los cultivos de S. phureja indica la necesidad de incorporar en los programas de certificación de tubérculos-semilla de S. phureja en Colombia el diagnóstico de este virus.

Viral diseases are one of the most limiting problems in the production of potato worldwide. Solanum phureja constitutes one of the most susceptible materials to viral diseases in Colombia; however, there are few studies on viruses infecting this crop. In the current study, we performed a molecular characterization of Potato virus V (PVV) that infects S. phureja, using different potato plots located in the province of Antioquia, using Next-Generation Sequencing (NGS), DAS-ELISA, real time RT-PCR (RT-qPCR) and RT-PCR. Results revealed variable levels of incidence among plots (6.7 %-86 %) and the presence of two slightly different variants (Var_A and Var_B) present in approximately 72 %:28 % ratio. These PVV strains have a genome of 9828 nt codifying for a polyprotein of 3066 aa and share high nucleotide sequence identity (99,7 % in their complete genome) with respect to PVV-Phureja, recently described in Colombia, but are very divergent with respect to currently available PVV genomes (82-83 %). The genome information was used to design two sets of primers, useful in the specific detection of this virus in S. phureja leaf samples through RT-PCR (459 bp) and RT-qPCR (89 bp, Ct=12.08-21.86; Tm=78.7 °C-80.2 °C). This study underscores the importance of including diagnostics of PVV in S. phureja tuber-seed certification programs in Colombia.

Serological Identification of Virus in Watermelon Production Fields in the Tocantins State

Watermelon (Citrullus lanatus) cultivated in almost all tropical and subtropical regions of the world, has its largest output in China, and then, according to FAO data, Turkey, Iran and Brazil, being one of the main crops cultivated in State of Tocantins, Brazil. In this work was investigated the occurrence and distribution of the watermelon viruses, totaling 752 samples taken in a stratified experimental design in four representative regions of production: Gurupi (150), Lagoa da Confusao (232), Formoso do Araguaia (265) and Porto Nacional (105). The sampling and collecting the leaves of plants with the presence of symptoms were performed once a week during the entire cultivation cycle. As a result, were observed by Dot-ELISA method, different types of viruses, such as Papaya ringspot W (PRSV-W), Zucchini yellow mosaic virus (ZYMV), Watermelon mosaic virus (WMV) (potyvirus), Cucumber mosaic virus ( CMV) (Cucumovirus) and Zucchini lethal chlorosis virus (ZLCV) (Tospovirus). Of these, PRSV-W was predominant (22%), followed by WMV (15%), ZLCV (11%), CMV (5%) and ZYMV (4%). Mixed infections with PRSV-W + WMV and PRSV-W + ZLCV were also observed around 20% frequency (expressed with symptoms differently from a single infection). The results provide important support for the program management viruses.

Detección molecular de potyvirus en hojas y minibulbillos de ajo, Allium sativum, asociados a un programa de producción de semilla limpia / Molecular detection of potyvirus in leaves and small bulbs of garlic, Allium sativum, associated a clean seed production program

El ajo (Allium sativum L) se reproduce vegetativamente utilizando bulbillos, condición que favorece la propagación de enfermedades, especialmente bacterias, hongos y virus que afectan la calidad y el rendimiento del cultivo. Por este motivo se implementó la identificación molecular por RT-PCR de los potyvirus LYSV y OYDV en el sistema de producción de semilla limpia de ajo en tres clones nacionales. En la fase de producción de semilla limpia mediante micropropagación, se estandarizó el establecimiento de meristemos de ajo. La presencia de potyvirus se analizó en 586 plántulas mediante ELISA y en 70 por RT-PCR. Para la RT-PCR se extrajo ARN a partir de microbulbillos y hojas de plántulas, obteniéndose 1.7 a 226 ng/microlitro de ARN y se sintetizó entre 35 a 50 ng de cADN. Los resultados obtenidos mostraron que el protocolo de desinfección produjo una viabilidad del 73.6%. El análisis ELISA presentó un saneamiento del 96.1% de las plántulas a potyvirus, mientras que con RT-PCR se identificó la presencia de LYSV en el 8.6% de las muestras evaluadas. El virus del enanismo amarrillo de la cebolla (OYDV) no fue detectado en ninguna de las muestras. Los resultados muestran que el cultivo in vitro de meristemos de ajo es una excelente alternativa para la producción de semilla, mostrando un 92% de eficiencia. Además, validan el diagnóstico eficiente del potyvirus LYSV en hojas y microbulbillos de ajo.

Garlic (Allium sativum L), reproduces vegetatively using bulbils, condition that favors the spread of diseases, especially bacteria, fungi and viruses, which affect the quality and crop yield. For this reason, the molecular identification by RT-PCR of potyvirus: LYSV and OYDV in the production system of clean seed garlic of three national clones were implemented. In the production phase of clean seed was establishing garlic meristems micropropagation. Potyvirus presence in 586 seedlings was analyzed by ELISA and for RT-PCR in 70. RNA was extracted from leaves and small bulbs, yielding 1.7 to 226 ng/μl, and with this RNA, between 35 to 50 ng of cDNA. The results showed that the disinfection protocol produced a 73.6% viability of plants. ELISA analysis showed 96% sanitation of seedling to potyvirus, whereas, Leek Yellow Strip Virus, LYSV was identified in 8.6% of samples used RT-PCR methodology. Onion yellow dwarf virus (OYDV) was not detected in any sample. The results show that the in vitro culture of meristem of garlic, is an excellent alternative for seed production, showing a 92% efficiency. Moreover, efficient diagnostics of LYSV potyvirus was validated in leaves and small bulbs of garlic.

Generación de anticuerpos policlonales para la detección de la variante genotípica GIII de PVY, en cultivos de tomate de Árbol y papa de Colombia / Generation of policlonal antibodies for detection of the PVY genotypic variant GIII in tamarillo and potato crops from Colombia

El potyvirus PVY es uno de los agentes causales más frecuentemente asociados a problemas virales en cultivos de papa y tomate de árbol en Colombia. Dada la importancia económica de las enfermedades causadas por PVY y a la necesidad de generar material de siembra certificado por su sanidad viral, es fundamental la generación de herramientas de diagnóstico que permitan la detección temprana de este virus. En este trabajo se reporta la obtención de anticuerpos policlonales específicos, útiles para la detección del genotipo III de PVY (GIII), una de las tres variantes que recientemente han sido reportadas en cultivos de papa y tomate de árbol de la región Andina de Colombia. Como antígeno, se utilizó un péptido sintético diseñado a partir de la región variable del extremo N-terminal del gen de la cápside viral. La sensibilidad de los anticuerpos fue evaluada mediante pruebas de ELISA y dot-blot utilizando péptidos sintéticos. Se realizó una prueba piloto para validar el uso de los anticuerpos a partir de plantas sintomáticas y asintomáticas obtenidas de una región donde confluyen cultivos de ambas solanéceas, encontrándose que los anticuerpos generados ofrecen mayores niveles de detección que los anticuerpos comerciales comúnmente utilizados para detectar los serotipos PVY-O,C y PVY-N de este virus.

PVY is one of the potyvirus more frequently associated with viral infections in tomato and tamarillo crops in Colombia. Due to the economic impact of PVY and the need to certify seeds as virus-free it is important to develop diagnostic tools that allow its premature detection. In this work, the obtention of antibodies detecting the genotype III of PVY is reported. This genotype is one of the three PVY variants infecting tamarillo and potato in the Andean region of Colombia. The N-terminal variable region of the coat protein was chosen as antigen for antibody production. The sensibility of these antibodies was tested by ELISA and dot-blot using synthetic peptides. A pilot test was performed on symptomatic and non-symptomatic plants from a mixed orchard of tamarillo and potato. The generated antibodies showed higher detection levels than the commercial antibodies commonly used to detect the PVY-O,C and PVY-N serotypes.

Molecular modeling and conformational analysis of native and refolded viral genome-linked protein of Cardamom mosaic virus.

The viral genome-linked protein (VPg) of Potyviruses is covalently attached to the 5’ end of the genomic RNA. Towards biophysical characterization, the VPg coding region of Cardamom mosaic virus (CdMV) was amplified from the cDNA and expressed in E. coli. Most of the expressed VPg aggregated as inclusion bodies that were solubilized with urea and refolded with L-arginine hydrochloride. The various forms of CdMV VPg (native, denatured and refolded) were purified and the conformational variations between these forms were observed with fluorescence spectroscopy. Native and refolded CdMV VPg showed unordered secondary structure in the circular dichroism (CD) spectrum. The model of CdMV VPg was built based on the crystal structure of phosphotriesterase (from Pseudomonas diminuta), which had the maximum sequence homology with VPg to identify the arrangement of conserved amino acids in the protein to study the functional diversity of VPg. This is the first report on the VPg of CdMV, which is classified as a new member of the Macluravirus genus of the Potyviridae family.

OBTENCIÓN DE ANTICUERPOS ESPECÍFICOS PARA LA DETECCIÓN DEL Tamarillo leaf malformation virus (TALMV) EN TOMATE DE ÁRBOL / Specific Antibodies to Detect Tamarillo leaf malformation virus (TaLMV) in Tamarillo

En Colombia el rendimiento del cultivo de tomate de árbol se ha visto seriamente afectado por la expansión de una enfermedad conocida como virosis de tomate de árbol. Esta patología se registró inicialmente en 1991 en el norte de Antioquia y su expansión ha alcanzado todas las regiones cultivadoras de este frutal en el país. Trabajos recientes han detectado la presencia de por lo menos dos especies del género Potyvirus (Potyviridae) asociadas a esta enfermedad en los cultivos de tomate de árbol de Antioquia: Potato virus Y (PVY) y Tamarillo leaf malformation virus (TaLMV, especie propuesta). Con el fin de reducir la diseminación de estos patógenos virales en el país, es necesario contar con herramientas de diagnóstico que permitan la certificación del material de siembra y la detección temprana en plantas asintomáticas. En este trabajo se obtuvieron anticuerpos policlonales específicos para la detección del virus TaLMV utilizando una región antigénica de 15 residuos de la cápside viral. La sensibilidad y especificidad de los anticuerpos anti-TaLMV fue evaluada mediante pruebas de ELISA y dot-blot utilizando proteína recombinante y péptidos sintéticos como controles. La utilidad de estos anticuerpos fue validada a partir de una prueba piloto de detección de TaLMV en muestras de plantas de tomate de árbol con y sin síntomas de virosis obtenidas en el oriente antioqueño. Los resultados serológicos fueron comparados con los niveles de detección que ofrece la técnica de RT-PCR con cebadores específicos para la cápside viral de TaLMV.

In Colombia, yields of tamarillo are seriously affected by a complex viral disease known as virosis. This pathology was first reported in 1991 in the north of Antioquia and currently affects all tamarillo growing regions in the country. Recent works have demonstrated the association of two potyviruses (potyviridae) with this disease: Potato virus Y (PVY) and Tamarillo leaf malformation virus (TaLMV, proposed species). Specific diagnostic tools are required for early asymptomatic detection of these viruses and tamarillo certification programs. In this study, we report the obtention of TaLMV specific antibodies using a 15 residues peptide mimicking the N-terminal coat protein. Specificity and sensitivity of the anti-TaLMV antibodies was determined by ELISA and dot-blot using recombinant protein and synthetic peptides as controls. The usefulness of these antibodies was validated from a preliminary trial of TaLMV detection in plant samples obtained from tamarillo crops in eastern Antioquia and results were compared with a TaMLV specific coat RT-PCR detection protocol.

Combining ability of summer-squash lines with different degrees of parthenocarpy and PRSV-W resistance

The aim was to assess heterosis in a set of 16 summer-squash hybrids, and evaluate the combining capacity of the respective parental lines, which differed as to the degree of parthenocarpy and resistance to PRSV-W (Papaya Ringspot Virus-Watermelon strain). The hybrids were obtained using a partial diallel cross design (4 x 4). The lines of parental group I were 1 = ABX-037G-77-03-05-01-01-bulk, 2 = ABX-037G-77-03-05-03-10-bulk, 3 = ABX-037G77-03-05-01-04-bulk and 4 = ABX-037G-77-03-05-05-01-bulk, and of group II, 1' = ABX-037G-77-03-05-04-08-bulk, 2' = ABX-037G-77-03-05-02-11-bulk, 3' = Clarice and 4' = Caserta. The 16 hybrids and eight parental lines were evaluated for PRSV-W resistance, parthenocarpic expression and yield in randomized complete-block designs, with three replications. Parthenocarpy and the resistance to PRSV-W were rated by means of a scale from 1 to 5, where 1 = non-parthenocarpic or high resistance to PRSV-W, and 5 = parthenocarpic or high susceptibility to PRSV-W. Both additive and non-additive gene effects were important in the expression of parthenocarpy and resistance to PRSV-W. Whereas estimates of heterosis in parthenocarpy usually tended towards a higher degree, resistance to PRSV-W was towards higher susceptibility. At least one F1 hybrid was identified with a satisfactory degree of parthenocarpy, resistance to PRSV-W and high fruit-yield.

Caracterizaciónsserológica y molecular de potyvrus asociados a la virosis del tomate de árbol en antioquia (Colomba)) / Serological and Molecular Characterization of Potyvirus Associated to the Viral Disease of Tamarillo in Antioquia (Colombia)

El tomate de árbol (Solanum betaceum) es una fruta andina altamente nutritiva, con propiedades organolépticas únicas para el procesamiento industrial y el mercado internacional. En Antioquia, Colombia, este cultivo presenta diferentes problemas fitosanitarios, siendo especialmente limitante la Virosis, causada por un complejo viral del que hacen parte entre otras, especies del género Potyvirus. En este trabajo se evaluaron mediante pruebas de ELISA los niveles de incidencia de este grupo viral en cultivos de siete zonas del departamento de Antioquia y se determinó la identidad taxonómica de dos de los potyvirus asociados al cultivo. Las pruebas serológicas muestran la presencia de potyvirus en seis de las siete zonas evaluadas, alcanzando niveles superiores al 80% de incidencia, siendo la excepción los cultivos del municipio de Jardín (8%). Pruebas serológicas con anticuerpos específicos para PVY, identificaron a este virus como uno de los presentes en algunas de las muestras sintomáticas colectadas; mientras que análisis de secuencias de amplicones obtenidos mediante RT-PCR, detectaron un nuevo potyvirus, para el que se propone el nombre Tamarillo Leaf Malformation Virus (TaLMV), aunque es necesario completar la secuencia de su genoma para confirmar la validez de esta hipótesis taxonómica. Esta investigación representa un avance importante en el conocimiento que se tiene en Colombia sobre los agentes causales virales del tomate de árbol. Sin embargo, es necesario profundizar en aspectos como los mecanismos de transmisión de estos virus y los efectos individuales y de su interacción sobre las variedades de este cultivo en el país.

Tomato tree (Solanum betaceum) is an andean fruit which, due to its high nutricious value and unique organoleptic properties, has very good potential for industrial processing and international marketing. In Antioquia, Colombia, this crop faces several phytosanitary problems, of which viral infections by species of the Potyvirus genus are the most limiting. In this work, potyvirus incidence levels was evaluated in seven regions of the Antioquia province using the ELISA assay. The taxomical identity of two potyvirus associated with this crop was also determined. Serological tests demonstrate the overall presence of potyvirus in six regions, with incidence levels above 80%. The only exception was the municipality of Jardin with an incidence of only 8%. Serological test specific to PVY virus, revealed its presence in many of the infected plants. DNA sequencing of RTPCR amplicons also showed the presence of a new potyvirus for which we propose the name Tamarillo Leaf Malformation Virus (TaLMV). However, to corroborate this taxonomical hypothesis it is necessary to complete the genome sequence of TaLMV. This research represents an important advance in the knowledge of viruses infecting tomato tree. However, future investigations are required to deepen further into the individual effects of each virus as well as the transmission mechanisms and interactions with different varieties of tomato tree.

Seleção de linhagens de melancia resistentes ao Watermelon mosaic virus e ao Papaya ringspot virus / Selection of resistant watermelon lines to Watermelon mosaic virus and Papaya ringspot virus

Foram avaliadas 20 linhagens de melancia, provenientes do cruzamento da cultivar comercial suscetível Crimson Sweet e da introdução PI 595201 resistente ao Watermelon mosaic virus (WMV) e Papaya ringspot virus (PRSV-W). As linhagens, e os parentais foram inoculados com o WMV ou com o PRSV-W em casa-de-vegetação distintas. Aos 35 e 49 dias após a primeira inoculação (DAI), as plantas foram avaliadas por meio de uma escala de notas, em que 1 (ausência de sintomas) a 5 (intenso mosaico e deformações foliares). Pelos resultados infere-se que, aos 35 DAI, as linhagens 1, 2 e 20 apresentaram resistência tanto para o WMV como para o PRSV-W, com médias de 1,95, 1,80 e 2,25 para o WMV, e de 2,50, 2,30 e 2,50 para o PRSV-W, respectivamente. As linhagens 5, 7 e 13 foram resistentes somente ao WMV e as plantas das linhagens 3, 10 e 18 para o PRSV-W. A reação das linhagens permaneceu em geral pouco alterada aos 49 DAI. A existência de linhagens resistentes somente ao WMV e somente ao PRSV-W, ao lado de linhagens resistentes a ambos os vírus, é indicativo de que as resistências ao WMV e ao PRSV-W não são controladas pelos mesmos genes.

Twenty advanced watermelon breeding lines, derived from the cross between cv. Crimson Sweet (susceptible) and PI 595201 (resistant to WMV and PRSV-W), were screened for resistance to both potyviruses. The twenty lines, among with Crimson Sweet and PI 595201, were inoculated with either WMV or PRSV-W, in two different greenhouse trials. Plants were evaluated for symptoms 35 and 49 days after the first inoculation (DAI), using a scale from 1 (no symptoms) to 5 (severe mosaic and foliar distortion). Evaluations at 35 DAI indicated that lines 1, 2 and 20 had good levels of resistance to both WMV and PRSV-W, with ratings of 1,95, 1,80 and 2,25 for WMV, and of 2,50, 2,30 and 2,50 for PRSV-W, respectively. Lines 5, 7 and 13 were resistant to WMV only, whereas lines 3, 10 and 18 were resistant to PRSV-W only. The reaction of the lines 49 DAI remained essentially unchanged. The existence of lines with resistance to WMV only and to PRSV-W only, along with lines with resistance to both viruses, indicates that resistance to WMV and PRSV-W are under control of different genes.