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Artículos de revistas sobre el tema "Sugarcane yellow leaf virus"

Autor: Grafiati

Publicado: 4 de junio de 2021

Última modificación: 12 de febrero de 2022

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1

Parmessur, Y., S. Aljanabi, S. Saumtally, and A. Dookun-Saumtally. "Sugarcane yellow leaf virus and sugarcane yellows phytoplasma: elimination by tissue culture." Plant Pathology 51, no. 5 (2002): 561–66. http://dx.doi.org/10.1046/j.1365-3059.2002.00747.x.

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2

Schenck, S., and A. T. Lehrer. "Factors Affecting the Transmission and Spread of Sugarcane yellow leaf virus." Plant Disease 84, no. 10 (2000): 1085–88. http://dx.doi.org/10.1094/pdis.2000.84.10.1085.

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Sugarcane, Saccharum spp. hybrid, is widely infected in the United States and many other countries with a yellowing and stunting disease called sugarcane yellow leaf syndrome. The causal agent, Sugarcane yellow leaf virus (ScYLV), is a Polerovirus of the Luteoviridae family. In this study, it was transmitted by the sugarcane aphid, Melanaphis sacchari, and also by the corn leaf aphid, Rhopalosiphum maidis, and the rice root aphid, R. rufiabdominalis. Two other aphids that infest sugarcane in Hawaii did not transmit the virus. Some Hawaiian sugarcane cultivars are susceptible to ScYLV, while ot

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3

Rao, G. P., R. K. Gaur, Maneesha Singh, et al. "Occurrence of sugarcane yellow leaf virus in india." Sugar Tech 2, no. 4 (2000): 37–38. http://dx.doi.org/10.1007/bf02995586.

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4

Ahmad, Youssef Abu, Monique Royer, Jean-Henrich Daugrois, et al. "Geographical Distribution of Four Sugarcane yellow leaf virus Genotypes." Plant Disease 90, no. 9 (2006): 1156–60. http://dx.doi.org/10.1094/pd-90-1156.

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Specific primer pairs were designed to distinguish four genotypes (BRA for Brazil, CUB for Cuba, PER for Peru, and REU for Réunion Island) of Sugarcane yellow leaf virus (SCYLV) by reverse transcription-polymerase chain reaction (RT-PCR). A unique genome fragment was amplified from each genotype, with the exception of genotypes BRA and PER that are phylogenetically relatively close and were designated genotype BRA-PER. These RT-PCR primers were then used to identify the SCYLV genotype(s) present in 18 different sugarcane growing locations in the world, and 245 leaf samples infected by the viru

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5

Viswanathan, R., and M. Balamuralikrishnan. "Detection of sugarcane yellow leaf virus, the causal agent of yellow leaf syndrome in sugarcane by DAS-ELISA." Archives Of Phytopathology And Plant Protection 37, no. 3 (2004): 169–76. http://dx.doi.org/10.1080/03235400410001730676.

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6

Nithya, Kadirvel, Balasubramaniam Parameswari, and Rasappa Viswanathan. "Mixed Infection of Sugarcane Yellow Leaf Virus and Grassy Shoot Phytoplasma in Yellow Leaf Affected Indian Sugarcane Cultivars." Plant Pathology Journal 36, no. 4 (2020): 364–77. http://dx.doi.org/10.5423/ppj.oa.06.2020.0092.

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7

Boukari, Wardatou, Claudia Kaye, Chunyan Wei, et al. "Field Infection of Virus-Free Sugarcane by Sugarcane Yellow Leaf Virus and Effect of Yellow Leaf on Sugarcane Grown on Organic and on Mineral Soils in Florida." Plant Disease 103, no. 9 (2019): 2367–73. http://dx.doi.org/10.1094/pdis-01-19-0199-re.

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Sugarcane yellow leaf virus (SCYLV), the causal agent of yellow leaf, is widespread in Florida. Two field trials were set up, one on organic soil and one on mineral soil, to investigate the rate and timing of sugarcane infection by SCYLV under field conditions and the effect of the virus on yield. Each trial consisted of plots planted with healthy or SCYLV-infected seed cane of two commercial cultivars. Virus prevalence varied from 83 to 100% in plots planted with infected seed cane regardless of cultivar, location, and crop season. On organic soil, plants of virus-free plots became progressiv

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8

Bertani, R. P., M. F. Perera, M. E. Arias, et al. "A Study of the Sugarcane Yellow Leaf Disease in Argentina." Plant Disease 98, no. 8 (2014): 1036–42. http://dx.doi.org/10.1094/pdis-12-13-1251-re.

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Yellow leaf disease, caused by Sugarcane yellow leaf virus (SCYLV), is widespread around the world but very little information is available on this viral disease in Argentina. Therefore, the aims of the study were to assess the presence of SCYLV, analyze its distribution in the main sugarcane production areas of Argentina, characterize the virus, and determine histological alterations caused by its presence. For this purpose, 148 sugarcane samples with and without symptoms were collected in 2011 and 2012 from the province of Tucumán. One additional sample was collected in Salta, a different ge

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9

Alegría, O. M., M. Chatenet, J. C. Girard, S. A. Saldarriaga, A. Nuget, and P. Rott. "First Report of Sugarcane yellow leaf virus in Peru." Plant Disease 84, no. 12 (2000): 1342. http://dx.doi.org/10.1094/pdis.2000.84.12.1342c.

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Two sugarcane cultivars, H 50-7209 and H 32-8560, have exhibited unusual, severe leaf yellowing for more than 18 years at Agro Industrial Paramonga S.A. (AIPSA) in Peru. In 1999, these varieties occupied about 4,600 ha (74% of the cultivated area), and almost all fields showed these symptoms. Symptoms first appear on the upper third of the leaf blades, which turns light green to light yellow in young canes up to 6 to 8 months of age. Between 10 and 16 months of age, the symptoms are visible on the spindle and first to third visible dewlap leaves. Tips and margins of older leaves become necroti

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10

Arocha, Y., L. Gonzalez, E. L. Peralta, and P. Jones. "First Report of Virus and Phytoplasma Pathogens Associated with Yellow Leaf Syndrome of Sugarcane in Cuba." Plant Disease 83, no. 12 (1999): 1177. http://dx.doi.org/10.1094/pdis.1999.83.12.1177b.

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Yellow leaf syndrome (YLS) has been seen recently in sugarcane (Saccharum sp.) in Cuba. The primary symptom is a yellow discoloration of the midrib that may spread from the midrib to the lamina in cane 6 months and older. In certain cultivars, such as CP 5243, EPC 17-395, and F31-156, a reddish coloration has been observed. In severe cases, plants are stunted and can be pulled easily. YLS was first reported from Hawaii, followed by Brazil, Florida, and Australia, where it is associated with a luteovirus: sugarcane yellow leaf virus (ScYLV). However, in South Africa, YLS is associated with a ph

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11

Viswanathan, R., R. Karuppaiah, P. Malathi, V. Ganesh Kumar, and C. Chinnaraja. "Diagnosis of Sugarcane yellow leaf virus in asymptomatic sugarcane by RT-PCR." Sugar Tech 11, no. 4 (2009): 368–72. http://dx.doi.org/10.1007/s12355-009-0063-z.

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12

Debibakas, S., S. Rocher, O. Garsmeur, et al. "Prospecting sugarcane resistance to Sugarcane yellow leaf virus by genome-wide association." Theoretical and Applied Genetics 127, no. 8 (2014): 1719–32. http://dx.doi.org/10.1007/s00122-014-2334-7.

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13

Chinnaraja, C., and R. Viswanathan. "Variability in yellow leaf symptom expression caused by the Sugarcane yellow leaf virus and its seasonal influence in sugarcane." Phytoparasitica 43, no. 3 (2015): 339–53. http://dx.doi.org/10.1007/s12600-015-0468-z.

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14

McAllister, C. D., J. W. Hoy, and T. E. Reagan. "Temporal Increase and Spatial Distribution of Sugarcane Yellow Leaf and Infestations of the Aphid Vector, Melanaphis sacchari." Plant Disease 92, no. 4 (2008): 607–15. http://dx.doi.org/10.1094/pdis-92-4-0607.

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Yellow leaf, caused by Sugarcane yellow leaf virus (ScYLV), is a potentially important disease of sugarcane first found in Louisiana during 1996. A survey during 2002 determined that ScYLV infection was present in all sugarcane-production areas of Louisiana. Virus was detected in 48% of 42 fields, and incidence averaged 15% in these fields. Disease progress curves determined in four fields during two growing seasons indicated that the greatest temporal increase of virus infection occurred during late spring and early summer and coincided with the initial infestation and increase of the virus v

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15

Avila, R., M. C. Arrieta, W. Villalobos, et al. "First Report of Sugarcane yellow leaf virus (ScYLV) in Costa Rica." Plant Disease 85, no. 8 (2001): 919. http://dx.doi.org/10.1094/pdis.2001.85.8.919c.

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In Costa Rica, sugarcane plants with symptoms similar to those described for yellow leaf syndrome (YLS) (1,2) were first observed in 1994 in research plots of imported material in the midland areas of San Carlos and Turrialba. Recently, the same symptoms have been observed in commercial plantations in Turrialba. Symptomatic plants were characterized by yellowing of the leaves and central veins, the yellowing being more intense near the leaf tips. In severe cases, veins became reddish, and necrosis developed along the leaf edges, beginning at the leaf tip and extending to the base of the leaf.

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16

ElSayed, Abdelaleim I., Ziad Soufi, Khalid M. Wahdan, and Ewald Komor. "Detection and Characterization of Phytoplasma and Sugarcane Yellow Leaf Virus Associated with Leaf Yellowing of Sugarcane." Journal of Phytopathology 164, no. 4 (2015): 217–25. http://dx.doi.org/10.1111/jph.12449.

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17

Filloux, D., E. Fernandez, J. C. Comstock, D. Mollov, P. Roumagnac, and P. Rott. "Viral Metagenomic-Based Screening of Sugarcane from Florida Reveals Occurrence of Six Sugarcane-Infecting Viruses and High Prevalence of Sugarcane yellow leaf virus." Plant Disease 102, no. 11 (2018): 2317–23. http://dx.doi.org/10.1094/pdis-04-18-0581-re.

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A viral metagenomics study of the sugarcane virome in Florida was carried out in 2013 to 2014 to analyze occurrence of known and potentially new viruses. In total, 214 sugarcane leaf samples were collected from different commercial sugarcane (Saccharum interspecific hybrids) fields in Florida and from other Saccharum and related species taken from two local germplasm collections. Virion-associated nucleic acids (VANA) metagenomics was used for detection and identification of viruses present within the collected leaf samples. VANA sequence reads were obtained for 204 leaf samples and all four p

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18

Lehrer, A. T., K. K. Wu, and E. Komor. "Impact of Sugarcane yellow leaf virus on growth and sugar yield of sugarcane." Journal of General Plant Pathology 75, no. 4 (2009): 288–96. http://dx.doi.org/10.1007/s10327-009-0172-2.

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19

Marwal, Avinash, and R. K. Gaur. "Phylogenetic and Recombination Analyses of Sugarcane yellow leaf virus isolates." Sugar Tech 22, no. 3 (2019): 540–45. http://dx.doi.org/10.1007/s12355-019-00783-0.

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20

Daugrois, J. H., I. Jean-Baptiste, B. E. L. Lockhart, M. S. Irey, M. Chatenet, and P. Rott. "First Report of Sugarcane Yellow Leaf Virus in the French West Indies." Plant Disease 83, no. 6 (1999): 588. http://dx.doi.org/10.1094/pdis.1999.83.6.588c.

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Unusually severe leaf yellowing symptoms, similar to those described for yellow leaf syndrome (1), have been observed in several sugarcane clones in Guadeloupe since 1994, and since 1997 in Martinique. Leaf samples exhibiting various types of yellowing were taken from five different sugarcane clones, and analyzed by immunosorbent electron microscopy. Spherical particles, 24 to 28 nm in diameter and characteristic of luteoviruses, were found in two of five samples. The two infected samples showed yellowing on the underside of the midrib and one had a pinkish coloration on the upper side. The pr

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21

Ahmad, Youssef Abu, Laurent Costet, Jean-Heinrich Daugrois, et al. "Variation in Infection Capacity and in Virulence Exists Between Genotypes of Sugarcane yellow leaf virus." Plant Disease 91, no. 3 (2007): 253–59. http://dx.doi.org/10.1094/pdis-91-3-0253.

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Two experiments, one in Guadeloupe and one in Réunion Island, were performed to transmit different genotypes of Sugarcane yellow leaf virus (SCYLV) to eight sugarcane cultivars differing in resistance to infection by the virus and to yellow leaf. Transmission was attempted from SCYLV-infected sugarcane plants or leaves to healthy tissue-cultured plantlets grown in vitro and with the aphid vector Melanaphis sacchari. After inoculation and elimination of insects with an insecticide, plantlets were transferred to Montpellier, France and grown in a greenhouse. Plants were tested for presence of SC

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22

Scagliusi, Sandra Mansur, and B. E. L. Lockhart. "Transmission, Characterization, and Serology of a Luteovirus Associated with Yellow Leaf Syndrome of Sugarcane." Phytopathology® 90, no. 2 (2000): 120–24. http://dx.doi.org/10.1094/phyto.2000.90.2.120.

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A previously uncharacterized luteovirus was associated with one form of yellow leaf syndrome (YLS), a widespread disease of sugarcane (Saccharum sp.). The virus was named Sugarcane yellow leaf luteovirus (ScYLV), and was identified in major sugarcane-producing areas of the world. Typical disease symptoms were reproduced when ScYLV was transmitted by Melanaphis sacchari or Rhopalosiphum maidis from infected to healthy sugarcane, suggesting that this virus may be the causal agent of one form of YLS. The only known hosts of ScYLV are Saccharum and Erianthus spp. Virions of ScYLV were 24 to 29 nm

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23

Lehrer, A. T., S. Schenck, S. L. Yan, and E. Komor. "Movement of aphid-transmitted Sugarcane yellow leaf virus (ScYLV) within and between sugarcane plants." Plant Pathology 56, no. 4 (2007): 711–17. http://dx.doi.org/10.1111/j.1365-3059.2007.01557.x.

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24

Singh, Deepti, Govind Pratap Rao, S. K. Snehi, S. K. Raj, R. Karuppaiah, and R. Viswanathan. "Molecular detection and identification of thirteen isolates of Sugarcane yellow leaf virus associated with sugarcane yellow leaf disease in nine sugarcane growing states of India." Australasian Plant Pathology 40, no. 5 (2011): 522–28. http://dx.doi.org/10.1007/s13313-011-0061-y.

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25

Bouallegue, M., M. Mezghani-Khemakhem, H. Makni, and M. Makni. "First Report of Sugarcane yellow leaf virus Infecting Barley in Tunisia." Plant Disease 98, no. 7 (2014): 1016. http://dx.doi.org/10.1094/pdis-12-13-1269-pdn.

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Sugarcane yellow leaf virus (ScYLV) causes severe leaf symptoms in sugarcane (Saccharum spp.). It is a single-stranded RNA virus assigned to the genus Polerovirus, family Luteoviridae (1). ScYLV is transmitted by two aphid species, Melanaphis sacchari and Rhopalosiphum maidis. Although barley (Hordeum vulgare), oats (Avena sativa), and wheat (Triticum spp.) are susceptible to ScYLV when experimentally inoculated (3), this virus, related serologically to Barley yellow dwarf virus (BYDV)-RPV (4), has never been detected naturally in these cereals. In this study, 240 barley leaves were randomly c

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26

Chatenet, M., C. Delage, M. Ripolles, M. Irey, B. E. L. Lockhart, and P. Rott. "Detection of Sugarcane yellow leaf virus in Quarantine and Production of Virus-free Sugarcane by Apical Meristem Culture." Plant Disease 85, no. 11 (2001): 1177–80. http://dx.doi.org/10.1094/pdis.2001.85.11.1177.

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Sugarcane yellow leaf virus (SCYLV) was detected for the first time in 1996 in the Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) sugarcane quarantine at Montpellier by reverse transcription-polymerase chain reaction (RT-PCR) in varieties from Brazil, Florida, Mauritius, and Réunion. Between 1997 and 2000, the virus was found by RT-PCR and/or tissue-blot immunoassay (TBIA) in additional varieties from Barbados, Cuba, Guadeloupe, Indonesia, Malaysia, Philippines, Puerto Rico, and Taiwan, suggesting a worldwide distribution of the pathogen. An excelle

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27

Vega, Jorge, Sandra M. M. Scagliusi, and Eugênio C. Ulian. "Sugarcane Yellow Leaf Disease in Brazil: Evidence of Association with a Luteovirus." Plant Disease 81, no. 1 (1997): 21–26. http://dx.doi.org/10.1094/pdis.1997.81.1.21.

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Evidence of the viral etiology of sugarcane yellow leaf disease (SCYLD), occurring in southeast Brazil, was obtained by light and electron microscopy combined with serology. Light microscopy using epifluorescence illumination showed an abnormal yellow-green fluorescing material in the phloem of SCYLD-affected plants that was rarely observed in control plants. Immunolocalization in tissue-printed (or -blotted) nitrocellulose membranes, using barley yellow dwarf virus (BYDV) serotype PAV antiserum, showed a weak but clearly positive reaction in the phloem. Isometric viruslike particles of 24 to

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28

Comstock, J. C., M. Pena, J. Vega, A. Fors, and B. E. L. Lockhart. "Report of Sugarcane yellow leaf virus in Ecuador, Guatemala, and Nicaragua." Plant Disease 86, no. 1 (2002): 74. http://dx.doi.org/10.1094/pdis.2002.86.1.74d.

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In 1998, sugarcane plants with symptoms similar to yellow leaf syndrome were observed in Ecuador, Guatemala, and Nicaragua. These plants showed yellowing of the central portion of the third to sixth leaves on the abaxial surface from the youngest expanding spindle leaf. Intense yellowing and necrosis of the leaf tip and the central portion of the leaf blade near the midrib occurred in severe cases. A tissue blot immunoassay was used to detect Sugarcane yellow leaf virus (SCYLV) in the midrib of the top visible dewlap leaf (2) using an antiserum specific to a Florida isolate of SCYLV (1). Since

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29

Zhu, Yun J., Heather McCafferty, Greg Osterman, et al. "Genetic transformation with untranslatable coat protein gene of sugarcane yellow leaf virus reduces virus titers in sugarcane." Transgenic Research 20, no. 3 (2010): 503–12. http://dx.doi.org/10.1007/s11248-010-9432-3.

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30

ElSayed, Abdelaleim Ismail, Ewald Komor, Moncef Boulila, Rasappa Viswanathan, and Dennis C. Odero. "Biology and management of sugarcane yellow leaf virus: an historical overview." Archives of Virology 160, no. 12 (2015): 2921–34. http://dx.doi.org/10.1007/s00705-015-2618-5.

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31

Gonçalves, Marcos C., Jorge Vega, Jurandi G. Oliveira, and Mara M. A. Gomes. "Sugarcane yellow leaf virus infection leads to alterations in photosynthetic efficiency and carbohydrate accumulation in sugarcane leaves." Fitopatologia Brasileira 30, no. 1 (2005): 10–16. http://dx.doi.org/10.1590/s0100-41582005000100002.

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Infection by Sugarcane yellow leaf virus (ScYLV) causes severe leaf symptoms in sugarcane (Saccharum spp.) hybrids, which indicate alterations in its photosynthetic apparatus. To gain an overview of the physiological status of infected plants, we evaluated chlorophyll a fluorescence and gas exchange assays, correlating the results with leaf metabolic surveys, i.e., photosynthetic pigments and carbohydrate contents. When compared to healthy plants, infected plants showed a reduction in potential quantum efficiency for photochemistry of photosystem (PSII) and alterations in the filling up of the

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32

Lehrer, Axel, Shih-Long Yan, Blanca Fontaniella, Abdelaleim ElSayed, and Ewald Komor. "Carbohydrate composition of sugarcane cultivars that are resistant or susceptible to Sugarcane yellow leaf virus." Journal of General Plant Pathology 76, no. 1 (2009): 62–68. http://dx.doi.org/10.1007/s10327-009-0210-0.

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33

Gilbert, R. A., N. C. Glynn, J. C. Comstock, and M. J. Davis. "Agronomic performance and genetic characterization of sugarcane transformed for resistance to sugarcane yellow leaf virus." Field Crops Research 111, no. 1-2 (2009): 39–46. http://dx.doi.org/10.1016/j.fcr.2008.10.009.

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34

Chinnaraja, C., and R. Viswanathan. "Quantification of sugarcane yellow leaf virus in sugarcane following transmission through aphid vector, Melanaphis sacchari." VirusDisease 26, no. 4 (2015): 237–42. http://dx.doi.org/10.1007/s13337-015-0267-7.

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35

Madugula, Suresh, and Uma Devi Gali. "Virus indexing for Sugarcane Yellow Leaf Virus (SCYLV) in field varieties and in vitro regenerated plantlets of sugarcane." Australasian Plant Pathology 46, no. 5 (2017): 433–39. http://dx.doi.org/10.1007/s13313-017-0505-0.

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36

Madugula, Suresh, Umadevi Gali, Raja Kumar Nalabolu, and Tirupathi Merugu. "Current Status of Yellow Leaf Disease (YLD) of Sugarcane Caused by Sugarcane Yellow Leaf Virus (ScYLV) in the states of Andhra Pradesh and Telangana." International Journal of Bio-resource and Stress Management 11, no. 1 (2020): 073–81. http://dx.doi.org/10.23910/ijbsm/2020.11.1.2060.

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37

ElSayed, A. I., M. Boulila, D. C. Odero, and E. Komor. "Phylogenetic and recombination analysis of sorghum isolates of Sugarcane yellow leaf virus." Plant Pathology 67, no. 1 (2017): 221–32. http://dx.doi.org/10.1111/ppa.12708.

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38

Wang, M. Q., D. L. Xu, R. Li, and G. H. Zhou. "Genotype identification and genetic diversity of Sugarcane yellow leaf virus in China." Plant Pathology 61, no. 5 (2012): 986–93. http://dx.doi.org/10.1111/j.1365-3059.2012.02591.x.

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39

Vaillant, Jean, Gavino Puggioni, Lance A. Waller, and Jean Daugrois. "A spatio-temporal analysis of the spread of sugarcane yellow leaf virus." Journal of Time Series Analysis 32, no. 4 (2011): 396–406. http://dx.doi.org/10.1111/j.1467-9892.2011.00730.x.

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40

Yang, Xiping, Sushma Sood, Ziliang Luo, James Todd, and Jianping Wang. "Genome-Wide Association Studies Identified Resistance Loci to Orange Rust and Yellow Leaf Virus Diseases in Sugarcane (Saccharum spp.)." Phytopathology® 109, no. 4 (2019): 623–31. http://dx.doi.org/10.1094/phyto-08-18-0282-r.

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Sugarcane (Saccharum spp.) supplies globally ∼80% of table sugar and 60% of bioethanol. Sugarcane orange rust and Sugarcane yellow leaf virus (SCYLV) are major sugarcane diseases, causing up to 50 and 40% yield losses, respectively. Sugarcane cultivars resistant to these diseases are needed to sustain sugarcane production in several regions. Dissecting DNA sequence variants controlling disease resistance provides a valuable tool for fulfilling a breeding strategy to develop resistant cultivars. In this study, we evaluated disease reactions to orange rust and SCYLV of a sugarcane diversity pane

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41

Viswanathan, R., M. Balamuralikrishnan, and R. Karuppaiah. "Identification of three genotypes of sugarcane yellow leaf virus causing yellow leaf disease from India and their molecular characterization." Virus Genes 37, no. 3 (2008): 368–79. http://dx.doi.org/10.1007/s11262-008-0277-2.

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42

Rassaby, L., J. C. Girard, O. Lemaire, et al. "Spread of Sugarcane yellow leaf virus in sugarcane plants and fields on the island of Reunion." Plant Pathology 53, no. 1 (2004): 117–25. http://dx.doi.org/10.1111/j.1365-3059.2004.00950.x.

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43

Lehrer, Axel T., and Ewald Komor. "Carbon dioxide assimilation by virus-free sugarcane plants and by plants which were infected by Sugarcane Yellow Leaf Virus." Physiological and Molecular Plant Pathology 73, no. 6 (2008): 147–53. http://dx.doi.org/10.1016/j.pmpp.2009.05.002.

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44

Kumar, Jitendra, Sachin Kumar, and Shahryar F. Kianian. "The Wheat Dwarf India Virus-Betasatellite Complex Has a Wider Host Range Than Previously Reported." Plant Health Progress 21, no. 2 (2020): 119–22. http://dx.doi.org/10.1094/php-10-19-0080-rs.

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Wheat dwarf India virus (WDIV) and associated alphasatellite and betasatellite have been documented to infect wheat (Triticum aestivum). Here, we report, for the first time, presence of WDIV and the associated Ageratum yellow leaf curl betasatellite (AYLCB) in barley (Hordeum vulgare) and sugarcane (Saccharum officinarum) in addition to wheat. However, surprisingly, the previously reported alphasatellites were not detected in the WDIV-positive barley, sugarcane, and wheat samples. The virus and betasatellite detected from barley, sugarcane, and wheat showed high levels of sequence identity to

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45

Perales-Rosas, Daniel, Ricardo Hernández-Pérez, Dagoberto Guillén-Sánchez, et al. "Detection of sugarcane yellow leaf virus and sugarcane mosaic virus in sorghum (Sorghum bicolor (L.) Moench) in the state of Morelos, México." Scientia Agropecuaria 9, no. 3 (2018): 423–27. http://dx.doi.org/10.17268/sci.agropecu.2018.03.14.

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46

ElSayed, Abdelaleim Ismail, Mohamed Fawzy Ramadan, and Ewald Komor. "Expression of sucrose transporter (ShSUT1) in a Hawaiian sugarcane cultivar infected with Sugarcane yellow leaf virus (SCYLV)." Physiological and Molecular Plant Pathology 75, no. 1-2 (2010): 56–63. http://dx.doi.org/10.1016/j.pmpp.2010.08.006.

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Korimbocus, J., S. Preston, C. Danks, I. Barker, D. Coates, and N. Boonham. "Production of Monoclonal Antibodies to Sugarcane Yellow Leaf Virus Using Recombinant Readthrough Protein." Journal of Phytopathology 150, no. 8-9 (2002): 488–94. http://dx.doi.org/10.1046/j.1439-0434.2002.00791.x.

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Gao, San-Ji, Yi-Hua Lin, Yong-Bao Pan, et al. "Molecular characterization and phylogenetic analysis of Sugarcane yellow leaf virus isolates from China." Virus Genes 45, no. 2 (2012): 340–49. http://dx.doi.org/10.1007/s11262-012-0774-1.

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49

Abu Ahmad, Y., L. Rassaby, M. Royer, et al. "Yellow leaf of sugarcane is caused by at least three different genotypes of sugarcane yellow leaf virus, one of which predominates on the Island of Réunion." Archives of Virology 151, no. 7 (2006): 1355–71. http://dx.doi.org/10.1007/s00705-005-0712-9.

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50

Amata, Ruth L., Emmanuel Fernandez, Denis Filloux, Darren P. Martin, Philippe Rott, and Philippe Roumagnac. "Prevalence of Sugarcane yellow leaf virus in Sugarcane-Producing Regions in Kenya Revealed by Reverse-Transcription Loop-Mediated Isothermal Amplification Method." Plant Disease 100, no. 2 (2016): 260–68. http://dx.doi.org/10.1094/pdis-05-15-0602-re.

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Resumen

Yellow leaf (YL) is a disease of sugarcane that is currently widespread throughout most American and Asian sugarcane-producing countries. However, its actual distribution in Africa remains largely unknown. A reverse-transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed to facilitate and improve the detection of Sugarcane yellow leaf virus (SCYLV), the causal agent of YL. The RT-LAMP assay was found to be comparable with or superior to conventional RT-polymerase chain reaction (PCR) for the detection of SCYLV genotypes CUB and BRA in infected sugarcane ‘C132-81’ and

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