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Prevalence of Sugarcane yellow leaf virus in Sugarcane-Producing Regions in Kenya Revealed by Reverse-Transcription Loop-Mediated Isothermal Amplification Method

Authors :
Denis Filloux
Philippe Roumagnac
Philippe Rott
Emmanuel Fernandez
Ruth Lodenyi Amata
Darren P. Martin
Kenya Agricultural & Livestock Research Organization (KALRO)
Biologie et Génétique des Interactions Plante-Parasite (UMR BGPI)
Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA)-Centre international d'études supérieures en sciences agronomiques (Montpellier SupAgro)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro)
Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)
Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)
University of Cape Town
Agropolis Fondation : 1101-004
African Women in Agricultural Research and Development (AWARD)
Source :
Plant Disease, Plant Disease, American Phytopathological Society, 2016, 100 (2), pp.260-268. ⟨10.1094/pdis-05-15-0602-re⟩
Publication Year :
2016
Publisher :
Scientific Societies, 2016.

Abstract

BGPI : équipe 7; International audience; 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 'SP71-6163', respectively. Additionally, 68 sugarcane samples that tested negative by RT-PCR were found positive by RT-LAMP, whereas the RT-LAMP assay failed to detect SCYLV in only 5 samples that tested positive by RT-PCR. Combining RT-PCR and RT-LAMP data enabled the detection of SCYLV in 86 of 183 Kenyan sugarcane plants, indicating high SCYLV prevalence throughout the country (ranging from 36 to 64% in individual counties). Seminested PCR assays were developed that enabled the amplification of a fragment encompassing the capsid protein coding region gene and its flanking 5' and 3' genomic regions. Sequences of this fragment for four Kenyan SCYLV isolates indicated that they shared 99.2 to 99.6% pairwise identity with one another and clearly clustered phylogenetically with SCYLV-BRA genotype isolates. To our knowledge, this is the first report of SCYLV in Kenya.

Details

ISSN :
19437692 and 01912917
Volume :
100
Database :
OpenAIRE
Journal :
Plant Disease
Accession number :
edsair.doi.dedup.....30c8f2aead4c4cfe545f62474e8db252
Full Text :
https://doi.org/10.1094/pdis-05-15-0602-re