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Use of next‐generation sequencing for the identification and characterization of M aize chlorotic mottle virus and S ugarcane mosaic virus causing maize lethal necrosis in K enya
Author(s) -
Adams I. P.,
Miano D. W.,
Kinyua Z. M.,
Wangai A.,
Kimani E.,
Phiri N.,
Reeder R.,
Harju V.,
Glover R.,
Hany U.,
SouzaRichards R.,
Deb Nath P.,
Nixon T.,
Fox A.,
Barnes A.,
Smith J.,
Skelton A.,
Thwaites R.,
Mumford R.,
Boonham N.
Publication year - 2013
Publication title -
plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.928
H-Index - 85
eISSN - 1365-3059
pISSN - 0032-0862
DOI - 10.1111/j.1365-3059.2012.02690.x
Subject(s) - biology , virus , virology , mottle , dna sequencing , plant virus , cucumber mosaic virus , strain (injury) , inoculation , polymerase chain reaction , genome , genetics , gene , horticulture , anatomy
The diagnosis of novel unidentified viral plant diseases can be problematic, as the conventional methods such as real‐time PCR or ELISA may be too specific to a particular species or even strain of a virus, whilst alternatives such as electron microscopy ( EM ) or sap inoculation of indicator species do not usually give species level diagnosis. Next‐generation sequencing ( NGS ) offers an alternative solution where sequence is generated in a non‐specific fashion and identification is based on similarity searching against G en B ank. The conventional and NGS techniques were applied to a damaging and apparently new disease of maize, which was first identified in K enya in 2011. ELISA and TEM provided negative results, whilst inoculation of other cereal species identified the presence of an unidentified sap transmissible virus. RNA was purified from material showing symptoms and sequenced using a R oche 454 GS ‐ FLX +. Database searching of the resulting sequence identified the presence of M aize chlorotic mottle virus and S ugarcane mosaic virus , a combination previously reported to cause maize lethal necrosis disease. Over 90% of both viral genome sequences were obtained, allowing strain characterization and the development of specific real‐time PCR assays which were used to confirm the presence of the virus in material with symptoms from six different fields in two different regions of K enya. The availability of these assays should aid the assessment of the disease and may be used for routine diagnosis. The work shows that next‐generation sequencing is a valuable investigational technique for rapidly identifying potential disease‐causing agents such as viruses.