African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12486

Full Length Research Paper

Occurrence and genetic variability of partial coat protein gene of Sweet potato leaf curl virus (SPLCV) in Kenya

Maina, S.
  • Maina, S.
  • Biosciences Eastern and Central Africa- International Livestock Research Institute Hub (BecA-ILRI Hub), P.O. Box 30709-00100, Nairobi, Kenya.
  • Google Scholar
Miano, D. W.
  • Miano, D. W.
  • College of Agriculture and Veterinary Sciences, University of Nairobi, P. O. Box 29053 00625, Nairobi, Kenya.
  • Google Scholar
Mbogo, E.
  • Mbogo, E.
  • Biotechnology Centre, Kenya Agricultural and Livestock Research Organization, P.O. BOX, 57811-00200, Nairobi, Kenya.
  • Google Scholar
Amimo, J. O.
  • Amimo, J. O.
  • College of Agriculture and Veterinary Sciences, University of Nairobi, P. O. Box 29053 00625, Nairobi, Kenya.
  • Google Scholar
Irungu, J.
  • Irungu, J.
  • Biotechnology Centre, Kenya Agricultural and Livestock Research Organization, P.O. BOX, 57811-00200, Nairobi, Kenya.
  • Google Scholar
Njiruh, P. N.
  • Njiruh, P. N.
  • Department of Agriculture Resource Management, Embu University College, P.O. Box 6, Embu Kenya.
  • Google Scholar


  •  Received: 02 May 2017
  •  Accepted: 09 June 2017
  •  Published: 08 November 2017

Abstract

A survey was conducted to determine the occurrence of sweet potato leaf curl virus (SPLCV) infecting sweet potato in Kenya. Vine cuttings of sweet potato were collected in 2011 from fields in Central, Western and Coastal regions of the country. The cuttings were grown in an insect-proof screen-house and scion grafted to Ipomoea setosa indicator plants. DNA was extracted from leaf samples of graft-inoculated I. serosa and tested for the presence of SPLCV by polymerase chain reaction (PCR) using degenerate and specific primers. The virus was detected in all the regions with incidence rates of 33, 17.0 and 2.6% from Western, Coastal and Central regions, respectively using specific primers. Coat protein gene AV1 from isolates collected from each region was sequenced and their comparison revealed >88.4% nucleotide identity. Phylogenetic grouping using nucleotide and amino acid sequences showed that four Kenyan isolates (Coast3, Central13, Coast15 and Western14) clustered together, while the other remaining five grouped a long with isolates from different parts of the world. The results reveal that Kenyan SPLCV isolates have a clear diversity and are also closely related with other isolates from different parts of the world. The wide distribution of the virus within the country means that urgent measures are needed to clean the farmers planting material to reduce possible losses incurred due to the presence of the virus. 

 

Key words: Sweet potato leaf curl virus, coat protein gene, virus, sweet potato, nucleotide, amino acid.