Assessment of cassava mosaic disease and field status of cassava begomoviruses in Kenya

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Research Paper 01/11/2021
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Assessment of cassava mosaic disease and field status of cassava begomoviruses in Kenya

Geofrey Sing’ombe Ombiro, Stephen Githiri, Douglas Miano, Elijah Ateka
Int. J. Agron. & Agric. Res. 19(5), 16-23, November 2021.
Copyright Statement: Copyright 2021; The Author(s).
License: CC BY-NC 4.0

Abstract

Cassava production in Kenya is affected by cassava mosaic disease caused by cassava mosaic begomoviruses (CMBs). This study was carried out in 2013 to determine the status of cassava mosaic begomoviruses in farmers’ fields in Kenya. The survey covered major cassava growing regions of Kenya of Coast, Eastern, Western and Nyanza. The survey covered a total of 88 fields in all the areas with the highest Cassava mosaic disease incidence 60.19% being reported in Western region and the least 34.66% recorded in Eastern Kenya. Using polymerase chain reaction (PCR) 5 begomoviruses were reported being present in Kneya namely ACMV, EACMV, EACMV-KE, DNA satellites and EACMV-UgV. The highest detections of ACMV 41.2% were recorded in Nyanza with no detections in Eastern. The peak 26.5% EACMV-KE detections were noted in Nyanza and the least 4.3% in Coast. Nyzanza reported the greatest count 70.6% of EACMV and the lowest count 36.6% noted in Western. The highest EACMV-UgV count was in Nyanza 41.2%. Sequencing was used to determine the genetic diversity of the cassava begomoviruses detected by PCR. Wide variability was seen for Kenyan EACMV isolates as they formed 2 independent groups. However, with regards to EACMV-KE, there was little variability forming a single cluster with bootstrap value of 99%. Of concern in the study was the high incidence of cassava begomoviruses in Nyanza region of Kenya, hence the need for efforts to mitigate the problem.

Bar ES, Bamkefa BA, Winter S, Dixon AGO. 2011. Distribution and current status of Cassava mosaic disease and Begomo-viruses in Guinea. Article in AJRTC 9(1), 17-23.

Bisimwa E, Walangululu J, Bragard C. 2012. Occurrence and Distribution of Cassava Mosaic Begomovirus Related to Agro-ecosystems in the Sud-kivu Province, Democratic Republic of Congo. Asian Journal of Plant Pathology 6, 1-12.

Bull SE, Briddon RW, Sserubombwe WS, Ngugi K, Markham PG, Stanley J. 2006. Genetic diversity and phylogeography of Cassava mosaic viruses in Kenya. Journal of General Virology 87, 3053-3065.

Chikoti PC, Ndunguru J, Melis R, Tairo F, Shanahan P, Sseruwagi P. 2013. Cassava mosaic disease and associated viruses in Zambia: occurrence and distribution. International Journal of pest Management 59, 63-72.

Chikoti PC, Tembo M, Chisola M, Ntawarahunga P, Ndunguru J. 2015. Status of Cassava mosaic disease and whitefly population in Zambia. African Journal of Biotechnology 14, 2539-2546.

Douglas A, 2004. Geographical, historical and political profiles of Nigeria pp 6-7.

Fauquetcm, Stanley J. 2003. Geminivirus classification and nomenclature: progress and problems. Ann Appl Biol 142, 165-189.

Fondong VN, Pita JS, Rey MEC. 2000. Evidence of the synergism between African cassava mosaic virus and a new double-recombinant geminivirus infecting cassava in Cameroon. J Gen Virol 1, 287-297.

Harimalala M, Chiroleu F, Giraud-Carrier C, Hoareau M, Zinga I, Randriamampianina JA, Lett J.-M. 2015. Molecular epidemiology of cassava mosaic disease in Madagascar. Plant Pathology, 64, 501-507. https://doi.org/10.1111/ppa.12277

Kathurima TM, Ateka EM, Nyende AB, Holton TA. 2016. The rolling circle amplification and next generation sequencing approaches reveal genome wide diversity of Kenyan cassava mosaic geminivirus. African Journal of Biotechnology 15, 2045-2052. https://doi.org/10. 5897/AJB2016.15357

Kenneth GM. 2007. Epidemiology of Cassava mosaic disease and molecular characterization of Cassava mosaic viruses and their associated whitefly vector in South Africa pp 2-9.

Mwatuni FM, Ateka EM, Karanja LS, Mwaura SK,  Obare IJ. 2015. Distribution of cassava mosaic geminiviruses and their associ- ated DNA satellites in Kenya. American Journal of Experimental Agricul- ture 9, 1-12. https://doi.org/10.9734/AJEA/2015/18473

Otim-Nape GW, Shaw MW, Thresh JM. 1994. The effects of African cassava mosaic geminivirus on the growth and yield of cassava in Uganda. Trop Sc 34, 43-54.

Owor B, Legg JP, Okao-Okuja G. 2005. The effect of cassava mosaic Gemini-viruses on symptom severity, growth and root yield of a cassava mosaic virus disease-susceptible cultivar in Uganda. Ann Appl Biol 145, 331-337.

Patil B, Fauquet CM. 2009. Cassava mosaic geminiviruses: actual knowledge and perspectives. Molecular Plant Pathology 10, 685–701. https://doi.org/10.1111/j.1364-3703.2009.00559.x

Sangare M, Atcham T, Olivier K, Bagui I, Traore A, Jeremie B, Thouakesseh Z. 2015. Classification of African mosaic virus infected Cassava leaves by the use of multi spectral imaging. Optics and phonic journals 5, 261-272.

Sseruwagi P, Sserubombwe WSS, Legg JPP, Ndunguru J, Thresh JMM. 2004. Methods of surveying the incidence and severity of cassava mosaic disease and whitefly vector populations on cassava in Africa: a review. Virus Research 100, 129-142. https://doi. org/10.1016/j.virusres.2003.12.021.

Swansonmm, Harrison BD. 1994. Properties, relationships and distribution of cassava mosaic geminiviruses. Trop Sc 34, 15-25.

Thresh JM, Fargette D, Otim-Nape GW. 1994. Effects of African cassava mosaic geminivirus on the yield of cassava. Trop Sc 34, 26-42.

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