New Disease Reports (2003) 8, 16.

First report of cassava mosaic disease and cassava mosaic geminiviruses in Gabon

J.P. Legg 1,2*, F. Ndjelassili 3 and G. Okao-Okuja 1

*jlegg@iitaesarc.co.ug

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Accepted: 27 Oct 2003

Cassava mosaic disease (CMD), arguably Africa's greatest plant protection problem, has been known to occur in Central/West Africa for more than 70 years. There is, however, no published record of the occurrence of CMD or the cassava mosaic geminiviruses (CMGs) that cause it from the central African country of Gabon. Significantly, however, the severe Uganda variant of East African cassava mosaic virus (EACMV-UG), associated with the African CMD pandemic, has been recorded from the Republic of Congo (Neuenschwander et al., 2002), bordering Gabon to the west.

Cassava fields were examined at 55 sites throughout Gabon in April and July 2003, in order to identify the CMGs associated with CMD and to determine if the pandemic associated EACMV-UG was present. At each site, 30 plants were examined and assessments made of CMD incidence, symptom severity, and the abundance of the whitefly vector, Bemisia tabaci (Genn.). At least two virus-diseased leaf samples were collected from each field for subsequent virus diagnosis. DNA was extracted from these samples on the day of collection using the method of Dellaporta et al. (1983). Virus diagnoses were subsequently made from DNA samples using both specific primer PCR (Zhou et al., 1997) and RFLP analysis involving restriction digestion by EcoRV and mluI of near full-length DNA-A fragments amplified using abutting primer PCR with universal geminivirus primers (Briddon & Markham, 1994).

ACMV was the most widely distributed CMG species, occurring at 53 of the 55 sites. EACMV was identified from a single site just south of Tchibanga in southern Gabon. EACMV-UG was detected in samples collected from 12 sites, all of which were in the eastern Provinces of Haute-Ogooué and Ogooué-Ivindo (Fig. 1). Of the 17 samples infected with EACMV-UG, 16 were mixed infections with ACMV. Symptom severity of plants infected by EACMV-UG (4.1) (Fig. 2) was significantly greater (χ2 = 44.4, df = 3, P < 0.001) than those infected by ACMV alone (2.8). Additionally, four of the five virus-sampled plants having current season whitefly-borne CMD were dual ACMV+EACMV-UG infections. These data comprise the first published record of CMGs in Gabon. The results also describe an early stage of spread of the EACMV-UG associated CMD pandemic into eastern Gabon, which now represents the pandemic's westernmost 'front'.

Figure1+
Figure 1: CMG infection zones in Gabon. Arrows indicate the presumed direction of spread of the EACMV-UG associated pandemic of severe CMD
Figure 1: CMG infection zones in Gabon. Arrows indicate the presumed direction of spread of the EACMV-UG associated pandemic of severe CMD
Figure2+
Figure 2: Severe CMD associated with mixed EACMV-UG+ACMV infection, Lekoni, Haut-Ogooué, Eastern Gabon
Figure 2: Severe CMD associated with mixed EACMV-UG+ACMV infection, Lekoni, Haut-Ogooué, Eastern Gabon

Acknowledgements

Grant assistance from the Office for US Foreign Disaster Assistance and technical help of Dr. M. Tindo and Mr. R. Obonyo are acknowledged.


References

  1. Briddon RW, Markham PG, 1994. Universal primers for the PCR amplification of dicot-infecting geminiviruses. Molecular Biotechnology 1, 202-5.
  2. Dellaporta SL, Wood JJ, Hicks JB. 1983. A plant DNA minipreparation: version II. Plant Molecular Biology Reporter 1, 19-21.
  3. Neuenschwander P, Hughes J d'A, Ogbe F, Ngatse JM, Legg JP. 2002. The occurrence of the Uganda Variant of East African cassava mosaic virus (EACMV-Ug) in western Democratic Republic of Congo and the Congo Republic defines the westernmost extent of the CMD pandemic in East/Central Africa. Plant Pathology 51, 384.
  4. Zhou X, Liu Y, Calvert L, Munoz C, Otim-Nape GW, Robinson DJ, Harrison BD. 1997. Evidence that DNA-A of a geminivirus associated with severe cassava mosaic disease in Uganda has arisen by interspecific recombination. Journal of General Virology 78, 2101-2111.

This report was formally published in Plant Pathology

©2003 The Authors