Genetic variability and population structure of Cercospora beticola, the causal agent of Cercospora leaf spot in sugarbeet, from four sugarbeet-growing regions of Greece were investigated using growth rate, pathogenicity, and mini- and microsatellite DNA fingerprinting. Mycelial growth and pathogenicity were very diverse within and between groups, and no correlation was found between these features and the geographic origin of the isolates. High diversity was found by micro- and minisatellite fingerprinting, with an average gene diversity of 0.21, and no significant differences among populations. Among the 46 isolates, 45 different genotypes were identified, showing a high degree of genotype diversity. Analysis of the genetic profiles provided no evidence for regional patterns of variation (ΦFST = 0.01, P = 0.261) and the analysis of molecular variation (AMOVA) revealed that genetic variability was due mainly to variations within (99%) rather than between (1%) populations. Such a low level of genetic differentiation is reflected by a migration rate value Nm of 4.7. The high migration rate cannot be referred to splash dispersed conidia. To justify the absence of a regional structure in these C. beticola populations, we must suppose the existence of a long-distance means of dispersal, such as seed transmission and/or man mediated transmission.

Analysis of genotipic diversity in Cercospora beticola Sacc. field isolates / M. Moretti, G. Karaoglanidis, M. Saracchi, A. Fontana, G. Farina. - In: ANNALS OF MICROBIOLOGY. - ISSN 1590-4261. - 56:3(2006), pp. 215-221. [10.1007/BF03175008]

Analysis of genotipic diversity in Cercospora beticola Sacc. field isolates

M. Moretti;M. Saracchi;G. Farina
2006

Abstract

Genetic variability and population structure of Cercospora beticola, the causal agent of Cercospora leaf spot in sugarbeet, from four sugarbeet-growing regions of Greece were investigated using growth rate, pathogenicity, and mini- and microsatellite DNA fingerprinting. Mycelial growth and pathogenicity were very diverse within and between groups, and no correlation was found between these features and the geographic origin of the isolates. High diversity was found by micro- and minisatellite fingerprinting, with an average gene diversity of 0.21, and no significant differences among populations. Among the 46 isolates, 45 different genotypes were identified, showing a high degree of genotype diversity. Analysis of the genetic profiles provided no evidence for regional patterns of variation (ΦFST = 0.01, P = 0.261) and the analysis of molecular variation (AMOVA) revealed that genetic variability was due mainly to variations within (99%) rather than between (1%) populations. Such a low level of genetic differentiation is reflected by a migration rate value Nm of 4.7. The high migration rate cannot be referred to splash dispersed conidia. To justify the absence of a regional structure in these C. beticola populations, we must suppose the existence of a long-distance means of dispersal, such as seed transmission and/or man mediated transmission.
Beta vulgaris; Microsatellite; Minisatellite; Pathogenicity; Population genetic
Settore AGR/12 - Patologia Vegetale
2006
http://www.springerlink.com/content/v562007356280051/
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/27225
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