Genetic diversity of the root‐knot nematode Meloidogyne ethiopica and development of a species‐specific SCAR marker for its diagnosis |
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| Authors: | V R Correa V S Mattos M R A Almeida M F A Santos M S Tigano P Castagnone‐Sereno R M D G Carneiro |
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| Institution: | 1. Embrapa Recursos Genéticos e Biotecnologia, , Brasília, DF, 70770‐900 Brazil;2. Departamento de Fitopatologia, Universidade de Brasília, , Brasília, DF, 70910‐900 Brazil;3. Institut Sophia Agrobiotech, INRA‐UMR1355, UNSA, CNRS‐UMR7254, , Sophia Antipolis, 06903 France |
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| Abstract: | Meloidogyne ethiopica is an important nematode pathogen causing serious economic damage to grapevine in Chile. In Brazil, M. ethiopica has been detected with low frequency in kiwifruit and other crops. The objectives of this study were to evaluate the intraspecific genetic variability of M. ethiopica isolates from Brazil and Chile using AFLP and RAPD markers and to develop a species‐specific SCAR‐PCR assay for its diagnosis. Fourteen isolates were obtained from different geographic regions or host plants. Three isolates of an undescribed Meloidogyne species and one isolate of M. ethiopica from Kenya were included in the analysis. The results showed a low level of diversity among the M. ethiopica isolates, regardless of their geographical distribution or host plant origin. The three isolates of Meloidogyne sp. showed a high homogeneity and clustered separately from M. ethiopica (100% bootstrap). RAPD screenings of M. ethiopica allowed the identification of a differential DNA fragment that was converted into a SCAR marker. Using genomic DNA from pooled nematodes as a template, PCR amplification with primers designed from this species‐specific SCAR produced a fragment of 350 bp in all 14 isolates of M. ethiopica tested, in contrast with other species tested. This primer pair also allowed successful amplification of DNA from single nematodes, either juveniles or females and when used in multiplex PCR reactions containing mixtures of other root‐knot nematode species, thus showing the sensitivity of the assay. Therefore, the method developed here has potential for application in routine diagnostic procedures. |
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| Keywords: | amplified fragment length polymorphisms diagnostic intraspecific diversity multiplex SCAR‐PCR
RAPD
root‐knot nematodes |
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