SummaryThe root-knot nematode Meloidogyne arenaria was found in Greece infecting balm (Melissa officinalis L.) and grapevine (Vitis vinifera L.). The isolate from balm was M. arenaria while the one from grapevine was a mixture of M. arenaria and M. javanica (prevalent species). This is the first report of the M. arenaria species in the country in which identification was based on biochemical methods and its occurrence on balm is a new host record.
Key words: esterase phenotypes; Melissa officinalis; Vitis viniferaRoot-knot nematodes (RKN), Meloidogyne spp., are among the most economically important nematodes in agriculture with a wide host range (Oka et al., 2000;Karssen & Moens, 2006). In Greece, RKN have been found in several areas and their identification was based on morphological and morphometric characters and/or differential host tests. Morphological identification of Meloidogyne species is a difficult task, even for qualified taxonomists with expertise in the genus, while esterase phenotypes of several RKN are species specific and can be used as reliable taxonomic characters (Esbenshade & Triantaphyllou, 1990;Pais & Abrantes, 1989). To date, the only records of Meloidogyne populations from Greece, in which biochemical and molecular methods were used for their identification, are referred to M. javanica (Treub) Chitwood and M. incognita (Kofoid and White) Chitwood found in vegetable crops (Tzortzakakis et al., 1999(Tzortzakakis et al., , 2005. In autumn 2004, galls of RKN were found in roots of grapevine (Vitis vinifera L.) and surrounding tomatoes and egg plants grown in a home yard in Crete (southern Greece). In summer 2005, some plants of a balm crop (Melissa officinalis L.) in Thrace (northern Greece) showed ……….. symptoms of stunting and wilting. The roots of the balm plants were examined and the presence of RKN galls was detected. Galled root samples of grapevine and balm plants were taken and egg masses were collected. The RKN isolates were bulked up by inoculating egg masses on to the susceptible tomato (Lycopersicon esculentum Mill.) cv ACE. Every two months the plants were uprooted and egg masses of each isolate were transferred to new plants. The plants were maintained in a controlled environment growth room with 16 h photoperiod at 23 -25 0 C.The identification of these RKN isolates was based on perineal patterns morphology and esterase phenotypes of females extracted from tomato infected roots (Hartmann & Sasser, 1985;Esbenshade & Triantaphyllou, 1985;Pais et al., 1986). The esterase phenotype designated as J3 and A2 were recognized in the isolate from grapevine and the phenotype A2 in the isolate from balm ( Fig. 1