INTRODUCTION Root-knot nematodes are serious pests of many cultivated crops around the word. The Meloidogyne spp. complex is one of the economically most important pests in Bulgaria Damage to tomato by Meloidogyne spp. was first observed in Bulgaria by Malkov (1903). Later research showed that these nematodes are widespread in the country (Stoyanov, 1980). To control the root-knot nematodes resistant varieties and chemicals are used (Stoyanov, 1989; Choleva et al., 2006; Salkova et al., 2006). The root-knot nematodes can be infected by fungi at different stages of their life cycles. Soils are a reservoir for microorganisms that are highly varied in activity and composition. Natural regulation of the soil densities of the root-knot nematodes occurs in monocropping areas. Our review of the literature on fungi associated with cyst and root-knot nematodes revealed that about 160 fungal species belonging to 70 genera had been reported on these nematodes (Qadri, 1989; Qadri & Saleh, 1990; De Leij & Kerry, 1991; Khan & Akram, 2000). Casual observations of populations of Meloidogyne spp. in southern Bulgaria revealed the presence of black eggs in some females. The purpose of the present investigation was to describe and isolate fungi from eggs of Meloidogyne spp. collected from a greenhouse in southern Bulgaria. These studies were conducted to assess the frequency of occurrence of the causative fungus in the nematodo-endemic areas. MATERIALS AND METHODS The experiment was undertaken at the Plant Protection Institute in Kostinbrod in 2002-2004. Monthly root samples were collected from a greenhouse previously identified as infested with Meloidogyne spp. The samples were taken on a zig-zag pattern over the field. Roots were washed free from soil with a fine jet of water. The females were picked off the roots and recorded whether infected or healthy. The egg numbers were determined per 1 g of roots by crushing the females. The healthy and diseased eggs were counted with the aid of a microscope (x400) in three replicates for each sampling time. The effects of parasites upon eggs in females were determined using the following two categories: (1) infested eggs--those developing a fungal colony and eggs that were not identifiable as juveniles or embryos, and (2) normal eggs--those containing embryos or second-stage juveniles (Lopez-Llorca & Boag, 1993). Part of the soil collected from the field was used in a pot experiment. Surface sterilized seeds (0.1 % mercuric chloride for 2 min) of tomato were sown in sterilized soil. Fifteen days after germination the seedlings were thinned to one per pot. Pots were filled with infested soil and planted with tomato seedlings (cv. Ideal) at the end of May. The plants were inoculated with freshly hatched juveniles of Meloidogyne spp. at a rate of 1500/pot. Three pots were removed at monthly intervals and 10 females were randomly chosen from each pot, rinsed several times in sterile water, and preserved at room temperature in sterile sand in glass vials. During January the females were separated from sand, crushed in water, and the numbers of the diseased and healthy eggs were recorded. Part of the soil collected from the infested field was steam-sterilized and put into 24 pots. A second set of 24 pots were filled with infested field soil. Tomato plants were placed in the pots and inoculated with 1500 juveniles/pot in a water suspension pipetted around the roots. From July onward the pots were examined more frequently and when the females emerged they were examined at x400 magnification to ascertain if there was any fungal infection. Weekly counts of healthy and diseased eggs were recorded in both of the sets in three replications. Fungi were isolated from the eggs. The surface of the egg-masses was sterilized by agitation for 3 min in 5 mL of 0.1% NaOCI, then removed and washed twice with sterile distilled water. …