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Females, males and second-stage juveniles of an unusual population of Meloidogyne exigua race 3 that only parasitises the rubber tree were examined by light and scanning electron microscopy. Previous molecular characterisation, using SCAR markers, showed consistency with other M. exigua populations from coffee. However, RAPD analysis showed high polymorphism (43.1-57.8%) but with 100% bootstrap support among populations from coffee and rubber tree. In addition, this population showed the main M. exigua esterase band (Rm: 1.5) and an additional band (Rm: 1.6) not detected in the coffee population. The morphology of this atypical population was very close to M. exigua from coffee in major diagnostic characters such as perineal pattern and male head region. However, minor differences occurred in morphological and morphometric features, particularly in the female and male stylet morphology. Cytogenetic studies confirmed the occurrence of meiotic parthenogenesis with haploid chromosome number (n = 18). [ABSTRACT FROM AUTHOR]

Thirteen Meloidogyne arenaria isolates representing two cytological types (3n = 51-56, 2n = 42-48) and four enzymatic phenotypes (esterase and malate dehydrogenase: A3N1, A2N1, A1N1, A2N3) were studied using different approaches. The analysis of molecular markers showed a high level of polymorphism among the isolates. The trees obtained with RAPD or ISSR polymorphisms showed concordant results and agree with morphological studies. By considering morphometrical and morphological features, it was possible to conclude that the isolate with enzymatic phenotype A2N3 race 1 was the M. arenaria described in 1949 by Chitwood and appearing clearly separated in the trees, as well as in the outgroups. The seven isolates with phenotype A2N1 from different localities and isolate A1N1 can be considered morphometrically typical of M. arenaria race 2 and they were apparently clustered by geographical origin. Morphologically, they differed from isolate A2N3 race 1. The two isolates with phenotype A3N1 appeared to be closely related to the isolate of M. morocciensis and, considering all of the features described for this species, were identified as such. The two isolates A2N3 race 2 were identified either as an atypical M. arenaria or an unidentified species (females and males having atypical stylets), and clustered together and separated from other M. arenaria isolates with high bootstrap support. The same M. arenaria isolates were tested with the species-specific molecular marker, type SCAR. A fragment of 420 bp was obtained for ten isolates of M. arenaria, including the atypical A2N3 race 2 and M. morocciensis. This fragment was not amplified for three typical A2N1 isolates of M. arenaria. [ABSTRACT FROM AUTHOR]

An obligate parasite bacterium of the root-knot nematode, Pasteuria penetrans strain P10, isolated from Meloidogyne incognita females on banana roots in Imperatriz Maranhão State, Brazil, was evaluated in glasshouse conditions, using two doses of a dry root bionematicide (107 endospores (5.0 g/seedling) and 106 endospores (0.5 g/seedling)) on seedlings of cv. Mundo Novo coffee. The soil in which coffee seedlings were raised was inoculated previously with these two doses of P. penetrans and after 2 months the plants were transferred to soils of different textures: clay-sandy soil (38% clay, 2% silt and 60% sand) and sandy soil (17% clay, 0% silt and 83% sand). When the coffee plants were 30 cm high, they were inoculated with 20 000 eggs/plant of M. incognita race 1. The coffee plants were examined 8, 16 and 24 months after nematode plant infestation. The effectiveness of the biological control was determined by the reduction of nematode reproduction factor, which ranged from 62 to 67% in clay-sandy soil and 80 to 85% in sandy soil. The mechanism of suppression caused by the bacterium was evaluated by the percentage of infected second-stage juveniles (J2), number of endospores attached/J2 and number of infected females. The high levels of suppression were related to time, increasing from 8 to 24 months, and to the percentage of sand in the soil. [ABSTRACT FROM AUTHOR]

Enzyme phenotypes, specifically esterases (EST) and malate dehydrogenase (MDH), were used to characterise different species of Meloidogyne from Chile. Esterase activity was highly polymorphic and was the most useful in the identification of the different species. Using this enzyme it is possible to characterise and identify M. ethiopica in about 80% of samples on grapevine, kiwi and tomatoes. Another three species, M. javanica, M. hapla and M. arenaria, were identified on tomatoes, kiwi and pomegranate with only one or a few populations. It was possible to detect minor atypical (unidentified) phenotypes, generally in mixed populations with M. ethiopica. Only the profiles N1 and H1 of MDH were detected. N1 was not specific and H1 allowed identification of M. hapla. Contaminated nursery stock has probably resulted in serious infestation by M. ethiopica in vineyards in various localities in Chile. [ABSTRACT FROM AUTHOR]

A new root-knot nematode parasitising coffee in the region of the Izalco volcano, Sansonate, El Salvador, is described as Meloidogyne izalcoensis n. sp. The suggested common name is El Salvador coffee root-knot nematode. The perineal pattern is characterised by the moderately high to high, squareish to rounded, dorsal arch, striae coarse, smooth to wavy, sometimes zigzaggy, usually without a distinct whorl, and similar to that of M. incognita and M. paranaensis. The female head region set off from body, sometimes annulated, and the labial disc has two prominent elevations or bumps on the ventral side that are slightly raised above the medial lips. The female stylet is robust, 15.0-16.0 μm long and with the DGO at 4.5-6.0 μm posterior to the knobs. Males have a high, round, head cap continuous with the body contour and the labial disc is fused with the medial lips to form an elongated structure. The head region is never marked by incomplete annulations. The stylet is robust, 23.0-26.0 μm long, and has rounded, backwardly sloping, knobs with the DGO located at 4.0-7.0 μm posteriorly. The stylet of second-stage juveniles is 12.0-13.0 μm long and the DGO is located 3.0-4.0 μm posterior to the stylet base; the tail is 45-48 μm long, conoid, with a rounded terminus. Biochemically, the esterase phenotype I4 (= Sa4) (Rm: 0.86, 0.96, 1.24, 1.30) is unique and is the most useful character to differentiate M. izalcoensis n. sp. from all other species. [ABSTRACT FROM AUTHOR]

Focuses on a study which characterized the different species of Meloidogyne nematode using enzyme phenotypes. Discussion on species characterization of the nematodes; Materials and methods; Results of the study.