Ralstonia solanacearum colonization of tomato roots infected by Meloidogyne incognita

Bacterial wilt, caused by Ralstonia solanacearum, is one of the most serious diseases of tomato (Solanum lycopersicum). Concomitant infection of R. solanacearum and root‐knot nematode Meloidogyne incognita increases the severity of bacterial wilt in tomato, but the role of this nematode in disease complexes involving bacterial pathogens is not completely elucidated. Although root wounding by root‐knot nematode infection seems to play an important role, it might not entirely explain the increased susceptibility of plants to R. solanacearum. In the present study, green fluorescent protein (GFP)‐labelled R. solanacearum distribution was observed in the root systems of the tomato cultivar Momotaro preinoculated with root‐knot nematode or mock‐inoculated with tap water. Fluorescence microscopy revealed that GFP‐labelled R. solanacearum mainly colonized root‐knot nematode galls, and little or no green fluorescence was observed in nematode‐uninfected roots. These results suggest that the gall induced by the nematode is a suitable location for the growth of R. solanacearum. Thus, it is crucial to control both R. solanacearum and root‐knot nematode in tomato production fields to reduce bacterial wilt disease incidence and effects.     

Integrated management of the root‐knot and reniform nematodes with cropping sequences and ploughing

In a 2 year crop rotation programme none of the 25 different cropping sequences was found to be effective in reducing the population of the root‐knot nematode, Meloidogyne incognita and the reniform nematode, Rotylenchulus reniformis. However it was observed that Fallow‐Cauliflower‐Sorghum‐Coriander (sequence no. 22) for reducing the root‐knot larvae population and Sorghum‐Wheat‐Horsegram‐Turnip (sequence no. 14) for the reducing of the reniform nematode population were comparatively beneficial. By and large, deep ploughing did not favour the multiplication of the both the test nematodes. The population of the nematodes was also reduced to a very low level when the field was left fallow.     

Pathogenicity of root knot nematode Meloidogyne incognita on okra and its management through botanicals

An investigation was carried out to study the pathogenicity of root knot nematode Meloidogyne incognita on okra and its management through various organic amendments. The inoculum level of 1000 juveniles per plant showed significant reduction in various plant growth parameters, which reveals that M. incognita is a potential pathogen of okra. With the increase in inoculums level of M. incognita (J₂), there was a progressive decrease in various plant growth parameters. The maximum reduction in plant growth parameters was observed at an inoculum level of 4000 juveniles per plant. The efficacy of five organic amendments viz. groundnut cake, castor cake, sunflower cake, linseed cake and sawdust was tested against root knot nematode M. incognita. Amending the soil with different oil cakes was found to be effective in reducing the nematode soil population, number of females, number of egg masses as well as root gall formation in okra. The highest increase in plant growth (13%) and maximum reduction in number of galls (54%), number of females (57%) and number of egg masses (55%) was recorded on application of groundnut cake.     

Polarographische Bestimmung von Chlorat-Rückständen im Boden und in der Pflanze

An increase in the inoculum level of root‐knot nematode, Meloidogyne incognita and the reniform nematode, Rotylenchulus reniformis resulted in a relative decrease in plant growth parameters of chickpea. Consequently water absorption capability of roots was impaired. M. incognita caused greater reduction than R. reniformis at the same inoculum level. In concomitant inoculation of M. incognita and R. reniformis there was greater suppression in plant growth of chickpea. The suppression in concomitant inoculations was less than the sum of the suppression caused by the same levels of inoculations of the individual species. The multiplication rate of the nematodes decreased as the inoculum level increased. The results also suggest competition for feeding sites between the two nematode species. The multiplication rate of one species progressively decrease with the increase in the inoculum levels of the other nematode.     

Genetic characterization of <Emphasis Type="Italic">Meloidogyne incognita</Emphasis> isolates from Turkey using sequence-related amplified polymorphism (SRAP)

Southern root knot nematode Meloidogyne incognita is the most widespread-species, causing serious yield losses in protected vegetables fields in the West Mediterranean region of Turkey. The knowledge of genetic variation within M. incognita is required for disease management and improvement of resistant varieties by breeding programs. In the present study, the isolates were classified into different groups based on sequence-related amplified polymorphism (SRAP) fingerprints. To our knowledge, this is the first study carried out on the characterization of M. incognita isolates using SRAP. The schematic diagram by tested primers to differentiate of M. incognita isolates was formed in discrimination of nematodes as an effective molecular tool since it is cost effective and easiness. Data presents a genetic variation on root-knot nematode species. These selected SRAP markers can be used to follow genetic structure and differentiation on M. incognita isolates in a certain region.     

Der Besatz von Beta-Rüubensaatgut rait Wurzelbranderregern und der Einfluß von Umweltfaktoren auf das Auftreten des samenbüurtigen Wurzelbrandes

The root knot nematode Meloidogyne incognita was controlled more effectively when P. lilacinus and G. mosseae were applied together in a pot experiment than either was applied alone. Inoculation of tomato plant with G. mosseae did not markedly increase the growth of plant infected with M. incognita. Inoculation of plant with G. mosseae and P. lilacinus together or alone resulted in a similar shoot and plant height. The highest root development was achieved when mycorrhizal plant were inoculated with P. lilacinus to combat root knot nematode. Inoculation of tomato plant with P. lilacinus suppressed galls/root system and eggs/egg masses, compared to seedling inoculated with M. incognita alone. The mycorrhizal colonization was not affected by inoculation of P. lilacinus.     

Über die Kallosebildung in Siebröhren von Kartoffelpflanzen in Abhängigkeit von Blattrollvirusinfektion und chemisch-physikalischen Bedingungen

All the cultivars of tomato tested were found to be infected with the root‐knot nematode, Meloidogyne incognita, however, to varying extent. There was also reducton in plant growth parameters accordingly. Further reduction in plant growth of tomato cultivars was recorded when plants also received the treatment with the heavy metal, lead, notwithstanding the fact that the presence of lead also reduced the root‐knot development. Tomato cv. Arka Vikas showed minimum reduction in plant growth with single or combined treatment with the nematode and the heavy metal.     

Effect of vesicular-arbuscular mycorrhiza on survival,penetration and development of root-knot nematode in tomato

Summary Effect of mycorrhizal colonisation byGlomus fasciculatum on survival, penetration and development of the root knot nematodeMeloidogyne incognita in tomato was studied. The number of giant cells formed in mycorrhizal plants was significantly low. Mycorrhizal roots did not prevent the penetration by nematode larvae. Root extract from the mycorrhizal plants brought about 50% mortality of the nematode larvae in four days time.     

A DNA probe which distinguishes Globodera pallida Pa2/3 from G. rostochiensis Ro1 and other cyst-forming nematodes

Abstract

A small DNA fragment (approx. 350 base pairs) from the genome of the potato cyst nematode Globodera pallida Pa2/3 was cloned in a bacterial plasmid. When used as a probe in dot-blot DNA hybridisations against a range of nematodes, the cloned DNA bound to G. pallida Pa2/3 but not to Globodera rostochiensis Rol. The cereal cyst nematode Heterodera avenae, the clover cyst nematode Heterodera trifolii, the root knot nematodes Meloidogyne hapla and Meloidogyne incognita, and the beet cyst nematode Heterodera schactii did not cross-hybridise. This probe can detect as few as six larvae of G. pallida.     

Efficacy of neem compost on root knot nematode pest of Lagos spinach,Celosia argentea

The effects of neem compost on root knot nematode, Meloidogyne incognita, pest of Lagos spinach, Celosia argentea, cv. TLV 8, was studied during 2010 and 2011 planting seasons on the field. The trial was conducted at the Teaching and Research Farm of Ladoke Akintola University of Technology, Ogbomoso, Nigeria. There were four treatments, replicated five times fitted into randomised complete block design. Neem compost was applied at 1.0, 1.5 and 2.0?tonnes/ha. Experimental plots, where no compost was applied served as the control. The result obtained shows that Lagos spinach treated with neem compost significantly (p?<?0.05) reduced the final soil nematode population and root infections (damage), with resultant improvement on crop growth and yield. The result of the chemical analysis of the neem compost revealed the presence of flavonoids, sterols, glycosides, alkaloids and saponins.     

Mykoplasmaähnliche Organismen in Früchten proliferationskranker Apfelbäume Kurze Mitteilung

The potential of an in vitro technique to study root‐knot nematode infection on banana roots was investigated. Regenerated banana plants were placed horizontally on Gamborg B5 (GB5)‐medium and incubated under a light‐dark regime of 16h‐8h. Temperature fluctuated between 24 and 33 °C. Banana roots were inoculated with Meloidogyne incognita race 1 coming from roots of a transgenic tomato (Lycopersicon esculentum cv. Moneymaker) grown on GB5‐medium at 28 °C in complete darkness. Root‐knots appeared on primary and secondary banana roots two to seven days after nematode inoculation. After 28 days, egg masses protruded through the cortex and two days later juveniles hatched and reinfected banana roots. This method holds promise for dynamic studies of banana root infection with root‐knot nematodes.     

The use of fluorescent reporter protein tagging to study the interaction between Root‐Knot Nematodes and Soft Rot Enterobacteriaceae

The study of plant parasitic nematodes such as Meloidogyne spp. and their interactions with phytopathogenic bacteria remains underexplored. One of the challenges towards establishing such interactions is the dependence on symptom development as a measure of interaction. In this study, mCherry was employed as a reporter protein to investigate the interaction between the soft rot Enterobacteriaceae (SRE) Pectobacterium carotovorum subsp. brasiliensis (Pcb) and root‐knot nematode (M. incognita). Pectobacterium carotovorum subsp. brasiliensis was transformed with pMP7604 generating Pcb_mCherry strain. This strain was shown to attach to the surface coat of M.incognita J2 at the optimum temperature of 28°C. This suggests that RKN juveniles may play a role in disseminating Pcb in soils that are heavily infested with Pcb. The presence of RKN juveniles was shown to play a role in introducing Pcb_mCherry into potato tubers potentially acting as a source of latent tuber infections.

Significance and Impact of the Study

This study uses fluorescent reporter protein tagging as a tool to demonstrate the interaction between root‐knot nematode (Meloidogyne incognita) and the soft rot Enterobacteriacea (Pectobacterium carotovorum subsp. brasiliensis). Introduction of Pectobacterium through wounds generated by second‐stage juveniles (J2) into potato tubers was demonstrated. These results suggest that RKN juveniles can facilitate latent infection of potato tubers in the soil. These findings have important implications in the management of RKN and SRE in seed potato production. Furthermore, this tool can be used to study other nematode–bacteria interactions that have not been previously studied.     

Biological control potential of plant growth‐promoting rhizobacteria suppression of Meloidogyne incognita on cotton and Heterodera glycines on soybean: A review

Over the past decade, we have seen an increasing market for biopesticides and an increase in number of microbial control studies directed towards plant‐parasitic nematodes. This literature survey provides an overview of research on biological control of two economically important plant‐parasitic nematodes, Meloidogyne incognita (Kofoid & White) Chitwood (southern root‐knot nematode) and Heterodera glycines Ichinohe (soybean cyst nematode) using spore‐forming plant growth‐promoting rhizobacteria (PGPR). In this review, the current biological control strategies for the management of those cotton and soybean nematodes, the mechanism of using BacillusPGPR for biological control of plant‐parasitic nematode including induced systemic resistance and antagonism and the future of biological control agents on management of plant‐parasitic nematodes are covered.     

Leaf herbivory counteracts nematode-triggered repression of jasmonate-related defenses in tomato roots

Shoot herbivores may influence the communities of herbivores associated with the roots via inducible defenses. However, the molecular mechanisms and hormonal signaling underpinning the systemic impact of leaf herbivory on root-induced responses against nematodes remain poorly understood. By using tomato (Solanum lycopersicum) as a model plant, we explored the impact of leaf herbivory by Manduca sexta on the performance of the root knot nematode Meloidogyne incognita. By performing glasshouse bioassays, we found that leaf herbivory reduced M. incognita performance in the roots. By analyzing the root expression profile of a set of oxylipin-related marker genes and jasmonate root content, we show that leaf herbivory systemically activates the 13-Lipoxigenase (LOX) and 9-LOX branches of the oxylipin pathway in roots and counteracts the M. incognita-triggered repression of the 13-LOX branch. By using untargeted metabolomics, we also found that leaf herbivory counteracts the M. incognita-mediated repression of putative root chemical defenses. To explore the signaling involved in this shoot-to-root interaction, we performed glasshouse bioassays with grafted plants compromised in jasmonate synthesis or perception, specifically in their shoots. We demonstrated the importance of an intact shoot jasmonate perception, whereas having an intact jasmonate biosynthesis pathway was not essential for this shoot-to-root interaction. Our results highlight the impact of leaf herbivory on the ability of M. incognita to manipulate root defenses and point to an important role for the jasmonate signaling pathway in shoot-to-root signaling.

Leaf herbivory counteracts the repression of jasmonate-related defenses triggered by a root knot nematode in tomato roots impairing the nematode performance via shoot-to-root jasmonate signaling     

Mode of action and efficacy of iprodione against the root‐knot nematode Meloidogyne incognita

The ban and restriction on the use of several synthetic chemicals for controlling plant parasitic nematodes, and concern about their side effects necessitate the availability of effective methods of control with low toxicity to humans and non‐target organisms. Therefore, efficacy and mode of action of iprodione, a dicarboximide fungicide, was evaluated against the root‐knot nematode Meloidogyne incognita, in vitro and in vivo conditions, in comparison with the nematicides fenamiphos, fosthiazate and oxamyl at 7.00, 1.66 and 1.66 mL/5 L water, respectively. In vitro, iprodione showed nematostatic rather than nematicidal activity against second‐stage juveniles of M. incognita in contrast to fenamiphos, fosthiazate and oxamyl which were nematicidal. In the in vivo experiment with tomato, iprodione controlled M. incognita less than fenamiphos, fosthiazate and oxamyl. No visual symptoms of phytotoxicity were observed. Therefore, iprodione can be a useful chemical for controlling nematode populations if included in an Integrated Pest Management program.     

Nematodes associated with some date palm cultivars in relation to soil type

A survey was conducted during 2010 and 2011 to study the distribution of nematodes associated with certain date palm cultivars in Nubaryia and Giza in Egypt. The results revealed that the root knot nematode, Meloidogyne incognita was found at high population density and frequency of occurrence on the surveyed date palm cultivars in sandy loam soil in Nubaryia. The highest population density and frequency of occurrence of the root knot nematode were found on date palm cv. Al-Ekhlas followed by cvs. Barhi, Samani and Zaghlool. The spiral nematode, Helicotylenchus was found in soil of Samani and Zaghlool only. In clay loamy soil in Giza, Helicotylenchus spp. and Rotylenchulus renformis were found in association with certain date palm cultivars. As for Rotylenchulus reniformis, it was found at the highest population density and frequency of occurrence in the rhizosphere of Hayani followed by Zaghlool, Samani and Barhi. As for Helicotylenchus, it was found that the highest population density, also, was in the rhizosphere of Hayani followed by Samani, Barhi and Zaghlool in a descending order.     

Integration of Glomus mosseae with Chromolaena odorata powder for suppression of Meloidogyne incognita on maize (Zea mays L.)

Meloidogyne incognita infestation on maize results in heavy yield loss in farmers’ field. Most of the varieties adopted by subsistence farmers in Nigeria are susceptible to M. incognita. Beside these, the cost of control exceeding the profit from the crop using nematicides and the pollution risk they pose to the environment has necessitated the need for alternatives. Pot and field experiments were, therefore, conducted to investigate the effects of Chromolaena odorata powder and Glomus mosseae (a mycorrhizal fungus) on M. incognita pathogenicity on maize. Hybrid Oba super II improved maize variety adopted by local farmers was selected for the study. Maize plants were grown with G. mosseae (5 spores/g of soil) and soil amended with C. odorata powder (1% w/w) singly and in combination. Two weeks after emergence, Test plants were inoculated with 5000 M. incognita eggs. Sixty days after planting, destructive samples were assessed for root gall symptom and severity, and nematode population. Results show that G. mosseae and C. odorata powder were effective in controlling the population of M. incognita and the root knot nematode symptom and gave the highest yield parameters in combination. Single application of G. mosseae and C. odorata powder was similar in the effect on M. incognita and maize yield. Combination of G. mosseae and C. odorata powder may become a viable alternative to nematicide in managing M. incognita pathogenicity on maize as C. odorata powder may serve as a carrier medium for G. mosseae.     

Divergent expression of cytokinin biosynthesis,signaling and catabolism genes underlying differences in feeding sites induced by cyst and root‐knot nematodes

Cyst and root‐knot nematodes are obligate parasites of economic importance with a remarkable ability to reprogram root cells into unique metabolically active feeding sites. Previous studies have suggested a role for cytokinin in feeding site formation induced by these two types of nematodes, but the mechanistic details have not yet been described. Using Arabidopsis as a host plant species, we conducted a comparative analysis of cytokinin genes in response to the beet cyst nematode (BCN), Heterodera schachtii, and the root‐knot nematode (RKN), Meloidogyne incognita. We identified distinct differences in the expression of cytokinin biosynthesis, catabolism and signaling genes in response to infection by BCN and RKN, suggesting differential manipulation of the cytokinin pathway by these two nematode species. Furthermore, we evaluated Arabidopsis histidine kinase receptor mutant lines ahk2/3, ahk2/4 and ahk3/4 in response to RKN infection. Similar to our previous studies with BCN, these lines were significantly less susceptible to RKN without compromising nematode penetration, suggesting a requirement of cytokinin signaling in RKN feeding site formation. Moreover, an analysis of ahk double mutants using CycB1;1:GUS/ahk introgressed lines revealed contrasting differences in the cytokinin receptors mediating cell cycle activation in feeding sites induced by BCN and RKN.     

Enhanced tolerance of Mentha arvensis against Meloidogyne incognita (Kofoid and White) Chitwood through mutualistic endophytes and PGPRs

The use of herbs in pharmaceutical preparation is ever increasing, and the demand for pesticides free material by the concern industries is on the rise. Consequently the need to grow disease-free plants using non-chemical fertilizers and pesticides is the need of the hour. Mentha arvensis cv. kosi is highly infested with Meloidogyne incognita (Kofoid and White) Chitwood, and severe oil yield loss occurs due to this nematode pest. Employing ecofriendly ways of nematode management, the mutualistic endophytes (Trichoderma harzianum strain Thu, Glomus intraradices) and plant growth promoting rhizobacteria (Bacillus megaterium and Pseudomonas fluorescens) were assessed individually and in combination on plant biomass, oil yield of menthol mint (M. arvensis cv. kosi), reproduction potential and population development of root knot nematode, M. incognita under glasshouse conditions. These microbes enhanced the plant biomass and percent oil yield both with and without M. incognita inoculation. Dual application of mutualistic fungal endophytes and Plant Growth Promoting Rhizobacteria (PGPRs) may be a wise option for enhancing the oil yield and tolerance of menthol mint against M. incognita infection.     

Genetic approaches to sustainable pest management in sugar beet (Beta vulgaris)

Sugar beet (Beta vulgaris) is an important arable crop, traditionally used for sugar extraction, but more recently, for biofuel production. A wide range of pests, including beet cyst nematode (Heterodera schachtii), root‐knot nematodes (Meloidogyne spp.), green peach aphids (Myzus persicae) and beet root maggot (Tetanops myopaeformis), infest the roots or leaves of sugar beet, which leads to yield loss directly or through transmission of beet pathogens such as viruses. Conventional pest control approaches based on chemical application have led to high economic costs. Development of pest‐resistant sugar beet varieties could play an important role towards sustainable crop production while minimising environmental impact. Intensive Beta germplasm screening has been fruitful, and genetic lines resistant to nematodes, aphids and root maggot have been identified and integrated into sugar beet breeding programmes. A small number of genes responding to pest attack have been cloned from sugar beet and wild Beta species. This trend will continue towards a detailed understanding of the molecular mechanism of insect–host plant interactions and host resistance. Molecular biotechnological techniques have shown promise in developing transgenic pest resistance varieties at an accelerated speed with high accuracy. The use of transgenic technology is discussed with regard to biodiversity and food safety.