Sensitivity to fluensulfone of inactivated Meloidogyne spp. second‐stage juveniles

2020 ◽  
Vol 76 (7) ◽  
pp. 2379-2387
Author(s):  
Yuji Oka
Keyword(s):  

2016 ◽  
Vol 37 (4) ◽  
pp. 1857 ◽  
Author(s):  
Sidiane Coltro-Roncato ◽  
José Renato Stangarlin ◽  
Affonso Celso Gonçalves Jr. ◽  
Odair José Kuhn ◽  
Edilaine Della Valentina Gonçalves ◽  
...  

Alternative methods for the control of nematodes, such as the use of plant secondary metabolites, can be explored for integrated pest management systems. The objective of this work was to assess the best solvent for obtaining allyl isothiocyanate from Crambe abyssinica leaves, and the effects of this extract on Meloidogyne incognita and M. javanica. Dry leaves of C. abyssinica at 200 mg L-1 were used to prepare extracts by using water (by infusion and grinding), acetone, water + ethanol (hydroalcoholic extraction), methanol, hexane, and chloroform as solvents. Following the evaporation of the solvents, the residue was resuspended in water for use in the experiments. Distilled water and chemical nematicide were used as control treatments. Once the most effective extracts were defined, the following dosages of dried crambe leaves were used: 0, 200, 300, 400, and 500 mg L-1. High performance liquid chromatography (HPLC) was used to quantify the allyl isothiocyanate present in the extracts. After the solvents evaporated, the residues were eluted with water and used in assays with 200 eggs for the hatching test or 200 second stage juveniles (J2) for mobility and mortality tests. The hydroalcoholic extract was the most effective in reducing the hatching of M. incognita and M. javanica juveniles, by 71.6 and 74.4 percentage points, respectively. The mortality of M. incognita and M. javanica in the hydroalcoholic extract was 93.2 and 64.4%, respectively, followed by the methanol extract (17.6 and 34%) and the extract obtained by grinding (9.2 and 28%). The hydroalcoholic extract at 250 mg L-1 showed high nematicidal effect. The HPLC analysis of the extracts revealed that only the methanol and hydroalcoholic extracts had allyl isothiocyanate, indicating that the inhibitory effects on the hatching, mobility, and mortality were not solely attributed to the presence of this compound.



Plants ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 699
Author(s):  
Christianna Meidani ◽  
Alexandros Savvidis ◽  
Evaggelia Lampropoulou ◽  
Aggeliki Sagia ◽  
Efstathios Katsifas ◽  
...  

A total of 461 indigenous Streptomycetes strains recovered from various Greek rhizosphere habitats were tested for their bioactivity. All isolates were examined for their ability to suppress the growth of 12 specific target microorganisms. Twenty-six were found to exert antimicrobial activity and were screened for potential nematicidal action. S. monomycini ATHUBA 220, S. colombiensis ATHUBA 438, S. colombiensis ATHUBA 431, and S. youssoufensis ATHUBA 546 were proved to have a nematicidal effect and thus were further sequenced. Batch culture supernatants and solvent extracts were assessed for paralysis on Meloidogyne javanica and Meloidogyne incognita second-stage juveniles (J2). The solvent extracts of S. monomycini ATHUBA 220 and S. colombiensis ATHUBA 438 had the highest paralysis rates, so these Streptomycetes strains were further on tested for nematodes’ biological cycle arrest on two Arabidopsis thaliana plants; the wild type (Col-0) and the katanin mutant fra2, which is susceptible to M. incognita. Interestingly, S. monomycini ATHUBA 220 and S. colombiensis ATHUBA 438 were able to negatively affect the M. incognita biological cycle in Col-0 and fra2 respectively, and increased growth in Col-0 upon M. incognita infection. However, they were ineffective against M. javanica. Fra2 plants were also proved susceptible to M. javanica infestation, with a reduced growth upon treatments with the Streptomyces strains. The nematicidal action and the plant-growth modulating abilities of the selected Streptomycetes strains are discussed.



2015 ◽  
Vol 33 (2) ◽  
pp. 147-150
Author(s):  
Érika CSS Correia ◽  
Norberto Silva ◽  
Marylia GS Costa ◽  
Silvia RS Wilcken

Lettuce is the main vegetable cultivated in Brazil, in volume and in marketed value. There are ranges of diseases which may affect lettuce crops, including those caused by root-knot nematodes (Meloidogyne spp.). We evaluated the reproductive potential of Meloidogyne enterolobii in 22 lettuce cultivars. The plants were inoculated with 5,000 eggs and eventuals second stage juveniles of nematode per pot, two days after the transplanting. 'Rutgers' tomato was used as standard for inoculum viability of M. enterolobii. We evaluated, 60 days after inoculation, the gall index, egg mass index and reproduction factor (RF). The 'Ithaca', 'Raider Plus', 'RS-1397', 'L-104', 'Challenge', 'IP-11', 'Classic', 'Salinas 88', 'Vanguard 75', 'Calona' and 'Desert Queen' were resistant to M. enterolobii with RF varying from 0.22 to 0.9, and the cultivars Lady Winterset, Robinson, Sonoma, Raider, Lucy Brown, Bnondaga, Summer Time, Taina, Sundevil and L-109 were susceptible to this nematode, with RF ranging from 1.06 to 5.73.



Plant Disease ◽  
2019 ◽  
Vol 103 (7) ◽  
pp. 1551-1558 ◽  
Author(s):  
Xia Li ◽  
Hai-Jing Hu ◽  
Jing-Yu Li ◽  
Cong Wang ◽  
Shuang-Lin Chen ◽  
...  

Root-knot nematodes (Meloidogyne spp.) cause serious crop losses worldwide. The colonization of tomato roots by endophytic bacteria Bacillus cereus BCM2 can greatly reduce Meloidogyne incognita damage, and tomato roots carrying BCM2 were repellent to M. incognita second-stage juveniles (J2). Here, the effects of BCM2 colonization on the composition of tomato root exudates was evaluated and potential mechanisms for BCM2-mediated M. incognita control explored using a linked twin-pot assay and GC-MS. On water agar plates, J2 preferentially avoided filter paper treated with tomato root exudates (organic phase only) from plants inoculated with BCM2, visiting these 67.1% less than controls. In a linked twin-pot assay, BCM2 treatment resulted in a 42.0% reduction in the number of nematodes in the soil, a 43.3% reduction in the number of galls and a 47.7% decrease in the density of M. incognita in root tissues. Analysis of root exudate composition revealed that BCM2 inoculation increased the number of components in exudates. Among these, 2,4-di-tert-butylphenol, 3,3-dimethyloctane, and n-tridecane secretions markedly increased. In repellency trials on water agar plates, J2 avoided 2,4-di-tert-butylphenol, n-tridecane, and 3,3-dimethyloctane at concentrations of 4 mmol/liter. In a linked twin-pot assay, inoculation with 2,4-di-tert-butylphenol or 3,3-dimethyloctane reduced the number of nematodes in the soil (by 54.9 and 70.6%, respectively), the number of galls (by 53.7 and 52.4%), and the number of M. incognita in root tissues (by 67.5 and 36.3%). BCM2 colonization in tomato roots affected the composition of root exudates, increasing the secretion of substances that appear to be repellent, thus decreasing M. incognita J2 infection of roots.



Nematologica ◽  
1997 ◽  
Vol 43 (1) ◽  
pp. 117-120 ◽  
Author(s):  
A.E.P. Christophers ◽  
M.N. Patel ◽  
J.A. Benson ◽  
V.W. Saka ◽  
A.A.F. Evans ◽  
...  


2005 ◽  
Vol 30 (6) ◽  
pp. 629-633 ◽  
Author(s):  
Liziane M. Lima ◽  
Maria F. Grossi-de-Sa ◽  
Railene A. Pereira ◽  
Rosane H.C. Curtis

Molecules expressed at the surface cuticle (SC) of plant parasitic nematodes represent the primary plant-nematode interface, and together with secreted-excreted (S-E) products are probably the first signals perceived by the host. These molecules, which are released into plant tissue, probably play important roles in the host-parasite interactions. Characterisation of these antigens will help in the identification of nematode targets useful for novel control strategies, which interfere with the nematode infection of plants. Three monoclonal (MAbs) and three polyclonal (PAbs) antibodies produced to S-E products of Meloidogyne spp. and Heterodera avenae were used to examine their reactivity towards M. incognita and/or M. arenaria second stage juveniles and adult females. The three PAbs showed cross-reactivity with M. incognita and M. arenaria. Antibody Roth-PC 373 strongly recognised molecules present in the SC, amphids and intestine, antibody Roth-PC 389 recognised the nematode amphids and metacorpus, while antibody Roth-PC 419 bound to molecules present in the subventral glands. Reactivity of the MAbs was only tested against M. arenaria. Monoclonal antibody Roth-MAb T116C1.1 showed intense reactivity with molecules present in the amphidial and phasmidial glands. Monoclonal antibodies Roth-MAb T46.2 and T42D.2 labeled the nematode amphids and molecules present in the nematode oesophagus (metacorpus), respectively.



2015 ◽  
Vol 3 (1) ◽  
pp. 1-5
Author(s):  
Ganesh Ghimire ◽  
Ranjana Gupta ◽  
Arvind K Keshari

Various concentrations of aqueous leaf extract of Lantana camara L. were assessed against second stage juveniles (J2) of Meloidogyne spp. (Goeldi, 1982) for its nematicidal potency in vitro conditions. Study showed 50% concentration of Lantana camara leaf extract at 48 hrs of incubation period and above showed effective in immobilizing second stage of larvae (J2) of Meloidogyne spp. The standard concentration ‘S’ (100%) of leaf extract was found to be highly nematostatic, 98.66% of nematode were found dead in 48 hrs. Similarly, 57.66% of nematode juveniles were found dead when applied 50% concentration in 48 hrs. Mean number of (J2) dead at 100% concentration for three time period was statistically significant highest at 48 hrs. So far, 50% concentration in 48 hrs and above was appropriate for controlling the root-knot nematode which seems as an alternative to chemical pesticides.



Plant Disease ◽  
2016 ◽  
Vol 100 (8) ◽  
pp. 1725-1734 ◽  
Author(s):  
Carla M. Maleita ◽  
Ana M. S. F. de Almeida ◽  
Nicola Vovlas ◽  
Isabel Abrantes

Meloidogyne megadora infects coffee trees, an economically important crop worldwide. The accurate identification of M. megadora is essential for the development of preventive measures to avoid the dispersion of this pathogen and establishment of efficient and sustainable integrated pest management programs. One M. megadora isolate was studied by biometrical, biochemical, and molecular characteristics (random amplified polymorphic DNA [RAPD] and PCR of internal transcribed spacer [ITS] region). Biometrical characteristics of M. megadora females, males, and second-stage juveniles were similar to the original description. Biochemical studies revealed a unique enzyme pattern for M. megadora esterases (Me3) that allowed for species differentiation. Three RAPD primers (OPG-4, OPG-5, and OPG-6) produced specific bands to all Meloidogyne spp. studied: M. megadora, M. arenaria, M. incognita, and M. javanica. Molecular analysis of the ITS region resulted in an amplification product of 700 bp. The phylogenetic relationship between M. megadora and several Meloidogyne spp. sequences was analyzed, revealing that M. megadora clearly differs from the most common root-knot nematode species. Based on the studies conducted, isozyme analysis remains a useful and efficient methodology for M. megadora identification when females are available. Further studies will be needed to convert the M. megadora differential DNA fragment obtained by RAPD and develop a species-specific sequence-characterized amplified region PCR assay for its diagnosis based on second-stage juveniles.



2014 ◽  
Vol 6 (3) ◽  
pp. 233-238
Author(s):  
Duc Hieu Duong ◽  
Xuan Quang Ngo ◽  
Dang Giap Do ◽  
Thi Anh Hong Le ◽  
Vu Thanh Nguyen ◽  
...  

Neem cake is a product of the cold pressing from the neem kernels to obtain neem oil. Bio-active substances from neem cake extracted solutions were evaluated for their potential to control the root knot nematodes and other pests of plants. In this study different concentrations of the solution extracted from neem cake was tested against the second stage juveniles of the plant parasitic nematode Meloidogyne spp. and four phytopathogenic fungi: Rhizoctonia solani, Sclerotium rolfsii, Collectotrichum spp. and Phytopthora capsici. Toxicity of neem cake extractions is represented by the EC50 value for the second-stage juvenile (J2) of Meloidogyne spp. and the four phytopathogenic fungi via Probit analysis. A 5% dilution of the solvent extracting from neem cake already caused 100% larval mortality after 24 hours exposure. Undiluted neem cake extraction effectively inhibited the growth of the four phytopathogenic fungi. The EC50 value of neem cake on J2-larvae of Meloidogyne nematode and on the fungi Rhizoctonia solani, Sclerotium rolfsii, Collectotrichum spp. and Phytophthora capsici was 0.51, 0.74, 0.30, 0.51 and 4.33%, respectively. Bánh dầu neem là sản phẩm của quá trình ép nhân hạt neem để lấy dầu. Các hoạt chất sinh học từ dịch chiết bánh dầu neem đã được đánh giá có tiềm năng lớn trong phòng trừ tuyến trùng nốt sưng và các loài dịch hại khác của nhiều loại cây trồng. Trong nghiên cứu này các nồng độ dịch chiết khác nhau của bánh dầu neem đã được thử nghiệm khả năng diệt tuyến trùng (ấu trùng tuổi 2 thuộc giống Meloidogyne spp.) và ức chế 4 loài nấm bệnh như: Rhizoctonia solani, Sclerotium rolfsii, Collectotrichum spp. và Phytopthora capsici. Độc tính của dịch chiết bánh dầu neem được biểu diễn bởi giá trị EC50 đối với ấu trùng tuổi 2 của tuyến trùng Meloidogyne spp. và các loài nấm bệnh thông qua phân tích Probit. Dịch chiết bánh dầu neem ở nồng độ 5% đã làm chết 100% cá thể IJ2 của Meloidogyne spp sau 24 giờ phơi nhiễm. Dịch nguyên chất bánh dầu neem ức chế cả 4 loài nấm bệnh. Giá trị EC50 của bánh dầu neem lên ấu trùng tuổi 2 của Meloidogyne spp và các loài nấm bệnh Rhizoctonia solani, Sclerotium rolfsii, Collectotrichum spp. and Phytophthora capsici tương ứng là 0.51, 0.74, 0.30, 0.51 và 4.33%.



Plant Disease ◽  
2007 ◽  
Vol 91 (7) ◽  
pp. 908-908 ◽  
Author(s):  
N. Viaene ◽  
D. B. Wiseborn ◽  
G. Karssen

The root-knot nematode, Meloidogyne minor, was described during 2004 after it was found on potato roots in a field in the Netherlands and in golf courses in England, Wales, and Ireland (2). Since it is associated with yellow patch disease in turf grass and causes deformation of potato tubers (2), it is important to know whether this organism is already widespread in these and neighboring countries. In addition, it has a relatively wide host range (2,4). A small survey conducted in Belgium was comprised of 10 golf courses geographically spread over the country. In each location, 3 to 9 samples were taken (one per green) consisting of 30 to 40 cores (1.5 × 20 cm deep). Nematodes were extracted from a 200-g subsample (containing roots) from each sample using zonal centrifugation (1). All Meloidogyne spp. were mounted on semipermanent slides and identified morphologically. M. minor was discovered in 3 of 6 samples taken in April 2006 from a golf course in Hasselt (northeastern Belgium). Between 41 and 50 M. minor per 100 g of soil were found together with M. naasi (7 to 20 individuals per 100 g of soil). Occurrence of M. minor together with other Meloidogyne species has been reported in natural and cultivated sites (2,4). Moreover, spores of Pasteuria spp. were clearly visible on 42% of the observed second-stage juveniles of M. minor, but not on those of M. naasi. The infected juveniles had between 2 and 15 spores attached to their cuticles. Additional juveniles were extracted from the soil samples and used for molecular identification by real-time PCR (2), which confirmed the presence of M. minor. There were no symptoms on the grass, consisting of a mixture of Agrostis stolonifera (10%), Festuca rubra (30%), and Poa annua (60%). Grass was sown in Rhine sand and heath land compost used for the construction of the greens in Hasselt. It could be that these soil amendments were infested with M. minor or that M. minor was introduced by other means, e.g., shoes, maintenance machinery, or golf equipment. On the other hand, the detection of M. minor in this small survey indicates that the species may be prevalent in golf courses in the region. The nematode has been found in several golf courses and sport fields in the United Kingdom and the Netherlands, including a golf course at Breda (close to the Belgian border) (3). The survey will be expanded to include grasslands and dune areas, the presumed natural habitat of M. minor. References: (1) G. A. Hendrickx. Nematologica 41:308, 1995. (2) G. Karssen et al. Nematology 6:59, 2004. (3) W. Lammers et al. Meloidogyne minor. Pest Risk Assessment. Online publication, www.minlnv.nl/pd - Schadelijke organismen, 2006. (4) S. J. Turner and C. C. Fleming. Comm. Appl. Biol. Sci. Ghent University 70:885, 2005.



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