scholarly journals OCCURRENCE OF MELOIDOGYNE JAVANICA PARASITING ROOTS AND NODULES OF PEANUTS IN PARAGUAY

Bragantia ◽  
1997 ◽  
Vol 56 (1) ◽  
pp. 87-89
Author(s):  
RUBENS RODOLFO ALBUQUERQUE LORDELLO ◽  
ANA INES LUCENA LORDELLO ◽  
IGNÁCIO JOSÉ DE GODOY

The root-knot nematode Meloidogyne javanica (Treub, 1885) Chitwood, 1949, was identified in roots, nodules and shells of peanut plants (Arachis hypogaea L.), cv. Florman-INTA, collected from a field in Menno colony, Chaco Central region of Paraguay. Infected plants were observed in patches, showing wilting and drying of vegetative parts. Peanut had been grown ininterruptly for many years in the same area and patches had already been observed in the preceding year in cv. Starr. Nematodes collected from roots in this field reproduced on tomato cultivar rutgers and peanut cultivar florunner and produced egg-masses on roots, nodules and shells of cultivar Florman. This is the first report on M. javanica parasiting peanut in Paraguay.

Plant Disease ◽  
2001 ◽  
Vol 85 (9) ◽  
pp. 1030-1030 ◽  
Author(s):  
S. H. Thomas ◽  
J. M. Fuchs ◽  
Z. A. Handoo

For several years, decline was observed in mature pecan (Carya illinoensis (F.A. Wangenheim) K. Koch) trees in an orchard in Dona Ana County, New Mexico despite normal fertilization and irrigation practices. Affected trees were growing in sandy soil in two widely separated irrigation terraces and exhibited chlorosis of foliage and substantial die-back of branches in the upper canopy. Examination of feeder roots revealed the presence of numerous small galls and egg masses, with root-knot nematode females often visibly protruding from root tissue. Attempts to culture the nematode on tomato (Lycopersicon esculentum Mill. ‘Rutgers’) were unsuccessful. Females and egg masses were collected from fresh pecan roots and sent to the USDA Nematology Laboratory in Beltsville, MD, in October 2000, where specimens were identified as Meloidogyne partityla Kleynhans (1) based on morphological examination. This is the first report of M. partityla from New Mexico, and the second report of this nematode outside South Africa. Starr et al. (2) first reported M. partityla from pecan in the United States in 1996, after recovering the nematode from five orchards in Texas. In their study, the host range of M. partityla was limited to members of the Juglandaceae, which may explain the inability of the New Mexico population to reproduce on tomato. Additional information is needed regarding distribution of this nematode within pecan-growing regions throughout North America. References: (1) K. P. N. Kleynhans. Phytophylactica 18:103, 1986. (2) J. L. Starr et al. J. Nematol. 28:565, 1996.


2018 ◽  
Vol 50 (4) ◽  
pp. 543-544 ◽  
Author(s):  
J. A. Brito ◽  
S. A. Subbotin ◽  
J. Desaeger ◽  
F. Achinelly ◽  
S. Qiu

Plant Disease ◽  
2014 ◽  
Vol 98 (9) ◽  
pp. 1286-1286 ◽  
Author(s):  
N. Walker

Meloidogyne marylandi is a nematode commonly associated with turfgrasses and has been reported to occur in Texas and Arkansas (1,3). In the fall of 2013, a stand of ultradwarf bermudagrass (Cynodon dactylon × C. transvaalensis) plants in a sand-based, research putting green in Stillwater, Oklahoma, exhibited symptoms of decline. Roots of the affected plants had small galls and upon staining of the root system, numerous egg masses were evident. Egg masses were collected, placed in water, and the morphology of 20 hatched, second-stage juveniles were examined. The characteristics of the juveniles were: body length averaged 393.1 ± 19.87 (range: 361 to 425) μm, mean width averaged 16.6 ± 0.7 (15.6 to 17.8) μm, stylet lengths averaged 12.1 ± 0.7 (10.4 to 12.9) μm, dorsal gland orifice from stylet base averaged 2.9 ± 0.4 (2.5 to 3.6) μm, tail lengths averaged 53.7 ± 3.8 (46.2 to 60.4) μm, and the hyaline region of the tails averaged 10.4 ± 1.1 (8.4 to 12.7) μm. Genomic DNA was extracted from six females that were removed from roots. Amplification and sequencing of the mitochondrial DNA region between COII and 16S rRNA genes was performed with primers 1RNAF (5′-TACCTTTGACCAATCACGCT-3′) and CO11R (5′-GGTCAATGTTCAGAAATTTGTGG-3′) as previously described (2). A PCR product approximately 510 bp in length was obtained and sequenced at the Oklahoma State University Core Facility. Sequences were compared with those in NCBI's nucleotide database using BLAST and had 97% identity with two sequences from M. marylandi (KC473862.1 and KC473863.1) and the next most similar species being M. graminis (JN241898.1) with 83% identity. To our knowledge, this is the first report of the root-knot nematode M. marylandi in Oklahoma. As bermudagrass becomes more commonly used for putting greens in the turfgrass transition zone, M. marylandi may become a more common and damaging pathogen in the region. References: (1) A. A. Elmi et al. Grass For. Sci. 55:166, 2000. (2) M. A. McClure et al. Plant Dis. 96:635, 2012. (3) J. L. Starr et al. Nematrop. 37:43, 2007.


HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 622a-622 ◽  
Author(s):  
W. R. Maluf ◽  
S. M. Azevedo ◽  
V.P. Campos

Heritabilities for resistance to root knot nematodes (Meloidogyne javanica and Meloidogyne incognita races 1, 2, 3, and 4) were studied in a population of 226 sweetpotato clones of diverse origin. For each nematode isolate tested, 128-cell speedling trays were filled with previously inoculated substrate (30000 eggs/1000 mL substrate). Sweetpotato clones suitably tagged and identified were randomly planted in the cells (one plant/cell), with a total of four plants per clone per isolate. Ninety days after inoculation, sweetpotato plants had their roots washed for substrate removal, and treated with 150 mg·L–1 Phloxine B to stain nematode egg masses. The number of egg masses per root was recorded, and plants were accordingly assigned scores from 0 (highly resistant) to 5 (highly susceptible). Broad-sense heritability estimates were 0.87, 0.91, 0.81, 0.95, and 0.93 respectively for resistance to M. javanica and races 1, 2, 3, and 4 of M. incognita. The frequencies of resistant genotypes were higher for M. javanica and lower for M. incognita race 2. Genotypic correlations (rG) among the resistances to the various Meloidogyne isolates utilized were weak, ranging from 0.11 to 0.57, suggesting independent genetic controls. Clones could be selected, however, with high levels of resistance to all nematode isolates tested. (This work was supported by CNPq, CAPES, FAPEMIG, and FAEPE/UFLA.)


2000 ◽  
Vol 27 (2) ◽  
pp. 78-82 ◽  
Author(s):  
P. Timper ◽  
C. C. Holbrook ◽  
H. Q. Xue

Abstract The peanut root-knot nematode (Meloidogyne arenaria, race 1) is a world-wide pest of peanut (Arachis hypogaea L.). Several moderately resistant genotypes have been identified in the cultivated peanut species. Our objective was to determine the expression of resistance for six of these genotypes. We examined four potential expressions of resistance—(a) fewer second-stage juveniles (J2) penetrate the roots, (b) fewer J2 establish functional feeding sites, (c) slower maturation, and (d) reduced fecundity (eggs per female). Seedlings of the susceptible cultivar Florunner and the resistant genotypes were inoculated with J2 of M. arenaria, and transplanted 3 d later to synchronize nematode development. Penetration was assessed at 3 and 10 d; development at 10 (or 12), 17, 22, and 27 d; and fecundity at 60 d after inoculation. The experiments were conducted in a greenhouse or growth chamber. The number of J2 within the roots was similar in resistant and susceptible peanut after 3 d; however, numbers were lower in two of the resistant genotypes than in Florunner after 10 d. A greater percentage of J2 failed to develop in all of the resistant genotypes (72 to 79%) than in Florunner (50%) after 17 d. Of the J2 that did begin to develop, the rate of maturation and fecundity was similar in resistant and susceptible genotypes. A lack of development indicates that the J2 failed to establish a feeding site. Therefore, the primary expression of resistance in the six peanut genotypes appears to be a reduction in the percentage of J2 that establish a functional feeding site. The decline in J2 after infection may be related to the failure to establish a feeding site.


2001 ◽  
Vol 28 (2) ◽  
pp. 80-84 ◽  
Author(s):  
C. C. Holbrook ◽  
T. G. Isleib

Abstract The U.S. maintains a large (> 8000 accessions) and genetically diverse collection of peanut (Arachis hypogaea L.) germplasm. It is costly to screen all accessions within this collection for traits that could be useful in cultivar development. The objective of this research was to identify countries of origin that are rich sources of resistance to important peanut diseases. This would allow peanut breeders to focus their efforts on smaller subsets of the germplasm collection. Accessions in the peanut core collection were evaluated for resistance to late (Cercosporidium personatum Berk. & M. A. Curtis) and early (Cercospora arachidicola Hori) leaf spot, tomato spotted wilt Tospovirus (TSWV), the peanut root-knot nematode [Meloidogyne arenaria (Neal) Chitwood race 1], and Cylindrocladium black rot (CBR)[Cylindrocladium crotalarie (Loos) Bell & Sobers]. These data then were examined to determine if genes for resistance clustered geographically. Several geographical areas that appear to be rich sources for disease-resistant genes were identified. China had a relatively large number of accessions with resistance to the peanut root-knot nematode. Peru appeared to be a rich source of material with resistance to CBR. Resistance to late leaf spot was more frequent than expected in accessions from Bolivia and Ecuador. Bolivia was also a valuable source of resistance to early leaf spot. Early leaf spot resistance also was more prevalent than expected in accessions from India, Nigeria, and Sudan. India, Israel, and Sudan were valuable origins for material with resistance to TSWV. Accessions with multiple disease resistance were most common in India, Mozambique, and Senegal. This information should enable plant breeders to utilize more efficiently the genes for disease resistance that are available in the U.S. germplasm collection.


1993 ◽  
Vol 20 (1) ◽  
pp. 66-71 ◽  
Author(s):  
N. A. Minton ◽  
T. B. Brenneman ◽  
K. Bondari ◽  
G. W. Harrison

Abstract The efficacy of fosthiazate, a new organophosphorus compound, against the peanut root-knot nematode (Meloidogyne arenaria (Neal) Chitwood), thrips (Frankliniella spp.), and southern stem rot (Sclerotium rolfsii Sacc.) in peanut (Arachis hypogaea L.) was studied for 2 years at Tifton, Georgia. Different rates and methods of applying granular and emulsifiable concentrate formulations of fosthiazate were compared with rates and methods of applying granular fenamiphos and aldicarb which were included as standard treatments. When compared with untreated controls, all treatments of all compounds increased peanut yield and reduced nematode galls on peanut roots, pods, and pegs and thrips damage to foliage significantly in both years. The treatments, however, varied in their effects on southern stem rot. Peanut yields from plots treated with equal rates of the granular and emulsifiable concentrate formulations of fosthiazate were similar. Yields of plots treated with fosthiazate at different rates compared favorably with those treated with comparable rates of fenamiphos and aldicarb. Fosthiazate increased peanut yield as much as 214% in 1990 and 64% in 1991, but yields varied with rates applied.


Plant Disease ◽  
2020 ◽  
Vol 104 (10) ◽  
pp. 2740-2740
Author(s):  
D. D. Nascimento ◽  
R. F. Gonsaga ◽  
A. Souza Pollo ◽  
L. S. M. Santos ◽  
R. J. Ferreira ◽  
...  

Plant Disease ◽  
2021 ◽  
Author(s):  
Saira Martínez-Salgado ◽  
Omar Romero-Arenas ◽  
Luis A. Morales-Mora ◽  
Alfonso Luna-Cruz ◽  
José A. Rivera-Tapia ◽  
...  

Peanut (Arachis hypogaea L.) is the third most important oilseed crop in the world. The cultivated area in Mexico is currently 52,046 ha with a production of 91,109 ton in 2018 (FAO, 2020). Puebla state ranks third in the national production with 9,313 ton (SIAP, 2020). In September 2019, typical symptoms of charcoal rot (Macrophomina phaseolina (Tassi) Goid.) were observed in about 50% of cultivar Virginia Champs peanuts, and it affecting 1.5 ha located in Chietla (18° 27' 39" N; 98° 37' 11" W), Puebla, Mexico. Diseased plants showed brown discoloration in stem and root rot, with chlorotic foliage, dark microsclerotia were observed on the stem and premature dying. To isolate the causal agent of these symptoms, 20 infected plants were recovered and processed in the laboratory. Ten pieces of stem and root tissue were selected from each plant, cut into small pieces 5-mm in length, superficially disinfested with 1% sodium hypochlorite for 3 min, followed by three rinses with sterile distilled water. Later, dried on sterile paper and placed on Petri plates containing potato dextrose agar (PDA) medium, which were kept at 28°C for 7 days (12 h light and 12 h dark). Four colonies were purified via hyphal tip culture, fungus was consistently isolated from the analyzed tissues; additional microcultures were prepared to observe phenotypic characteristics. Colonies showed dense growth, with a gray initial mycelium, becoming black after 7 days. Microesclerotia with spherical to oblong in shape were observed after 5 days on PDA, with a black coloration, measuring an average of 74 µm width × 110 µm length (n=40). Phylogenetic analysis was conducted by amplification and sequencing of the internal transcribed spacer (ITS) region with the ITS5 and ITS4 primers (White et al. 1990). The obtained sequences were deposited in GenBank database under accession numbers: MW585378, MW585379, MW585380, and MW585381 containing approximately 601 bp of the ITS1-5.8S-ITS2 region (complete sequence); they were 99% identical with the reference sequence of Macrophomina phaseolina (GenBank accession KF951698) isolated in Phaseolus vulgaris from Mexico. Based on the symptoms in the field, colony morphology, color, and shape of the microsclerotia, and molecular identification, the fungus was identified as M. phaseolina (Tassi) Goid. The pathogenicity test was performed on peanut plants cultivar Virginia Champs grown on plastic pots with an autoclaved peat/soil mixture under greenhouse conditions (70% relative humidity and 28°C). Fifty two-month-old peanut plants were inoculated using the toothpick method. The toothpicks were previously sterilized and then placed in Petri plates with each of the four colonies of M. phaseolina until colonization. Small wounds were made with those toothpicks in the roots, and a sterile toothpick was used in the control plants, the assays were performed twice. After three weeks, the inoculated plants exhibited symptoms of wilting chlorosis on the leaves and brown to dark brown discoloration of the vascular ring, while control plants remained healthy. M. phaseolina was re-isolated from symptomatic root tissues and identified by phylogenetic approach, fulfilling Koch’s postulates. To date, this fungus affects at least 372 hosts globally causing yield losses. Although in Mexico this fungus has been documented in Glycine max, Ipomoea batatas, Phaseolus vulgaris, Physalis ixocarpa, Saccharum officinarum, Sesamum indicum, Solanum melongena, S. tuberosum, and Sorghum bicolor (Farr and Rossman 2021). However, there are no reports of M. phaseolina as a potential pathogen on peanut; therefore, according to our knowledge, this is the first report of this fungus affecting A. hypogaea in Mexico.


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