The relationship of crops grown in rotation or in succession has increased every day and the use of antagonistic plants and/or non-host plants is one of the most efficient practices of integrated management of nematodes. This study aimed to evaluate the efficiency of crotalaria (Crotalaria spectabilis Roth) and millet [Pennisetum glaucum (L.) Leeke] ‘ADR 300’ in reducing the population of Meloidogyne incognita and M. javanica and in increasing the productivity of okra [Abelmoschus esculentus (L.) Moench] when cultivated in succession. The experiment was conducted in an area cultivating okra (host culture) in rotation, with a history of severe infestation by phytonematoids. The experimental design involved randomized blocks with six treatments and four replicates, with the following treatments: T1, 15 kg.ha-1 of millet seeds; T2, 30 kg.ha-1 of crotalaria; T3, 10 kg.ha-1 of millet + 20 kg.ha-1 of crotalaria; T4, 20 kg.ha-1 of millet + 6 kg.ha-1 of crotalaria; T5, 6 kg.ha-1 of millet + 36 kg.ha-1 of crotalaria; and T6, control. The nematode populations in the soil and roots were evaluated about 60 d after planting okra, and the yield was evaluated at the end of the crop cycle. Simple treatment with millet or crotalaria reduced the nematode population by 61% and 72%, respectively. The millet-crotalaria intercropping treatments reduced the nematode population by up to 85% compared with the control. In terms of productivity, there was an increase of 787 kg.ha-1 in the millet treatment and 2,109 kg.ha-1 in the intercropping treatments. Both the single cultivation of crotalaria or millet and the consortia of crotalaria and millet were effective in controlling the root-knot nematodes, and increased the productivity of okra.
The production of common bean (Phaseolus vulgaris L.) may be compromised by a variety of pests and diseases, with root-knot nematodes standing out among the soil-borne pathogens that cause significant losses. It was assessed the reaction of common bean genotypes to the reproduction of these nematodes, with emphasis on the two species most frequently found parasitizing the crop: Meloidogyne javanica and Meloidogne incognita. The experiments were conducted in a greenhouse, using a completely randomized design, with 26 treatments (genotypes), ten replications and plot consisting of a pot containing one plant. Each plot was inoculated with 1,000 eggs and second-stage juveniles and assessed at 62 days after the inoculation, when the final populations were estimated. The genotypic resistance was determined based on two criteria: reproduction factor and index. All the genotypes were susceptible to M. incognita according to both assessment criteria. The IAC Alvorada, IAC Imperador, BRS Esplendor and BRS Esteio cultivars, although may be classified as resistant to M. javanica by the reproduction factor, are classified only as moderately resistant if the assessment criterion is the reproduction index.
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The soybean cyst nematode (SCN), Heterodera glycines, is present in more than 150 municipalities in Brazil, and the long persistence of the cysts in the soil combined with the severe degree of parasitism induces high soybean production losses. The objective of this study was to evaluate the biofumigant effect of Crambe abyssinica on the SCN population in the second soybean crop season. The experiment was conducted on a rural property whose soil was naturally infested with SCN. Crambe abyssinica was planted in the second crop season following harvest, and in the subsequent crop season, 4 soybean varieties, 2 resistant and 2 susceptible to SCN, were planted. The nematode population was evaluated every month for 90 days after planting. In the second crop season, when C. abyssinica was in the field, there was a significant decrease in the number of adult SCN females and cysts. During the 90-day period after C. abyssinica cultivation, when plant residues were incorporated into the soil and the area was planted with soybeans, both the number of adult SCN females / 10 g roots and the number of cysts decreased. This result indicates that C. abyssinica reduced the nematode population during its time in the field.
In 2019, during a nematologic survey in Jaboticabal, Brazil, root-knot nematode Meloidogyne incognita parasitizing hops ( Humulus lupulus ) was identified with based on morphological characters of adults, esterase phenotypes ( n = 16), and molecular analysis. Modified Koch’s postulates was carried out and after 90 days, the average total population recovered had different stages of development, with a reproductive factor (RF) of 4.81. This is the first report of H. lupulus as a host of M. incognita in the state of São Paulo and in Brazil.
The sweetpotato (Ipomoea batatas L., Convolvulaceae family) originated in Latin America and is currently cultivated worldwide. The storage roots, rich in calories, have made this crop one of the main caloric sources for low-income populations, especially in developing countries. Brazil annually produces about 805,000 tons, with the Northeast region responsible for 34% of this production (Albuquerque et al. 2020). In October 2019, sweetpotato plants cv. Campina, from a field in the region of Touros, state of Rio Grande do Norte (RN), Brazil (5°12’31”S 35°34’42”W), presented deformed storage roots, with galls, typical of root-knot nematodes. The roots were sent to the Nematology Laboratory (LabNema) where 14,032 eggs and 3,312 second-stage juveniles (J2s) of Meloidogyne sp., in 10 g of roots, were recovered. The species of adults was identified through morphological, biochemical, and phylogenetic analysis. The perineal region of females (n = 10) presented an oval shape, with a high and semi-trapezoidal dorsal arch and streak-free perivulval region. The labial region of males (n=10) presented high and rounded head cap, labial region slightly set off from the body, without annulations. The morphological characters were compatible with the original description of Meloidogyne enterolobii (Yang and Eisenback 1983). The phenotype of esterase isoenzymes showed two major bands (VS1-S1) also characteristic of M. enterolobii (Esbenshade and Triantaphyllou 1985). Sequences of 18S rDNA (~1200bp) of individual females (Holterman et al. 2006) obtained from sweetpotatoes before (SPme1 and 2) and after inoculation (SPme3 and 6), and from guava, used as M. enterolobii species control, were submitted to Bayesian analysis. The sequences presented genetic diversity among them resulting from seven SNPs (Single Nucleotide Polymorphism) and 99.4 to 99.9% identity with M. enterolobii sequences deposited in the NCBI GenBank (accession numbers MW209034-MW209039). The pathogenicity test was carried out under greenhouse conditions, in which 3,000 eggs and J2s from the original population isolated of M. enterolobii were inoculated in sweetpotato seedlings cv. Campina (n = 6). After three months, the roots presented galls and deformations typical of root-knot nematodes, while non-inoculated plants did not present any symptoms. An average of 15,900 eggs and J2s of M. enterolobii (RF = 5.3) were recovered from the roots, proving that sweetpotatoes were a host of this species. Meloidogyne enterolobii is known to cause great damage to sweetpotato (Ye et al. 2020). In Brazil, Meloidogyne nematode had been reported once, isolated from a sweetpotato field in the Ceara state and the species suggested by the authors according to esterase electrophoresis was M. enterolobii. Nonetheless, the authors did not present taxonomic, isoenzyme phenotypes and molecular species identification integratively, nor included pathogenicity tests (Silva et al. 2016). Therefore, it is the first time that M. enterolobii, with reliable identification by different methods, including sequencing, was detected in commercial sweetpotato fields in the RN state and in Brazil. The local farmers reported that this nematode deforms the storage roots which make them useless for commercialization, resulting in minimal losses of 50% of production in the infested areas. Furthermore, as sweetpotatoes are vegetatively propagated, the spread of this nematode through planting material is favored. Considering the importance of this crop in Brazil, this report is essential for control measures of this pathogen to be taken in order to avoid its spread to other regions.
Sugarcane crops Saccharum spp. (Poales: Poaceae) produces different derivatives to the world: sugar, ethanol and bioenergy. Despite the application of pesticides, insect pests still cause economic losses, among these the pink sugarcane mealybug Saccharicoccus sacchari (Cockerell, 1895) (Hemiptera: Pseudococcidae) causing direct and indirect damage to the plant. This study assess the virulence of three entomopathogenic nematodes (EPNs) species and their symbiont bacteria against the pink sugarcane mealybug, under laboratory conditions. Fourteen treatments represented by control (distilled water), Heterorhabditis bacteriophora Poinar, 1976 (HB EN01) (Rhabditida: Heterorhabditidae), Steinernema rarum (Doucet, 1986) (PAM25) and Steinernema carpocapsae Weiser, 1955 (All) (Rhabditida: Steinermatidae) at concentrations of 25, 50, 75 and 100 infective juveniles (IJs)/insect, and the standard chemical product, thiamethoxam, were assayed. In a second experiment, the bacteria Photorhabdus luminescens (Thomas and Poinar, 1979), Xenorhabdus szentirmaii Lengyel, 2005 and Xenorhabdus nematophila (Poinar and Thomas, 1965) (Enterobacterales: Morganellaceae) at 3.0 x 109 cells/ml were assessed for each treatment. Ten replications were stablished, each one counting ten females/mealybugs inside a 10 cm Petri dish, amounting 100 individuals/treatment. All treatments were kept under stable conditions (25±1 ºC, H 70±10%, in the dark). All nematodes species infected S. sacchari. Steinerma rarum (PAM25) provided the highest mortality against the pink sugarcane mealybug (79.25%), followed by H. bacteriophora (HB EN01) (58.25%) and S. carpocapsae (All) (42.50%) (P<0.001). The mortality rate caused by X. szentirmaii, P. luminescens and X. nematophila were 40, 45 and 20%, respectively. Steinerma rarum (PAM25) has conditions to be a potential agent to be incorporate into the integrated pest management in sugarcane.
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