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Adjustment of inoculum levels for the evaluation of carrot genotypes resistance to Meloidogyne incognita

Ajuste de níveis de inóculo para avaliação da resistência de genótipos de cenoura a Meloidogyne incognita

ABSTRACT

One of the main phytopathogens that cause enormous economic losses in several agricultural species, including carrots, are the root-knot nematodes belonging to the genus Meloidogyne. Thus, in order to identify the best population level for inoculum of the root-knot nematode (Meloidogyne incognita) for maximum expression of symptoms of this nematode attack on carrots, an experiment was carried out to evaluate the carrot cultivar Brasília (CBR) and the population Pop-750 (CRO). The experiment was carried out in a greenhouse at Embrapa Vegetable, Brasília-DF, in 5 L pots, with six replications, in a 4x2 factorial scheme in a completely randomized design, in the dosages of 0, 1, 5 and 10 thousand eggs and occasional juveniles of 2nd stage (E+J2R). ‘Rutgers’ susceptible tomato cultivar was used as control to verify inoculum efficiency. Inoculation was carried out 30 days after sowing and evaluation 60 days after inoculation. Gall index (GI), egg mass index (EMI), number of eggs plus occasional second stage juveniles per gram of root (E+J2R) and reproduction factor (RF) were performed. There were differences between genotypes and between inoculum levels for all variables evaluated. For CRO, inoculum levels of M. incognita from 1,000 E+J2 the plants already manifested symptoms and changes in all evaluated variables, with ideal levels around 5 to 7 thousand E+J2R, above 7 thousand E+J2R nematode multiplication to express symptoms decreased. For CBR the response variables E+J2 at root and RF inoculum levels close to 5 thousand E+J2R also present the best results, but when the characterization is based on the evaluation of GI and EMI, suitable inoculum levels would be close to 9 and 12 thousand E+J2R.

Keywords:
Daucus carota; resistance; root-knot nematodes; dose

RESUMO

Um dos principais fitopatógenos que causam prejuízos econômicos em diversas espécies agrícolas, inclusive cenoura, são os nematoides-das-galhas, pertencentes ao gênero Meloidogyne. Assim, com o objetivo de identificar o melhor nível populacional de inóculo de Meloidogyne incognita para a máxima expressão de sintomas do ataque de nematoides-das-galhas em cenoura, foi realizado um experimento que avaliou os genótipos de cenoura cv. Brasília (CBR) e a população Pop-750 (CRO). O experimento foi conduzido em casa de vegetação da Embrapa Hortaliças, Brasília-DF em vasos de 5 L, com seis repetições, em esquema fatorial 4x2 em delineamento inteiramente casualizado, nas dosagens de 0, 1, 5 e 10 mil ovos e eventuais juvenis de segundo estádio (O+J2R). O tomateiro suscetível ‘Rutgers’ foi utilizado como testemunha para verificar eficiência do inóculo. A inoculação foi realizada 30 dias após a semeadura e, a avaliação, 60 dias após a inoculação. Foi realizada a avaliação dos índices de galhas (IG) e de massas de ovos (IMO), do número de ovos mais eventuais juvenis de segundo estádio por grama de raiz (O+J2R) e do fator de reprodução (FR). Houve diferenças entre os genótipos e entre os níveis de inóculo para todas as variáveis avaliadas. Para CRO, os níveis de inóculo de M. incognita a partir de mil O+J2 as plantas já manifestaram sintomas e alterações para todas as variáveis avaliadas, com os níveis ideais em torno de 5 a 7 mil O+J2R, sendo que acima de 7 mil O+J2R a multiplicação do nematoide para expressar sintomas diminuiu. Para a CBR, as variáveis índices O+J2R na raiz e FR, os níveis de inóculo próximos a 5 mil O+J2R também apresentam os melhores resultados. Quando a caracterização for baseada na avaliação da formação de galha (IG) e massa de ovos (IMO), os níveis de inóculo adequados seriam entre 9 e 12 mil O+J2R.

Palavras-chave:
Daucus carota; resistência; nematoides-das-galhas; dose

Carrot (Daucus carota) is the most important species of the Apiaceae family due to its social and economic significance. Worldwide more than 39 million tons are produced in an area of 1.1 million hectares, with an average yield of 35 t/ha. China is the largest producing country, achieving a value of 18 million tons (FAO, 2020FAO. Faostats - FAO Statistical Databases. 2020. Avaliable in: Avaliable in:http://www.fao.org/faostat/en/#data/QCL/visualize . acesseced in: Jun.24 2020.
http://www.fao.org/faostat/en/#data/QCL/...
). In Brazil, carrot is among the most popular and consumed vegetables, with an annual volume of 700 thousand tons grown in an estimated area of 20,000 hectares. This carrot growing area is represented primarily by the Alto Paranaíba region in Minas Gerais State, which encompasses half of the country production volume, followed by Marilândia do Sul (Paraná state), Caxias do Sul (Rio Grande do Sul state), Cristalina (Goiás state), and Irecê (Bahia state) (IBGE, 2017INSTITUTO BRASILEIRO DE GEOGRAFIA E ESTATÍSTICA- IBGE. Horticultura: número de estabelecimentos agropecuários e quantidade produzida por produtos da horticultura, 2017. Available at:<https://sidra.ibge.gov.br/tabela/6619#resultado> accessed at: 23/08/2019.; Cunha et al., 2021CUNHA, TGD; VISÔTTO, LE; PINHEIRO, LM; GOD, PIVG; ROSA, JMO; OLIVEIRA, CMG; LOPES, EA. 2021. Distribution of Meloidogyne species in carrot in Brazil. Ciência Rural 51: e20200552. Available at https://doi.org/10.1590/0103-8478cr20200552.
https://doi.org/10.1590/0103-8478cr20200...
).

Several diseases can occur during the carrot growing stages, but root-knot nematodes (RKN) are of particular interest, given that these plant-parasitic nematodes cause significant losses not only in the afore mentioned regions but as well as in all global carrot production areas (Viljoen et al., 2019VILJOEN, JJF; LABUSCHAGNE, N; FOURIE, H; SIKORA, RA. 2019. Biological control of the root-knot nematode Meloidogyne incognita on tomatoes and carrots by plant growth-promoting rhizobacteria. Tropical Plant Pathology 44: 284-291. Available at https://doi.org/10.1007/s40858-019-00283-2.
https://doi.org/10.1007/s40858-019-00283...
). The amplitude of these damages goes from discarding of products classified as unsuitable for marketing, up to areas suffering from recurring infestation, as a result of lack of sound agricultural practices, or its complete abandonment (Pinheiro, 2017PINHEIRO, JB. 2017. Nematoides em hortaliças. 1. ed. Brasília-DF: Embrapa. 194p.).

Meloidogyne incognita, M. javanica, and M. hapla are the major RKN species responsible for carrot losses in Brazil (Cunha et al., 2021CUNHA, TGD; VISÔTTO, LE; PINHEIRO, LM; GOD, PIVG; ROSA, JMO; OLIVEIRA, CMG; LOPES, EA. 2021. Distribution of Meloidogyne species in carrot in Brazil. Ciência Rural 51: e20200552. Available at https://doi.org/10.1590/0103-8478cr20200552.
https://doi.org/10.1590/0103-8478cr20200...
). Their attack is characterized by cell hyperplasia and hypertrophy of the taproots, compromising its classification (Charchar et al., 2000CHARCHAR, JM; VIEIRA, JV; FACION, CE. 2000. Controle de nematoides das galhas em cenoura através de rotação. Fitopatologia Brasileira 5: 329-336.), though in certain circumstances the weight loss is not evident, resulting mostly in forking (Huang et al., 1986HUANG, SP; DELLA VECHHIA, PT; FERREIRA, PE. 1986. Varietal response and estimates of heritability of resistance to Meloidogyne javanica in carrots. Journal of Nematology18: 406-501.). RKN can also induce galling, plant stunting, and root fasciculation (Cunha et al., 2021CUNHA, TGD; VISÔTTO, LE; PINHEIRO, LM; GOD, PIVG; ROSA, JMO; OLIVEIRA, CMG; LOPES, EA. 2021. Distribution of Meloidogyne species in carrot in Brazil. Ciência Rural 51: e20200552. Available at https://doi.org/10.1590/0103-8478cr20200552.
https://doi.org/10.1590/0103-8478cr20200...
). The use of chemical control is not recommended given the fact that its efficiency is uncertain and also expensive (Pinheiro, 2017PINHEIRO, JB. 2017. Nematoides em hortaliças. 1. ed. Brasília-DF: Embrapa. 194p.). Additionally, in Brazil, there are few nematicides registered for carrots, with most of them being highly toxic and pollutant, making this practice inappropriate (Silva et al., 2011SILVA, GO; PINHEIRO, JB; VIEIRA, JV; CARVALHO, ADF. 2011. Seleção para resistência de genótipos de cenoura aos nematoides-das-galhas. Horticultura Brasileira 29: 335-341. Available at https://doi.org/10.1590/S0102-05362011000300013.
https://doi.org/10.1590/S0102-0536201100...
). Crop rotation with legumes, brassicas, or grasses previous to carrot cultivation is being used as a control measure (Charchar & Aragão, 2003CHARCHAR, JM; ARAGÃO, FAS. 2003. Sequência de cultivos no controle de Meloidogyne javanica em campo. Nematologia Brasileira 27: 81-86.). However, this practice is not effective in all situations, besides making the production system more complex.

Thus, improving genetic resistance is considered the best method to overcome RKN. Sources of resistance in carrots have been identified since 1982 by Embrapa Vegetables, and as a result the cultivars Brasília and Tropical were released in the ’80s (Pinheiro, 2017PINHEIRO, JB. 2017. Nematoides em hortaliças. 1. ed. Brasília-DF: Embrapa. 194p.). Boiteux et al. (2000BOITEUX, LS; BELTER, GJ; ROBERTS, AP; SIMON, WP. 2000. RAPD Linkage map of the genomic region encompassing the root-knot nematode (Meloidogyne javanica) resistance locus in carrot. Theoretical and Applied Genetics 100: 439-446. Available athttps://doi.org/10.1007/s001220050057.
https://doi.org/10.1007/s001220050057...
) identified the MJ-1 gene located in chromosome 8 in two carrot genotypes derived from ‘Brasília’ (891091 and 971252). This gene expresses a complete resistance to M. javanica and a partial resistance to M. incognita. Other (Quantitative Trait locus - QTLs) were identified in chromosomes 1, 2, 8, and 9, that explained 27.3% of the genetic effects, all considered of additive nature (Parsons et al., 2015PARSONS, J; MATTHEWS, W; IORIZZO, M; ROBERTS, P; SIMON, P. 2015. Meloidogyne incognita nematode resistance QTL in carrot. Molecular Breeding 35: 1-11. Available at https://doi.org/10.1007/s11032-015-0309-2.
https://doi.org/10.1007/s11032-015-0309-...
). More recently, another gene was identified in the genotype PI 652188, called Mj-2, and also located in chromosome 8. This gene confers a high level of resistance to M. javanica and M. incognita compared to the ‘Imperator 58’ used as susceptible control (Ali et al., 2014ALI, A; MATTHEWS, WC; CAVAGNARO, PF; IORIZZO, M; ROBERTS, PA; SIMON, PW. 2014. Inheritance and mapping of Mj-2, a new source of root-knot nematode (Meloidogyne javanica) resistance in carrot. Journal Heredity 105: 288-291. Available athttps://doi.org/10.1093/jhered/est090.
https://doi.org/10.1093/jhered/est090...
).

Even though resistance sources to RKN are well known, difficulties in the evaluation of progenies in field conditions are patent (Silva et al., 2011SILVA, GO; PINHEIRO, JB; VIEIRA, JV; CARVALHO, ADF. 2011. Seleção para resistência de genótipos de cenoura aos nematoides-das-galhas. Horticultura Brasileira 29: 335-341. Available at https://doi.org/10.1590/S0102-05362011000300013.
https://doi.org/10.1590/S0102-0536201100...
). These difficulties comprise the visual identification of individual characteristics of resistant plants, in addition to the effects of environmental conditions, resulting in values of heritability close to zero, making the selection process compromised.

Studies in the literature report inoculation doses ranging from 1,000 (Viljoen et al., 2019VILJOEN, JJF; LABUSCHAGNE, N; FOURIE, H; SIKORA, RA. 2019. Biological control of the root-knot nematode Meloidogyne incognita on tomatoes and carrots by plant growth-promoting rhizobacteria. Tropical Plant Pathology 44: 284-291. Available at https://doi.org/10.1007/s40858-019-00283-2.
https://doi.org/10.1007/s40858-019-00283...
) to 50,000 (Simon et al., 2000SIMON, P; MATTHEWS, W: ROBERTS, P. 2000. Evidence for simply inherited dominant resistance to Meloidogyne javanica in carrot. 2000. Theoretical and Applied Genetics100: 735-742. Available athttps://doi.org/10.1007/s001220051346
https://doi.org/10.1007/s001220051346...
) eggs and eventual second-instar juveniles in experiments evaluating carrots. However, this amount varies according to the purpose of the work. It should be noted that low doses may not cause symptoms and high doses may lead to competition between individuals, also with negative effects on the appearance of symptoms.

This study aimed at the adjustment of inoculum levels for the expression of plant reaction to M. incognita by analyzing the resistance and susceptibility of carrot genotypes from breeding populations derived from cultivar Brasília (CBR), and from population Pop-750 (CRO).

MATERIAL AND METHODS

The experiment was held from May 21 to October 29, 2019, at Embrapa Vegetables, Brasília-DF, Brazil (15°55’54”S; 48°08’40”W, 1.014 m altitude ) in a glass-glazed greenhouse. It consisted of a completely randomized design with a factorial scheme (4x2) with six replications. Four inoculum levels (0; 1.000; 5.000 and 10.000) containing eggs and eventual second-stage juveniles (E+J2R) of M. incognita represented the first factor and two breeding populations, Pop-750 of purple skin color identified as (CRO), and from cv. Brasília of orange skin color identified as (CBR) represented the second factor.The tomato cv. Rutgers, susceptible to RKN, was used as control to verify the inoculum viability. Sowing was made in 5 L pots filled with a sterilized substrate mixture of subsurface soil (a clayey red Oxisol commonly encountered in the Cerrado Biome region), washed sand, manure, and carbonized rice hulls, in a proportion of 1:1:1:1. It was fertilized with 300 g of 4-30-16 NPK formulation, and 300 g of calcined ground dolomitic limestone per 300 kg of this mixture. All other cultural practices to maintain the plants (irrigation, top dressing fertilizers, and others) were done according to Coyne & Ross (2014COYNE, DL; ROSS, JL. 2014. Protocol for nematode resistance screening: Root knot nematodes, Meloidogyne spp. (Ibadan, Nigeria: International Institute of Tropical Agriculture (IITA)), 27p.).

Thirty days after sowing (30 DAS) thinning was performed, leaving two plants per pot, to proceed the inoculation. The inoculum was maintained in tomato plants and was extracted according to Boneti & Ferraz (1981BONETI, JI; FERRAZ, S. 1981. Modificações no método de Hussey e Barker para extração de ovos de Meloidogyne exigua em raízes de cafeeiro. Fitopatologia Brasileira 6: 533.) methodology. Afterward, the suspension was calibrated to contain the afore said levels, being diluted in 5 mL water, and applied around the plant’s stalk. Sixty days after the inoculation (60 DAI), the root system was washed thoroughly, preserving the galls and eggs. All infected roots were stained with phloxine B for J2 and egg masses, respectively.

Egg mass index (EMI) was obtained according to Taylor & Sasser (1978TAYLOR, AL; SASSER, JN. 1978. Biology, identification and control of root-knot nematodes (Meloidogyne species). Raleigh, US: North Carolina State University. 111p.) using a scoring scale from 0 to 5, wherein: 0 = roots without egg masses; 1 = presence of 1 to 2 egg masses; 2 = presence of 3 to 10 egg masses; 3 = presence of 11 to 30 egg masses; 4 = presence of 31 to 100 egg masses and 5 = presence of more than 100 galls or egg masses. Gall index (GI) was quantified according to Taylor & Sasser (1978) likewise, using the afore mentioned scoring scale for the number of galls. The reproduction factor (RF) was obtained by dividing the initial and final nematode population (RF = Pf/Pi), considering the initial population (Pi) the one inoculated and the final population (Pf) present (Oostenbrink, 1966OOSTENBRINK, M.1966. Major characteristic of the relation between nematodes and plants. Wageningen: Medelingen Landbowhogeschool. 46p.). Data were subjected to analysis of variance (ANOVA), and transformation of √(x + 0.5) was used to approximate the residuals to a normal distribution to enable homoscedasticity. The inoculum levels were analyzed by regression. All computations were performed using SAS/GLM (Statistical Analysis System, Cary, NC, USA).

RESULTS AND DISCUSSION

The significance of the inoculum levels was expressed by regression curves (Figures 1 to 4). Concerning the GI (Figure 1), crescent levels resulted in a quadratic fit for CRO and CRB, with a coefficient of determination (R²) presenting values of 0.93 and 0.70, respectively, which show the usefulness of both models. As for CRO, the level of 6,948 resulted in a higher E+J2R value. Thus, values superior to this would decrease GI number. At the same time, for CBR the maximum value of 11,902 E+J2R is fundamentally close to the higher inoculum level evaluated. These results are consistent with those reported previously for carrot genotypes/cultivars. Silva et al. (2011SILVA, GO; PINHEIRO, JB; VIEIRA, JV; CARVALHO, ADF. 2011. Seleção para resistência de genótipos de cenoura aos nematoides-das-galhas. Horticultura Brasileira 29: 335-341. Available at https://doi.org/10.1590/S0102-05362011000300013.
https://doi.org/10.1590/S0102-0536201100...
) described that it was possible to distinguish resistant genotypes from susceptible ones using an inoculum level of 6,000 E+J2R, with progenies from ‘Brasília’ regarded as tolerant when compared to the control ‘Kuronan’. Yet, the authors stated that improvements in this methodology were still necessary for the selection of superior progenies, aiming at precise results.

Figure 1
Regression fitting for the variable gall index scores observed in carrot genotypes under different Meloidogyne incognita inoculum levels. Brasília, Embrapa Hortaliças, 2019.

GI is a primary character for the evaluation of resistance in carrot progenies, substantiated by several studies (Boiteux et al., 2004BOITEUX, SL; HYMAN, JR; BACH, IC; FONSECA, MEN; MATTHEWS, WC; ROBERTS, P A; SIMON, PW. 2004. Employment of flanking codominant STS markers to estimate allelic substitution effects of a nematode resistance locus in carrot. Euphytica136: 37-44. Available at https://doi.org/10.1023/B:EUPH.0000019508.78153.dd.
https://doi.org/10.1023/B:EUPH.000001950...
). A high correlation between egg production and gall formation allows the identification of resistant carrot genotypes (lines or populations) based on this characteristic. Seo et al. (2014SEO, Y; PARK, J; KIM, YS; PARK, Y; KIM, YH. 2014. Screening and histopathological characterization of Korean carrot lines for resistance to the root-knot nematode Meloidogyne incognita. The Plant Pathology Journal 30: 75-81. Available at https://doi.org/10.5423/PPJ.OA.08.2013.0082.) evaluated 170 carrot lines about their resistance to M. incognita race 1, inoculating 1,000 E+J2R, evaluating the GI 7 weeks after inoculation, observing values ranging from 0.20 to 4.20.

For the EMI (Figure 2), similar results to GI were observed, hence, CRO displayed a larger quantity with a peak of around 7,000 E+J2R. After this inoculum level, symptoms began to become less evident. For CBR, there was no maximum expression at the evaluated inoculum levels. The estimate to obtain the maximum expression of EMI in Brasília would be 11,472 E+J2. Khan et al. (2018KHAN, F; ASIF, M; KHAN, A; SIDDIQU, M. 2018. Screening of carrot cultivars against root-knot nematode Meloidogyne incognita. Indian Phytopathology 71: 415-421. Available at https://doi.org/10.1007/s42360-018-0052-9.
https://doi.org/10.1007/s42360-018-0052-...
) evaluated 13 carrot cultivars utilizing an inoculum level of 3,000 E+J2R of M. incognita. These authors identified, with varying degrees of resistance, that all main roots showed symptoms. Thus, they emphasize that the management of this RKN in production fields is a challenge and requires a combination of genetic and cultural methods.

Figure 2
Regression fitting for the variable egg mass index scores observed in carrot genotypes under different Meloidogyne incognita inoculum levels. Brasília, Embrapa Hortaliças, 2019.

Regarding the E+J2R per g of roots (Figure 3), in all inoculum levels evaluated, CRO presented higher values compared to CBR. Yet an equivalent fitting was observed, where increasing the inoculum would result in E+J2R values being elevated in different proportions for both genotypes. An inoculum level of 6,329 E+J2 would result in a approximate population of 25 E+J2R per gram of roots, considering the higher quantity of this RKN present in the roots.

Figure 3
Regression fitting for the variable E+J2R/g of roots scores observed in carrot genotypes under different Meloidogyne incognita inoculum levels. Brasília, Embrapa Hortaliças, 2019.

The reduction of E+J2R values from certain inoculum levels can be explained mostly by competition, as a result of higher levels that interfere in the infection and multiplication of RKN. Jaiteh et al. (2012JAITEH, F; KWOSEH, C; AKROMAH, R. 2012. Evaluation of tomato genotypes for resistance to root-knot nematodes. African Crop Science Journal 20: 41-49.) described this effect in a tomato trial with inoculum levels of 100 to 2,000 E+J2 of Meloidogyne spp., which was also noticed by Kayani et al. (2017KAYANI, MZ; MUKHTAR, T; HUSSAIN, MA. 2017. Effects of southern root knot nematode population densities and plant age on growth and yield parameters of cucumber. Crop Protection, 92: 207-212. Available athttps://doi.org/10.1016/j.cropro.2016.09.007.
https://doi.org/10.1016/j.cropro.2016.09...
) with cucumber genotypes inoculated with levels ranging from 500 to 8,000 E+J2 of Meloidogyne incognita.

For comparison purposes, the susceptible tomato ‘Rutgers’ used to verify the efficiency of the inoculum, presented a mean value of 103 E+J2R per gram of roots. Carrot is classified as one of the most susceptible vegetable species, with high E+J2R values, like the obtained in tomato, okra, eggplant, and green peas, but lesser compared to cauliflower, radish, and cabbage (Anwar & McKenry, 2010ANWAR, SA; MCKENRY, MV. 2010. Incidence and reproduction of Meloidogyne incognita on vegetable crop genotypes. Pakistan Journal of Zoology 42: 135-141.). The lower number of E+J2R per gram of roots of the present work may be associated with the high and intermediate resistance of CBR and CRO, respectively, pointing to the resistance of the genotypes that form their derivate population against M. incognita.

The RF values (Figure 4) observed for both CBR and CRO, were inferior to 1. This denotes a lesser quantity of nematodes per root compared to the inoculated treatments, therefore, proving a populational reduction of M. incognita of these genotypes, mainly CBR, that behaved as more tolerant. An inoculum level of 5,959 E+J2 would result in a Rf value of 0.30. These low Rf values obtained from genotypes derived from ‘Brasília’ are commonly observed when compared to other parental lines.

Figure 4
Regression fitting for the variable reproduction factor (Rf) scores observed in carrot genotypes under different Meloidogyne incognita inoculum levels. Brasília, Embrapa Hortaliças, 2019.

Pop-750 is derived from a crossing between ‘BRS Planalto’ (also derived from ‘Brasília’) and ‘Cosmic’, being selected for six successive cycles for resistance to leaf blight diseases and against premature bolting, but not directly selected to RKN. A high susceptibility level of ‘Cosmic’ was identified by Pinheiro (2017PINHEIRO, JB. 2017. Nematoides em hortaliças. 1. ed. Brasília-DF: Embrapa. 194p.) where severe symptoms in the taproots were described. Contrarily, the resistance of genotypes derived from ‘Brasília’ to RKN is largely discussed in other works (Singh et al., 2019SINGH, S; KALIA, P; MANGAL, M; CHINTHAGUNTI, H; CHUG, C; MISHRA, S; RAO, U. 2019. In vitro screening technique and polymorphic DNA markers for introgression of root knot nematode resistance in tropical carrot. Indian Journal of Horticulture 76: 430-437. Available at https://doi.org/10.5958/0974-0112.2019.00069.0
https://doi.org/10.5958/0974-0112.2019.0...
; Simon et al., 2000SIMON, P; MATTHEWS, W: ROBERTS, P. 2000. Evidence for simply inherited dominant resistance to Meloidogyne javanica in carrot. 2000. Theoretical and Applied Genetics100: 735-742. Available athttps://doi.org/10.1007/s001220051346
https://doi.org/10.1007/s001220051346...
). This cultivar is a standard parent for RKN resistance in breeding programs in Brazil and other countries. As an example, populations 891091 and 971252 possess a complete resistance level to M. javanica obtained in the USA (Boiteux et al., 2004BOITEUX, SL; HYMAN, JR; BACH, IC; FONSECA, MEN; MATTHEWS, WC; ROBERTS, P A; SIMON, PW. 2004. Employment of flanking codominant STS markers to estimate allelic substitution effects of a nematode resistance locus in carrot. Euphytica136: 37-44. Available at https://doi.org/10.1023/B:EUPH.0000019508.78153.dd.
https://doi.org/10.1023/B:EUPH.000001950...
). So, when GI and EMI are evaluated, a higher inoculum level is necessary to differentiate tolerant progenies, which can be obtained by utilizing ‘Brasília’ as a source of resistance.

In the evaluation of populations with different degrees of resistance to nematodes, the inoculum level must be adequate for each response variable evaluated and for each genotype studied. In the inoculation process for carrot populations like CRO, with a lower tolerance level to RKN, the most adequate levels of inoculum ranged from 5,000 to 7,000 eggs and eventual second stage juveniles of M. incognita, to obtain the maximum manifestation of nematological characters. Levels higher than 7,000 would decrease multiplication efficiency, due to competition for feeding sites. Regarding carrot genotypes with resistance degrees comparable to ‘Brasília’, which is known to have resistance to M. javanica and tolerance to M. incognita (Boiteux et al., 2004BOITEUX, SL; HYMAN, JR; BACH, IC; FONSECA, MEN; MATTHEWS, WC; ROBERTS, P A; SIMON, PW. 2004. Employment of flanking codominant STS markers to estimate allelic substitution effects of a nematode resistance locus in carrot. Euphytica136: 37-44. Available at https://doi.org/10.1023/B:EUPH.0000019508.78153.dd.
https://doi.org/10.1023/B:EUPH.000001950...
), for the quantification of the number of E+J2R per gram of roots and RF, inoculum levels close to 5,000 are sufficient to maximize the expressions of nematode variables. Inoculation levels higher than that will present the same competition for feeding sites. However, when the characterization is based on the evaluation of gall index (GI) and egg mass index (EMI), the appropriate inoculum level would range between 9,000 to 12,000 E+J2 to maximize symptoms. This necessity for higher levels of inoculum for this RKN species multiplication is partially explained by the tolerance mechanism of cultivar Brasília.

ACKNOWLEDGEMENTS

To Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) by the first author’s scientific initiation scholarship.

REFERENCES

  • ALI, A; MATTHEWS, WC; CAVAGNARO, PF; IORIZZO, M; ROBERTS, PA; SIMON, PW. 2014. Inheritance and mapping of Mj-2, a new source of root-knot nematode (Meloidogyne javanica) resistance in carrot. Journal Heredity 105: 288-291. Available athttps://doi.org/10.1093/jhered/est090.
    » https://doi.org/10.1093/jhered/est090
  • ANWAR, SA; MCKENRY, MV. 2010. Incidence and reproduction of Meloidogyne incognita on vegetable crop genotypes. Pakistan Journal of Zoology 42: 135-141.
  • BOITEUX, LS; BELTER, GJ; ROBERTS, AP; SIMON, WP. 2000. RAPD Linkage map of the genomic region encompassing the root-knot nematode (Meloidogyne javanica) resistance locus in carrot. Theoretical and Applied Genetics 100: 439-446. Available athttps://doi.org/10.1007/s001220050057.
    » https://doi.org/10.1007/s001220050057
  • BOITEUX, SL; HYMAN, JR; BACH, IC; FONSECA, MEN; MATTHEWS, WC; ROBERTS, P A; SIMON, PW. 2004. Employment of flanking codominant STS markers to estimate allelic substitution effects of a nematode resistance locus in carrot. Euphytica136: 37-44. Available at https://doi.org/10.1023/B:EUPH.0000019508.78153.dd.
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Publication Dates

  • Publication in this collection
    03 Oct 2022
  • Date of issue
    Jul-Sep 2022

History

  • Received
    19 Apr 2022
  • Accepted
    24 Aug 2022
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