Characterization of type and genetic diversity among soybean cyst nematode differentiators

NOTE

Characterization of type and genetic diversity among soybean cyst nematode differentiators

Éder Matsuo^I; Tuneo SediyamaI, ^*; Rosângela D'Arc de Lima Oliveira^II; Cosme Damião Cruz^III; Rita de Cássia Teixeira Oliveira^IV

^IUFV/CCA - Depto. de Fitotecnia, Av. Peter Henry Rolfs, s/n - Campus Universitário - 36570-000 - Viçosa, MG - Brasil

^IIUFV/CCA - Depto. de Fitopatologia

^IIIUFV/CCB - Depto. de Biologia Geral

^IVBacuri Pesquisa e Melhoramento, R. Aimorés, 290 - 36570-000 - Viçosa, MG - Brasil

ABSTRACT

The development of soybean cyst nematode, Heterodera glycines Ichinohe, resistant genotypes with high yields has been one of the objectives of soybean (Glycine max (L.) Merrill) breeding programs. The objective of this study was to characterize the pathotype of soybean cyst nematodes and analyze the genetic diversity of ten differentiator lines ('Lee 74', Peking, Pickett, PI 88788, PI 90763, PI 437654, PI 209332, PI 89772, PI 548316 and 'Hartwig'). Inoculum was obtained from plants cultivated in field soil in Viçosa, state of Minas Gerais, Brazil. Thirty-four days after inoculating each plant with 4,000 eggs, the number of females, female index, total number of eggs, number of eggs per female, reproduction factor, plant height, number of nodes, fresh and dry matter weights were assessed. The differential lines were first grouped with Scott-Knott test. Subsequently, the genetic diversity was evaluated using dendrograms, graphic analysis and the Tocher grouping method. The inoculum of H. glycines obtained from NBSGBP-UFV was characterized as HG Type 0. The differentiating lines were divergent, and PI 89772, PI 437654, 'Hartwig' and 'Peking' had the greatest potential for use in breeding programs.

Keywords:Glycine max, Heterodera glycines, soybean breeding, resistant cultivars

Introduction

The soybean cyst nematode (SCN), Heterodera glycines Ichinohe, was detected in Brazil for the first time in the 1991/1992 growing season (Lima et al., 1992; Lordello et al., 1992; Monteiro and Moraes, 1992). It is currently present in ten Brazilian states, in an estimated area of over 2.0 million hectares (EMBRAPA, 2008). The grain yield losses in these locations can reach 90 %, depending on the degree of infestation, cultivar susceptibility, soil fertility and nematode race (Dhingra et al., 2009).

Control strategies include crop rotation, use of resistant soybean (Glycine max (L.) Merrill) cultivars, and the combination of these methods has been shown to be adequate (EMBRAPA, 2008). Several studies have endeavored to identify cultivars with SCN resistance in breeding programs (Dias et al., 2009).

In addition to the seven differential lines used to characterize pathogenic variability of SCN (Niblack et al., 2006), genotypes used periodically as resistance sources in breeding programs can be included to assess their potential to increase resistance (Niblack et al., 2006). The success of a breeding program is enhanced by the inclusion of genetic variability in the working population (Cruz and Carneiro, 2006). In plant breeding, studies to estimate genetic diversity has been made as of Matsuo et al. (2009) in soybean; Conde et al. (2011) in wheat and Leão et al. (2011) in grape.

The objective of this study was to characterize the HG type of our SCN populations, and to analyze the genetic diversity among the differentiating lines.

Materials and Methods

The experiment was conducted in a greenhouse in Viçosa, Minas Gerais State, Brazil (20°45'14'' S; 42°52'54'' W; 649 m a.s.l.). A randomized complete design with six replications was used and the experimental unit consisted of one plant. During the experiment, the average temperature was 27.7 ºC.

Infested soil with H. glycines was collected from the Nematode Bank of the Soybean Genetic Breeding Program at the Universidade Federal de Viçosa, (NBSGBP-UFV). The Nematode Bank was formed in 1996 from field soil collected from different Brazilian areas cropped with soybean. To maintain the SCN sample in the NBSGBP-UFV, a susceptible soybean cultivar was planted at least twice a year. Soybean cultivar was usually grown 'FT-Estrela'. Among the different sample present in the NBSGBP-UFV, were used those previously characterized as race 3 in 1998 by Silva et al. (1999c).

The cyst nematode was multiplied from 3 dm³ soil from each sample of the NBSGBP-UFV that were homogenized and distributed in the pots. The soil from each sample, after 34 days with susceptible soybean plants, was mixed between the different samples, race 3, used in this study, which resulted in an infested homogeneous soil. This SCN was maintained in a greenhouse using the susceptible soybean cultivar 'Quartzo'.

To obtain the eggs, the plants were removed from the pots and the root systems placed in a 0.84 mm (20 mesh) over 0.15 mm (100 mesh) pore sieves, and then washed with a strong jet of running water. The females retained in the 0.15 mm (100 mesh) pore sieve were transferred to a 0.15 mm (100 mesh) over 0.025 mm (500 mesh) pore sieve where they were squashed. The eggs retained in the 0.025 mm (500 mesh) pore sieve were transferred to a beaker for later quantification by microscope. The eggs concentration was determined by counting in a Peters counting chamber and the suspension standardized to 1,000 eggs mL^-1.

The differentiating lines seeds 'Peking', 'Pickett' 'PI 88788, PI 90763, PI 437654, PI 209332, PI 89772, PI 548316 and 'Hartwig' plus 'Lee 74' (susceptible standard), provided by Embrapa Soja, were germinated in a sand bed previously sterilized with methyl bromide. At the VE stage (Fehr and Caviness, 1977), the plants were standardized (by size and vigor) and transplanted to ceramic pots containing 0.8 dm³ of sand and clay soil (55 %: 21 %: 24 % of sand:silt:clay) mixture (1:1) (v/v) that had been sterilized with methyl bromide.

Each pot received 4,000 eggs ten days after planting, distributed in four 2 cm deep holes in the soil made with a glass rod, 2 cm from the main stem.

The root system of each inoculated plant was removed from the soil 34 days after inoculation and washed under a strong jet of running water in 0.84 mm (20 mesh) pore sieves attached to another 0.09 mm (160 mesh) pore sieves. Females retained in the 0.09 mm (160 mesh) pore sieves were collected with water in a beaker and counted in a plastic counting plate with a grid base under a stereoscopic microscope (20X). The female index (FI) was used to determine the race in the sample (Riggs and Schmitt, 1988; Dias et al., 1998) and to HG Type characterization according to Niblack et al. (2002). In addition to the number of females, number of eggs, number of eggs per female, reproduction factor (Oostenbrink, 1966), the plant height, number of nodes, fresh and dry matter weight were also assessed.

Number of females, number of eggs and number of eggs per female were transformed in before analysis of variance and the means of all the traits assessed, except for the reproduction factor, were grouped by the Scott-Knott test (p < 0.05). The differential lines were later analyzed for genetic diversity based on the traits related to resistance (number of females, number of eggs and number of eggs per female) and agronomic traits (plant height, number of nodes, fresh and dry matter weights). The dissimilarity among the hosts was estimated by the Mahlanobis distance. The genetic diversity was studied by a dendrogram using UPGMA (Unweighted Pair Group Method with Arithmetic Mean), graphic analysis following the canonic variables and differentiating lines were grouped by the Tocher optimization method. The statistical analyses were performed by the Programa Genes: Estatística experimental e matrizes (Cruz, 2006) and Programa Genes: Diversidade Genética (Cruz, 2008).

Results and Discussion

The female indices were 6.4, 1.9, 1.1, 1.0, and 0.0 %, respectively to 'Pickett', 'Peking', PI88788, PI90763, and 'Hartwig'. Thus, the inoculum from the NBSGBP-UFV was confirmed as belonging to race 3 (Riggs and Schmitt, 1988). In the HG Type characterization of this inoculum (Niblack et al., 2002) a female index (FI) of less than 10 % was obtained for all indicator lines, showing that the isolate was a Type 0 (zero) (Table 1).

The SCN population from the NBSGBP-UFV was first characterized as race 3 (Silva et al., 1999c). H. glycines is a species with amphmitic reproduction where the females can attract and be fertilized by more than one male. This can result in genetic variability in the soybean cyst nematode population in the field (Triantaphyllou and Esbenshade, 1990). The use of resistant cultivars is the most economic and popular control method used by the producers (Dias et al., 2009). However, over time changes in the physiological race may occur due to selection pressure (Triantaphyllou, 1975; Schmitt and Noel, 1984; Santana et al., 2009). Our results were similar to those as Silva et al. (1999a,b).

In the soybean cyst nematode HG type classification system, 'Lee 74' was used as susceptible standard and indicator lines including of seven sources of resistance to SCN most commonly used by the soybean genetic breeding programs in the United States of America (Niblack et al., 2002) plus 'Hartwig' (Dias et al., 2009). Lines can be added in the HG-type characterization used as resistance sources in other breeding programs (Niblack et al., 2002). This is a great advantage because the genetic make-up of the nematode population can be more thoroughly characterized for resistance to SCN. Furthermore, the test gives information on the potential of the population to adapt or respond to selection pressure resulting in loss of effectiveness of resistance. The nematode population present in the NBSGBP-UFV sample did not multiply in any of the eight indicator lines so these sources could therefore be used as SCN resistance sources in breeding programs whose cropping area present H. glycines population similar to the NBSGBP-UFV.

Lee 74 cultivar supported the greatest mean number of females (348.0), followed by the group formed by 'Pickett' and PI 548316. There was a greater egg production in 'Lee 74' than PI 88788, PI 90763, PI 437654, PI 209332, and 'Hartwig' which had the smallest egg production. Moreover, 'Lee 74' also differed (p < 0.05) from Pickett, Peking, PI 89772, and PI 548316 in egg number. The reproduction factor ranged from 0.00 in 'Hartwig' to 8.02 in 'Lee 74' (Table 2).

Among the agronomic characteristics, the plant height in 'Peking' had the lowest mean (38.92 cm) and was different (p < 0.05) from the other groups. 'Lee 74', 'Pickett', PI 88788, PI 209332, and PI 89772 formed a group with means ranging from 86-114.5 cm. 'Lee 74', 'Pickett', and 'Hartwig' formed the group with the highest means for number of nodes while the group with the lowest means was formed by 'Peking', PI 90763, PI 437654, PI 89772, and PI 548316. Similar performance was observed in the differentiating lines for the fresh and dry matter weights, where 'Lee 74', 'Pickett', 'Peking', PI 88788, PI 89772, and 'Hartwig' formed the group with the highest means (Table 2).

'Lee 74' was the most dissimilar (100 % dissimilarity) compared to the other genotypes, relative to the traits related to SCN resistance (Figure 1A). 'Peking', 'Pickett', PI 88788, PI 90763, PI 437654, PI 209332, PI 89772, PI 548316, and 'Hartwig' were similar, at the magnitude of < 10 %. Among these, the most similar were PI 88788 and PI 437654, followed by 'Peking', PI 89773, and PI 209332. When only the agronomic traits were considered (Figure 1B) there was greater dissimilarity among the differentiating lines. Three pairs presented dissimilarity less than 10 %, namely 'Pickett' and PI 209332, PI 90763 and PI 548316, and 'Lee74' and PI 88788. 'Hartwig' was the most dissimilar (100 %) among those assessed and 'Peking' presented 90 % dissimilarity in relation to the other hosts. When the dendrogram was analyzed that considered all the traits assessed (Figure 1C) the most dissimilar performance was observed in 'Lee 74' (100 %) followed by 'Hartwig' (> 10 % and < 20 % dissimilarity). The other genotypes presented less than 10 % dissimilarity.

The first two eigenvalues explained at least 88 % of the total variation. Using the canonic variables for traits related to resistance (Figure 2A), 'Lee 74' was the most distant graphically and had greatest divergence among the differentiating lines. 'Pickett' and 'Hartwig' were the most divergent of the remaining differentials, followed by PI 548316 and 'Hartwig'. When all traits were considered similar performance was observed from 'Lee 74' (Figure 2C) and 'Hartwig' was the most divergent. A different result among the differentiating lines is presented in Figure 2B that considered when the agronomic traits were considered alone, they diverged more amongst each other, except for 'Hartwig' and 'Peking' that presented greater graphic distance. In the grouping analysis, only two groups formed in Figure 1A and 1C. In group I nine differentiating lines (90 % of the genotypes assessed) and in group II, 'Lee 74' were seen. In Figure 2B, four groups formed: group I formed by 'Lee 74', 'Pickett', PI 88788, PI 90763, PI 437654, PI 209332, and PI 548316 that represented 70 % of the genotypes assessed, group II by PI 89772, group III by 'Hartwig' and group IV by 'Peking', each represented by 10 % of the genotypes.

Using resistance sources in the development of high-yielding disease resistant soybean cultivars has been one of the main objectives of many soybean breeding programs. The development of effective SCN-resistant cultivars is one of the greatest contributions of plant breeding (Sediyama et al. (2009). The improved cultivars carry genes that can express high yield, wide adaptation and good resistance/tolerance to biotic or abiotic factors (EMBRAPA, 2008). In addition, desirable agronomic traits have also been considered by geneticists and breeders.

About 50 resistant soybean cultivars are available to Brazilian producers and annually new cultivars are presented on the market. The most used strategy to incorporate SCN resistance is line selection from populations derived from hybridizations among adapted genotypes and North American resistant cultivars (Dias et al., 2009). The success of a breeding program lies in the existence of genetic variability in the working population, that is, breeders have recommended intercrossing among superior and divergent cultivars to form the base population (Cruz and Carneiro, 2006). With this, 'Hartwig', 'Peking', PI 437654, and PI 89772 appear to be good options as parents because they present resistance to SCN, genetic divergence compared to the other differentiating lines based on the agronomic traits, and they present many desirable agronomic traits. The progenies developed by hybridization from these resistance sources with susceptible cultivars could present different resistance genes. Young (1982), Luedders (1983) and Young (1994) stressed the importance of rotating cultivars with different resistance sources in nematode management. Cultivar rotation can be important to prevent cultivar yield suppression and the practice should be accompanied to maintain the SCN population density below the economic threshold (Young, 1994).

After incorporating resistance, the recently released cultivars in Brazil substituted the North American cultivars as resistance sources (Dias et al., 2009) because they present both agronomic adaptations to Brazilian cropping conditions and SCN resistance. Although nematode resistance is generally identified and characterized based on nematode reproduction inhibition, the main objective for the development of resistance is protection of the crop yield. Releasing a resistant, but little productive, cultivar will probably not meet the producers requirements (Starr and Roberts, 2004). Resistance can be considered an advance in the genetic quality of the cultivar, which may contribute to maintaining or increasing yield.

Acknowledgments

To the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq-Brazil) for financial support in carrying out this study (MSc and research productivity grants).

Received February 25, 2011

Accepted October 14, 2011

Edited by: Cláudio Marcelo Gonçalves de Oliveira

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Publication Dates

• Publication in this collection
  29 Feb 2012
• Date of issue
  Apr 2012

History

• Received
  25 Feb 2011
• Accepted
  14 Oct 2011