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Crop Science 40:1168-1171 (2000)
© 2000 Crop Science Society of America

PLANT GENETIC RESOURCES

Level and Geographical Distribution of Resistance to Meloidogyne arenaria in the U.S. Peanut Germplasm Collection

C.Corley Holbrook, Michael G. Stephenson and A.William Johnson

USDA-ARS, P.O. Box 748, Coastal Plain Exp. Stn., Tifton, GA 31793 USA

holbrook{at}tifton.cpes.peachnet.edu


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 Materials and methods
 Results and discussion
 REFERENCES
 
The peanut root-knot nematode [Meloidogyne arenaria (Neal) Chitwood race 1] causes significant economic losses in many peanut (Arachis hypogaea L.) production areas of the world. The objectives of this study were (i) to examine the peanut core collection to identify sources of resistance, (ii) to estimate the level of resistance that occurs in the U.S. germplasm collection, and (iii) to examine the geographical distribution for resistance in peanut germplasm. Seven hundred forty-one accessions from the core collection were tested in greenhouse trials. The egg-mass rating for cultivar Florunner, the susceptible check, was 4.0 on a 1.0 to 5.0 scale with a nematode reproduction rate of 15496 eggs per gram of fresh root weight. Fifty-six accessions exhibited an egg-mass rating of <=2.5. Thirty-six core accessions showed a reduction in root galling, egg-mass rating, egg count per root system, and egg count per gram of root in comparison to Florunner. Twenty-one accessions showed a 70% reduction in egg count per root system and per gram of root, and two accessions showed a 90% reduction of these variables in comparison with Florunner. The 56 resistant indicators from screening the core collection identified 39 clusters in the entire germplasm collection that should be examined more thoroughly. China and Japan appear to be valuable geographical sources for resistance to this nematode.


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 Materials and methods
 Results and discussion
 REFERENCES
 
THE ROOT-KNOT NEMATODE causes significant economic losses in many peanut production areas of the world. Chemicals for control of this pest are becoming increasingly limited, and the development of peanut cultivars with resistance would be desirable.

Only moderate levels of resistance have been observed in naturally occurring germplasm of A. hypogaea. Holbrook and Noe (1992) evaluated 1321 peanut plant introductions for resistance to M. arenaria and identified 17 accessions that supported fewer egg masses and seven genotypes that supported less egg production per gram of fresh root weight compared with the cultivar Florunner. Holbrook et al. (1996) evaluated 1000 plant introductions and identified eight additional accessions that had significantly higher levels of resistance (lower egg mass rating) than Florunner. Although none of the eight had a significantly higher level of resistance than those reported by Holbrook and Noe (1992), two of the eight exhibited significantly higher yield than all others when grown in soil heavily infested with M. arenaria.

More desirable sources of resistance to M. arenaria may exist in A. hypogaea since less than one-third of the germplasm collection has been examined for resistance based on nematode reproduction. A core collection has been selected to represent the U.S. germplasm collection of peanut (Holbrook et al., 1993). Theoretically this core collection could be used to more efficiently identify desirable traits, such as nematode resistance, in the entire collection (Brown, 1989; Frankel, 1984). Data on resistance to late leaf spot [Phaeoisariopsis personata (Berk. & M.A. Curtis) Arx. syn. Cercosporidium personatum (Berk. & M.A. Curtis)] for the entire collection was used to empirically evaluate the peanut core collection (Holbrook and Anderson, 1995). The results demonstrated that the use of the peanut core collection would have improved the efficiency of identifying resistance to late leaf spot in the entire collection.

Very high levels of resistance to M. arenaria exist in related Arachis spp. (Nelson et al., 1989; Holbrook and Noe, 1990). The level of resistance thus far observed in A. hypogaea has not been as high as that observed in wild species or interspecific material derived from these species. Screening of the peanut core collection should indicate whether high levels of resistance to M. arenaria occur in A. hypogaea.

The objectives of this study were (i) to use the core collection to identify sources of resistance (ii) to estimate the level of resistance available in the germplasm collection of A. hypogaea, and (iii) to examine the geographical distribution for resistance in peanut germplasm to indicate areas within the collection for further study.


    Materials and methods
 TOP
 ABSTRACT
 INTRODUCTION
 Materials and methods
 Results and discussion
 REFERENCES
 
The peanut core collection consists of 831 accessions (Holbrook et al., 1993). Seed was available for 741 accessions, and these accessions were tested for resistance to M. arenaria by the greenhouse screening technique described by Holbrook et al. (1983) with five replications (5 plants). Plants were grown in steam-pasteurized loamy sand (85% sand, 11% silt, 4% clay). Each plant was inoculated with 3500 eggs of M. arenaria race 1, which had been cultured on tomato (Lycopersicon esculentum Mill. cv. Rutgers). Nematode inoculum was prepared using the NaOCl method (Hussey and Barker, 1973) and applied 10 d after planting.

Approximately 90 d after inoculation, plants were uprooted and washed clean of soil. The roots were placed in 1000-mL beakers containing 300 mL of phloxine B solution for 3 to 5 min (Daykin and Hussey, 1985). Each plant was indexed for root galls and egg masses on the following scale: 0 = no galls or no egg masses, 1 = 1 to 2, 2 = 3 to 10, 3 = 11 to 30, 4 = 31 to 100, 5 = more than 100 galls or egg masses per root system (Taylor and Sasser, 1978).

Means for egg mass ratings were calculated and resistant selections were made based on a mean rating of less than or equal to three (<=30 egg masses). These resistant selections were further evaluated in a greenhouse experiment that was planted on 20 Dec. 1996 in a randomized complete-block design with seven replications. Germinated seedlings were inoculated with 3500 eggs 10 d after planting. Egg-masses and root-gall ratings were measured on 25 and 26 March, as described above. Roots from four replications were blotted dry and weighed, and eggs were collected with NaOCl (Hussey and Barker, 1973) and counted.

Data were subjected to analysis of variance and genotypic means were compared by Fisher's protected least significant difference (LSD). Unless otherwise stated, all differences referred to in the text were significant at P <= 0.05.

For each country of origin represented by at least one nematode resistant core accession, the expected number of resistant accessions was calculated. Expected values were calculated by multiplying the number of accessions in the core collection from each country of origin by the percentage of resistant accessions in the core collection. Chi-square analysis was used to test for significant deviations from expected.


    Results and discussion
 TOP
 ABSTRACT
 INTRODUCTION
 Materials and methods
 Results and discussion
 REFERENCES
 
These studies resulted in the identification of 56 accessions from the core collection that had an egg mass rating of 2.5 or less (Table 1) . Eggs were not counted for 13 of these accessions. The number of eggs per root system for five accessions was not different from Florunner, although four of these had fewer eggs per gram of root than the susceptible cultivar. Thirty-six core accessions showed a significant reduction in galling, egg-mass rating, egg count per root system, and egg count per gram of root in comparison with the susceptible cultivar Florunner.


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Table 1 Meloidogyne arenaria reproduction and root galling on resistant selections from screening the peanut core collection

 
None of the resistant accessions identified in these studies had lower galling, egg-mass rating, egg count per root system, and eggs per gram of root than the resistant accessions previously identified by Holbrook and Noe (1992), and Holbrook et al. (1996) (Table 1). However, the sources of resistance identified from the core collection may provide unique genes for resistance or they may provide genes for resistance in combination with more acceptable agronomic characteristics.

Extremely high levels of resistance to M. arenaria are available in related Arachis spp. (Baltensperger et al., 1986; Nelson et al., 1989; Holbrook and Noe, 1990). Starr et al. (1995) observed high levels of resistance (<97% reduction of eggs per gram of roots compared with the susceptible recurrent parent) in F2 individuals from the second, third, and fourth backcross generations derived from the resistant parent TxAG-7 (Simpson et al., 1993). None of the A. hypogaea accessions identified in our studies showed a level of resistance as high as the highest levels observed in wild species or interspecific material derived from these species. Twenty-one accessions from the core collection showed a 70% reduction in eggs per root system and in eggs per gram of root in comparison with Florunner (Table 1). Two of these accessions (PI 269064 and PI 295747) showed a 90% reduction in these variables compared with Florunner.

Theoretically, the reaction of a core accession should serve as an indicator for the cluster in the entire germplasm collection from which the accession was selected. The frequency of additional resistant accessions should be higher in clusters with resistant indicator values. Resistant indicators from screening the core collection identified 39 clusters in the entire germplasm collection that should be examined more thoroughly (Table 2) . Screening material from these clusters would require examining 871 accessions.


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Table 2 Clusters that should be examined for resistance to the peanut root-knot nematode on the basis of screening of the peanut core collection

 
Previous research showed that a two-stage screening program for resistance to late leaf spot using this core collection would have identified 54% of the resistant accessions in the entire collection (Holbrook and Anderson, 1995). Based on available data, similar results should be expected for resistance to M. arenaria. Sixteen peanut accessions have been reported to have moderate resistance (Holbrook and Noe, 1992; Holbrook et al., 1996). Eight of these accessions would have been identified and eight accessions would not have been identified by the two-stage core screening approach.

The only striking geographical pattern observed were relatively large numbers of resistant accessions from China and Japan (Table 3) . Eleven of the resistant accessions identified were from China. This was 20% of the resistant accessions, whereas <4% of the germplasm collection originated from China. Seven percent of the resistant accessions were from Japan, although <2% of the germplasm collection originated from Japan.


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Table 3 Geographical distribution of resistance to Meloidogyne arenaria observed in the peanut core collection

 

    ACKNOWLEDGMENTS
 
The contributions and technical support of Jamie Day, David Clements, Vickie Hogan, Jimmy Laska, Dannie Mauldin, Betty Tyler, and Billy Wilson are gratefully acknowledged. This work was supported in part by funds from the Georgia Peanut Commission.

Received for publication July 29, 1999.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 Materials and methods
 Results and discussion
 REFERENCES
 




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This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF) Free
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Right arrow Citing Articles via HighWire
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Right arrow Articles by Holbrook, C.C.
Right arrow Articles by Johnson, A.W.
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Right arrow Articles by Holbrook, C.C.
Right arrow Articles by Johnson, A.W.
Agricola
Right arrow Articles by Holbrook, C.C.
Right arrow Articles by Johnson, A.W.


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