scholarly journals A Comprehensive Review of the Major Genes Conditioning Resistance to Anthracnose in Common Bean

HortScience ◽  
2004 ◽  
Vol 39 (6) ◽  
pp. 1196-1207 ◽  
Author(s):  
James D. Kelly ◽  
Veronica A. Vallejo
Keyword(s):  
Common Bean ◽  
Resistance Genes ◽  
Durable Resistance ◽  
Gene Pyramiding ◽  
Resistance Breeding ◽  
Gene Clusters ◽  
Allelic Series ◽  
Multiple Alleles ◽  
Differential Cultivars ◽  
Major Resistance Genes

Resistance to anthracnose in common bean is conditioned primarily by nine major independent genes, Co-1 to Co-10 as the Co-3/Co-9 genes are allelic. With the exception of the recessive co-8 gene, all other nine are dominant genes and multiple alleles exist at the Co-1, Co-3 and Co-4 loci. A reverse of dominance at the Co-1 locus suggests that an order of dominance exists among individual alleles at this locus. The nine resistance genes Co-2 to Co-10 are Middle American in origin and Co-1 is the only locus from the Andean gene pool. Seven resistance loci have been mapped to the integrated bean linkage map and Co-1 resides on linkage group B1; Co-2 on B11, Co-3 on B4; Co-4 on B8; Co-6 on B7; and Co-9 and Co-10 are located on B4 but do not appear to be linked. Three Co-genes map to linkage groups B1, B4 and B11 where clusters with genes for rust resistance are located. In addition, there is co-localization with major resistance genes and QTL that condition partial resistance to anthracnose. Other QTL for resistance may provide putative map locations for the major resistance loci still to be mapped. Molecular markers linked to the majority of major Co-genes have been reported and these provide the opportunity to enhance disease resistance through marker-assisted selection and gene pyramiding. The 10 Co-genes are represented in the anthracnose differential cultivars, but are present as part of a multi-allelic series or in combination with other Co-genes, making the characterization of more complex races difficult. Although the Co-genes behave as major Mendelian factors, they most likely exist as resistance gene clusters as has been demonstrated on the molecular level at the Co-2 locus. Since the genes differ in their effectiveness in controlling the highly variable races of the anthracnose pathogen, the authors discuss the value of individual genes and alleles in resistance breeding and suggest the most effective gene pyramids to ensure long-term durable resistance to anthracnose in common bean.

scholarly journals Marker-assisted pyramiding of two major broad-spectrum bacterial blight resistance genes,Xa21andXa33into an elite maintainer line of rice, DRR17B

2018 ◽  
Author(s):  
CH Balachiranjeevi ◽  
S Bhaskar Naik ◽  
V Abhilash Kumar ◽  
G Harika ◽  
H.K Mahadev Swamy ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Bacterial Blight ◽  
Durable Resistance ◽  
Gene Pyramiding ◽  
Resistance Breeding ◽  
Fertility Restorer ◽  
Rice Varieties ◽  
Homozygous Condition ◽  
Specific Pcr ◽  
High Level

AbstractBacterial blight (BB) disease reduces the yield of rice varieties and hybrids considerably in many tropical rice growing countries like India. The present study highlights the development of durable BB resistance into the background of an elite maintainer of rice, DRR17B, by incorporating two major dominant genes,Xa21andXa33through marker-assisted backcross breeding (MABB). Through two sets of backcrosses, the two BB resistance genes were transferred separately to DRR17B. In this process, at each stage of backcrossing, foreground selection was carried out for the target resistance genes and for non-fertility restorer alleles concerning the major fertility restorer genesRf3andRf4, using gene-specific PCR-based markers, while background selection was done using a set of 61 and 64 parental polymorphic SSR markers respectively. Backcross derived lines possessing eitherXa21orXa33along with maximum genome recovery of DRR17B were identified at BC3F1generation and selfed to develop BC3F2s. Plants harboringXa21orXa33in homozygous condition were identified among BC3F2s and were intercrossed with each other to combine both the genes. The intercross F1plants (ICF1) were selfed and the intercross F2(ICF2) plants possessing bothXa21andXa33in homozygous condition were identified with the help of markers. They were then advanced further by selfing until ICF4generation. Selected ICF4lines were evaluated for their resistance against BB with eight virulent isolates and for key agro-morphological traits. Six promising two-gene pyramiding lines of DRR17B with high level of BB resistance and agro-morphological attributes similar or superior to DRR17B with complete maintenance ability have been identified. These lines with elevated level of durable resistance may be handy tool for BB resistance breeding.

scholarly journals Gene Pyramiding for Achieving Enhanced Resistance to Bacterial Blight, Blast, and Sheath Blight Diseases in Rice

2020 ◽  
Vol 11 ◽  
Author(s):  
Jegadeesan Ramalingam ◽  
Chandavarapu Raveendra ◽  
Palanisamy Savitha ◽  
Venugopal Vidya ◽  
Thammannagowda Lingapatna Chaithra ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Bacterial Blight ◽  
Durable Resistance ◽  
Gene Pyramiding ◽  
Resistance Breeding ◽  
Sheath Blight ◽  
Potential Donor ◽  
Broad Spectrum Resistance ◽  
Combine Blast ◽  
High Degree

Bacterial blight, blast, and sheath blight are the commonest diseases causing substantial yield loss in rice around the world. Stacking of broad-spectrum resistance genes/QTLs into popular cultivars is becoming a major objective of any disease resistance breeding program. The varieties ASD 16 and ADT 43 are the two popular, high yielding, and widely grown rice cultivars of South India, which are susceptible to bacterial blight (BB), blast, and sheath blight diseases. The present study was carried out to improve the cultivars (ASD 16 and ADT 43) through introgression of bacterial blight (xa5, xa13, and Xa21), blast (Pi54), and sheath blight (qSBR7-1, qSBR11-1, and qSBR11-2) resistance genes/QTLs by MABB (marker-assisted backcross breeding). IRBB60 (xa5, xa13, and Xa21) and Tetep (Pi54; qSBR7-1, qSBR11-1, and qSBR11-2) were used as donors to introgress BB, blast, and sheath blight resistance into the recurrent parents (ASD 16 and ADT 43). Homozygous (BC3F3 generation), three-gene bacterial blight pyramided (xa5 + xa13 + Xa21) lines were developed, and these lines were crossed with Tetep to combine blast (Pi54) and sheath blight (qSBR7-1, qSBR11-1, and qSBR11-2) resistance. In BC3F3 generation, the improved pyramided lines carrying a total of seven genes/QTLs (xa5 + xa13 + Xa21 + Pi54 + qSBR7-1 + qSBR11-1 + qSBR11-2) were selected through molecular and phenotypic assay, and these were evaluated for resistance against bacterial blight, blast, and sheath blight pathogens under greenhouse conditions. We have selected nine lines in ASD 16 background and 15 lines in ADT 43 background, exhibiting a high degree of resistance to BB, blast, and sheath blight diseases and also possessing phenotypes of recurrent parents. The improved pyramided lines are expected to be used as improved varieties or used as a potential donor in breeding programs. The present study successfully introgressed Pi54, and qSBR QTLs (qSBR7-1, qSBR11-1, and qSBR11-2) from Tetep and major effective BB-resistant genes (xa5, xa13, and Xa21) from IRBB60 into the commercial varieties for durable resistance to multiple diseases.

scholarly journals Identification of Random Amplified Polymorphic DNA Markers Linked to the Co-4 Resistance Gene to Colletotrichum lindemuthianum in Common Bean

2000 ◽  
Vol 90 (7) ◽  
pp. 758-761 ◽  
Author(s):  
Maricilia C. Cardoso de Arruda ◽  
Ana Lilia Alzate-Marin ◽  
José Mauro Chagas ◽  
Maurilio Alves Moreira ◽  
Everaldo Gonçalves de Barros
Keyword(s):  
Common Bean ◽  
Resistance Genes ◽  
Rapd Markers ◽  
Random Amplified Polymorphic Dna ◽  
Durable Resistance ◽  
Colletotrichum Lindemuthianum ◽  
Sources Of Resistance ◽  
Repulsion Phase ◽  
Bean Anthracnose ◽  
Major Resistance Genes

New cultivars of the common bean (Phaseolus vulgaris) with durable resistance to anthracnose can be developed by pyramiding major resistance genes using marker-assisted selection. To this end, it is necessary to identify sources of resistance and molecular markers tightly linked to the resistance genes. The objectives of this work were to study the inheritance of resistance to anthracnose in the cultivar TO (carrying the Co-4 gene), to identify random amplified polymorphic DNA (RAPD) markers linked to Co-4, and to introgress this gene in the cultivar Rudá. Populations F1, F2, F2:3, BC1s, and BC1r from the cross Rudá × TO were inoculated with race 65 of Colletotrichum lindemuthianum, causal agent of bean anthracnose. The phenotypic ratios (resistant/susceptible) were 3:1 in the F2 population, 1:1 in the BC1s, and 1:0 in the BC1r, confirming that resistance to anthracnose in the cultivar TO was monogenic and dominant. Six RAPD markers linked to the Co-4 gene were identified, four in the coupling phase: OPY20830C (0.0 centimorgan [cM]), OPC08900C (9.7 cM), OPI16850C (14.3 cM), and OPJ011,380C (18.1 cM); and two in the repulsion phase: OPB031,800T (3.7 cM) and OPA18830T (17.4 cM). OPY20830C and OPB031,800T, used in association as a codominant pair, allowed the identification of the three genotypic classes with a high degree of confidence. Marker OPY20830C, which is tightly linked to Co-4, is being used to assist in breeding for resistance to anthracnose.

scholarly journals Identification of Phaeoisariopsis griseola pathotypes from five States in Brazil

2002 ◽  
Vol 27 (1) ◽  
pp. 78-81 ◽  
Author(s):  
ALOISIO SARTORATO
Keyword(s):  
Phaseolus Vulgaris ◽  
Common Bean ◽  
Resistance Genes ◽  
Leaf Spot ◽  
Angular Leaf Spot ◽  
Phaeoisariopsis Griseola ◽  
Moist Chamber ◽  
Differential Cultivars ◽  
Pathogenic Variability ◽  
Resistant Genotypes

Due to the increased importance of angular leaf spot of common bean (Phaseolus vulgaris) in Brazil, monitoring the pathogenic variability of its causal agent (Phaeoisariopsis griseola) is the best strategy for a breeding program aimed at developing resistant genotypes. Fifty one isolates of P. griseola collected in five Brazilian States were tested on a set of 12 international differential cultivars in the greenhouse. When inoculated plants showed symptoms but no sporulation was observed, they were transferred to a moist chamber for approximately 20-24 h. After this period of time, if no sporulation was observed, the plants were considered resistant; otherwise, they were considered susceptible. From the fifty-one tested isolates, seven different pathotypes were identified. No Andean pathotypes were identified; consequently, all isolates were classified as Middle American pathotypes. Pathotype 63-31 was the most widespread. Pathotype 63-63 overcame resistance genes present in all differential cultivars and also the resistance gene(s) present in the cultivar AND 277. This fact has important implications for breeding angular leaf spot resistance in beans, and suggests that searching for new resistance genes to angular leaf spot must be pursued.

scholarly journals Race structure of cowpea witchweed (Striga gesnerioides) in West Africa and its implications for Striga resistance breeding of cowpea

Weed Science ◽  
2020 ◽  
Vol 68 (2) ◽  
pp. 125-133 ◽  
Author(s):  
Erik W. Ohlson ◽  
Michael P. Timko
Keyword(s):  
West Africa ◽  
Resistance Genes ◽  
Broad Spectrum ◽  
Genetic Relatedness ◽  
Durable Resistance ◽  
Resistance Breeding ◽  
Differential Resistance ◽  
African Countries ◽  
Sources Of Resistance ◽  
Striga Gesnerioides

AbstractCowpea witchweed [Striga gesnerioides (Willd.) Vatke] is a primary constraint of cowpea [Vigna unguiculata (L.) Walp.] production in West Africa. Previously, seven S. gesnerioides races were classified based upon host specificity and genotypic profiling. Because race number and distribution are dynamic systems influenced by gene flow, genetic drift, and natural selection, a thorough investigation of S. gesnerioides diversity and the effectiveness of known sources of resistance in cowpea is needed to develop varieties with durable and broad-spectrum Striga resistance. In this study, we screened seven cowpea lines against 58 unique S. gesnerioides populations collected from across nine West African countries. Individuals from 10 S. gesnerioides populations were genotyped with simple sequence repeat (SSR) markers. We identified six races of S. gesnerioides based on their parasitism of the seven cowpea lines with known differential resistance genotypes. No cowpea line was resistant to all 58 Striga populations and none of the Striga populations were able to overcome the resistance of all seven lines. A novel race, SG6, of the parasite collected from Kudu, Nigeria, was found to overcome more cowpea resistance genes than any previously reported race. SSR analysis indicates that Striga populations are highly differentiated and genetic relatedness generally corresponds with geographic proximity rather than their host compatibility. Due to the dearth of broad-spectrum resistance found among Striga-resistant cowpea lines, there exists a need to stack multiple Striga resistance genes in order to confer broad-spectrum and durable resistance.

scholarly journals Recent Strategies for Detection and Improvement of Brown Planthopper Resistance Genes in Rice: A Review

Plants ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 1202
Author(s):  
Bello Sani Haliru ◽  
Mohd Y. Rafii ◽  
Norida Mazlan ◽  
Shairul Izan Ramlee ◽  
Isma’ila Muhammad ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Large Scale ◽  
Insect Pest ◽  
Durable Resistance ◽  
Brown Planthopper ◽  
Gene Clusters ◽  
Nilaparvata Lugens ◽  
Scale Production ◽  
Rice Varieties ◽  
Resistant Genes

Brown planthopper (BPH; Nilaparvata lugens Stal) is considered the main rice insect pest in Asia. Several BPH-resistant varieties of rice have been bred previously and released for large-scale production in various rice-growing regions. However, the frequent surfacing of new BPH biotypes necessitates the evolution of new rice varieties that have a wide genetic base to overcome BPH attacks. Nowadays, with the introduction of molecular approaches in varietal development, it is possible to combine multiple genes from diverse sources into a single genetic background for durable resistance. At present, above 37 BPH-resistant genes/polygenes have been detected from wild species and indica varieties, which are situated on chromosomes 1, 3, 4, 6, 7, 8, 9, 10, 11 and 12. Five BPH gene clusters have been identified from chromosomes 3, 4, 6, and 12. In addition, eight BPH-resistant genes have been successfully cloned. It is hoped that many more resistance genes will be explored through screening of additional domesticated and undomesticated species in due course.

scholarly journals Identification of Clusters that Condition Resistance to Anthracnose in the Common Bean Differential Cultivars AB136 and MDRK

2017 ◽  
Vol 107 (12) ◽  
pp. 1515-1521 ◽  
Author(s):  
Ana Campa ◽  
Noemí Trabanco ◽  
Juan José Ferreira
Keyword(s):  
Linkage Group ◽  
Common Bean ◽  
Resistance Genes ◽  
Correct Identification ◽  
Genetic Dissection ◽  
Breeding Programs ◽  
Anthracnose Resistance ◽  
Differential Cultivars ◽  
The Common ◽  
Or Genes

The correct identification of the anthracnose resistance systems present in the common bean cultivars AB136 and MDRK is important because both are included in the set of 12 differential cultivars proposed for use in classifying the races of the anthracnose causal agent, Colletrotrichum lindemuthianum. In this work, the responses against seven C. lindemuthianum races were analyzed in a recombinant inbred line population derived from the cross AB136 × MDRK. A genetic linkage map of 100 molecular markers distributed across the 11 bean chromosomes was developed in this population to locate the gene or genes conferring resistance against each race, based on linkage analyses and χ2 tests of independence. The identified anthracnose resistance genes were organized in clusters. Two clusters were found in AB136: one located on linkage group Pv07, which corresponds to the anthracnose resistance cluster Co-5, and the other located at the end of linkage group Pv11, which corresponds to the Co-2 cluster. The presence of resistance genes at the Co-5 cluster in AB136 was validated through an allelism test conducted in the F2 population TU × AB136. The presence of resistance genes at the Co-2 cluster in AB136 was validated through genetic dissection using the F2:3 population ABM3 × MDRK, in which it was directly mapped to a genomic position between 46.01 and 47.77 Mb of chromosome Pv11. In MDRK, two independent clusters were identified: one located on linkage group Pv01, corresponding to the Co-1 cluster, and the second located on LG Pv04, corresponding to the Co-3 cluster. This report enhances the understanding of the race-specific Phaseolus vulgaris–C. lindemuthianum interactions and will be useful in breeding programs.

scholarly journals Genetic Analysis of the Resistance to Eight Anthracnose Races in the Common Bean Differential Cultivar Kaboon

2011 ◽  
Vol 101 (6) ◽  
pp. 757-764 ◽  
Author(s):  
Ana Campa ◽  
Ramón Giraldez ◽  
Juan José Ferreira
Keyword(s):  
Common Bean ◽  
Resistance Genes ◽  
Specific Resistance ◽  
Pathogenic Fungus ◽  
Gene Clusters ◽  
Colletotrichum Lindemuthianum ◽  
Anthracnose Resistance ◽  
Complementary Gene ◽  
Or Gene ◽  
Dominant Genes

Resistance to the eight races (3, 7, 19, 31, 81, 449, 453, and 1545) of the pathogenic fungus Colletotrichum lindemuthianum (anthracnose) was evaluated in F3 families derived from the cross between the anthracnose differential bean cultivars Kaboon and Michelite. Molecular marker analyses were carried out in the F2 individuals in order to map and characterize the anthracnose resistance genes or gene clusters present in Kaboon. The analysis of the combined segregations indicates that the resistance present in Kaboon against these eight anthracnose races is determined by 13 different race-specific genes grouped in three clusters. One of these clusters, corresponding to locus Co-1 in linkage group (LG) 1, carries two dominant genes conferring specific resistance to races 81 and 1545, respectively, and a gene necessary (dominant complementary gene) for the specific resistance to race 31. A second cluster, corresponding to locus Co-3/9 in LG 4, carries six dominant genes conferring specific resistance to races 3, 7, 19, 449, 453, and 1545, respectively, and the second dominant complementary gene for the specific resistance to race 31. A third cluster of unknown location carries three dominant genes conferring specific resistance to races 449, 453, and 1545, respectively. This is the first time that two anthracnose resistance genes with a complementary mode of action have been mapped in common bean and their relationship with previously known Co- resistance genes established.

scholarly journals Identification of a RAPD marker linked to the Co-6 anthracnose resistant gene in common bean cultivar AB 136

2000 ◽  
Vol 23 (3) ◽  
pp. 633-637 ◽  
Author(s):  
Ana Lilia Alzate-Marin ◽  
Henrique Menarim ◽  
José Mauro Chagas ◽  
Everaldo Gonçalves de Barros ◽  
Maurilio Alves Moreira
Keyword(s):  
Common Bean ◽  
Rapd Markers ◽  
Rapd Marker ◽  
Durable Resistance ◽  
Gene Pyramiding ◽  
Dominant Gene ◽  
Segregation Ratio ◽  
Colletotrichum Lindemuthianum ◽  
Bean Cultivar ◽  
Common Bean Cultivar

The pathogenic variability of the fungus Colletotrichum lindemuthianum represents an obstacle for the creation of resistant common bean (Phaseolus vulgaris L.) varieties. Gene pyramiding is an alternative strategy for the development of varieties with durable resistance. RAPD markers have been proposed as a means to facilitate pyramiding of resistance genes without the need for multiple inoculations of the pathogens. The main aims of this work were to define the inheritance pattern of resistance present in common bean cultivar AB 136 in segregating populations derived from crosses with cultivar Rudá (susceptible to most C. lindemuthianum races) and to identify RAPD markers linked to anthracnose resistance. The two progenitors, populations F1 and F2, F2:3 families and backcross-derived plants were inoculated with race 89 of C. lindemuthianum under environmentally controlled greenhouse conditions. The results indicate that a single dominant gene, Co-6, controls common bean resistance to this race, giving a segregation ratio between resistant and susceptible plants of 3:1 in the F2, 1:0 in the backcrosses to AB 136 and 1:1 in the backcross to Rudá. The segregation ratio of F2:3 families derived from F2 resistant plants was 1:2 (homozygous to heterozygous resistant). Molecular marker analyses in the F2 population identified a DNA band of approximately 940 base pairs (OPAZ20(940)), linked in coupling phase at 7.1 cM of the Co-6 gene. This marker is being used in our backcross breeding program to develop Rudá-derived common bean cultivars resistant to anthracnose and adapted to central Brazil.

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