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Colletotrichum sublineola is a destructive fungal pathogen that causes anthracnose in sorghum. Senegalese sorghum germplasm is currently being considered as an option of sources for genetic resistance. In a recent study, Senegalese sorghum accessions were evaluated for response to a mixture of Texas isolates of C. sublineola at the 8-leaf stage in the greenhouse. As a comparison, 159 Senegalese sorghum accessions at the 1-leaf developmental stage were evaluated against a single Texas isolate of C. sublineola (FSP53) using an excised-leaf assay. A genome-wide association study (GWAS) was conducted based on the phenotypic data acquired to discover genetic variation associated with response to C. sublineola using 193,727 single nucleotide polymorphisms (SNPs) throughout the genome. Sorghum seedlings tended to be more resistant when compared with sorghum plants inoculated at the 8-leaf stage in the greenhouse in previous experiments. Based on the highest score evaluated in the 1-leaf developmental stage excised leaf assay for each accession, 16 accessions were labeled as susceptible. GWAS identified the SNP locus S01_72868925 that is associated with protein kinase domain // Leucine rich repeat N-terminal domain at a level of confidence that surpassed Bonferroni correction. Along with the SNP locus S01_72868925, other top SNP loci were also associated with genes that are known to play critical roles in plant defense or plant stress responses. [ABSTRACT FROM AUTHOR]

Anthracnose caused by the fungal pathogen C. sublineola is an economically important constraint on worldwide sorghum production. The most effective strategy to safeguard yield is through the introgression of resistance alleles. This requires elucidation of the genetic basis of the different resistance sources that have been identified. In this study, 223 recombinant inbred lines (RILs) derived from crossing anthracnose-differentials QL3 (96 RILs) and IS18760 (127 RILs) with the common susceptible parent PI609251 were evaluated at four field locations in the United States (Florida, Georgia, Texas, and Puerto Rico) for their anthracnose resistance response. Both RIL populations were highly susceptible to anthracnose in Florida and Georgia, while in Puerto Rico and Texas they were segregating for anthracnose resistance response. A genome scan using a composite linkage map of 982 single nucleotide polymorphisms (SNPs) detected two genomic regions of 4.31 and 0.85 Mb on chromosomes 4 and 8, respectively, that explained 10–27% of the phenotypic variation in Texas and Puerto Rico. In parallel, a subset of 43 RILs that contained 67% of the recombination events were evaluated against anthracnose pathotypes from Arkansas (2), Puerto Rico (2) and Texas (4) in the greenhouse. A genome scan showed that the 7.57 Mb region at the distal end of the short arm of chromosome 5 is associated with the resistance response against the pathotype AMP-048 from Arkansas. Comparative analysis identified the genomic region on chromosome 4 overlaps with an anthracnose resistance locus identified in another anthracnose-differential line, SC414-12E, indicating this genomic region is of interest for introgression in susceptible sorghum germplasm. Candidate gene analysis for the resistance locus on chromosome 5 identified an R-gene cluster that has high similarity to another R-gene cluster associated with anthracnose resistance on chromosome 9. [ABSTRACT FROM AUTHOR]

A total of 377 lines from Sorghum Association Panel (SAP) grouped into 10 subpopulations based on eight phenotypic traits, including flag leaf width, terminal branch length, flag leaf height, and flowering time and genetic data were evaluated for grain mold resistance by inoculating them with Alternaria alternata alone, a mixture of A. alternata, Fusarium thapsinum, and Curvularia lunata, and untreated water-sprayed control during 2010, 2013–2015 growing seasons at the Texas A&M AgriLife Research Farm, Burleson County, Texas. Each accession was evaluated at least twice. Eleven accessions exhibited grain mold severity ratings of 2 or less, indicating that they were resistant to highly resistant to the disease when challenged with A. alternata alone, 7 lines identified as such when inoculated with a mixture of A. alternata, F. thapsinum, and C. lunata, and 17 resistant lines were identified under the untreated control. Three lines PI533871, PI576130, and PI656036 exhibited resistant to highly resistant response to grain mold across treatments. When the 10 subpopulations were compared for disease response, accessions within subpopulation 4 had the lowest overall grain mold severity ratings, indicating that this subpopulation (zerazera/caudatum racial type) harbors genes that may contribute to grain mold resistance. A genome-wide association study with over 79,000 single-nucleotide polymorphic (SNP) loci from a publicly available genotype by sequencing dataset available for the (SAP) lines was conducted to identify genomic regions associated with grain mold resistance response based on the individual and combined treatments. In most cases, the top-scoring SNPs were mapped to the nearest or a nearby annotated gene with precedence for a role in host defense. [ABSTRACT FROM AUTHOR]

Key message: SNPs identify prospective genes related to response to Colletotrichum sublineola (anthracnose) in the sorghum association panel lines. Sorghum association panel (SAP) lines were scored over several years for response to Colletotrichum sublineola, the causal agent of the disease anthracnose. Known resistant and susceptible lines were included each year to verify successful inoculation. Over 79,000 single-nucleotide polymorphic (SNP) loci from a publicly available genotype by sequencing dataset available for the SAP lines were used with TASSEL association mapping software to identify chromosomal locations associated with differences in disease response. When the top-scoring SNPs were mapped to the published sorghum genome, in each case, the nearest annotated gene has precedence for a role in host defense. [ABSTRACT FROM AUTHOR]

Sporisorium reilianum causes head smut in sorghum and maize and exists in two formae speciales, Sporisorium reilianum f. sp. reilianum and Sporisorium reilianum f. sp. zeae that have preference for sorghum and maize, respectively. Infection requires the formation of a dikaryon between sporidia of compatible mating types, leading to a change from yeast-like to hyphal growth within the host plant. This switching is controlled through mating type loci. A total of 66 sorghum isolates of S. reilianum collected from fields in different geographic regions and 2 maize isolates were examined for mating compatibility, leading to the establishment of haploid cultures with three different alleles at the a mating type locus, as verified by gene expression. Interestingly, a mating compatibility was detected between maize and sorghum isolates. Comparison of amino acid sequences, deduced from nucleotide sequencing of pheromone precursor genes of sorghum to the corresponding components in maize, showed 100% similarity of pheromone components mfa1.2, mfa2.1, mfa3.1 and 97% for mfa1.3, mfa3.2 and mfa2.3. Only 1 amino acid substitution was detected in sorghum mfa1.3. To assay host preference in relationship to whole genome polymorphism, six amplified fragment length polymorphism (AFLP) selective primer combinations were used on DNA of S. reilianum isolates. High genetic polymorphism (61%) was observed between sorghum and maize isolates. The resultant dendrogram constructed using neighbor-joining (NJ) analysis grouped maize isolates into one cluster with high similarity (>88%) while sorghum isolates grouped into four clusters suggesting that genetic differentiation contributes to host specific populations of S. reilianum. [ABSTRACT FROM AUTHOR]

An amendment to this paper has been published and can be accessed via a link at the top of the paper. [ABSTRACT FROM AUTHOR]