Endophytic Microorganisms Associated with Reversion of Silverleaf Disease Symptoms in Apple.

Silverleaf is caused by the fungus Chondrostereum purpureum, which produces wood necrosis and foliar silvering in woody plants. Field observations and studies in apple have shown the reversion of foliar symptoms. Because plants were clones and received identical agronomical management, it was hypothesized that reversion is driven by endophytic microbiota. Thus, the objectives of this study were to compare healthy, diseased, and reverted plants with respect to their physiology, endophytic microbial communities, antagonistic ability of their endophytes against C. purpureum, and defense genes expression. Water potential, stomatal conductance, chlorophyll content, and fluorescence were measured. Endophytic bacterial and fungal DNA were analyzed by denaturing gradient gel electrophoresis, and community richness and similarity were calculated. Wood cores were collected and bacterial and fungal endophytes were isolated and confronted with C. purpureum-virulent strains in dual-culture assays. Defense genes expression was measured by quantitative PCR. Results indicated that there were no differences in physiological parameters between healthy and reverted plants, except for fluorescence, and both type of plants differed from diseased ones. Bacterial and fungal community richness was similar in healthy and reverted plants and higher than in diseased ones. Endophytes from reverted and healthy plants showed high antagonism to C. purpureum. Furthermore, nonexpressor of pathogenesis-related gene 1 expression was upregulated in reverted plants, whereas phenylalanine ammonia lyase and polygalacturonase-inhibiting protein genes showed higher values in diseased plants. Overall, physiological, molecular, and microbial characteristics were similar between healthy and reverted plants, and both differed from diseased ones. Therefore, reversion of symptoms is associated with changes in the endophytic microbiota, which seems to be a promising source of biological control agents against C. purpureum.

A PCR-Based Method for the Rapid Detection of Chondrostereum purpureum in Apple.

Silverleaf caused by the basidiomycete Chondrostereum purpureum affects numerous woody species, including fruit tree crops like apple, resulting in wood necrosis and foliar silvering. There are no curative alternatives for this disease, and its management is by prevention methods. Therefore, the aim of this study was to develop a rapid diagnostic tool for the detection and identification of C. purpureum directly from woody tissues to help distinguish the pathogen from other basidiomycetes that are commonly found on apple. The silverleaf pathogen was isolated from different hosts and locations, and Koch's postulates were performed by inoculating the isolates on apple cuttings and measuring internal necrosis. A previously described APN 1 pair of primers specificity was also tested against 25 C. purpureum isolates in this study, using other wood rotting species as negative controls. Seven virulent isolates were inoculated on apple cuttings, and DNA was extracted from the cuttings' sawdust and amplified using APN 1, after 22 days of incubation. To prove the efficiency of the method in the field, DNA from healthy nursery plants inoculated with two virulent isolates, and naturally infected plants showing different levels of foliar symptoms, were tested. Presence of the fungus was verified by reisolation on APDA in all assays. Koch's postulates indicated that all C. purpureum isolates were pathogenic, showing different virulence levels, and APN 1 primers were able to discriminate them from other basidiomycetes. The method was also able to detect C. purpureum from artificially inoculated plants as well as naturally infected ones, demonstrating that the protocol may become a rapid minimally destructive diagnostic tool to detect the pathogen without the need to isolate it from tissues, and thus taking measures to prevent its dissemination.

First Report of Fusarium sporotrichioides Causing Foliar Spots on Forage Corn in Chile.

In southern Chile, forage corn (Zea mays L.) is grown for feeding animals in milk diaries and livestock production. In December 2010, corn plants with small circular spots on leaves were collected from three fields located in Río Negro (Los Lagos region). Symptoms began as small, circular white to brown spots of 5 to 10 mm on different parts of the leaf and necrotic tissue with irregular brown to burgundy margins on the border and tip of the leaf. Estimated visual severity was ~5 to 40% for each leaf from field samples. Twelve small blocks of tissue were taken from the edge of necrotic spots from infected leaves, surface disinfected (2 min in 95% ethanol, 2 min in 0.5% NaOCl, followed by three rinses with sterile distilled water), and then placed on PDA and incubated for 7 days at 24 ± 1°C. Seventy five percent of the sampled tissues developed fungal colonies and a 4-mm3 block of agar that contained the advancing hyphal edge of each colony was transferred to PDA and carnation leaf agar and incubated for 10 days at 24 ± 1°C. Colonies were fast growing with pink-white and dense mycelia; with a carmine red color on the undersurface of the plate and orange sporodochia; polyphialides abundant; microconidia abundant, oval or pear-shaped or spindle-shaped, thin walled, hyaline, often with a papilla at the base, and 5.5 to 12.2 × 2.0 to 3.2 µm. Macroconidia were sickle-shaped, 3 to 5 septate, moderately curved to straight, hyaline, thick walled, and 20.5 to 42.9 × 3.5 to 5.0 µm. Morphology of colonies and conidia matched the description of Fusarium sporotrichioides Sherb. (3). Identity of the fungus was confirmed by molecular characterization of the ITS and 18SrRNA regions (universal primers ITS4/5 and NS1/2, respectively) and the ß-tubulin gene (primers Bt1a/Bt1b) of three isolates. BLAST searches of the obtained sequences had between 99 to 100% homology with several isolates of F. sporotrichioides from GenBank (Accession Nos. KC866343 to KC866351). Pathogenicity tests were conducted by dispensing 10 µl of a prepared spore suspension (107 spores/ml) on corn leaves (16 leaves). Negative controls were corn leaves inoculated with sterile distilled water. Inoculated corn leaves were kept at 25 ± 1°C in glass bell jars and monitored for the onset of symptoms for 10 days. The test was conducted twice. Additionally, 20 corn plants of four hybrid lines were inoculated with ~5 ml of a spore suspension (104 macroconidia/ml) 2 months after seeding under field conditions in Valdivia, Los Ríos region, Chile. Seventy five days after sowing, similar lesions to those initially observed on field infected leaves were observed on inoculated leaves but not on water controls. Under field conditions, an extended damage on borders of basal leaves and spots on stems and cobs was observed. The pathogen was reisolated from infected tissues, thereby fulfilling Koch's postulates. F. sporotrichioides is a frequent pathogen in corn silage (1) and cereal crops (3,4), and produces trichothecene mycotoxins that cause toxicosis in animals (2,3). To our knowledge, this is the first report of F. sporotrichioides causing foliar spot on forage corn in Chile and this disease could represent a serious risk of mycotoxin contamination in this crop. References: (1) H. Baath et al. Arch. Tierernahr. 40:397, 1990. (2) A. E. Desjardins et al. Phytopathology 79:170, 1989. (3) J. F. Leslie and B. A. Summerell. Page 256 in: The Fusarium Laboratory Manual. Blackwell Publishing Professional, Hoboken, NJ, 2006. (4) R. H. Vargo et al. Plant Dis. 70:629, 1986.