First Report of Alternaria alternata and Fusarium spp. Causing Brown Apical Necrosis in Walnut Fruit in Southern Chile

Author(s):  
Ernesto Antonio Moya-Elizondo ◽  
María Jose Lagos ◽  
Juan G. San Martín ◽  
Braulio E. Ruiz

This is the first report of Alternaria alternata and Fusarium spp. causing brown apical necrosis (BAN) in walnut fruit in southern Chile. English walnut (Juglans regia L.) is the second most widely grown fruit in Chile. The bacterial pathogen Xanthomonas arboricola pv. juglandis affects walnut production in Chile and has been associated with apical necrosis symptom and premature fruit drop; this research focused on determining if fungal pathogens were associated with this damage. The presence of BAN in commercial walnut orchards in southern Chile reveals the need for improved phytosanitary programs to control this disease.

Plant Disease ◽  
2002 ◽  
Vol 86 (6) ◽  
pp. 599-602 ◽  
Author(s):  
A. Belisario ◽  
M. Maccaroni ◽  
L. Corazza ◽  
V. Balmas ◽  
A. Valier

In 1998, a severe fruit drop was observed in Italy, principally on cv. Lara Persian (English) walnut (Juglans regia). Dropped fruit showed a brown patch at the blossom end and blackening and rot of inner tissues. The disease, called brown apical necrosis (BAN), was investigated on fruit collected in Italy and France in 1999. In 2000, studies were carried out in three walnut orchards located in Italy and in France to substantiate the etiology of BAN. Isolations performed from inner diseased fruit tissues yielded several fungi, in decreasing frequency of isolation: species of Fusarium and Alternaria, and one species each of Cladosporium, Colletotrichum, and Phomopsis. However, only Fusarium spp. were recovered from stigmas of BAN-affected fruit. The fungi associated with BAN-diseased fruit and species composition differed among locations and over time, confirming results obtained in previous investigations. The species of Fusarium used in pathogenicity tests reproduced BAN-disease symptoms when inoculated on fruit, whereas an Alternaria alternata isolate caused only limited necrosis of the style. However, the role of the other fungi commonly isolated from BAN-diseased fruit remains to be defined. The walnut blight pathogen, Xanthomonas arboricola pv. juglandis, occasionally was isolated from BAN-diseased fruit. No correlation was found between the extent of external brown patches and the size of inner lesions. Repeated isolations from and inoculations of fruit demonstrated that BAN can be considered a complex disease, and the inner infections originate from the style of the fruit.


Plant Disease ◽  
2011 ◽  
Vol 95 (12) ◽  
pp. 1565-1570 ◽  
Author(s):  
Concepció Moragrega ◽  
Josep Matias ◽  
Neus Aletà ◽  
Emilio Montesinos ◽  
Mercé Rovira

Etiological and epidemiological aspects of apical necrosis of walnut fruit were studied on cultivars Chandler, Franquette, and Hartley in a Spanish walnut orchard during 2007 and 2008. Affected fruit showed brown necrosis beginning at the blossom end of nuts; these symptoms differed from lesions of common blight of walnut (Xanthomonas arboricola pv. juglandis). X. arboricola pv. juglandis was consistently isolated from apical lesions throughout the growing season. Field isolates reproduced symptoms observed in the orchard when inoculated on immature detached walnut fruit in the laboratory. Sporadic occurrence of Fusarium spp. and Alternaria spp., mainly in dropped fruit, was attributed to secondary colonization of apical lesions that were originally caused by X. arboricola pv. juglandis. Apical necrosis and common blight were similar in disease epidemiology and cultivar susceptibility; a major increase in epidemics occurred at initial fruit development, and cvs. Chandler and Hartley were more affected than cv. Franquette. Our results suggest that apical necrosis is a new manifestation of walnut blight characterized by distinct symptoms and severe premature fruit drop.


Plant Disease ◽  
1999 ◽  
Vol 83 (7) ◽  
pp. 696-696 ◽  
Author(s):  
A. Belisario ◽  
E. Forti ◽  
L. Corazza ◽  
H. A. van Kesteren

A foliar disease of English walnut (Juglans regia L.) was observed in 1998 in an orchard in northern Italy. Symptoms consisted of circular, necrotic spots bordered with concentric zones of darker tissue. Average lesion diameter was 20 mm, although lesions could extend to half of the leaflet lamina. A fungus identified as Alternaria alternata (Fr.:Fr.) Keissl. (1) was observed on the necrotic tissue and was consistently isolated from the margins of the necrosis. Conidia from leaves were brown, ellipsoid to ovoid (primary conidia 28 to 60 × 8 to 15 μm; secondary conidia 10 to 30 × 7 to 13 μm), with walls often ornamented, 1 to 6 transversely septate and 0 to 3 longitudinally septate. For pathogenicity tests, three isolates were grown on potato dextrose agar for 2 weeks. Inoculations were performed on detached, surface-sterilized, healthy J. regia leaflets. Four drops (5 μl each) of a sterile water suspension of 1 × 105 conidia per ml were placed on each leaflet; three leaves per isolate were used. Leaves were incubated in a moist chamber. After 10 days, leaf spots similar to the original symptoms developed on all the inoculated points for all three isolates, and the pathogen was reisolated. Control leaflets inoculated with sterile, distilled water remained symptomless. The experiment was performed three times and the results were similar. Alternaria alternata is a well-known pathogen on many crops but a few records report this fungus as a causal agent of leaf spot on deciduous trees. This is the first report of A. alternata on English walnut. Reference: (1) E. G. Simmons. Mycotaxon 37:79, 1990.


Plant Disease ◽  
2003 ◽  
Vol 87 (3) ◽  
pp. 315-315 ◽  
Author(s):  
A. Belisario ◽  
M. Maccaroni ◽  
A. M. Vettraino ◽  
A. Vannini

English (Persian) walnut (Juglans regia), among the most widely cultivated species of Juglans worldwide, is cultivated primarily for fruit production but also for timber. In the last 10 years, walnut decline causing leaf yellowing, sparse foliage, overall decline, and plant death has increased in Italian commercial orchards. In Italy, Phytophthora cactorum, P. cambivora, P. cinnamomi, and P. cryptogea are associated with this disease (1,4). Over the last 5 years, P. cinnamomi was the most widely isolated and destructive species (1). Recently, a different species of Phytophthora was isolated from diseased roots and soil from around lateral roots of 10 declining trees in two orchards in the Veneto Region of northern Italy. Another species of Phytophthora was isolated consistently from rotted roots of declining walnut trees in two orchards in the Campania Region of southern Italy. Phytophthora spp. were isolated directly from plant material or Rhododendron spp. leaf baiting on soil samples with PARBhy selective medium (10 mg of pimaricin, 250 mg of ampicillin [sodium salt], 10 mg of rifampicin, 50 mg of hymexazol, 15 mg of benomyl, 15 g of malt extract, 20 g of agar in 1,000 ml of H2O). Two species of Phytophthora were identified based on morphological and cultural characteristics (2). The species from trees in the Veneto Region was identified as P. nicotianae. All isolates produced papillate, spherical to obturbinate, occasionally caducous sporangia with short pedicels, terminal and intercalary chlamydospores, and were mating type A2. The species isolated from trees in the Campania Region was identified as P.citricola. Isolates were homothallic, produced semipapillate, persistent, obclavate to obpyriform sporangia, occasionally with two apices, and antheridia paragynous. Identifications were confirmed by comparing restriction fragment length polymorphism patterns of the internal transcribed spacer region of rDNA with those obtained from previously identified species of Phytophthora. Pathogenicity of two isolates each of P. citricola and P. nicotianae was tested on 2-year-old potted walnut seedlings. Inocula were prepared by inoculating sterilized millet seeds moistened with V8 broth with plugs of mycelium and incubated for 4 weeks at 20°C in the dark. Infested seeds were added to potting soil at a rate of 3% (wt/vol). One day later, pots were flooded for 48 h to promote sporulation. Ten noninoculated seedlings were used as the control. Symptoms were assessed 2 months after inoculation. Seedlings inoculated with P. nicotianae developed necrosis of feeder and lateral roots, but only limited infection of taproots. Seedlings inoculated with P. citricola developed necroses at the insertion points of lateral roots. All four isolates produced visible damage to lateral roots on inoculated plants. P. nicotianae and P. citricola were reisolated from respectively infected roots. Results from these inoculations confirmed P. nicotianae and P. citricola as root pathogens of English walnut. Both species were associated with walnut decline as reported in the United States (3). To our knowledge, this is the first report of P. nicotianae and P. citricola on J. regia in Europe. References: (1) A. Belisario et al. Petria 11:149. (2) D. C. Erwin and O. K. Ribeiro. Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN, 1996. (3) M. E. Matheron and S. M. Mircetich. Phytopathology 75:977, 1985. (4) A. M. Vettraino et al. Plant Dis. 86:328, 2002.


2010 ◽  
pp. 449-452 ◽  
Author(s):  
A. Belisario ◽  
A. Santori ◽  
G. Potente ◽  
A. Fiorin ◽  
B. Saphy ◽  
...  

Plant Disease ◽  
2010 ◽  
Vol 94 (10) ◽  
pp. 1267-1267 ◽  
Author(s):  
F. P. Trouillas ◽  
J. R. Úrbez-Torres ◽  
F. Peduto ◽  
W. D. Gubler

California produces 99% of the U.S. English walnut crop with more than 30 cultivars on ~89,000 ha. Production for 2008 was ~436,000 tons with a value of $527 million. In early summer of 2009 and 2010, branch and twig dieback of English walnut (Juglans regia L.) was detected in orchards in Yolo County and submitted to our diagnostic laboratory. Disease symptoms included death of twig tips, branch dieback, wood lesions, and canker formation. Pycnidia were embedded within the bark of dead twigs. Conidia from pycnidia were hyaline, fusoid-ellipsoidal, widest usually in the middle, and 21 to 24 (–27) × 5 to 7 μm (n = 30). Isolations from cankers yielded the fungus Neofusicoccum mediterraneum Crous, M.J. Wingf. & A.J.L. Phillips (1). Fungal colonies of N. mediterraneum grew light olive green to gray on potato dextrose agar, becoming dark olive green with age. Identification of fungal isolates was confirmed by sequence comparison of Californian isolates with ex-type (CBS 121558) sequences in GenBank (3) using the internal transcribed spacer region of the rDNA, a portion of the β-tubulin gene, and part of the translation elongation factor. Sequences of Californian isolates (GenBank HM443604–HM443609) were identical to the ex-type sequences for all three genes. Previous studies in California reported the occurrence and pathogenicity of N. mediterraneum into grapevine (Vitis vinifera L.) (3) and almond trees (Prunis dulcis L.) (2). Inderbitzin et al (2) investigated the host range of N. mediterraneum in California and reported the occurrence of pycnidia on English walnut trees. However, this study did not investigate the pathogenicity of N. mediterraneum on this host. In the current study, the pathogenicity of N. mediterraneum in J. regia cvs. Hartley and Chandler was investigated in an orchard at UC Davis using two fungal isolates. Pathogenicity tests were performed by inoculating eight 2- to 4-year-old branches of mature J. regia trees. Inoculations were made in June 2009 with a 5-mm cork borer to remove bark and placing an 8-day-old 5-mm-diameter agar plug bearing fresh mycelium of the fungal isolates directly into the fresh wound, mycelium side down. An additional eight branches of each cultivar were inoculated with noncolonized agar plugs to serve as controls. Inoculated wounds were covered with petroleum jelly and wrapped with Parafilm to retain moisture. Branches were harvested after 10 months of incubation and checked for canker development. The extent of vascular discoloration was measured in each branch and isolations were made from the edge of discolored tissue to confirm Koch's postulates. Statistical analyses were performed with analysis of variance and Dunnett's t-test to assess significant differences in the extent of vascular discoloration between inoculations with N. mediterraneum and the control. Necrosis length for the two isolates averaged 131.5 mm in Hartley branches and 110 mm in the Chandler branches. Average necrosis lengths in the control branches were 18.5 mm and 16.7 mm, respectively, significantly lower (P < 0.05) than the average necrosis length found in branches inoculated with N. mediterraneum. Fungal recovery was 75% in both varieties. To our knowledge, this study is the first report of N. mediterraneum as a pathogen of J. regia trees in California. References: (1) P. W. Crous et al. Fungal Planet 19, 2007. (2) P. Inderbitzin et al. Mycologia. Online publication. doi:10.3852/10-006, 2010. (3) J. R. Úrbez-Torres et al. Plant Dis. 94:785, 2010.


Plant Disease ◽  
2000 ◽  
Vol 84 (5) ◽  
pp. 592-592 ◽  
Author(s):  
W. Chen ◽  
W. J. Swart

Cultivation of English walnut (Juglans regia L.) has considerable economic potential in South Africa. In February 1999, die-back of walnut trees was observed on ≈30% of trees in an orchard in Gauteng Province, South Africa. Die-back was associated with characteristic cankers and discoloration of the cambial tissue of twigs and young branches. Fifty pieces of discolored tissue from the margins of cankers of five trees were transferred to potato dextrose agar (PDA) after surface-sterilization with 0.5% NaOCl. Fungal colonies emerged from all 50 pieces of diseased tissue. Fungi recovered included Fusarium solani (74.5%), Alternaria tenuissima (17.3%), and a Phoma sp. (6.2%). Small pieces of sterile cheesecloth (10 × 5 mm) were cultured on PDA with an isolate of F. solani from infected walnut trees. Colonized pieces of cheesecloth were applied to stems (≈5-mm diameter) of nine potted J. regia plants in a glasshouse. Each stem was wounded by lightly scraping off a length of bark (5 × 5 mm). Colonized cheesecloth was wrapped around the wound and covered with Parafilm to prevent desiccation of mycelia in the cheesecloth. Nine walnut stems were similarly treated with sterile cheesecloth pieces to serve as control treatments. After 4 weeks, die-back of foliage was observed in all plants artificially inoculated with F. solani. Cheesecloth pieces and surrounding bark were removed, and the length and width of each cambial lesion was measured. The mean area of cambial lesions (length by width) resulting from artificial inoculations was 27.3 × 8.5 mm. None of the control plants developed any symptoms. Koch's postulates were confirmed by consistently reisolating F. solani from inoculated plants. A similar disease of black walnut (J. nigra) was reported by Carlson et al. (1) from five central states in the United States. Our findings represent the first report of F. solani as a causal agent of stem canker of English walnut in South Africa. Reference: (1) J. C. Carlson et al. N. J. Appl. For. 10:1, 1993.


Plant Disease ◽  
2011 ◽  
Vol 95 (6) ◽  
pp. 773-773 ◽  
Author(s):  
K. Q. Yang ◽  
W. W. Qu ◽  
X. Liu ◽  
H. X. Liu ◽  
L. Q. Hou

Brown apical necrosis (BAN) of walnut (Juglans regia L.) causes premature fruit drop and yield losses and has been reported to be an important walnut production problem in Spain, Italy, France, and Turkey (1,2). A number of organisms have been associated with BAN on walnut: Xanthomonas arboricola pv. juglandis, Fusarium spp., and Alternaria spp. (3). Since the spring of 2007, BAN was observed in 50 to 60% of the trees in walnut orchards in Taian City and Laiwu City, Shandong Province, China. Surface-disinfested tissue from premature walnut fruits was placed onto potato dextrose agar. Alternaria spp., X. arboricola pv. juglandis, and Pantoea agglomerans (formerly Enterobacter agglomerans) were isolated 76, 35, and 45% of the time, respectively. The P. agglomerans cultures formed a yellow lawn and were rod shaped with the body length of 1.5 to 3.0 μm, width of 0.5 to 1.0 μm, and four to six flagella. In biochemical tests, these bacteria were gram negative, lactose positive, and indole negative. Genomic DNA was extracted from one HXJ isolate and the 16S rRNA gene sequence (GenBank Accession No. HM016799) was obtained using universal primers 27F and 1492R. HM016799 had 99% sequence identity with P. agglomerans accessions in GenBank (GU477762, GQ494018, FJ756355, and AB004757). To confirm pathogenicity, HXJ isolate (108 CFU·ml–1) was inoculated at the bottom of the stigma within 5 days after florescence (DAF) and in premature fruit wounded with a needle within 30 DAF in 2008 to 2010. Stigmas injected with only sterile water served as controls. The bacteria were inoculated into three replicate 9-year-old plants of the walnut cv. Xiangling. Forty nuts on each plant were inoculated. The plants were grown in Shandong Province, China (36°09′59″N, 117°13′30″E). Ten days after inoculation, typical internal BAN symptoms were observed on all treated nuts and the controls were still healthy. In the inoculated stigmas, necrosis of stigma and style spread to internal tissues and reached the kernel. In treated premature fruit, internal tissues became necrotic and blackish and eventually led to nut drop. The same bacterium was reisolated from the inoculated tissue. On the basis of morphological, physiological, and biochemical characteristics and sequencing of the 16S rRNA gene, the bacterium was identified as P. agglomerans. To our knowledge, this is the first report of P. agglomerans causing internal type BAN of walnut in China or worldwide. References: (1) A. Belisario et al. Plant Dis. 6:599, 2002. (2) G. Bouvet. Acta Hortic. 705:447, 2005. (3) C. Moragrega and H. Özaktan. J. Plant Pathol. 92:S1.67, 2010.


Plant Disease ◽  
2017 ◽  
Vol 101 (2) ◽  
pp. 382
Author(s):  
Y. Q. Cheng ◽  
Y. T. Ming ◽  
B. W. Yang ◽  
T. Liu ◽  
J. F. Liu

2000 ◽  
Vol 10 (1) ◽  
pp. 127-130
Author(s):  
William H. Krueger

English walnut (Juglans regia, L.) is a monoecious species bearing staminate and pistillate flowers separately on the same tree. Walnuts are generally self-fruitful, cross-compatible and dichogamous, having incomplete overlap of pollen shed and female receptivity. It is this characteristic which led to the recommendation that about 10% of the trees in a commercial planting be a cultivar with a pollen shed period overlapping pistillate flower receptivity of the main cultivar. Excessive pollen load has been implicated in the `Serr' cultivar in pistillate flower abortion (PFA), the loss of the female flowers early in the season before fruit drop due to lack of pollination. PFA can be reduced and yield improved in `Serr' orchards by reducing pollen load. This can be accomplished by pollinizer removal, or catkin removal at the beginning of pollen shed by mechanical shaking. In years of significant bloom overlap between staminate and pistillate bloom, PFA can be further reduced and yield improved by removing `Serr' catkins. PFA occurs to a lesser extent in other cultivars such as `Chico', `Chandler', `Vina' and `Howard'. This information has led to the reevaluation of pollinizer recommendations. Research focused on optimum pollinizer levels in `Chandler', a cultivar of increasing importance to the California walnut industry, has been inconclusive. Lack of pollinizers may impact yields to a greater extent in the in the northern San Joaquin Valley and Sacramento Valley than in the southern San Joaquin Valley. In any case the previously recommended 10% appears to be excessive. Two to three percent is probably adequate to limit losses due to lack of pollination without resulting in excessive PFA, and is currently being recommended by extension farm advisors and specialists. Factors to consider when determining the number of pollinators to plant include: cultivar susceptibility to PFA, walnut pollen load in the area and local pollination and fruit set experiences.


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