Early blight disease caused by Alternaria sp. is one of the most devastating diseases of
Solanaceous crops widely distributed in Sudan. The aim of this study was to determine the
genetic variation among different Alternaria isolates recovered from different Solanaceae
crops showing typical symptoms of early blight disease. Infected leaves of tomato, potato,
eggplant and pepper were collected from different geographical zones in Sudan. The recovered
fungal isolates were identified to the genus level based on cultural and morphological
characteristics. Five representative isolates were sent to the CABI Bioscience, U.K. for confirmation.
The genetic relationship among the isolates was determined using the amplified
fragments length polymorphism (AFLP) technique and the generated data were used to
create similarity matrices using the PAST 3.01 software package. Dendrograms were constructed
based on Jaccard’s similarity coefficients. A total of 70 fungal isolates was recovered
from the tested plants and all of them showed morphological characteristics typical
of Alternaria spp. The conidia appeared in multiple-branched chains with spore sizes in
the range of 2.38−13.09 μm × 12.30−43.63 μm. Therefore, the isolates were identified as
Alternaria alternata (Fr.) Keissl. The identification was then confirmed by CABI.AFLPbased
dendrogram which revealed five clusters with a significant cophenetic correlation
coefficient (r = 0.834) between the dendrogram and the original similarity matrix irrespective
of their geographical origins. Eighteen (75%) of the Alternaria isolated from tomato
leaves were clustered together in cluster I and five isolates formed two separate clusters,
viz. cluster IV (T-Kh5 and T-H1) and cluster V (T-H4 and T-Med2). The remaining isolate,
T-Am5, grouped with one of the potato isolates in cluster III. The other isolates which were
recovered from potato, pepper and eggplants were all separated from the tomato isolates
in the largest cluster.
Field surveys were performed in winter and spring rape crops of agricultural companies and individual farmers during the period of 2001–2003. A questionnaire was completed for each experimental field, giving a description of the crop. The incidence and severity of fungal diseases were estimated annually in 14–18 winter and spring rape crops. Seed samples were taken from each field and composition fungal communities on harvested seed was estimated. Alternaria blight and Phoma stem canker were present on stems of all investigated winter and spring rape cultivars and Alternaria blight occurred on siliques in all experimental years. In 2001, most favourable year for spread of diseases, Alternaria blight damaged 87.2 100% of winter rape and 100% of spring rape siliques, maximum disease severity was 6.66 and 7.24%, respectively. All cultivars of winter and spring rape were susceptible to Alternaria blight. Phoma stem canker was more often found on stems of spring oilseed rape – up to 98% of stems with symptoms of Phoma stem canker. Seed fungal infection level was 10.0–100% in winter rape and 16.0–93.6% in spring rape seed samples. The most frequent fungi on seeds of winter and spring oilseed rape were Alternaria spp. and Cladosporium spp.
Black mold and green mold caused by Alternaria alternata and Penicillium digitatum, respectively, are the most important decay pathogens of tomato fruits during storage. Our research was aimed to control tomato phytopathogenic fungi A. alternata and P. digitatum in vitro and in vivo by using natural nanomaterials rosmarinic acid (RA-NPs) at concentrations of 0.3 and 0.6 mM, glycyrrhizic acid (GA-NPs) and glycyrrhizic acid ammounium salt (GAS-NPs) (0.1–0.2 mM). Characterizations of the tested nanoparticles were carried out by using dynamic light scattering which revealed that synthesized nanoparticles had particle sizes of less than 100 nm. In vitro studies revealed that the three tested nanoparticles reduced the growth of A. alternata and P. digitatum. Glycyrrhizic acid nanoparticles were the most effective in reducing the growth of the two tested pathogens followed by RA-NPs at 0.6 mM. Observations of A. alternata and P. digitatum by scanning electron microscopy (SEM) showed severe damage in the hyphae and deformities in the conidia due to the effect of the tested nanoparticles. In vivo results showed that, dipping tomato fruits as a post-harvest treatment in all of the tested nanoparticles at different concentrations, then stored at 10 ± 1°C and 90–95% relative humidity (RH) for 20 days greatly reduced the disease severity of infected fruits with the two tested pathogens. GA-NPs at 0.2 mM significantly reduced the development of black mold rot on tomato fruits. RA-NPs at 0.6 mM had the best effect in controlling P. digitatum of all naturally and artificially inoculated tomato fruits. Also, individual treatments of tomato fruits with RA-NPs, GA-NPs and GAS-NPs significantly reduced postharvest losses of fruit since they delayed decay and maintained fruit quality characteristics such as fruit firmness, titratable acidity and total soluble solids during cold storage.
Mycoherbicides are special biotechnology products which contain fungi or fungal metabolites as nonchemical alternatives thereby reducing the input of harmful chemicals to control noxious weeds. The present communication emphasizes on the potential of an indigenous isolate of Alternaria alternata ITCC 4896 as a mycoherbicide for the global weed – Parthenium hysterophorus. Of the various spore concentrations tested by in vitro Detached Leaf Bioassay, 1x106 spores/ml was the most effective inducing 89.2% leaf area damage on the 7th day and was further tested by Whole Plant Bioassay. Both in vitro Detached Leaf Bioassay and Whole Plant Bioassay exhibited a similar trend in disease development showing 50% damage at 96 hours post treatment. However, 100% mortality was observed in the Whole Plant Bioassay on the 7th day. This is the very first report on the bioweedicidal potential of A. alternata ITCC 4896 (LC#508) for use as a mycoherbicide for P. hysterophorus.
Genetically modified Bt cotton (Gossypium hirsutum) leaves with typical symptoms of Alternaria early blight disease resembling that of tomato and potato were observed in the main cotton growing schemes in Sudan. Symptoms on leaves appeared as either brown 2leaf spot with gray centers or leaf blight with concentric rings. Pathogenicity tests using isolates with both symptoms showed that the isolated fungi were highly pathogenic to both G. hirsutum and G. barbadense cotton varieties. Alternaria alternata isolated from infected tomato and potato leaves with early blight symptoms was included for comparison. Microscopic examination showed that the mean length of conidia from cotton, tomato and potato isolates ranged from 26.25 to 45.45 μm, while the width ranged from 9.56 to 13.64 μm. The mean number of transverse septa among all isolates was 3.4 to 5.7 and the peak length ranged from 3.75 to 7.8 μm. Based on morphological characteristics the two isolates from cotton were identified as A. alternata. Genomic DNA was extracted directly from fungal cultures grown on potato dextrose agar (PDA) plates using a Zymo Research Quick DNA kit. A species-specific primer using the internal transcribed spacer ribosomal DNA (ITS rDNA) PCR scoring indicated the presence of A. alternata using primer pair ITS4/ITS5. Amplifications of the internal transcribed spacer region of 600 bp revealed 100% identity of the isolated fungus from cotton with A. alternata from tomato and potato. These data oblige us to reconsider the presence of A. alternata in the four main cotton growing schemes in Sudan while these symptoms have always been described for tomato and potato early blight disease.