In the years 2000–2003 under Polish climatic conditions early blight occurred at different level of incidence on over 90.6% of surveyed fields. Time of disease appearance in different regions was closely related to climatic conditions. On average, early blight appeared on potato plants 59.3 days after planting, earlier than late blight. In the years 2001–2003, efficacy of six selected fungicides in early blight control was examined in field conditions. Experiments carried out in the Department of Potato Protection and Seed Science of Plant Breedingand Acclimatization Institute. Field trials located in two sites – at Bonin and Stare Olesno revealed much slower development of early blight on these fields where chemical protection was applied as compared to untreated control. Efficacy of plant protection program carried out in Bonin over three years varied from 40% to 63.9%. Effectiveness of selected products was higher in Stare Olesno at higher infection pressure, and ranged from 49.8% to 66.6%. However, efficiency of chemical protection in early blight suppressing is not as satisfactory as in late blight control. In field experiments good control of early blight resulted in tuber yield increase. In Bonin yield increase varied from 5.5 to 24.2% and in Stare Olesno from 12.2 to 34.4%.
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.
Potato (Solanum tuberosum L.), an important food crop in the world, is susceptible to many fungal pathogens including Alternaria solani and Fusarium oxysporum causing Fusarium wilt and early blight diseases. Mycoparasitic fungi like Trichoderma encode chitinases, cell wall degrading enzymes, with high antifungal activity against a wide range of phytopathogenic fungi. In this study, a binary vector harboring endochitinase gene of ~1,000 bp was constructed and used to transform potato nodes through Agrobacterium-mediated transformation. Out of several primary transformants, two transgenic potato lines were verified for transgene insertion and integration by Southern blot. In a pot experiment for Fusarium resistance, the transgenic potato lines didn’t show any symptoms of disease, instead they remained healthy post infection. The transgenic potato lines exhibited 1.5 fold higher mRNA expression of endochitinase at 7 days as compared to 0 day post fungus inoculation. It was evident that the mRNA expression decreased over days of inoculation but was still higher than at 0 day and remained stable upto 30 days post inoculation. Similarly, for A. solani infection assay, the mRNA expression of the endochitinase gene was 3 fold higher 7 days post inoculation compared to expression at 0 day. Although the expression decreased by1.2 fold during subsequent days post infection, it remained stable for 30 days, suggesting that protection in transgenic potato plants against fungal pathogens was achieved through an increase in endochitinase transcript.