scholarly journals First Report of Alternaria alternata Causing Leaf Blight of Potatoes in South Africa

Plant Disease ◽  
2011 ◽  
Vol 95 (3) ◽  
pp. 363-363 ◽  
Author(s):  
J. E. van der Waals ◽  
B. E. Pitsi ◽  
C. Marais ◽  
C. K. Wairuri

During recent growing seasons, a new leaf blight was observed on potatoes (Solanum tuberosum L.) in various production regions in South Africa. Symptoms were observed before early blight, from 50 to 60 days after emergence of the potato plants. Typical leaf symptoms were small, circular, brown lesions, first visible on the abaxial sides of leaves. Lesions resembled those of early blight, but were smaller and did not show concentric rings. During favorable environmental conditions, severe infections were seen as coalesced lesions and blighted leaves and stems. Such severe infections occurred in seasons when high humidity, leaf wetness, and warm temperatures were present. Yield losses as much as 40% were reported on approximately 50 20-ha pivots in various potato-growing regions, particularly Ceres, Eastern Free State, KwaZulu Natal, and Mpumalanga, due to this leaf blight because conventional fungicidal spray programs did not adequately control the disease. Isolations from leaf lesions were made on V8 juice agar under aseptic conditions. The fungus, Alternaria alternata (Fr.) Kreissler, was consistently isolated and preliminarily identified on the basis of morphological characteristics. Dark brown conidia were produced in chains on conidiophores. Conidia had short beaks and ranged from 20 to 60 × 9 to 18 μm. Morphological identification was confirmed by amplification of the internal transcribed spacer (ITS) region. Primers used were AAF2 (5′-TGCAATCAGCGTCAGTAACAAAT-3′) and AAR3 (5′-ATGGATGCTAGACCTTTGCTGAT-3′), specifically designed for identification of A. alternata (4). PCR products were sequenced and the identity of isolates confirmed by a BLAST search on the GenBank database. Koch's postulates were conducted by inoculation of healthy potato leaves of cv. BP1. Spores at a concentration of 106 spores per ml were suspended in an oil/surfactant mixture and sprayed onto leaves until runoff. Control plants were sprayed with a sterile oil/surfactant mixture until runoff. Plants were covered by polyethylene bags for 2 days to achieve high humidity levels and maintained in a greenhouse at 25 ± 2°C. Three days after inoculation, plants were exposed to a moisture regimen simulating that of in-field irrigation. Plants were placed in a fogging chamber twice a week for 1 h at a time. Leaf blight symptoms similar to those observed on diseased potato plants in the field began to develop 3 weeks after inoculation. Isolations made from these lesions consistently yielded A. alternata. Control plants did not develop any symptoms. Five plants were used for each treatment and the experiment was repeated twice. Leaf blight on potatoes caused by A. alternata has previously been reported in Israel, (2), Brazil (1), and North America (3). To our knowledge, this is the first report of A. alternata causing leaf blight on potatoes in South Africa. Future research will focus primarily on management of this disease. References: (1) L. S. Boiteux and F. J. B. Reifschneider. Plant Dis. 78:101. 1994. (2) S. Droby et al. Phytopathology 74:537, 1984. (3) W. W. Kirk et al. Plant Dis. Manage. Rep. 2:V065:1, 2007. (4) P. Konstantinova et al. Mycol. Res. 106:23, 2002.

Plant Disease ◽  
2015 ◽  
Vol 99 (11) ◽  
pp. 1652-1652 ◽  
Author(s):  
W. Bihon ◽  
M. Cloete ◽  
A. Gerrano ◽  
P. Adebola ◽  
D. Oelofse

Plant Disease ◽  
2020 ◽  
Vol 104 (10) ◽  
pp. 2725
Author(s):  
Qin Wang ◽  
Qing-Shu Luan ◽  
Jian-Jun Wang ◽  
Xu Jiang ◽  
Gang Chen

Plant Disease ◽  
2008 ◽  
Vol 92 (3) ◽  
pp. 484-484 ◽  
Author(s):  
N. van den Berg ◽  
S. Serfontein ◽  
B. Christie ◽  
C. Munro

In September of 2005 and 2006, macadamia (Macadamia integrifolia Maiden & Betche) orchards in Tzaneen, Modjadji, Politsi, and Levubu in the Northern Province and Kiepersol in Mpumalanga, South Africa were surveyed and sampled to determine the causal agent of raceme blight. Symptoms appeared during early bloom and were present on racemes of all developmental stages. Early signs were necrotic tips of the peduncle that often curved to one side with necrosis spreading upward, resulting in the so-called “rat tail”. Unopened flowers were also affected. In severe cases, the entire inflorescence (flowers and peduncle) was necrotic and eventually flowers abscised. Occasionally, infection began with single flowers as small water-soaked specks on the flower, with no symptoms on the green peduncle. Diseased racemes were covered with olive gray patches of mycelia and abundant conidia. Flowers with blight symptoms were collected, surface disinfested with 70% ethanol for 2 min, and left to dry. Thirty isolations were made from the interface of the lesion and healthy tissue, plated onto 50% potato dextrose agar (PDA) (Biolab, Merck Laboratories, Wadeville, South Africa) with 19 g of agar per liter, and incubated at 25°C for 5 days. Direct isolations from diseased material were done by picking up conidia and placing them on PDA. A fungus was isolated consistently and identified morphologically as Cladosporium cladosporioides (Fresen.) de Vries based on the velvety olive-brown with almost black reverse colony color and dimensions and color of conidia and conidiophores. Conidia formed in long branched chains that readily disarticulate, mostly aseptate, elliptical to limoniform, 3 to 10.5 (3 to 7) × 2 to 5 (3 to 4) μm. Conidia were pale to olive brown and smooth to verruculose. Ramoconidia were 0-1 septate, 2.5 to 5 μm wide, up to 28 μm long, smooth or sometimes minutely verruculose. Conidiophores were pale to olive brown, macro- and micronemateus, smooth or sometimes verruculose, and of various lengths up to 320 μm long and 2 to 6 μm wide. To confirm pathogen identity, the ITS 1 and ITS 4 regions were sequenced, which had 100% homology to the 18S rRNA of C. cladosporioides (GenBank Accession No. DQ 124142.1). Pathogenicity trials were conducted in the field. Fungal isolates were grown on PDA for 6 days, spores were harvested, and a suspension was made (106 spores ml–1). Twenty macadamia inflorescences (cv. Beaumont) were dipped in the suspension for 1 s, covered with plastic bags containing wet cotton wool, and covered with paper bags. Inflorescences in different stages (petal fall, knee stage, and closed) were inoculated. Control treatments were dipped in sterile water. After 2 to 3 days, the bags were removed. Symptoms developed on all 20 inflorescences and in all cases, the bottom of the inflorescence blighted, resulting in the typical rat tail symptom. C. cladosporioides was reisolated from all surface-disinfested infected material plated on PDA. Control inflorescences developed no symptoms. Isolate PPRI 8376 was deposited with the National Collection of Fungi, Plant Protection Research Institute, Pretoria, South Africa. The disease is prevalent during wet periods and 5 to 10% of flowers were infected. The disease has increasingly been seen in orchards over the last two seasons and under favorable wet, humid conditions, severe infections have resulted in 100% flower loss. To our knowledge, this is the first report of C. cladosporioides causing raceme blight on macadamia in South Africa.


Plant Disease ◽  
2016 ◽  
Vol 100 (5) ◽  
pp. 1021-1021
Author(s):  
L. X. Zhang ◽  
Y. R. Shi ◽  
J. H. Yu ◽  
H. Xu ◽  
G. J. Tan

2007 ◽  
Vol 73 (5) ◽  
pp. 377-378 ◽  
Author(s):  
Chandan Kumar Maiti ◽  
Surjit Sen ◽  
Amal Kanti Paul ◽  
Krishnendu Acharya

Plant Disease ◽  
2020 ◽  
Vol 104 (6) ◽  
pp. 1868-1868
Author(s):  
Y. L. Liu ◽  
J. R. Tang ◽  
C. L. Wang ◽  
Y. H. Zhou

Plant Disease ◽  
2014 ◽  
Vol 98 (10) ◽  
pp. 1431-1431 ◽  
Author(s):  
J. P. Dube ◽  
M. Truter ◽  
J. E. van der Waals

Since the first report of brown spot of potatoes (Solanum tuberosum) caused by Alternaria alternata (Fr.) Keissl in South Africa (3), disease intensity has steadily increased. No fungicides are registered for control of brown spot of potatoes in South Africa but growers attempt to control the disease with products registered for early blight, which include various QoI fungicides. Failure to control brown spot with QoI fungicides led to an investigation on putative development of resistance among A. alternata populations. In the summer of 2012, diseased leaves were collected from five potato growing regions. Isolations were made from the margin of brown spot lesions by plating surface disinfested tissue on V8 agar medium (200 ml V8 juice, 3 g CaCO3, 20 g agar). Plates were incubated at 25°C in darkness for 7 days, purified, and single-spore cultures transferred to fresh potato dextrose agar (PDA) plates. Identity of isolates was confirmed using conidial morphology and PCR amplification using species-specific primers AAF2 and AAR3 (1). Eight A. alternata isolates (PPRI 13607, 13608, 13609, 13610, 13611, 13612, 13613, and 13614) were obtained and screened for sensitivity to azoxystrobin in vitro by evaluating relative conidial germination on media amended with 0, 1.0, 2.5, 5.0, 10, 25, 50, 75, 85, and 100 μg of azoxystrobin per ml of media. The dose effect of the fungicide on germination and the EC50 of each isolate were computed using the probit analysis. Isolates were subjected to DNA extraction and the partial cytochrome b (cyt b) was amplified using primer pair CBF1 and CBR2 (2). PCR products were transformed into DH5α competent cells using a pGEM-T Easy vector. Both strands of the cloned fragments were sequenced using primers T7 and SP6 (4). Isolates PPRI 13611 and 13614 had low EC50 values of 0.11 and 0.23 μg/ml, respectively, and a mean EC50 of 0.17 μg/ml, showing their relative sensitivity to azoxystrobin. The other six isolates had EC50 values ranging from 51.88 to 114.92 μg/ml, and a mean EC50 of 71.60 μg/ml, showing their resistance to azoxystrobin. Sequence analysis of the partial cyt b gene showed strong association of resistance in isolates PPRI 13607, 13608, 13609, 13610, 13612, and 13613 to a base substitution resulting in an amino acid substitution at position 143 (G143A). Isolates PPRI 13611 and 13614 did not exhibit this mutation. Although resistance has been reported on other crops where QoI fungicides, including azoxystrobin, have been used to control different pathogens, this is the first report of resistance to a QoI fungicide in field isolates of A. alternata from potatoes in South Africa. Identification of resistance will help to explain failure to control this disease using QoI fungicides. Further monitoring of resistance to azoxystrobin and other QoI fungicides is warranted. References: (1) P. Konstantinova et al. Mycol. Res. 106:23, 2002. (2) Z. Ma et al. Pesticide Biochem. Phys. 77:66, 2003. (3) J. van der Waals et al. Plant Dis. 95:363, 2011. (4) E. Youssef et al. DNA Seq. 11:541, 2001.


Plant Disease ◽  
2021 ◽  
Author(s):  
Azim Syahmi Zafri ◽  
Rita Muhamad ◽  
Aswad Wahab ◽  
Anis Syahirah Mokhtar ◽  
Erneeza Mohd Hata

Weeds may act as inoculum reservoirs for fungal pathogens that could affect other economically important crops (Karimi et al. 2019). In February 2019, leaves of the ubiquitous invasive weed, Parthenium hysterophorus L. (parthenium weed) exhibiting symptom of blight were observed at Ladang Infoternak Sg. Siput (U), a state–owned livestock center in Perak, Malaysia. Symptoms appeared as irregularly shaped, brown–to–black necrotic lesions across the entire leaf visible from both surfaces, and frequently on the older leaves. The disease incidence was approximately 30% of 1,000 plants. Twenty symptomatic parthenium weed leaves were collected from several infested livestock feeding plots for pathogen isolation. The infected tissues were sectioned and surface–sterilized with 70% ethyl alcohol for 1 min, rinsed three times with sterile distilled water, transferred onto potato dextrose agar, and incubated at 25°C under continuous dark for 7 days. Microscopic observation revealed fungal colonies with similar characteristics. Mycelium was initially white and gradually changed to pale orange on the back of the plate but later turned black as sporulation began. Conidia were spherical or sub–spherical, single–celled, smooth–walled, 12 to 21 μm diameter (mean = 15.56 ± 0.42 μm, n= 30) and were borne on a hyaline vesicle. Based on morphological features, the fungus was preliminarily identified as Nigrospora sphaerica (Sacc) E. W. Mason (Wang et al. 2017). To confirm identity, molecular identification was conducted using isolate 1SS which was selected as a representative isolate from the 20 isolates obtained. Genomic DNA was extracted from mycelia using a SDS–based extraction method (Xia et al. 2019). Amplification of the rDNA internal transcribed spacer (ITS) region was conducted with universal primer ITS1/ITS4 (White et al. 1990; Úrbez–Torres et al. 2008). The amplicon served as a template for Sanger sequencing conducted at a commercial service provider (Apical Scientific, Malaysia). The generated sequence trace data was analyzed with BioEdit v7.2. From BLASTn analysis, the ITS sequence (GenBank accession number. MN339998) had at least 99% nucleotide identity to that of N. sphaerica (GenBank accession number. MK108917). Pathogenicity was confirmed by spraying the leaf surfaces of 12 healthy parthenium weed plants (2–months–old) with a conidial suspension (106 conidia per ml) collected from a 7 day–old culture. Another 12 plants served as a control treatment and received only sterile distilled water. Inoculation was done 2 h before sunset and the inoculated plants were covered with plastic bags for 24 h to promote conidial germination. All plants were maintained in a glasshouse (24 to 35°C) for the development of the disease. After 7 days, typical leaf blight symptoms developed on the inoculated plants consistent with the symptoms observed in the field. The pathogen was re–isolated from the diseased leaves and morphological identification revealed the same characteristics as the original isolate with 100% re–isolation frequency, thus, fulfilling Koch’s postulates. All leaves of the control plants remained symptomless and the experiment was repeated twice. In Malaysia, the incidence of N. sphaerica as a plant pathogen has been recorded on several important crops such as watermelon and dragon fruit (Kee et al. 2019; Ismail and Abd Razak 2021). To our knowledge, this is the first report of leaf blight on P. hysterophorus caused by N. sphaerica from this country. This report justifies the significant potential of P. hysterophorus as an alternative weed host for the distribution of N. sphaerica. Acknowledgement This research was funded by Universiti Putra Malaysia (UPM/GP–IPB/2017/9523402). References Ismail, S. I., and Abd Razak, N. F. 2021. Plant Dis. 105:488. Karimi, K., et al. 2019. Front Microbiol. 10:19. Kee, Y. J., et al. 2019. Crop Prot. 122:165. Úrbez–Torres, J. R., et al. 2008. Plant Dis. 92:519. Wang, M., et al. 2017. Persoonia 39:118. White, T. J. et al. 1990. Page 315 in: PCR Protocols: A Guide to Methods and Applications. Academic Press, San Diego, CA. Xia, Y., et al. 2019. Biosci Rep. 39:BSR20182271.


2010 ◽  
Vol 76 (4) ◽  
pp. 284-286 ◽  
Author(s):  
Manjunath Hubballi ◽  
Sevugapperumal Nakkeeran ◽  
Thiruvengadam Raguchander ◽  
Lingan Rajendran ◽  
Perumal Renukadevi ◽  
...  

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