Anthracnose is major disease of pepper (Capsicum annum) in the tropics and causes severe damage both in the field and postharvest. In Brazil, this disease is caused by Colletotrichum acutatum, C. boninense, C. capsici, C. coccodes, and C. gloeosporioides, where the first species is responsible for 70% of all occurrences (3). Recently, C. acutatum has been considered a species complex (1); thus, the aim of this study was to verify the etiology of anthracnose on peppers using a morphological and molecular approaches. In 2011, pepper fruits with typical symptoms of anthracnose (dark, sunken spots with concentric rings of orange conidial masses) were collected in Viçosa, Minas Gerais, Brazil. A single spore isolate was obtained on potato dextrose agar (PDA), and the derived culture was deposited in the Coleção de Culturas de Fungos Fitopatogênicos “Prof. Maria Menezes” (code CMM-4200). The upper side colonies on PDA were gray, cotton-like, and pale gray to pale orange. Conidia were hyaline, aseptate, smooth, straight, cylindrical with round ends or occasionally with end ± acute, 12.5 to 17 μm long and 3.5 to 4 μm wide on synthetic nutrient deficient agar. The isolate was morphologically typical of species belonging to the C. acutatum complex. Molecular identification of the pathogen was carried out and sequences of the regions internal transcribed spacer (ITS), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and β-tubulin (βt) were obtained and deposited in GenBank (Accession Nos. KJ541821 to KJ541823). A search in the Q-bank fungi database using the ITS, βt, and GAPDH sequences retrieved C. scovillei with 100% identity for all three genes. This pathogen was previously reported in Capsicum spp. only in Thailand, Indonesia, and Japan (1,2). To confirm pathogenicity, drops with 105 spores/ml were deposited in 10 artificially wounded fruits (cv. Itapuã 501 and Melina). In control fruits, drops of sterilized water were deposited onto wounds. The fruits were covered for one day with a transparent plastic bag with moisture supplied by a wet filter paper. The fruits were detached and mature. The bags were removed, and the fruits were incubated for 10 days in a growth chamber at 25°C with a photoperiod of 12 h. After 4 days, gray-brown to black sunken spots with concentric rings were observed on 100% of the wounded fruits that had been inoculated. No disease was observed on the control fruits. The fungus C. scovillei was successfully re-isolated from symptomatic fruits to fulfill Koch's postulates. To our knowledge, this is the first report of anthracnose on pepper fruit caused by C. scovillei in Brazil. Due to the diversity of species that cause anthracnose in Capsicum, future studies using morphological and molecular tools are essential for the correct identification of Colletotrichum spp. on pepper in Brazil. References: (1) U. Damm et al. Stud. Mycol. 73:37, 2012. (2) T. Kanto et al. J. Gen. Plant. Pathol. 80:73, 2014. (3) M. J. Z. Pereira et al. Hortic. Bras. 29:569, 2011.
This study compared different temperatures and dormancy-reversion procedures for preservation of Phakopsora pachyrhizi uredospores. The storage temperatures tested were room temperature, 5°C, )20°C and )80°C. Dehydrated and non-dehydrated uredospores were used, and evaluations for germination (%) and infectivity (no. of lesions⁄cm 2 ) were made with fresh harvested spores and after 15, 29, 76, 154 and 231 days of storage. The dormancy-reversion procedures evaluated were thermal shock (40°C⁄5 min) followed or not by hydration (moist chamber⁄24 h). Uredospores stored at room temperature were viable only up to a month of storage, regardless of their hydration condition. Survival of uredospores increased with storage at lower temperatures. Dehydration of uredospores prior to storage increased their viability, mainly for uredospores stored at 5°C, )20°C and )80°C. At 5°C and )20°C, dehydrated uredospores showed increases in viability of at least 47 and 127 days, respectively, compared to non-dehydrated spores. Uredospore germination and infectivity after storage for 231 days (7.7 months), could only be observed at )80°C, for both hydration conditions. At this storage temperature, dehydrated and non-dehydrated uredospores exhibited 56 and 28% of germination at the end of the experiment, respectively. Storage at )80°C also maintained uredospore infectivity, based upon levels of infection frequency, for both hydration conditions. Among the dormancyreversion treatments applied to spores stored at )80°C, those involving hydration allowed recoveries of 85 to 92% of the initial germination.
RESUMOObjetivou-se detectar a influência do estádio fenológico e da idade da folha de soja na infecção por Phakopsora pachyrhizi, agente causal da ferrugem asiática (FA). Plantas das cultivares BRS 154 e BRS 258 foram inoculadas, com suspensão de 10 5 urediniósporos/mL, nos estádios fenológicos V 3 , R 1 e R 5 . Após 24 horas de câmara úmida, as plantas foram acondicionadas em condições de casa de vegetação por 20 dias. Avaliou-se o período latente médio (PLM) e a severidade. Para a avaliação da suscetibilidade de trifólios à FA utilizou-se a cultivar BRS 154 (V 5 ). A inoculação foi realizada nos quatro primeiros trifólios. Aos 15 dias após a inoculação, os folíolos foram avaliados quanto à severidade, tamanho médio de lesão e freqüência de infecção. O estádio das plantas de soja não influenciou no PLM. As cultivares BRS 154 e BRS 258 tiveram PLM de 8 e 9 dias, respectivamente. As cultivares não se diferenciaram quanto à severidade da doença. Não houve diferença de severidade nos estádios V 3 e R 1 , porém, os valores de severidade nesses estádios foram superiores ao valor de severidade no estádio R 5 , na avaliação realizada 8 dias após a inoculação. Em relação à suscetibilidade de folhas, o trifólio mais velho apresentou maiores valores de doença. Palavras-chave: Glycine max, ferrugem asiática, estádios de inoculação. ABSTRACT Influence of soybean phenological stage and leaflets age on infection by Phakopsora pachyrhiziThis work was conducted to study the influence of soybean growth stage and leaf age on the infection of Phakopsora pachyrhizi, the soybean rust pathogen. Soybean plants (cv. BRS 154 and BRS 258) at the V 3 , R 1 and R 5 growth stages were inoculated with a 1 x 10 5 urediniospores per mL suspension. After a period of 24 hours in dew chambers, all plants were removed from the chambers and placed under greenhouse conditions for 20 days. Mean latent period (PLM) and disease severity were estimated. The susceptibility of trifoliate leaves to soybean rust was estimated on cv. BRS 154 at the growth stage R 5 . Pathogen inoculation was done at the first four trifoliate leaves. Fifteen days after inoculation, leaflets of each trefoil were evaluated for disease severity, lesion mean size and infection frequency. Plants' growth stage did not influence the PLM. Cultivars BRS 154 and BRS 258 presented PLM of 8 and 9 days, respectively. There was no difference in disease severity at the growth stages V 3 and R 1 , but those values were higher than at the R 5 growth stage, 8 days after inoculation. The oldest trefoil showed the highest disease values.
Objetivou-se determinar a taxa de transporte de população de fungos associados às sementes de pinhão manso, a patogenicidade desses microrganismos a plântulas e frutos e a transmissibilidade fruto-semente e semente-plântula. Avaliaram-se a taxa de transporte, por meio de blotter test, de sementes produzidas nos estados de Minas Gerais, São Paulo, Bahia e Tocantins. As sementes foram submetidas aos tratamentos: sem desinfestação com tegumento (SDCT), sem desinfestação sem tegumento (SDST), com desinfestação com tegumento (CDCT) e com desinfestação sem tegumento (CDST). A incidência (%) dos fungos foi avaliada sob microscópio estereoscópico binocular. Para o teste de patogenicidade em plântulas e frutos inocularam-se suspensões de 10(6) esporos e discos de BDA com micélio, respectivamente. Para os fungos fitopatogênicos avaliaram-se a transmissibilidade fruto-semente e semente-plântula. O tratamento SDCT permitiu a detecção de maior número de fungos. Os fungos identificados foram Colletotrichum gloeosporioides, C. capsici, Curvularia sp., Verticillium sp., Fusarium sp., Penicillium sp., Aspergillus sp., A. niger e Rhizopus sp. Apenas as espécies de Colletotrichum são patogênicas às plântulas e frutos. Para ambas espécies há transmissibilidade fruto-semente, entretanto não é observada transmissão semente-plântula.
This study aimed to elucidate the infection process of Botrytis cinerea on eucalypt leaves. Tests were conducted to evaluate the influence of leaf side (adaxial or abaxial), leaf age and luminosity on conidial germination, appressorium formation and grey mould (GM) severity. The adaxial and abaxial surfaces of detached eucalypt leaves were inoculated with a conidial suspension of B. cinerea and kept under constant light or dark. Subsequently, the adaxial surface of young and old leaves was inoculated and kept in the dark. To evaluate the percentage of conidia germination and appressorium formation, leaf samples were collected 6 hours after inoculation (hai), clarified (alcohol and chloral hydrate) and evaluated under a light microscope. The severity of GM was assessed 10 days after inoculation. For scanning electron microscopy analysis, samples were collected from 2 to 168 hai. A higher percentage of conidia germination (92%) and GM severity (21%) occurred on the adaxial surfaces of leaves kept in the dark. There was no statistical difference between the surfaces of young and old leaves for conidia germination. No appressorium was formed by B. cinerea. The GM severity on young leaves (17.3%) was 34 times higher than on old leaves (0.5%). The micrographs showed germinating conidia emitting 1–4 germ tubes in samples at 4 hai. The fungus penetration occurred through intact leaf surfaces, and both extra‐ and intracellular colonization of the mesophyll cells by the hyphae of the pathogen were observed at 120 hai. Sporulation occurred on the adaxial and abaxial surfaces (macronematous conidiophores) and below the epidermis (micronematous conidiophores).
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