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Chlamydospores of Phytophthora ramorum were used to infest field soil at densities ranging from 0.2 to 42 chlamydospores/cm3 soil. Recovery was determined by baiting with rhododendron leaf discs and dilution plating at time 0 and after 30 days of storage at 4°C, as recommended by USDA‐APHIS. Baiting was slightly more sensitive than dilution plating in recovering P. ramorum immediately following infestation of soil and allowed detection from samples infested with as little as 0.2 chlamydospores/cm3 compared with 1 chlamydospore/cm3 for dilution plating. After 30 days of infested soil storage at 4°C, P. ramorum was detected at significantly (P = 0.05) higher levels than at time 0 with both recovery methods. The results indicate that storage of P. ramorum‐infested soil at 4°C may allow for pathogen activity, such as sporangia production, which may enhance recovery from soil. 相似文献
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Francesco Citiulo Gary P. Moran David C. Coleman & Derek J. Sullivan 《FEMS yeast research》2009,9(7):1051-1060
Candida albicans and Candida dubliniensis are the only Candida sp. that have been observed to produce chlamydospores. The function of these large, thick-walled cells is currently unknown. In this report, we describe the production and purification of chlamydospores from these species in defined liquid media. Staining with the fluorescent dye FUN-1 indicated that chlamydospores are metabolically active cells, but that metabolic activity is undetectable in chlamydospores that are >30 days old. However, 5–15-day-old chlamydospores could be induced to produce daughter chlamydospores, blastospores, pseudohyphae and true hyphae depending on the incubation conditions used. Chlamydospores that were preinduced to germinate were also observed to escape from murine macrophages following phagocytosis, suggesting that these structures may be viable in vivo . Mycelium-attached and purified chlamydospores rapidly lost their viability in water and when subjected to dry stress, suggesting that they are unlikely to act as long-term storage structures. Instead, our data suggest that chlamydospores represent an alternative specialized form of growth by C. albicans and C. dubliniensis . 相似文献
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Chlamydospores are vital asexual resting cells, which allow most of the Fusarium pathogenic strains to retain their longevity, thus ensuring survival of viable reproductive cells. This study suggested that both abiotic – extreme temperature and growth media, and biotic – antagonistic Bacillus amyloliquefaciens SMCD 518 and mycoparasititic Acremonium strictum SMCD 504 are natural stressors able to shift chlamydospores formation in Fusarium graminearum and F. sporotrichioides under in vitro conditions. In F. sporotrichioides, Minimal Conversion Media (MCM) with mannitol supplement induced high chlamydospore size, and chain abundance at optimal 21°C and extreme 37°C temperatures, respectively. F. graminearum showed low chlamydospore formation on MCM–mannitol, even when exposed to 37°C under prolonged 5 days incubation. Generally, F. sporotrichioides has higher chlamydospore abundance, longer chlamydospore chain, and production rapidity compared to F. graminearum in both abiotic and biotic treatments. However, biocontrol bacteria and mycoparasite posed minimal effects on chlamydospore formation, as compared to abiotic stressors, thus controlling the Fusaria but not triggering them to generate chlamydospores as protection shields. 相似文献
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从国内不同烟区分离获得烟草根黑腐病菌根串珠霉45个野生型和11个白色变异菌株,参照Punja & Sun的分群鉴定方法,对这56个菌株进行了分群鉴定。结果表明:中国根串珠霉分离株存在明显形态变异,共划分出6个群,其中群Ⅰ、Ⅱ、Ⅲ为野生型,群Ⅳ、Ⅴ为白色变异型;另有白色变异型HLL-1¢不同于其他各群,将其建为新群—群Ⅵ。统计分析发现,群Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ及Ⅵ的分离频率分别占42.9%、33.9%、3.6%、16.0%、1.8%和1.8%。群Ⅰ主要分布重庆和云南,群Ⅱ在5个调查省市均有分布,群Ⅲ、群Ⅴ仅分布 相似文献
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Antonella Torosantucci Letizia Angiolella Antonio Cassone 《FEMS microbiology letters》1984,24(2-3):335-339
Abstract 2-Deoxy- d -glucose (dGlc) is able to inhibit both N -acetyl-hexosamine-induced chlamydosporogenesis and N -acetyl-glucosamine- or proline-induced germ-tube formation in Candida albicans . This inhibition is exerted also at dGlc concentrations which do not affect growth in the yeast form and do not reduce either the uptake or the incorporation of N-acetyl- d -glucosamine (GlcNAc) into yeast or hyphal cell material. Inhibition of germtube formation by dGlc does not occur in serum and is fully reversed by glucose. It is suggested that dGlc acts as a potent antimorphogenic effector in C. albicans . 相似文献
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Evaluation of SOC for the presumptive identification of Candida albicans and Cryptococcus neoformans
SOC, a fungal growth medium composed of SolrythR, oxgall, and caffeic acid, was evaluated as a medium to provide rapid, differential identification of Candida albicans and Cryptococcus neoformans. Using a variety of common isolation media to produce the yeast inocula, the germ tube methods tested ranked in the following order of decreasing sensitivity: SOC (97%±1), serum (92%±5), rabbit coagulase plasma with EDTA in combination with tryptic soy broth (89%±5), TOC (89%±6), and rabbit coagulase plasma with EDTA (83%±4). In chlamydospore production, SOC also proved to be the most sensitive after 24 h incubation: SOC (96%±2), TOC (80%±2), and cornmeal-Tween 80 agar (14%±3). Other medically important yeasts showed normal patterns of growth within 24 h on SOC, thus assisting in their identification.Eighty strains of Cryptococcus neoformans showed characteristic brown pigmentation on SOC and TOC within 18 h, while all other species of the genus Cryptococcus and 229 Candida isolates did not show a change in pigmentation. 相似文献
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