Temperature Effects on the Onset of Sporulation by Phytophthora ramorum on Rhododendron ‘Cunningham's White’

The effect of temperature and moist period on the onset of sporangia production by Phytophthora ramorum on Rhododendron ‘Cunningham's White’ was examined with misted detached leaves held in humid chambers. Following wound inoculation with sporangia, leaves were pre‐incubated at 20°C for either 24 or 72 h prior to placement at six different temperatures (4, 10, 15, 20, 25 and 30°C). The overall mean moist period required for first occurrence of sporulation over all six temperatures was 3.24 days with the 24‐h pre‐incubation time, compared with 1.49 days for the 72‐h pre‐incubation time. Following 24 h pre‐incubation at 20°C and at an incubation temperature of 15°C, sporangia were first collected from leaves following a 24 h incubation. At 10 and 20°C, sporangia were first collected after 48 h, whereas at 4, 25 and 30°C, sporangia were first collected after 3 days. Following 72 h pre‐incubation at 20°C, sporulation generally occurred within 1 day, even at temperatures such at 4 and 30°C that are suboptimal for sporulation. The highest levels of P. ramorum sporulation were observed at 20°C. P. ramorum formed sporangia on host tissue under moist conditions within the same time frame reported for P. phaseoli, P. palmivora and P. nicotianae, but substantially more slowly than certain other species such as P. infestans. Quantifying moisture and temperature conditions for initiation of sporangia production provides knowledge which leads to a greater understanding of the epidemic potential of P. ramorum.     

Effects of Inoculum Density and Wounding on Stem Infection of Three Eastern US Forest Species by Phytophthora ramorum

Seedlings of three Eastern US forest species Quercus rubra (northern red oak), Quercus prinus (chestnut oak) and Acer rubrum (red maple) were inoculated by applying Phytophthora ramorum sporangia to stems at different inoculum densities with and without wounding. Disease occurred in all treatments involving wounds, and no disease was observed in unwounded treatments. Younger seedlings (2–3 years old) did not differ significantly from older seedlings (5–6 years old) in disease incidence, but older seedlings sustained smaller lesions compared with younger seedlings. For both old and young seedlings, disease on wounded stems was observed down to the lowest sporangia concentration utilized (500 sporangia/ml for old seedlings and 100 sporangia/ml for young seedlings). The results show that in the presence of wounding, even very low sporangia concentrations can result in disease, and further suggest that wounding caused by insects and other factors may play an important role in P. ramorum epidemiology in forest environments.     

The effect of salinity on the survival,growth, sporulation and infection of Phytophthora ramorum

Phytophthora ramorum has been found in waterways outside infested nurseries, but little is known about its behavior in water. This study examined the effect of salinity on survival, growth, sporulation, and infection. P. ramorum survival and growth was negatively correlated with salt concentration (range of 0–45 g l⁻¹), but showed a level of tolerance even at 45 g l⁻¹. No sporangia were observed in cultures with higher than 20 g l⁻¹ of salt and zoospores were not released from sporangia above 14 g l⁻¹. Water sources with different salinity were used to understand the environment where P. ramorum can survive and infect host material. Water from natural bodies and water amended with different salt concentrations were added to P. ramorum-infested sand and baited with rhododendron leaf disks. Infection decreased with increasing salt concentration and increased with higher initial concentration of P. ramorum. This research helps to better understand the effects of water quality on survival and infectivity of P. ramorum, expanding the potential survey range.     

Inoculum Density Relationships for Infection of Some Eastern US Forest Species by Phytophthora ramorum

Our objectives were to establish inoculum density relationships between P. ramorum and selected hosts using detached leaf and whole‐plant inoculations. Young plants and detached leaves of Quercus prinus (Chestnut oak), Q. rubra (Northern red oak), Acer rubrum (red maple), Kalmia latifolia (mountain laurel) and Rhododendron ‘Cunningham's White’ were dip‐inoculated with varying numbers of P. ramorum sporangia, and the total number of diseased and healthy leaves recorded following incubation at 20°C and 100% relative humidity. Calibration threshold estimates for obtaining 50% infected leaves based on linear analysis ranged from 36 to 750 sporangia/ml for the five hosts. Half‐life (LD50) estimates (the number of spores for which the per cent of diseased leaves reaches 50% of its total) from asymptotic regression analysis ranged from 94 to 319 sporangia/ml. Statistically significant differences (P = 0.0076) were observed among hosts in per cent infection in response to increased inoculum density. Inoculum threshold estimates based on studies with detached leaves were comparable to those obtained using whole plants. The results provide estimates of inoculum levels necessary to cause disease on these five P. ramorum hosts and will be useful in disease prediction and for development of pest risk assessments.     

DEVELOPMENT OF ENDOPHYTIC FRANKIA SPORANGIA IN FIELD- AND LABORATORY-GROWN NODULES OF COMPTONIA PEREGRINA AND MYRICA GALE

Field-collected nodules of Comptonia peregrina (L.) Coult. and Myrica gale L. (Myricaceae), infected by the nitrogen-fixing actinomycete Frankia sp., were of two types: those that lacked sporangia entirely, designated spore(-), and those that showed extensive sporangial development, designated spore(+). In spore(+) nodules of C. peregrina, sporangia began to develop after the differentiation of endophytic vesicles and the concomitant onset of nitrogenase activity. At the onset of sporangial differentiation, infected host cells appeared healthy. However, endophytic vesicles and host cell cytoplasm and nuclei began to senesce rapidly as sporangia developed. Staining of sectioned material with the fluorescent stain Calcofluor White suggested that vesicles, hyphae and young sporangia were enclosed within a host-derived encapsulation layer, but mature sporangia were no longer encapsulated. In both C. peregrina and M. gale, vesicles were more short-lived in spore(+) than in spore(-) nodules. Field-collected spore(+) M. gale nodules exhibited a pronounced seasonality of sporangial formation. Sporangia began to differentiate in June, after the formation of vesicles and became more prominent in late summer. Inter- and intraspecific cross-inoculations suggest that the ability to form sporangia in the symbiotic state is controlled by endophytic strain type rather than host genotype or host/endophyte combination. The host may, however, influence the number and seasonal appearance of sporangia formed.     

未来气候变化下栎树猝死病菌在中国的适生性分析

基于中国国家有害生物检疫信息平台的有关记录和文献以及WoldClim网站,获取栎树猝死病菌的地理分布数据及气候数据,并用SPSS软件和刀切法筛选主导环境变量。利用MaxEnt生态位模型和ArcGIS软件,对栎树猝死病菌现代和未来情景下在我国的潜在适生区进行预测,并计算和绘制栎树猝死病菌高风险区质心转移轨迹。通过不同年份和不同气候情况下的受试者工作特征曲线(ROC)的训练集和测试集受试者工作特征曲线下面积(AUC)值均大于0.91,说明MaxEnt模型准确并适用于预测栎树猝死病菌在我国的潜在分布,同时结合其主要寄主植物的地理分布进一步增强预测模型的可信度。预测结果表明,最冷季度降水量、最冷季度平均温度、最干季度平均温度和年均降水量是影响栎树猝死病菌分布的主要环境变量。而2030s(2021—2040年)、2050s(2041—2060年)和2070s(2061—2080年)在3种气候情景下(SSP1-2.6、SSP2-4.5、SSP5-8.5),栎树猝死病菌的潜在适生区相较于现代情景下都有所增加。此外,高风险区面积在3个年代3种情景下的面积增长率均高于45%。高风险区质心变化的预测结果表...     

Frankia-Alnus incana symbiosis: Effect of endophyte on nitrogen fixation and biomass production

The efficiency of different FinnishFrankia strains as symbionts onAlnus incana (L.) Moench was evaluated in inoculation experiments by measuring nitrogen fixation and biomass production. Since all available pure cultures ofFrankia are of the Sp⁻ type (sporangia not formed in nodules), but the dominant nodule endophyte ofA. incana in Finland is of the Sp⁺ type (sporangia formed in nodules), crushed nodules of thisFrankia type were included. The Sp⁻ pure cultures, whether originating fromA. incana orA. glutinosa, produced with one exception, similar biomass withA. incana. The highest biomass was produced with an American reference strain fromA. viridis crispa. Using Sp⁺ nodule homogenates fromA. incana as inoculum, the biomass production was only one third of that produced by Sp⁻ pure cultures from the same host. Hence, through selection of the endophyte it is possible to exert a considerable influence on the productivity ofAlnus incana.     

Enhanced Recovery of Phytophthora ramorum from Soil Following 30 Days of Storage at 4°C

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.     

进境德国云杉原木中夹带栎树猝死病菌的检疫鉴定

[目的] 检测自德国进境云杉原木夹杂的水青冈植物叶片上是否携带栎树猝死病菌。[方法] 采用磁珠法提取水青冈植物叶片DNA,根据巢式PCR方法和DNA序列测定分析方法,进行栎树猝死病菌的检测。[结果] 采用巢式PCR方法,能够扩增出约280 bp的特异性条带;DNA序列测定表明,该DNA序列与GenBank中多个栎树猝死病菌分离物DNA序列相似性达99%,位于同一个发育分支。[结论] 样品中检出栎树猝死病菌,这是我国口岸首次从进境德国云杉原木中截获栎树猝死病菌。     

ENDOPHYTE-HOST ASSOCIATIONS IN FORAGE GRASSES. XV. CLUSTERING OF STROMATA-BEARING INDIVIDUALS OF AGROSTIS HIEMALIS INFECTED BY EPICHLOË TYPHINA

Population studies involving the grass Agrostis hiemalis infected with the endophytic fungus Epichloë typhina were made. Grass individuals were assessed for infection state (presence or absence of fungus), number of culms and fungal stromata, and location within plot. Using clustering and ANOVA procedures available in SAS, geometric groups were identified and analyzed. The tendency of plants to bear stromata was found to be significant with respect to both the plot (P < 0.05) and the cluster (P < 0.0001) within which plants occurred. A cultural study was made of the endophytes from one of the plots. Here isolates from a cluster containing stroma-bearing grass individuals were found to grow more rapidly than those from grass clusters without stromata on a variety of sugars naturally available in vivo. Histological studies of the host demonstrate that the endophyte is seed transmitted in a comparable fashion to endophytes in other grasses. It is suggested that the clustering of stromata-bearing plants in Agrostis hiemalis is the result of the presence of aggressive strains of endophyte within proximally located plants.     

Oligosaccharide side chains of wall molecules are essential for cell-wall lysis in Chlamydomonas reinhardtii

The glycoproteins of the cell walls of Chlamydomonas are lysed during the reproductive cycle by proteases (autolysins) which are specific for their substrates. The autolysin which digests the wall of sporangia to liberate the zoospore daughter cells in the vegetative life cycle is a collagenase-like enzyme which attacks only selected domains in its wall substrates containing (hydroxy)-proline clusters. Cell-wall fractions obtained by salt-extraction (NaClO₄) and oxidizing agents (NaClO₂) and the insoluble residue were tested as substrates. The most-crosslinked insoluble inner part of the wall is the best substrate for the sporangia autolysin. Oligosaccharides obtained from the insoluble cell-wall fraction of sporangia by hydrolysis with Ba(OH)₂ inhibit autolysin action. We conclude that the oligosaccharide side chains of wall substrates are essential for forming the reactive enzyme-substrate complex.Abbreviations CSW chlorite-soluble cell-wall fraction - ICW insoluble cell-wall fraction - PSW salt-soluble fraction - SDS-PAGE sodium dodecyl sulfate-polyacrylamide gel electrophoresis     

Examining the strength and possible causes of the relationship between fire history and Sudden Oak Death

Fire can be a dominant process in the ecology of forest vegetation and can also affect forest disease dynamics. Little is known about the relationship between fire and an emerging disease epidemic called Sudden Oak Death, which is caused by a new pathogen, Phytophthora ramorum. This disease has spread across a large, fire-prone portion of California, killing great numbers of oaks and tanoaks and infecting most associated woody plants. Suitable hosts cover a much broader geographic range, raising concern over where the disease may spread. To understand the strength and potential sensitivities of a fire–disease relationship, we examined geographic patterns of confirmed P. ramorum infections in relation to past fire history. We found these infections to be extremely rare within the perimeter of any area burned since 1950. This finding is not caused by spatial bias in sampling for the disease, and is robust to variation in host abundance scenarios and to aggregation of closely spaced sampling locations. We therefore investigated known fire-related factors that could result in significantly lower incidence of the disease in relatively recently burned landscapes. Chemical trends in post-fire environments can influence the success of pathogens like P. ramorum, either by increasing plant nutrient stress or by reducing the occurrence of chemicals antagonistic to Phytophthoras. Succession in the absence of fire leads to greater abundance of host species, which will provide increased habitat for P. ramorum; this will also increase intraspecific competition where these trees are abundant, and other density-dependent effects (e.g. shading) can reduce resource allocation to defenses. Despite these findings about a fire–disease relationship, a much deeper understanding is necessary before fire can be actively used as a tool in slowing the epidemic.     

Development of the zoosporangia ofSynchytrium endobioticum,the causal agent of potato wart disease

Summary An ultrastructural study of zoosporangium development ofSynchytrium, endobioticum (Schilb.) Perc. is presented. Emphasis is placed on the location of the parasitic fungal thallus in the potato host cell, on the specific location of organelles in relation to the developing zoosporangial wall, and on the host cell reaction to the fungal infection. The cytoplasmic organization of the individual sporangia after division of the zoosporangium into a sorus of sporangia is characterized by numerous similarly sized nuclei, well developed dictyosomes, and the presence of many lipid bodies of variable size. Cytoplasmic microtubules are observed to flare out from the functional kinetosome both before and after zoospore cleavage.The ultrastructural details of zoosporangium development are used to revaluate the life cycle ofS. endobioticum as described from light microscopic observations made early in the century (Curtis 1921;Köhler 1923, 1932;Percival 1910).     

The Effect of Exposure to Decreasing Relative Humidity on the Viability of Phytophthora ramorum sporangia

Sporangia of three isolates of Phytophthora ramorum representing three different clonal lineages were subjected to relative humidity (RH) levels between 80 and 100% for exposure periods ranging from 1 to 24 h at 20°C in darkness. Plastic containers (21.5 × 14.5 × 5 cm) were used as humidity chambers with 130 ml of glycerine solution added to each container. Glycerine concentrations corresponded to 100, 95, 90, 85 and 80% RH based on refractive index measurements. Sporangia suspensions were pipeted onto nitrile mesh squares (1.5 × 1.5 cm, 15 micron pore size) which were placed in the humidity chambers and incubated at 20°C in darkness. Following exposure periods of 1, 2, 4, 8, 12 and 24 h, mesh squares were inverted onto Petri dishes of selective medium and sporangia germination assessed after 24 and 48 h. At 100% RH, we observed a mean value of 88% germination after 1 h exposure declining to 18% germination following 24 h incubation. At 95% RH, a steeper decline in germination was noted, with means ranging from 79% at 1 h to less than 1% at 24 h exposure. At 90% RH, no germination was noted after 8 or more h exposure, and values were 57%, 22% and 3% germination for the 1, 2 and 4 h exposures, respectively. Germination was only observed at 1 h exposure for both the 85% RH treatment (52% germination) and the 80% RH treatment (38% germination). The three isolates responded similarly over the range of RH values tested. The germination response of P. ramorum sporangia to RH values between 80% and 100% was comparable to that reported for other Phytophthora species. Knowledge of conditions that affect P. ramorum sporangia germination can shed light on pathogenesis and epidemic potential and lead to improved control recommendations.     

In vivo studies evaluating commercial biofungicide suppression of blight caused by Phytophthora ramorum in selected ornamentals

Phytophthora ramorum is a regulated pathogen in North America, which causes ramorum blight on nursery stock resulting in the implementation of costly quarantine and eradication measures. Earlier studies showed some biofungicides could inhibit growth and reduce the disease in vitro. The objective of this study was to evaluate the effect of commercial biofungicides on in vivo disease development and plant growth on four nursery species when inoculated with three isolates representing each of the NA1, NA2 and EU1 lineages of the pathogen. The plant species were Gaultheria shallon, Rubus spectabilis, Rhododendron caucasicum x R. ponticum var. album and Cornus sericea. Prior to pathogen inoculation, plants were pretreated with Aliette® (standard fungicide), Actigard 50WG Plant Activator®, Actinovate® SP, Sonata®, Serenade®, Plant Helper®, SoilGard® 12G and Pro Mix BX Biofungicide?. A suspension containing 7000 sporangia ml^?1 was used to inoculate plants. Disease severity and foliar biomass were recorded 14 days after inoculation. Actinovate was the only product able to reduce disease severity by about 50% and improve plant growth of the susceptible hosts. Its effectiveness differed by isolate. Several other biofungicides and the standard fungicide provided suppression of disease and improved plant growth but their effectiveness was dependent on host species, product and isolate. None of the products prevented disease and generally the level of control obtained was lower than would be acceptable for a commercial nursery. In addition to assessing the disease control products, it was also observed that rhododendron, salal and salmonberry were highly susceptible hosts of P. ramorum with PR05-001 (NA2) being the most aggressive isolate on them.     

The specific identity and the life history of JapaneseSyringoderma (Syringodermatales,phaeophyceae)

Observations on JapaneseSyringoderma from Rishiri Island, which had been previously identified asS. australe, were made based on newly collected fertile material. These results and comparisons with the type specimen ofSyringoderma abyssicola (=Chlanidophora abyssicola) revealed that the Rishiri Island plants should be identified asSyringoderma abyssicola. Syringoderma abyssicola from Rishiri Island formed unilocular sporangia among the paraphyses on the fan-shaped blades in winter. The first products (uni-spores) in the unilocular sporangia form flagella, and soon after form cell walls before release. Then these reduced gametophytes divide into tetrads and form swarmers, each of which contains a chloroplast with a stigma. These swarmers germinate into branched filaments, from which thicker erect filaments of apical growth tissue. At 5–10 C these erect filaments formed fan-shaped blades under long-day conditions, and unilocular sporangia under short-day conditions corresponding respectively to spring and winter at Rishiri Island. Accordingly, the seasonal growth pattern of the species is considered to be controlled by responses to photoregime and temperature. Dedicated to the memory of the late Professor Muneao Kurogi.     

Germination of the resting sporangia ofPhysoderma maydis,the causal agent ofPhysoderma disease of maize

Summary The structural and developmental characteristics of the resting sporangium in uniflagellate phycomycetes, together with the type of zoospore, are of high taxonomic value. Among these fungi, however, only a few electron microscopic investigations have been published on this topic, mainly due to technical problems. In the present study ofPhysoderma maydis (Blastocladiales) these problems were overcome as the resting sporangia in this species are formed synchronously, in large numbers, the germination is readily induced and the impermeability of the resting sporangium wall can be circumvented by shaking the prefixed sporangia with glass beads.The germination of the resting sporangia ofP. maydis is described by correlative light and electron microscopic studies and discussed in relation to related investigations on sporogenesis: The germination process starts by a breakdown of large electron-dense accretions found in the resting stage. Simultaneously, the peripheral location of the lipid bodies is lost. The large operculum is pushed open by a protrusion of the inner sporangial wall; an additional wall layer is formed during this process. Synaptonemal complexes are found in the nuclei at this stage, as are nuclear division figures which suggests anEuallomyces type of life cycle for this fungus. Cleavage vesicles, formed from dictyosomes or endoplasmic reticulum, ultimately separate the sporangial content into meiospores. The sequential assembly of organelles into the side body complex is described. Sequestering of the ribosomes into a nuclear cap is interpreted as taking place immediately prior to zoospore discharge.     

THE DEVELOPMENT AND CYTOLOGY OF THE EPIBIOTIC PHASE OF PHYSODERMA PULPOSUM

Lingappa , Yamuna . (U. Michigan, Ann Arbor.) The development and cytology of the epibiotic phase of Physoderma pulposum. Amer. Jour. Bot. 46(3) : 145-150. Illus. 1959.—Physoderma pulposum, a chytrid parasite on Chenopodium album L. and Atriplex patula L., has a zoosporangial epibiotic phase. The latter consists of extramatrical sporangia and intramatrical bushy rhizoids, both enclosed in large protruding galls. The sporangia are subspherical, up to 350μ in diameter, and may produce hundreds of planospores. If planospores settle on the host surface, they develop narrow germ tubes which penetrate the epidermal cells and develop into rhizoids. The planospore body, however, remains on the host surface and develops into a mature epibiotic sporangium in about 20-25 days at 16°C., 12-15 days at 20-25°C., or 6-8 days at 30°C. During development, its nucleus and daughter nuclei divide mitotically with intranuclear spindles until the sporangium contains several hundred nuclei. This is followed by progressive cleavage which delimits the planospore rudiments. When mature sporangia are placed in fresh water, the planospores are quickly formed within 1 hr. at 25°C. and begin to swarm within the sporangia. They escape in large numbers through an opening formed by the deliquescence of a papillum in the sporangial wall. The planospores are subspherical or elongate, 3-5 × 4-6 μ, and each has an eccentric orange-yellow refractive globule and a flagellum 18-22 μ in length. The electron micrographs of the flagella indicate that the flagella are absorbed from tip backward during encystment of the planospores. By periodic inoculation of the host plants with planospores from epibiotic sporangia, as well as from germinating resting sporangia, generation after generation of epibiotic sporangia have been obtained for 4 years. This proves the existence of a eucarpic, epibiotic, ephemeral zoosporangial phase in P. pulposum. Field observations on the duration and sequence of development of the fungus indicate that the endobiotic resting sporangial phase always follows the epibiotic phase. The results of infection experiments also indicate that the epi- and endobiotic phases belong to one and the same fungus, P. pulposum.     

Sporangial structure inPhytophthora is disrupted after high pressure freezing

Summary The effects of high pressure on the ultrastructure of sporangia ofPhytophthora cinnamomi andP. palmivora have been examined by comparing sporangia frozen in a Balzers hyperbaric freezer or pressurized in a French pressure cell with sporangia plunge frozen at ambient pressure. Both freeze fixation methods provided excellent preservation of most cell structures, but one organelle type seen in plunge frozen material, the large peripheral vesicle (LPV), was not observed in high pressure frozen sporangia. Instead, these sporangia contained large irregularly shaped structures which exhibit the patterns of spatial distribution and, forP. cinnamomi, the monoclonal antibody binding characteristic of LPVs. These findings suggest that some factor of the hyperbaric freezing process causes LPVs to be degraded. Sporangia ofP. cinnamomi that had been pressurized in a French pressure cell also exhibited large structures with the spatial distribution and monoclonal antibody binding characteristic of LPVs. The apparent expansion of LPVs that follows from both pressurizing treatments causes considerable passive disruption of sporangial structure. This is the first report of a major disturbance of cell structure from use of the Balzers hyperbaric freezer, and reflects the lability, noted in previous work, of LPVs inPhytophthora.