scholarly journals Sources of Inoculum for Phytophthora ramorum in a Redwood Forest

2008 ◽  
Vol 98 (8) ◽  
pp. 860-866 ◽  
Author(s):  
J. M. Davidson ◽  
H. A. Patterson ◽  
D. M. Rizzo

Sources of inoculum were investigated for dominant hosts of Phytophthora ramorum in a redwood forest. Infected trunks, twigs, and/or leaves of bay laurel (Umbellularia californica), tanoak (Lithocarpus densiflorus), and redwood (Sequoia sempervirens) were tested in the laboratory for sporangia production. Sporangia occurred on all plant tissues with the highest percentage on bay laurel leaves and tanoak twigs. To further compare these two species, field measurements of inoculum production and infection were conducted during the rainy seasons of 2003-04 and 2004-05. Inoculum levels in throughfall rainwater and from individual infections were significantly higher for bay laurel as opposed to tanoak for both seasons. Both measurements of inoculum production from bay laurel were significantly greater during 2004-05 when rainfall extended longer into the spring, while inoculum quantities for tanoak were not significantly different between the 2 years. Tanoak twigs were more likely to be infected than bay laurel leaves in 2003-04, and equally likely to be infected in 2004-05. These results indicate that the majority of P. ramorum inoculum in redwood forest is produced from infections on bay laurel leaves. Years with extended rains pose an elevated risk for tanoak because inoculum levels are higher and infectious periods continue into late spring.

2011 ◽  
Vol 101 (4) ◽  
pp. 492-501 ◽  
Author(s):  
Jennifer M. Davidson ◽  
Heather A. Patterson ◽  
Allison C. Wickland ◽  
Elizabeth J. Fichtner ◽  
David M. Rizzo

The transmission ecology of Phytophthora ramorum from bay laurel (Umbellularia californica) leaves was compared between mixed-evergreen and redwood forest types throughout winter and summer disease cycles in central, coastal California. In a preliminary multisite study, we found that abscission rates of infected leaves were higher at mixed-evergreen sites. In addition, final infection counts were slightly higher at mixed-evergreen sites or not significantly different than at redwood sites, in part due to competition from other foliar pathogens at redwood sites. In a subsequent, detailed study of paired sites where P. ramorum was the main foliar pathogen, summer survival of P. ramorum in bay laurel leaves was lower in mixed-evergreen forest due to lower recovery from infected attached leaves and higher abscission rates of infected leaves. Onset of inoculum production and new infections of bay laurel leaves occurred later in mixed-evergreen forest. Mean inoculum levels in rainwater and final infection counts on leaves were higher in redwood forest. Based on these two studies, lower summer survival of reservoir inoculum in bay laurel leaves in mixed-evergreen forest may result in delayed onset of both inoculum production and new infections, leading to slower disease progress in the early rainy season compared with redwood forest. Although final infection counts also will depend on other foliar pathogens and disease history, in sites where P. ramorum is the main foliar pathogen, these transmission patterns suggest higher rates of disease spread in redwood forests during rainy seasons of short or average length.


2007 ◽  
Vol 97 (7) ◽  
pp. 850-856 ◽  
Author(s):  
Daniel K. Manter ◽  
Rick G. Kelsey ◽  
Joseph J. Karchesy

Phytophthora ramorum, causal agent of sudden oak death, is responsible for widespread oak mortality in California and Oregon, and has the potential to infect 100 or more species. Symptoms range from stem girdling and shoot blight to leaf spotting. In this study, we examined the physiological impacts of P. ramorum infection on Rhododendron macrophyllum. In stem-inoculated plants, photosynthetic capacity (Vcmax) significantly declined by ≈21% 3 weeks after inoculation in visibly asymptomatic leaves. By 4 weeks, after the development of significant stem lesions and loss in water transport capacity, water stress led to stomatal closure and additional declines in photosynthetic capacity. We also report the isolation, characterization, and biological activity of two P. ramorum elicitins. Both elicitins were capable of inducing a hypersensitive-like response in one incompatible (Nicotiana tabacum SR1) and three compatible hosts (R. macrophyllum, Lithocarpus densiflorus, and Umbellularia californica). Infiltration of leaves from all three compatible hosts with both P. ramorum elicitins caused significant declines in chlorophyll fluorescence (Fv /Fm). For all four species, the loss of photosynthetic capacity was directly proportional to H+ uptake and ethylene production, two common components of the hypersensitive response. This is the first report of elicitins causing photosynthetic declines in compatible hosts independent of plant water stress.


2007 ◽  
Vol 97 (10) ◽  
pp. 1366-1375 ◽  
Author(s):  
E. J. Fichtner ◽  
S. C. Lynch ◽  
D. M. Rizzo

Recovery of Phytophthora ramorum from soils throughout sudden oak death-affected regions of California illustrates that soil may serve as an inoculum reservoir, but the role of soil inoculum in the disease cycle is unknown. This study addresses the efficacy of soil baiting, seasonal pathogen distribution under several epidemiologically important host species, summer survival and chlamydospore production in soil, and the impact of soil drying on pathogen survival. The efficacy of rhododendron leaves and pears as baits for detection of soilborne propagules were compared. Natural inoculum associated with bay laurel (Umbellularia californica), tanoak (Lithocarpus densiflorus), and redwood (Sequoia sempervirens) were determined by monthly baiting. Summer survival and chlamydospore production were assessed in infected rhododendron leaf disks incubated under bay laurel, tanoak, and redwood at either the surface, the litter/soil interface, or in soil. Rhododendron leaf baits were superior to pear baits for sporangia detection, but neither bait detected chlamydospores. Most inoculum was associated with bay laurel and recovery was higher in soil than litter. Soil-incubated inoculum exhibited over 60% survival at the end of summer and also supported elevated chlamydospore production. P. ramorum survives and produces chlamydospores in forest soils over summer, providing a possible inoculum reservoir at the onset of the fall disease cycle.


Plant Disease ◽  
2003 ◽  
Vol 87 (3) ◽  
pp. 315-315 ◽  
Author(s):  
S. K. Murphy ◽  
D. M. Rizzo

During August 2002, Phytophthora ramorum S. Werres & A.W.A.M. de Cock was isolated from branches <2.0 cm in diameter on a canyon live oak (Quercus chrysolepis) in Mt. Tamalpais State Park, Marin County, CA. The shrub was a cluster of stems <1 m in diameter and 1 m high. Similar cankers were observed on small branches of adjacent canyon live oaks and there was dieback of the branches distal to the lesions. Many tanoak (Lithocarpus densiflorus), California bay laurel (Umbellularia californica), and evergreen huckleberry (Vaccinium ovatum) were also infected by P. ramorum at this site. The isolate was identified as P. ramorum by its abundant chlamydospores and caducous, semi-papillate sporangia and internal transcribed spacer (ITS) rDNA sequences identical to those of isolates of P. ramorum from Quercus spp., tanoak, and Rhododendron (1,3). To test for pathogenicity, two greenhouse trials (5 seedlings per trial plus controls) were conducted on 20- to 24-month-old canyon live oak seedlings. Coast live oak (Q. agrifolia, section Lobatae) seedlings were included in the trials as a comparison because the species is known to be susceptible (1). Stems (approximately 1 cm in diameter) were wound inoculated (1). After 6 weeks, lesion lengths in the cambium of canyon live oak averaged 17.2 mm (range 16 to 30 mm), which was significantly greater (analysis of variance [ANOVA], P < 0.05) in both trials than those of control inoculations (mean = 6 mm). Coast live oak seedlings inoculated at the same time had mean lesion lengths of 22.6 mm (range 15 to 30 mm). P. ramorum was recovered from 100% of inoculated stems. Canyon live oak has a wide geographic range within California, but is not common in the areas currently affected by P. ramorum. We have not observed disease symptoms or unusual mortality on overstory canyon live oaks. Although a number of understory canyon live oaks at the site on Mt. Tamalpais were apparently infected, the long-term effect of P. ramorum infection on understory trees remains unclear. To our knowledge, this is the first report of infection by P. ramorum of an oak species outside of the section Lobatae (red oaks); canyon live oak is classified in the section Protobalanus (intermediate or golden cup oaks) (2). Oaks in the section Quercus (white oaks) have not been observed to be infected by P. ramorum in the field. References: (1) D. M. Rizzo et al. Plant Dis. 86:205, 2002. (2) P. Manos et al. Mol. Phylogenet. Evol. 12:333, 1999. (3) S. Werres et al. Mycol. Res. 105:1155, 2001.


Plant Disease ◽  
2002 ◽  
Vol 86 (11) ◽  
pp. 1274-1274 ◽  
Author(s):  
J. M. Davidson ◽  
M. Garbelotto ◽  
S. T. Koike ◽  
D. M. Rizzo

Phytophthora ramorum S. Werres & A.W.A.M. de Cock was isolated from three Douglas-fir (Pseudotsuga menziesii) saplings in a mixedevergreen forest in Sonoma County, California. Symptoms on these saplings included cankers on small branches (0.5 to 1 cm in diameter) resulting in wilting of new shoots, dieback of branches, and loss of leaves as much as 15 cm from the twig tip. Symptoms were observed on most saplings growing in the same area. On several smaller saplings (<1 m tall), P. ramorum infection resulted in the death of the leader and the top several whorls of branches. Isolates were identified as P. ramorum by their abundant chlamydospores and caducous, semi-papillate sporangia (2) and internal transcribed spacer rDNA sequences identical to those of isolates of P. ramorum from Quercus spp., Lithocarpus densiflorus, and Rhododendron (1,2). To test for pathogenicity, foliage inoculations were conducted on seedlings in two trials by misting 30 leaves per trial (five leaves per seedling plus controls) with sterile distilled water and pinning inoculum plugs, taken from the margin of P. ramorum cultures, to the upper surface of leaves. Inoculation resulted in lesions ranging between 1 and 12 mm long, and P. ramorum was recovered from 47% of inoculated leaves. Symptoms were not restricted to inoculated leaves, and in 26 single-leaf inoculations, lesions 17 to 85 mm long developed on branches (five mm in diameter) adjacent to the inoculated leaf. Isolation success from branch lesions was 50%, despite the fact that such lesions were apparently disjunct from the small 1-mm lesions developing on inoculated leaves. Stems of Douglas-fir seedlings (approximately 1 cm in diameter) were wound inoculated (1) in two trials consisting of 10 inoculated seedlings per trial plus 10 controls. After 6 weeks, lesion lengths in the cambium averaged 38 mm (range 12 to 62 mm), and three seedlings were completely girdled. P. ramorum was recovered from 75% of inoculated stems. Mean lesion lengths on seedlings inoculated with P. ramorum were significantly greater (P < 0.05) in both trials than those of control inoculations (mean 9 mm) based on analysis of variance. We have not observed unusual mortality or disease symptoms on overstory Douglas-fir trees in natural forests. The importance of P. ramorum branch tip dieback for growth and reproduction of Douglas-fir is unknown. Douglas-fir is present in many forests in California and Oregon already infested by P. ramorum, yet we have found infection of plants at only one location. At this site, symptomatic Douglas-fir saplings were surrounded by bay laurel (Umbellularia californica) trees with extremely high levels of P. ramorum infection. P. ramorum is known to sporulate prolifically on bay laurel leaves. More studies are necessary to determine if the incidence of P. ramorum in Douglas-fir extends to other locations or if it is limited to this one locale. References: (1) D. M. Rizzo et al. Plant Disease 86:205, 2002. (2) S. Werres et al. Mycol. Res. 105:1155, 2001.


Author(s):  

Abstract A new distribution map is provided for Phytophthora ramorum Werres, de Cock & Man in't Veld. Oomycota: Pythiales. Hosts include California black oak (Quercus kelloggii), California live oak (Quercus agrifolia), Rhododendron, shreve oak (Quercus parvula var. shrevei), tanoak (Lithocarpus densiflorus) and Viburnum. Information is given on the geographical distribution in Europe (Belgium, Denmark, France, Germany, Ireland, Italy, Netherlands, Norway, Poland, Slovenia, Spain, Sweden, Switzerland, UK) and North America (Canada (British Columbia), USA (California, Florida, Georgia, Louisiana, Oregon, South Carolina, Tennessee, Virginia, Washington)).


2014 ◽  
Vol 15 (1) ◽  
pp. 36-40 ◽  
Author(s):  
Nina Shishkoff

Growth-inhibiting fungicides are used routinely to control common and regulated Oomycete pathogens. This study investigated whether such fungicides could affect detection of Phytophthora ramorum from plant tissue, both foliage and roots. Whole plants of Rhododendron × ‘Cunningham's White’ were inoculated with P. ramorum and treated 3 days later with fosetyl-Al, mefenoxam, or propamocarb. The foliage was sampled over time to see if fungicides prevented successful culturing of the pathogen from infected leaf tissue or interfered with detection using real-time PCR or ELISA. Mefenoxam significantly reduced the ability to culture the pathogen from leaves for the first 6 weeks while recovery from leaves treated with other fungicides did not differ from water-treated controls; detection using PCR or ELISA was not affected by fungicide application. The roots of Viburnum cuttings were inoculated with P. ramorum and then treated 4 days later with fosetyl-Al, mefenoxam, or propamocarb. The amount of inoculum in flow through water samples taken weekly for 5 weeks was quantified and percent root colonization determined at the end of the experiment. Propamocarb had no effect on inoculum production or root infection, while viable inoculum production was significantly decreased in fosetyl-Al- or mefenoxam-treated plants over 5 weeks, and root colonization was significantly decreased. Accepted for publication 23 January 2014. Published 18 March 2014.


2009 ◽  
Vol 39 (9) ◽  
pp. 1766-1776 ◽  
Author(s):  
Bradley R. Collins ◽  
Jennifer L. Parke ◽  
Barb Lachenbruch ◽  
Everett M. Hansen

Tanoak ( Lithocarpus densiflorus (Hook. and Arn.) Rehder) is highly susceptible to sudden oak death, a disease caused by the oomycete Phytophthora ramorum Werres, De Cock & Man in’t Veld. Symptoms include a dying crown, bleeding cankers, and, eventually, death of infected trees. The cause of mortality is not well understood, but recent research indicates that water transport is reduced in infected trees. One possible mechanism causing the reduction in hydraulic conductivity is the presence of tyloses in xylem vessels. The development of tyloses was studied in relation to hydraulic conductivity in P. ramorum-infected sapwood. Inoculated logs showed a greater abundance of tyloses than noninoculated logs after 4 weeks. Inoculated trees with xylem infections had significantly more tyloses than noninoculated trees. In addition, the increase in number of tyloses was associated with a decrease in specific conductivity, suggesting that tyloses induced by infection with P. ramorum may interfere with stem sap flow. Over time, tylosis development increased in tissues farther from the inoculation site, in advance of the vertical spread of infection. The results suggest that infected sapwood contains numerous tyloses, which could significantly impede stem water transport.


2007 ◽  
Vol 97 (12) ◽  
pp. 1558-1567 ◽  
Author(s):  
J. L. Parke ◽  
E. Oh ◽  
S. Voelker ◽  
E. M. Hansen ◽  
G. Buckles ◽  
...  

Isolation, detection with diagnostic polymerase chain reaction (PCR), and microscopy demonstrated the presence of Phytophthora ramorum in the sapwood of mature, naturally infected tanoak (Lithocarpus densiflorus) trees. The pathogen was strongly associated with discolored sapwood (P < 0.001), and was recovered or detected from 83% of discolored sapwood tissue samples. Hyphae were abundant in the xylem vessels, ray parenchyma, and fiber tracheids. Chlamydospores were observed in the vessels. Studies of log inoculation indicated that P. ramorum readily colonized sapwood from inoculum placed in the bark, cambium, or sapwood. After 8 weeks, radial spread of P. ramorum in sapwood averaged 3.0 to 3.3 cm and axial spread averaged 12.4 to 18.8 cm. A field study was conducted to determine if trees with infected xylem had reduced sap flux and reduced specific conductivity relative to noninfected control trees. Sap flux was monitored with heat-diffusion sensors and tissue samples near the sensors were subsequently tested for P. ramorum. Adjacent wood sections were excised and specific conductivity measured. Both midday sap flux and specific conductivity were significantly reduced in infected trees versus noninfected control trees. Vessel diameter distributions did not differ significantly among the two treatments, but tyloses were more abundant in infected than in noninfected trees. Implications for pathogenesis, symptomology, and epidemiology are discussed.


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