Cronartium ribicola. [Descriptions of Fungi and Bacteria].

Author(s):  
G. F. Laundon

Abstract A description is provided for Cronartium ribicola. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Pycnia and aecia on numerous members of Pinus sect. Strobus (= sect. Cembra) (white pines) especially P. albicaulis, P. lambertiana, P. monticola and P. strobus; uredia and telia on almost all Ribes and Grossularia species, the cultivated black currant being particularly susceptible. DISEASE: White pine blister rust, currant rust. Causes stem cankers on pines and leaf lesions on currants. GEOGRAPHICAL DISTRIBUTION: Asia, Europe and N. America (CMI Map 6, ed. 3). TRANSMISSION: Overwinters almost exclusively on pines from which aeciospores may be blown hundreds of kilometres (7: 813) to infect Ribes leaves through stomata (Spaulding, 1922). In contrast, basidiospores (38: 393) travel only a few hundred metres to infect pine needles through stomata (Patton & Johnson, 1970), from where the mycelium grows into the stem to form cankers. The importation of large quantities of white pine seedlings from Europe at the turn of the century carried the disease to N. America (Spaulding, 1922; 1929).

1996 ◽  
Vol 72 (6) ◽  
pp. 637-638 ◽  
Author(s):  
Jean A. Bérubé

White pine seedlings were treated with triadimefon two weeks prior to natural inoculation with Cronartium ribicola and were observed for two growth seasons. During the second growth season in the greenhouse the incidence of blister rust symptoms was 70.8% for the untreated controls, whereas only 3.8% of the treated seedlings showed symptoms of blister rust. Triadimefon offers effective protection against white pine blister rust infection and would enable the production of bare root seedlings in areas prone to blister rust infection.


2000 ◽  
Vol 10 (3) ◽  
pp. 567-569 ◽  
Author(s):  
Stanislaw Pluta ◽  
Agata Broniarek-Niemiec

Field resistance to white pine blister rust (WPBR) (Cronartium ribicola J. C. Fischer) was investigated on 53 black currant (Ribes nigrum L.) genotypes (cultivars and breeding selections) in 1998 and 1999. Uredia did not form on the black currant `Titania' and 17 advanced selections during field evaluations made at the Experimental Orchard at Dabrowice, near Skierniewice, Poland.


Plant Disease ◽  
2010 ◽  
Vol 94 (4) ◽  
pp. 461-464 ◽  
Author(s):  
D. T. Dalton ◽  
J. D. Postman ◽  
K. E. Hummer

Hosts for the fungus Cronartium ribicola, causal agent of white pine blister rust (WPBR), include five-needle pines as aecial hosts, and currants and gooseberries as uredinial/telial hosts. Aeciospores produced on diseased pine, and urediniospores produced on diseased Ribes plants, can infect Ribes foliage. Resistance and susceptibility for both spore types have been reported for Ribes; however, the comparative infectivity of these spore types on clonal Ribes nigrum genotypes is under-described. Immunity, resistance, and susceptibility to WPBR resides at a clonal level in Ribes. Previous studies have emphasized fungal diversity or forestry considerations, rather than horticultural aspects. The objective of this study was to determine if aeciospores and urediniospores were equally infective to specific genotypes of black currant, Ribes nigrum, with differential responses. A family of 51 black currant genotypes from a cross between a known-immune cultivar containing the Cr gene and a susceptible cultivar was examined. Single-leaf softwood cuttings of each of these genotypes were artificially inoculated with a spore solution and incubated in airtight plastic containers within a growth chamber. Inoculations were replicated three times for each spore type. Twenty-two of the F1 genotypes did not develop uredia after artificial inoculation. These may be immune; 22 developed uredia after exposure to both types of inoculum, and were susceptible; whereas seven exhibited differential responses and may have some mechanism for resistance to WPBR other than the Cr gene. The infectivity of aeciospores and urediniospores was not significantly different on specific Ribes genotypes. Either spore type can therefore be considered equally effective as inoculum when screening for WPBR resistance or immunity in horticultural settings.


1998 ◽  
Vol 28 (3) ◽  
pp. 412-417 ◽  
Author(s):  
Abul KM Ekramoddoullah ◽  
Joanne J Davidson ◽  
Doug W Taylor

A 19-kDa protein, Pin m III, was recently shown to be associated with overwintering and frost hardiness of western white pine (Pinus monticola Dougl. ex D. Don) seedlings. Here, we report that this protein is up-regulated by the fungus Cronartium ribicola Fisch, the causal agent of white pine blister rust in western white pine trees. Between 1991 and 1994, bark samples of mature western white pine trees (resistant with no stem cankers and susceptible with stem cankers) were collected in winter, spring, and fall. Proteins were extracted and analyzed by Western immunoblot utilizing specific rabbit polyclonal anti-Pin l I (a homologue of Pin m III) antibodies. During all collection dates, but particularly in the spring, susceptible trees had more Pin m III than resistant trees. In July 1995, 43 previously inoculated 7-year-old white pine seedlings were also analyzed. In all susceptible seedlings (cankered) tested, cankered tissue had high levels of Pin m III, and samples collected from the outside edge of the canker margin had low levels of Pin m III; this protein was also detected in some healthy bark of cankered trees. Since the level of Pin m III in healthy white pine trees is normally lowest in summer months, the high level Pin m III in summer samples of infected tissues is a consequence of the fungal infection.


Plant Disease ◽  
2011 ◽  
Vol 95 (12) ◽  
pp. 1589-1589 ◽  
Author(s):  
Z. A. Frederick ◽  
S. Villani ◽  
K. D. Cox ◽  
L. Los ◽  
J. Allen

Since the relaxation of federal sanctions on the planting of Ribes crops because of the development of white pine blister rust (WPBR) immune Ribes cultivars (3), a small industry for the production of Ribes fruit for fresh and processing markets was established in New York and surrounding New England states. The majority of Ribes acreage in the region is planted to a WPBR immune black currant R. nigrum cv. Titania. From 2008 to June 2011, symptoms resembling those caused by WPBR pathogen Cronartium ribicola were observed at a large (>12 ha) R. nigrum cv. Titania planting in Preston, CT. In 2008, infection was restricted to a single field (100% incidence), but in 2009, all fields suffered from premature defoliation by late July. In 2010 and 2011, there was considerable incidence (>85%), but premature defoliation was kept in check by chemical management. Symptoms began as chlorotic lesions (0.5 to 4.3 mm in diameter) on both sides of the leaf. These chlorotic lesions had margins delineated by leaf veins and many developed necrotic (0.3 to 0.9 mm in diameter) centers on the upper surface of leaves within 2 to 3 weeks. The undersides of lesions developed blisters containing orange uredinia (0.1 to 0.33 mm in diameter) with smooth peridia that broke with the production of yellow-orange urediniospores (30 × 15 to 25 μm). Symptoms and signs were consistent with published descriptions of C. ribicola (1) and with WPBR infections on highly susceptible R. nigrum cv. Ben Alder planted at the New York State Agricultural Experiment Station in Geneva. Additional confirmation was provided by sequencing the two internal transcribed spacer (ITS) regions and the 5.8S gene (GenBank Accession No. JN587805; 98% identity with No. DQ533975) in the nuclear ribosomal repeat using primers ITS1-F and ITS4 as described previously (2,4). Furthermore, an attempt was made to confirm pathogenicity in the greenhouse by inoculating shoots of potted nursery stock of R. nigrum cv. Titania. Shoots were inoculated by rubbing leaves with either an uninfected currant leaf or a currant leaf from Preston, CT sporulating with urediniospores. Plants were subsequently misted with dH20 and covered with plastic bags for 24 h. Plants were watered biweekly and kept in a greenhouse with 39 to 65% relative humidity at 21 to 26°C. Shoots were monitored for symptom development on a weekly basis. After 3 weeks, 2 of the 10 plants inoculated with infected leaves developed chlorotic lesions and uredinia identical to those on leaves from Preston, CT, while all others remained healthy. Although not easily reproducible in a greenhouse, the breakdown of immunity in R. nigrum cv. Titania was observed for the last 4 years in Connecticut. Given that WPBR immunity was one of the conditions for legalized planting of Ribes, the breakdown of immunity has potentially deleterious implications particularly for nearby states like Massachusetts and New York, in which the Ribes industries are expanding. Moreover, Ribes growers may need to rely on chemical management programs to manage WPBR in the future. References: (1) G. B. Cummins. Illustrated Genera of Rust Fungi. Burgess Publishing Company, Minneapolis, MN, 1959. (2) M. Gardes and T. D. Bruns. Mol. Ecol. 2:113, 1993. (3) S. McKay. Hortic. Technol. 10:562, 2000. (4) T. J. White et al. PCR Protocols: A Guide to Methods and Applications. Academic Press, Inc., San Diego, CA, 1990.


2000 ◽  
Vol 10 (3) ◽  
pp. 555-556 ◽  
Author(s):  
Margie Luffman

The search for appropriate white pine blister rust (WPBR) (Cronartium ribicola J.C. Fischer) resistant germplasm to use in black currant (Ribes nigrum L.) breeding programs began in 1935 in Ottawa. Crosses were made in 1938 and 1939 with three different Ribes L. species and two standard black currant cultivars. The resulting seedlings from these crosses were evaluated for rust resistance. Three promising selections resulted from this program and were named `Coronet', `Crusader' and `Consort'.


PLoS ONE ◽  
2016 ◽  
Vol 11 (5) ◽  
pp. e0154267 ◽  
Author(s):  
Jun-Jun Liu ◽  
Danelle Chan ◽  
Yu Xiang ◽  
Holly Williams ◽  
Xiao-Rui Li ◽  
...  

2004 ◽  
Vol 21 (2) ◽  
pp. 61-68 ◽  
Author(s):  
Jerome A. Krueger ◽  
Klaus J. Puettmann

Abstract White pine seedlings were underplanted under a range of overstory densities in a hardwood stand in northern Minnesota. Vegetation surrounding seedlings was left untreated (control), weeded annually, or completely removed through monthly weeding. After 4 years, the benefit of weeding woody competition for diameter growth of seedlings was limited to areas with relatively open overstory conditions. Seedling height growth was reduced in areas with higher overstory density, but improved through weeding treatments that removed woody vegetation. The removal of herbaceous vegetation did not improve growth of seedlings in any conditions. Open growing conditions created by overstory removal and weed control resulted in higher incidences of seedling injuries, e.g., through infection by white pine blister rust. Conditions for pine bark adelgids also were enhanced in areas with low overstory densities and weeding treatments. The incidence for white pine weevil seems to follow a similar pattern, although the number of trees infected was minimal. Results show that improving growing conditions through management of the overstory and understory vegetation improves seedling growth rates, but must be balanced with potentially higher incidences of seedling injuries under more open conditions.


1998 ◽  
Vol 13 (2) ◽  
pp. 60-63 ◽  
Author(s):  
R. S. Hunt

Abstract Survey lines were located in areas that had been pruned to control blister rust (Cronartium ribicola) 10 yr previously and adjacent control (unpruned) areas in 10 stands of western white pine. Stands were classified as densely stocked, moderately stocked, or open. Cankers were tallied and their position noted. The success of pruning varied from stand to stand. Since the stands had not been pruned at an early age, there was only a 4 and 5% reduction in threatening cankers and stem cankers respectively, as few new cankers were initiated. Stands with the greatest increase in cankering had Ribes spp., were open grown, or possessed a high component of small white pine. Repruning these specific stands may be worthwhile, but in general, entering stands again to do either pruning or scribing would produce few additional healthy trees. Doing both treatments, however, may significantly enhance the number of healthy stems. To optimize the benefits of pruning, stands should be entered early and pruning should continue until a sufficient number of stems are pruned to a height of 3 m to ensure full stocking. Other species may be impediments to spore movement within stands, and thus they should not be pruned. Dense stands initially had less rust than open stands and could be entered later, but once spaced, they also need to be pruned to 3 m to minimize rust infection. West. J. Appl. For: 13(2):60-63.


2007 ◽  
Vol 85 (3) ◽  
pp. 299-306 ◽  
Author(s):  
Bryce A. Richardson ◽  
Paul J. Zambino ◽  
Ned B. Klopfenstein ◽  
Geral I. McDonald ◽  
Lori M. Carris

The white-pine blister rust fungus, Cronartium ribicola Fisch. in Rabenh., continues to spread in North America, utilizing various aecial (primary) and telial (alternate) hosts, some of which have only recently been discovered. This introduced pathogen has been characterized as having low genetic diversity in North America, yet it has demonstrated a capacity to invade diverse environments. The recent discovery of this rust fungus on the telial host Pedicularis racemosa Dougl. ex Benth., raises questions of whether this host association represents a recent acquisition by C. ribicola or a long-standing host association that was overlooked. Here we explore two questions: (i) is host specialization detectable at a local scale and (ii) is the capacity to infect Pedicularis racemosa local or widespread? Genetic analysis of C. ribicola isolates from different aecial and telial hosts provided no evidence for genetic differentiation and showed similar levels of expected heterozygosity within a geographic population. An inoculation test showed that diverse C. ribicola sources from across North America had the capacity to infect Pedicularis racemosa. These results support a hypothesis that ability to infect Pedicularis racemosa is common in C. ribicola from North America. Utilization of Pedicularis racemosa by C. ribicola may be dependent on the co-occurrence of this host, inoculum, and favorable environments.


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