Dynamics of bioluminescence by Armillaria gallica, A. mellea and A. tabescens

Mycologia ◽  
2007 ◽  
Vol 99 (3) ◽  
pp. 341-350 ◽  
Author(s):  
Jeanne D. Mihail ◽  
Johann N. Bruhn
Keyword(s):  
2006 ◽  
Vol 55 (4) ◽  
pp. 583-583 ◽  
Author(s):  
D. Prodorutti ◽  
L. Palmieri ◽  
D. Gobbin ◽  
I. Pertot

Mycologia ◽  
2000 ◽  
Vol 92 (5) ◽  
pp. 894-899 ◽  
Author(s):  
Brett Hodnett ◽  
James B. Anderson

Plant Disease ◽  
2011 ◽  
Vol 95 (10) ◽  
pp. 1255-1262 ◽  
Author(s):  
Nicholas J. Brazee ◽  
Robert L. Wick ◽  
Phillip M. Wargo

We hypothesized that Armillaria gallica, which is abundant in oak-dominated forests, is more successful at oxidizing and metabolizing polyphenols than A. calvescens, which is mostly restricted to maple-dominated forests. Isolates were challenged with up to seven concentrations of tannic acid (TA), gallic acid (GA), and black oak root bark extracts (RBE). Six concentrations of glucose and ethanol were also tested to determine the influence of available carbon on growth. Colony area and biomass values were analyzed using a GLM and Tukey's HSD test. When challenged with 0.12% concentrations of TA, GA, and RBE, A. gallica produced a significantly larger biomass in all treatments and larger colony areas in four of the five treatments compared to control values. A. gallica also produced a significantly larger number of rhizomorphs than A. calvescens on RBE medium. In contrast, A. calvescens generated significantly larger biomass over control treatments only when RBE was added, and values were substantially less compared to A. gallica. Growth of both species was significantly greater when ethanol was added, especially on GA medium, while glucose had little effect. Results from this study suggest that A. gallica is better at oxidizing and metabolizing polyphenols than A. calvescens.


2010 ◽  
Vol 40 (3) ◽  
pp. 536-548 ◽  
Author(s):  
J. A. McLaughlin ◽  
T. Hsiang

DNA sequences (~3 kb long) extending from the intergenic spacer 1 (IGS1) region to the 18S gene were obtained for isolates of Armillaria ostoyae , Armillaria calvescens , Armillaria gallica , and Armillaria sinapina . Additional investigation of 16 A. ostoyae, 11 Armillaria gemina , 21 A. calvescens, 18 A. gallica, and 15 A. sinapina isolates produced 117 sequences spanning the 3′ end of the IGS1 through the 5S gene and into the 5′ end of the IGS2 region. Additional sequences spanning the 3′ IGS2 to 5′ 18S gene region were obtained for two A. ostoyae, three A. gemina, two A. calvescens, two A. gallica, and three A. sinapina isolates. This is the first report of complete IGS2 sequences from Armillaria spp. A species identification protocol involving species-specific primers and restriction fragment length polymorphism analysis was devised based on species-specific polymorphisms. The protocol successfully identified all 16 A. ostoyae, 11 A. gemina, three of three Armillaria mellea , 18 A. gallica, 14 of 15 A. sinapina (11/12 diploid and 3/3 haploid), and 14 of 21 A. calvescens (13/15 diploid and 1/6 haploid) isolates included in this study. To the best of our knowledge, this success rate has not been matched by other methods.


2003 ◽  
Vol 107 (4) ◽  
pp. 408-412 ◽  
Author(s):  
Diane Cope Peabody ◽  
Robert B. Peabody ◽  
Maura Geens Tyrrell ◽  
Matthew J. Towle ◽  
Elizabeth M. Johnson

1995 ◽  
Vol 99 (6) ◽  
pp. 641-647 ◽  
Author(s):  
D.B. Carvalho ◽  
M.L. Smith ◽  
J.B. Anderson

Plant Disease ◽  
2017 ◽  
Vol 101 (1) ◽  
pp. 255 ◽  
Author(s):  
M.-S. Kim ◽  
N. R. Fonseca ◽  
R. D. Hauff ◽  
P. G. Cannon ◽  
J. W. Hanna ◽  
...  

Plant Disease ◽  
2010 ◽  
Vol 94 (12) ◽  
pp. 1503-1503 ◽  
Author(s):  
M.-S. Kim ◽  
J. W. Hanna ◽  
N. B. Klopfenstein

The loss and decline of native tree species caused by invasive plant pathogens is a major threat to the endangered endemic forests of the Hawaiian Islands (3). Thus, it is critical to characterize existing pathogens to evaluate potential invasiveness. In August 2005, rhizomorphs and mycelial bark fans of genet HI-4 were collected from dead/declining, mature trees of introduced Monterey pine (Pinus radiata) on the southern flank of Mauna Kea, Hawaii (approximately 19°42′55″N, 155°26′48″W, elevation 2,175 m). In March of 2008, three additional genets (HI-11, HI-13, and HI-16) were collected as rhizomorphs at a site named Pu'u La'au (west slope of the Mauna Kea Forest Reserve area, approximately 19°50′00″N, 155°35′35″W, elevation 2,275 to 2,550 m), approximately 20 km west-northwest of the HI-4 collection. These genets were collected from apparently healthy loblolly pine (Pinus taeda) that were introduced, apparently healthy māmane (Sophora chrysophylla; an endemic tree species of Hawaii), dead and dying māmane, and apparently healthy Methley plum (Prunus cerasifera × Prunus salicina) that was planted. All isolates were determined to have identical sequences in the intergenic spacer-1 rDNA region (GenBank Accession No. DQ995357). On the basis of somatic paring tests against North American Armillaria tester strains and 99% nucleotide sequence identities to GenBank Accession Nos. AY190245 and AY190246, these isolates were identified as Armillaria gallica. Past surveys have noted A. mellea sensu lato and A. nabsnona on numerous hosts in Hawaii, including māmane (3,4). However, to our knowledge, this is the first confirmed report of A. gallica in Hawaii, where it was found on māmane, Monterey pine, loblolly pine, and Methley plum. A. gallica has been widely categorized as a beneficial saprophyte, an opportunistic pathogen, or an aggressive pathogen (2). A recent study suggests that A. gallica can be highly pathogenic in some areas of the eastern United States and it is an important component of forest decline (2), especially under increasing stressors such as climate change. The isolation of A. gallica from declining stands on both introduced and endemic hosts under drought conditions suggests this pathogen is a contributing factor to forest decline on the island of Hawaii. Because the māmane tree is an important component of the native forest stands and essential to the endangered palila bird (Loxioides bailleui), which feeds almost exclusively on its green seeds (1), continued monitoring of Armillaria root disease is warranted. References: (1) P. C. Banko et al. J. Chem. Ecol. 28:1393, 2002. (2) N. J. Brazee and R. L. Wick. For. Ecol. Manage. 258:1605, 2009. (3) R. E. Burgan and R. E. Nelson. USDA For. Serv. Tech. Rep. PSW-3, 1972. (4) J. W. Hanna et al. Plant Dis. 91:634, 2007.


2020 ◽  
Vol 51 (4) ◽  
pp. 1539-1552 ◽  
Author(s):  
Mengtao Zhan ◽  
Menghua Tian ◽  
Weiguang Wang ◽  
Ganpeng Li ◽  
Xiaokai Lu ◽  
...  

1998 ◽  
Vol 28 (1) ◽  
pp. 141-149 ◽  
Author(s):  
T M Frontz ◽  
D D Davis ◽  
B A Bunyard ◽  
D J Royse

Restriction fragment length polymorphism analysis (RFLP) of the intergenic region (IGR-1) between the 3 ' end of the 26S ribosomal RNA gene and the 5 ' end of the 5S rRNA gene was used to identify 39 isolates of Armillaria species collected from live or recently dead bigtooth aspen (Populus grandidentata Michx.) trees and sucker sprouts in the Tioga State Forest, Pennsylvania. The unknown isolates were identified by comparing their restriction fragment patterns with 18 isolates of known Armillaria species common to the northeastern United States. Twenty of the unknown isolates (50%) were identified as either Armillaria gallica or Armillaria calvescens. Eighteen (46%) of the isolates were identified as Armillaria ostoyae. One isolate of Armillaria sinapina was obtained from a recently dead aspen tree. One isolate of Armillaria mellea, considered to be the most divergent of the Armillaria species, was obtained from basidiomes fruiting on a recently dead aspen tree near Berwick, Pennsylvania. In some instances, amplification of DNA was possible by adding mycelial scrapes directly to the polymerase chain reaction (PCR) mix, thus precluding the need for DNA extraction. Advancements in RFLP analysis may offer a method able to provide rapid and precise identification of most North American and European Armillaria isolates.


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