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1.
Mycologia ; 110(5): 948-961, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30240340

RESUMO

Species of Laccaria (Hydnangiaceae, Basidiomycota) are important in forest ecosystems as ectomycorrhizal fungi. Nine of the 75 described Laccaria species worldwide been reported from Korea. Most of these have European and North American names, and their identities are based solely on morphological features. To evaluate the taxonomy of Korean Laccaria, we used 443 specimens collected between 1981 and 2016 in a phylogenetic analysis based on sequence data from nuc rDNA internal transcribed spacer ITS1-5.8S-ITS2 rDNA (ITS) region, nuc 28S rDNA (28S), RNA polymerase II subunit 2 (rpb2), and translation elongation factor 1-α (tef1). Ten Laccaria species were identified. Three of these were previously reported from Korea: L. bicolor, L. tortilis, and L. vinaceoavellanea. Laccaria alba, L. japonica, and L. murina are confirmed as new reports from Korea. Lastly, four new Laccaria species are described: L. araneosa, L. parva, L. torosa, and L. versiforma. This study supports the general contention that Asian species of ectomycorrhizal fungi may not be conspecific with morphologically similar species from Europe and North America. Furthermore, identification based on morphology alone is often unreliable in Laccaria due to considerable overlap of characters among species. Thus, use of molecular methods is necessary for effective identification. Illustrations of the four newly described species and a taxonomic key to species of Laccaria in Korea are provided.


Assuntos
Carpóforos/crescimento & desenvolvimento , Laccaria/classificação , Micorrizas/classificação , Filogenia , Análise por Conglomerados , DNA Fúngico/química , DNA Fúngico/genética , DNA Ribossômico/química , DNA Ribossômico/genética , DNA Espaçador Ribossômico/química , DNA Espaçador Ribossômico/genética , Coreia (Geográfico) , Laccaria/citologia , Laccaria/genética , Laccaria/crescimento & desenvolvimento , Microscopia , Microscopia Eletrônica de Varredura , Micorrizas/citologia , Micorrizas/genética , Micorrizas/crescimento & desenvolvimento , Fator 1 de Elongação de Peptídeos/genética , RNA Polimerase II/genética , RNA Ribossômico 28S/genética , RNA Ribossômico 5,8S/genética , Análise de Sequência de DNA , Esporos Fúngicos/citologia , Esporos Fúngicos/ultraestrutura
2.
Fungal Biol ; 121(11): 939-955, 2017 11.
Artigo em Inglês | MEDLINE | ID: mdl-29029701

RESUMO

Purple Laccaria are ectomycorrhizal basidiomycetes associated with temperate forests all over the Northern Hemisphere in at least two taxa: Laccaria amethysteo-occidentalis in North America, and L. amethystina complex in Eurasia, as shown by Vincenot et al. (2012). Here, we combine a further study of the genetic structure of L. amethystina populations from Europe to southwestern China and Japan, using neutral Single Sequence Repeat (SSR; microsatellite) markers; and a systematic description of two novel Asian species, namely Laccaria moshuijun and Laccaria japonica, based on ecological, morphological, and molecular criteria (rDNA sequences). Population genetics provides evidence of the ancient isolation of three regional groups, with strong signal for speciation, and suggests a centre of origin of modern populations closest to present-day Chinese populations. Phylogenetic analyses confirm speciation at the molecular level, reflected in morphological features: L. moshuijun samples (from Yunnan, China) display strongly variable cheilocystidia, while L. japonica samples (from Japan) present distinctive globose to subglobose spores and clavate cheilocystidia. This study of a species complex primarily described with an extremely wide ecological and geographical range sheds new light on the biodiversity and biogeography of ectomycorrhizal fungi.


Assuntos
Laccaria/classificação , Laccaria/isolamento & purificação , Repetições de Microssatélites , Filogenia , Filogeografia , China , DNA Fúngico/química , DNA Fúngico/genética , DNA Espaçador Ribossômico/química , DNA Espaçador Ribossômico/genética , Europa (Continente) , Japão , Laccaria/citologia , Laccaria/genética , Microscopia , Análise de Sequência de DNA
3.
Mol Plant Microbe Interact ; 28(3): 261-73, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25338146

RESUMO

The coordinated transcriptomic responses of both mutualistic ectomycorrhizal (ECM) fungi and their hosts during the establishment of symbiosis are not well-understood. This study characterizes the transcriptomic alterations of the ECM fungus Laccaria bicolor during different colonization stages on two hosts (Populus trichocarpa and Pseudotsuga menziesii) and compares this to the transcriptomic variations of P. trichocarpa across the same time-points. A large number of L. bicolor genes (≥ 8,000) were significantly regulated at the transcriptional level in at least one stage of colonization. From our data, we identify 1,249 genes that we hypothesize is the 'core' gene regulon necessary for the mutualistic interaction between L. bicolor and its host plants. We further identify a group of 1,210 genes that are regulated in a host-specific manner. This variable regulon encodes a number of genes coding for proteases and xenobiotic efflux transporters that we hypothesize act to counter chemical-based defenses simultaneously activated at the transcriptomic level in P. trichocarpa. The transcriptional response of the host plant P. trichocarpa consisted of differential waves of gene regulation related to signaling perception and transduction, defense response, and the induction of nutrient transfer in P. trichocarpa tissues. This study, therefore, gives fresh insight into the shifting transcriptomic landscape in both the colonizing fungus and its host and the different strategies employed by both partners in orchestrating a mutualistic interaction.


Assuntos
Regulação Fúngica da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Laccaria/genética , Populus/microbiologia , Pseudotsuga/microbiologia , Transcriptoma , Proteínas Fúngicas/genética , Perfilação da Expressão Gênica , Laccaria/citologia , Laccaria/fisiologia , Micorrizas/citologia , Micorrizas/genética , Micorrizas/fisiologia , Análise de Sequência com Séries de Oligonucleotídeos , Proteínas de Plantas/genética , Raízes de Plantas/citologia , Raízes de Plantas/genética , Raízes de Plantas/imunologia , Raízes de Plantas/microbiologia , Populus/citologia , Populus/genética , Populus/imunologia , Pseudotsuga/citologia , Pseudotsuga/genética , Pseudotsuga/imunologia , Regulon/genética , Transdução de Sinais , Especificidade da Espécie , Simbiose
4.
Plant Physiol ; 151(4): 1991-2005, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19854859

RESUMO

The early phase of the interaction between tree roots and ectomycorrhizal fungi, prior to symbiosis establishment, is accompanied by a stimulation of lateral root (LR) development. We aimed to identify gene networks that regulate LR development during the early signal exchanges between poplar (Populus tremula x Populus alba) and the ectomycorrhizal fungus Laccaria bicolor with a focus on auxin transport and signaling pathways. Our data demonstrated that increased LR development in poplar and Arabidopsis (Arabidopsis thaliana) interacting with L. bicolor is not dependent on the ability of the plant to form ectomycorrhizae. LR stimulation paralleled an increase in auxin accumulation at root apices. Blocking plant polar auxin transport with 1-naphthylphthalamic acid inhibited LR development and auxin accumulation. An oligoarray-based transcript profile of poplar roots exposed to molecules released by L. bicolor revealed the differential expression of 2,945 genes, including several components of polar auxin transport (PtaPIN and PtaAUX genes), auxin conjugation (PtaGH3 genes), and auxin signaling (PtaIAA genes). Transcripts of PtaPIN9, the homolog of Arabidopsis AtPIN2, and several PtaIAAs accumulated specifically during the early interaction phase. Expression of these rapidly induced genes was repressed by 1-naphthylphthalamic acid. Accordingly, LR stimulation upon contact with L. bicolor in Arabidopsis transgenic plants defective in homologs of these genes was decreased or absent. Furthermore, in Arabidopsis pin2, the root apical auxin increase during contact with the fungus was modified. We propose a model in which fungus-induced auxin accumulation at the root apex stimulates LR formation through a mechanism involving PtaPIN9-dependent auxin redistribution together with PtaIAA-based auxin signaling.


Assuntos
Arabidopsis/crescimento & desenvolvimento , Arabidopsis/microbiologia , Ácidos Indolacéticos/metabolismo , Laccaria/fisiologia , Micorrizas/fisiologia , Populus/crescimento & desenvolvimento , Populus/microbiologia , Arabidopsis/citologia , Arabidopsis/efeitos dos fármacos , Transporte Biológico/efeitos dos fármacos , Polaridade Celular/efeitos dos fármacos , Contagem de Colônia Microbiana , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Laccaria/citologia , Laccaria/genética , Laccaria/crescimento & desenvolvimento , Modelos Biológicos , Mutação/genética , Micorrizas/citologia , Micorrizas/efeitos dos fármacos , Micorrizas/genética , Análise de Sequência com Séries de Oligonucleotídeos , Ftalimidas/farmacologia , Populus/citologia , Populus/genética , Transdução de Sinais/efeitos dos fármacos , Fatores de Tempo
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