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1.
Mycologia ; 110(5): 948-961, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30240340

RESUMEN

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.


Asunto(s)
Cuerpos Fructíferos de los Hongos/crecimiento & desarrollo , Laccaria/clasificación , Micorrizas/clasificación , Filogenia , Análisis por Conglomerados , ADN de Hongos/química , ADN de Hongos/genética , ADN Ribosómico/química , ADN Ribosómico/genética , ADN Espaciador Ribosómico/química , ADN Espaciador Ribosómico/genética , Corea (Geográfico) , Laccaria/citología , Laccaria/genética , Laccaria/crecimiento & desarrollo , Microscopía , Microscopía Electrónica de Rastreo , Micorrizas/citología , Micorrizas/genética , Micorrizas/crecimiento & desarrollo , Factor 1 de Elongación Peptídica/genética , ARN Polimerasa II/genética , ARN Ribosómico 28S/genética , ARN Ribosómico 5.8S/genética , Análisis de Secuencia de ADN , Esporas Fúngicas/citología , Esporas Fúngicas/ultraestructura
2.
Fungal Biol ; 121(11): 939-955, 2017 11.
Artículo en Inglés | MEDLINE | ID: mdl-29029701

RESUMEN

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.


Asunto(s)
Laccaria/clasificación , Laccaria/aislamiento & purificación , Repeticiones de Microsatélite , Filogenia , Filogeografía , China , ADN de Hongos/química , ADN de Hongos/genética , ADN Espaciador Ribosómico/química , ADN Espaciador Ribosómico/genética , Europa (Continente) , Japón , Laccaria/citología , Laccaria/genética , Microscopía , Análisis de Secuencia de ADN
3.
Mol Plant Microbe Interact ; 28(3): 261-73, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25338146

RESUMEN

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.


Asunto(s)
Regulación Fúngica de la Expresión Génica , Regulación de la Expresión Génica de las Plantas , Laccaria/genética , Populus/microbiología , Pseudotsuga/microbiología , Transcriptoma , Proteínas Fúngicas/genética , Perfilación de la Expresión Génica , Laccaria/citología , Laccaria/fisiología , Micorrizas/citología , Micorrizas/genética , Micorrizas/fisiología , Análisis de Secuencia por Matrices de Oligonucleótidos , Proteínas de Plantas/genética , Raíces de Plantas/citología , Raíces de Plantas/genética , Raíces de Plantas/inmunología , Raíces de Plantas/microbiología , Populus/citología , Populus/genética , Populus/inmunología , Pseudotsuga/citología , Pseudotsuga/genética , Pseudotsuga/inmunología , Regulón/genética , Transducción de Señal , Especificidad de la Especie , Simbiosis
4.
Plant Physiol ; 151(4): 1991-2005, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19854859

RESUMEN

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.


Asunto(s)
Arabidopsis/crecimiento & desarrollo , Arabidopsis/microbiología , Ácidos Indolacéticos/metabolismo , Laccaria/fisiología , Micorrizas/fisiología , Populus/crecimiento & desarrollo , Populus/microbiología , Arabidopsis/citología , Arabidopsis/efectos de los fármacos , Transporte Biológico/efectos de los fármacos , Polaridad Celular/efectos de los fármacos , Recuento de Colonia Microbiana , Perfilación de la Expresión Génica , Regulación de la Expresión Génica de las Plantas/efectos de los fármacos , Laccaria/citología , Laccaria/genética , Laccaria/crecimiento & desarrollo , Modelos Biológicos , Mutación/genética , Micorrizas/citología , Micorrizas/efectos de los fármacos , Micorrizas/genética , Análisis de Secuencia por Matrices de Oligonucleótidos , Ftalimidas/farmacología , Populus/citología , Populus/genética , Transducción de Señal/efectos de los fármacos , Factores de Tiempo
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