RESUMO
In July-August 2019, seven Armillaria isolates (derived from rhizomorphs and mycelial fans of infected roots) were collected in association with woody hosts in the central Mexico: states of Guanajuato (MEX204), Jalisco (MEX206, MEX208, MEX209), and Michoacan (MEX211, MEX214, MEX216). All seven isolates were identified as Armillaria gallica based on translation elongation factor 1α (tef1) gene sequences (GenBank accession Nos.: MN839636 - MN839642 for MEX204, MEX206, MEX208, MEX209, MEX211, MEX214, and MEX216) and somatic pairing tests against known tester isolates. GenBank nucleotide BLAST results showed tef1 similarity for all isolates was highest for with A. gallica (≥ 97%; GenBank Accession Nos. KF156775 and KF156772). In replicated pairings against three tester isolates each for A. gallica, A. mellea, and A. mexicana, all isolates showed the highest compatibility with A. gallica (67-100%), with lower compatibility against A. mellea and A. mexicana, with 3-11% and 2-11%, respectively. Variations in compatibility among different tester isolates could reflect cryptic speciation within A. gallica (Klopfenstein et al., 2017). In Tarimoro, Guanajuato, MEX204 was isolated from infected Quercus jonesii (20°13'46.2"N 100°42'51.1"W, elevation 2286 m) that displayed root disease symptoms/signs (wilting/defoliation and mycelial fans within the roots). In a forested area of Mazamitla, Jalisco, MEX206 was isolated from infected Quercus laevis (19°54´52"N 103°00´07"W, elevation 2564 m) with root disease symptoms/signs (e.g., wilting, foliar chlorosis, and mycelial fans within the root crown); MEX208 was isolated from infected Pinus pseudostrobus (19°54´53"N 102°59´54"W, elevation 2554 m) with basal resinosis and mycelial fans; and MEX209 was collected from a symptomless P. devoniana (19°54'13.1"N 103°00'14.1"W, elevation 2566 m). In Zinapecuaro, Michoacan, MEX211 (19°53'28.8"N 100°39'44.0"W, elevation 2587 m) was isolated from infected Malus domestica with root disease that resulted in mortality; in Hidalgo, Michoacan, MEX214 (19°46'49"N 100°39'25.2"W, elevation 2961 m) and MEX216 (19°46'58"N 100°39'24"W, elevation 2958 m) were isolated from infected P. devoniana and P. teocote, respectively, which both displayed root disease symptoms/signs (basal resinosis and mycelial fans). Previously, A. gallica was reported in the State of Mexico, Veracruz, Oaxaca, Mexico (Elías-Román et al. 2013; Klopfenstein et al. 2014), but this represents the first report of A. gallica in Guanajuato, Jalisco, and Michoacan, Mexico. In contrast to other regions of North America (e.g., Bruhns et al. 2000), A. gallica was demonstrated to be a virulent pathogen on peach (Prunus persica) in central Mexico (Elías-Román et al. 2013). Unfortunately, tree seedlings cannot be used for Armillaria pathogenicity tests in a greenhouse or nursery; however, all root-diseased trees in this report showed Armillaria mycelial fans under the bark of a living tree, which are reliable indicators of pathogenicity, and no other root diseases were found. This report demonstrates that A. gallica is distributed across central Mexico, where it is associated with disease on Quercus, Pinus, and Malus. Such information is critical to increase our understanding of Armillaria root disease across diverse geographic regions and climates.
RESUMO
Armillaria mexicana (Agaricales, Physalacriaceae) is described as a new species based on morphology, DNA sequence data, and phylogenetic analyses. It clearly differs from previously reported Armillaria species in North, Central, and South America. It is characterized by the absence of fibulae in the basidioma, abundant cheilocystidia, and ellipsoidal, hyaline basidiospores that are apparently smooth under light microscope, but slightly to moderately rugulose under scanning electron microscope. It is differentiated from other Armillaria species by macromorphological characters, including annulus structure, pileus and stipe coloration, and other structures. DNA sequence data (nuc rDNA internal transcribed spacers [ITS1-5.8S-ITS2 = ITS], 28S D-domain, 3' end of 28S intergenic spacer 1, and translation elongation factor 1-α [TEF1]) show that A. mexicana sequences are quite distinct from sequences of analogous Armillaria species in GenBank. In addition, sequences of ITS of the A. mexicana ex-type culture reveal an ITS1 of 1299 bp and an ITS2 of 582 bp, the longest ITS regions reported thus far in fungi. Phylogenetic analysis based on TEF1 sequences place A. mexicana in a well-separated, monophyletic clade basal to the polyphyletic A. mellea complex.
Assuntos
Armillaria/classificação , Armillaria/isolamento & purificação , Armillaria/citologia , Armillaria/genética , Análise por Conglomerados , DNA Fúngico/química , DNA Fúngico/genética , DNA Ribossômico/química , DNA Ribossômico/genética , DNA Espaçador Ribossômico/química , DNA Espaçador Ribossômico/genética , México , Microscopia , Microscopia Eletrônica de Varredura , Fator 1 de Elongação de Peptídeos/genética , Filogenia , RNA Ribossômico 28S/genética , Análise de Sequência de DNARESUMO
The rust fungus, Puccinia psidii, is a devastating pathogen of introduced eucalypts (Eucalyptus spp.) in Brazil where it was first observed in 1912. This pathogen is hypothesized to be endemic to South and Central America and to have first infected eucalypts via a host jump from native guava (Psidium guajava). Ten microsatellite markers were used to genotype 148 P. psidii samples from eucalypts and guava plus five additional myrtaceous hosts across a wide geographic range of south-eastern Brazil and Uruguay. Principal coordinates analysis, a Bayesian clustering analysis and a minimum-spanning network revealed two major genetic clusters among the sampled isolates, one associated with guava and another associated with eucalypts and three additional hosts. Multilocus genotypes infecting guava differed by multiple mutational steps at eight loci compared with those infecting eucalypts. Approximate Bayesian computation revealed that evolutionary scenarios involving a coalescence event between guava- and eucalypt-associated pathogen populations within the past 1000 years are highly unlikely. None of the analyses supported the hypothesis that eucalypt-infecting P. psidii in Brazil originated via host jump from guava following the introduction of eucalypts to Brazil approximately 185 years ago. The existence of host-associated biotypes of P. psidii in Brazil indicates that this diversity must be considered when assessing the invasive threat posed by this pathogen to myrtaceous hosts worldwide.