ABSTRACT
Species of Diaporthe are considered important plant pathogens, saprobes, and endophytes on a wide range of plant hosts. Several species are well-known on grapevines, either as agents of pre- or post-harvest infections, including Phomopsis cane and leaf spot, cane bleaching, swelling arm and trunk cankers. In this study we explore the occurrence, diversity and pathogenicity of Diaporthe spp. associated with Vitis vinifera in major grape production areas of Europe and Israel, focusing on nurseries and vineyards. Surveys were conducted in Croatia, Czech Republic, France, Hungary, Israel, Italy, Spain and the UK. A total of 175 Diaporthe strains were isolated from asymptomatic and symptomatic shoots, branches and trunks. A multi-locus phylogeny was established based on five genomic loci (ITS, tef1, cal, his3 and tub2), and the morphological characters of the isolates were determined. Preliminary pathogenicity tests were performed on green grapevine shoots with representative isolates. The most commonly isolated species were D. eres and D. ampelina. Four new Diaporthe species described here as D. bohemiae, D. celeris, D. hispaniae and D. hungariae were found associated with affected vines. Pathogenicity tests revealed D. baccae, D. celeris, D. hispaniae and D. hungariae as pathogens of grapevines. No symptoms were caused by D. bohemiae. This study represents the first report of D. ambigua and D. baccae on grapevines in Europe. The present study improves our understanding of the species associated with several disease symptoms on V. vinifera plants, and provides useful information for effective disease management.
ABSTRACT
This study introduces two new families, one new genus, 22 new species, 10 new combinations, four epitypes, and 16 interesting new host and / or geographical records. Cylindriaceae (based on Cylindrium elongatum) is introduced as new family, with three new combinations. Xyladictyochaetaceae (based on Xyladictyochaeta lusitanica) is introduced to accommodate Xyladictyochaeta. Pseudoanungitea gen. nov. (based on P. syzygii) is described on stems of Vaccinium myrtillus (Germany). New species include: Exophiala eucalypticola on Eucalyptus obliqua leaf litter, Phyllosticta hakeicola on leaves of Hakea sp., Setophaeosphaeria citricola on leaves of Citrus australasica, and Sirastachys cyperacearum on leaves of Cyperaceae (Australia); Polyscytalum chilense on leaves of Eucalyptus urophylla (Chile); Pseudoanungitea vaccinii on Vaccinium myrtillus (Germany); Teichospora quercus on branch tissue of Quercus sp. (France); Fusiconidium lycopodiellae on stems of Lycopodiella inundata, Monochaetia junipericola on twig of Juniperus communis, Myrmecridium sorbicola on branch tissues of Sorbus aucuparia, Parathyridaria philadelphi on twigs of Philadelphus coronarius, and Wettsteinina philadelphi on twigs of Philadelphus coronarius (Germany); Zygosporium pseudogibbum on leaves of Eucalyptus pellita (Malaysia); Pseudoanungitea variabilis on dead wood (Spain); Alfaria acaciae on leaves of Acacia propinqua, Dictyochaeta mimusopis on leaves of Mimusops caffra, and Pseudocercospora breonadiae on leaves of Breonadia microcephala (South Africa); Colletotrichum kniphofiae on leaves of Kniphofia uvaria, Subplenodomus iridicola on Iris sp., and Trochila viburnicola on twig cankers on Viburnum sp. (UK); Polyscytalum neofecundissimum on Quercus robur leaf litter, and Roussoella euonymi on fallen branches of Euonymus europaeus (Ukraine). New combinations include: Cylindrium algarvense on leaves of Eucalyptus sp. (Portugal), Cylindrium purgamentum on leaf litter (USA), Cylindrium syzygii on leaves of Syzygium sp. (Australia), Microdochium musae on leaves of Musa sp. (Malaysia), Polyscytalum eucalyptigenum on Eucalyptus grandis × pellita (Malaysia), P. eucalyptorum on leaves of Eucalyptus (Australia), P. grevilleae on leaves of Grevillea (Australia), P. nullicananum on leaves of Eucalyptus (Australia), Pseudoanungitea syzygii on Syzygium cordatum leaf litter (South Africa), and Setophaeosphaeria sidae on leaves of Sida sp. (Brazil). New records include: Sphaerellopsis paraphysata on leaves of Phragmites sp., Vermiculariopsiella dichapetali on leaves of Melaleuca sp. and Eucalyptus regnans, and Xyladictyochaeta lusitanica on leaf litter of Eucalyptus sp. (Australia); Camarosporidiella mackenziei on twigs of Caragana sp. (Finland); Cyclothyriella rubronotata on twigs of Ailanthus altissima, Rhinocladiella quercus on Sorbus aucuparia branches (Germany); Cytospora viticola on stems of Vitis vinifera (Hungary); Echinocatena arthrinioides on leaves of Acacia crassicarpa (Malaysia); Varicosporellopsis aquatilis from garden soil (Netherlands); Pestalotiopsis hollandica on needles of Cupressus sempervirens (Spain), Pseudocamarosporium africanum on twigs of Erica sp. (South Africa), Pseudocamarosporium brabeji on branch of Platanus sp. (Switzerland); Neocucurbitaria cava on leaves of Quercus ilex (UK); Chaetosphaeria myriocarpa on decaying wood of Carpinus betulus, Haplograhium delicatum on decaying Carpinus betulus wood (Ukraine). Epitypes are designated for: Elsinoë mimosae on leaves of Mimosa diplotricha (Brazil), Neohendersonia kickxii on Fagus sylvatica twig bark (Italy), Caliciopsis maxima on fronds of Niphidium crassifolium (Brazil), Dictyochaeta septata on leaves of Eucalyptus grandis × urophylla (Chile), and Microdochium musae on leaves of Musa sp. (Malaysia).
ABSTRACT
Lemon balm is a well-known perennial, medicinal and culinary herb, and also a melliferous plant that is grown commercially in many parts of the world including Hungary. In October 2009, symptoms of powdery mildew infection were observed on lemon balm plants grown in several gardens in Budapest, Maklár, and Eger, Hungary, as well as in Ghenci, Romania. Abundant mycelium and conidial sporulation was observed on both leaf surfaces and stems. Conidia were produced in chains and were ellipsoid-ovoid to subcylindrical, measured 29 to 44 × 15 to 18 µm, and germinated with germ tubes produced apically or subapically on conidia. The basal septa of the conidiophores were sometimes displaced from the point of branching. The width of their foot cells increased from base to top and sometimes enlarged considerably at a particular point. Hyphal appressoria were nipple shaped. On the basis of these characteristics, the pathogen was identified as an Oidium sp. belonging to the subgenus Reticuloidium. The teleomorph stage was not found. To precisely identify the pathogen, DNA was extracted from mycelia collected from single leaves collected in Budapest and Ghenci with a Qiagen (Valencia, CA) DNeasy Plant Kit. The internal transcribed spacer (ITS) sequences of the nrDNA were amplified and sequenced as described in Jankovics et al. (3). The two ITS sequences, deposited in GenBank under Accession Nos. HM156493 and HM156494, were identical to several ITS sequences of Golovinomyces biocellatus, such as AB307675, AF011291, and EU035602. Thus, the pathogen was identified as G. biocellatus based on the host plant species, anamorph morphology, and ITS sequence. It was clearly distinguished from Neoerysiphe galeopsidis, another powdery mildew species known to infect lemon balm in Europe (1). Specimens were deposited under Accession Nos. HAL 2369F and HAL 2370F at the Herbarium of Martin Luther University, Halle, Germany. Pathogenicity tests were carried out in cabinets within a controlled environment as described for other powdery mildews in Jankovics et al. (3) using five potted healthy lemon balm plants bought from a nursery. The first powdery mildew colonies appeared 7 to 10 days after inoculation, and 2 to 3 weeks later, nearly all the leaves and stems of the three inoculated plants became covered with powdery mildew mycelium. Light microscopy confirmed that the pathogen was the anamorph of G. biocellatus. The two noninoculated plants remained healthy. This confirmed the pathogenicity of the fungus collected from the field to lemon balm. G. biocellatus has long been known to infect lemon balm in some European countries and elsewhere (1), but was not listed as a pathogen of this plant species in Hungary (4). However, it was reported from Romania, a neighboring country, more than 30 years ago (2). This suggests that G. biocellatus might have occurred in Hungary on lemon balm during the past decades without being reported in the literature. References: (1) U. Braun. Beih. Nova Hedwigia 89:1, 1987. (2) O. Constantinescu and G. Negrean. Sydowia 29:75, 1976-77. (3) T. Jankovics et al. Phytopathology 98:529, 2008. (4) Sz. Nagy and L. Kiss. Acta Phytopathol. Entomol. Hung. 41:79, 2006.
