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Orchid seeds depend on colonization by orchid mycorrhizal (OM) fungi for their germination; therefore, the orchids and OM fungi have long maintained a close relationship (e.g., formation of the hyphal mass structure, peloton) during their evolution. In the present study, we isolated new partitiviruses from OM fungi; partitivirus were separately found in different subcultures from the same fungi. Partitiviruses have been believed to lack an RNA silencing suppressor (RSS), which is generally associated with viral pathogenicity, because most partitiviruses isolated so far are latent in both plants and fungi. However, we found that the coat protein (CP) of our partitiviruses indeed had RSS activity, which differed among the virus isolates from OM fungi; one CP showed RSS activity in both plants and fungi, while another CP showed no activity. The family Partitiviridae include viruses isolated from plants and fungi, and it has been suggested that these viruses may occasionally be transmitted between plant and fungal hosts. Given that there are several reports showing that viruses can adapt to nonhost using strong RSS, we here discussed the idea that partitiviruses may be better able to migrate between the orchid and fungus probably through the pelotons formed in the orchid cells, if host RNA silencing is suppressed by partitivirus RSS.

Tuber infection of Phytophthora infestans often occurs at harvest. However, it is difficult to accurately estimate the population densities of P. infestans in soil, especially Japanese soil. In the present study, P. infestans DNA was extracted from soil samples using a modified CTAB-bead method and quantified using real-time PCR to accurately, rapidly and easily estimate the P. infestans population densities in upland soils in Japan. P. infestans was well quantified in eleven types of soil samples, including nine types of upland soils in Japan, that were artificially inoculated with a zoosporangia suspension. The amounts of P. infestans DNA estimated by the real-time PCR were proportional to the inoculum densities. In the non-controlled experimental potato field, P. infestans population densities in soil corresponded to the development of symptoms and were correlated with the number of lesions on the potato foliage. These results imply that the proposed real-time PCR assay is suitable for the estimation or monitoring of P. infestans population densities in upland soils in Japan. The population densities at the ridge bottoms were larger than those at any other location in commercial potato fields. These results were similar to those of a previous report using a bioassay. Moreover, a correlation between DNA quantity and inoculum potential was observed. In conclusion, the real-time PCR assay developed in this study is suitable for indirect estimation of the inoculum potential of P. infestans .

Failure to sprout due to seed-tuber rot is a serious problem for autumn potato seedling cultivation in Nagasaki Prefecture, Japan. In this study, five strains were isolated from rotten seed tubers sampled in 2015; when tubers were inoculated with these strains, the tubers developed rot and failed to sprout. We identified these strains as Fusarium acuminatum, Fusarium commune, and the known agent of potato dry rot, Fusarium oxysporum based on morphological and DNA sequencing analyses. F. commune and F. acuminatum were identified as causal agents of potato dry for the first time in the world and in Japan, respectively.

The virulence of 29 isolates of Phytophthora infestans collected in potato fields in Hokkaido, Japan, in 2013 and 2014, was tested for race identification. Thirteen different races were identified, each of which had five to eight virulence factors. All of the isolates caused a virulent reaction against plants with R1 and R7, and most of the isolates caused a virulent reaction against plants with R3, R4, R10, and R11. On the other hand, no isolate was virulent against plants with R9. These results demonstrate that the current Japanese P. infestans population is more complex than the population in the 1990s from the viewpoint of race.

In Hokkaido potato fields, tubers produced from the plants with leaf curl symptoms caused by potato leaf roll virus (PLRV) were noted to be more densely covered with Rhizoctonia sclerotia. This observation led us to hypothesize that potato infected with PLRV would have an increased susceptibility to Rhizoctonia solani . To test this hypothesis, in a pot experiment, we inoculated PLRV-infected mother tubers with Rhizoctonia . As a result, PLRV-infected plants produced significantly fewer and smaller tubers than virus-free plants did, suggesting that PLRV-infected plants are more susceptible than virus-free plants to R. solani . Virus-free seed tubers should thus be used to reduce Rhizoctonia diseases.

Twenty-nine isolates of Thanatephorus cucumeris (Rhizoctonia solani) AG-2-2 IV were collected from the roots, petioles, and leaves of diseased sugar beets in Hokkaido, Japan. We examined the genetic variation of the field isolates using somatic compatibility grouping of progeny (cultured isolates derived from induced basidiospores) based on analysis of hyphal anastomosis reactions (i.e., hyphal perfect fusion) and inter-simple sequence repeats (ISSRs). The number of somatic compatibility groups (SCGs) of single basidiospore isolates was strongly correlated with the host plant tissue from which the parental isolates were obtained. Parental isolates from roots and petioles tended to be genetically heterogeneous and generated plural SCGs, whereas isolates (except for two non-self-anastomosing isolates) from leaves tended to be homogeneous and generated a single SCG. Heterogeneous sibling basidiospore isolates yielded homogeneous progeny within a few generations. These findings were supported by the results of ISSR analysis, which showed that the homogeneous isolates generated progeny with the same genotype, whereas heterogeneous isolates generated progeny with different genotypes. However, like SCGs, ISSR genotypes of heterogeneous progeny tended to be homogeneous within two or three generations. Additionally, we examined clonal diversity during the basidiospore infection process over a 2-year period. A heterogeneous isolate generated a large number of progeny SCGs, thereby increasing clonal diversity. In contrast, progeny SCGs were almost all the same in a homogeneous isolate plot with a few exceptions. These results indicate that infection of T. cucumeris basidiospores play a role in the clonal diversity of AG-2-2 IV isolates, as indicated by progeny SCGs in the field.

Microsatellite markers were tested to rapidly discriminate five Japanese genotypes (US-1, JP-1, JP-2, JP-3, and JP-4) of Phytophthora infestans . Collected from 1958 to 2007, 111 isolates of Japanese P. infestans were examined using a fluorescent-labeled primer and capillary electrophoresis. Microsatellite marker Pi26 generated specific products for each genotype without any differences in terms of isolation area or year for a particular genotype. The Pi26 marker is a powerful tool for obtaining information on the structure of Japanese populations of P. infestans .

Phytophthora infestans is the causal agent of potato late blight. Genotypes of Japanese populations of P. infestans have been classified as US-1, JP-1, JP-2, JP-3, and JP-4 based on analyses of DNA polymorphisms. These populations may have been introduced to Japan by the migration of P. infestans from other countries and by domestic changes produced through sexual and asexual propagation. Resistance to late blight has been an ongoing desire of potato farmers in Japan and elsewhere. Recurrent backcrossing of Solanum demissum to varieties of S. tuberosum has been used to transfer late blight resistance. Many varieties carry the R1 gene, whereas others carry R2, R3, and/or R4. However, R genes provided only transient resistance to late blight. New races rapidly overcome R-gene-mediated resistance. The R genes of potato generally encode receptors that recognize secretory effector (Avr) proteins produced by P. infestans. These effector proteins induce robust resistance in potato varieties containing R genes, while they suppress resistance in potato varieties lacking R genes. Conserved molecules from Phytophthora species such as fatty acids, glucans, and elicitins also act as elicitors in Solanaceae species. These P. infestans-derived elicitors induce defensive reactions, including the accumulation of phytoalexins and hypersensitive cell death. A future challenge will be to combine our accumulated knowledge with that from other scientific fields to develop a disease management approach for late blight.

We explored the effects of harvest damage on potatoes infected with Phytophthora infestans in 2015 and 2016. Injured tubers were inoculated with zoosporangia suspensions and incubated at 18°C in the dark for 4 weeks. In 2015 and 2016, 38.5% and 74.4%, respectively, of injured tubers inoculated with P. infestans rotted and hyphal masses were apparent on the tuber surfaces. Tubers in the uninjured group rarely rotted even when there were numerous P. infestans zoosporangia on the inoculated tuber surface. The percentage of rotten tubers in the injured/no inoculation group caused by other types of fungi or bacteria increased rapidly, to approximately 20% within one week; however, there was very little increase during the subsequent incubation. Conversely, the percentage of rotten tubers increased with incubation time in the injured/inoculation group and this phenomenon was significant in 2015. These results imply that not only the presence of P. infestans but also surface harvest injuries affect potato storage rot. Storage rot can be minimized by reducing surface injuries and/or decreasing blighted plant material and the population density of P. infestans in the soil at the time of harvest during commercial potato production.

Five Pythium species ( Pythium irregulare , P. mamillatum , P. myriotylum , P. spinosum and P. ultimum var. ultimum ) were isolated from the hypocotyls and roots of kidney bean plants with damping-off from a commercial field and from experimental plots that have undergone either continuous cropping with kidney bean or rotational cropping with arable crops. In inoculation tests, all five Pythium species were pathogenic to kidney bean. This is the first report of damping-off of kidney bean caused by Pythium species; we named this disease damping-off of kidney bean.