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Hatomi, H.

Publications and source records attributed to Hatomi, H..

4 recordsLinked to original sources

Bulk sample testing by real-time PCR for detecting Diaporthe destruens-infected seedlings of sweet potatoes

Foot rot disease of sweet potato is a fungal disease that causes serious damage to sweet potato production. It is especially important to check the health of seedlings as there is a risk that if the seed tubers or stem seedlings infected with foot rot pathogen are introduced into the production fields, it will rapidly spread throughout the fields. We have already developed a real-time PCR method to diagnose sweet potatoes contaminated with foot rot pathogen. In this study, to apply this method to the bulk sample testing, we provided examples on estimating the "probability of detection (POD)" for detecting bulk samples, and determining the number of subgroups and the number of samples in each subgroup for the bulk sample testing. Our results indicate that, for tubers, when testing between 100 and 1200 fragments per bulk sample, the lowest detection rate was approximately 81% at 800 fragments. For stems, when testing between 100 and 600 fragments, the lowest detection rate was approximately 83% at 500 fragments. Based on the estimated POD, the required sample size for bulk testing was calculated as follows: for the impermissible threshold proportion of contamination of infected plants (p) of 1%, between 390 and 624 samples are needed, while for p of 0.1%, between 3,840 and 6,228 samples are required. The bulk sample testing method using real-time PCR demonstrated in this study will become a powerful quality testing method for checking the health of sweet potato seedlings, and will make a significant contribution to sweet potato production.

plant biology↗

Investigation of host plant contact with Diaphorina citri (Hemipreta: Psyllidae) by detecting D. citri-derived environmental DNA

Citrus greening (Huanglongbing) disease has serious impacts on citrus production. Field monitoring of the Asian citrus psyllid Diaphorina citri (Hemiptera: Psyllidae), a vector of citrus greening disease, is essential to prevent the invasion and spread of this disease. This study reported a new method for determining the presence of D. citri and traces of contact with host plants by collecting leaves of host plants from the survey area and detecting the environmental DNA (eDNA) derived from D. citri. The results showed that the method can determine the presence of D. citri. As D. citri-derived eDNA is contained in DNA solutions of plants with a history of contact with D. citri, we succeeded in detecting not only genes conserved in D. citri mitochondria but also genes of D. citri symbiont organisms consisting of Wolbachia, Wolbachia phage, Candidatus Carsonella sp., and Candidatus Profftella sp. Diaphorina citri-derived eDNA could be detected in host plants even after only 10 min of contact with D. citri and could still be detected 6 months after contact. This technology has the potential to trace D. citri from their traces without individual detection and is expected to greatly contribute to the early detection and invasion warning of citrus greening disease in the future.

molecular biology↗

Draft Genome Sequences of 10 Strains of Pseudomonas syringae pv. actinidiae Biovar 1: A Major Kiwifruit Bacterial Canker Pathogen in Japan

Several groups (biovars) of the kiwifruit bacterial canker pathogen, Pseudomonas syringae pv. actinidiae, are found in Japan. Here, we sequenced and compared the 10 genomes of biovar 1, the major group in Japan, which is known as the phaseolotoxin producer. The kiwifruit bacterial canker pathogen, Pseudomonas syringae pv. actinidiae (Psa), was first described in Japan in 1989 (1). Subsequently, Psa was found in other kiwifruit-producing countries (2). Based on comparative analyses (2-4), Psa was categorized into several groups (biovars). The first Japanese group was named biovar 1 (Psa1), which was also later found in Italy and Korea. This biovar produces phaseolotoxin (2), a phytotoxin that inhibits arginine biosynthesis in host plants and results in bacterial canker symptom development. On the Psa1 chromosome, a large number of genes involved in phaseolotoxin biosynthesis are accumulated in an approximately 23 kb region (argK-tox cluster), which is contained in an exogenous genomic island (tox island) that Psa1 acquired in the past (2). However, some Psa1 strains found in Ehime Prefecture, Japan (the Ehime isolates) do not produce phaseolotoxin, although they seem to possess the argK-tox cluster (5). On the other hand, several Psa1 strains preserved in the NARO Genebank (https://www.gene.affrc.go.jp/index_en.php) may lack this cluster (2). Here, we selected 10 strains (Table 1) that represent Psa1 diversity and conducted comparative genome analyses. O_TBL View this table: org.highwire.dtl.DTLVardef@f2cdbdorg.highwire.dtl.DTLVardef@a16c33org.highwire.dtl.DTLVardef@1c68baborg.highwire.dtl.DTLVardef@1fbb077org.highwire.dtl.DTLVardef@fe901e_HPS_FORMAT_FIGEXP M_TBL O_FLOATNOTable 1.C_FLOATNO O_TABLECAPTIONGenome data and accession numbers of 10 strains of Pseudomonas syringae pv. actinidiae biovar 1. C_TABLECAPTION C_TBL

genomics↗