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991.
Keisuke Tomioka Yuuri Hirooka Toshirou Nagai Hiroyuki Sawada Takayuki Aoki Toyozo Sato 《Journal of General Plant Pathology》2011,77(4):266-268
Severe blight of potted seedlings of monkshood caused by Plectosporium tabacinum was found in glasshouses in Kagawa Prefecture in southwest Japan in May 2001. Root rot and browning of stem bases were followed
by wilting and yellowing of leaves, then blighting of leaves, flower buds and stems. A fungus was isolated from diseased plants
and confirmed to cause the disease. The new disease was named “Plectosporium blight of monkshood”. 相似文献
992.
Shin-ichi Shimizu Takao Ito Takanori Miyoshi Yasunobu Tachibana Tsutae Ito 《Journal of General Plant Pathology》2011,77(6):326-330
Universal primers to detect Satsuma dwarf virus (SDV), including distantly related strains Citrus mosaic virus (CiMV), Navel orange infectious mottling virus (NIMV), and
Hyuganatsu virus (HV), were tested in a convenient one-step RT-PCR assay. SDV was the most broadly detected using uSDVup/uSDVdo
primers that specifically targeted a nucleotide sequence in the 3′-noncoding region that is conserved in both segmented RNAs
1 and 2 of SDV among the tested primers. Nucleotide sequence analysis confirmed that the amplified RT-PCR products could be
derived from RNAs 1 or 2 of SDV variants, some of which had interesting genetic diversity. 相似文献
993.
Ryo Kubota Mark A. Schell Gabriel D. Peckham Joanne Rue Anne M. Alvarez Caitilyn Allen Daniel M. Jenkins 《Journal of General Plant Pathology》2011,77(3):182-193
New rapid diagnostic methods are urgently needed to discriminate the quarantine pathogen Ralstonia solanacearum (Rs) race 3 biovar 2 (R3B2) from other populations of Rs that lack the adaptation to cause bacterial wilt disease in temperate
regions. We used an in silico bioinformatic approach to identify several genome sequences potentially specific to R3B2 strains. Primer sets were designed
to PCR-amplify sequences in these regions, and four sets were ultimately shown to be >99% accurate for detection of R3B2 strains.
On the basis of these results, several primers were designed to enable development of a loop-mediated isothermal amplification
assay that was rapid, technologically simple, and essentially 100% accurate for identification of R3B2 when applied to a comprehensive
collection of geographically diverse Rs strains. We fortuitously found that a sequence in one of the “R3B2-specific” regions
has ~90% identity to a sequence present in strains of the blood disease bacterium (BDB), a member of the Rs species complex
that infects banana. Alignments of these sequences allowed design of a second PCR primer set that proved 100% accurate for
identification of BDB strains when tested on the 22 BDB strains available to us. These results demonstrate the power of in silico genomic subtraction for rapid identification of population-specific DNA sequences and for the development of simple, reliable
detection methods for Rs subpopulations. 相似文献
994.
Syed Jawad Ahmad Shah Shaukat Hussain Musharaf Ahmad Farhatullah Iftikhar Ali Muhammad Ibrahim 《Journal of General Plant Pathology》2011,77(3):174-177
Fifty wheat varieties along with Jupateco-73 and Morocco were studied for the expression of leaf tip necrosis (LTN), a trait
linked with the durable rust resistance gene pair Lr34/Yr18. LTN was frequent (i.e., ≥6) in nine replications of a field experiment over 3 years in 17 genotypes, and the varieties were
considered positive for LTN. In molecular analyses of these varieties, having relative severity values up to 78 for yellow
rust and 45 for leaf rust, the 150-bp Lr34/Yr18-linked allele was consistently amplified. Expression of LTN in six of nine replications is an appropriate threshold for predicting
the presence of Lr34/Yr18 gene pair, and genotypes can be selected using this trait. 相似文献
995.
Jun Ohnishi Toshio Kitamura Fumihiro Terami Ken-ichiro Honda 《Journal of General Plant Pathology》2011,77(1):54-59
The ability of the whitefly Bemisia tabaci to transmit two strains of Tomato yellow leaf curl virus, the Israel and Mild strains, was studied after serial transfers of individual whiteflies that were viruliferous for both
strains to tomato plants. After single whiteflies had successive acquisition feedings first on a single plant infected with
one strain and then on a plant infected with the other strain, the single whiteflies later transmitted intermittently one,
the other, or both strains to the test plants during serial transfers at 1-day intervals. Because both strains were found
in the head, abdomen, and legs dissected from whiteflies during the retention period after the two successive acquisition
feedings, both strains apparently circulate from midgut cells to salivary glands through the hemolymph. 相似文献
996.
Kuko Fuke Kana Takeshita Nanako Aoki Toshiyuki Fukuhara Mayumi Egusa Motoichiro Kodama Hiromitsu Moriyama 《Journal of General Plant Pathology》2011,77(4):248-252
Strains of the Japanese pear pathotype of Alternaria alternata were screened for double-stranded RNAs (dsRNAs). Four strains had several dsRNAs; strain N18 was associated with several
dsRNAs and had impaired growth phenotypes such as irregular mycelium and abnormal pigmentation. We isolated dsRNA-cured isolates
from strain N18 by single-conidium isolation. The dsRNA-cured isolates had recovered normal growth and pigmentation. Enlarged
vesicles were observed in mycelial cells of the original dsRNA-carrying N18 strain. DAPI nuclear staining revealed regression
of the nuclei in dsRNA-carrying N18 cells. These results indicate that the dsRNAs might have negative effects, such as apoptosis-like
cell death, on the host fungus. 相似文献
997.
Shinpei Banno Hidenari Saito Hiroshi Sakai Toshihiko Urushibara Kentaro Ikeda Takeshi Kabe Isao Kemmochi Makoto Fujimura 《Journal of General Plant Pathology》2011,77(5):282-291
Verticillium longisporum and V. dahliae, causal agents of Verticillium wilt, are spreading through the cabbage fields of Gunma Prefecture. Using the V. longisporum-specific intron within the 18S rDNA and differences between ITS 5.8S rDNA sequences in Japanese isolates of V. longisporum and V. dahliae, we developed three quantitative nested real-time (QNRT) PCR assays. The QNRT-PCR quantification of V. longisporum or V. dahliae in cabbage field soil was consistent with the severity of Verticillium wilt disease in those fields. In field trials of resistant
cultivar YR Ranpo grown for three seasons in soil infested with the pathogen, disease severity and pathogen density in the
soil were significantly reduced in a field moderately contaminated by V. dahliae, but only slightly reduced in a highly contaminated field. These results suggest that continuous cultivation of a resistant
cultivar is an effective way to reduce the pathogen population. QNRT-PCR assays provide a powerful analytical tool to evaluate
the soil population dynamics of V. longisporum and V. dahliae for disease management. 相似文献
998.
Here Fusarium oxysporum was killed in exudates obtained from soil biologically disinfested with ethanol, indicating that physical interaction with
soil microorganisms was not essential. Because acetic acid was confirmed to accumulated during the treatment, we evaluated
the effect of acetic acid amendment against the pathogen in plastic containers. A drop in the soil redox potential seemed
to be correlated with the fungicidal efficacy of acetic acid. Under reductive soil conditions, metal ions such as Mn2+ and Fe2+ formed, and the pathogen was effectively suppressed in Mn2+ and Fe2+ solution. Therefore, Fe2+ and Mn2+ may be the agents that induce suppression of the pathogen during biological soil disinfestation. 相似文献
999.
Background
Safflower (Carthamus tinctorius L.) is a difficult crop to genetically transform being susceptible to hyperhydration and poor in vitro root formation. In addition to traditional uses safflower has recently emerged as a broadacre platform for the production of transgenic products including modified oils and pharmaceutically active proteins. Despite commercial activities based on the genetic modification of safflower, there is no method available in the public domain describing the transformation of safflower that generates transformed T1 progeny.Results
An efficient and reproducible protocol has been developed with a transformation efficiency of 4.8% and 3.1% for S-317 (high oleic acid content) and WT (high linoleic acid content) genotypes respectively. An improved safflower transformation T-DNA vector was developed, including a secreted GFP to allow non-destructive assessment of transgenic shoots. Hyperhydration and necrosis of Agrobacterium-infected cotyledons was effectively controlled by using iota-carrageenan, L-cysteine and ascorbic acid. To overcome poor in vitro root formation for the first time a grafting method was developed for safflower in which ~50% of transgenic shoots develop into mature plants bearing viable transgenic T1 seed. The integration and expression of secreted GFP and hygromycin genes were confirmed by PCR, Southern and Western blot analysis. Southern blot analysis in nine independent lines indicated that 1-7 transgenes were inserted per line and T1 progeny displayed Mendelian inheritance.Conclusions
This protocol demonstrates significant improvements in both the efficiency and ease of use over existing safflower transformation protocols. This is the first complete method of genetic transformation of safflower that generates stably-transformed plants and progeny, allowing this crop to benefit from modern molecular applications.1000.
Antonio Evidente Rossitza Rodeva Anna Andolfi Zornitsa Stoyanova Carmen Perrone Andrea Motta 《European journal of plant pathology / European Foundation for Plant Pathology》2011,130(2):173-182
Recently, a new fungal disease caused by Diaporthe angelicae (anamorph Phomopsis foeniculi) has been found with increasingly frequency on fennel (Foeniculum vulgare) in Bulgaria. Using a bioassay-guided isolation and purification procedure, different metabolites were isolated from the
fungal culture filtrates. They were identified by spectroscopic methods as nectriapyrone, a pentaketide monoterpenoid, and
altersolanols A and J and macrosporin, three octaketides anthracenones. Leaf puncture bioassay was applied on detached tomato
leaves to prove the phytotoxic activity of the fractions and of pure compounds. Nectriapyrone and altersolanols A and J showed
a modulated phytotoxicity, while macrosporin was not toxic. Altersolanol A was the most active compound. 相似文献