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  • 1
    Online Resource
    Online Resource
    Wiley ; 2008
    In:  Molecular Plant Pathology Vol. 9, No. 4 ( 2008-07), p. 403-423
    In: Molecular Plant Pathology, Wiley, Vol. 9, No. 4 ( 2008-07), p. 403-423
    Abstract: Taxonomy:   Superkingdom Prokaryota; Kingdom Monera; Domain Bacteria; Phylum Firmicutes (low‐G+C, Gram‐positive eubacteria); Class Mollicutes; Candidatus (Ca.) genus Phytoplasma. Host range:   Ca. Phytoplasma comprises approximately 30 distinct clades based on 16S rRNA gene sequence analyses of ~200 phytoplasmas. Phytoplasmas are mostly dependent on insect transmission for their spread and survival. The phytoplasma life cycle involves replication in insects and plants. They infect the insect but are phloem‐limited in plants. Members of Ca. Phytoplasma asteris (16SrI group phytoplasmas) are found in 80 monocot and dicot plant species in most parts of the world. Experimentally, they can be transmitted by approximately 30, frequently polyphagous insect species, to 200 diverse plant species. Disease symptoms:   In plants, phytoplasmas induce symptoms that suggest interference with plant development. Typical symptoms include: witches’ broom (clustering of branches) of developing tissues; phyllody (retrograde metamorphosis of the floral organs to the condition of leaves); virescence (green coloration of non‐green flower parts); bolting (growth of elongated stalks); formation of bunchy fibrous secondary roots; reddening of leaves and stems; generalized yellowing, decline and stunting of plants; and phloem necrosis. Phytoplasmas can be pathogenic to some insect hosts, but generally do not negatively affect the fitness of their major insect vector(s). In fact, phytoplasmas can increase fecundity and survival of insect vectors, and may influence flight behaviour and plant host preference of their insect hosts. Disease control:   The most common practices are the spraying of various insecticides to control insect vectors, and removal of symptomatic plants. Phytoplasma‐resistant cultivars are not available for the vast majority of affected crops.
    Type of Medium: Online Resource
    ISSN: 1464-6722 , 1364-3703
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2008
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    SSG: 12
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  • 2
    In: The Plant Journal, Wiley, Vol. 50, No. 1 ( 2007-04), p. 149-158
    Abstract: The receptor importin‐α mediates the nuclear import of functionally diverse cargo proteins that contain arginine/lysine‐rich nuclear localization signals (NLSs). Functional homologs of importin‐α have been characterized in a wide range of species including yeast, human and plants. However, the differential cargo selectivity of plant importin‐α homologs has not been established. To advance nuclear import studies conducted in plant cells, we have developed a method that allows importin‐α‐dependent nuclear import to be assayed in Nicotiana benthamiana. We employed virus‐induced gene silencing (VIGS) to knock down the expression of two importin‐α homologs, NbImp α 1 and NbImp α 2 , which we identified from N. benthamiana. Agro‐infiltration was then used to transiently express the NLS‐containing proteins Arabidopsis thaliana fibrillarin 1 (AtFib1) and the Nuk6, Nuk7 and Nuk12 candidate effector proteins of the oomycete plant pathogen Phytophthora infestans . In this manner, we demonstrate importin‐α‐dependent nuclear import of Nuk6 and Nuk7 . In contrast, the nuclear import of Nuk12 and AtFib1 was unaffected in cells of NbImp α ‐ silenced plants . These data suggest that P. infestans Nuk6 and Nuk7 proteins are dependent on one or more α‐importins for nuclear import. Our VIGS‐based assay represents a powerful new technique to study mechanisms underlying the transport of proteins from cytoplasm to nucleus in plants.
    Type of Medium: Online Resource
    ISSN: 0960-7412 , 1365-313X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2007
    detail.hit.zdb_id: 2020961-7
    SSG: 12
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  • 3
    In: Molecular Microbiology, Wiley, Vol. 77, No. 6 ( 2010-09), p. 1406-1415
    Type of Medium: Online Resource
    ISSN: 0950-382X
    Language: English
    Publisher: Wiley
    Publication Date: 2010
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  • 4
    In: Molecular Ecology Resources, Wiley, Vol. 21, No. 1 ( 2021-01), p. 316-326
    Abstract: Woolly apple aphid (WAA, Eriosoma lanigerum Hausmann) (Hemiptera: Aphididae) is a major pest of apple trees ( Malus domestica , order Rosales) and is critical to the economics of the apple industry in most parts of the world. Here, we generated a chromosome‐level genome assembly of WAA—representing the first genome sequence from the aphid subfamily Eriosomatinae—using a combination of 10X Genomics linked‐reads and in vivo Hi‐C data. The final genome assembly is 327 Mb, with 91% of the assembled sequences anchored into six chromosomes. The contig and scaffold N50 values are 158 kb and 71 Mb, respectively, and we predicted a total of 28,186 protein‐coding genes. The assembly is highly complete, including 97% of conserved arthropod single‐copy orthologues based on Benchmarking Universal Single‐Copy Orthologs ( busco ) analysis. Phylogenomic analysis of WAA and nine previously published aphid genomes, spanning four aphid tribes and three subfamilies, reveals that the tribe Eriosomatini (represented by WAA) is recovered as a sister group to Aphidini + Macrosiphini (subfamily Aphidinae). We identified syntenic blocks of genes between our WAA assembly and the genomes of other aphid species and find that two WAA chromosomes (El5 and El6) map to the conserved Macrosiphini and Aphidini X chromosome. Our high‐quality WAA genome assembly and annotation provides a valuable resource for research in a broad range of areas such as comparative and population genomics, insect–plant interactions and pest resistance management.
    Type of Medium: Online Resource
    ISSN: 1755-098X , 1755-0998
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2406833-0
    SSG: 12
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  • 5
    In: Molecular Ecology, Wiley, Vol. 28, No. 18 ( 2019-09), p. 4228-4241
    Abstract: Aphids present an ideal system to study epigenetics as they can produce diverse, but genetically identical, morphs in response to environmental stimuli. Here, using whole genome bisulphite sequencing and transcriptome sequencing of the green peach aphid ( Myzus persicae ), we present the first detailed analysis of cytosine methylation in an aphid and investigate differences in the methylation and transcriptional landscapes of male and asexual female morphs. We found that methylation primarily occurs in a CG dinucleotide (CpG) context and that exons are highly enriched for methylated CpGs, particularly at the 3′ end of genes. Methylation is positively associated with gene expression, and methylated genes are more stably expressed than unmethylated genes. Male and asexual female morphs have distinct methylation profiles. Strikingly, these profiles are divergent between the sex chromosome and the autosomes; autosomal genes are hypomethylated in males compared to asexual females, whereas genes belonging to the sex chromosome, which is haploid in males, are hypermethylated. Overall, we found correlated changes in methylation and gene expression between males and asexual females, and this correlation was particularly strong for genes located on the sex chromosome. Our results suggest that differential methylation of sex‐biased genes plays a role in aphid sexual differentiation.
    Type of Medium: Online Resource
    ISSN: 0962-1083 , 1365-294X
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2019
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    detail.hit.zdb_id: 1126687-9
    SSG: 12
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  • 6
    In: New Phytologist, Wiley, Vol. 202, No. 3 ( 2014-05), p. 838-848
    Abstract: Phytoplasmas are insect‐transmitted bacterial phytopathogens that secrete virulence effectors and induce changes in the architecture and defense response of their plant hosts. We previously demonstrated that the small (± 10 kDa) virulence effector SAP 11 of A ster Y ellows phytoplasma strain W itches' B room ( AY ‐ WB ) binds and destabilizes Arabidopsis CIN ( CINCINNATA ) TCP ( TEOSINTE ‐ BRANCHED , CYCLOIDEA , PROLIFERATION FACTOR 1 AND 2) transcription factors, resulting in dramatic changes in leaf morphogenesis and increased susceptibility to phytoplasma insect vectors. SAP 11 contains a bipartite nuclear localization signal ( NLS ) that targets this effector to plant cell nuclei. To further understand how SAP 11 functions, we assessed the involvement of SAP 11 regions in TCP binding and destabilization using a series of mutants. SAP 11 mutants lacking the entire N ‐terminal domain, including the NLS , interacted with TCP s but did not destabilize them. SAP 11 mutants lacking the C ‐terminal domain were impaired in both binding and destabilization of TCP s. These SAP 11 mutants did not alter leaf morphogenesis. A SAP 11 mutant that did not accumulate in plant nuclei ( SAP 11Δ NLS ‐ NES ) was able to bind and destabilize TCP transcription factors, but instigated weaker changes in leaf morphogenesis than wild‐type SAP 11. Overall the results suggest that phytoplasma effector SAP 11 has a modular organization in which at least three domains are required for efficient CIN ‐ TCP destabilization in plants.
    Type of Medium: Online Resource
    ISSN: 0028-646X , 1469-8137
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 208885-X
    detail.hit.zdb_id: 1472194-6
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  • 7
    In: New Phytologist, Wiley, Vol. 198, No. 4 ( 2013-06), p. 1178-1190
    Abstract: Small RNA s play important roles in resistance to plant viruses and the complex responses against pathogens and leaf‐chewing insects. We investigated whether small RNA pathways are involved in A rabidopsis resistance against a phloem‐feeding insect, the green peach aphid ( M yzus persicae ). We used a 2‐wk fecundity assay to assess aphid performance on A rabidopsis RNA silencing and defence pathway mutants. Quantitative real‐time polymerase chain reaction was used to monitor the transcriptional activity of defence‐related genes in plants of varying aphid susceptibility. High‐performance liquid chromatography‐mass spectrometry was employed to measure the accumulation of the antimicrobial compound camalexin. Artificial diet assays allowed the assessment of the effect of camalexin on aphid performance. M yzus persicae produces significantly less progeny on A rabidopsis micro RNA (mi RNA ) pathway mutants. Plants unable to process mi RNA s respond to aphid infestation with increased induction of PHYTOALEXIN DEFICIENT3 ( PAD 3 ) and production of camalexin. Aphids ingest camalexin when feeding on A rabidopsis and are more successful on pad3 and cyp79b2 / cyp79b3 mutants defective in camalexin production. Aphids produce less progeny on artificial diets containing camalexin. Our data indicate that camalexin functions beyond antimicrobial defence to also include hemipteran insects. This work also highlights the extensive role of the mi RNA ‐mediated regulation of secondary metabolic defence pathways with relevance to resistance against a hemipteran pest.
    Type of Medium: Online Resource
    ISSN: 0028-646X , 1469-8137
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2013
    detail.hit.zdb_id: 208885-X
    detail.hit.zdb_id: 1472194-6
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