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1.
PLoS One ; 14(8): e0221182, 2019.
Article in English | MEDLINE | ID: mdl-31412079

ABSTRACT

The pepper weevil, Anthonomus eugenii, is a major pest on Capsicum species. Apart from natural spread, there is a risk of spread via international pepper trade. In the Netherlands, a pepper weevil outbreak occurred in 2012 and affected six greenhouses producing different sweet pepper varieties. The following year, a pepper weevil outbreak occurred in Italy. To trace the origin of the Dutch outbreak and to establish if the Dutch and Italian outbreaks were linked, we determined the mitogenomes of A. eugenii specimens collected at outbreak locations, and compared these with specimens from the native area, and other areas where the pest was introduced either by natural dispersal or via trade. The circular 17,257 bp A. eugenii mitogenome comprises thirteen mitochondrial genes typically found in insect species. Intra-species variation of these mitochondrial genes revealed four main mitochondrial lineages encompassing 41 haplotypes. The highest diversity was observed for specimens from its presumed native area (i.e. Mexico). The Dutch outbreak specimens represented three highly similar haplotypes, suggesting a single introduction of the pest. The major Dutch haplotype was also found in two specimens from New Jersey. As the Netherlands does not have pepper trade with New Jersey, it is likely that the specimens sampled in New Jersey and those sampled in the Netherlands originate from a shared source that was not included in this study. In addition, our analysis shows that the Italian and Dutch outbreaks were not linked. The mitochondrial genome is a useful tool to trace outbreak populations and the methodology presented in this paper could prove valuable for other invasive pest species, such as the African fruit moth Thaumatotibia leucotreta and emerald ash borer Agrilus planipennis.


Subject(s)
Capsicum/parasitology , Genome, Insect , Genome, Mitochondrial , Haplotypes , Plant Diseases , Weevils/genetics , Animals , Mexico , Netherlands , Plant Diseases/genetics , Plant Diseases/parasitology
2.
Mol Plant Microbe Interact ; 27(1): 30-9, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24006884

ABSTRACT

Aphids are phloem-feeding insects that, like other plant parasites, deliver effectors inside their host to manipulate host responses. The Myzus persicae (green peach aphid) candidate effectors Mp10 and Mp42 were previously found to reduce aphid fecundity upon intracellular transient overexpression in Nicotiana benthamiana. We performed functional analyses of these proteins to investigate whether they activate defenses through similar activities. We employed a range of functional characterization experiments based on intracellular transient overexpression in N. benthamiana to determine the subcellular localization of Mp10 and Mp42 and investigate their role in activating plant defense signaling. Mp10 and Mp42 showed distinct subcellular localization in planta, suggesting that they target different host compartments. Also, Mp10 reduced the levels of Agrobacterium-mediated overexpression of proteins. This reduction was not due to an effect on Agrobacterium viability. Transient overexpression of Mp10 but not Mp42 activated jasmonic acid and salicylic acid signaling pathways and decreased susceptibility to the hemibiotrophic plant pathogen Phytophthora capsici. We found that two candidate effectors from the broad-host-range aphid M. persicae can trigger aphid defenses through different mechanisms. Importantly, we found that some (candidate) effectors such as Mp10 interfere with Agrobacterium-based overexpression assays, an important tool to study effector activity and function.


Subject(s)
Aphids/genetics , Gene Expression Regulation, Plant/genetics , Insect Proteins/genetics , Nicotiana/parasitology , Plant Diseases/parasitology , Plant Immunity , Agrobacterium/physiology , Animals , Aphids/physiology , Genetic Markers/genetics , Host-Parasite Interactions , Insect Proteins/metabolism , Microscopy, Confocal , Plant Diseases/immunology , Plant Leaves/cytology , Plant Leaves/immunology , Plant Leaves/parasitology , Plant Leaves/physiology , Real-Time Polymerase Chain Reaction , Recombinant Fusion Proteins , Nicotiana/cytology , Nicotiana/immunology , Nicotiana/physiology , Transcription, Genetic
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