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38 results for “Helicoverpa armigera.”
Virome of Helicoverpa armigera, Tuta absoluta, Nezara viridula
<p>Virome of Helicoverpa armigera, Tuta absoluta, Nezara viridula</p>
CRISPR/Cas9 mediated knockout of ABCC1 confers resistance to Bacillus thuringiensis toxin Cry2Ab in Helicoverpa armigera
<p>This data contains the Bt and insecticide bioassay results of ABCC1 knockout and wild-type strain of <em>Helicoverpa armigera</em>. Bioassay results revealed that the HaABCC1-KO strain exhibited >60-fold resistance to Cry2Ab toxin compared with the susceptible XJ strain, while no resistance has been recorded for Cry1Ab, Cry1Ac and Vip3A. Furthermore, the inheritance of <em>H. armigera</em> resistance to Cry2Ab was autosomal and completely recessive, significantly associated with the 4-nt deletion mutation of ABCC1 in the HaABCC1-KO strain. The relative growth of HaABCC1-KO and XJ strain also confirmed the role of <em>HaABCC1 </em>on the toxicity of Cry2Ab.</p>
Data from: High nucleotide diversity and limited linkage disequilibrium in Helicoverpa armigera facilitates the detection of a selective sweep
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Data from: Oxidative stress delays development and alters gene expression in the agricultural pest moth, Helicoverpa armigera
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Data from: Invasion origin, rapid population expansion, and the lack of genetic structure of cotton bollworm (Helicoverpa armigera) in the Americas
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Data from: Assessing the role of non-cotton refuges in delaying Helicoverpa armigera resistance to Bt cotton in West Africa
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Data from: Population structure and gene flow in the global pest, Helicoverpa armigera
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Identification and expression profiling of Helicoverpa armigera microRNAs and their possible role in the regulation of digestive protease genes
GEO Series GSE61503. Helicoverpa armigera. 12 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Genome scale analysis of host-virus mRNA differential expression in Helicoverpa zea insect cells infected by H. armigera baculovirus from early till late infection
GEO Series GSE44184. Helicoverpa zea; Helicoverpa armigera. 8 samples. Type: Expression profiling by array.
Transcriptional responses underlying the hormetic and detrimental effects of gossypol on Helicoverpa armigera
GEO Series GSE33080. Helicoverpa armigera. 32 samples. Type: Expression profiling by array.
Transcriptional analysis of physiological pathways in a generalist herbivore: responses to different host plants and plant structures by the cotton bollworm (CBW) Helicoverpa armigera [CottonStructure
GEO Series GSE34344. Helicoverpa armigera. 40 samples. Type: Expression profiling by array.
Transcriptional analysis of physiological pathways in a generalist herbivore: responses to different host plants and plant structures by the cotton bollworm (CBW) Helicoverpa armigera [DifferentHost]
GEO Series GSE34346. Helicoverpa armigera. 48 samples. Type: Expression profiling by array.
Helicoverpa armigera gene expression on gossypol suppelemented diet, larval gut and rest of body
GEO Series GSE77619. Helicoverpa armigera. 24 samples. Type: Expression profiling by array.
Transcriptional analysis of physiological pathways in a generalist herbivore: responses to different host plants and plant structures by the cotton bollworm (CBW) Helicoverpa armigera
GEO Series GSE34349. Helicoverpa armigera. 72 samples. Type: Expression profiling by array.
Histone deacetylase 3: A potential target fight against Helicoverpa armigera
GEO Series GSE215090. Helicoverpa armigera. 6 samples. Type: Expression profiling by high throughput sequencing.
Dynamic transcriptome analysis and volatile profiling of Gossypium hirsutum in response to the cotton bollworm Helicoverpa armigera
GEO Series GSE62158. Gossypium arboreum; Gossypium barbadense; Gossypium hirsutum; Gossypium raimondii. 24 samples. Type: Expression profiling by array.
A Real-time PCR assay for rapid identification of Helicoverpa armigera (Lepidoptera: Noctuidae) from closely related species
<p>The bollworm, <em>Helicoverpa armigera</em> is one of the most important agricultural pests in the world. Diagnosis of this species morphologically is difficult from the similar species <em>H. assulta</em>, <em>H. punctigera and H. zea </em>as the adults are identified based on genitalia morphology and larval identification is limited due to shared morphological characters. To provide an accurate diagnosis of New Zealand border interceptions we have developed and validated a real-time PCR assay to identify <em>H. armigera </em>from commonly occurring exotic <em>Helicoverpa</em> species, <em>H. assulta</em> and <em>H. zea</em>. The newly designed primers and probe were optimised, and the assay demonstrated its specificity to <em>H. armigera</em> with no false positives observed in the non-target species tested in this study. The specificity of the assay was tested against 64 samples of Lepidoptera from 14 countries including 48 <em>Helicoverpa </em>samples. The sensitivity of the assay showed it can detect up to 1 copy /µL of the DNA fragment. Therefore, this assay can be used for rapid detection of <em>H. armigera</em>, which is imperative in quarantine application to determine the presence of exotic species regardless of its life stage.</p>
Helicoverpa armigera flights record during the research period in the region of Beja
<p>Record of the flights of Helicoverpa armigera males by pheromone monitoring in the region of Beja.</p>
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