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20 results for “Haemaphysalis longicornis”
Fig. 6 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 6 Phenotype associated with dynein, kinesin, isocitrate dehydrogenase and citrate synthase mRNA subjected to RNAi in female ticks via injection with the corresponding dsRNA. a Dynein dsRNA injection. b Kinesin dsRNA injection. c Isocitrate dehydrogenase dsRNA injection. d Citrate synthase dsRNA injection. e GFP dsRNA injection, control. f No injection, control. Scale-bars: 5 mm
Fig. 7 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 7 Digital micrographs of salivary gland acinar morphological changes in unfed female H. longicornis after RNAi.The time at which the tick bit the host and began sucking blood was recorded as day 0. a–e Dynein dsRNA injection. f–j Kinesin dsRNA injection. k–o Isocitrate dehydrogenase dsRNA injection. p–t Citrate synthase dsRNA injection. u–y GFP dsRNA injection, control. Scale-bars: 25 µm
Fig. 4 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 4 KEGG pathway enrichment analysis of the differentially expressed proteins in 5 different Clusters. Terms with a P-value <0.05 were used to draw the column diagrams. a–e KEGG pathway enrichment for the proteins in Cluster 1 to Cluster 5
Fig. 3 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 3 GO functional annotations for all the differentially expressed proteins. a–c GO annotations of differentially expressed proteins in the salivary glands of partially fed ticks compared with unfed ticks (115:114). d–f GO annotations of differentially expressed proteins in the salivary glands of mated semi-engorged ticks compared with partially fed ticks (116:115). g–i GO annotations of differentially expressed proteins in the salivary glands of engorged ticks compared with mated semi-engorged ticks (117:116). Abbreviations: BP, biological process; CC, cellular component; MF, molecular function; CO, cellular component organization or biogenesis
Fig. 5 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 5 RT-qPCR analyzed the mRNA expression levels of dynein, kinesin, isocitrate dehydrogenase, and citrate synthase during the four feeding stages of salivary gland development
Fig. 2 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 2 Statistics and cluster analysis for the identified proteins and their expression levels in the salivary glands of female H. longicornis. a Venn diagram showing the number of proteins (with CV <20%) identified in the three experiments. b Venn diagram showing the number of proteins with quantitative information. c Cluster analysis according to trends in protein expression in the salivary glands of female ticks
Fig. 1 in Salivary gland proteome analysis of developing adult female HaemaphYSaliS longiCorniS ticks: molecular motor and TCA cycle-related proteins play an important role throughout development
Fig. 1 Workflow for quantitative proteomics analysis of changes in protein expression in the salivary glands of female H. longicornis during the blood-feeding process
Environmental variables serve as predictors of the exotic and invasive Asian longhorned tick (Haemaphysalis longicornis Neumann): an approach for targeted tick surveillance
<p>Since the 2017 discovery of established populations of the Asian longhorned tick, (<em>Haemaphysalis longicornis </em>Neumann) in the United States, populations continue to be detected in new areas. For this exotic and invasive species, capable of transmitting a diverse repertoire of pathogens and blood-feeding on a variety of host species, there remains a lack of targeted information on how to best prepare for this tick and understand when and where it occurs. To fill this gap, we conducted two years of weekly tick surveillance at four farms in Tennessee (three <em>H. longicornis</em>-infested and one without) to identify environmental factors associated with each questing life stage, to investigate predictors of abundance, and to determine the likelihood of not collecting ticks at different life stages. A total of 46,770 ticks were collected, of which 12,607 <em>H. longicornis</em> and five other tick species were identified. Overall, abundance of <em>H. longicornis </em>was associated with spring and summer seasons, forested environments, relative humidity and barometric pressure, sunny conditions, and in relation with other tick species. The likelihood of not collecting <em>H. longicornis</em> was associated with day length and barometric pressure. Additional associations for different life stages were also identified and included other tick species, climatic variables, and environmental conditions. Here, we demonstrated that environmental variables can be useful to predict the presence of questing <em>H. longicornis</em> and provide ideas on how to use this information to develop a surveillance plan for different southeastern areas with and without infestations.</p>
Environmental variables serve as predictors of the exotic and invasive Asian longhorned tick (Haemaphysalis longicornis Neumann): an approach for targeted tick surveillance
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Detection and response to <em>Haemaphysalis longicornis</em> and <em>Theileria orientalis</em> Ikeda on a cow-calf farm in Tennessee (USA)
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Figure 2 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 2 SEM photos of male H.longicornis from a colony started with specimens from Jeju-teukbyeoljachido, Republic of Korea. (Accession # RML48803) a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 4 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 4 SEM photos of larval H.longicornis from a colony started with specimens from Queensland, Australia (Accession # RML58949). a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 3 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 3 SEM photos of nymphal H.longicornis from a colony started with specimens from Jeju-teukbyeoljachido, Republic of Korea (Accession # RML48803). a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
Figure 1 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 1 SEM photos of female H.longicornis from a colony started with specimens from Jeju-teukbyeoljachido, Republic of Korea (Accession # RML48803) a dorsal full body b dorsal capitulum c ventral full body d ventral capitulum.
A microRNA profile of saliva and role of miR-375 in Haemaphysalis longicornis (Ixodida: Ixodidae)
GEO Series GSE123407. Haemaphysalis longicornis. 1 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Transcriptome profile of Haemaphysalis longicornis (Acari: Ixodidae) exposed to C. citratus essential oil and citronellal
GEO Series GSE176275. Haemaphysalis longicornis. 21 samples. Type: Expression profiling by high throughput sequencing.
Figure 5 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 5 Pictorial key to adults of Haemaphysalis spp. occurring in North America.
Figure 7 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 7 Pictorial key to larvae of Haemaphysalis spp. occurring in North America.
Figure 6 from: Egizi AM, Robbins RG, Beati L, Nava S, Evans CR, Occi JL, Fonseca DM (2019) A pictorial key to differentiate the recently detected exotic Haemaphysalis longicornis Neumann, 1901 (Acari, Ixodidae) from native congeners in North America. ZooKeys 818: 117-128. https://doi.org/10.3897/zookeys.818.30448
Figure 6 Pictorial key to nymphs of Haemaphysalis spp. occurring in North America.
Induction and suppression of Haemaphysalis longicornis ticks antiviral RNA interference responses by arthropod-borne RNA viruses (RNA-Seq)
GEO Series GSE165139. Haemaphysalis longicornis. 9 samples. Type: Expression profiling by high throughput sequencing.
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