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53 results for “Rhipicephalus”
Figure 1. A in The Caspian red deer, Cervus elaphus maral (Mammalia: Cervidae): a new host record for Rhipicephalus (Boophilus) annulatus (Acari: Ixodidae) in northern Iran
Figure 1. A combined phylogenetic tree constructed using Bayesian Inference method based on ITS2/16S rRNA sequence data of Rhipicephalus (Boophilus) species in this study with sequences originated from various part of world retrieved from GenBank database. The main R. (B.) annulatus clade separated by a vertical double headed line. The taxa were defined with a name of species, country, GenBank accession number (taxon of the present study is bold). Posterior probability values inserted in the place of nodes. Branch lengths are proportional to the evolutionary changes. Rhipicephalus sanguineus assigned as outgroup taxon.
Fig. 1 in Identification and characterization of Rhipicephalus (Boophilus) microplus candidate protective antigens for the control of cattle tick infestations
Fig. 1 Antibody response in vaccinated cattle. Bovine serum antibody titers to recombinant antigens were determined by ELISA in cattle vaccinated with ubiquitin, subolesin, Bm86, and adjuvant/ saline control. Antibody titers in immunized cattle were expressed as the OD450 nm value for the highest serum dilution (1:1,000) and compared between vaccinated and control cattle using an ANOVA test (*P<0.05). The time of vaccination shots (arrows) and tick infestation are indicated
Fig. 1 in The Rhipicephalus appendiculatus tick vector of Theileria parva is absent from cape buffalo (Syncerus caffer) populations and associated ecosystems in northern Uganda
Fig. 1 Map showing the sampling sites. The three national parks are indicated with red dots and the cattle sampling sites adjacent to the parks depicted as green dots
Fig. 2 Infected R in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 2 Infected R. appendiculatus adult ticks feeding on a silicone membrane. a A representation of adult ticks attached to a silicone membrane. b Detection of tick salivary gland infected with T. parva via p104 PCR. Amplicons were visualized in 2% agarose gel
Fig. 5 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 5 Determination of the minimum dose of T. parva sporozoites from the in vitro tick feeding system sufficient to infect bovine lymphocytes in vitro. Lymphocytes were probed with anti-PIM monoclonal antibody. a Unstimulated and ConA-stimulated negative controls. b Flow cytometric detection of infected lymphocytes exposed to tenfold serial dilutions of T. parva sporozoites isolated from the in vitro tick feeding system
Fig. 4 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 4 Demonstration of infectivity of secreted T. parva sporozoites collected from the in vitro tick feeding system. a Flow cytometric detection of cultured T. parva-infected lymphocytes. b Immunocytochemistry demonstrating T. parva schizont formation in bovine lymphocytes. Lymphocytes were probed with monoclonal antibodies: left panel, isotype control; right panel, anti-PIM. Red indicates antibody-specific reactivity to T. parva within bovine lymphocytes. Scale bar: 20 µm
Fig. 3 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 3 Immunohistochemical detection of T. parva salivary gland acinus colonization in adult ticks. Tick sections were probed with monoclonal antibodies: a anti-PIM; b anti-p67; c isotype control. Red indicates antibody-specific reactivity to T. parva colonies. Scale bar: 50 µm
Fig. 1 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 1 Infection of R. appendiculatus via acquisition feeding on a T. parva-infected calf. a Calf was infected via subcutaneous inoculation with T. parva salivary gland stabilate. The calf developed severe fever beginning 10 days post-infection. Red arrow indicates nymphal tick application and green arrows indicate collection of replete nymphs. b Detection of T. parva via p104 PCR. Amplicons were visualized in 2% agarose gel
Figure 2 in Histological structures of the midguts of adult Rhipicephalus bursa and Rhipicephalus turanicus ticks (Acari: Ixodidae)
Figure 2. Histology of the digestive tract of the midgut of Rhipicephalus bursa. Í: muscle layer, R: caecae, Ḩ: stem (generative) cell, gdc: granular digestive cell, ddc: densely granulated digestive cell. X400, H&E.
Figure 1 in Histological structures of the midguts of adult Rhipicephalus bursa and Rhipicephalus turanicus ticks (Acari: Ixodidae)
Figure 1. Histology of the digestive tract of the midgut of Rhipicephalus turanicus. Í: muscle layer, R: caecae, Ḩ: stem (generative) cell, gdc: granular digestive cell, ddc: densely granulated digestive cell, hc: host cell, mt: Malpighian tube. X400, H&E.
Figure 6 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 6. The biogeographic analysis of the Rhipicephalus sanguineus complex with S-DIVA and BBM analysis based on mt 12S rDN.
Figure 3 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 3. Phylogenetic tree of sequences obtained by mt 12S rDNA from this study and sequences of GenBank. Haplotypes obtained from this study are indicated with TRY codes and highlighted in bold.
Figure 4 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 4. Phylogenetic tree of sequences obtained by ITS2 from this study and sequences of GenBank. Haplotypes obtained from this study are indicated with TRY codes and highlighted in bold. Different haplotypes of the same individual are labeled as TRY-1 and TRY-2 on the phylogenetic tree.
Figure 2 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 2. Phylogenetic tree of sequences obtained by mt 16S rDNA from this study and sequences of GenBank. Haplotypes obtained from this study are indicated with TRY codes and highlighted in bold.
Figure 5 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 5. The biogeographic analysis of the Rhipicephalus sanguineus complex with S-DIVA and BBM analysis based on mt 16S rDNA.
Figure 1 in An update on the phylogeny and biogeographical history of Rhipicephalus sanguineus complex
Figure 1. Map of collecting sites. (The map was generated using QGIS 3.22.2 software.)
Data from: Prevalence of and potential risk factors for multiple resistance to acaricides in <em>Rhipicephalus (Boophilus) microplus</em> ticks: A survey in the state of Rio Grande do Sul, Brazil
Open the record for dataset details and reuse information.
Data from: Geographic distribution of the invasive cattle tick Rhipicephalus microplus, a country-wide survey in Benin
The cattle tick Rhipicephalus microplus is currently invading the West African region, and little information is available on the spread of this exotic tick in this region. We set out a country-wide field survey to determine its current distribution in Benin. Ticks were collected on cattle from 106 farms selected by random sampling covering all regions of the country. Rhipicephalus annulatus was found on 70 % of all farms, R. decoloratus on 42 %, R. geigyi on 58 %, and R. microplus on 49 %. There is a clear geographic separation between the indigenous Rhipicephalus species and R. microplus. Rhipicephalus annulatus occurs mainly in the northern departments, but it was also observed in lower numbers in locations in the south. The presence of R. decoloratus is limited to the northern region, and in most locations, this tick makes up a small proportion of the collected ticks. The tick R. geigyi tends to be dominant, but occurs only in the four northern departments. The observations concerning R. microplus are entirely different, this species occurs in the southern and central region. The results of this survey confirm the invasive character and displacement properties of R. microplus, since in less than a decade it has colonized more than half of the country and has displaced indigenous ticks of the same genus in many of the sampled locations.
Supplementary material 12 from: Paez-Triana L, Herrera G, Vega L, Garcia-Corredor D, Pulido Medellín MO, Paniz-Mondolfi A, Muñoz M, Ramírez JD (2023) Metagenomic exploration of endosymbionts and pathogens in the tropical lineage of Rhipicephalus sanguineus sensu lato (s.l.) ticks in Colombia. Metabarcoding and Metagenomics 7: e109085. https://doi.org/10.3897/mbmg.7.109085
p-values obtained between departments and sexes within each department using the Wilcoxon test on the relative abundances of pathogens and endosymbionts
Supplementary material 3 from: Paez-Triana L, Herrera G, Vega L, Garcia-Corredor D, Pulido Medellín MO, Paniz-Mondolfi A, Muñoz M, Ramírez JD (2023) Metagenomic exploration of endosymbionts and pathogens in the tropical lineage of Rhipicephalus sanguineus sensu lato (s.l.) ticks in Colombia. Metabarcoding and Metagenomics 7: e109085. https://doi.org/10.3897/mbmg.7.109085
Significant differences in the relative abundances of assigned reads in Bacteria and Archaea between departments and sexes of the various genera found in the samples
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