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14 results for “Sarcoptes scabiei”
Fig. 2. 3 in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 2. 3-Dimensional models of A) S. scabiei mite survival from laboratory data (Arlian et al., 1984a), and B) the estimated mite survival from GAM fit to the laboratory data (R2 = 0.834).
Fig. 5. A in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 5. A) Estimated mite survival within burrows across the eastern (low mange prevalence) and western (high mange prevalence) survey areas. B) The relationship between estimated mite survival and the elevation of burrows from the eastern and western areas.
Fig. 4 in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 4. Relationship of burrow A) length, B) depth, C) elevation, and D) field trip number, to estimated mite survival time within burrow.
Fig. 3 in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 3. Temporal profiles of A) air temperature, B) relative humidity, and C) estimated mite survival within wombat burrows and outside at the burrow entrances. D) Average estimated mite survival time at burrow entrances and within burrows (n = 33).
Fig. 6 in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 6. Seasonal variation in estimated mite survival within wombat burrows. Note: in winter, the burrows were sampled with a different method (data loggers) compared to the spring and summer (robotic vehicle, the WomBot).
Fig. 1 in Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei
Fig. 1. Location of study area at Musselroe Wind Farm, Cape Portland. Map of DPIPWE spotlight survey transect routes, red: west transect, blue: east transect. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Infestation, histology, and molecular confirmation of Sarcoptes scabiei in an Andean porcupine (Coendou quichua) from the Central Andes of Colombia
Fig. 1. Coendou quichua with macroscopic lesions corresponding to hyperkeratosis and alopecia, which extend ventrally from the chest to the inguinal region and base of the tail, hyperkeratosis is also observed in the mandible and the fore and hind limbs up to the carpal and tarsal joints (A, B). Histopathological microphotographs of mangy skin of C. quichua, with the presence of tunnels with (black arrow heads) and without (white arrow heads) mites (Sarcoptes scabiei) in the stratum corneum (C) and skin with predominance of hyperkeratosis (hyp) and acanthosis (ac) (D). Light micrographs of: S. scabiei eggs (E). Dorsal view of a female with the presence of robust dorsal setae (ds), numerous and conspicuous triangular cuticular spines (cs) on its dorsal surface (F). Ventral view of a female with the presence of the legs short, with legs I and II bear a stalked empodium (e) that terminate in a broad pad, and the two hind pairs of legs (III and IV) terminate in long setae or bristles (s) (G). Ventral view of a male with the legs I, II and III bear a stalked empodium (e) that terminate in a broad pad and the last pair (IV) of legs terminate in long setae (s) (H). ch (chelicerae), p (pedipalps).
Fig. 2 in Infestation, histology, and molecular confirmation of Sarcoptes scabiei in an Andean porcupine (Coendou quichua) from the Central Andes of Colombia
Fig. 2. Histological microphotographs of the development of the mite S. scabiei in the skin of the porcupine C. quichua. Permanent burrows dug by fertilized adult females, with the presence of a developing egg and the shell of another hatched egg (A, B). Burrows with the presence of three eggshells (sh) and feces (fe), where between two and three eggs are laid daily (C). Developing eggs within burrows in the stratum corneum of the skin, which hatch approximately 3–4 days after oviposition (D–F). Developing larvae in the superficial layer of the skin (G, H). Nymph burrowing just below the skin surface to moult into an adult in 3–4 days (I). Side-axial view of an adult female specimen of S. scabiei in a tunnel in the superficial epidermis. The mites have a short and broad gnathosoma (gn), globose idiosoma, short and conical legs I and II, with a delicate chitinous coating (le). Structures associated with the female reproductive system, spermatheca (sp), ovarian nutrient cell (ONC) located inside the ovary (ov), vitellogenic oocyte (oc) in the oviduct (ovd), as well as chorional gland (chg) close to oviporus (op) are visible (J).
Fig. 3 in Infestation, histology, and molecular confirmation of Sarcoptes scabiei in an Andean porcupine (Coendou quichua) from the Central Andes of Colombia
Fig. 3. Wild mammals with sarcoptic mange (S. scabiei) in South America.
Supplementary materials from: Histone deacetylase 2 and 3 of Sarcoptes scabiei: Characterization of a potential drug target
Open the record for dataset details and reuse information.
Data from: The cascading pathogenic consequences of Sarcoptes scabiei infection that manifest in host disease
Open the record for dataset details and reuse information.
Transcriptome analysis of the host immune responses to Sarcoptes scabiei
GEO Series GSE178563. Homo sapiens. 8 samples. Type: Expression profiling by high throughput sequencing.
Sarcoptes scabiei Mites Modulate Gene Expression In Human Skin Equivalents
GEO Series GSE48459. Homo sapiens. 14 samples. Type: Expression profiling by array.
PCR (Polymerase Chain Reaction) Assay for Diagnosis of Sarcoptes Scabiei
ClinicalTrials.gov study NCT02254564. IPD Sharing: NO. Countries: 1. Publications: 0.
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