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opencc-by-4.0May 2021View details →

Figure 8 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella

Figure 8. Levels of IgG (A), sCD4 (B), sCD8 (C), cytokines IFN-γ (D), IL-10 (E), IL-17 (F) and TGF-β1 (G) in chicken sera were measured using ELISA. Chickens of group rEtCHP18905-50 μg and group rEtCHP18905-100 μg were immunized with 50 μg or 100 μg of rEtCHP18905 protein, respectively. Challenged and unchallenged groups were immunized with PBS and served as controls. The IgG titers and the concentrations of sCD4, sCD8, and cytokines are expressed as Min to Max. (*p <0.05, **p <0.01, ***p <0.001; ns, p> 0.05).

Figure 5 in Quantitative phosphoproteomic analysis of chicken DF-1 cells infected with Eimeria tenella, using tandem mass tag (TMT) and parallel reaction monitoring (PRM) mass spectrometry

Figure 5. KEGG pathways of the differentially expressed phosphorylated proteins. The abscissa indicates the first 10 significantly enriched KEGG pathways and the ordinate indicates the significance of enriched KEGG pathways, the more left, the more significant.

Figure 4 in Quantitative phosphoproteomic analysis of chicken DF-1 cells infected with Eimeria tenella, using tandem mass tag (TMT) and parallel reaction monitoring (PRM) mass spectrometry

Figure 4. Gene ontology annotations of the differentially expressed phosphorylated proteins. The abscissa indicates the enriched GO functional classification, including biological process (A), cellular component (B), and molecular function (C). The ordinate indicates the size of the significance of corresponding to each entry, the more left, the more significant.

Figure 3 in Quantitative phosphoproteomic analysis of chicken DF-1 cells infected with Eimeria tenella, using tandem mass tag (TMT) and parallel reaction monitoring (PRM) mass spectrometry

Figure 3. Clustering heatmap of different expression phosphorylated peptides. Each row represents a phosphorylated peptide segment, each column represents a group of samples. The logarithmic value (logarithmic transformation based on 2) of the significantly differentially expressed phosphorylated peptides in different samples is displayed in the clustering heatmap in different colors. Red represents significant upregulation of phosphorylated peptides; blue represents significant down-regulation of phosphorylated peptides.

Figure 2 in Quantitative phosphoproteomic analysis of chicken DF-1 cells infected with Eimeria tenella, using tandem mass tag (TMT) and parallel reaction monitoring (PRM) mass spectrometry

Figure 2. Volcano plots from different group comparisons. The abscissa indicates difference multiple (logarithmic transformation based on 2), the ordinate indicates the significant of difference (logarithmic transformation based on 10). The red point is significantly upregulated phosphorylated peptide segment, the blue point is significantly downregulated phosphorylated peptide segment and the gray point is a phosphorylated peptide segment with no significant difference.

opencc-by-4.0Dec 2021View details →

Рис. 2. Ооцисты кокциΔий роΔа Eimeria, Isospora, Octosporella моΔифицированные, световая микроскопия (размеры увеΛичены в 400 раз, 1 ΔеΛение равно 10 мкм). A — ооцисты Eimeria изоΛированные из Testudo graeca из Апшеронской попуΛяции; B — ооцисты Isospora изоΛированные из Testudo graeca из Апшеронской попуΛяции; С — ооцисты Isospora изоΛированные из Teniadactylus caspius из Апшеронской попуΛяции; D — ооцисты Octosporella изоΛированные из Paralaudakia caucasia из Гобустанской попуΛяции. Автор: С. О. МамеΔова Fig. 2. Eimeria, Isospora, Octosporella oocysts (Magnification 1000 x, each segment corresponds to 10 μm): A — oocysts Eimeria found in Testudo graeca from Absheron population; B — oocysts Isospora found in Testudo graeca from Absheron population; C — oocysts Isospora found in Teniadactylus caspius from Absheron population; D — oocysts Octosporella found in Paralaudakia caucasia from Gobustan population. Author: S. O. Mamedova in Intestinal coccidia (Apicomplexa: Coccidia) in reptiles of Azerbaijan and anthropogenic influences on their prevalence

Рис. 2. Ооцисты кокциΔий роΔа Eimeria, Isospora, Octosporella моΔифицированные, световая микроскопия (размеры увеΛичены в 400 раз, 1 ΔеΛение равно 10 мкм). A — ооцисты Eimeria изоΛированные из Testudo graeca из Апшеронской попуΛяции; B — ооцисты Isospora изоΛированные из Testudo graeca из Апшеронской попуΛяции; С — ооцисты Isospora изоΛированные из Teniadactylus caspius из Апшеронской попуΛяции; D — ооцисты Octosporella изоΛированные из Paralaudakia caucasia из Гобустанской попуΛяции. Автор: С. О. МамеΔова Fig. 2. Eimeria, Isospora, Octosporella oocysts (Magnification 1000 x, each segment corresponds to 10 μm): A — oocysts Eimeria found in Testudo graeca from Absheron population; B — oocysts Isospora found in Testudo graeca from Absheron population; C — oocysts Isospora found in Teniadactylus caspius from Absheron population; D — oocysts Octosporella found in Paralaudakia caucasia from Gobustan population. Author: S. O. Mamedova

opencc-by-4.0Apr 2016View details →

Fig. 1 in Morphological and molecular characterization of Eimeria purpureicephali n. sp. (Apicomplexa:Eimeriidae) in a red-capped parrot (Purpureicephalus spurius, Kuhl, 1820) in Western Australia

Fig. 1. Nomarski interference-contrast photomicrographs of E. purpureicephali n. sp. oocysts showing spheroidal to subspheroidal sporocysts (scale bar = 20 Mm) (1—5) and line drawing of the sporulated oocyst of E. purpureicephali n. sp. Scale bar = 20 Mm (6).

Fig. 6 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 6. Histopathologic sections of ceca which were obtained from dead chicks infected with Eimeria spp. Arrowhead indicates macrogametocytes with a prominent wall-forming body (A), and arrows indicate zygotes or early oocysts, which are surrounded by an oocyst wall (A and B). Pathological lesions could not be observed because of severe degradation after death. Scale bars indicate 20 μm.

Fig. 3 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 3. Phylogram of E. uekii, type B, other Eimeria spp., and related parasites (Cyclospora spp.) inferred by the neighbor-joining method using partial 18S rRNA gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Cystoisospora spp. are used as an outgroup taxon.

Fig. 4 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 4. Phylogram of E. uekii, type B, and other related Eimeria spp. inferred by the neighbor-joining method using partial mitochondrial cytochrome c oxidase subunit I gene sequences. Accession numbers and derived hosts are shown in parentheses. Scale bar represents substitutions per nucleotide, and bootstrap values are indicated (> 1000). Toxoplasma gondii is used as an outgroup taxon.

Fig. 2 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 2. Eimeria oocysts detected in the feces of Japanese rock ptarmigans. (A) E. uekii and (B) type B. Scale bars indicate 10 μm.

Fig. 1 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 1. Location of three sampled areas in Japan, Mt. Tateyama (36̊35′N, 137̊36′E), Norikuradake (36̊6′N, 137̊33′E), and Kitadake (35̊40′N, 138̊14′E) (triangle boxes 1–3).

Fig. 5 in Molecular identification of two Eimeria species, E. uekii and E. raichoi as type B, in wild Japanese rock ptarmigans, Lagopus muta japonica

Fig. 5. Composite line drawing of oocyst of Eimeria raichoi n. sp (previously referred as type B). Scale bars indicate 10 μm.

Fig. 3. Seasonal detection rate for E. uekii, type B in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 3. Seasonal detection rate for E. uekii, type B, and mixed Eimeria spp. oocyst infection in both adults and chicks in 2006 and 2007. Numbers in parentheses below months indicate the total number of fecal samples analyzed. Data for the number of chicks (23 in 2006 and 11 in 2007) were only available for August.

Fig. 1 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 1. Seasonal prevalence of Eimeria spp. infection in Japanese rock ptarmigans from April to November in 2006 and 2007. (a) and (b) show the prevalence of infection in adult birds and chicks, respectively. Numbers above bars indicate the total number of fecal samples analyzed.

Fig. 2 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 2. Photomicrograph of eimerian oocysts detected in the feces of Japanese rock ptarmigans; (a) E. uekii and (b) type B. The scale bar indicates 20 μm.

Fig. 6 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 6. Average monthly environmental temperatures on the windward and leeward slopes of Mt. Tateyama from 2006 to 2007. The temperatures on the windward slopes were not measured in April. The table below the graph shows monthly maximum and minimum temperatures.

Fig. 5 in Surveillance of Eimeria species in wild Japanese rock ptarmigans, Lagopus muta japonica, and insight into parasitic seasonal life cycle at timberline regions of the Japanese Alps

Fig. 5. Sporulation rate for Eimeria spp. (mainly E. uekii) after incubation at different temperatures for 48 h. Dark bars indicate sporulation rates of> 85% after incubation for 24 h.

opencc-by-4.0Dec 2013View details →

Figs 1–6 in Eimeria spp. (Apicomplexa: Eimeriidae) in Black Caiman Melanosuchus niger (Crocodilia: Alligatoridae) from the Amazon Region, Brazil, with a Description of Two New Coccidian Species

Figs 1–6. Nomarski interference micrographs of sporulated coccidia oocysts found in black caimans faeces × 1,000. 1–2 – Eimeria nigeri n. sp.; 3–4 – Eimeria portovelhensis n. sp.; 5–6 – Eimeria paraguayensis. FIL – filament from the area of the Stieda body, OR – oocyst residuum, OW – oocyst wall, RB – refractile body, SB – Stieda body, SR – sporocyst residuum.