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31 results for “Coccidia”
Figure 5 in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 5. Bayesian phylogenetic relationships of fish-infecting Goussia and Choleoeimeria spp. based on partial 18S rDNA. Selected sequences represent different morphology types (epicellular, leucisci, dispersed, and nodular) defined by Rosenthal et al. (2016). Hammondia hammondi was used as an outgroup. Posterior probability is indicated at branch sites. Accession numbers follow species names in parentheses.
Figure 4 in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 4. Light micrographs of coccidia of Goussia bayae n. sp. in hepatic bile ducts of white perch, Morone americana. (A) Developing stages of coccidia epicellular to biliary epithelium. (B) Microgamont (Mi), macrogamont (Ma), and meront (Me) along epithelium. (C) Longitudinal view of bile duct with developing coccidia along epithelium (arrow) and sporulating oocysts (O) in lumen. (D). Cross-section of enlarged bile duct with numerous developing and mature coccidia.
Figure 7 in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 7. Bayesian phylogenetic relationships of mitochondrial genes cytochrome oxidase 1 (COI) and cytochrome oxidase b (Cytb). Babesia microti was used as the outgroup. Accession numbers follow species names in parentheses.
Figure 1 in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 1. Photomicrographs of oocysts of Goussia bayae n. sp. from the gallbladder of white perch, Morone americana. (A) Nomarski differential interference contrast image of mature oocysts with micropyle (m) and refractile bodies (arrow) in sporocysts. (B) Histological preparation of oocysts with sporocysts containing paired sporozoites with densely stained nuclei (arrow).
Figure 3 in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 3. Light micrographs of coccidia of Goussia bayae n. sp. in the gallbladder of white perch, Morone americana. (A) Severe coccidiosis in gallbladder. Note that numerous oocysts were removed with the bile for differential interference contrast microscopy before histological processing. (B) Developing stages of coccidia along epithelium (arrow) and sporulating oocysts in the lumen. (C) Microgamont (Mi), macrogamont (Ma), and meront (Me) epicellular to biliary epithelium, with oocysts (O) in the lumen.
Figure 4 in An ultrastructural study on the merogonic stages of Goussia senegalensis (Faye, 1988) Diouf and Toguebaye, 1993 (Apicomplexa, Coccidia) from the liver of Pagellus bellottii (Pisces, Teleostei)*
Figure 4. Enclosure of merozoites (Mz) by endomerogony. The limiting membranes (Lm) elongate to surround each nucleus (N) and a part of the cytoplasm. Many invaginations (I) can be seen, some of them forming the pellicle (boxed area). HcN = host cell nucleus, and Pv = parasitophorous vacuole. Scale: 2 µm.
Figure 5 in An ultrastructural study on the merogonic stages of Goussia senegalensis (Faye, 1988) Diouf and Toguebaye, 1993 (Apicomplexa, Coccidia) from the liver of Pagellus bellottii (Pisces, Teleostei)*
Figure 5. Detail of formation of the pellicle (Pe) shown in the boxed area of Figure 4. A double membrane forms around the new merozoites (Mz). The inner membrane (Im) is from the limiting membrane (Lm) of the merozoite by invagination (I), and the outer membrane (Om) is from the inner membrane of the meront. N = nucleus, Pv = parasitophorous vacuole. Scale: 2 µm.
Figure 6 in An ultrastructural study on the merogonic stages of Goussia senegalensis (Faye, 1988) Diouf and Toguebaye, 1993 (Apicomplexa, Coccidia) from the liver of Pagellus bellottii (Pisces, Teleostei)*
Figure 6. Endodyogeny: meront dividing into 2 merozoites (Mz). The pellicle (Pe) begins forming by invagination (I). Cr = cytoplasm residuum, HcN = host cell nucleus, Mi = mitochondrion, N = nucleus. Scale: 2.8 µm.
Fig. 2 in Detection and quantification of house mouse Eimeria at the species level - Challenges and solutions for the assessment of coccidia in wildlife
Fig. 2. Phylogenetic trees based on 18S rRNA and COI sequences. Sequences of 18S A) and COI B) were used to infer the molecular identification of wild-derived isolates of Eimeria. In both phylogenies, our isolates clustered in three groups one close to E. falciformis (red), other close to E. ferrisi (green) and finally one to E. vermiformis (yellow). Numbers in the branches represent the Bayesian posterior probability and the non-parametric bootstrap value. In bold are indicate the reference sequences for each species. CE and IL make reference to sequence derived from cecum or ileum tissue DNA, respectively. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Figure 2. Goussia bayae n in Newly Described Coccidia Goussia Bayae From White Perch Morone Americana: Morphology And Phylogenetics Support Emerging Taxonomy Of Goussia Within Piscine Hosts
Figure 2. Goussia bayae n. sp. Line drawing of a sporulated oocyst.
Immunoenhancing effects of Montanide adjuvant on recombinant coccidia antigen vaccination against Eimeria spp. and comparative microarray analysis of intestinal lymphocytes
GEO Series GSE40743. Gallus gallus. 8 samples. Type: Expression profiling by array.
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