1.Hematology, cytochemistry and ultrastructure of blood cells in fishing cat (Felis viverrina).
Kreangsak PRIHIRUNKIT ; Chaleow SALAKIJ ; Suntaree APIBAL ; Nual Anong NARKKONG
Journal of Veterinary Science 2007;8(2):163-168
Hematological, cytochemical and ultrastructural features of blood cells in fishing cat (Felis viverrina) were evaluated using complete blood cell counts with routine and cytochemical blood stains, and scanning and transmission electron microscopy. No statistically significant difference was found in different genders of this animal. Unique features of blood cells in this animal were identified in hematological, cytochemical and ultrastructural studies. This study contributes to broaden hematological resources in wildlife animals and provides a guideline for identification of blood cells in the fishing cat.
Animals
;
Animals, Zoo
;
Blood Cells/*cytology/ultrastructure
;
Felis/*blood
;
Female
;
Histocytochemistry/veterinary
;
Male
;
Microscopy, Electron, Scanning/veterinary
;
Microscopy, Electron, Transmission/veterinary
;
Thailand
2.Heterosporis anguillarum infections in farm cultured eels (Anguilla japonica) in Korea.
Seong Joon JOH ; Yong Kuk KWON ; Min Chul KIM ; Min Jeong KIM ; Hyuk Man KWON ; Jung Won PARK ; Jun Hun KWON ; Jae Hong KIM
Journal of Veterinary Science 2007;8(2):147-149
Ten eels (Anguilla japonica) from a fish farm in Korea were examined and diagnosed with a Heterosporis infection. The gross lesions on the trunk were uneven and the concave parts were pasty. Histopathologically, lyses of the trunk muscles, degenerative muscle fibers and the scattered spores were observed. The sporophorocyst (SPC) contained several spores with a variety of shapes. Some SPC were disrupted and the spores in the SPC were scattered in the muscle tissues. Macrophages existed near the scattered spores. Electron microscopy revealed special structures such as sporophorocyst containing various developmental parasitic stages such as meronts, sporonts, sporophorous vesicles and spores.
*Anguilla
;
Animals
;
Aquaculture
;
Fish Diseases/*parasitology/pathology
;
Histocytochemistry/veterinary
;
Korea
;
Microscopy, Electron, Scanning Transmission/veterinary
;
Microsporidia/*growth & development/ultrastructure
;
Microsporidiosis/parasitology/pathology/*veterinary
;
Muscular Diseases/parasitology/pathology/*veterinary
3.Expression of E-cadherin in pig kidney.
Su Youn LEE ; Sun M HAN ; Ji Eun KIM ; Ku Yong CHUNG ; Ki Hwan HAN
Journal of Veterinary Science 2013;14(4):381-386
E-cadherin is a cell adhesion molecule that plays an important role in maintaining renal epithelial polarity and integrity. The purpose of this study was to determine the exact cellular localization of E-cadherin in pig kidney. Kidney tissues from pigs were processed for light and electron microscopy immunocytochemistry, and immunoblot analysis. E-cadhedrin bands of the same size were detected by immunoblot of samples from rat and pig kidneys. In pig kidney, strong E-cadherin expression was observed in the basolateral plasma membrane of the tubular epithelial cells. E-cadherin immunolabeling was not detected in glomeruli or blood vessels of pig kidney. Double-labeling results demonstrated that E-cadherin was expressed in the calbindin D28k-positive distal convoluted tubule and H(+)-ATPase-positive collecting duct, but not in the aquaporin 1-positive, N-cadherin-positive proximal tubule. In contrast to rat, E-cadherin immunoreactivity was not expressed at detectable levels in the Tamm-Horsfall protein-positive thick ascending limb of pig kidney. Immunoelectron microscopy confirmed that E-cadherin was localized in both the lateral membranes and basal infoldings of the collecting duct. These results suggest that E-cadherin may be a critical adhesion molecule in the distal convoluted tubule and collecting duct cells of pig kidney.
Animals
;
Blotting, Western/veterinary
;
Cadherins/*genetics/metabolism
;
Cell Membrane/*metabolism/ultrastructure
;
*Gene Expression Regulation
;
Kidney/*metabolism
;
Male
;
Microscopy, Electron, Transmission/veterinary
;
Sus scrofa/*genetics/metabolism
4.Transmission electron microscopy for characterization of acrosomal damage after Percoll gradient centrifugation of cryopreserved bovine spermatozoa.
Leticia Z OLIVEIRA ; Vera F M HOSSEPIAN DE LIMA ; Marcelo A LEVENHAGEN ; Ricarda M DOS SANTOS ; Terezinha I ASSUMPCAO ; Jose O JACOMINI ; Andre F C DE ANDRADE ; Rubens P DE ARRUDA ; Marcelo E BELETTI
Journal of Veterinary Science 2011;12(3):267-272
The objective of this study was to characterize acrosomal ultrastructure following discontinuous Percoll gradient centrifugation of cryopreserved bovine sperm. Semen was collected from six bulls of different breeds and three ejaculates per bull were evaluated. Frozen semen samples were thawed and the acrosomal region of sperm cells was evaluated by transmission electron microscopy (TEM) before (n = 18) and after (n = 18) Percoll centrifugation. The evaluation of 20 sperm heads from each of the 36 samples analyzed ensured that a large number of cells were investigated. The data were subjected to analysis of variance at a level of significance of 5%. Percoll centrifugation reduced the percentage of sperm exhibiting normal acrosomes (from 61.77 to 30.24%), reduced the percentage of sperm presenting atypical acrosome reactions (from 28.38 to 4.84%) and increased the percentage of sperm exhibiting damage in the acrosome (from 6.14 to 64.26%). The percentage of sperm with typical acrosome reactions was not significantly different before (3.70%) and after (0.67%) centrifugation. TEM distinguished four different types of acrosomal status and enabled ultrastructural characterization of acrosomal injuries. The percentage of sperm exhibiting normal acrosomes decreased and damage in the acrosome was the most frequent acrosomal injury with the Percoll gradient centrifugation protocol utilized.
Acrosome/*pathology/ultrastructure
;
Animals
;
Cattle/*physiology
;
Cell Membrane/*pathology/ultrastructure
;
Cell Separation/veterinary
;
Centrifugation, Density Gradient/veterinary
;
Cryopreservation/veterinary
;
Male
;
Microscopy, Electron, Transmission/veterinary
;
Povidone/*adverse effects
;
Silicon Dioxide/*adverse effects
;
Spermatozoa/pathology/ultrastructure
5.Immunolocalization of anion exchanger 1 (Band 3) in the renal collecting duct of the common marmoset.
Ji Hyun SONG ; Yong Hwan KIM ; Tae Cheon KANG ; Moo Ho WON ; Jun Gyo SUH ; Byung Hwa HYUN ; Yang Seok OH ; Si Yun RYU ; Ju Young JUNG
Journal of Veterinary Science 2007;8(4):329-333
The purpose of this study was to determine the expression and distribution of band 3 in the collecting duct and connecting tubules of the kidney of the marmoset monkey (Callithrix jacchus), and to establish whether band 3 is expressed in type A intercalated cells. The intracellular localization of band 3 in the different populations of intercalated cells was determined by double-labeling immunohistochemistry. Immunohistochemical microscopy demonstrated that band 3 is located in the basolateral plasma membranes of all type A intercalated cells in the connecting tubule (CNT), cortical collecting duct (CCD), and outer medullary collecting duct (OMCD) of the marmoset. However, type B intercalated cells and non-A/ non-B intercalated cells did not show band 3 labeling. Electron microscopy of the CNT, CCD and OMCD confirmed the light microscopic observation of the basolateral plasma membrane staining for band 3 in a subpopulation of interacted cells. Basolateral staining was seen on the plasma membrane and small coated vesicles in the perinuclear structure, some of which were located in the Golgi region. In addition, there was no labeling of band 3 in the mitochondria of the CNT, CCD and in OMCD cells. The intensity of the immunostaining of the basolateral membrane was less in the CNT than in the CCD and OMCD. In contrast, band 3 immunoreactivity was greater in the intracellular vesicles of the CNT. From these results, we suggest that the basolateral Cl-/HCO3- exchanger in the monkey kidney is in a more active state in the collecting duct than in the CNT.
Animals
;
Anion Exchange Protein 1, Erythrocyte/*metabolism
;
Callithrix/*metabolism
;
Gene Expression Profiling/veterinary
;
*Gene Expression Regulation
;
Immunohistochemistry/veterinary
;
Kidney Tubules/cytology/physiology/ultrastructure
;
Kidney Tubules, Collecting/cytology/*metabolism/ultrastructure
;
Male
;
Microscopy, Electron, Transmission/veterinary
6.Preliminary study on apoptosis of DEF cells induced by new type gosling viral enteritis virus (NGVEV) infection.
Shun CHEN ; An-Chun CHENG ; Ming-Shu WANG ; Yi ZHOU
Chinese Journal of Virology 2008;24(5):396-400
The characteristics changes of apoptosis of Duck Embryo Fibroblasts (DEF) cells induced by New type gosling viral enteritis virus, NGVEV) were observed by means of HE staining, electron microscopy and Annexin V-FITC/PI fluorescent staining. During 24-48 h post infection (pi), the difference of morphological change between infected DEF cells and the mock infected cells was invisible. At 72 h pi, the nuclear chromatin was getting condensed through HE staining; apoptotic morphological change such as abnormal shape of the nucleus, condensation of the cytoplasm and chromatin were observed under electron microscope; and the early apoptotic cells (Annexin V-FITC positive and PI negative) were detected under fluorescence microscope. At 96-120 h pi, by means of HE staining and electron microscopy, the advanced morphological change of apoptosis such as formation of different kinds of apoptotic bodies, and shrink of the DEF cells and nucleus were detected; under fluorescence microscope the different stages of the apoptotic DEF can be easily distinguished: early apoptotic cells (Annexin V-FITC postive and pi negative), advanced or late apoptotic cells (both Annexin V-FITC and PI positive), necrosis cells or dead cells (Annexin V-FITC negative and PI positive). This investigation shows that NGVEV might induce apoptosis and form characteristic apoptotic morphological changes in the DEF cells. NGVEV inducement of apoptosis may be an important mechanism of efficient dissemination of virus progeny.
Adenoviridae
;
physiology
;
Animals
;
Annexin A5
;
analysis
;
Apoptosis
;
Ducks
;
embryology
;
Enteritis
;
veterinary
;
virology
;
Fibroblasts
;
cytology
;
virology
;
Geese
;
virology
;
Microscopy, Electron, Transmission
;
Poultry Diseases
;
virology
7.Pathology of non-thermal irreversible electroporation (N-TIRE)-induced ablation of the canine brain.
John H ROSSMEISL ; Paulo A GARCIA ; John L ROBERSTON ; Thomas L ELLIS ; Rafael V DAVALOS
Journal of Veterinary Science 2013;14(4):433-440
This study describes the neuropathologic features of normal canine brain ablated with non-thermal irreversible electroporation (N-TIRE). The parietal cerebral cortices of four dogs were treated with N-TIRE using a dose-escalation protocol with an additional dog receiving sham treatment. Animals were allowed to recover following N-TIRE ablation and the effects of treatment were monitored with clinical and magnetic resonance imaging examinations. Brains were subjected to histopathologic and ultrastructural assessment along with Bcl-2, caspase-3, and caspase-9 immunohistochemical staining following sacrifice 72 h post-treatment. Adverse clinical effects of N-TIRE were only observed in the dog treated at the upper energy tier. MRI and neuropathologic examinations indicated that N-TIRE ablation resulted in focal regions of severe cytoarchitectural and blood-brain-barrier disruption. Lesion size correlated to the intensity of the applied electrical field. N-TIRE-induced lesions were characterized by parenchymal necrosis and hemorrhage; however, large blood vessels were preserved. A transition zone containing parenchymal edema, perivascular inflammatory cuffs, and reactive gliosis was interspersed between the necrotic focus and normal neuropil. Apoptotic labeling indices were not different between the N-TIRE-treated and control brains. This study identified N-TIRE pulse parameters that can be used to safely create circumscribed foci of brain necrosis while selectively preserving major vascular structures.
Animals
;
Brain/metabolism/*pathology/surgery/ultrastructure
;
Caspase 3/metabolism
;
Caspase 9/metabolism
;
Dogs
;
Electroporation/veterinary
;
Magnetic Resonance Imaging/methods
;
Microscopy, Electron, Transmission
;
Necrosis/metabolism/pathology
;
Neurosurgical Procedures/*adverse effects
8.Comparison of characteristics of SVCV strains isolated in China and in Europe.
Long-ying GAO ; Hong LIU ; Xiu-jie SHI ; Jun-qiang HE ; Yu-lin JIANG
Chinese Journal of Virology 2009;25(1):47-51
In the nationwide epidemiological investigation, SVCV-741 was for the first time isolated in Beijing region, China in 2003, and designated as SVCV Asian strain. In this paper, we compared SVCV-741 (Asian strains isolated in China) with SVCV-10/3 (Europe reference strain) on their physico-chemical, biological and morphological characteristics. The results indicated that there were no distinct differences between two SVCV strains on phycico-chemical and morphological characteristics. The main existing differences were: (1) The stability of SVCV-741 to temperature in cell culture was higher than that of SVCV-10/3, which might have some evolutionary and biological implication of SVCV; (2) No SVC outbreak ever occurred caused by SVCV-741;Furthermore we found that both SVCV-741 and SVCV-10/3 grew faster and produced higher virus titer in CO cells than other cell lines. It indicated that CO cell lines might be useful tool for SVCV research.
Animals
;
Carps
;
virology
;
Cell Line
;
China
;
Europe
;
Fish Diseases
;
virology
;
Fishes
;
Microscopy, Electron, Transmission
;
Reverse Transcriptase Polymerase Chain Reaction
;
Rhabdoviridae Infections
;
veterinary
;
virology
;
Vesiculovirus
;
genetics
;
growth & development
;
isolation & purification
;
ultrastructure
9.Clinical use of a ceramide-based moisturizer for treating dogs with atopic dermatitis.
Ji Young JUNG ; Eui Hwa NAM ; Seol Hee PARK ; Seung Hee HAN ; Cheol Yong HWANG
Journal of Veterinary Science 2013;14(2):199-205
In humans, skin barrier dysfunction is thought to be responsible for enhanced penetration of allergens. Similar to conditions seen in humans, canine atopic dermatitis (CAD) is characterized by derangement of corneocytes and disorganization of intercellular lipids in the stratum corenum (SC) with decreased ceramide levels. This study was designed to evaluate the effects of a moisturizer containing ceramide on dogs with CAD. Dogs (n = 20, 3~8 years old) with mild to moderate clinical signs were recruited and applied a moisturizer containing ceramide for 4 weeks. Transepidermal water loss (TEWL), skin hydration, pruritus index for canine atopic dermatitis (PICAD) scores, and canine atopic dermatitis extent and severity index (CADESI) scores of all dogs were evaluated. Skin samples from five dogs were also examined with transmission electron microscopy (TEM) using ruthenium tetroxide. TEWL, PICAD, and CADESI values decreased (p < 0.05) and skin hydration increased dramatically over time (p < 0.05). Electron micrographs showed that the skin barrier of all five dogs was partially restored (p < 0.05). In conclusion, these results demonstrated that moisturizer containing ceramide was effective for treating skin barrier dysfunction and CAD symptoms.
Animals
;
Ceramides/*therapeutic use
;
Cholesterol/*therapeutic use
;
Dermatitis, Atopic/complications/drug therapy/physiopathology/*veterinary
;
Dog Diseases/*drug therapy/etiology/physiopathology
;
Dogs
;
Emollients/*therapeutic use
;
Epidermis/drug effects/physiopathology/ultrastructure
;
Fatty Acids, Nonesterified/*therapeutic use
;
Female
;
Male
;
Microscopy, Electron, Transmission/veterinary
;
Pruritus/drug therapy/etiology/physiopathology/veterinary
;
Republic of Korea
;
Ruthenium Compounds/chemistry
;
Water Loss, Insensible/drug effects
10.Apoptosis induced in vivo by new type gosling viral enteritis virus.
Shun CHEN ; Anchun CHENG ; Mingshu WANG ; Dekang ZHU ; Renyong JIA ; Qihui LUO ; Hengmin CUI ; Yi ZHOU ; Yin WANG ; Zhiwen XU ; Zhengli CHEN ; Xiaoyue CHEN ; Xiaoyu WANG
Journal of Veterinary Science 2011;12(4):333-339
In this study, apoptosis was induced by new type gosling viral enteritis virus (NGVEV) in experimentally infected goslings is reported in detail for the first time. After 3-day-old goslings were orally inoculated with a NGVEV-CN strain suspension, the time course of NGVEV effects on apoptotic morphological changes of the internal tissues was evaluated. These changes were observed by histological analysis with light microscopy and ultrastructural analysis with transmission electron microscopy. DNA fragmentation was assessed with a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay and DNA ladder analysis. A series of characteristic apoptotic morphological changes including chromatin condensation and margination, cytoplasmic shrinkage, plasma membrane blebbing, and formation of apoptotic bodies were noted. Apoptosis was readily observed in the lymphoid and gastrointestinal organs, and sporadically occurred in other organs after 3 days post-infection (PI). The presence and quantity of TUNEL-positive cells increased with infection time until 9 days PI. DNA extracted from the NGVEV-infected gosling cells displayed characteristic 180~200 bp ladders. Apoptotic cells were ubiquitously distributed, especially among lymphocytes, macrophages, monocytes, and epithelial and intestinal cells. Necrosis was subsequently detected during the late NGVEV-infection phase, which was characterized by cell swelling, plasma membrane collapse, and rapidly lysis. Our results suggested that apoptosis may play an important role in the pathogenesis of NGVE disease.
*Adenoviridae/classification/pathogenicity
;
Adenoviridae Infections/pathology/*veterinary/virology
;
Animals
;
*Anseriformes
;
*Apoptosis
;
Bird Diseases/*virology
;
DNA Fragmentation
;
Enteritis/*veterinary/virology
;
Epithelial Cells/cytology/virology
;
In Situ Nick-End Labeling
;
Intestines/cytology/virology
;
Leukocytes/cytology/virology
;
Lymphoid Tissue/cytology/virology
;
Macrophages
;
Microscopy, Electron, Transmission