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
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Animals, Zoo
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Blood Cells/*cytology/ultrastructure
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Felis/*blood
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Female
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Histocytochemistry/veterinary
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Male
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Microscopy, Electron, Scanning/veterinary
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Microscopy, Electron, Transmission/veterinary
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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
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Animals
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Aquaculture
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Fish Diseases/*parasitology/pathology
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Histocytochemistry/veterinary
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Korea
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Microscopy, Electron, Scanning Transmission/veterinary
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Microsporidia/*growth & development/ultrastructure
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Microsporidiosis/parasitology/pathology/*veterinary
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Muscular Diseases/parasitology/pathology/*veterinary
3.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
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Animals
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Cattle/*physiology
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Cell Membrane/*pathology/ultrastructure
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Cell Separation/veterinary
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Centrifugation, Density Gradient/veterinary
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Cryopreservation/veterinary
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Male
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Microscopy, Electron, Transmission/veterinary
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Povidone/*adverse effects
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Silicon Dioxide/*adverse effects
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Spermatozoa/pathology/ultrastructure
4.Eggshell apex abnormalities associated with Mycoplasma synoviae infection in layers.
Eun Ok JEON ; Jong Nyeo KIM ; Hae Rim LEE ; Bon Sang KOO ; Kyeong Cheol MIN ; Moo Sung HAN ; Seung Baek LEE ; Yeon Ji BAE ; Jong Suk MO ; Sun Hyung CHO ; Chang Hee LEE ; In Pil MO
Journal of Veterinary Science 2014;15(4):579-582
Eggs exhibiting eggshell apex abnormalities (EAA) were evaluated for changes in shell characteristics such as strength, thickness, and ultrastructure. Mycoplasma synoviae (MS) infection was confirmed by serological assay along with isolation of MS from the trachea and oviduct. Changes in eggshell quality were shown to be statistically significant (p < 0.01). We also identified ultrastructural changes in the mammillary knob layer by Scanning Electron Microscopy. While eggs may seem to be structurally sound, ultrastructural evaluation showed that affected eggs do not regain their former quality. In our knowledge, this is the first report describing the occurrence of EAA in Korea.
Animals
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Chickens
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Egg Shell/microbiology/*ultrastructure
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Microscopy, Electron, Scanning/veterinary
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Mycoplasma Infections/microbiology/*veterinary
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Mycoplasma synoviae/*physiology
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Poultry Diseases/*microbiology
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Republic of Korea
5.Larval Gnathostoma hispidum detected in the red banded odd-tooth snake, Dinodon rufozonatum rufozonatum, from China.
Shin Hyeong CHO ; Tong Soo KIM ; Yoon KONG ; Byoung Kuk NA ; Woon Mok SOHN
The Korean Journal of Parasitology 2007;45(3):191-198
A total of 205 larval gnathostomes were collected from 18 (22.5%) of 80 red banded odd-tooth snakes, Dinodon rufozonatum rufozonatum, which had been smuggled from China and confiscated at Customs in Busan, Republic of Korea. In order to identify the species, some of the larvae were observed by a light microscope and a scanning electron microscope (SEM). The larvae were 2.18 x 0.29 mm in average size, and had a pair of lips at the anterior end, a muscular esophagus, 2 pairs of cervical sacs, and brownish intestines. The head bulb was characteristically equipped with 4 rows of hooklets; the average number of hooklets in each respective row was 38.6, 40.5, 41.5, and 43.7. In SEM views, the mouth evidenced a pair of lateral lips of equal size in a half-moon shape. Each lip featured a couple of labial papillae and a small amphid located between the 2 papillae. The hooklets on the head bulb had single-pointed, posteriorly-curved tips. The cuticular spines were larger and more densely distributed on the anterior part of the body, and decreased gradually in size and number toward the posterior body. On the basis of these morphological characteristics, the larvae were identified as the third stage larvae of Gnathostoma hispidum.
Animals
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China
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Colubridae/*parasitology
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Gnathostoma/*isolation & purification/pathogenicity/*ultrastructure
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Larva/ultrastructure
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Microscopy, Electron, Scanning/veterinary
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Muscles/parasitology
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Species Specificity
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Spirurida Infections/parasitology/*veterinary
6.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
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Blotting, Western/veterinary
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Cadherins/*genetics/metabolism
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Cell Membrane/*metabolism/ultrastructure
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*Gene Expression Regulation
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Kidney/*metabolism
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Male
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Microscopy, Electron, Transmission/veterinary
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Sus scrofa/*genetics/metabolism
7.Site adaptations of Acanthogyrus (Acanthosentis) tilapiae: Observations through light and scanning electron microscopy.
Mahmoud E BAYOUMY ; Osman K ABD EL-HADY ; Hussein AM OSMAN
Journal of Veterinary Science 2006;7(4):339-342
Acanthogyrus (Acanthosentis) tilapiae parasites were collected from the intestines of 300 fish belonging to three tilapia species sourced at the River Nile, Giza, Egypt. The proboscis of the parasite was characterized by three rows of hooks that curved towards the posterior of the body. The first row is supported by unmodified hooks. The parasite tegument has a series of alternative folds and a large number of pores. Sensory ganglia are located on the surface of the proboscis and body. Acanthogyrus (Acanthosentis) tilapiae provokes an aggressive host response indicated by hyperplasia of the intestinal goblet cells and focal eosinophil infiltrations. This acanthocephalan parasite shows a highly modified adaptation to its site of host infection.
Acanthocephala/*anatomy & histology/*physiology/ultrastructure
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Adaptation, Physiological
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Animals
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*Cichlids
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Egypt
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Female
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Fish Diseases/*parasitology
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Histocytochemistry/veterinary
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Intestines/parasitology
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Male
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Microscopy, Electron, Scanning/veterinary
8.Inherited canine copper toxicosis in Australian Bedlington Terriers.
Changbaig HYUN ; Lucio John FILIPPICH
Journal of Veterinary Science 2004;5(1):19-28
Inherited copper toxicosis in Bedlington Terriers (CTBT) is a copper associated hepatopathy caused by an autosomal recessive genetic defect of gene involving copper metabolism. To compare clinical and histopathological findings with previous reports and to expand our knowledge for future genetic studies, 18 terriers were clinically and histopathologically examined in this study. Pedigree information and dietary history were obtained from the owners before a thorough clinical examination was undertaken. Following the examination, a blood sample was collected for haematology, biochemistry and genetic analysis and a urine sample for urinalysis. Seven dogs were also liver biopsied for histopathology, histochemistry and electron microscopy. In this study, plasma alanine transaminase (ALT) activity was highly concordant with DNA marker test results and was the most reliable and sensitive biochemical test measured. Also clinical and biochemical copper toxicosisaffected states were noticed in a genotyped carrier dog. Histopathological and electron microscopy findings showed that the severity of the lesion was more closely correlated to the presence of clinical signs than to hepatic copper concentration. In addition, the involvement of apoptosis and p53 gene was observed in electron microscopy. The general findings related to CT-BT in this study was similar to those previously reported except few differences in histopathology and electron microscopy.
Alanine Transaminase/blood
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Animals
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Biopsy/veterinary
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Blood Chemical Analysis/veterinary
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Copper/*metabolism
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Dog Diseases/*genetics/*metabolism
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Dogs
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Female
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Histocytochemistry/veterinary
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Leukocyte Count/veterinary
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Liver/metabolism/pathology/ultrastructure
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Male
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Metal Metabolism, Inborn Errors/*genetics/metabolism/pathology/*veterinary
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Microscopy, Electron/veterinary
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Urinalysis/veterinary
9.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
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Anion Exchange Protein 1, Erythrocyte/*metabolism
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Callithrix/*metabolism
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Gene Expression Profiling/veterinary
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*Gene Expression Regulation
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Immunohistochemistry/veterinary
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Kidney Tubules/cytology/physiology/ultrastructure
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Kidney Tubules, Collecting/cytology/*metabolism/ultrastructure
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Male
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Microscopy, Electron, Transmission/veterinary
10.Morphology and histology of the adult Paramphistomum gracile Fischoeder, 1901.
Busaba PANYARACHUN ; Arin NGAMNIYOM ; Prasert SOBHON ; Panat ANURACPREEDA
Journal of Veterinary Science 2013;14(4):425-432
In the present study, we evaluated the histological morphology of the adult Paramphistomum (P.) gracile. Adult flukes with bodies 5~15 mm in length and 2~7 mm in width were subjected to histological analysis. Longitudinal and transversal serial-sections were stained with hematoxylin and eosin, and examined. The body surface and longitudinal section of P. gracile were also assessed using scanning electron microscopy. In this species, the anterior sucker and posterior sucker (acetabulum) were present on an anterior and posterior part of the body, respectively. The major folds were located in the areas of the anterior sucker, genital canal, and posterior sucker. The fluke membrane was spineless at the tegument surface and in the tegument tissue. Histological data showed structural-systematic characteristics of the digestive tract, reproductive tract, excretory tract, copulatory organs, connective tissues, and muscle tissues. We attempted to elucidate the histological characteristics of P. gracile that might increase the knowledge and understanding of rumen fluke morphology.
Animals
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Cattle
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Cattle Diseases/*parasitology/pathology
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Female
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Male
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Microscopy, Electron, Scanning/veterinary
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Rumen/parasitology
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Stomach Diseases/parasitology/pathology/*veterinary
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Thailand
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Trematoda/*anatomy & histology/isolation & purification/ultrastructure
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Trematode Infections/parasitology/pathology/*veterinary