Effects of anti-arthritis preparations on gene expression and enzyme activity of cyclooxygenase-2 in cultured equine chondrocytes     

Tung JT  Venta PJ  Eberhart SW  Yuzbasiyan-Gurkan V  Alexander L  Caron JP 《American journal of veterinary research》2002,63(8):1134-1139

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Antibody-induced internalization of viral glycoproteins in pseudorabies virus-infected monocytes and role of the cytoskeleton: a confocal study     

Van de Walle GR  Favoreel HW  Nauwynck HJ  Van Oostveldt P  Pensaert MB 《Veterinary microbiology》2002,86(1-2):51-57

Addition of pseudorabies virus (PrV)-specific polyclonal immunoglobulins to PrV-infected monocytes induces internalization of plasma membrane anchored viral glycoproteins. This process may interfere with antibody-dependent cell lysis and resembles the well-studied physiological endocytosis process. A confocal study was designed to investigate whether the major cellular components, involved in physiological endocytosis (clathrin, actin, dynein and microtubules), play a role in this virological internalization process. In order to visualize the interaction of endosomes, which contain the internalized viral glycoproteins, with clathrin, actin, dynein and microtubules, a double labeling of viral glycoproteins and different cellular proteins was performed. Porcine monocytes were inoculated with the PrV-strain 89V87 at a multiplicity of infection of 50 for 13h. After the addition of FITC-labeled porcine polyclonal PrV-specific antibodies, cells were fixed with para-formaldehyde at different time points and afterwards permeabilized. The different cellular components were visualized with monoclonal antibodies and a Texas Red-conjugate, with the exception of actin, which was stained with phalloidin-Texas Red. The cells were analyzed by confocal microscopy. A clear co-localization was observed between the viral glycoproteins and clathrin and dynein during the internalization process. The microtubules were in close contact with the internalized vesicles. For actin no co-localization could be observed. It can be stated that clathrin, dynein and microtubules, important components during physiological endocytosis, are also of importance during the antibody-induced internalization of viral glycoproteins.  相似文献   

Genetic characterization of 2 novel feline caliciviruses isolated from cats with idiopathic lower urinary tract disease     

Rice CC  Kruger JM  Venta PJ  Vilnis A  Maas KA  Dulin JA  Maes RK 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》2002,16(3):293-302

Feline caliciviruses (FCVs) are potential etiologic agents in feline idiopathic lower urinary tract disease (I-LUTD). By means of a modified virus isolation method, we examined urine obtained from 28 male and female cats with nonobstructive I-LUTD, 12 male cats with obstructive I-LUTD, and 18 clinically healthy male and female cats. All cats had been routinely vaccinated for FCV. Two FCVs were isolated; I (FCV-U1) from a female cat with nonobstructive I-LUTD, and another (FCV-U2) from a male cat with obstructive I-LUTD. To determine the genetic relationship of FCV-U1 and FCV-U2 to other FCVs. capsid protein gene RNA was reverse transcribed into cDNA, amplified, and sequenced. Multiple amino acid sequence alignments and phylogenetic trees were constructed for the entire capsid protein, hypervariable region E, and the more conserved (nonhypervariable) regions A, B, D, and F. When compared to 23 other FCV isolates with known biotypes, the overall amino acid sequence identity of the capsid protein of FCV-U1 and FCV-U2 ranged from 83 to 96%; identity of hypervariable regions C and E ranged from 58 to 85%. Phylogenetically, FCV-U1 clearly separated from other FCV strains in phenograms based on nonhypervariable regions. In contrast, FCV-U2 consistently segregated with the Urbana strain in all phenograms. Clustering of isolates by geographic origin was most apparent in phenograms based on nonhypervariable regions. No clustering of isolates by biotype was apparent in any phenograms. Our results indicate that FCV-UI and FCV-U2 are genetically distinct from other known vaccine and field strains of FCV.  相似文献   

Effects of time and concentration on mortality of phosphine-resistant Sitophilus oryzae (L) fumigated with phosphine     

Daglish GJ  Collins PJ  Pavic H  Kopittke RA 《Pest management science》2002,58(10):1015-1021

The effects of exposure period and phosphine concentration on mortality of susceptible and resistant Sitophilus oryzae (L) were investigated. Although S oryzae is one of the world's most serious pests of stored grain there are few data on the practical significance of phosphine resistance in this species. The strains investigated were an Australian susceptible strain, a homozygous resistant strain exhibiting a level of resistance common in Australia and an unselected field strain from China with a much stronger resistance. Fumigations were carried out at 25 degrees C on adults and mixed-age cultures. For adults of all three strains and mixed-age cultures of the susceptible and resistant Australian strains, the relationship between concentration and time could be described by equations of the form Cnt = k. In all cases n < 1, indicating that time was a more important variable than concentration. In all fumigations of adults the resistant strains were harder to kill than the susceptible strain. However, in fumigations of mixed-age cultures, which contained the tolerant pupal stage, the difference between susceptible and resistant strains was more pronounced at lower concentrations than higher concentrations. For example, at 0.02 mg litre-1 the estimated LT99.9 for mixed-age cultures of the Australian resistant strain (27 days) is 3.4 times that of the susceptible strain (8 days), but at 1 mg litre-1 there is no difference between the two strains (4 days). Limited data on the Chinese resistant strain supported this finding. Twenty-three days exposure at 0.02 mg litre-1 had no effect on mixed-age cultures of this strain, but there were no survivors after 5 days exposure to 1 mg litre-1.  相似文献   

The effects of cooling and vitrification of embryos from mares treated with equine follicle-stimulating hormone on pregnancy rates after nonsurgical transfer   总被引：1，自引：0，他引：1  

Jason Hudson DVM  Patrick M. McCue DVM  PhD  Elaine M. Carnevale DVM  PhD  Susan Welch MS  Edward L. Squires PhD 《Journal of Equine Veterinary Science》2006,26(2):51-54

Equine embryos can remain viable for 12 to 24 hours when cooled and stored at 5°C.¹ Cryopreservation of embryos would allow for long-term preservation of genetic material and more efficient management of embryo recipients. This study compared pregnancy rates after transfer of equine embryos vitrified within 1 hour of collection or cooled for 12 to 19 hours before vitrification. Mares (N = 40) were superovulated using equine follicle-stimulating hormone (eFSH). Embryos were recovered 6.5 days after ovulation or 8 days after human chorionic gonadotropin. Forty morulae or early blastocysts with a grade of 1 to 2 and <300 mm in diameter were randomly assigned to 1 of 2 treatments: Group 1 (n = 20), washed 4 times in a commercial holding medium and then vitrified; Group 2 (n = 20), washed 3 times and then stored in the same holding medium at 5°C to 8°C in a passive cooling device for 12 to 19 hours before being vitrified. To thaw, embryos were warmed by holding the straw in air at room temperature for 10 seconds and then submerged in a water bath (20°C to 22°C) for an additional 10 seconds. The contents of the straw were transferred directly into a recipient that had ovulated 4 to 6 days previously. There were no differences (P > .05) in embryo diameter, grade, or morphology score between treatment groups before vitrification. Pregnancy rates (day 16) were not different (P > .05) between embryos vitrified immediately after collection (15 of 20; 75%) and embryos cooled for 12 to 19 hours before vitrification (13 of 20; 65%). Based on these results, small equine embryos (<300 mm) can be stored at 5°C to 8°C for 12 to 19 hours before vitrification without a significant loss of viability.  相似文献   

Granulosa Cell Tumors of the Equine Ovary     

Patrick M. McCue  Janet F. Roser  Coralie J. Munro  Irwin K.M. Liu  Bill L. Lasley 《Veterinary Clinics of North America: Equine Practice》2006

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Further evidence that in African acacia,white is a warning colour to herbivores: the white pseudo-galls of Vachellia seyal     

Jeremy Midgley  Huyam Altayeb  Patrick Mbosso 《African Journal of Range and Forage Science》2016,33(2):127-129

Pseudo-galls of three East African acacia (Vachellia) species were compared to determine the correlates of gall colour and their potential defensive functions. Although all three species produce white thorns, the pseudo-galls of V. gerrardii and V. drepanolobium are dark coloured. In contrast, pseudo-galls of V. seyal var. fistula are white. Associated with this, they are thin-walled and poorly used by aggressive mutualistic ants. We suggest that this weak functionality is compensated for by the highly visible white colour. This aposematism may also involve mimicry as only the fistula variety of V. seyal has galls and only this variety co-occurs with other Vachellia species that have functional galls. Vachellia seyal seyal does not have pseudo-galls and this variety does not occur with other Vachellia species that have pseudo-galls.  相似文献   

Fetal mummification in a mare     

Patrick M. McCue DVM  PhD  Dirk K. Vanderwall DVM  PhD  Edward L. Squires PhD 《Journal of Equine Veterinary Science》1997,17(5):267-269

A single mummified fetus was removed from the uterus of a 23-year-old mare that had been bred approximately 30 months previously. The mare had received supplemental progestin therapy for approximately 150 days after ovulation. This case represents the longest recorded occurrence of fetal mummification in the mare. Progestion administration may have contributed to the initial retention of the fetus in the uterus.  相似文献   

Structural and physiological studies of paraquat-resistant Conyza     

Kevin C. Vaughn  E.Patrick Fuerst 《Pesticide biochemistry and physiology》1985,24(1):86-94

Structural and physiological studies were conducted with a population of Conyza bonariensis (L.) Cronq. that segregates into paraquat-resistant and -susceptible biotypes. Leaf disks from resistant seedlings, when incubated on 10 μM paraquat for 24 hr, exhibited little difference from the control disks incubated on H₂O as measured by conductivity change, malondialdehyde formation, or plastid ultrastructure. Leaf disks from the susceptible seedlings incubated on 10^?5M paraquat for 24 hr were uniformly bleached, had elevated malondialdehyde content, and leaked more electrolytes than control disks. Plastids of the susceptible biotype incubated on 10^?5M paraquat for 24 hr were swollen organelles with gross rearrangements of the lamella system. Most of the chloroplasts from the central area of the leaf disk of the resistant biotype incubated on a paraquat solution were structurally normal. Swollen plastids and plastids with twisted lamellae were also noted, although much less frequently. Plastids from the edges of the leaf disks of paraquat-resistant clones were structurally similar to those found throughout the leaf disks in susceptible seedlings. When the size of the leaf disk was increased, paraquat-resistant clones exhibited more “resistance” toward paraquat compared to similar-sized leaf disks of the susceptible seedlings. These data are consistent with the hypothesis that the paraquat-resistant seedlings have an altered uptake and/or compartmentalization of paraquat. Superoxide dismutase isozymes, which were previously considered to be related to paraquat resistance in Conyza, did not correlate with the segregation of paraquat resistance in this population.  相似文献   

Charcoal affects early development and hormonal concentrations of somatic embryos of hybrid larch     

von Aderkas P  Label P  Lelu MA 《Tree physiology》2002,22(6):431-434

Embryogenic tissue of hybrid larch (Larix x marschlinsii Coaz) was multiplied on Medium M (modified MSG medium supplemented with the plant growth regulators (PGRs) 2,4-dichlorophenoxyacetic acid (2,4-D; 9 microM) and N-6-benzyladenine (2.25 microM)). After 1 week, cultures were transferred to either MSG lacking PGRs (Medium C-) or MSG lacking PGRs but supplemented with 1% activated charcoal (Medium C+). Embryos were sampled after 1 week on Medium M, C- or C+. Embryos were analyzed by ELISA for abscisic acid (ABA), abscisic acid-glucose ester, 2,4-D, indole-3-acetic acid (IAA), indole-3-aspartate (IAAsp), zeatin (Z), zeatin riboside (ZR), isopentenyladenine (iP) and isopentenyladenosine (iPA). Transfer of embryos to Medium C+ reduced the embryo concentrations of 2,4-D and iPA, but resulted in elevated concentrations of IAA, IAAsp, ABA, Z, ZR and iP. Charcoal reduced 2,4-D concentrations of embryos by an order of magnitude greater than PGR-free medium alone. Charcoal affected embryo concentrations of five of the eight PGRs quantified. Use of either C+ or C- medium as part of the maturation protocols also affected germination and plantlet establishment of the embryos. A 1-week treatment on Medium C+ positively influenced plantlet establishment and generally reduced variability during both germination and plantlet establishment.  相似文献