Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “SWINE”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 739 records · Page 41Linked to original sources

Experimental infection of weanling pigs with A-swine influenza virus. I. Epidemiology and serological response.

Naturally occurring swine influenza is caused by a strain of virus closely related to influenza strains isolated from man in 1918 and later. Information is lacking on certain aspects of the epidemiology of swine influenza that, if obtained, might shed some light on the epidemiology of human influenza, particularly with respect to inter-epidemic reservoirs and shedders of the virus. In a first series of experiments undertaken by the authors pigs were experimentally infected intranasally with swine influenza virus and the course of clinical infection, spread by contact, and the serological response of infected animals were studied. Observations were also made on persons in contact with the infected swine to determine whether cross-transmission occurred. Respiratory and feverish clinical signs of the disease were observed in infected animals. Contact infection of several animals in the same piggery occurred, as revealed by serological tests, although the contact-infected pigs showed no clinical signs. There was some but not highly significant serological evidence of human infection in laboratory workers and animal handlers exposed to swine influenza virus. Some pigs infected as weanlings developed specific antibodies that lasted for 1(1/2) years of observation. Antibody titres decreased markedly towards the end of 1 year in animals of a lower age at the time of infection (42 days old), as compared with older animals (52-77 days) in which there were lesser decreases in titre.

Animals↗

Immunity to Lancefield's group E Streptococcus: passive protection of swine.

Healthy swine from one source were randomly allotted to 3 groups of 3 pigs each. Troup I and II pigs were parenterally dosed with serum obtained from swine in the convalescent stage of streptococcic lymphadenitis of swine. Group III pigs were contact controls. The swine of all groups were orally exposed to Lancefield's group E Streptococcus sp. During the next 3 weeks, the controls evidenced little resistance to the development of streptococcic lymphadenitis of swine, whereas the principals evidenced considerable resistance to development of the disease.

Agglutinins↗

Sarcocystis infections in Georgia swine.

Tissues from 168 mature sows obtained at slaughter in northern and southern Georgia were examined for infection with Sarcocystis spp. Digestion techniques revealed zoites in 28 (16.5%) sows. Infected meat was fed to laboratory-reared dogs, cats, raccoons (Procyon lotor), and opossums (Didelphis marsupialis). Dogs and raccoons shed sporocysts (8.3 mum X 11.2 mum) 12 to 14 days after infection. Cats and opossums were refractory to infection. Sarcocystis-free pigs were infected with 50,000 sporocysts of swine-dog origin. Tissues from laboratory-infected swine were fed to dogs and raccoons. Both species shed sporocysts 14 days later. This is the 1st time in which a definitive host has been demonstrated for species of Sarcocystis occurring in North American swine. The raccoon constitutes a new definitive host for S suicanis Erber 1977. In contrast to previously reported low prevalences of Sarcocystis infections in swine, the relatively high prevalence reported here indicates that S suicanis may be of importance to swine producers in Georgia.

Animals↗

Prevalence and distribution of Sarcocystis sp among wild swine of southeastern United States.

Digestive techniques revealed Sarcocystis sp infection in 62 of 192 (32%) wild swine collected in Alabama, Arkansas, Georgia, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, Virginia, and West Virginia. Sarcosporidia were not detected in wild swine of Florida and were rarely found in the lower coastal plains of Georgia, Mississippi, and South Carolina. Swine from mountainous terrain in North Carolina, Tennessee, and West Virginia and bottomland floodplain regions of Alabama, Arkansas, and Louisiana were most frequently infected. Infections by sarcocystis sp may have been spread via swine relocated from mountainous regions to some other locales. Upon ingestion of infected pork from wild swine of Tennessee and West Virginia, dogs, but not cats, shed sporocysts morphometrically identical to Sarcocystis suicanis.

Animal Population Groups↗

Cell-mediated immune responses in swine from a herd infected with Brucella suis.

Cell-mediated immune (CMI) responses in swine naturally infected with Brucella suis biotype 3, swine suckling an infected sow and Brucella-noninfected swine were studied by an in vitro lymphocyte transformation procedure. The antigen used was a soluble antigen prepared from killed cells of B suis biotype 3. Lymphocytes were prepared from peripheral swine blood by the Ficoll-Hypaque technique, suspended in RPMI-1640 medium (1.5 X 10(6) lymphocytes/ml), cultured with B suis-soluble antigen or concanconcanavalin A, and incubated for 6 days. Sixteen hours prior to termination of incubation, cultures were labeled with 1 muCi of [3H]thymidine and, after harvesting, were assayed for [3H]thymidine incorporation into DNA by liquid scintillation spectrometry. Agglutination tests were conducted on sera collected simultaneously with samples for lymphocyte-stimulation tests. The B suis-soluble antigen elicited specific stimulation in lymphocytes from infected pigs. On a group basis, there was high correlation between the amount of serum antibodies and specific lymphocyte stimulation, but on an individual animal basis, there was little correlation of the results of both systems in infected swine. There was high correlation between recovery of Brucella from the tissues of animals and the degree of CMI response. Suckling pigs from an infected sow did not develop CMI responses, as measured by our system.

Agglutination Tests↗

Possible factors influencing immunoglobulin A concentration in swine colostrum.

The immunoglobulin (Ig) A concentration in swine colostrum was determined by the single radial immunodiffusion method, using 157 samples collected from the same number of farm-raised sows in the Yamaguchi Prefecture of Japan during 1976 and 1977. The mean IgA value was 12.26 +/- 3.30 mg/ml, and the maximum and minimum values were 28.14 mg/ml and 5.63 mg/ml, respectively. To determine factors influencing the IgA concentration in swine colostrum, the following items were analyzed in the present study: season, district, breed, number of parturitions, udder section from which samples were collected, kind of feed, vaccinations of swine (erysipelas live-organism vaccine, hog cholera live-virus vaccine, Japanese encephalitis live-virus vaccine, and transmissible gastroenteritis live-virus vaccine), type of farming, and number of sows raised on a farm. Relationships between the IgA concentration in swine colostrum and each of these 12 items were analyzed. Of the 12 items, breed and number of parturitions were the most influential on the IgA concentration in colostra of farm-raised sows. Season, district, and vaccination with transmissible gastroenteritis live-virus vaccine were moderately influential. Udder section, kind of feed, vaccinations of swine (erysipelas live-organism vaccine, hog cholera live-virus vaccine, and Japanese encephalitis live-virus vaccine), type of farming, and number of farm-raised sows were slightly influential. The multiple correlation coefficient obtained was 0.5887 (P greater than 0.05).

Animal Feed↗

Application of a leukocyte migration-inhibition agarose test to swine dysentery.

Cell-mediated immunity (CMI) was demonstrated in swine naturally affected with swine dysentery (SD) by a leukocyte migration-inhibition agarose test (LMAT). Migration of leukocytes from SD-affected pigs was inhibited in the presence of soluble antigen of Treponema hyodysenteriae, whereas migration of leukocytes from noninfected swine was not inhibited by exposure to the same antigen. Cell-mediated immunity was detected initially after the appearance of clinical signs of the disease, and a peak migration index (MI) of 0.11 (P less than 0.01) was detected at 2 weeks thereafter. The MI gradually decreased over the remaining 3 weeks of the experiment. Humoral antibody correlated well with CMI, since both showed maximum production within the same time interval. Leukocytes of swine naturally affected with SD 4 months previously had a significant MI response of 0.73 (P less than 0.05), whereas uninfected swine of comparable age and weight showed a MI of 0.94 that was not significant (P less than 0.05). The results indicated that the LMAT may be useful for the diagnosis of SD.

Animals↗

Bone marrow culture and transduction of stem cells in a miniature swine model.

Recombinant retroviral vectors, engineered to express the beta-chain gene of swine major histocompatibility complex class II DR, were developed for the genetic modification of swine hematopoietic stem cells (HSC). The expression of these vectors in swine bone marrow has been studied both in culture and after bone marrow transplantation. In addition, myeloid progenitor colony assays were performed on swine umbilical cord blood as part of a study to identify alternative sources of HSC for somatic gene transfer, revealing the presence of both granulocyte macrophage colony forming-units (CFU-GM) and CFU-Mix at frequencies comparable to those found in juvenile swine bone marrow.

Age Factors↗

Vesicular exanthema of swine and San Miguel sea lion virus.

San Miguel sea lion virus (SMSV), recently isolated from marine mammals, and vesicular exanthema of swine virus (VESV), which caused epizootics of vesicular exanthema of swine (VES) over a period of 24 years (1932 to 1956), may be the same virus. This finding is of particular interest because the source of the original VES epizootic was never identified, swine were the only known natural host of VESV, and VESV was thought to have been eradicated. The SMSV has been shown to be enzootic in 2 species of marine mammals found off the coast of California and to cause lesions in swine that are indistinguishable from those caused by VESV. Therefore, we should be alert to recognize situations in which swine might become exposed to SMSV and to consider SMSV in differential diagnoses of vesicular conditions.

Animals↗

Use of polymerase chain reaction to detect swine influenza virus in nasal swab specimens.

Rapid and accurate detection of a virus in a population is a critical factor in the eventual treatment and/or control of the virus. In this study, we examined use of the polymerase chain reaction (PCR) to detect swine influenza virus in nasal swab specimens from infected pigs. This approach was first standardized, using viral RNA purified by guanidinium/phenol-chloroform extraction and placed in the same transport medium as the swabs. By using highly conserved primers for the swine H1 hemagglutinin, we amplified a 591-base pair fragment that was analyzed by use of agarose gel electrophoresis, Southern blot, and DNA sequencing. To evaluate PCR as a potential diagnostic tool for detection of swine influenza virus infection, we obtained nasal swab specimens from experimentally infected pigs. Amplification by PCR and reamplification of extracted samples with internal primers yielded detectable bands for an amount of virus less than that required to infect embryonating chicken eggs. We also tested swab specimens from pigs involved in 3 separate, natural episodes of swine influenza. These swab specimens were extracted, amplified and reamplified, producing visible bands on the gel and in Southern blots. We performed Southern blot analyses on all PCR products, to confirm that they were from viral H1 RNA. We also cloned and sequenced a 591-base pair product from 1 specimen and found that it was 100% identical to the hemagglutinin gene sequence of A/Sw/Ind/1726/88. Results indicate that PCR can be used to detect swine influenza virus, even in nasal swab specimens, the specimen typically collected for diagnosis of virus infection.

Animals↗

Classical swine fever virus: independent induction of protective immunity by two structural glycoproteins.

To study which proteins of classical swine fever virus (CSFV) are able to confer protective immunity in swine, N-terminal autoprotease, viral core protein, and the three structural glycoproteins were expressed via vaccinia virus recombinants (VVR). CSFV proteins synthesized in cells infected with VVR showed migration characteristics on sodium dodecyl sulfate gels identical to those of their respective CSFV counterparts. Apparently authentic dimerization of the recombinant glycoproteins was observed. The glycoproteins E0 and E2 were detected on the surfaces of VVR-infected cells. In protection experiments, swine were immunized with the different VVR, and the generation of humoral immune response was monitored. Only animals vaccinated with VVR expressing E0 and/or E2 resisted a lethal challenge infection with CSFV. Glycoprotein E0 represents a second determinant for the induction of protective immunity against classical swine fever.

Animals↗

Swine chromosomal DNA quantification by bivariate flow karyotyping and karyotype interpretation.

Human and swine chromosomes were analyzed separately and as a mix to obtain bivariate flow karyotypes. They were normalized to each other in order to use the human chromosomal DNA content as standard. Our results led to the characterization of the "DNA line" in swine identical to the human "DNA line." Estimation of the DNA content in mega-base pairs of the swine chromosomes is proposed. Chromosomal assignment to the various resolved peaks on the bivariate swine flow karyotype is suggested from the relation between DNA content quantified by flow cytometry and chromosomal size. Swine chromosomes 1, 13, 6, 5, 10, 16, 11, 18, and Y were assigned to peaks A, B, C, K, L, N, O, Q, and Y, respectively. Peaks D and E were assumed to contain chromosomes 2 and 14, but without specific assignment. Similarly, P and M peaks were expected to correspond to chromosomes 12 and 17. Of the remaining chromosomes (3, 7, X, 8, 15, 9, and 4), chromosomes 3, 7, and X, which were assigned previously to peaks F, G, and H, respectively, led us to deduce that chromosomes 15 and 8 belonged to peaks I and J, and chromosomes 9, 4, and X to peak H.

Animals↗

Grafted swine neuroepithelial stem cells can form myelinated axons and both efferent and afferent synapses with xenogeneic rat neurons.

Neuroepithelial stem cells derived from the swine mesencephalic neural tube were examined regarding their eligibility for neural xenografting as a donor material, with the aim of evaluating myelinated axon formation and both types of synaptic formation with xenogeneic host neurons as part of possible neural circuit reconstruction. The mesencephalic neural tube tissues were dissected out from swine embryos at embryonic days 17 and 18 and were implanted immediately into the striatum of the Parkinsonian model rat. The swine-derived grafts had many nestin-positive rosette-forming, neurofilament-positive, and tyrosine hydroxylase-positive cells in the rat striatum. Electron microscopic study revealed both efferent and afferent synaptic formations in the donor-derived immature neurons or tyrosine hydroxylase-positive donor cells in the grafts. Myelinated axons, both positive and negative for swine-specific neurofilament antibody, were mingled together in the graft. These results indicated that implanted neuroepithelial stem cells could survive well and divide asymmetrically into both nestin-expressing precursors and differentiated neurochemical marker-expressing neurons in the xenogeneic rat striatum, with the help of an immunosuppressant. Donor-derived immature neurons formed both efferent and afferent synapses with xenogeneic host neurons, and donor-derived axons were myelinated, which suggests that implanted swine neuroepithelial stem cells could possibly restore damaged neuronal circuitry in the diseased brain.

Animals↗

Pharmacokinetics of polychlorinated biphenyl components in swine and sheep after a single oral dose.

Single-dose oral administration of a commercial polychlorinated biphenyl product containing 54% chlorine provided data with which to plot the time course of total polychlorinated biphenyl and individual components in the blood of swine and sheep. Pharmacokinetic parameters describing absorption from the gut and elimination from a two-compartment body system were determined for the components in swine and sheep. The absorption half-time for total polychlorinated biphenyl in swine was 1.13 hr while that for sheep was 3.83 hr. The half-time for disposition of total polychlorinated biphenyl from the central compartment was 4.4 hr in swine and 7.7 hr in sheep; the apparent biological half-life was 62.4 hr in swine and 78.8 hr in sheep. Individual components varied significantly from each other and from total polychlorinated biphenyl in all parameters.

Animals↗

Analysis of tilmicosin in swine liver extracts by liquid chromatography/atmospheric pressure chemical ionization mass spectrometry.

Tilmicosin is a semisynthetic macrolide antibiotic used in the treatment of respiratory disease in cattle and swine. The technique of liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (LC/APCI-MS) was employed in an on-line capacity for the analysis of tilmicosin in extracts from spiked swine liver. Increasing the potential in the cone/skimmer region of the ion source resulted in an increased abundance of unique structurally indicating fragment ions of tilmicosin. Three ions, [M+H]+ and two diagnostic fragment ions were chosen for confirmation of the presence of tilmicosin in swine liver tissue extracts using the mass spectrometer in selected-ion monitoring mode. The ion abundance ratios arising from any given combination of ions in data acquired from extracts of swine liver tissue spiked with tilmicosin at 5 and 10 ppm were within +/- 10% of the corresponding mean standard abundance ratio, and duplicate sample analyses exhibited < 10% relative standard deviation. These results suggest the potential for the application of LC/APCI-MS as a confirmatory technique for tilmicosin in swine liver.

Animals↗

Swine and dynamic ultrasound models for trauma ultrasound testing of surgical residents.

BACKGROUND: Trauma ultrasound workshops have been recommended for training surgical residents. We assessed the teaching effectiveness of the workshop, comparing swine and dynamic patient ultrasound models. MATERIALS AND METHODS: MCQ exams on ultrasound physics and practical skills tests with and without pericardial or peritoneal fluid using four swines and eight dynamic patient ultrasound videos were used to compare pre- and postworkshop performance in 18 surgical residents (Group I) and a matched control group of 18 (Group II). Paired t tests and unpaired t tests for paired and unpaired data, respectively, were used for analysis with a P < 0.05 being considered statistically significant. RESULTS: Mean scores (% correct response) +/- SD were as follows (*P < 0.05 vs Group I). [table: see text] For the swine model, the best scores were with pericardial fluid (25.0% pre vs 69.4% post in Group I) and the worst scores were with RUQ fluid (5.6% pre vs 22.2% post in Group I). Postworkshop dynamic video scores were always higher than the swine model scores in Group I (100% correct video scores for pericardial fluid). CONCLUSIONS: This study confirms the trauma ultrasound workshop teaching effectiveness. For testing, the swine model (especially RUQ) was more difficult. In postcourse evaluation, the dynamic human video was considered more relevant, realistic, and less costly for repeated testing of the residents.

Animals↗

The effects of mycotoxins, fumonisin B1 and aflatoxin B1, on primary swine alveolar macrophages.

Mycotoxins were fungal metabolites that were widely present in feed and food; some of them were known to associate with human and animal disease. In the present study, the effects of fumonisin B1 (FmB1) and aflatoxin B1 (AFB1) on swine alveolar macrophages (AM) were examined by exposing primary cultures of swine AM to various concentrations of mycotoxins. Incubation of AM with 5 microg/ml of FmB1 for 72 h led to a reduction in the number of viable cells to 65% of the control levels. In the presence of 1.5 microg/ml of AFB1, the viability of AM falls to less than 41% of controls after 24 h exposure. FmB1, but not AFB1, induced the apoptosis of swine AM with evidence of DNA laddering and nuclear fragmentation. However, both FmB1 and AFB1 exposure induced the expression of apoptosis-related heat shock protein 72 (HSP 72) in AM. Swine AM treated with 50 ng/ml of FmB1 and 100 ng/ml of AFB1 for 24 h led to a reduction in phagocytic ability to approximately 55 and 36% of the control levels, respectively. Incubation of AM with FmB1 (2 and 10 microg/ml) for 24 h dramatically decreased the mRNA levels of interleukin-1beta (IL-1beta) and tumor necrosis factor-alpha (TNF-alpha). However, AFB1 treatment did not affect the expression of IL-1beta and TNF-alpha mRNA. The results suggest that both FmB1 and AFB1 are immunotoxic to swine AM but that they exert their toxic effects via different biochemical mechanisms.

Aflatoxin B1↗

Characterization of mucin glycoprotein-specific translation products from swine and human trachea, pancreas and colon.

RNA was isolated from cultured swine trachea epithelial cells and mucus-secreting tumor cell lines from human pancreas, lung and colon by extraction with guanidine isothiocyanate. Poly(A)+mRNA rich fractions were purified by repeated chromatography on oligo (dT)-cellulose columns and they were translated in a cell-free rabbit reticulocyte system. Translation products labelled with 35S-methionine were isolated by immunoprecipitation with specific antibodies to the polypeptide chains of mucin glycoproteins and they were analyzed by SDS-PAGE and fluorography. A single principal polypeptide band of 67 kDa was found in all cases when the immunoprecipitates were washed with buffer containing bovine serum albumin and unlabeled deglycosylated mucin glycoprotein. The intensity of the 67 kDa band decreased when unlabeled deglycosylated mucin glycoprotein was added to the translation mixture before immunoprecipitation. Affinity purified monospecific antibodies elicited against chemically deglycosylated polypeptide chains of purified mucin glycoproteins from human and swine trachea and Cowper's gland were all equally effective in immunoprecipitating the 67 kDa translation product. Monospecific antibodies directed against the glycosylated and unglycosylated regions of the polypeptide chain yielded single bands with a molecular size of 67 kDa in each case. Peptide profiles obtained by digestion of the 67 kDa translation product with S. aureus V-8 protease were identical to those obtained with deglycosylated human and swine trachea mucin glycoproteins. These studies clearly demonstrate that the translation product of swine trachea and human lung, colon and pancreatic mucin glycoprotein gene is a single polypeptide chain of 67 kDa. The relative size and properties of the translation products synthesized with poly (A)+RNA isolated from mucus-secreting cells derived from three different tissues are similar to those of mucin glycoproteins purified directly from mucus secretions of human and swine trachea epithelium.

Animals↗