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At least 865 records · Page 48Linked to original sources
PubMed1994

Expressed swine VH genes belong to a small VH gene family homologous to human VHIII.

The sequences of 34 swine H chain V-regions expressed with either IgG, IgA, or IgM C regions in adult swine and newborn piglets are described and compared. Sixteen of these V-regions were cloned by using a specific leader primer whereas 18 were cloned by anchored PCR. According to the operational criterion of VH family classification, i.e., > 80% DNA sequence similarity, all sequences belong to a homogeneous VH gene family. A total of 31 additional VH-bearing C mu clones obtained by anchored PCR from colostrum-deprived newborn piglets hybridized equally with a probe for C mu and a pan-VH probe. When the consensus sequence of the expressed swine VH genes were compared with those of VH gene for humans (VHI, II, III), mouse (VHI, II, III), rabbit, and chicken, swine VH genes seem to have common ancestry with the human VHIII family, rabbit VH genes, and the single functional VH gene of the chicken. The leader peptides of all clones obtained by anchored PCR showed < 1% variability, and the deduced amino acid sequences from aa4 to aa25 in all 34 clones are identical. Framework (FR)1 and FR2 are conserved whereas FR3 shows greater variability. A total of 23 of 30 JH sequences were identical, suggesting preferential use of one JH. This frequent, putative JH sequence is not similar to any JH gene in humans. Identical genomic Southern hybridization patterns, each with 13 bands of differing intensity and regardless of stringency, were obtained when either a leader or a pan-specific VH probe was used. Analyses of individual genomic bands by single strand conformational polymorphism and sequence analysis suggest that the number of VHIII-related genes in the swine genome is < 20.

Amino Acid Sequence↗
PubMed1996

Double gallbladder of swine.

In research on the reduplication of the pig gallbladder, a total of 297,531 swine from 130 breeders were surveyed at a slaughter house (Ozu Health Center, Ehime Prefecture, Japan) between October 1993 and December 1995. The swine were 6-7 months old and their body weights ranged from 95 to 120 kg. Twenty-nine swine were found to have reduplication of the gallbladder. Of these 19 were females, nine were males and the sex of one was not identified. The second sac was smaller than main one. Eleven cases were diverticulum of a cystic duct (Type I). Diverticulum of the neck of the main gallbladder of six cases also gave rise to the second gallbladder (Type II). A sac attached to the neck of the main gallbladder via a small cystic duct in seven cases was another type of reduplication (Type III). Connection of the second sac to the middle of the hepatic duct via a small cystic duct was seen in three cases (Type IV). The positions of these small sacs to the main gallbladder were right (13 cases), left (II cases) and ventral (three cases). The fundus of one gallbladder were divided and resulted in double sacs (Type V). One second sac was set apart from the main gallbladder and attached to a hepatic duct of lateral left lobe of the liver (Type VI). One specimen of the Type III gallbladder had two additional small sacs as diverticulum of the cystic duct. Compared to occurrences in humans and the Japanese monkey, the ratio of gallbladder reduplication to normal system anatomy in swine was extremely low. It was similar to the ratio of spleen reduplication in swine (1/10,000).

Animals↗
PubMed1977

Aortic intimal changes in aging swine.

Aortic intimal lesions in aging swine contained smooth muscle, monocyte-like and unclassifiable cells. The most frequent cellular constituent was the smooth muscle cell that had slightly different features than those in the media. Monocyte-like and unclassified cells appeared largely in the innermost layer of the intima; both types of cells were ultrastructurally similar in appearance except the former had heterophagic vacuoles and overall resemblance to circulating monocytes in shape and size. These cells seemed to preexist in aortic lesions of untreated, aging swine. The intima-media strips of the grossly normal thoracic aortas in 3 1/2 year old swine showed significantly higher contents of cholesterol, triglycerides, phospholipids and total lipids than those of a 6 month old swine. Three to four month old cultured aortic cells accumulated extracellular components, such as fibriles, electron dense substances and cellular debris, which appeared similar to the extracellular matrix of aortic plaques in aged swine.

Aging↗
PubMed1997

Advances in gender preselection in swine.

Gender preselection using isolated populations of X- and Y-chromosome bearing spermatozoa that have been separated on the basis of DNA content is currently possible in swine and other farm animals, as well as in humans. Semen from most livestock species can now be successfully separated into predominantly X or Y sperm populations before their use for intra-tubal insemination, deep-uterine insemination or for in vitro fertilization (IVF) to produce sexed offspring. Birth of progeny of the desired sex in cattle, sheep and swine under semi-practical conditions has successfully validated the sexing technology. Spermatozoa are separated on the basis of inherent differences in DNA content in the X- and Y-chromosome bearing sperm population using modified flow cytometry/cell sorting technology. Spermatozoa are stained with Hoechst 33342 which binds to the DNA in an amount proportional to the amount of DNA present in the individual spermatozoa. Over 300 animals from various species at several locations have been born using the USDA-Beltsville Sperm Sexing Technology for separating X and Y spermatozoa. Sex ratios are shifted from the normal 50:50 to 85 to 90% of one sex or the other. In swine, offspring have been born as the result of surgical intratubal insemination of separated spermatozoa and also from IVF and embryo transfer. At the present time, standard swine artificial insemination techniques are not optimized for use with the small numbers of flow cytometrically separated X or Y sperm populations. Cattle, swine and rabbit offspring have been reproduced through the second generation with normal morphology and reproductive function. Numerous improvements have been made in the sexing technology since it was first reported in 1989. Increasing the speed of the sexing process to make the application of the technology available to a larger segment of the livestock industry is paramount, even with insemination technology designed for small numbers of spermatozoa.

Animals↗
PubMed1998

[Health effects of airborne pollutants, particularly in swine confinement stalls, from the viewpoint of occupational medicine].

From the point of view of occupational respiratory medicine, an overview on potential health effects of airborne pollutants particularly in swine confinement houses is presented. Airway diseases are the most frequent occupational disorders among farmers in many countries around the world including Germany. Due to various methodological reasons, epidemiological studies in farming populations are more difficult to perform than among non-farmers. Major constituents of swine confinement dust include bacteria, endotoxin, mites, fungal spores, and animal dander. Gaseous pollutants include ammonia, methane, and hydrogen sulfide. In a variety of cross-sectional studies, high prevalences of respiratory symptoms and non-obstructive (and obstructive) bronchitis and Organic Dust Toxic Syndrome have been reported in pig farmers. Nasal and bronchial provocation challenges with swine confinement dust include influx of neutrophils and other inflammatory cells as well as mediators. In cross-sectional and longitudinal studies, endotoxin turns out as the probably most relevant parameter associated with lung function impairment. Further studies are clearly needed focusing on the prognosis of non-obstructive bronchitis in swine farmers and on health effects of reducing airborne contaminants in swine confinement houses.

Adolescent↗
PubMed1997

A BIR motif containing gene of African swine fever virus, 4CL, is nonessential for growth in vitro and viral virulence.

An African swine fever virus (ASFV) gene with similarity to viral and cellular inhibitor of apoptosis genes (iap) has been described in the African isolate Malawi Lil-20/1 (ORF 4CL) and a cell-culture-adapted European virus, BA71V (ORF A224L). The similarity of the ASFV gene to genes involved in inhibiting cellular apoptosis suggested the gene may regulate apoptosis in ASFV-infected cells and thus may function in ASFV virulence and/or host range. Sequence analysis of additional African and European pathogenic isolates demonstrates that this gene is highly conserved among both pig and tick ASFV isolates and that its similarity to iap genes is limited to the presence of a single IAP repeat motif (BIR motif) in the ASFV gene. To study gene function, a 4CL gene deletion mutant, delta 4CL, was constructed from the pathogenic Malawi Lil-20/1 isolate. Growth characteristics of delta 4CL in swine macrophage cell cultures were indistinguishable from those of parental virus. Infected macrophage survival time and the induction and magnitude of apoptosis in virus-infected macrophages were comparable for cells infected with either delta 4CL or parental virus. In infected swine, delta 4CL exhibited an unaltered Malawi Lil-20/1 virulence phenotype. These data indicate that, although highly conserved among ASFV isolates, the 4CL gene is nonessential for growth in macrophage cell cultures in vitro and for pig virulence. Additionally, despite its limited similarity to JAP genes, 4CL exhibits no anti-apoptotic function in infected macrophage cell cultures. The high degree of gene conservation among ASFV isolates, together with the apparent lack of function in the swine host, suggests 4CL may be a host range gene involved in aspects of infection in the arthropod host, ticks of the genus Ornithodoros.

African Swine Fever↗
PubMed1993

African swine fever virus specific porcine cytotoxic T cell activity.

African swine fever virus (ASFV) specific, cytotoxic T lymphocyte (CTL) activity has been studied in a protection model in which SLA inbred miniature swine are experimentally inoculated with a naturally occurring, non-fatal ASFV isolate (NHV). Peripheral blood mononuclear cells (PBMC) from such infected swine show significant activity in CTL assays, using cultured ASFV-infected porcine blood derived macrophages as target cells. This CTL activity is elicited from PBMC by in vitro restimulation of effector cells with low doses (multiplicity of infection = 0.1) of the homologous virus isolate for 48 to 72 h. For SLAc/c effectors, this CTL activity appears to be SLA class I restricted because (1) blocking target cell antigens with monoclonal antibodies (mAb) against SLA class I antigens causes a major reduction in CTL activity; (2) there is preferential lysis of SLA class I matched, ASFV infected targets; and (3) depletion of effector cells with CD8 specific mAb and complement causes a reduction in CTL activity. The CTL activity is ASFV specific for all pigs tested in that infected macrophages are preferentially lysed as compared to normal (non-infected) cultured macrophages or macrophages infected with hog cholera virus (HCV). Lysis of macrophages infected with different ASFV isolates revealed that there is marked lysis of macrophages infected with the virulent L60 isolate but less lysis of macrophages infected with the DR-II and Tengani isolates. In summary, our data show that ASFV specific CTL activity is triggered in swine infected with the NHV ASFV isolate.

African Swine Fever Virus↗
PubMed1995

Production and purification of recombinant African swine fever virus attachment protein p12.

The conditions for cultivation of Spodoptera frugiperda (Sf9) insect cells for production of recombinant baculoviruses have been studied, to scale-up and improve the efficiency of the process for production of the African swine fever virus attachment protein p12 in the baculovirus expression system. It was shown that the total virus and recombinant protein production in insect cells infected with the Acp12 recombinant baculovirus were slightly dependent on cell density, but largely dependent on the serum concentration, in the case of suspended cells, but not in static monolayer cultures. The yield of recombinant protein p12 exceeded 50 mg per 1 of 2 x 10(9) cells, representing more than 10% of total cell proteins, a level > 20-fold higher than that observed with other eukaryotic expression systems. The presence of p12 in the cytoplasmic fraction of infected cells has allowed the purification of the protein by a simple two-step procedure of aqueous phase partition and octyl-glucoside solubilization. The recombinant protein p12 was able to inhibit, in a dose-dependent manner, the African swine fever virus production in swine macrophages infected with a number of different virus isolates, including attenuated, virulent, highly passaged on tissue culture, and non-haemadsorbing strains, indicating a fundamental role for p12 in the early interaction of the virus with the natural target cell receptors. However, pigs immunized with purified recombinant p12 did not develop protective immunity against African swine fever.

African Swine Fever Virus↗
PubMed1984

Evaluation of the indirect hemagglutination assay as a practical serodiagnostic test for mycoplasmal pneumonia of swine.

Sera from swine experimentally or naturally infected with Mycoplasma hyopneumoniae (the etiological agent of mycoplasmal pneumonia of swine, MPS) were tested by the indirect hemagglutination assay (IHA), the enzyme-linked immunosorbent assay (ELISA) and the complement fixation (CF) test. The IHA detected antibody at comparable times and levels to the other 2 serological tests following experimentally-induced infection. In the late antibody response (greater than or equal to 86 days post-infection), the ELISA titres were higher than either the IHA or the CF test. The IHA appeared least satisfactory when it was used to test sera from commercial swine herds. When 1000 sera were tested, the IHA was positive for only 30 (22%) of 135 sera which were positive by the ELISA and the CF test. The IHA titres were low; 20 of the 30 sera had a titre of only 10. The end-points for the IHA were difficult to read for sera of this low titre. The relationship between positive IHA results for the herd sera obtained at necropsy, and the occurrence of gross or microscopic lesions typical of MPS was poor (41 and 50% agreement, respectively). An agreement of 39% was noted between positive IHA results and the localization of mycoplasmal antigens by an indirect immunofluorescence (IIF) test. However, IHA results correlated significantly (P less than 0.05) with gross and microscopic lesions, but not with the IIF test. No significant correlation was noted between the IHA (or the other 2 serologic tests) and the cultural isolation of M. hyopneumoniae or M. flocculare. On the basis of these results, the IHA appears to have limited promise as a practical test for the diagnosis of MPS in commercial swine herds because of the low titres observed, poor correlation of the IHA and other indicators of MPS, the necessarily subjective determination of end-points, and other inherent technical limitations of the test.

Animals↗
PubMed2000

A tissue culture system to study respiratory ciliary epithelial adherence of selected swine mycoplasmas.

An in vitro culture system for swine tracheal epithelial cells was developed to study the adherence of swine mycoplasmas. Swine tracheal epithelial cells were isolated by enzymatic digestion and cultured on microporous membranes. Growth medium was placed under the membrane support to create air-liquid interface feeding resulting in the cells growing cilia and microvilli on the apical surface. Two strains of Mycoplasma hyopneumoniae (pathogenic strain 91-3 and non-pathogenic type strain J) and two strains of Mycoplasma flocculare (type strain Ms42 and field isolate 7160T) were used in this study. The morphology of the cultured tracheal cells was evaluated by transmission electron microscopy. Adherence of M. hyopneumoniae and M. flocculare and damage to the cilia were demonstrated using scanning electron microscopy. The pathogenic M. hyopneumoniae strain 91-3 adhered to cilia inducing obvious damage. The non-pathogenic M. hyopneumoniae strain J did not adhere to mature cilia. Both M. flocculare strains Ms42 and 7160T adhered to mature and budding cilia. No obvious ciliary damage was observed with strain Ms42. Minimal damage consisting of a slight tangling of the cilia occurred after adherence by strain 7160T. This model will enable us to further study the role of adherence of mycoplasmas on the pathogenesis of swine pneumonia.

Animals↗
PubMed1993

A sero-epizootiological study of porcine respiratory coronavirus in Belgian swine.

A porcine respiratory coronavirus (PRCV), antigenically closely related to transmissible gastroenteritis virus (TGEV), appeared in the European swine population in 1984. The present serological study was performed to obtain insight into the epizootiology of PRCV and of TGEV. PRCV-induced neutralizing antibodies were found in 90.6 per cent of the 160 sera collected from sows at slaughter, demonstrating the enzootic appearance of PRCV in the Belgian swine population. A serological study of fattening swine on 33 farms revealed that 11 farms situated in an area with a high farm density (all farms within 4 km2) and 11 on 22 closed breeding-fattening farms situated in areas with a low farm density (only one to four farms per 12 km2) were infected with PRCV throughout the year, whereas the other 11 closed breeding-fattening farms were temporarily free of PRCV. PRCV disappeared from the farms mainly in spring and summer. All the 11 farms became reinfected in autumn or winter, indicating that PRCV is regularly reintroduced in farms in the colder seasons. There was no correlation between the herd size and the temporary disappearance of PRCV from farms. It was observed on some farms that PRCV could infect pigs shortly after weaning in the presence of declining maternal antibodies, indicating that PRCV can persist on a farm by regularly infecting newly weaned pigs. TGEV-specific antibodies were found in 7.6 per cent of the 160 sera from the slaughterhouse sows. TGEV-specific antibodies were also detected in sera from fattening swine of 5 of the above mentioned 33 farms. TGEV-outbreaks were not observed on these farms.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1996

Classical swine fever virus (CSFV) envelope glycoprotein E2 containing one structural antigenic unit protects pigs from lethal CSFV challenge.

Envelope glycoprotein E2, formerly called E1 or gp51-54, of classical swine fever virus (CSFV) expressed in insect cells protects swine from classical swine fever. Monoclonal antibodies directed against epitopes of domains B and C and subdomain A1 are neutralizing. The domains are located on two structural antigenic units in a proposed model of the antigenic structure of E2. One unit consists of nonconserved antigenic domains B and C and the other contains highly conserved antigenic domain A. We produced several mutant E2 proteins by use of the baculovirus expression system. Two selected mutants were E2 proteins in which one of the two structural antigenic units, unit B/C or unit A, was deleted. The protective capacity of the mutant E2 proteins was investigated in an immunization experiment in pigs. Titres of the neutralizing responses in pigs immunized with mutant E2 proteins were all comparable with that of intact E2. These vaccinated pigs were protected against an intranasal lethal CSFV challenge, indicating that the immune response induced by one structural antigenic unit of E2 can protect pigs against classical swine fever.

Animals↗
PubMed2004

African swine fever virus multigene family 360 and 530 genes affect host interferon response.

African swine fever virus (ASFV) multigene family 360 and 530 (MGF360/530) genes affect viral growth in macrophage cell cultures and virulence in pigs (L. Zsak, Z. Lu, T. G. Burrage, J. G. Neilan, G. F. Kutish, D. M. Moore, and D. L. Rock, J. Virol. 75:3066-3076, 2001). The mechanism by which these novel genes affect virus-host interactions is unknown. To define MGF360/530 gene function, we compared macrophage transcriptional responses following infection with parental ASFV (Pr4) and an MGF360/530 deletion mutant (Pr4 Delta 35). A swine cDNA microarray containing 7,712 macrophage cDNA clones was used to compare the transcriptional profiles of swine macrophages infected with Pr4 and Pr4 Delta 35 at 3 and 6 h postinfection (hpi). While at 3 hpi most (7,564) of the genes had similar expression levels in cells infected with either virus, 38 genes had significantly increased (>2.0-fold, P < 0.05) mRNA levels in Pr4 Delta 35-infected macrophages. Similar up-regulation of these genes was observed at 6 hpi. Viral infection was required for this induced transcriptional response. Most Pr Delta 35 up-regulated genes were part of a type I interferon (IFN) response or were genes that are normally induced by double-stranded RNA and/or viral infection. These included monocyte chemoattractant protein, transmembrane protein 3, tetratricopeptide repeat protein 1, a ubiquitin-like 17-kDa protein, ubiquitin-specific protease ISG43, an RNA helicase DEAD box protein, GTP-binding MX protein, the cytokine IP-10, and the PKR activator PACT. Differential expression of IFN early-response genes in Pr4 Delta 35 relative to Pr4 was confirmed by Northern blot analysis and real-time PCR. Analysis of IFN-alpha mRNA and secreted IFN-alpha levels at 3, 8, and 24 hpi revealed undetectable IFN-alpha in mock- and Pr4-infected macrophages but significant IFN-alpha levels at 24 hpi in Pr4 Delta 35-infected macrophages. The absence of IFN-alpha in Pr4-infected macrophages suggests that MGF360/530 genes either directly or indirectly suppress a type I IFN response. An inability to suppress host type I IFN responses may account for the growth defect of Pr4 Delta 35 in macrophages and its attenuation in swine.

African Swine Fever↗
PubMed1999

Eradication of Mycoplasma hyopneumoniae from infected swine herds joining the LSO 2000 health class.

The study was conducted in order to determine if eradication of swine enzootic pneumoniae (SEP) had succeeded with different variants of partial depopulation during the eradication programme on swine farrowing farms joining a health class, LSO 2000. The farms in the health class need to be free from swine enzootic pneumoniae, swine dysentery, sarcoptic mange and atrophic rhinitis. Twenty-one eradication attempts for M. hyopneumoniae were carried out using different variants based on separating adult animals for 2 weeks from infected young pigs which were not returned to the herd. The infected young pigs were kept in the same building (variant 1) in 4 herds and on the same compound (variant 2) as disease-free pigs in 12 herds. The infected young pigs were finally all sold. In 5 herds only adult animals were present during the eradication (variant 3). The eradication attempt succeeded in 81% and failed or remained uncertain in 19% of the herds. The result was confirmed with 1) frequent clinical follow-up of the health status in the herds (both the farrowing and the finishing units) joining the LSO 2000 health class 2) milk and/or blood serology. Possible causes of the failure of the eradication attempt were described: a short distance between infected and uninfected animals, the time period between diagnosis of SEP and initiation of the programme, the age of the youngest animal kept on the farm, the period of time when animals with different status were reared close to each other, the medications used, the cleaning of the facilities during the programme and the season. Further, a good cooperation between the farmer, the local veterinarian and the animal health service of the slaughterhouse was an essential part of the initiation and the follow-up of the programme. The secondary aim of the study was to collect information about the expenses during the programme. Only 57% of the farmers gave some estimates for the expenses on their farms. For variants 1, 2 and 3 the expenses were 879, 1110 and 1274 FIM per sow (1 USD = 5.5 FIM), respectively (p > 0.1).

Animal Husbandry↗
PubMed1991

Detection of African swine fever virus by a biotinylated DNA probe: assay on cell cultures and field samples.

African swine fever virus was detected in various samples using a molecular hybridization technique. A fragment located in a constant area of the viral genome was biotin-labelled. This probe, when present at a concentration of 100 ng/ml of the hybridization solution, could detect 10 pg of target DNA immobilized on nitrocellulose with cellular DNA and RNA. The virus was evidenced after being passaged on monkey kidney cells, either 8 h post-inoculation (pi) if the multiplicity of infection (MOI) was at least 1 hemadsorbing unit (HAd) per cell, or 24 h later if the inoculum was diluted up to 10(-3) HAd per cell. When passaged on pig leukocytes with a MOI of 0.1 HAd per cell, the virus was evidenced 12 h pi, or 24 h pi with a MOI of 10(-2) HAd per cell. The probe did not hybridize with another DNA virus passaged on cells, neither did it react with non-infected blood or ham, but did so if African swine fever virus was resuspended with the samples. The spleen from uninfected pig and the lymph nodes from a pig which had died from hog cholera were found to be negative, whereas the spleen from a pig which had died of African swine fever was positive. These samples were also tested with a 32P-labelled probe whose sensitivity was 10-fold higher. A non-radioactive probe could be used both for the sensitive and specific diagnosis of African swine fever and the detection of the virus in an epidemiological survey.

African Swine Fever↗
PubMed1987

[Trial of the intensity and duration of swine fever immunity in pigs].

Comparative testing of the intensity and the continuity of immunity against swine fever was carried out with pigs producers of serum against edema disease and swine erysipelas, vaccinated with an untreated and a freeze-dried K vaccine. Control infection studies revealed that serum-producing pigs with regard to edema disease, immunized with a freeze-dried and an untreated lapinized K vaccine, could acquire sufficiently stable immunity from the 6th to the 9th month following immunization both in the beginning and at the end of the exploitation period. So far as the intensity and the continuity of immunity of pigs producing serum against erysipelas are concerned the animals were shown to acquire sufficiently stable immunity against swine fever when vaccination was carried out with a freeze-dried K vaccine, while not all of the pigs treated with an untreated K vaccine were protected from swine fever upon control challenging. Therefore, instead of immunization with an untreated K vaccine as many as 400 immunization doses of the freeze-dried K vaccine could be used.

Animals↗
PubMed1980

Experimental transmission of African swine fever virus by Ornithodoros coriaceus, an argasid tick indigenous to the United States.

Three ticks, indigenous to the United States, were assessed for their ability to maintain and transmit African swine fever virus (ASFV). Amblyomma americanum and A cajennense adults and nymphs maintained virus for 4 to 7 days after engorging on infected swine blood; however, virus was not carried through the subsequent molt of nymphs and it was not transmitted vertically to the eggs and larvae of the infected females. On refeeding of the ticks, infection was not transmitted to healthy swine. Ornithodoros coriaceus adult females also did not show transovarial transmission of two strains of ASFV. Nymphs, however, maintained virus for 77 to 118 days through a molting stage and transmitted one strain of the virus (Lisbon 60) to healthy swine.

African Swine Fever↗
PubMed1995

Retrospective evaluation of production characteristics in Sinclair miniature swine--44 years later.

Three hundred seventy-one litter records collected between 1985 and 1993 from 156 Sinclair S-1 miniature sows, a Hormel-derived strain of miniature swine, were retrospectively analyzed and compared with published records for 1950 to 1952 and 1963 to 1965. The effect of several variables such as season and month of parturition, age of sow, parity, and litter size on reproductive parameters of the Sinclair miniature swine were evaluated. The mean and standard error of the mean for litter size, number of liveborn, number of stillborn, and litter size at weaning of the Sinclair S-1 miniature swine were 7.20 +/- 0.12, 6.57 +/- 0.12, 0.63 +/- 0.06, and 5.75 +/- 0.12 piglets respectively. From a total of 2,436 liveborn piglets, 2,133 (87.56%) were weaned. The litter size at birth was similar to that previously reported for this strain of swine, whereas the litter size at weaning increased (P < 0.001) from 4.7 piglets during 1963 to 1965 to 5.8 piglets in our study. The average birth weight decreased (P < 0.001) from 0.90 kg in 1950 to 1952 and 0.72 kg in 1963 to 1965 to 0.59 kg in our study. Reproductive variables that had a considerable effect on the miniswine reproduction included month of parturition, age of sow, parity, and litter size. Primiparous sows had the smallest litter size and lowest number of weaned piglets. Sows during their second and third parity or sows between 2 and 4 years old had the best reproductive performances. Litter size and number of stillborn increased with parity and age of sow, resulting in fewer piglets weaned in older sows.(ABSTRACT TRUNCATED AT 250 WORDS)

Aging↗