<p>The aim was to characterize 100 coagulase positive staphylococci isolates originating from pig carcasses from Swedish slaughterhouses by biotyping, antibiotic susceptibility testing, typing with pulsed field gel electrophoresis (PFGE) and real-time PCR-screening of the enterotoxin genes sea, sec, seg and sei in order to evaluate the impact on human health. The biotyping classified 56 as non host specific (NHS), 29 as human biotype, five as poultry, one as ovine, one as bovine biotype and eight were unclassified (UCF). Susceptibility testing to 16 antibiotics revealed that 49% of the isolates were resistant to penicillin, which the biotype human dominated among these isolates. The results from the PFGE showed correlation between the biotypes and the pulsotypes obtained with several groups with identical strains. The results from the 47 isolates tested for enterotoxins were that the combination of seg and sei was the most common but sea and sec were also detected. There were slaughterhouses that had certain biotypes and penicillin resistance linked to them.</p>

Diabetes is a major health problem worldwide, and there is substantial interest in developing xenogeneic islet transplantation as a potential treatment. The potential to relieve the demand on an inadequate supply of human pancreata is dependent upon the efficiency of techniques for isolating and culturing islets from the source pancreata. Porcine islets are favored for xenotransplantation, but mature pigs (>2 years) present logistic and economic challenges, and young pigs (3-6 months) have not yet proven to be an adequate source. In this study, islets were isolated from 20 juvenile porcine pancreata (similar to 3 months; 25 kg Yorkshire pigs) immediately following procurement or after 24 h of hypothermic machine perfusion (HMP) preservation. The resulting islet preparations were characterized using a battery of tests during culture in silicone rubber membrane flasks. Islet biology assessment included oxygen consumption, insulin secretion, histopathology, and in vivo function. Islet yields were highest from HMP-preserved pancreata (2,242 +/- 449 IEQ/g). All preparations comprised a high proportion (>90%) of small islets (<100 mu m), and purity was on average 63 +/- 6%. Morphologically, islets appeared as clusters on day 0, loosely disaggregated structures at day 1, and transitioned to aggregated structures comprising both exocrine and endocrine cells by day 6. Histopathology confirmed both insulin and glucagon staining in cultures and grafts excised after transplantation in mice. Nuclear staining (Ki-67) confirmed mitotic activity consistent with the observed plasticity of these structures. Metabolic integrity was demonstrated by oxygen consumption rates=175 +/- 16 nmol/min/mg DNA, and physiological function was intact by glucose stimulation after 6-8 days in culture. In vivo function was confirmed with blood glucose control achieved in nearly 50% (8/17) of transplants. Preparation and culture of juvenile porcine islets as a source for islet transplantation require specialized conditions. These immature islets undergo plasticity in culture and form fully functional multicellular structures. Further development of this method for culturing immature porcine islets is expected to generate small pancreatic tissue-derived organoids termed "pancreatites," as a therapeutic product from juvenile pigs for xenotransplantation and diabetes research.

Doctor of Philosophy / Department of Diagnostic Medicine/Pathobiology / Raymond R. R. Rowland / Emerging viral diseases threaten the health of the US swineherd and have the potential to impact the industry. Parvoviruses are capable of infecting birds, livestock and humans, however, in swine, parvoviruses cause reproductive failure and contribute to a devastating set of diseases termed porcine circovirus associated disease (PCVAD). Here, a divergent porcine parvovirus, porcine parvovirus 7 (PPV7), distantly related to known parvovirus sequences, was identified in market pigs in the US. The PPV7 non-structural protein displayed 42.4% similarity to Eidolon helvum parvovirus 2 and 37.9% similarity to turkey parvovirus. Conserved parvovirus replicase motifs including three rolling circle replication (RCR), two NTP-binding motifs and a helicase- binding domain, were present in PPV7. Analysis by qPCR of 182 porcine samples found 16 (8.6%) positive, suggesting moderate nucleic acid prevalence in US swine. Paramyxoviruses are capable of infecting various species including cattle, pigs and humans, causing respiratory disease and importantly, can overcome species barriers causing disease. In 2013, a novel paramyxovirus sequence was described in Hong Kong, China in slaughterhouse pigs, and subsequently named porcine parainfluenza virus 1 (PPIV1). The second study identifies two complete PPIV1 genomes in US pigs originating in Oklahoma and Nebraska that display 90.0-95.3% identity to the Chinese strains. Molecular analysis by qPCR resulted in 6.1% prevalence in 279 porcine respiratory samples. Further serological analysis revealed 66.1% of 59 porcine sera samples were positive by PPIV1 F ELISA. Eleven 3-week old nursery pigs from a PPIV1 naturally infected herd were monitored for signs of infection. No clinical signs were seen in the animals, however, six pigs and the lungs of one animal tested qPCR positive by the conclusion of the study. Taken together, PPIV1 is moderately prevalent in US swine-herds. Previously known to infect avian species, canines and swine, recent reports have identified circoviruses in bats, mink, and human feces. In pigs, porcine circovirus 2 (PCV2) is essential to PCVAD, a group of diseases including reproductive failure, respiratory disease complex (PRDC), porcine dermatitis and nephropathy syndrome (PDNS) and postweaning multisystemic wasting syndrome (PMWS). Additionally, PCV2 nucleic acid has been detected in mammalian species other than swine such as cattle and mink. The final study focuses on the identification and characterization of a divergent circovirus, porcine circovirus 3, identified in aborted mummies taken from sows displaying clinical and histological signs of PDNS. Putative capsid and replicase open reading frames display 37% and 55% identity to PCV2, respectively. A retrospective study of 48 PDNS cases, PCV2 negative by immunohistochemistry (IHC), identified 45 positive and 60% of a subset, positive for PCV3 by IHC. Molecular and serological prevalence studies revealed 12.5% nucleic acid and 55% antibody prevalence in US swine samples. Collectively, these studies identify emerging porcine viruses with the potential to cause disease using metagenomic sequencing. The results of these studies will help to mitigate the risk attributed to emerging swine viruses causing disease outbreaks.

As lesões cutâneas e queimaduras são considerados os principais causadores de danos e perdas dos tecidos moles. Em casos severos de trauma, os processos naturais de regeneração são insuficientes no reparo dos danos, resultando em lesões cutâneas crônicas. A desvitalização de matrizes homólogas ou heterólogas é uma alternativa para a produção de matrizes dérmicas. A pele porcina é bastante similar à pele humana, podendo ser utilizada como matriz de colágeno na regeneração de tecido mole. Além disso, ela tem como constituinte principal o colágeno tipo I, e, assim, pode ser utilizada em queimaduras de segundo grau. Este trabalho teve como objetivo a preparação e caracterização de matrizes extracelulares de colágeno tipo I por meio de hidrólise alcalina e reticulação com glutaraldeído (GA). As matrizes de colágeno foram obtidas a partir da hidrólise alcalina de pele porcina, com posterior reticulação com GA, em diferentes concentrações (0-0,1%) e tempos de reação (15 e 45 min). As matrizes foram caracterizadas através de determinação do conteúdo de elastina, estabilidade biológica (tripsina), Calorimetria Exploratória Diferencial (DSC), termogravimetria (TG/DTG), Microscopia Eletrônica de Varredura (MEV) e citotoxicidade in vitro. Através da determinação do conteúdo de elastina, foi possível determinar a massa média de colágeno presente nas matrizes, a qual foi de 95,2?0,2% (m/m), e a massa média de elastina, que foi de 4,8?0,2% (m/m), e também verificar que independente do tratamento, a elastina estava presente nas matrizes. O ensaio de estabilidade biológica mostrou que o tratamento com GA diminui a biodegradação do material; sendo obtidos porcentagens de degradação que variaram de 83,6%?1,1 (0% GA) a 46,1%?0,7 (0,085%-45min), indicando, assim, que com o aumento da concentração de GA e do tempo de reação, há uma diminuição da porcentagem de degradação. Pela análise termogravimétrica, foi observado que o colágeno presente nas matrizes tornou-se mais estável termicamente em conseqüência do aumento do grau de reticulação e, portanto, mais resistentes à degradação térmica. Os resultados de DSC confirmam os de termogravimetria devido ao aumento nos valores das temperaturas de desnaturação das matrizes em função do aumento do tempo de reação e da concentração de GA. Pela análise das fotomicrografias, pôde ser observado que após a reticulação com GA, as fibras de colágeno tornam-se mais organizadas e definidas; e essa definição torna-se maior com o aumento da concentração de GA. Os resultados de citotoxicidade in vitro mostraram que as matrizes analisadas são citotóxicas possivelmente devido a gordura remanescente, sendo necessário a realização de um pré-tratamento. Assim, a preparação de matrizes derivadas de pele porcina com diferentes tempos de degradação, as quais podem ser utilizadas na reconstrução de tecidos moles, é viável. / Cutaneous lesions and burns are considered the main causes of damage of soft tissues. In severe cases of trauma, the natural processes of regeneration are insufficient in the repair of the damage, resulting in chronic cutaneous lesions. Desvitalization of homologous or heterologous matrices is an alternative for the production of dermal matrices. The porcine skin is quite similar to the human skin and can be used as collagen matrix in soft tissue regeneration. Besides, it contains type I collagen as the main constituent and thus, it can be used in second degree burns. The objective of this work was the preparation and characterization of type I collagen extracellular matrices with alkaline hydrolysis and glutaraldehyde (GA) crosslinking. The collagen matrices were obtained from the alkaline hydrolysis of porcine skin, with subsequent GA crosslinking, in different concentrations (0 - 0,1%) and reaction time (15 and 45 min). Matrices were characterized by determination of the elastin content, biological stability (trypsin), differential scanning calorimetry (DSC), termogravimetry (TG/DTG), scanning electron microscopy (SEM) and a preliminar assay of in vitro cytotoxicity. Elastin and collagen content were 4,8±0,2% (m/m) and 95,2±0,2% (m/m), respectively. Biological stability results showed that GA crosslinking reduces matrix biodegradation; as degradation varied from 83,6%±1,1 (0% GA) to 46,1%±0,7 (0,085% - 45min), demonstrating, thus, that with the increase of GA concentration and reaction time, there was a decrease of degradation. For termogravimetric analysis it was observed that the collagen present in the matrices become termically more resistant as a consequence of the increasing crosslink degree and, therefore, more resistant to thermal degradation. DSC results, similar to termogravimetric ones, showed an increase in denaturation temperatures as a function of increasing reaction time and GA concentration. SEM analysis showed that after the GA crosslinking, collagen fibers become more organized and defined; and that definition improved with increasing GA concentration. Preliminar assay of in vitro cytotoxicity showed that treated matrices are cytotoxic possibly due to remaining fat, being necessary the accomplishment of a pre-treatment. Therefore, porcine skin matrices preparation with different degradation times, which can be used in the soft tissue reconstruction, are viable.

A utilização e o desenvolvimento de biomateriais para a regeneração tecidual são de grande importância, principalmente para a área médica e odontológica. Matrizes de colágeno derivadas de tecidos de origem animal são utilizadas devido o colágeno apresentar características como biodegradabilidade e biocompatibilidade. Essas matrizes podem ser obtidas a partir de várias fontes, sendo uma delas o pericárdio porcino, que apresenta vantagens como grande disponibilidade, baixo custo, fácil obtenção e possibilidade de sofrer modificações químicas. Além disso, tecidos de origem suína são muito similares aos tecidos humanos, podendo ser utilizados para a produção de biomateriais para a regeneração de tecido mole. Este trabalho teve como objetivo a preparação de membranas acelulares derivadas de pericárdio porcino por hidrólise alcalina em diferentes tempos, para posterior utilização em engenharia de tecido. As membranas de colágeno foram obtidas por hidrólise alcalina de pericárdio porcino durante 4, 8, 12 e 24 h e caracterizadas por análise histológica, microscopia eletrônica de varredura (MEV), avaliação da citoxicidade in vitro, estabilidade biológica in vitro (colagenase), titulação potenciométrica, porcentagem de absorção de água, calorimetria exploratória diferencial (DSC), termogravimetria (TG), análise térmica dinâmico-mecânica (DMTA) e ensaios de tração. A análise histológica mostrou que após 4h de hidrólise as células foram removidas das membranas. A avaliação da citotoxicidade in vitro mostrou que as membranas preparadas neste trabalho não são citotóxicas. Os ensaios de estabilidade biológica in vitro por colagenase mostraram que as membranas hidrolisadas degradaram mais rapidamente que a não hidrolisada e, quando comparadas com matrizes derivadas de pericárdio bovino, as derivadas de pericárdio porcino foram mais resistentes à degradação por colagenase. A titulação potenciométrica possibilitou determinar o número de grupos carboxílicos das membranas e o incremento desses grupos por molécula de colágeno. Os resultados mostraram que houve um aumento no número de grupos carboxílicos tituláveis nas membranas hidrolisadas e, consequentemente, houve um aumento do número de cargas negativas incorporadas na molécula de colágeno. As membranas hidrolisadas apresentaram uma maior absorção de água, uma diminuição das temperaturas de desnaturaçãoe e menor estabilidade térmica em função do aumento do tempo de hidrólise. Os ensaios de tração mostraram que após a hidrólise alcalina as membranas apresentaram maiores valores de resistência à tração e que a deformação é dependente do tempo de hidrólise alcalina. Esses resultados mostraram que a preparação de membranas de colágeno derivadas de pericárdio porcino com diferentes tempos de hidrólise alcalina é um procedimento viável para ser utilizado na produção de biomateriais para engenharia de tecido. / The use and development of biomaterials for tissue regeneration are of great importance, especially for medical and dental care. Collagen matrices derived from animal tissues are widely used because collagen has characteristics such as biodegradability and biocompatibility. These matrices can be obtained from various sources, such as porcine pericardium, which is a tissue that can be used due its low cost, wide availability and because it can be chemically modified. Besides, porcine tissues are very similar to human tissue and can be used to produce biomaterials for soft tissue regeneration. The aim of this study was the preparation and characterization acellular membranes by alkaline hydrolysis of porcine pericardium. Membranes were characterized by histological analysis, scanning electron microscopy (SEM), in vitro cytotoxicity evaluation, in vitro biological stability (collagenase), potentiometric titration, water absorption percentage, differential scanning calorimetry (DSC), thermogravimetry (TG), dynamic mechanical thermal analysis (DMTA) and tensile tests. Histological analysis showed that after 4h of hydrolysis, cells were totally removed from matrices. In vitro cytotoxicity showed that all matrices prepared in this work are not cytotoxic. In vitro biological stability tests (collagenase) showed that the hydrolyzed membranes degraded more quickly than the non hydrolized matrix and more resistant to collagenase degradation when compared to matrices derived from bovine pericardium. The potentiometric titration allowed the determination carboxylic groups and the increase of these groups per collagen molecule. Hydrolyzed matrices had an increase in water absorption, a decrease in denaturation temperature and a small decrease in thermal stability with the increase of hydrolysis time. Tensile tests showed that after alkaline hydrolysis matrices showed higher tensile strength and the deformation was independent of the time of alkaline hydrolysis. These results showed that the preparation of collagen biological matrices derived from porcine pericardium with different times of alkaline hydrolysis is a viable procedure to be subsequently used in the production of biomaterials for tissue engineering.

Porcine Reproductive and Respiratory Syndrome (PRRS) is, globally, one of the costliest of diseases to the pig industry. Despite enormous efforts, methods such as vaccination strategies and herd management have failed to fully control the disease. Exploiting the genetic variation in host response could be included as part of a multifaceted approach to mitigate the devastating impact of this disease. Establishing the presence of genetic variation and its underlying genetic architecture are key to implementing genomic selection, which is considered a viable and safe long-term disease control strategy. This thesis explores the effect of natural PRRSV outbreaks on the reproductive performance of sows, and the underlying genetic influences on it. Litter records were available from two farms, where Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) outbreaks had been confirmed using ELISA. One farm had full pedigree information, but for both farms 60K SNP genotypes were available. In both farms, performance records could be partitioned into an epidemic and non-epidemic phase using a previously established threshold method. The partitioning also identified a period of high reproductive failure not coinciding with a diagnosed PRRSV outbreak on one farm. This period was isolated and analysed separately. Linear mixed models were used to explore both genetic and non-genetic factors contributing to differences in reproductive performance associated with the two phases. This analysis identified five disease indicator traits identified showing significant differences (>95% CI) in least squares means between the epidemic and non-epidemic phase. These were the number of mummified, stillborn, dead and alive piglets per litter and the fraction of the total born dead. Alternative statistical models that accounted for differences in the severity of the individual PRRSV outbreaks were also considered throughout. Despite differences in the estimates associated with different models and farms, in general very low heritability estimates were obtained for these disease indicator traits during the non-epidemic phase, whereas the traits were found moderately heritable during the epidemic phase. Two genome wide association analyses methods were used to explore the distribution of the genetic effects throughout the genome: Family-based Score Test for Association (FASTA) and Genome-wide Rapid Analysis using Mixed Model and Regression (GRAMMAR). In addition, regional associations were studied using Regional Heritability Mapping (RHM). Associations were then further characterised using Measured Genotype (MG) analyses. Genome-wide significant associations were identified for five SNPs and one region. The regional association spans the region previously identified in an experimental challenge experiment of growing pigs, in association with viral load and weight gain. Different patterns of linkage disequilibrium (LD) are observed which may explain why this study and others failed to find single SNP effects at this location. One genome wide significant SNP on SSC15 was found between two previously identified SNPs associated with PRRSV mortality. Five further putative SNP associations are indicated by RHM and subsequent measured genotype analysis, two of which flank previously reported associations and indicate an epistatic effect, observed in several traits. In summary, this study showed that reproductive performance of sow is considerably reduced during PRRSV outbreaks and the genetics of the sow significantly affects variance in survival and mortality. Several novel genomic regions associated with the reproductive performance of sows in the absence and during PRRSV outbreaks have been identified in this study. In addition to these, the results suggest the region on SSC4 previously associated with PRRSV viral load and weight gain may also affect foetal mortality. These results demonstrate the potential for genomic selection to be used to mitigate PRRSV related reproductive losses, the greatest financial exposure faced by the pig industry. In addition, RHM is directly shown to capture genetic variance, where single SNP methods fail to identify an effect, highlighting the usefulness of this tool as a method to identify genomic regions with significant effect on production traits.

These studies were conducted to examine the influence of several variables on the growth hormone binding protein (GHBP) in serum of pigs. Continuous long term porcine somatotropin (pST) injections (daily for 6-7 wk) increased GHBP activity (p < .05). However, periodic short term pST injections (daily, every second d or every fourth d for 2 wk) did not cause significant change in GHBP levels (p > .40). No difference was observed between fed animals and animals fasted for 5 days (p > .3). Between 0 and 6 mo of age boar and gilt serum GHBP activity were not significantly different from each other, but increased significantly with age in both sexes(p < .0001). There was no significant correlation between serum GHBP and body weight in this study (p > .30). In pregnant sows, GHBP concentrations were highest at the beginning (day 72) of the third trimester (p< .05). These values were compared with information in the literature on serum growth hormone (GH) concentrations and GH receptor activity under similar conditions. Growth hormone receptor activity reported by other researchers and GHBP activity appear to vary concurrently except during fasting which may indicate alternate regulation of either the GHBP or the GH receptor. / Graduation date: 1992

Alors que les biologistes moléculaires poursuivent les travaux de transgénèse animale depuis plusieurs décennies déjà et que des instances réglementaires américaines et canadiennes étudient actuellement la possibilité d'introduire sur le marché des animaux transgéniques destinés à l'alimentation, force est de constater que très peu de travaux en sciences de l'environnement menés dans une perspective globale santé et société permettent d'appréhender la genèse, les enjeux et les impacts de l'introduction éventuelle d'animaux transgéniques de boucherie dans les cheptels et donc dans l'environnement et dans les assiettes. Notre étude porte plus spécifiquement sur l'introduction éventuelle de porcs transgéniques censée remédier aux problèmes de surplus de phosphore résultant de certaines stratégies d'intensification croissante de la production porcine. Bien que ce mémoire ne soit pas centré sur l'analyse politique et économique de la production porcine au Québec, c'est néanmoins dans ce contexte que nous examinerons cette application de la transgénèse animale en agriculture et les stratégies de légitimation dont on tente d'enrober ces développements sociotechniques. Le porc transgénique hypophosphorique en question, nommé Enviropig™ permettrait, selon ses promoteurs, d'atténuer certains impacts environnementaux associés au surplus de phosphore ingéré et rejeté par les bêtes dans leurs excréments, désormais gérés sous forme de lisiers. Techniquement, les glandes salivaires de certains de ces porcs transgéniques peuvent produire une enzyme appelée phytase permettant la digestion puis l'absorption du phosphore alimentaire diminuant alors le contenu en phosphore de certains de ces porcs de 56 à 75% dans les matières fécales. Dans un contexte où la mesure des types et des niveaux de risques que représente la transgénèse pour la santé environnementale, humaine et animale ne fait pas consensus au sein de la communauté scientifique, il nous est apparu essentiel, en l'absence manifeste de contre-expertise indépendante, d'examiner si un tel porc est compatible avec une agriculture durable dont se réclame cet « Enviropig™ ». Ainsi, suite à une vaste revue de littérature, en s'inspirant des approches écosanté et cycle de vie, nous analysons certains risques associés à un tel porc transgénique susceptibles de toucher plus largement d'autres d'animaux de boucherie transgéniques, tout en identifiant les principaux impacts sur la production porcine. Notre analyse porte également sur les zones d'ombre des dispositifs d'évaluations scientifiques et des politiques publiques dans le domaine. En examinant cette question de l'introduction du porc transgénique, dans le contexte global des pratiques d'élevage de ce secteur agro-industriel très concentré et dominé par quelques grands intégrateurs et multinationales de la transformation, nous mettrons également en évidence le caractère peu viable d'une telle stratégie. ______________________________________________________________________________ MOTS-CLÉS DE L’AUTEUR : Transgénèse, Porc transgénique, Production porcine, Élevage et agriculture durable, Développement durable, Risques, Politiques publiques, Approche écosanté.

To investigate the physiological action of follistatin in the swine ovary a recombinant porcine follistatin (rpFS) with apparent molecular weights of 39, 46, 48, and 50 kDa was expressed and characterized. The rpFS crossreacted with antibodies against native porcine follistatin and with activin A. One rpFS isotype was purified by monoclonal antibody affinity chromatography (rp-305 a.a. FS). In porcine granulosa cell cultures, rp-305 a.a. FS suppressed estradiol-17<math> <f> <g>b</g></f> </math> accumulation (ED50 = 0.9 <math> <f> <g>m</g></f> </math>g/ml) independent of activin. Gilts were vaccinated against rpFS to determine the effect of follistatin immunoneutralization on litter size or ovulation rate. In Experiment 1, forty-seven gilts were vaccinated four times with rpFS (FS n = 23) or with a control vaccine (CTL n = 24). The naturally matured, cycling gilts were bred and piglet numbers were recorded at farrowing. FS vaccination did not increase total litter size. However, grouping by low (<math> <f> <=</f> </math>1:400 n = 16) or high anti-follistatin antibody titer (>1:400 n = 7) responses showed an increased litter size in gilts with a high titer (total piglets: FS high titer = 13.0 ± 0.8; FS low titer = 10.8 ± 0.6; CTL 11.4 ± 0.5; p = 0.08). In Experiment 2, sixty-nine gilts were vaccinated three times with rpFS (n = 35) or CTL (n = 34) vaccines. The gilts were induced and synchronized into estrus using PG600, <math> <f> <rm>PGF<inf>2<g>a</g></inf></rm></f> </math> and boar exposure; cycling gilts received a fourth vaccination. Reproductive tracts were collected two weeks after the second observed estrus (FS n = 14, CTL n = 15). FS vaccination did not increase the number of corpora lutea (FS = 13.2 ± 0.5, CTL = 14.5 ± 0.7) or corpora albicantia (FS = 12.1 ± 1.9, CTL = 12.3 ± 2.0), but appeared to effect normal ovarian morphology increasing the number of blood-filled follicles and corpora lutea. In conclusion, rp-305 a.a. FS appears to negatively affect estradiol accumulation 'in vitro'. Vaccination against follistatin in naturally cycling gilts enhanced litter size. Follistatin vaccination of pharmacologically induced gilts did not increase ovulation rate, but biological effects were apparent suggesting that pharmacological induction of estrus may have confounded the follistatin vaccination treatment.

The aim was to characterize 100 coagulase positive staphylococci isolates originating from pig carcasses from Swedish slaughterhouses by biotyping, antibiotic susceptibility testing, typing with pulsed field gel electrophoresis (PFGE) and real-time PCR-screening of the enterotoxin genes sea, sec, seg and sei in order to evaluate the impact on human health. The biotyping classified 56 as non host specific (NHS), 29 as human biotype, five as poultry, one as ovine, one as bovine biotype and eight were unclassified (UCF). Susceptibility testing to 16 antibiotics revealed that 49% of the isolates were resistant to penicillin, which the biotype human dominated among these isolates. The results from the PFGE showed correlation between the biotypes and the pulsotypes obtained with several groups with identical strains. The results from the 47 isolates tested for enterotoxins were that the combination of seg and sei was the most common but sea and sec were also detected. There were slaughterhouses that had certain biotypes and penicillin resistance linked to them.