Vaccination against ETEC in pigs

Enterotoxigenic Escherichia coli (ETEC) that bear F4 fimbriae on their surface (F4+ ETEC) are a major cause of postweaning diarrhoea (PWD) in pigs. The F4 fimbriae enable the bacteria to colonize the small intestine and subsequently, to produce enterotoxins causing diarrhoea. Consequently, an F4-specific secretory IgA response at the intestinal mucosa that neutralizes the fimbriae is desired for protection against postweaning diarrhoea

Maltose-binding protein is a potential carrier for oral immunizations

In humans and most animal species such as pigs, vaccination via the oral route is a prerequisite for induction of a protective immunity against enteropathogens. Hereto, live attenuated microorganisms can be used. However, these microorganisms often are either too attenuated to induce sufficient intestinal immunity or are still too virulent resulting in clinical signs. We previously demonstrated that it is possible to induce immunity against enteropathogens by targeting antigen towards enterocytes. Maltose-binding protein (MBP) is part of the maltose/maltodextrin system of Escherichia coli. MBP is a relatively small protein (42.5 kDa) approximately 3 × 4 × 6.5 nm in size with surface residues capable of both hydrogen bonding interactions and hydrophobic interactions. Recombinant proteins are often fused to MPB to improve their yield and to increase their solubility. In mice, these fusion proteins showed an enhanced immunogenicity following systemic immunization. More recently, this has been attributed to interaction of MBP with TLR4 on dendritic cells (DCs). TLR4 is also expressed in the enterocytes of the gut. Therefore, we examined if oral administration of MPB-FedF to 4-week-old pigs could be used to induce an immune response against F18+ verotoxigenic E. coli in pigs. Also we examined if the oral administration of MBP to pigs is able to induce an immune response. In both experiments cholera toxin was used as oral adjuvant

Evaluation of parasite antigens in Elisa for the detection of toxoplasma infection in pigs

One-third of the human world population is infected with the protozoan parasite Toxoplasma gondii Toxoplasmosis is an old disease but is still very underreported and neglected disease

The adjuvant effect of Gantrez®AN nanoparticles on oral vaccination of pigs and mice with F4 fimbriae is strongly influenced by polymer degradation

We analysed the adjuvant effect of Gantrez nanoparticles NP on oral immunisation of pigs and mice with F4 fimbriae. The animals were vaccinated with F4, F4 encapsulated in Gantrez NP, called gF4 NP, or F4 + empty Gantrez NP, called F4 + gNP, and intragastrically infected with F4+ ETEC. The adjuvant effect of Gantrez®AN nanoparticles on oral vaccination of pigs and mice with F4 fimbriae is strongly influenced by polymer degradation

T. gondii strains and their dosage influence the parasitic load in tissues of experimentally infected pigs

One of the major routes of a Toxoplasma gondii infection in humans is the consumption of raw or undercooked meat. In the present study, we compared the parasitic load induced by 2 different T. gondii strains in the tissues of experimentally infected 6 weeks old pigs. In the first experiment, pigs were orally infected with 3000 tissue cysts of IPB-Gangji strain. The pigs were euthanized 2 and 6 months after infection, and the following samples were tested by bio-assay and qPCR: brain, heart and several skeletal muscles. Two months after infection, all samples tested positive with both tests. Remarkably, after 6 month no cysts were detected in tenderloin and ham, while brain and heart tissue remained infectious. In the second experiment, pigs were infected orally with a low (700 cysts) and a high (6000) dose of T. gondii IPB-Gangji cysts and euthanized after 4 months. The parasitic load was much higher in the low dose group than in the high dose group, as determined by qPCR. In most animals various samples tested negative in both groups, with the exception of the intercostals muscles. Last experiment was repeated with a low and a high dose of the T. gondii IPB-LR strain. Here, all samples remained infectious with no significant difference in parasitic load between both groups. The parasitic load was higher in brain and heart tissue compared to the skeletal muscles. In bio-assay, numerous mice died from the inoculated samples from pigs infected with the IPB-Gangji strain. Ascites and lungs tested T. gondii positive by qPCR. When inoculated with samples from pigs infected with the IPB-LR strain, no mice died from acute T. gondii infection