<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>44</volume><submitter>Crombe F</submitter><pubmed_abstract>At present, the immune response of pigs in relation to Staphylococcus aureus carriage is poorly understood. This study was aimed at investigating the dynamics of the anti-staphylococcal humoral immune response in methicillin-susceptible S. aureus (MSSA)-positive piglets and at assessing the effect of the experimental introduction of a methicillin-resistant S. aureus (MRSA) Sequence Type (ST) 398 strain. Therefore, serum samples were collected at different times from 31 weaned piglets originating from four different sows. Twenty-four out of the 31 piglets were challenged with MRSA ST398. The serum samples were analyzed for IgG antibodies to 39?S. aureus antigens, using a multiplex bead-based assay (xMAP technology, Luminex Corporation). Though antibody responses showed broad inter-individual variability, serological results appeared to be clustered by litter of origin. For most antigens, an age-related response was observed with an apparent increase in antibody titers directed against staphylococcal microbial surface components recognizing adhesive matrix molecules (MSCRAMM), which have been shown to play a role in S. aureus colonization. In most animals, antibody titers directed against staphylococcal toxins or immune-modulating proteins decreased with age, possibly reflecting the absence of bacterial invasion. The introduction of MRSA ST398 did not elicit a significant humoral immune reaction.This study describes, for the first time, the humoral immune response in weaned pigs colonized with S. aureus.</pubmed_abstract><journal>Veterinary research</journal><pagination>4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3558462</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Serological profiles in nursery piglets colonized with Staphylococcus aureus.</pubmed_title><pmcid>PMC3558462</pmcid><pubmed_authors>Van Wamel WJ</pubmed_authors><pubmed_authors>Barbe K</pubmed_authors><pubmed_authors>Butaye P</pubmed_authors><pubmed_authors>Haesebrouck F</pubmed_authors><pubmed_authors>Crombe F</pubmed_authors><pubmed_authors>de Vogel CP</pubmed_authors><pubmed_authors>Hermans K</pubmed_authors><pubmed_authors>Vanderhaeghen W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serological profiles in nursery piglets colonized with Staphylococcus aureus.</name><description>At present, the immune response of pigs in relation to Staphylococcus aureus carriage is poorly understood. This study was aimed at investigating the dynamics of the anti-staphylococcal humoral immune response in methicillin-susceptible S. aureus (MSSA)-positive piglets and at assessing the effect of the experimental introduction of a methicillin-resistant S. aureus (MRSA) Sequence Type (ST) 398 strain. Therefore, serum samples were collected at different times from 31 weaned piglets originating from four different sows. Twenty-four out of the 31 piglets were challenged with MRSA ST398. The serum samples were analyzed for IgG antibodies to 39?S. aureus antigens, using a multiplex bead-based assay (xMAP technology, Luminex Corporation). Though antibody responses showed broad inter-individual variability, serological results appeared to be clustered by litter of origin. For most antigens, an age-related response was observed with an apparent increase in antibody titers directed against staphylococcal microbial surface components recognizing adhesive matrix molecules (MSCRAMM), which have been shown to play a role in S. aureus colonization. In most animals, antibody titers directed against staphylococcal toxins or immune-modulating proteins decreased with age, possibly reflecting the absence of bacterial invasion. The introduction of MRSA ST398 did not elicit a significant humoral immune reaction.This study describes, for the first time, the humoral immune response in weaned pigs colonized with S. aureus.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Jan</publication><modification>2021-02-21T07:28:05Z</modification><creation>2019-03-27T01:04:02Z</creation></dates><accession>S-EPMC3558462</accession><cross_references><pubmed>23339425</pubmed><doi>10.1186/1297-9716-44-4</doi></cross_references></HashMap>