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1.
Vet Parasitol ; 223: 153-8, 2016 Jun 15.
Article in English | MEDLINE | ID: mdl-27198794

ABSTRACT

Haemonchus contortus (H. contortus) is a haematophagous parasite which causes important economic losses in small ruminants. On the island of Gran Canaria, two sheep breeds coexist which differ in their susceptibility to the infection with H. contortus; the resistant Canaria Hair Breed (CHB) sheep and the susceptible Canaria Sheep (CS) breed. The major target of resistance mechanisms in CHB sheep are directed to the adult parasite stage, reducing the worm burden, and decreased length and fecundity of surviving worms. Mucosal IgA (mIgA) has been shown to be an important regulator of immunity in Haemonchus and Teladorsagia infections; through correlations with larval stages where such mechanisms as antibody-dependent cell cytotoxicity and enzyme inhibition may mediate resistance. Here for the first time, we demonstrate a significant negative correlation between mIgA and adult worm length and fecundity only in the resistant CHB sheep. In contrast, and as reported in other sheep breeds, mIgA was only negatively correlated against the larval stage in the more susceptible CS breed. This study suggests mIgA may play a role in resistance to both larval and adult stages.


Subject(s)
Haemonchiasis/veterinary , Haemonchus/classification , Immunoglobulin A/metabolism , Intestinal Mucosa/metabolism , Sheep Diseases/parasitology , Animals , Haemonchiasis/immunology , Haemonchiasis/parasitology , Intestinal Mucosa/parasitology , Sheep , Sheep Diseases/immunology
2.
J Comp Pathol ; 154(2-3): 165-8, 2016.
Article in English | MEDLINE | ID: mdl-26922858

ABSTRACT

Mycoplasma hyopneumoniae (Mh) is a bacterium that specifically infects the surface of bronchi and bronchioles of pigs without invading the host cells, and it is considered to be the primary agent of porcine enzootic pneumonia (PEN). The present study investigates the morphological and immunohistological changes induced in bronchiolar epithelium by Mh infection. Lungs from 20 pigs with naturally occurring Mh pneumonia were compared with those from 10 uninfected controls. Bronchiolar epithelial height, inflammatory infiltration, hyperplasia of bronchus-associated lymphoid tissue (BALT) and mucin subtype MUC5AC-producing cells significantly increased in all infected animals. Mh antigen was detected in association with the cilia of the bronchial and bronchiolar epithelium. Interleukin (IL)-5 and IL-13 were expressed consistently by epithelial and mononuclear cells of the airways of infected animals. The expression of these cytokines in the bronchial and bronchiolar tissues is related to the histological changes of PEN.


Subject(s)
Interleukin-13/biosynthesis , Interleukin-5/biosynthesis , Pneumonia of Swine, Mycoplasmal/metabolism , Pneumonia of Swine, Mycoplasmal/pathology , Respiratory Mucosa/metabolism , Animals , Bronchioles/metabolism , Bronchioles/pathology , Immunohistochemistry , Mycoplasma hyopneumoniae , Respiratory Mucosa/pathology , Sus scrofa , Swine
3.
Parasite Immunol ; 33(7): 401-10, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21585398

ABSTRACT

Malaria caused by Plasmodium falciparum is a major cause of global infant mortality, and there is currently no licensed vaccine that provides protection against infection or disease. Several P. falciparum vaccine targets have undergone early testing, but many more candidates remain with little data to support their development. Plasmodium falciparum Merozoite Surface Protein 6 (PfMSP6) is a candidate of particular interest because it is a member of the PfMSP3 multi-gene family, raising the possibility that vaccine-induced immune responses could cross-react across multiple family members. However, few immunoepidemiological studies of PfMSP6 have been carried out to measure domain-specific anti-PfMSP6 responses. This study investigated anti-PfMSP6 responses in P. falciparum-infected individuals from the Peruvian Amazon, using two different PfMSP6 N-terminal allele antigens and a single C-terminal domain antigen, and compared the responses with both PfMSP6 genotyping data and anti-PfMSP3 response data that had been previously generated for the same samples. Anti-PfMSP6 responses were detected despite the low transmission setting, but were less frequent and of considerably lower intensity than anti-PfMSP3 responses. There was a positive correlation between anti-PfMSP3 and PfMSP6 responses, suggesting that the possibility that PfMSP3 family antigens could induce cross-reactive responses requires further detailed investigation.


Subject(s)
Antibodies, Protozoan/blood , Antigens, Protozoan/immunology , Malaria, Falciparum/epidemiology , Malaria, Falciparum/immunology , Membrane Proteins/immunology , Plasmodium falciparum/immunology , Protozoan Proteins/immunology , Antigens, Protozoan/genetics , Cross Reactions , Enzyme-Linked Immunosorbent Assay , Humans , Immunoglobulin G/blood , Membrane Proteins/genetics , Peru/epidemiology , Plasmodium falciparum/genetics , Protozoan Proteins/genetics , Seroepidemiologic Studies
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