ABSTRACT
Mastitis, an inflammation of the mammary gland affecting milk production and quality in dairy herds, is often associated with Staphylococcus spp. in goats. Neutrophils are crucial in combating infections by migrating into milk and deploying various defense strategies, including the release of neutrophil extracellular traps (NETs) composed of DNA, histones, and bactericidal proteins. This study investigated whether NETs are released by goat neutrophils stimulated in vitro by Staphylococcus aureus and Staphylococcus warneri, two common pathogens of goat mastitis. PMNs were isolated from blood from healthy adult goats. We evaluated goat NET formation by stimulating cells with: phorbol 12-myristate 13-acetate (PMA) as a positive control, cytochalasin for inhibition of actin polymerization, S. aureus, and S. warneri. NET formation was observed in response to chemical stimulation and bacterial presence, effectively trapping pathogens. Variations in NET formation between S. aureus and S. warneri suggest pathogen-specific responses. These findings suggest that the formation of NETs may be an important complementary mechanism in the defense against mastitis in goats. In conclusion, this study unveils a novel defense mechanism in goats, indicating the role of NETs against S. aureus and S. warneri in mastitis.
Subject(s)
Extracellular Traps , Goat Diseases , Goats , Mastitis , Neutrophils , Staphylococcal Infections , Staphylococcus aureus , Animals , Goats/immunology , Extracellular Traps/immunology , Female , Mastitis/veterinary , Mastitis/immunology , Mastitis/microbiology , Goat Diseases/immunology , Goat Diseases/microbiology , Neutrophils/immunology , Staphylococcus aureus/immunology , Staphylococcal Infections/veterinary , Staphylococcal Infections/immunology , Staphylococcus/immunologyABSTRACT
This study evaluated the effects of injectable trace minerals (ITM) on antioxidant and immune response, resistance to endoparasites, health and growth of newborn Boer kids. Forty-six Boer kids [24 males and 22 females; 3.94±1.03kg of body weight (BW); 6.2±2.4 d of age] were enrolled in the study. Kids were stratified by type of birth (twins or singlet), sex, and BW and assigned to 1 of 2 treatments: one subcutaneous injection (0.1mL/4.5kg of BW) of (1) saline solution or (2) ITM (60, 10, 5, and 15mg/mL of Zn, Mn, Se and Cu, respectively). Blood samples were collected on d 0, 7, 14, 28 and 56. Feces samples were collected on d 56 and BW on d 0, 28 and 56. Kids were checked daily for signs of diarrhea. ITM kids had greater (P<0.01) plasma concentration of superoxide dismutase and tended (P=0.06) to have greater plasma concentration of glutathione peroxidase. ITM kids had greater (P=0.05) concentration of eosinophils, but no differences (P≥0.11) were observed for other hemogram variables. The ITM application did not affect (P≥0.11) the EPG count. However, ITM kids had less (P=0.02) cumulative incidence of diarhea until d 42 (3.85 vs. 25.93±6.8% for ITM vs. Saline kids, respectively) but no differences (P>0.10) were observed after d 42. The ITM application did not affect (P≥0.40) the growth of kids (0.071 vs. 0.065±0.005kg/day for ITM vs. Saline kids, respectively). Thus, the ITM application, increased the plasma concentration of antioxidant enzymes and eosinophils, decreased the incidence of diarrhea only in the middle of the experiment, but did not affected the EPG count and growth of Boer kids.(AU)
Este estudo avaliou os efeitos de microminerais injetáveis (ITM) na resposta antioxidante e imune, resistência a endoparasitas, saúde e crescimento de cabritos Boer recém-nascidos. Quarenta e seis cabritos [24 fêmeas e 22 machos; 3,94±1,03kg de peso corporal (PC); 6,2±2,4 dias de idade] foram incluídos no estudo. Os animais foram estratificados por tipo de nascimento (gêmeos ou singular), sexo e peso ao nascimento (PN) e atribuídas a 1 de 2 tratamentos. Uma injeção subcutânea (0,1ml/4,5 de PC de (1) Solução salina ou (2) ITM (60,10,5 e 15mg/ml de Zn, Mn, Se e Cu, respectivamente). As amostras de sangue foram coletadas nos dias 0, 7, 14, 28 e 56. As amostras de fezes foram coletadas no dia 56 e PC nos dias 0, 28 e 56. Os recém-nascidos foram verificados diariamente quanto a sinais de diarreia. Os cabritos ITM apresentaram maior (P<0.01) concentração de superóxido desmutase no plasma e tenderam (P=0,06) a ter maior concentração de glutationa peroxidase no plasma. Os animais ITM apresentaram maior (P=0,05) concentração de eosinófilos, mas não foram observadas diferenças (P≥0.11) para outras variáveis do hemograma. A aplicação de ITM não afetou (P≥0.11) a contagem de EPG. No entanto, os cabritos ITM apresentaram menor incidência cumulativa de diarreia (P=0,02) ate d 42 (3,85 vs. 25,93±6,8% para animais ITM vs. animais salina, respectivamente), mas nenhuma diferença (P>0.10) foi observada após d 42. A aplicação do ITM não afetou (P≥0.40) o crescimento dos animais (0.071 vs. 0.065±0.005kg/dia para ITM vs. Salina, respectivamente). Assim, a aplicação do ITM aumentou a concentração plasmática de enzimas antioxidantes e eosinófilos, diminuiu a incidência de diarreia somente na metade do experimento, mas não afetou a contagem de OPG e crescimento de cabritos Boer recém-nascidos.(AU)
Subject(s)
Animals , Infant, Newborn , Superoxide Dismutase , Goats/immunology , Enzymes , Glutathione Peroxidase , Injections , Antioxidants , Body Weight , Parturition , DiarrheaABSTRACT
This study evaluated the effects of injectable trace minerals (ITM) on antioxidant and immune response, resistance to endoparasites, health and growth of newborn Boer kids. Forty-six Boer kids [24 males and 22 females; 3.94±1.03kg of body weight (BW); 6.2±2.4 d of age] were enrolled in the study. Kids were stratified by type of birth (twins or singlet), sex, and BW and assigned to 1 of 2 treatments: one subcutaneous injection (0.1mL/4.5kg of BW) of (1) saline solution or (2) ITM (60, 10, 5, and 15mg/mL of Zn, Mn, Se and Cu, respectively). Blood samples were collected on d 0, 7, 14, 28 and 56. Feces samples were collected on d 56 and BW on d 0, 28 and 56. Kids were checked daily for signs of diarrhea. ITM kids had greater (P<0.01) plasma concentration of superoxide dismutase and tended (P=0.06) to have greater plasma concentration of glutathione peroxidase. ITM kids had greater (P=0.05) concentration of eosinophils, but no differences (P≥0.11) were observed for other hemogram variables. The ITM application did not affect (P≥0.11) the EPG count. However, ITM kids had less (P=0.02) cumulative incidence of diarhea until d 42 (3.85 vs. 25.93±6.8% for ITM vs. Saline kids, respectively) but no differences (P>0.10) were observed after d 42. The ITM application did not affect (P≥0.40) the growth of kids (0.071 vs. 0.065±0.005kg/day for ITM vs. Saline kids, respectively). Thus, the ITM application, increased the plasma concentration of antioxidant enzymes and eosinophils, decreased the incidence of diarrhea only in the middle of the experiment, but did not affected the EPG count and growth of Boer kids.(AU)
Este estudo avaliou os efeitos de microminerais injetáveis (ITM) na resposta antioxidante e imune, resistência a endoparasitas, saúde e crescimento de cabritos Boer recém-nascidos. Quarenta e seis cabritos [24 fêmeas e 22 machos; 3,94±1,03kg de peso corporal (PC); 6,2±2,4 dias de idade] foram incluídos no estudo. Os animais foram estratificados por tipo de nascimento (gêmeos ou singular), sexo e peso ao nascimento (PN) e atribuídas a 1 de 2 tratamentos. Uma injeção subcutânea (0,1ml/4,5 de PC de (1) Solução salina ou (2) ITM (60,10,5 e 15mg/ml de Zn, Mn, Se e Cu, respectivamente). As amostras de sangue foram coletadas nos dias 0, 7, 14, 28 e 56. As amostras de fezes foram coletadas no dia 56 e PC nos dias 0, 28 e 56. Os recém-nascidos foram verificados diariamente quanto a sinais de diarreia. Os cabritos ITM apresentaram maior (P<0.01) concentração de superóxido desmutase no plasma e tenderam (P=0,06) a ter maior concentração de glutationa peroxidase no plasma. Os animais ITM apresentaram maior (P=0,05) concentração de eosinófilos, mas não foram observadas diferenças (P≥0.11) para outras variáveis do hemograma. A aplicação de ITM não afetou (P≥0.11) a contagem de EPG. No entanto, os cabritos ITM apresentaram menor incidência cumulativa de diarreia (P=0,02) ate d 42 (3,85 vs. 25,93±6,8% para animais ITM vs. animais salina, respectivamente), mas nenhuma diferença (P>0.10) foi observada após d 42. A aplicação do ITM não afetou (P≥0.40) o crescimento dos animais (0.071 vs. 0.065±0.005kg/dia para ITM vs. Salina, respectivamente). Assim, a aplicação do ITM aumentou a concentração plasmática de enzimas antioxidantes e eosinófilos, diminuiu a incidência de diarreia somente na metade do experimento, mas não afetou a contagem de OPG e crescimento de cabritos Boer recém-nascidos.(AU)
Subject(s)
Animals , Infant, Newborn , Superoxide Dismutase , Goats/immunology , Enzymes , Glutathione Peroxidase , Injections , Antioxidants , Body Weight , Parturition , DiarrheaABSTRACT
The objective was to determine, through indirect immunofluorescence reaction (RIFI, 1:64), the occurrence of IgG antibodies to Toxoplasma gondii and the risk factors associated with infection in goats in the state of Sergipe. To this study were used 675 samples of blood of animals from 41 farms of the three state mesoregions from 2013 to 2014. The occurrence of seropositive goats was 30.07%, with 90.24% of farms with seropositive animals. The distribution of titers obtained was 37.93%, 11.82%, 17.24%, 18.22%, and 17.77% for 64, 128, 512 and 1024 respectively. The risk factors observed were farms that did not have facilities (p=0.000, OR=2.30, CI 95%=1.41-3.74), with flooded soils (p=0.011, OR=2.94, CI 95%=1.27-6.79), which provided feed on the ground (p=0.032, OR=1.69, CI 95%=1.04-2.74), in uncovered cages (p=0.032, OR=1.69, CI 95%=1.04-2.74), pasture-based feed (p=0.003, OR=3.52, CI 95%=1.53-8.09), with access from cats to (p=0.031, OR=1.45, CI 95%=1.03-2.04) and introduced new breeders in the last five years (p=0.036, OR=1.58, CI 95%=1.02-2.74).(AU)
O objetivo desse estudo foi determinar, através da reação de imunofluorescência indireta (RIFI, 1:64), a ocorrência de anticorpos IgG para o Toxoplasma gondii e os fatores de risco associados à infecção em rebanhos caprinos do estado de Sergipe, a partir de 675 amostras de sangue de animais de 41 propriedades das três mesorregiões do estado entre os anos de 2013 e 2014. A ocorrência de caprinos soropositivos foi de 30,07% com 90,24% de propriedades com animais soropositivos. A distribuição dos títulos obtidos foi de 37,93%, 11,82%, 17,24%, 18,22% e 17,77% para 64, 128, 512 e 1024 respectivamente. Os fatores de riscos observados foram propriedades que não possuíam instalações (p=0,000, OR=2,30, IC 95%=1,41-3,74), com terrenos alagados (p=0,011, OR=2,94, IC 95%=1,27-6,79), que disponibilizam a ração no chão (p=0,032, OR=1,69, IC 95%=1,04-2,74), em cochos descobertos (p=0,000, OR=1,97, IC 95%=1,32-2,94), alimentação à base de pastagem (p=0,003, OR=3,52, IC 95%=1,53-8,09), com acesso de gatos à fonte de água (p=0,031, OR=1,45, IC 95%=1,03-2,04) e que introduziram novos reprodutores nos últimos cinco anos (p=0,036, OR=1,58, IC 95%=1,02-2,74).(AU)
Subject(s)
Animals , Toxoplasma/isolation & purification , Goats/immunology , Toxoplasmosis, Animal/immunology , Toxoplasmosis, Animal/epidemiology , Serologic Tests , Risk FactorsABSTRACT
The objective was to determine, through indirect immunofluorescence reaction (RIFI, 1:64), the occurrence of IgG antibodies to Toxoplasma gondii and the risk factors associated with infection in goats in the state of Sergipe. To this study were used 675 samples of blood of animals from 41 farms of the three state mesoregions from 2013 to 2014. The occurrence of seropositive goats was 30.07%, with 90.24% of farms with seropositive animals. The distribution of titers obtained was 37.93%, 11.82%, 17.24%, 18.22%, and 17.77% for 64, 128, 512 and 1024 respectively. The risk factors observed were farms that did not have facilities (p=0.000, OR=2.30, CI 95%=1.41-3.74), with flooded soils (p=0.011, OR=2.94, CI 95%=1.27-6.79), which provided feed on the ground (p=0.032, OR=1.69, CI 95%=1.04-2.74), in uncovered cages (p=0.032, OR=1.69, CI 95%=1.04-2.74), pasture-based feed (p=0.003, OR=3.52, CI 95%=1.53-8.09), with access from cats to (p=0.031, OR=1.45, CI 95%=1.03-2.04) and introduced new breeders in the last five years (p=0.036, OR=1.58, CI 95%=1.02-2.74).(AU)
O objetivo desse estudo foi determinar, através da reação de imunofluorescência indireta (RIFI, 1:64), a ocorrência de anticorpos IgG para o Toxoplasma gondii e os fatores de risco associados à infecção em rebanhos caprinos do estado de Sergipe, a partir de 675 amostras de sangue de animais de 41 propriedades das três mesorregiões do estado entre os anos de 2013 e 2014. A ocorrência de caprinos soropositivos foi de 30,07% com 90,24% de propriedades com animais soropositivos. A distribuição dos títulos obtidos foi de 37,93%, 11,82%, 17,24%, 18,22% e 17,77% para 64, 128, 512 e 1024 respectivamente. Os fatores de riscos observados foram propriedades que não possuíam instalações (p=0,000, OR=2,30, IC 95%=1,41-3,74), com terrenos alagados (p=0,011, OR=2,94, IC 95%=1,27-6,79), que disponibilizam a ração no chão (p=0,032, OR=1,69, IC 95%=1,04-2,74), em cochos descobertos (p=0,000, OR=1,97, IC 95%=1,32-2,94), alimentação à base de pastagem (p=0,003, OR=3,52, IC 95%=1,53-8,09), com acesso de gatos à fonte de água (p=0,031, OR=1,45, IC 95%=1,03-2,04) e que introduziram novos reprodutores nos últimos cinco anos (p=0,036, OR=1,58, IC 95%=1,02-2,74).(AU)
Subject(s)
Animals , Toxoplasma/isolation & purification , Goats/immunology , Toxoplasmosis, Animal/immunology , Toxoplasmosis, Animal/epidemiology , Serologic Tests , Risk FactorsABSTRACT
Algae are a rich source of bioactive compounds and health properties that have been narrowly explored in goat production systems. The aim of this study was to determine the effect of feeding diets supplemented with Sargassum spp. on antioxidant status and immune parameters in goat kids. The diets were as follows: control (basal diet without alga), Sargassum spp. 2.5% (Ss2.5), and Sargassum spp. 5% (S5) fed over a 70-day period. A total of 11 body tissues, intestinal mucus, and blood serum were sampled at necropsy. Protein content, superoxide dismutase (SOD), catalase (CAT), myeloperoxidase (MPO), lysozyme, and anti-protease activities were determined, as well as immunoglobulin A (IgA) and immunoglobulin G (IgG). The results indicated that Sargassum spp. supplementation increased protein content in six tissues. Antioxidant activities (SOD and CAT) and immune-related (lysozyme, MPO, and anti-protease) activities were statistically higher (P < 0.05) in Sargassum spp. groups compared with control in several tissues, intestinal mucus, and serum. Imunoglobulin A levels in intestinal mucus were higher (P < 0.05) in Sargassum spp.-supplemented groups than the control group. In conclusion, diet supplementation of Sargassum spp. improves the antioxidant status and enhances the immune parameters in goats. Sargassum spp. dietary supplementation is proposed as strategy to strengthen antioxidant status and stimulate the immune system, which helps in the control of opportunistic pathogens in goats.
Subject(s)
Adjuvants, Immunologic/metabolism , Antioxidants/metabolism , Diet/veterinary , Goats/immunology , Goats/metabolism , Sargassum/chemistry , Animal Feed/analysis , Animals , Dietary Supplements/analysis , Dose-Response Relationship, Drug , Goats/growth & development , Random Allocation , Seaweed/chemistryABSTRACT
Beta-glucans from yeast can induce trained immunity in in vitro and in vivo models. Intraperitoneal doses of ß-glucans in mammals have shown to induce trained immunity, but the training effects of orally administering ß-glucans are unknown. Newborn goats are susceptible to infections in the neonatal stage, so the induction of trained immunity could improve animal survival. This study aimed to describe the in vitro effects of immunological training by ß-glucan from Debaryomyces hansenii (ß-Dh) on caprine monocytes, as well as its in vivo effects using oral doses on newborn goats upon challenge with lipopolysaccharide (LPS). Hence in vitro, goat monocytes trained with ß-Dh up-regulated the gene expression of macrophage surface markers (CD11b and F4/80) whereas enhanced cell survival and high phagocytic ability was found upon LPS challenge. In the in vivo experiment, newborn goats stimulated with two doses (day -7 and - 4) of ß-Dh (50 mg/kg) and challenged (day 0) with LPS showed an increase in respiratory burst activity, IL-1ß, IL-6, and TNFα production in plasma, and transcription of the macrophage surface markers. This study has demonstrated for the first time that trained immunity was induced with oral doses of ß-glucan upon LPS challenge in mammals using newborn goats.
Subject(s)
Debaryomyces/physiology , Goats/immunology , Macrophages/immunology , Monocytes/immunology , beta-Glucans/metabolism , Administration, Oral , Animals , Animals, Newborn , Cells, Cultured , Cytokines/metabolism , Immunity, Innate , Inflammation Mediators/metabolism , Lipopolysaccharides/metabolism , Phagocytosis , Respiratory Burst , beta-Glucans/immunologyABSTRACT
A selection of commercially available antibodies, targeted against markers employed in studies of mammary gland biology, was tested to determine their reactivity in goat mammary tissue and the derived tissue cultures. Expression of the markers smooth muscle actin (SMA), selected keratins (KRT) 5, 14, 18, and 19, CD24 molecule (CD24), epithelial cell adhesion molecule (EPCAM), mucin 1 (MUC1), integrin subunit alpha 6 (ITGA6; CD49F), integrin subunit beta 1 (ITGB1; CD29), cyclin dependent kinase inhibitor 1A (CDKN1A; p21), membrane metalloendopeptidase (MME; CD10), progesterone receptor (PGR), estrogen receptor 1 (ESR1), and vimentin (VIM) was first assessed on mRNA level, using reverse transcription PCR (RT-PCR). The reactivity of the antibodies in the tissue sections and the derived tissue cultures was determined using immunofluorescence. The result of this study is a list of commercially available antibodies, raised mostly against human antigens, which also recognize orthologous goat antigens and are useful for characterization of different mammary cell types. Additionally, primers that are functional in detecting expression of mammary lineage markers in goat mammary mRNA isolates were validated. The suggested antibodies, PCR primers, and the described methods are of practical value for researchers interested in characterization and isolation of cell types comprising mammary tissue of goats and probably other ruminants.(AU)
Subject(s)
Animals , Goats/immunology , Biomarkers/analysis , Epithelial Cells/immunology , Polymerase Chain Reaction/methods , Fluorescent Antibody Technique/veterinaryABSTRACT
Debaryomyces hansenii-derived ß-glucan has shown immunostimulant effect on aquaculture species and recently on goat peripheral blood leukocytes. Moreover, the marine yeast D. hansenii CBS 8339 has demonstrated to enhance fish immune response. Nonetheless, the associated immune signaling pathways induced by ß-glucan from this marine yeast have not been characterized yet. This study described the effects of ß-glucan from D. hansenii CBS 8339 against challenge with Escherichia coli and activation of possible mechanisms on goat peripheral blood leukocytes. The proton nuclear magnetic resonance spectra showed that D. hansenii had ß-(1,3)(1,6)-glucan. The phagocytic ability enhanced after E. coli challenge, and nitric oxide production increased before and after challenge in leukocytes stimulated with D. hansenii ß-glucan. In addition, an early gene expression stimulation was found related to ß-glucan recognition by TLR2 and Dectin-1 receptors, intracellular regulation by Syk, TRAF6, MyD88 and transcription factor NFκB, and effector functions of pro-inflammatory cytokine, such as IL-1ß and TNF-α. Interestingly, simulation with D. hansenii-derived ß-glucan increased leukocyte viability after E. coli challenge. In conclusion, ß-glucan from D. hansenii CBS 8339 reduced cytotoxic effects of E. coli and modulated signaling pathways and innate immune response in goat peripheral blood leukocytes.
Subject(s)
Debaryomyces/chemistry , Goats/immunology , Immunologic Factors/pharmacology , Leukocytes/immunology , beta-Glucans/pharmacology , Animals , Aquatic Organisms/chemistry , Cell Survival/drug effects , Cell Survival/immunology , Cells, Cultured , Cytokines/immunology , Escherichia coli/immunology , Goats/microbiology , Immunity, Innate/drug effects , Immunologic Factors/isolation & purification , Leukocytes/drug effects , Leukocytes/metabolism , Leukocytes/microbiology , Phagocytosis/drug effects , Phagocytosis/immunology , Primary Cell Culture , Signal Transduction/drug effects , Signal Transduction/immunology , beta-Glucans/isolation & purificationABSTRACT
The exact influence of caprine arthritis encephalitis virus (CAEV) infection on blood and milk polymorphonuclear leukocytes (PMNLs) and monocyte/macrophages of goats remains unclear. Thus, the present study sought to explore the blood and milk PMNL and monocyte/macrophage functions in naturally CAEV-infected goats. The present study used 18 healthy Saanen goats that were segregated according to sera test outcomes into serologically CAEV negative (n=8; 14 halves) and positive (n=10; 14 halves) groups. All milk samples from mammary halves with milk bacteriologically positive outcomes, somatic cell count ≥2×106cellsmL-1, and abnormal secretions in the strip cup test were excluded. We evaluated the percentage of blood and milk PMNLs and monocyte/macrophages, the viability of PMNLs and monocyte/macrophages, the levels of intracellular reactive oxygen species (ROS) and the nonopsonized phagocytosis of Staphylococcus aureus and Escherichia coli by flow cytometry. In the present study, a higher percentage of milk macrophages (CD14+) and milk polymorphonuclear leukocytes undergoing late apoptosis or necrosis (Annexin-V+/Propidium iodide+) was observed in CAEV-infected goats; we did not find any further alterations in blood and milk PMNL and monocyte/macrophage functions. Thus, regarding our results, the goats naturally infected with CAEV did not reveal pronounced dysfunctions in blood and milk polymorphonuclear leukocytes and monocytes/macrophages.
Subject(s)
Arthritis-Encephalitis Virus, Caprine/immunology , Goat Diseases/virology , Lentivirus Infections/veterinary , Macrophages/immunology , Monocytes/immunology , Neutrophils/immunology , Animals , Female , Goat Diseases/blood , Goat Diseases/immunology , Goats/blood , Goats/immunology , Goats/virology , Lentivirus Infections/blood , Lentivirus Infections/immunology , Milk/cytology , Milk/immunology , Milk/virologyABSTRACT
The mammalian hair follicle (HF) is a unique, highly regenerative organ with a distinct developmental cycle. Cashmere goat (Capra hircus) HFs can be divided into two categories based on structure and development time: primary and secondary follicles. To identify differentially expressed genes (DEGs) in the primary and secondary HFs of cashmere goats, the RNA sequencing of six individuals from Arbas, Inner Mongolia, was performed. A total of 617 DEGs were identified; 297 were upregulated while 320 were downregulated. Gene ontology analysis revealed that the main functions of the upregulated genes were electron transport, respiratory electron transport, mitochondrial electron transport, and gene expression. The downregulated genes were mainly involved in cell autophagy, protein complexes, neutrophil aggregation, and bacterial fungal defense reactions. According to the Kyoto Encyclopedia of Genes and Genomes database, these genes are mainly involved in the metabolism of cysteine and methionine, RNA polymerization, and the MAPK signaling pathway, and were enriched in primary follicles. A microRNA-target network revealed that secondary follicles are involved in several important biological processes, such as the synthesis of keratin-associated proteins and enzymes involved in amino acid biosynthesis. In summary, these findings will increase our understanding of the complex molecular mechanisms of HF development and cycling, and provide a basis for the further study of the genes and functions of HF development.
Subject(s)
Gene Expression Regulation, Developmental , Gene Regulatory Networks , Goats/genetics , Hair Follicle/metabolism , Transcriptome , Animals , Autophagy , Electron Transport , Female , Gene Expression Profiling , Gene Ontology , Goats/growth & development , Goats/immunology , Hair Follicle/growth & development , Immunity, Innate/genetics , Keratins/genetics , MAP Kinase Signaling System/genetics , MAP Kinase Signaling System/immunology , MicroRNAs/genetics , Mitochondrial Proteins/genetics , Molecular Sequence Annotation , Sequence Analysis, RNAABSTRACT
The objective of present study was to determine the prevalence of natural caprine fasciolosis in the Mixteca region of Mexico using coproantigen and serum IgG1 ELISA tests for comparative purposes. A total of 1070 serum and faecal samples were analyzed for IgG1 antibodies and coproantigens, using ELISA with E/S products as antigen and a monoclonal antibody-based sandwich ELISA. Prevalence of 73.46% was found using the serological ELISA and a percentage of 77.20 was found for coproantigen ELISA. The diagnostic sensitivity and specificity for serum ELISA were 86.7% and 96.4%, and for the coproantigen ELISA they were 93.1% and 97.8%, respectively. The seropositive samples were further categorized as low, medium, or high positivity. Results show a great proportion of low and medium positive goats when the serum ELISA test was used. Correlation coefficients between coproantigens and seropositivity were statistically significant (P < 0.01) for low seropositivity (r = 0.93) and medium seropositivity (r = 0.84). The accuracy of faecal antigen ELISA was higher compared to indirect ELISA serological test. Two ELISAs were shown to be useful for demonstrating the current status of F. hepatica infection in the endemic areas and can be employed in studies on epidemiology as well as anthelmintics treatment for preventing economic loss and the risk of transmission to humans.
Subject(s)
Enzyme-Linked Immunosorbent Assay/veterinary , Fascioliasis/veterinary , Goat Diseases/blood , Goat Diseases/diagnosis , Immunoglobulin G/blood , Animals , Antigens/immunology , Biomarkers/blood , Enzyme-Linked Immunosorbent Assay/methods , Fascioliasis/blood , Fascioliasis/diagnosis , Female , Goat Diseases/immunology , Goats/blood , Goats/immunology , Immunoglobulin G/immunology , Male , Mexico , Reproducibility of Results , Sensitivity and SpecificityABSTRACT
O objetivo deste trabalho foi avaliar a transferência de imunidade passiva de cabras, que pariram com mastite, para seus respectivos cabritos. Os animais foram distribuídos em dois grupos, a saber: grupo 1 (GI), constituído por cabritos, filhos de cabras sem isolamento microbiológico em ambas as glândulas mamárias, e grupo 2 (GII), composto por cabritos, filhos de cabras com resultado positivo à lactocultura, em pelo menos uma das glândulas mamárias. Foram coletadas amostras de colostro e sangue à parição, bem como às 24 e às 48 horas após o parto/nascimento. O diagnóstico e o monitoramento da mastite nos animais foram realizados por meio do California Mastitis Test (CMT), contagem de células somáticas e isolamento microbiológico. A proteína total foi mensurada pelo método do biureto, e as concentrações de imunoglobulina A (IgA), imunoglobulina G (IgG), transferrina, albumina e haptoglobina por meio da eletrofoerese em gel de poliacrilamida contendo dodecil sulfato de sódio (SDS-PAGE). Os agentes mais isolados na cultura microbiológica foram os Staphylococcus coagulase negativa. Não houve diferença significativa (P<0,05) entre os valores médios de imunoglobulina G (IgG) nos cabritos provenientes de cabras com mastite quando comparados aos recém-nascidos oriundos de cabras livres de infecções intramamárias. Da mesma forma, a atividade de gamaglutamiltransferase (GGT) não mostrou diferença entre os grupos em todos os momentos avaliados. A ingestão de colostro decorrente de cabras com mastite não causou falha na transferência de imunidade passiva nos respectivos conceptos.
The aim of this study was to evaluate the transfer of passive immunity goats kidded with mastitis to their kids. The animals were divided into two groups, namely: Group 1 (GI) containing kids, sons of goats without microbiological isolation in both mammary glands, and Group 2 (GII), composed of kids, sons of goats with positive result to lactoculture in at least one of mammary glands. Colostrum samples and blood were collected after delivery, 24 and 48 hours after delivery / birth. The diagnosis and monitoring of mastitis in animals were performed using the California Mastitis Test (CMT), somatic cell count and microbiological isolation. Total protein was measured by the biuret method, and the concentrations of immunoglobulin A (IgA), immunoglobulin G (IgG), transferrin, albumin and haptoglobin through eletrofoerese polyacrylamide gel containing sodium dodecyl sulfate (SDS-PAGE). The agents most isolated in microbiological culture were coagulase-negative Staphylococcus. There was no significant difference (p <0.05) between the acquisition of immunoglobulin G (IgG) in goats from goats with mastitis compared to infants originating free goat mammary infections. Similarly the gamma glutamyl transferase (GGT) was equal in the comparison between groups in all evaluated moments. The colostrum intake resulting from goats with mastitis caused no failure in the passive transfer of immunity in their fetuses.
Subject(s)
Animals , Goats/immunology , Immunization, Passive/veterinary , Mastitis/immunology , Mastitis/veterinary , Ruminants , Staphylococcus/pathogenicity , Coagulase/analysis , Cell Count/veterinary , Mammary Glands, Animal/abnormalities , ImmunoglobulinsABSTRACT
O objetivo deste trabalho foi avaliar a transferência de imunidade passiva de cabras, que pariram com mastite, para seus respectivos cabritos. Os animais foram distribuídos em dois grupos, a saber: grupo 1 (GI), constituído por cabritos, filhos de cabras sem isolamento microbiológico em ambas as glândulas mamárias, e grupo 2 (GII), composto por cabritos, filhos de cabras com resultado positivo à lactocultura, em pelo menos uma das glândulas mamárias. Foram coletadas amostras de colostro e sangue à parição, bem como às 24 e às 48 horas após o parto/nascimento. O diagnóstico e o monitoramento da mastite nos animais foram realizados por meio do California Mastitis Test (CMT), contagem de células somáticas e isolamento microbiológico. A proteína total foi mensurada pelo método do biureto, e as concentrações de imunoglobulina A (IgA), imunoglobulina G (IgG), transferrina, albumina e haptoglobina por meio da eletrofoerese em gel de poliacrilamida contendo dodecil sulfato de sódio (SDS-PAGE). Os agentes mais isolados na cultura microbiológica foram os Staphylococcus coagulase negativa. Não houve diferença significativa (P<0,05) entre os valores médios de imunoglobulina G (IgG) nos cabritos provenientes de cabras com mastite quando comparados aos recém-nascidos oriundos de cabras livres de infecções intramamárias. Da mesma forma, a atividade de gamaglutamiltransferase (GGT) não mostrou diferença entre os grupos em todos os momentos avaliados. A ingestão de colostro decorrente de cabras com mastite não causou falha na transferência de imunidade passiva nos respectivos conceptos.(AU)
The aim of this study was to evaluate the transfer of passive immunity goats kidded with mastitis to their kids. The animals were divided into two groups, namely: Group 1 (GI) containing kids, sons of goats without microbiological isolation in both mammary glands, and Group 2 (GII), composed of kids, sons of goats with positive result to lactoculture in at least one of mammary glands. Colostrum samples and blood were collected after delivery, 24 and 48 hours after delivery / birth. The diagnosis and monitoring of mastitis in animals were performed using the California Mastitis Test (CMT), somatic cell count and microbiological isolation. Total protein was measured by the biuret method, and the concentrations of immunoglobulin A (IgA), immunoglobulin G (IgG), transferrin, albumin and haptoglobin through eletrofoerese polyacrylamide gel containing sodium dodecyl sulfate (SDS-PAGE). The agents most isolated in microbiological culture were coagulase-negative Staphylococcus. There was no significant difference (p <0.05) between the acquisition of immunoglobulin G (IgG) in goats from goats with mastitis compared to infants originating free goat mammary infections. Similarly the gamma glutamyl transferase (GGT) was equal in the comparison between groups in all evaluated moments. The colostrum intake resulting from goats with mastitis caused no failure in the passive transfer of immunity in their fetuses.(AU)
Subject(s)
Animals , Ruminants/immunology , Goats/immunology , Mastitis/immunology , Mastitis/veterinary , Staphylococcus/pathogenicity , Immunization, Passive/veterinary , Cell Count/veterinary , Mammary Glands, Animal/abnormalities , Immunoglobulins , Coagulase/analysisABSTRACT
Background: Toxoplasma gondii is a coccidium, obligate intracellular protozoan, with complex life cycle, affecting virtually all-animal species homoeothermics. Goats are considered susceptible to infection by T. gondii, alterations being reported as pathological fetal death (with subsequent reabsorption), abortion, mummification, and/or the birth of weak goats. Because of these consequences to the animal, the disease is investigated throughout the Brazilian territory. Therefore, the aim of this study was to estimate the seroprevalence of Toxoplasma gondii antibodies and identify risk factors in goats. Materials, Methods & Results: It were collected 654 blood samples from goats distributed on west and mountainous regions of Santa Catarina, Brazil. The number municipalities with the highest numbers of goats were used, with an expected prevalence of 25%, error of 3.2% and confidence level of 95%. All collected samples were tested by indirect immunofluorescence assay (IFA), and 216 (33.02%; 95% CI 29.43-36.77) had antibodies against T. gondii (IFA 1: 64). Titration 1:64 was observed more frequently (60.2%; 130/216) among seropositive animals. The region with the highest prevalence was the west, i.e., more prone to infections present, with 1.16 more chances than the mountainous region. Animals Boer were more likely to T. gondii infection, being race is a risk factor for [...](AU)
Subject(s)
Animals , Toxoplasma/immunology , Risk Factors , Goats/immunology , Goats/virology , Nervous System Diseases/veterinary , Fluorescent Antibody Technique, Indirect/veterinary , Cats/parasitologyABSTRACT
Background: Toxoplasma gondii is a coccidium, obligate intracellular protozoan, with complex life cycle, affecting virtually all-animal species homoeothermics. Goats are considered susceptible to infection by T. gondii, alterations being reported as pathological fetal death (with subsequent reabsorption), abortion, mummification, and/or the birth of weak goats. Because of these consequences to the animal, the disease is investigated throughout the Brazilian territory. Therefore, the aim of this study was to estimate the seroprevalence of Toxoplasma gondii antibodies and identify risk factors in goats. Materials, Methods & Results: It were collected 654 blood samples from goats distributed on west and mountainous regions of Santa Catarina, Brazil. The number municipalities with the highest numbers of goats were used, with an expected prevalence of 25%, error of 3.2% and confidence level of 95%. All collected samples were tested by indirect immunofluorescence assay (IFA), and 216 (33.02%; 95% CI 29.43-36.77) had antibodies against T. gondii (IFA 1: 64). Titration 1:64 was observed more frequently (60.2%; 130/216) among seropositive animals. The region with the highest prevalence was the west, i.e., more prone to infections present, with 1.16 more chances than the mountainous region. Animals Boer were more likely to T. gondii infection, being race is a risk factor for [...]
Subject(s)
Animals , Goats/immunology , Goats/virology , Nervous System Diseases/veterinary , Risk Factors , Toxoplasma/immunology , Cats/parasitology , Fluorescent Antibody Technique, Indirect/veterinaryABSTRACT
Objetivou-se avaliar a sanidade da glândula mamária em cabras e ovelhas no período de lactação e definir o perfil de resistência e sensibilidade aos antibióticos a espécie Staphylococcus aureus coagulase positiva. Utilizou-se 42 cabras e 36 ovelhas procedentes do Agreste e Zona da Mata de Alagoas. Realizou-se o exame clínico da glândula mamária e em seguida detectou-se as mastites por meio dos testes da caneca telada e California Mastitis Test (CMT). Observou-se nas cabras a mastite clínica em 15,48 % (13/84) e mastite subclínica 65,48 % (55/84). Detectou-se em ovelhas mastite clínica em 19,44 % (14/72) e mastite subclínica 27,78 % (20/72). As amostras positivas para mastite subclínica e que confirmaram no microbiológico foram 83,63 % (46/55) para caprinos e 90 % (18/20) para ovinos. Identificou-se 60 microrganismos na mastite clínica e subclínica caprina, sendo Staphylococcus sp. a bactéria mais frequente 41,66 % (25/60) e na mastite ovina foram identificadas 45 amostras, o que prevaleceu foi Staphylococcus sp. 60 % (27/45). As bactérias isoladas do gênero Staphylococcus sp. foram submetidas ao teste de coagulase e as amostras positivas foram submetidas ao teste de sensibilidade a fitoterápicos e antibióticos convencionais. Observou-se nas amostras de mastite caprina, sensibilidade de 25% aos fitoterápicos Cupania impressi- nervia Acev. - Rodr e Mabea piriri Aubl. e de 16,67 % aos fitoterápicos Ipomoea purga e Zanthxylum rhoifolium Lam. - Rutaceae, nos antimicrobianos convencionais o de maior efeito foi Gentamicina (91,67 %), a maior resistência foi ao antimicrobiano Penicilina (70,83 %). Detectou-se nas amostras de mastite ovina 100 % de sensibilidade ao fitoterápico Cupania impressinervia Acev - Rodr, seguido de Mabea piriri Aubl. com 70%, os fitoterápicos Zanthxylum rhoifolium Lam. - Rutaceae e Ipomoea purga foram eficazes in vitro contra 65 % e 60%, respectivamente. Dentre os antimicrobianos convencionais os de maior eficácia foram Gentamicina (95 %) e Sulfa+Trimetoprim (90 %). Conclui-se que a mastite subclínica é a forma mais comum da mastite, sendo de etiologia contagiosa e que a bactéria responsável pela maioria dos casos é Staphylococcus sp. produzindo diversos tipos de doenças infectocontagiosas em humanos.
Subject(s)
Animals , Goats/immunology , Mastitis , Phytotherapeutic Drugs , Sheep/immunology , StaphylococcusABSTRACT
DRA encodes the alpha chain of the DR heterodimer, is closely linked to DRB and is considered almost monomorphic in major histocompatibility complex region. In this study, we identified the exon 2 of DRA to evaluate the immunogenetic diversity of Chinese south indigenous goat. Two single nucleotide polymorphisms in an untranslated region and one synonymous substitution in coding region were identified. These data suggest that high immunodiversity in native Chinese population.
Subject(s)
Goats/genetics , HLA-DR alpha-Chains/genetics , Polymorphism, Genetic , Animals , Animals, Domestic , China , Exons , Goats/classification , Goats/immunology , HLA-DR alpha-Chains/immunology , Introns , Open Reading Frames , Untranslated RegionsABSTRACT
Eleven commercially available PE-labeled anti-human (IL-1-α, IL-6, IL-8, TNF-α, IL-17A, IL-5, IL-10, IL-12 and IL-13) and anti-mouse (IL-10, TNF-α) cytokine monoclonal antibodies (mAbs) were tested for cross-reactivity with cattle, goat, and sheep cytokines. Cross-reactivity was assessed by comparative analysis with the standard reactivity of the target species. Our data demonstrated that anti-human IL-1-α, IL-6, IL-8, IL-17A and IL-10 mAbs cross-react with all ruminant species tested. Anti-human IL-5 mAb showed a strong cross-reactivity with cattle and goat IL-5, while anti-human TNF-α mAb showed a selective cross-reactivity with goat TNF-α. No cross-reactivity with the ruminant cytokines was observed for anti-human IL-12 and IL-13 mAbs or for the two anti-mouse cytokine mAbs tested. The present study demonstrated the cross-reactivity of various anti-human cytokine mAbs with cattle, sheep, and goat cytokines, increasing the range of immunological biomarkers for studies in veterinary medicine.
Subject(s)
Antibodies, Monoclonal/immunology , Biomarkers/blood , Cross Reactions/immunology , Cytokines/immunology , Animals , Cattle , Cross Reactions/genetics , Cytokines/genetics , Goats/immunology , Humans , Mice , Sheep/immunologyABSTRACT
Goats are susceptible to brucellosis and the detection of Brucella-infected animals is carried out by serological tests. In other ruminant species, polymorphisms in microsatellites (Ms) of 3' untranslated region (3'UTR) of the solute carrier family 11 member A1 (SLC11A1) gene were associated with resistance to Brucella abortus infection. Goats present two polymorphic Ms at the 3'UTR end of SLC11A1 gene, called regions A and B. Here, we evaluated if polymorphisms in regions A and/or B are associated with Brucella infection in goats. Serum (for the detection of Brucella-specific antibodies) and hair samples (for DNA isolation and structure analysis of the SLC11A1 gene) were randomly collected from 229 adult native goats from the northwest of Argentina. Serological status was evaluated by buffer plate antigen test (BPAT) complemented by the fluorescent polarization assay (FPA), and the genotype of the 3'UTR of the SLC11A1 gene was determined by capillary electrophoresis and confirmed by sequence analysis. Polymorphisms in regions A and B of the 3'UTR SLC11A1 gene were found statistically significant associated with protection to Brucella infection. Specifically, the association study indicates statistical significance of the allele A15 and B7/B7 genotype with absence of Brucella-specific antibodies (p=0.0003 and 0.0088, respectively). These data open a promising opportunity for limiting goat brucellosis through selective breeding of animals based on genetic markers associated with natural resistance to B. melitensis infection.