Allison Milby-Blackledge, Yuhua Farnell, Christina Swaggerty, Morgan Farnell
{"title":"甘露聚糖-低聚糖益生元对肉鸡肠炎沙门氏菌盲肠定植和免疫应答的影响。","authors":"Allison Milby-Blackledge, Yuhua Farnell, Christina Swaggerty, Morgan Farnell","doi":"10.1016/j.psj.2025.105931","DOIUrl":null,"url":null,"abstract":"<p><p>Salmonella causes 1.35 million cases of foodborne illness in the United States annually. We hypothesized that the administration of ActiveMOS®, a prebiotic mannan-oligosaccharide (MOS) product, would reduce Salmonella Enteritidis (SE) cecal colonization and improve immune function in young broilers. The objectives of this study were to assess the effects of MOS on SE cecal colonization, serum cytokines, lipopolysaccharide (LPS), and immunoglobulin M (IgM). This study consisted of two independent 14 d trials. Day-of-hatch broilers (n = 240/trial) were evenly distributed across eight floor pens and randomly assigned to four treatments. Treatments were as follows: control (0.0), 1.0, 1.5, and 2.0 kg of MOS/metric ton (MT) of feed. Broilers were orally gavaged with PBS for unchallenged treatments or SE for challenged treatments at 7 d of age. Birds were euthanized one week post gavage. Salmonella Enteritidis cecal colonization, serum pro-inflammatory cytokines- interferon gamma (IFNγ), interleukin-2 (IL-2), IL-6, IL-16, IL-21; anti-inflammatory/regulatory cytokines- IFNα, IL-10; chemokines- regulated on activation, normal T-cell expressed and secreted (RANTES), macrophage inflammatory protein-1β (MIP-1β), MIP-3α; colony-stimulating factors- macrophage colony-stimulating factor (M-CSF); and growth factors- vascular endothelial growth factor (VEGF), IgM titers, and LPS concentrations were evaluated. Data were analyzed via a two-way ANOVA with an α = 0.05. In the first trial, Salmonella was significantly reduced by 1.07 and 0.84 log in the 1.5 kg/MT and 2.0 kg/MT MOS inclusions, respectively. In trial two, a significant 1.14 log reduction of SE in the 1.5 kg/MT MOS diet was observed. For unchallenged birds, all MOS treatments decreased IFNα levels. However, in the control basal diet, levels of IFNα were significantly diminished in SE challenged chicks. Decreased expression of IL-16 and MIP-1β was detected (p < 0.05) in SE challenged broilers compared to unchallenged birds. Levels of RANTES were significantly increased in 1.0 kg/MT and 2.0 kg/MT MOS inclusions compared to all other diets. No significant differences were observed with any other cytokines or LPS. The isotype IgM was reduced in all treatments compared to the control diet in both unchallenged and SE challenged birds, suggesting depressed humoral immunity when MOS was fed. Although a mechanism of action was not determined, these data suggest that MOS at the 1.5 kg/MT inclusion was efficacious in reducing SE.</p>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 12","pages":"105931"},"PeriodicalIF":4.2000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of a prebiotic mannan-oligosaccharide on Salmonella Enteritidis cecal colonization and immune response of broiler chickens.\",\"authors\":\"Allison Milby-Blackledge, Yuhua Farnell, Christina Swaggerty, Morgan Farnell\",\"doi\":\"10.1016/j.psj.2025.105931\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Salmonella causes 1.35 million cases of foodborne illness in the United States annually. We hypothesized that the administration of ActiveMOS®, a prebiotic mannan-oligosaccharide (MOS) product, would reduce Salmonella Enteritidis (SE) cecal colonization and improve immune function in young broilers. The objectives of this study were to assess the effects of MOS on SE cecal colonization, serum cytokines, lipopolysaccharide (LPS), and immunoglobulin M (IgM). This study consisted of two independent 14 d trials. Day-of-hatch broilers (n = 240/trial) were evenly distributed across eight floor pens and randomly assigned to four treatments. Treatments were as follows: control (0.0), 1.0, 1.5, and 2.0 kg of MOS/metric ton (MT) of feed. Broilers were orally gavaged with PBS for unchallenged treatments or SE for challenged treatments at 7 d of age. Birds were euthanized one week post gavage. Salmonella Enteritidis cecal colonization, serum pro-inflammatory cytokines- interferon gamma (IFNγ), interleukin-2 (IL-2), IL-6, IL-16, IL-21; anti-inflammatory/regulatory cytokines- IFNα, IL-10; chemokines- regulated on activation, normal T-cell expressed and secreted (RANTES), macrophage inflammatory protein-1β (MIP-1β), MIP-3α; colony-stimulating factors- macrophage colony-stimulating factor (M-CSF); and growth factors- vascular endothelial growth factor (VEGF), IgM titers, and LPS concentrations were evaluated. Data were analyzed via a two-way ANOVA with an α = 0.05. In the first trial, Salmonella was significantly reduced by 1.07 and 0.84 log in the 1.5 kg/MT and 2.0 kg/MT MOS inclusions, respectively. In trial two, a significant 1.14 log reduction of SE in the 1.5 kg/MT MOS diet was observed. For unchallenged birds, all MOS treatments decreased IFNα levels. However, in the control basal diet, levels of IFNα were significantly diminished in SE challenged chicks. Decreased expression of IL-16 and MIP-1β was detected (p < 0.05) in SE challenged broilers compared to unchallenged birds. Levels of RANTES were significantly increased in 1.0 kg/MT and 2.0 kg/MT MOS inclusions compared to all other diets. No significant differences were observed with any other cytokines or LPS. The isotype IgM was reduced in all treatments compared to the control diet in both unchallenged and SE challenged birds, suggesting depressed humoral immunity when MOS was fed. Although a mechanism of action was not determined, these data suggest that MOS at the 1.5 kg/MT inclusion was efficacious in reducing SE.</p>\",\"PeriodicalId\":20459,\"journal\":{\"name\":\"Poultry Science\",\"volume\":\"104 12\",\"pages\":\"105931\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poultry Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1016/j.psj.2025.105931\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1016/j.psj.2025.105931","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Evaluation of a prebiotic mannan-oligosaccharide on Salmonella Enteritidis cecal colonization and immune response of broiler chickens.
Salmonella causes 1.35 million cases of foodborne illness in the United States annually. We hypothesized that the administration of ActiveMOS®, a prebiotic mannan-oligosaccharide (MOS) product, would reduce Salmonella Enteritidis (SE) cecal colonization and improve immune function in young broilers. The objectives of this study were to assess the effects of MOS on SE cecal colonization, serum cytokines, lipopolysaccharide (LPS), and immunoglobulin M (IgM). This study consisted of two independent 14 d trials. Day-of-hatch broilers (n = 240/trial) were evenly distributed across eight floor pens and randomly assigned to four treatments. Treatments were as follows: control (0.0), 1.0, 1.5, and 2.0 kg of MOS/metric ton (MT) of feed. Broilers were orally gavaged with PBS for unchallenged treatments or SE for challenged treatments at 7 d of age. Birds were euthanized one week post gavage. Salmonella Enteritidis cecal colonization, serum pro-inflammatory cytokines- interferon gamma (IFNγ), interleukin-2 (IL-2), IL-6, IL-16, IL-21; anti-inflammatory/regulatory cytokines- IFNα, IL-10; chemokines- regulated on activation, normal T-cell expressed and secreted (RANTES), macrophage inflammatory protein-1β (MIP-1β), MIP-3α; colony-stimulating factors- macrophage colony-stimulating factor (M-CSF); and growth factors- vascular endothelial growth factor (VEGF), IgM titers, and LPS concentrations were evaluated. Data were analyzed via a two-way ANOVA with an α = 0.05. In the first trial, Salmonella was significantly reduced by 1.07 and 0.84 log in the 1.5 kg/MT and 2.0 kg/MT MOS inclusions, respectively. In trial two, a significant 1.14 log reduction of SE in the 1.5 kg/MT MOS diet was observed. For unchallenged birds, all MOS treatments decreased IFNα levels. However, in the control basal diet, levels of IFNα were significantly diminished in SE challenged chicks. Decreased expression of IL-16 and MIP-1β was detected (p < 0.05) in SE challenged broilers compared to unchallenged birds. Levels of RANTES were significantly increased in 1.0 kg/MT and 2.0 kg/MT MOS inclusions compared to all other diets. No significant differences were observed with any other cytokines or LPS. The isotype IgM was reduced in all treatments compared to the control diet in both unchallenged and SE challenged birds, suggesting depressed humoral immunity when MOS was fed. Although a mechanism of action was not determined, these data suggest that MOS at the 1.5 kg/MT inclusion was efficacious in reducing SE.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.