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Modulation of Chicken Intestinal Immune Gene Expression by Small Cationic Peptides as Feed Additives during the First Week Posthatch

机译:孵化后第一周小阳离子肽作为饲料添加剂对鸡肠道免疫基因表达的调控

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摘要

We have been investigating modulation strategies tailored around the selective stimulation of the host's immune system as an alternative to direct targeting of microbial pathogens by antibiotics. One such approach is the use of a group of small cationic peptides (BT) produced by a Gram-positive soil bacterium, Brevibacillus texasporus. These peptides have immune modulatory properties that enhance both leukocyte functional efficiency and leukocyte proinflammatory cytokine and chemokine mRNA transcription activities in vitro. In addition, when provided as a feed additive for just 4 days posthatch, BT peptides significantly induce a concentration-dependent protection against cecal and extraintestinal colonization by Salmonella enterica serovar Enteritidis. In the present studies, we assessed the effects of feeding BT peptides on transcriptional changes on proinflammatory cytokines, inflammatory chemokines, and Toll-like receptors (TLR) in the ceca of broiler chickens with and without S. Enteritidis infection. After feeding a BT peptide-supplemented diet for the first 4 days posthatch, chickens were then challenged with S. Enteritidis, and intestinal gene expression was measured at 1 or 7 days postinfection (p.i.) (5 or 11 days of age). Intestinal expression of innate immune mRNA transcripts was analyzed by quantitative real-time PCR (qRT-PCR). Analysis of relative mRNA expression showed that a BT peptide-supplemented diet did not directly induce the transcription of proinflammatory cytokine, inflammatory chemokine, type I/II interferon (IFN), or TLR mRNA in chicken cecum. However, feeding the BT peptide-supplemented diet primed cecal tissue for increased (P ≤ 0.05) transcription of TLR4, TLR15, and TLR21 upon infection with S. Enteritidis on days 1 and 7 p.i. Likewise, feeding the BT peptides primed the cecal tissue for increased transcription of proinflammatory cytokines (interleukin 1β [IL-1β], IL-6, IL-18, type I and II IFNs) and inflammatory chemokine (CxCLi2) in response to S. Enteritidis infection 1 and 7 days p.i. compared to the chickens fed the basal diet. These small cationic peptides may prove useful as alternatives to antibiotics as local immune modulators in neonatal poultry by providing prophylactic protection against Salmonella infections.
机译:我们一直在研究围绕选择性刺激宿主免疫系统量身定制的调节策略,以替代通过抗生素直接靶向微生物病原体的方法。一种这样的方法是使用由革兰氏阳性土壤细菌德氏短杆菌(Brevibacillus texasporus)产生的一组小阳离子肽(BT)。这些肽具有免疫调节特性,可增强体外白细胞功能效率以及白细胞促炎细胞因子和趋化因子mRNA转录活性。此外,当作为饲料添加剂在孵化后仅4天提供时,BT肽可显着诱导针对肠沙门氏菌血清肠炎沙门氏菌的盲肠和肠外定殖的浓度依赖性保护。在本研究中,我们评估了饲喂BT肽对有或没有肠炎沙门氏菌感染的肉鸡盲肠中促炎细胞因子,炎性趋化因子和Toll样受体(TLR)转录变化的影响。孵化后头4天以补充BT肽的饮食为食,然后将鸡用肠炎沙门氏菌攻击,并在感染后(p.i。)(5或11天)的1或7天测量肠道基因表达。通过定量实时PCR(qRT-PCR)分析先天免疫mRNA转录本的肠道表达。相对mRNA表达的分析表明,补充BT肽的饮食不能直接诱导鸡盲肠中促炎性细胞因子,炎性趋化因子,I / II型干扰素(IFN)或TLR mRNA的转录。但是,在补充肠炎沙门氏菌感染后第1天和第7天,喂食补充了BT肽的饮食引发的盲肠组织,可使TLR4,TLR15和TLR21的转录增加(P≤0.05)。同样,饲喂BT肽可引发盲肠组织,以增强促炎细胞因子(白介素1β[IL-1β],IL-6,IL-18,I和II型IFN)和炎症趋化因子(CxCLi2)的转录。肠感染1到7天与喂基础饮食的鸡相比。通过提供针对沙门氏菌感染的预防性保护,这些小的阳离子肽可被证明可替代抗生素作为新生儿家禽中的局部免疫调节剂。

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