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首页> 外文期刊>Clinical and vaccine immunology: CVI >Modulation of chicken intestinal immune gene expression by small cationic peptides as feed additives during the first week posthatch
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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:小阳离子肽作为饲料添加剂在第一个星期后通过小阳离子肽调节鸡肠道免疫基因表达

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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宿主免疫系统选择性刺激的调制策略,以此作为抗生素直接靶向微生物病原体的替代方法。一种方法是使用一组由革兰氏阳性土壤细菌Brevibacillus texasporus产生的小阳离子肽(BT)。这些肽具有免疫调节特性,可在体外增强白细胞功能效率和白细胞促炎细胞因子和趋化因子mRNA转录活性。另外,当作为饲料添加剂提供仅4​​天后的饲料添加剂时,BT肽会显着诱导浓度依赖性保护,以防止沙门氏菌肠血清肠肠肠染式和肠外结肠化。在目前的研究中,我们评估了喂养BT肽对促炎细胞因子,炎症趋化因子和Toll样受体(TLR)对肉鸡鸡的CECA的影响,伴有和没有肠肠链球菌感染。在后4天喂食BT肽补充的饮食后,然后用肠链球菌对鸡进行挑战,并在感染后1或7天(P.I.)(5或11天)测量肠道基因表达。通过定量实时PCR(QRT-PCR)分析了先天免疫mRNA转录本的肠道表达。对相对mRNA表达的分析表明,补充BT肽的饮食并未直接诱导促炎细胞因子,炎性趋化因子,I型干扰素(IFN)或TLR mRNA的转录。然而,在第1天和第7页的肠链球菌感染后,喂食BT肽补充的饮食引发的盲肠组织,以增加TLR4,TLR15和TLR21的转录(P≤0.05)。同样,喂食BT肽在盲肠组织中提高了促炎细胞因子的转录(白介素1β[IL-1β],IL-6,IL-6,IL-18,I型和II型IFN)和炎性趋化因子(CXCLI2),响应S。 Enteritidis感染1和7天P.I.与喂养基础饮食的鸡相比。这些小的阳离子肽可能被证明是新生儿家禽中局部免疫调节剂的替代方法,通过提供预防性保护沙门氏菌感染。

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