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Protective effect of CpG-DNA against mastitis induced by Staphylococcus aureus infection in a rat model.

机译:CpG-DNA对大鼠金黄色葡萄球菌感染所致乳腺炎的保护作用。

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A mastitis model in rats, induced by Staphylococcus aureus infection, was established and the protective effect of CpG-DNA on this model was determined. A S. aureus suspension containing 2 x 10(3) CFU.mL(-1) (SL group), 2 x 10(5) CFU.mL(-1) (SH group) or 100 microL PBS (CON group) was inoculated into the mammary glands of rats 72 h after parturition. The rats were euthanized at 24 h post-infection. The histopathologic changes in mammary tissue from SL were mild, whereas the structural changes of the mammary gland from SH were severe and polymorphonuclear leukocytes (PMNs) accumulated in mammary alveoli. Interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha) and N-acetyl-beta-d-Glucosaminidase (NAGase) in mammary tissue from SH were significantly increased, however, those from SL were not significantly changed. Therefore, 2 x 10(5) CFU.mL(-1) was selected to test the potential protective effect of CpG-DNA on mammary glands. CpG-DNA (200 microg) or PBS (100 microL) controls were intramuscularly injected right after parturition of rats. At 72 h post-partum, 2 x 10(5) CFU.mL(-1)of S. aureus (100 microL) were inoculated into the mammary gland of all rats and at pre-infection (0 h), 8, 16, 24, 48 and 72 h after inoculation six rats were euthanatized. CpG-DNA induced more rapid migration of PMNs from blood to mammary tissue at the initial stage of infection, stimulated the secretion of IL-6 and TNF-alpha at different time points, reduced viable S. aureus in mammary tissue and decreased the activity of NAGase. CpG-DNA also promoted the expression of its specific receptor TLR-9 mRNA in mammary tissue. In conclusion, CpG-DNA protected against S. aureus mastitis in a rat model.
机译:建立了由金黄色葡萄球菌感染引起的大鼠乳腺炎模型,并确定了CpG-DNA对该模型的保护作用。含有2 x 10(3)CFU.mL(-1)(SL组),2 x 10(5)CFU.mL(-1)(SH组)或100 microL PBS(CON组)的金黄色葡萄球菌悬液为分娩后72小时接种到大鼠的乳腺中。在感染后24小时对大鼠实施安乐死。 SL的乳腺组织的组织病理学改变是轻度的,而SH的乳腺的结构改变是严重的,并且乳腺肺泡中积累了多形核白细胞(PMNs)。 SH乳腺组织中的白细胞介素6(IL-6),肿瘤坏死因子-α(TNF-α)和N-乙酰基-β-d-葡萄糖苷酶(NAGase)显着增加,而SL的乳腺组织中无明显变化。因此,选择2 x 10(5)CFU.mL(-1)来测试CpG-DNA对乳腺的潜在保护作用。大鼠分娩后立即肌内注射CpG-DNA(200微克)或PBS(100微升)对照。产后72小时,将2 x 10(5)CFU.mL(-1)的金黄色葡萄球菌(100 microL)接种到所有大鼠的乳腺中,并在感染前(0 h),8、16接种后24、48和72小时,对六只大鼠实施安乐死。在感染初期,CpG-DNA诱导PMN从血液更快速地迁移至乳腺组织,在不同时间点刺激IL-6和TNF-α的分泌,减少乳腺组织中金黄色葡萄球菌的活力,并降低其活性。 NAGase。 CpG-DNA还促进了其特异性受体TLR-9 mRNA在乳腺组织中的表达。总之,CpG-DNA可在大鼠模型中预防金黄色葡萄球菌乳腺炎。

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