Zhu Yumin, Fan Hongjie, Miao Jinfeng, Zou Sixiang
College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, PR China.
Vet J. 2008 Mar;175(3):369-78. doi: 10.1016/j.tvjl.2007.01.027. Epub 2007 Apr 3.
A mastitis model in rats, induced by Escherichia coli infection, was established and the protective effect of Cytosine-phosphate-Guanosine (CpG)-DNA was determined. An E. coli suspension containing either 2 x 10(3) colony forming units (CFU)mL(-1)(EL group), 2 x 10(5)CFU mL(-1) (EH group), or (as controls) 100 microL phosphate buffer saline (CON group), was inoculated into the mammary glands 72 h after parturition. The rats were euthanased 24 h post-infection. The histopathological changes in mammary tissue in the EL group were mild, whereas the structural changes in the EH group were severe and polymorphonuclear leukocytes (PMNs) had accumulated in the mammary alveoli. Interleukin (IL)-6 and tumour necrosis factor (TNF)-alpha and N-acetyl-beta-d-glucosaminidase (NAGase) were significantly increased in the mammary tissue from the EH group but not significantly changed in the EL group. On the basis of these findings, the potential protective effect of CpG-DNA on mammary glands was tested using a 2 x 10(5)CFU mL(-1) suspension. An intramuscular injection of either CpG-DNA (200 microg) or PBS (100 microL) was given immediately after parturition. At 72 h post-partum, 2 x 10(5)CFU mL(-1)E. coli (100 microL) were inoculated into the mammary glands of all rats. At pre-infection (0 h), and 8, 16, 24, 48 and 72 h after inoculation six rats were euthanased. CpG-DNA induced more rapid migration of PMNs from the 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 E. coli in mammary tissues and decreased the activity of NAGase. CpG-DNA also promoted the expression of its specific receptor TLR-9 mRNA in mammary tissue. The study showed that CpG-DNA protected against E. coli mastitis in this rat model.
建立了由大肠杆菌感染诱导的大鼠乳腺炎模型,并确定了胞嘧啶-磷酸-鸟嘌呤(CpG)-DNA的保护作用。将含有2×10³菌落形成单位(CFU)mL⁻¹(EL组)、2×10⁵CFU mL⁻¹(EH组)的大肠杆菌悬液,或(作为对照)100μL磷酸盐缓冲盐水(CON组),在产后72小时接种到乳腺中。感染后24小时对大鼠实施安乐死。EL组乳腺组织的组织病理学变化轻微,而EH组的结构变化严重,多形核白细胞(PMN)在乳腺腺泡中积聚。EH组乳腺组织中白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α和N-乙酰-β-D-氨基葡萄糖苷酶(NAGase)显著增加,而EL组无显著变化。基于这些发现,使用2×10⁵CFU mL⁻¹的悬液测试了CpG-DNA对乳腺的潜在保护作用。产后立即肌肉注射CpG-DNA(200μg)或PBS(100μL)。在产后72小时,将2×10⁵CFU mL⁻¹的大肠杆菌(100μL)接种到所有大鼠的乳腺中。在感染前(0小时)以及接种后8、16、24、48和72小时,对6只大鼠实施安乐死。CpG-DNA在感染初期诱导PMN从血液更快地迁移到乳腺组织,在不同时间点刺激IL-6和TNF-α的分泌,减少乳腺组织中活的大肠杆菌数量并降低NAGase的活性。CpG-DNA还促进其特异性受体TLR-9 mRNA在乳腺组织中的表达。该研究表明,在该大鼠模型中CpG-DNA对大肠杆菌性乳腺炎具有保护作用。