Piper Clare, Casey Pat G, Hill Colin, Cotter Paul D, Ross R Paul
Department of Microbiology, University College Cork, College Road, Cork, Ireland.
Int J Microbiol. 2012;2012:806230. doi: 10.1155/2012/806230. Epub 2012 Jan 12.
The objective of this study was to investigate the in vivo activity of the lantibiotic lacticin 3147 against the luminescent Staphylococcus aureus strain Xen 29 using a murine model. Female BALB/c mice (7 weeks old, 17 g) were divided into groups (n = 5) and infected with the Xen 29 strain via the intraperitoneal route at a dose of 1 × 10(6) cfu/animal. After 1.5 hr, the animals were treated subcutaneously with doses of phosphate-buffered saline (PBS; negative control) or lacticin 3147. Luminescent imaging was carried 3 and 5 hours postinfection. Mice were then sacrificed, and the levels of S. aureus Xen 29 in the liver, spleen, and kidneys were quantified. Notably, photoluminescence and culture-based analysis both revealed that lacticin 3147 successfully controlled the systemic spread of S. aureus in mice thus indicating that lacticin 3147 has potential as a chemotherapeutic agent for in vivo applications.
本研究的目的是使用小鼠模型研究羊毛硫抗生素乳酸乳球菌素3147对发光金黄色葡萄球菌菌株Xen 29的体内活性。将雌性BALB/c小鼠(7周龄,17克)分成若干组(n = 5),并通过腹腔注射途径以1×10(6) cfu/动物的剂量感染Xen 29菌株。1.5小时后,给动物皮下注射磷酸盐缓冲盐水(PBS;阴性对照)或乳酸乳球菌素3147。在感染后3小时和5小时进行发光成像。然后处死小鼠,并对肝脏、脾脏和肾脏中金黄色葡萄球菌Xen 29的水平进行定量。值得注意的是,光致发光和基于培养的分析均显示,乳酸乳球菌素3147成功地控制了小鼠体内金黄色葡萄球菌的全身扩散,因此表明乳酸乳球菌素3147有作为体内应用化疗药物的潜力。