Van Horn D L, Davis S D, Hyndiuk R A, Alpren T V
Invest Ophthalmol Vis Sci. 1978 Nov;17(11):1076-86.
Uniformly severe corneal infections were produced in guinea pigs by intracorneal injection of about 10 viable Pseudomonas aeruginosa. After a brief lag period, multiplication of bacteria was rapid, reaching geometric means of 280,000 after 24 hr and of 5 million after 48 hr. Within 8 hr after inoculation, polymorphonuclear leukocytes (PMNs) began to infiltrate the anterior two thirds of the stroma. Stromal cells adjacent to the injection site became necrotic and appeared to be engulfed by PMNs. By 14 to 16 hr, an abscess containing a dense aggregate of PMNs and multiplying bacteria developed in the central stroma. By 16 to 24 hr, collagen breakdown was apparent within and around the abscess. Ultrastructural evidence of collagen breakdown included loss of intact collagen fibrils, tactoid formation, and accumulation of amorphous electron-dense material. The area of liquefactive necrosis gradually enlarged, and many corneas perforated after 3 to 4 days. Because the course of infection is highly reproducible, this model should prove useful for many studies of experimental Pseudomonas keratitis.
通过向豚鼠角膜内注射约10个活的铜绿假单胞菌,可在豚鼠身上产生均匀严重的角膜感染。经过短暂的滞后期后,细菌迅速繁殖,24小时后达到几何平均数280,000,48小时后达到500万。接种后8小时内,多形核白细胞(PMN)开始浸润角膜基质的前三分之二。注射部位附近的基质细胞坏死,似乎被PMN吞噬。到14至16小时,中央基质中形成了一个含有密集PMN聚集物和繁殖细菌的脓肿。到16至24小时,脓肿内及周围的胶原分解明显。胶原分解的超微结构证据包括完整胶原纤维的丧失、触觉小体形成和无定形电子致密物质的积累。液化性坏死区域逐渐扩大,许多角膜在3至4天后穿孔。由于感染过程具有高度可重复性,该模型应被证明对许多实验性铜绿假单胞菌角膜炎的研究有用。