Pinna Antonio, Usai Donatella, Sechi Leonardo A, Molicotti Paola, Zanetti Stefania, Carta Arturo
Institute of Ophthalmology, Section of Experimental and Clinical Microbiology, University of Sassari, Sassari, Italy.
Cornea. 2008 Apr;27(3):320-6. doi: 10.1097/ICO.0b013e31815c5a3f.
In microbial keratitis associated with contact lens use, Pseudomonas is the most common etiologic agent. The purpose of this study was to report on the microbiological findings of 8 P. aeruginosa strains isolated from contact lens-associated corneal ulcers.
Scrapings from contact lens-related corneal ulcers were inoculated for culture. Identification and antibiotic susceptibility testing were performed by using the Vitek system (bioMérieux). The Pseudomonas' ability to form biofilm; produce gelatinase, elastase, and alkaline protease; and adhere to and invade human corneal epithelial cells was studied. Polymerase chain reaction with enterobacterial repetitive intergenic consensus primers (ERIC-PCR) was used to establish clonal relationship between the different isolates.
All the strains showed multiple antibiotic resistance (resistance to 4 or more antibiotics), but all were susceptible to aminoglycosides and fluoroquinolones. Biofilm production was weak in 5 cases and absent in the remaining 3 cases. All isolates were able to produce alkaline protease and gelatinase but not elastase. Adherence to human corneal epithelial cells was poor (0-15 bacteria/cell) in 5 cases and medium (16-60 bacteria/cell) in 3 cases. Five isolates were found to be efficient invaders (>1000 CFU/mL). ERIC-PCR showed 8 different genetic patterns.
Because multiresistant Pseudomonas isolates are common, we recommend antibiotic susceptibility testing in all cases of Pseudomonas keratitis so that, if there is no response to initial empiric treatment, antibiotics can be modified according to susceptibility results. The ability to produce alkaline protease and gelatinase and invade the corneal epithelium may play a major role in the pathogenesis of contact lens-related P. aeruginosa keratitis. Also, ERIC-PCR seems to be an inexpensive, fast, reproducible, and discriminatory DNA typing tool for effective epidemiologic surveillance of P. aeruginosa isolates potentially transmissible between patients with ocular infections.
在与隐形眼镜使用相关的微生物性角膜炎中,铜绿假单胞菌是最常见的病原体。本研究的目的是报告从与隐形眼镜相关的角膜溃疡中分离出的8株铜绿假单胞菌菌株的微生物学研究结果。
采集与隐形眼镜相关的角膜溃疡刮片进行培养。使用Vitek系统(生物梅里埃公司)进行鉴定和抗生素敏感性测试。研究了铜绿假单胞菌形成生物膜的能力;产生明胶酶、弹性蛋白酶和碱性蛋白酶的能力;以及黏附和侵袭人角膜上皮细胞的能力。使用肠杆菌重复基因间共有引物聚合酶链反应(ERIC-PCR)来确定不同分离株之间的克隆关系。
所有菌株均表现出多重耐药性(对4种或更多抗生素耐药),但均对氨基糖苷类和氟喹诺酮类敏感。5例生物膜产生较弱,其余3例未产生生物膜。所有分离株均能产生碱性蛋白酶和明胶酶,但不能产生弹性蛋白酶。5例对人角膜上皮细胞的黏附能力较差(0 - 15个细菌/细胞),3例中等(16 - 60个细菌/细胞)。发现5株分离株是有效的侵袭菌(>1000 CFU/mL)。ERIC-PCR显示出8种不同的基因模式。
由于多重耐药的铜绿假单胞菌分离株很常见,我们建议在所有铜绿假单胞菌角膜炎病例中进行抗生素敏感性测试,以便在初始经验性治疗无反应时,可根据药敏结果调整抗生素。产生碱性蛋白酶和明胶酶以及侵袭角膜上皮的能力可能在与隐形眼镜相关的铜绿假单胞菌角膜炎的发病机制中起主要作用。此外,ERIC-PCR似乎是一种廉价、快速、可重复且具有鉴别力的DNA分型工具,可用于对眼部感染患者之间可能传播的铜绿假单胞菌分离株进行有效的流行病学监测。