Cholesterol as treatment for pneumococcal keratitis: Cholesterol-specific inhibition of pneumolysin in the cornea

被引:27
|
作者
Marquart, Mary E. [1 ]
Monds, Kathryn S. [1 ]
McCormick, Clare C. [1 ]
Dixon, Sherrina N. [1 ]
Sanders, Melissa E. [1 ]
Reed, Julian M. [1 ]
McDaniel, Larry S. [1 ]
Caballero, Armando R. [1 ]
O'Callaghan, Richard J. [1 ]
机构
[1] Univ Mississippi, Med Ctr, Dept Microbiol, Jackson, MS 39216 USA
关键词
D O I
10.1167/iovs.07-0017
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. The purpose of this study was to determine whether cholesterol, the host cell receptor for pneumolysin of Streptococcus pneumoniae, could effectively treat pneumococcal keratitis. METHODS. New Zealand White rabbits were intrastromally injected with 105 colony-forming units (CFUs) of S. pneumoniae D39. Corneas were treated with topical drops of 1% cholesterol every 2 hours beginning 25 hours after infection and were examined by slit lamp microscopy 24, 36, and 48 hours after infection. Rabbits were killed, and CFUs were recovered from the corneas after the final slit lamp examination (SLE). Minimal inhibitory concentration (MIC) assays of cholesterol against bacteria were performed. Specific inhibition of pneumolysin by cholesterol in the rabbit cornea was tested by intrastromal injection of pneumolysin with or without cholesterol and was compared with cholesterol inhibition of pneumolysin in vitro using hemolysis assays with rabbit erythrocytes. RESULTS. Corneas treated with cholesterol had significantly lower SLE scores 48 hours after infection than corneas treated with vehicle (P = 0.0015). Treated corneas also had significantly less log,. CFUs than vehicle-treated corneas (P = 0.0006). Cholesterol at a 1% concentration was bactericidal to bacteria in vitro, and lower concentrations of cholesterol were partially inhibitory in a concentration-dependent manner. Cholesterol also specifically inhibited 1 mu g pneumolysin in vivo and up to 50 ng pneumolysin in vitro. CONCLUSIONS. Topical cholesterol is an effective treatment for S. pneumoniae keratitis. Cholesterol not only inhibits pneumolysin, it is also bactericidal.
引用
收藏
页码:2661 / 2666
页数:6
相关论文
共 50 条
  • [41] Liver-specific induction of Abcg5 and Abcg8 stimulates reverse cholesterol transport in response to ezetimibe treatment
    Altemus, Jessica B.
    Patel, Shailendra B.
    Sehayek, Ephraim
    METABOLISM-CLINICAL AND EXPERIMENTAL, 2014, 63 (10): : 1334 - 1341
  • [42] Cholesterol esterification inhibition and imatinib treatment synergistically inhibit growth of BCR-ABL mutation-independent resistant chronic myelogenous leukemia
    Bandyopadhyay, Shovik
    Li, Junjie
    Traer, Elie
    Tyner, Jeffrey W.
    Zhou, Amy
    Oh, Stephen T.
    Cheng, Ji-Xin
    PLOS ONE, 2017, 12 (07):
  • [43] Stereo specific platelet inhibition by the natural LXR agonist 22(R)-OH-cholesterol and its fluorescence labelling with preserved bioactivity and chiral handling in macrophages
    Schaffer, Stephanie
    Tandon, Raman
    Zipse, Hendrik
    Siess, Wolfgang
    Schmidt, Andreas
    Jamasbi, Janina
    Karshovska, Ela
    Steglich, Wolfgang
    Lorenz, Reinhard
    BIOCHEMICAL PHARMACOLOGY, 2013, 86 (02) : 279 - 285
  • [44] INHIBITION OF CHOLESTEROL 7-ALPHA-HYDROXYLASE BY AN ANTIBODY TO A MALE-SPECIFIC FORM OF CYTOCHROME-P-450 FROM SUBFAMILY P450IIC
    ELDREDGE, ER
    JACKSON, B
    SUCKLING, KE
    WOLF, CR
    BIOCHEMICAL JOURNAL, 1989, 262 (01) : 91 - 95
  • [45] Site-Specific MicroRNA-33 Antagonism by pH-Responsive Nanotherapies for Treatment of Atherosclerosis via Regulating Cholesterol Efflux and Adaptive Immunity
    Li, Chenwen
    Dou, Yin
    Chen, Yidan
    Qi, Yuantong
    Li, Lanlan
    Han, Songling
    Jin, Taotao
    Guo, Jiawei
    Chen, Jianhong
    Zhang, Jianxiang
    ADVANCED FUNCTIONAL MATERIALS, 2020, 30 (42)
  • [46] Seeking Novel Targets for Improving In Vivo Macrophage-Specific Reverse Cholesterol Transport: Translating Basic Science into New Therapies for the Prevention and Treatment of Atherosclerosis
    Julve, Josep
    Llaverias, Gemma
    Blanco-Vaca, Francisco
    Escola-Gil, Joan C.
    CURRENT VASCULAR PHARMACOLOGY, 2011, 9 (02) : 220 - 237
  • [47] Identification of a Tissue-specific Very Long-chain Acyl-CoA Synthetase Involved in the Inhibition of ATP-Citrate Lyase (ACL) by ETC-1002: A Novel Mechanism for Cholesterol Biosynthesis Inhibition in the Liver
    Pinkosky, Stephen L.
    Newton, Roger S.
    Birch, Carolyn M.
    Filippov, Sergey
    Groot, Pieter H.
    Lalwani, Narendra D.
    CIRCULATION, 2015, 132
  • [48] MOUSE-LIVER MICROSOMAL CHOLESTEROL EPOXIDE HYDROLASE - A SPECIFIC-INHIBITION OF ITS ACTIVITY BY 5,6-ALPHA-IMINO-5-ALPHA-CHOLESTAN-3-ALPHA-OL
    WATABE, T
    KOMATSU, T
    ISOBE, M
    TSUBAKI, A
    CHEMICO-BIOLOGICAL INTERACTIONS, 1983, 44 (1-2) : 143 - 154
  • [49] Liver-specific inhibition of acyl-coenzyme A:cholesterol acyltransferase 2 with antisense oligonucleotides limits atherosclerosis development in apolipoprotein B100-only low-density lipoprotein receptor-/- mice
    Bell, Thomas A., III
    Brown, J. Mark
    Graham, Mark J.
    Lemonidis, Kristina A.
    Crooke, Rosanne M.
    Rudel, Lawrence L.
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (08) : 1814 - 1820
  • [50] INHIBITION OF CHOLESTEROL-BIOSYNTHESIS IN CHINESE-HAMSTER OVARY CELLS BY 4,4,10-BETA-TRIMETHYL-TRANS-DECAL-3-BETA-OL - SPECIFIC 2,3-OXIDOSQUALENE CYCLASE INHIBITOR
    CHANG, TY
    SCHIAVONI, ES
    MCCRAE, KR
    NELSON, JA
    SPENCER, TA
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1979, 254 (22) : 1258 - 1263