Previous Article | Next Article 
Infection and Immunity, July 1999, p. 3348-3356, Vol. 67, No. 7
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Pathogenesis of Gram-Positive Bacterial
Endophthalmitis
Michelle C.
Callegan,1,2
Mary C.
Booth,1,2,3
Bradley D.
Jett,1,2,
and
Michael S.
Gilmore1,2,3,*
Department of
Ophthalmology,1 Department of
Microbiology and Immunology,2 and
Molecular Pathogenesis of Eye Infections Research Center, Dean
A. McGee Eye Institute,3 University of Oklahoma
Health Sciences Center, Oklahoma City, Oklahoma
Received 21 December 1998/Returned for modification 3 February
1999/Accepted 12 April 1999
The severity of endophthalmitis has been associated generally with
the virulence of the offending pathogen. However, precisely what
constitutes the virulence in intraocular infections remains ill
defined. We therefore sought to identify the basis for virulence for
three common ocular pathogens (Bacillus cereus,
Enterococcus faecalis, and Staphylococcus
aureus) in terms of intraocular growth rates, bacterial
localization patterns, and the contribution of cell walls and secreted
products to the pathogenesis of endophthalmitis. Rabbit eyes were
injected intravitreally with (i) viable B. cereus, E. faecalis, or S. aureus, (ii) metabolically inactive
B. cereus, E. faecalis, or S. aureus, (iii) sacculus preparations from each strain, or (iv)
culture fluid containing products secreted by each strain. Eyes were
assessed at various times following injection by slit lamp
biomicroscopy, electroretinography (ERG), bacterial and inflammatory
cell enumeration, and histology. B. cereus endophthalmitis followed a more rapid and virulent course than E. faecalis
or S. aureus endophthalmitis, eliminating retinal
responsiveness, as measured by ERG, by 12 h. Analysis of bacterial
localization revealed that B. cereus uniquely migrated
rapidly from posterior to anterior segment during infection. Although
injection of neither metabolically inactive bacteria nor cell wall
sacculi greatly affected ERG, significant intraocular inflammation was
observed. Injection of B. cereus or S. aureus
culture fluids caused both significant reductions in retinal
responsiveness and significant intraocular inflammation, paralleling
that seen in natural infections. The results demonstrate that toxins,
intraocular localization, and, to a lesser extent, the intraocular host
response to cell walls all contribute to the pathogenesis of B. cereus, S. aureus, and E. faecalis
endophthalmitis in a pathogen-specific manner. The key pathophysiologic
differences in these intraocular diseases highlight opportunities for
optimizing conventional therapies and deriving new ones.
*
Corresponding author. Mailing address: Department of
Ophthalmology, University of Oklahoma Health Sciences Center, 608 Stanton L. Young Blvd., Oklahoma City, OK 73104. Phone: (405) 271-1084. Fax: (405) 271-8128. E-mail: mgilmore{at}aardvark.ou.edu.

Present address: Department of Biology, Oklahoma Baptist
University, Shawnee,
Okla.
Infection and Immunity, July 1999, p. 3348-3356, Vol. 67, No. 7
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Moyer, A. L., Ramadan, R. T., Novosad, B. D., Astley, R., Callegan, M. C.
(2009). Bacillus cereus-Induced Permeability of the Blood-Ocular Barrier during Experimental Endophthalmitis. IOVS
50: 3783-3793
[Abstract]
[Full Text]
-
Wiskur, B. J., Hunt, J. J., Callegan, M. C.
(2008). Hypermucoviscosity as a Virulence Factor in Experimental Klebsiella pneumoniae Endophthalmitis. IOVS
49: 4931-4938
[Abstract]
[Full Text]
-
Bouillaut, L., Perchat, S., Arold, S., Zorrilla, S., Slamti, L., Henry, C., Gohar, M., Declerck, N., Lereclus, D.
(2008). Molecular basis for group-specific activation of the virulence regulator PlcR by PapR heptapeptides. Nucleic Acids Res
36: 3791-3801
[Abstract]
[Full Text]
-
Johnson, B. T., Shaw, L. N., Nelson, D. C., Mayo, J. A.
(2008). Extracellular proteolytic activities expressed by Bacillus pumilus isolated from endodontic and periodontal lesions. J Med Microbiol
57: 643-651
[Abstract]
[Full Text]
-
Wiskur, B. J., Robinson, M. L., Farrand, A. J., Novosad, B. D., Callegan, M. C.
(2008). Toward Improving Therapeutic Regimens for Bacillus Endophthalmitis. IOVS
49: 1480-1487
[Abstract]
[Full Text]
-
Moyer, A. L., Ramadan, R. T., Thurman, J., Burroughs, A., Callegan, M. C.
(2008). Bacillus cereus Induces Permeability of an In Vitro Blood-Retina Barrier. Infect. Immun.
76: 1358-1367
[Abstract]
[Full Text]
-
Saile, E., Koehler, T. M.
(2006). Bacillus anthracis Multiplication, Persistence, and Genetic Exchange in the Rhizosphere of Grass Plants.. Appl. Environ. Microbiol.
72: 3168-3174
[Abstract]
[Full Text]
-
Engelbert, M., Gilmore, M. S.
(2005). Fas Ligand but Not Complement Is Critical for Control of Experimental Staphylococcus aureus Endophthalmitis. IOVS
46: 2479-2486
[Abstract]
[Full Text]
-
Perkins, S. L., Han, D. P., Burke, J. M., Schlievert, P. M., Wirostko, W. J., Tarasewicz, D. G., Skumatz, C. M. B.
(2004). Intravitreally Injected Human Immunoglobulin Attenuates the Effects of Staphylococcus aureus Culture Supernatant in a Rabbit Model of Toxin-Mediated Endophthalmitis. Arch Ophthalmol
122: 1499-1506
[Abstract]
[Full Text]
-
Minnaard, J., Lievin-Le Moal, V., Coconnier, M.-H., Servin, A. L., Perez, P. F.
(2004). Disassembly of F-Actin Cytoskeleton after Interaction of Bacillus cereus with Fully Differentiated Human Intestinal Caco-2 Cells. Infect. Immun.
72: 3106-3112
[Abstract]
[Full Text]
-
Callegan, M. C., Kane, S. T., Cochran, D. C., Gilmore, M. S., Gominet, M., Lereclus, D.
(2003). Relationship of plcR-Regulated Factors to BacillusEndophthalmitis Virulence. Infect. Immun.
71: 3116-3124
[Abstract]
[Full Text]
-
Callegan, M. C., Cochran, D. C., Kane, S. T., Gilmore, M. S., Gominet, M., Lereclus, D.
(2002). Contribution of Membrane-Damaging Toxins to Bacillus Endophthalmitis Pathogenesis. Infect. Immun.
70: 5381-5389
[Abstract]
[Full Text]
-
Mylonakis, E., Engelbert, M., Qin, X., Sifri, C. D., Murray, B. E., Ausubel, F. M., Gilmore, M. S., Calderwood, S. B.
(2002). The Enterococcus faecalis fsrB Gene, a Key Component of the fsr Quorum-Sensing System, Is Associated with Virulence in the Rabbit Endophthalmitis Model. Infect. Immun.
70: 4678-4681
[Abstract]
[Full Text]
-
Callegan, M. C., Engelbert, M., Parke, D. W. II, Jett, B. D., Gilmore, M. S.
(2002). Bacterial Endophthalmitis: Epidemiology, Therapeutics, and Bacterium-Host Interactions. Clin. Microbiol. Rev.
15: 111-124
[Abstract]
[Full Text]
-
Callegan, M. C., Parke II, D. W., Gilmore, M. S., Liu, S., Steidl, S. M.
(2001). Corticosteroid and Antibiotic Therapy for Bacillus Endophthalmitis. Arch Ophthalmol
119: 1391-1392
[Full Text]
-
ROBERTS, G., HOMER, K.A., TARELLI, E., PHILPOTT-HOWARD, J., DEVRIESE, L.A., BEIGHTON, D.
(2001). Distribution of endo-{beta}-N-acetylglucosaminidase amongst enterococci. J Med Microbiol
50: 620-626
[Abstract]
[Full Text]
-
Mundy, L. M., Sahm, D. F., Gilmore, M.
(2000). Relationships between Enterococcal Virulence and Antimicrobial Resistance. Clin. Microbiol. Rev.
13: 513-522
[Abstract]
[Full Text]
-
Beecher, D. J., Olsen, T. W., Somers, E. B., Wong, A. C. L.
(2000). Evidence for Contribution of Tripartite Hemolysin BL, Phosphatidylcholine-Preferring Phospholipase C, and Collagenase to Virulence of Bacillus cereus Endophthalmitis. Infect. Immun.
68: 5269-5276
[Abstract]
[Full Text]
-
Beecher, D. J., Wong, A. C. L.
(2000). Tripartite haemolysin BL: isolation and characterization of two distinct homologous sets of components from a single Bacillus cereus isolate. Microbiology
146: 1371-1380
[Abstract]
[Full Text]
-
Callegan, M. C., Booth, M. C., Jett, B. D., Gilmore, M. S.
(1999). Pathogenesis of Gram-Positive Bacterial Endophthalmitis. Infect. Immun.
67: 3348-3356
[Abstract]
[Full Text]
-
Callegan, M. C., Jett, B. D., Hancock, L. E., Gilmore, M. S.
(1999). Role of Hemolysin BL in the Pathogenesis of Extraintestinal Bacillus cereus Infection Assessed in an Endophthalmitis Model. Infect. Immun.
67: 3357-3366
[Abstract]
[Full Text]