Role of swarming migration in the pathogenesis of Bacillus endophthalmitis

被引:36
作者
Callegan, Michelle C.
Novosad, Billy D.
Ramirez, Raul
Ghelardi, Emilia
Senesi, Sonia
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Ophthalmol, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73104 USA
[3] Dean A McGee Eye Inst, Oklahoma City, OK USA
[4] Univ Pisa, Dipartimento Patol Sperimentale Biotechnol Med In, I-56100 Pisa, Italy
关键词
D O I
10.1167/iovs.06-0301
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. Bacillus cereus causes one of the most rapidly blinding forms of bacterial endophthalmitis. Migration of B. cereus throughout the eye during endophthalmitis is a unique aspect of this disease that may contribute to intraocular virulence. This study was conducted to analyze the contribution of swarming and intraocular migration to the pathogenesis of experimental endophthalmitis. METHODS. Eyes were injected intravitreally with 100 colony-forming units (CFU) of either wild-type, nonswarming, or swarming-complemented strains of B. cereus. Pathogenicity was compared throughout the course of infection by biomicroscopy, histology, electroretinography, and bacterial and inflammatory cell quantitation. RESULTS. Wild-type, nonswarming, and swarming-complemented B. cereus strains grew to a similar number in the vitreous throughout the course of infection. Unlike the wildtype and swarming-complemented strains, the nonswarming mutant did not migrate to the anterior segment during infection. The rate of decrease in retinal responses of eyes infected with the all strains was similar, resulting in near complete elimination of retinal function by 12 hours. All Bacillus strains caused similar degrees of posterior segment inflammation and retinal destruction. However, the accumulation of inflammatory cells in the anterior chamber, hyphemae, and corneal ring abscesses did not occur in eyes infected with the nonswarming mutant. CONCLUSIONS. The deficiency in swarming had little effect on retinal function loss or the overall course or severity of experimental B. cereus endophthalmitis. However, a deficiency in swarming prevented Bacillus from migrating to the anterior segment, leading to less severe anterior segment disease.
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页码:4461 / 4467
页数:7
相关论文
共 27 条
[1]  
AFFELDT JC, 1987, OPHTHALMOLOGY, V94, P407
[2]   THE ROLE OF SWARM CELL-DIFFERENTIATION AND MULTICELLULAR MIGRATION IN THE UROPATHOGENICITY OF PROTEUS-MIRABILIS [J].
ALLISON, C ;
EMODY, L ;
COLEMAN, N ;
HUGHES, C .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (05) :1155-1158
[3]   ABILITY OF PROTEUS-MIRABILIS TO INVADE HUMAN UROTHELIAL CELLS IS COUPLED TO MOTILITY AND SWARMING DIFFERENTIATION [J].
ALLISON, C ;
COLEMAN, N ;
JONES, PL ;
HUGHES, C .
INFECTION AND IMMUNITY, 1992, 60 (11) :4740-4746
[4]  
ALLISON C, 1992, MOL MICROBIOL, V6, P1583
[5]   Evidence for contribution of tripartite hemolysin BL, phosphatidylcholine-preferring phospholipase C, and collagenase to virulence of Bacillus cereus endophthalmitis [J].
Beecher, DJ ;
Olsen, TW ;
Somers, EB ;
Wong, ACL .
INFECTION AND IMMUNITY, 2000, 68 (09) :5269-5276
[6]   Chemotaxis in Vibrio cholerae [J].
Boin, MA ;
Austin, MJ ;
Häse, CC .
FEMS MICROBIOLOGY LETTERS, 2004, 239 (01) :1-8
[7]   Bacillus endophthalmitis:: Roles of bacterial toxins and motility during infection [J].
Callegan, MC ;
Kane, ST ;
Cochran, DC ;
Novosad, B ;
Gilmore, MS ;
Gominet, M ;
Lereclus, D .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46 (09) :3233-3238
[8]   Role of hemolysin BL in the pathogenesis of extraintestinal Bacillus cereus infection assessed in an endophthalmitis model [J].
Callegan, MC ;
Jett, BD ;
Hancock, LE ;
Gilmore, MS .
INFECTION AND IMMUNITY, 1999, 67 (07) :3357-3366
[9]   Relationship of plcR-regulated factors to Bacillus endophthalmitis virulence [J].
Callegan, MC ;
Kane, ST ;
Cochran, DC ;
Gilmore, MS ;
Gominet, M ;
Lereclus, D .
INFECTION AND IMMUNITY, 2003, 71 (06) :3116-3124
[10]   Contribution of membrane-damaging toxins to Bacillus endophthalmitis pathogenesis [J].
Callegan, MC ;
Cochran, DC ;
Kane, ST ;
Gilmore, MS ;
Gominet, M ;
Lereclus, D .
INFECTION AND IMMUNITY, 2002, 70 (10) :5381-5389