In vitro cellular toxicity predicts Pseudomonas aeruginosa virulence in lung infections

被引:96
作者
Sawa, T
Ohara, M
Kurahashi, K
Twining, SS
Frank, DW
Doroques, DB
Long, T
Gropper, MA
Wiener-Kronish, JP
机构
[1] Univ Calif San Francisco, Inst Cardiovasc Res, Dept Anesthesia, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Inst Cardiovasc Res, Dept Med, San Francisco, CA 94143 USA
[3] Med Coll Wisconsin, Dept Microbiol, Milwaukee, WI 53226 USA
关键词
D O I
10.1128/IAI.66.7.3242-3249.1998
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The role of quorum sensing by Pseudomonas aeruginosa in producing cytotoxicity has not been fully investigated. Strains of P. aeruginosa have been characterized as having an invasive or a cytotoxic phenotype (S. M. J. Fleiszig et al., Infect. Immun. 65:579-586, 1997). We noted that the application of a large inoculum of the invasive strain 6291 caused cytotoxicity of cultured epithelial cells. To investigate this dose-related cytotoxicity, we compared the behavior of 6294 to that of another invasive strain, PAO1, and determined whether the cytotoxicity could be related to quorum sensing. Both invasive strains, 6291 and PAO1, appear to have quorum-sensing systems that were operative when large doses of bacteria were applied to cultured lung epithelial cells or instilled into the lungs of animals. Nonetheless, only 6294 was cytotoxic. Cytotoxicity induced by 6294 correlated with increased elastase production. These experiments suggest that there are multiple mechanisms for the induction of cytotoxicity, pathology, and mortality in vivo. However, in vivo cytotoxicity and mortality, but not pathology, could be predicted by quantitative in vitro cellular damage experiments utilizing a range of bacteria-to-cell ratios. It appears that quorum sensing may inversely correlate with virulence in that strains that produced PAI [N-(3-oxododecanoyl) homoserine lactone] also appeared to attract more polymorphonuclear leukocytes in vivo and were possibly eliminated more quickly. In addition, exoproduct production in bacteriological medium in vitro may differ significantly from exoproduct expression from infections in vivo or during cocultivation of bacteria with tissue culture cells.
引用
收藏
页码:3242 / 3249
页数:8
相关论文
共 34 条
[1]  
Brewer C, 1996, CHEST, V109, P1019
[2]   SYNTHESIS OF MULTIPLE EXOPRODUCTS IN PSEUDOMONAS-AERUGINOSA IS UNDER THE CONTROL OF RHLR-RHLI, ANOTHER SET OF REGULATORS IN STRAIN PAO1 WITH HOMOLOGY TO THE AUTOINDUCER-RESPONSIVE LUXR-LUXI FAMILY [J].
BRINT, JM ;
OHMAN, DE .
JOURNAL OF BACTERIOLOGY, 1995, 177 (24) :7155-7163
[3]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[4]  
Craven D E, 1996, Semin Respir Infect, V11, P32
[5]   The involvement of cell-to-cell signals in the development of a bacterial biofilm [J].
Davies, DG ;
Parsek, MR ;
Pearson, JP ;
Iglewski, BH ;
Costerton, JW ;
Greenberg, EP .
SCIENCE, 1998, 280 (5361) :295-298
[6]   DIVERSE PSEUDOMONAS-AERUGINOSA GENE-PRODUCTS STIMULATE RESPIRATORY EPITHELIAL-CELLS TO PRODUCE INTERLEUKIN-8 [J].
DIMANGO, E ;
ZAR, HJ ;
BRYAN, R ;
PRINCE, A .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (05) :2204-2210
[7]  
DUNN M, 1995, CLIN CHEST MED, V16, P95
[8]   Histopathologic and microbiologic aspects of ventilator-associated pneumonia [J].
Fabregas, N ;
Torres, A ;
ElEbiary, M ;
Ramirez, J ;
Hernandez, C ;
Gonzalez, J ;
delaBellacasa, JP ;
deAnta, J ;
RodriguezRoisin, R .
ANESTHESIOLOGY, 1996, 84 (04) :760-771
[9]   NOSOCOMIAL PNEUMONIA IN VENTILATED PATIENTS - A COHORT STUDY EVALUATING ATTRIBUTABLE MORTALITY AND HOSPITAL STAY [J].
FAGON, JY ;
CHASTRE, J ;
HANCE, AJ ;
MONTRAVERS, P ;
NOVARA, A ;
GIBERT, C .
AMERICAN JOURNAL OF MEDICINE, 1993, 94 (03) :281-288
[10]   ExoU expression by Pseudomonas aeruginosa correlates with acute cytotoxicity and epithelial injury [J].
FinckBarbancon, V ;
Goranson, J ;
Zhu, L ;
Sawa, T ;
WienerKronish, JP ;
Fleiszig, SMJ ;
Wu, C ;
MendeMueller, L ;
Frank, DW .
MOLECULAR MICROBIOLOGY, 1997, 25 (03) :547-557