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Klebsiella pneumoniae: Selected Virulence Factors that Contribute to Pathogenicity

Published online by Cambridge University Press:  02 January 2015

Anita K. Highsmith*
Affiliation:
Hospital Infections Program, Center for Infectious Diseases, Centers for Disease Control, Atlanta, Georgia
William R. Jarvis
Affiliation:
Hospital Infections Program, Center for Infectious Diseases, Centers for Disease Control, Atlanta, Georgia
*
Nosocomial Infections Laboratory Branch, Hospital Infections Program, Center for Infectious Diseases, Centers for Disease Control, Atlanta, GA 30333

Abstract

Klebsiella pneumoniae infections occur in humans of all ages, however the highest risk groups appear to be infants, the elderly and the immunocompromised. One or more virulence factors may contribute to pathogenicity in humans. In this article we review three factors that may mediate virulence: cell wall receptors, capsular polysaccharide, and endotoxin.

First, the presence of cell wall receptors enables K. pneumoniae to attach to the host cell, thereby altering the bacterial surface so that phagocytosis by polymorphonuclear leukocytes and macrophages is impaired and invasion of the non-phagocytic host cell is facilitated. Second, invasion of the host cell is also facilitated by the large polysaccharide capsule surrounding the bacterial cell; in addition this capsule acts as a barrier and protects the bacteria from phagocytosis. Third, K. pneumoniae produces an endotoxin that appears to be independent of factors that determine receptors and capsular characteristics. Marked interspecies differences in endotoxin production may correlate with virulence. Although some or all of these factors may ultimately determine virulence, the interaction of these factors in vivo has made it difficult to assess the relative contribution of any one of these virulence factors. The pathogenic mechanisms of K. pneumoniae that ultimately determine virulence remain unclear and will require further study.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1985

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References

1. Fader, RC, Avots-Avotins, AE, Davis, CP: Evidence for pili-mediated adherence of Klebsiella pneumoniae to rat bladder epithelial cells in vitro. Infect Immun 1979; 25:729737.Google Scholar
2. Fader, RC, Davis, CP: Klebsiella pneumoniae induced experimental pyelitis: The effect of piliation on infectivity. J Urol 1982; 128:197201.Google Scholar
3. Pruzzo, C, Valisena, S, Satta, G: Laboratory and wild-type Klebsiella pneumoniae strains carrying mannose-inhibitable adhesions and receptors for coliphages T3 and T7. Infect Immun 1983;39:520527.Google Scholar
4. Pruzzo, C, Debbia, EA, Satta, G: Identification of the major adherence ligand of Klebsiella pneumoniae in the receptor for coliphage T7 and alteration of Klebsiella adherence properties by lysogenic conversion. Infect Immun 1980; 30:562571.CrossRefGoogle ScholarPubMed
5. Pruzzo, C, Debbia, E, Satta, G: Mannose-inhibitable adhesions and T3-T7 receptors of Klebsiella pneumoniae inhibit phagocytosis and intracellular killing by human polymorphonuclear leukocytes. Infect Immun 1982; 36:949957.Google Scholar
6. Ehrenworth, L, Baer, H: The pathogenicity of Klebsiella pneumoniae for mice: The relationship to the quantity and rate of production of type specific capsular polysaccharide. J Bacteriol 1956; 72:713717.Google Scholar
7. Julianelle, LA: A biological classification of Encapsulate pneumoniae (Friedlanders bacillus) . J Exp Med 1926; 44:113128.Google Scholar
8. DuBose, RJ, Hirsch, JG: Bacterial and Mycotic Infections of Man, ed 4. Philadelphia, JB Lippincott Company, 1965.Google Scholar
9. Cryz, SJ Jr, Furer, E, Germanier, R: Experimental Klebsiella pneumoniae burn wound sepsis: Role of capsular polysaccharide. Infect Immun 1984; 43:440441.Google Scholar
10. Domenico, P, Johanson, WG Jr, Straus, DC: Lobar pneumoniae in rats produced by clinical isolates of Klebsiella pneumoniae . Infect Immun 1982; 37:327335.Google Scholar
11. Kato, N, Kato, O, Nahashima, I: Effect of capsule polysaccharide of Klebsiella pneumoniae on host resistance to bacterial infections. I. Induction of increased susceptibility to infections in mice. Japanese Journal of Microbiology 1976; 20:163172.Google Scholar
12. Nakashima, I, Kobayashi, T, Kato, N: Alterations in the antibody response to bovine serum albumin by capsular polysaccharide of Klebsiella pneumoniae . J Immunol 1971; 107:11121121.Google Scholar
13. Luderwitz, O, Jana, K, Wheat, R: Somatic and capsular antigen of gram-negative bacteria in, Comprehensive Biochemistry, 26A Amsterdam, Elsevier, 1968; 105228.Google Scholar
14. Highsmith, AK, Jarvis, WR, Vukajovich, S, et al: Endotoxin production of Klebsiella pneumoniae as a virulence factor in disease. Proceedings of the Annual Meeting of the American Society for Microbiology. St. Louis, Missouri, 1984.Google Scholar
15. Heiander, I, Saxen, H, Salkinoja-Salonen, M, et al: Pulmonary toxicity of endotoxins: Comparison of lipopolysaccharices from various bacterial species. Infect Immun 1982; 35:528532.Google Scholar
16. Morrison, DC, Ulevitch, RJ: The effects of bacterial endotoxin on host mediation systems. Am J Pathol 1978; 93:525618.Google ScholarPubMed
17. Michalek, SM, Moore, RN, McGhee, JR, et al: The primary role of lymphoreticular cells in the mediation of host responses to bacterial endotoxin. J Infect Dis 1980; 141:5563.Google Scholar
18. Slack, JM, Snyder, IS: Bacteria and Human Disease. Chicago, Year Book Medical Publishers, Inc., 1978.Google Scholar
19. Jarvis, WR, Highsmith, AK: Bacterial growth and endotoxin production in lipid emulsion. J Clin Microbiol 1984; 19:1720.Google Scholar