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Abstract 


Streptococcus pneumoniae is a causative agent for bacterial pneumonia, otitis media, meningitis, and bacteremia. Mechanisms for acquisition of iron by this organism under low-iron conditions were investigated. Siderophore production was not detected by either chemical or biological methods. Its utilization of iron-containing compounds found in human hosts was tested. Both hemin and hemoglobin supported the full growth of S. pneumoniae in a culture lacking other iron sources, while lactoferrin and transferrin failed to do so. A mutant defective in hemin utilization was isolated and was less virulent than wild-type S. pneumoniae in experimental animals.

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Infect Immun. 1993 Dec; 61(12): 5401–5405.
PMCID: PMC281331
PMID: 8225615

Hemin utilization is related to virulence of Streptococcus pneumoniae.

Abstract

Streptococcus pneumoniae is a causative agent for bacterial pneumonia, otitis media, meningitis, and bacteremia. Mechanisms for acquisition of iron by this organism under low-iron conditions were investigated. Siderophore production was not detected by either chemical or biological methods. Its utilization of iron-containing compounds found in human hosts was tested. Both hemin and hemoglobin supported the full growth of S. pneumoniae in a culture lacking other iron sources, while lactoferrin and transferrin failed to do so. A mutant defective in hemin utilization was isolated and was less virulent than wild-type S. pneumoniae in experimental animals.

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  • Adams TJ, Vartivarian S, Cowart RE. Iron acquisition systems of Listeria monocytogenes. Infect Immun. 1990 Aug;58(8):2715–2718. [Europe PMC free article] [Abstract] [Google Scholar]
  • Bagg A, Neilands JB. Molecular mechanism of regulation of siderophore-mediated iron assimilation. Microbiol Rev. 1987 Dec;51(4):509–518. [Europe PMC free article] [Abstract] [Google Scholar]
  • BARDSDALE WL, PAPPENHEIMER AM., Jr Phage-host relationships in nontoxigenic and toxigenic diphtheria bacilli. J Bacteriol. 1954 Feb;67(2):220–232. [Europe PMC free article] [Abstract] [Google Scholar]
  • Berry AM, Yother J, Briles DE, Hansman D, Paton JC. Reduced virulence of a defined pneumolysin-negative mutant of Streptococcus pneumoniae. Infect Immun. 1989 Jul;57(7):2037–2042. [Europe PMC free article] [Abstract] [Google Scholar]
  • Daskaleros PA, Stoebner JA, Payne SM. Iron uptake in Plesiomonas shigelloides: cloning of the genes for the heme-iron uptake system. Infect Immun. 1991 Aug;59(8):2706–2711. [Europe PMC free article] [Abstract] [Google Scholar]
  • Dyer DW, McKenna W, Woods JP, Sparling PF. Isolation by streptonigrin enrichment and characterization of a transferrin-specific iron uptake mutant of Neisseria meningitidis. Microb Pathog. 1987 Nov;3(5):351–363. [Abstract] [Google Scholar]
  • Evans SL, Arceneaux JE, Byers BR, Martin ME, Aranha H. Ferrous iron transport in Streptococcus mutans. J Bacteriol. 1986 Dec;168(3):1096–1099. [Europe PMC free article] [Abstract] [Google Scholar]
  • Ferrante A, Rowan-Kelly B, Paton JC. Inhibition of in vitro human lymphocyte response by the pneumococcal toxin pneumolysin. Infect Immun. 1984 Nov;46(2):585–589. [Europe PMC free article] [Abstract] [Google Scholar]
  • Gillespie SH. Aspects of pneumococcal infection including bacterial virulence, host response and vaccination. J Med Microbiol. 1989 Apr;28(4):237–248. [Abstract] [Google Scholar]
  • Hanson MS, Hansen EJ. Molecular cloning, partial purification, and characterization of a haemin-binding lipoprotein from Haemophilus influenzae type b. Mol Microbiol. 1991 Feb;5(2):267–278. [Abstract] [Google Scholar]
  • Hantke K. Regulation of ferric iron transport in Escherichia coli K12: isolation of a constitutive mutant. Mol Gen Genet. 1981;182(2):288–292. [Abstract] [Google Scholar]
  • Herrington DA, Sparling PF. Haemophilus influenzae can use human transferrin as a sole source for required iron. Infect Immun. 1985 Apr;48(1):248–251. [Europe PMC free article] [Abstract] [Google Scholar]
  • Kilian M, Mestecky J, Schrohenloher RE. Pathogenic species of the genus Haemophilus and Streptococcus pneumoniae produce immunoglobulin A1 protease. Infect Immun. 1979 Oct;26(1):143–149. [Europe PMC free article] [Abstract] [Google Scholar]
  • Law D, Wilkie KM, Freeman R, Gould FK. The iron uptake mechanisms of enteropathogenic Escherichia coli: the use of haem and haemoglobin during growth in an iron-limited environment. J Med Microbiol. 1992 Jul;37(1):15–21. [Abstract] [Google Scholar]
  • McKee AS, McDermid AS, Baskerville A, Dowsett AB, Ellwood DC, Marsh PD. Effect of hemin on the physiology and virulence of Bacteroides gingivalis W50. Infect Immun. 1986 May;52(2):349–355. [Europe PMC free article] [Abstract] [Google Scholar]
  • Mickelsen PA, Sparling PF. Ability of Neisseria gonorrhoeae, Neisseria meningitidis, and commensal Neisseria species to obtain iron from transferrin and iron compounds. Infect Immun. 1981 Aug;33(2):555–564. [Europe PMC free article] [Abstract] [Google Scholar]
  • Otto BR, Sparrius M, Verweij-van Vught AM, MacLaren DM. Iron-regulated outer membrane protein of Bacteroides fragilis involved in heme uptake. Infect Immun. 1990 Dec;58(12):3954–3958. [Europe PMC free article] [Abstract] [Google Scholar]
  • Paton JC, Ferrante A. Inhibition of human polymorphonuclear leukocyte respiratory burst, bactericidal activity, and migration by pneumolysin. Infect Immun. 1983 Sep;41(3):1212–1216. [Europe PMC free article] [Abstract] [Google Scholar]
  • Paton JC, Lock RA, Hansman DJ. Effect of immunization with pneumolysin on survival time of mice challenged with Streptococcus pneumoniae. Infect Immun. 1983 May;40(2):548–552. [Europe PMC free article] [Abstract] [Google Scholar]
  • Paton JC, Rowan-Kelly B, Ferrante A. Activation of human complement by the pneumococcal toxin pneumolysin. Infect Immun. 1984 Mar;43(3):1085–1087. [Europe PMC free article] [Abstract] [Google Scholar]
  • Payne SM. Iron and virulence in the family Enterobacteriaceae. Crit Rev Microbiol. 1988;16(2):81–111. [Abstract] [Google Scholar]
  • Perry RD, Brubaker RR. Accumulation of iron by yersiniae. J Bacteriol. 1979 Mar;137(3):1290–1298. [Europe PMC free article] [Abstract] [Google Scholar]
  • Russell LM, Holmes RK. Initial characterization of the ferric iron transport system of Corynebacterium diphtheriae. J Bacteriol. 1983 Sep;155(3):1439–1442. [Europe PMC free article] [Abstract] [Google Scholar]
  • Schneider R, Hantke K. Iron-hydroxamate uptake systems in Bacillus subtilis: identification of a lipoprotein as part of a binding protein-dependent transport system. Mol Microbiol. 1993 Apr;8(1):111–121. [Abstract] [Google Scholar]
  • Schwyn B, Neilands JB. Universal chemical assay for the detection and determination of siderophores. Anal Biochem. 1987 Jan;160(1):47–56. [Abstract] [Google Scholar]
  • Snow GA. Mycobactins: iron-chelating growth factors from mycobacteria. Bacteriol Rev. 1970 Jun;34(2):99–125. [Europe PMC free article] [Abstract] [Google Scholar]
  • Stahl WL, O'Toole RD. Pneumococcal neuraminidase: purification and properties. Biochim Biophys Acta. 1972 May 12;268(2):480–487. [Abstract] [Google Scholar]
  • Stoebner JA, Payne SM. Iron-regulated hemolysin production and utilization of heme and hemoglobin by Vibrio cholerae. Infect Immun. 1988 Nov;56(11):2891–2895. [Europe PMC free article] [Abstract] [Google Scholar]
  • Tai SP, Krafft AE, Nootheti P, Holmes RK. Coordinate regulation of siderophore and diphtheria toxin production by iron in Corynebacterium diphtheriae. Microb Pathog. 1990 Oct;9(4):267–273. [Abstract] [Google Scholar]
  • Yeowell HN, White JR. Iron requirement in the bactericidal mechanism of streptonigrin. Antimicrob Agents Chemother. 1982 Dec;22(6):961–968. [Europe PMC free article] [Abstract] [Google Scholar]
  • Zimmermann L, Angerer A, Braun V. Mechanistically novel iron(III) transport system in Serratia marcescens. J Bacteriol. 1989 Jan;171(1):238–243. [Europe PMC free article] [Abstract] [Google Scholar]
  • Zimmermann L, Hantke K, Braun V. Exogenous induction of the iron dicitrate transport system of Escherichia coli K-12. J Bacteriol. 1984 Jul;159(1):271–277. [Europe PMC free article] [Abstract] [Google Scholar]

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