Abstract
Haemophilus influenzae has the ability to obtain iron from human transferrin via two bacterial cell surface transferrin binding proteins, Tbp1 and Tbp2. Although a wide array of strains have been shown to express these receptor proteins, two studies have recently identified a series of isolates which appeared to lack the ability to bind transferrin. Included in this group were the members of a cryptic genospecies of nontypeable biotype IV strains which appear to possess a tropism for female urogenital tissues and are major etiologic agents of neonatal and postpartum bacteremia due to H. influenzae. The present study employed oligonucleotide primers specific for genes encoding the Tbp proteins of a type b biotype I strain of H. influenzae to probe the genomic DNAs of isolates from the previous studies. The tbpA and tbpB genes which encode Tbp1 and Tbp2, respectively, were detected in all of the strains tested either by PCR amplification directly or by Southern hybridization analysis. All of the strains displayed a transferrin binding phenotype, and affinity isolation of receptor proteins with transferrin-conjugated Sepharose recovered Tbp1 and/or Tbp2 from 11 of 14 strains, including 2 of the nontypeable biotype IV strains. In addition, all of the strains were capable of growing on human transferrin specifically, indicating that the mechanism of iron assimilation from transferrin is functional and is not siderophore mediated. These results confirm the presence of tbp genes in all of the invasive H. influenzae isolates characterized to date, suggesting that Tbp-mediated iron acquisition is important in disease which initiates from either the respiratory or urogenital mucosa.
Full Text
The Full Text of this article is available as a PDF (521.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Albritton W. L., Brunton J. L., Meier M., Bowman M. N., Slaney L. A. Haemophilus influenzae: comparison of respiratory tract isolates with genitourinary tract isolates. J Clin Microbiol. 1982 Nov;16(5):826–831. doi: 10.1128/jcm.16.5.826-831.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barcak G. J., Chandler M. S., Redfield R. J., Tomb J. F. Genetic systems in Haemophilus influenzae. Methods Enzymol. 1991;204:321–342. doi: 10.1016/0076-6879(91)04016-h. [DOI] [PubMed] [Google Scholar]
- Crosa J. H. Genetics and molecular biology of siderophore-mediated iron transport in bacteria. Microbiol Rev. 1989 Dec;53(4):517–530. doi: 10.1128/mr.53.4.517-530.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Friesen C. A., Cho C. T. Characteristic features of neonatal sepsis due to Haemophilus influenzae. Rev Infect Dis. 1986 Sep-Oct;8(5):777–780. doi: 10.1093/clinids/8.5.777. [DOI] [PubMed] [Google Scholar]
- Gonzalez G. C., Caamano D. L., Schryvers A. B. Identification and characterization of a porcine-specific transferrin receptor in Actinobacillus pleuropneumoniae. Mol Microbiol. 1990 Jul;4(7):1173–1179. doi: 10.1111/j.1365-2958.1990.tb00692.x. [DOI] [PubMed] [Google Scholar]
- Gray-Owen S. D., Loosmore S., Schryvers A. B. Identification and characterization of genes encoding the human transferrin-binding proteins from Haemophilus influenzae. Infect Immun. 1995 Apr;63(4):1201–1210. doi: 10.1128/iai.63.4.1201-1210.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hardie K. R., Adams R. A., Towner K. J. Transferrin-binding ability of invasive and commensal isolates of Haemophilus spp. J Med Microbiol. 1993 Sep;39(3):218–224. doi: 10.1099/00222615-39-3-218. [DOI] [PubMed] [Google Scholar]
- Herrington D. A., Sparling P. F. Haemophilus influenzae can use human transferrin as a sole source for required iron. Infect Immun. 1985 Apr;48(1):248–251. doi: 10.1128/iai.48.1.248-251.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holland J., Langford P. R., Towner K. J., Williams P. Evidence for in vivo expression of transferrin-binding proteins in Haemophilus influenzae type b. Infect Immun. 1992 Jul;60(7):2986–2991. doi: 10.1128/iai.60.7.2986-2991.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Irwin S. W., Averil N., Cheng C. Y., Schryvers A. B. Preparation and analysis of isogenic mutants in the transferrin receptor protein genes, tbpA and tbpB, from Neisseria meningitidis. Mol Microbiol. 1993 Jun;8(6):1125–1133. doi: 10.1111/j.1365-2958.1993.tb01657.x. [DOI] [PubMed] [Google Scholar]
- Kilian M. A taxonomic study of the genus Haemophilus, with the proposal of a new species. J Gen Microbiol. 1976 Mar;93(1):9–62. doi: 10.1099/00221287-93-1-9. [DOI] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Morton D. J., Musser J. M., Stull T. L. Expression of the Haemophilus influenzae transferrin receptor is repressible by hemin but not elemental iron alone. Infect Immun. 1993 Oct;61(10):4033–4037. doi: 10.1128/iai.61.10.4033-4037.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morton D. J., Williams P. Siderophore-independent acquisition of transferrin-bound iron by Haemophilus influenzae type b. J Gen Microbiol. 1990 May;136(5):927–933. doi: 10.1099/00221287-136-5-927. [DOI] [PubMed] [Google Scholar]
- Murphy T. F., Kirkham C., Sikkema D. J. Neonatal, urogenital isolates of biotype 4 nontypeable Haemophilus influenzae express a variant P6 outer membrane protein molecule. Infect Immun. 1992 May;60(5):2016–2022. doi: 10.1128/iai.60.5.2016-2022.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Musser J. M., Barenkamp S. J., Granoff D. M., Selander R. K. Genetic relationships of serologically nontypable and serotype b strains of Haemophilus influenzae. Infect Immun. 1986 Apr;52(1):183–191. doi: 10.1128/iai.52.1.183-191.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Otto B. R., Verweij-van Vught A. M., MacLaren D. M. Transferrins and heme-compounds as iron sources for pathogenic bacteria. Crit Rev Microbiol. 1992;18(3):217–233. doi: 10.3109/10408419209114559. [DOI] [PubMed] [Google Scholar]
- Pidcock K. A., Wooten J. A., Daley B. A., Stull T. L. Iron acquisition by Haemophilus influenzae. Infect Immun. 1988 Apr;56(4):721–725. doi: 10.1128/iai.56.4.721-725.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quentin R., Goudeau A., Wallace R. J., Jr, Smith A. L., Selander R. K., Musser J. M. Urogenital, maternal and neonatal isolates of Haemophilus influenzae: identification of unusually virulent serologically non-typable clone families and evidence for a new Haemophilus species. J Gen Microbiol. 1990 Jul;136(7):1203–1209. doi: 10.1099/00221287-136-7-1203. [DOI] [PubMed] [Google Scholar]
- Quentin R., Musser J. M., Mellouet M., Sizaret P. Y., Selander R. K., Goudeau A. Typing of urogenital, maternal, and neonatal isolates of Haemophilus influenzae and Haemophilus parainfluenzae in correlation with clinical source of isolation and evidence for a genital specificity of H. influenzae biotype IV. J Clin Microbiol. 1989 Oct;27(10):2286–2294. doi: 10.1128/jcm.27.10.2286-2294.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosenau A., Sizaret P. Y., Musser J. M., Goudeau A., Quentin R. Adherence to human cells of a cryptic Haemophilus genospecies responsible for genital and neonatal infections. Infect Immun. 1993 Oct;61(10):4112–4118. doi: 10.1128/iai.61.10.4112-4118.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schryvers A. B. Identification of the transferrin- and lactoferrin-binding proteins in Haemophilus influenzae. J Med Microbiol. 1989 Jun;29(2):121–130. doi: 10.1099/00222615-29-2-121. [DOI] [PubMed] [Google Scholar]
- Schryvers A. B., Morris L. J. Identification and characterization of the transferrin receptor from Neisseria meningitidis. Mol Microbiol. 1988 Mar;2(2):281–288. doi: 10.1111/j.1365-2958.1988.tb00029.x. [DOI] [PubMed] [Google Scholar]
- Shurin S. B., Anderson P., Zollinger J., Rathbun R. K. Pathophysiology of hemolysis in infections with Hemophilus influenzae type b. J Clin Invest. 1986 Apr;77(4):1340–1348. doi: 10.1172/JCI112439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stein D. C., Silver L. E., Clark V. L., Young F. E. Construction and characterization of a new shuttle vector, pLES2, capable of functioning in Escherichia coli and Neisseria gonorrhoeae. Gene. 1983 Nov;25(2-3):241–247. doi: 10.1016/0378-1119(83)90228-7. [DOI] [PubMed] [Google Scholar]
- Stevenson P., Williams P., Griffiths E. Common antigenic domains in transferrin-binding protein 2 of Neisseria meningitidis, Neisseria gonorrhoeae, and Haemophilus influenzae type b. Infect Immun. 1992 Jun;60(6):2391–2396. doi: 10.1128/iai.60.6.2391-2396.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stull T. L. Protein sources of heme for Haemophilus influenzae. Infect Immun. 1987 Jan;55(1):148–153. doi: 10.1128/iai.55.1.148-153.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Baker C. J., Quinones F. J., Hollis D. G., Weaver R. E., Wiss K. Nontypable Haemophilus influenzae (biotype 4) as a neonatal, maternal, and genital pathogen. Rev Infect Dis. 1983 Jan-Feb;5(1):123–136. doi: 10.1093/clinids/5.1.123. [DOI] [PubMed] [Google Scholar]
- Weinberg E. D. Iron and infection. Microbiol Rev. 1978 Mar;42(1):45–66. doi: 10.1128/mr.42.1.45-66.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu R., Schryvers A. B. Transferrin receptors on ruminant pathogens vary in their interaction with the C-lobe and N-lobe of ruminant transferrins. Can J Microbiol. 1994 Jul;40(7):532–540. doi: 10.1139/m94-086. [DOI] [PubMed] [Google Scholar]