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Comparative Analysis of the Structures of the Outer Membrane Protein P1 Genes from Major Clones of Haemophilus Influenzae Type B

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Journal Infect Immun
Date 1989 Nov 1
PMID 2572549
Citations 12
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Abstract

P1 outer membrane proteins from Haemophilus influenzae type b are heterogeneous antigenically and with respect to apparent molecular weight in sodium dodecyl sulfate-polyacrylamide gel electrophoresis. For determination of the molecular basis for the differences in the P1 proteins, the genes for the P1 proteins from strain 1613, representative of outer membrane protein subtype 3L, and strain 8358, representative of outer membrane protein subtype 6U, were cloned, sequenced, and compared with the previously reported gene for the P1 protein from strain MinnA, a strain with the outer membrane protein subtype 1H. These prototype strains are representatives of the three major clonal families of H. influenzae type b responsible for invasive disease in diverse areas of the world. The nucleotide sequences of the P1 genes from strains 1613 and 8358 were 94 and 90% identical to the MinnA sequence, respectively. The derived amino acid sequences were 91 and 86% identical, respectively. Heterogeneity between the MinnA and 1613 proteins was largely localized to two short variable regions; the protein from strain 8538 contained a third variable region not observed in the other P1 proteins. Thus, the outer membrane protein P1 genes are highly conserved; the variable regions may code for the previously demonstrated strain-specific antigenic determinants.

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References
1.
Rodrigues L, Schneerson R, Robbins J . Immunity to Hemophilus influenzae type b. I. The isolation, and some physicochemical, serologic and biologic properties of the capsular polysaccharide of Hemophilus influenzae type b. J Immunol. 1971; 107(4):1071-80. View

2.
Weinberg G, Ghafoor A, Ishaq Z, Nomani N, Kabeer M, Anwar F . Clonal analysis of Hemophilus influenzae isolated from children from Pakistan with lower respiratory tract infections. J Infect Dis. 1989; 160(4):634-43. DOI: 10.1093/infdis/160.4.634. View

3.
Loeb M, Smith D . Outer membrane protein composition in disease isolates of Haemophilus influenzae: pathogenic and epidemiological implications. Infect Immun. 1980; 30(3):709-17. PMC: 551373. DOI: 10.1128/iai.30.3.709-717.1980. View

4.
Barenkamp S, Munson Jr R, Granoff D . Subtyping isolates of Haemophilus influenzae type b by outer-membrane protein profiles. J Infect Dis. 1981; 143(5):668-76. DOI: 10.1093/infdis/143.5.668. View

5.
Barenkamp S, Munson Jr R, Granoff D . Comparison of outer-membrane protein subtypes and biotypes of isolates of Haemophilus influenzae type b. J Infect Dis. 1981; 144(5):480. DOI: 10.1093/infdis/144.5.480. View