Affiliation:
1. Department of Pediatrics and Communicable Diseases, University of Michigan Medical School,1 and
2. Department of Epidemiology, University of Michigan School of Public Health,2 Ann Arbor, Michigan
Abstract
ABSTRACT
Adherence of
Haemophilus influenzae
to epithelial cells plays a central role in colonization and is the first step in infection with this organism. Pili, which are large polymorphic surface proteins, have been shown to mediate the binding of
H. influenzae
to cells of the human respiratory tract. Earlier experiments have demonstrated that the major epitopes of
H. influenzae
pili are highly conformational and immunologically heterogenous; their subunit pilins are, however, immunologically homogenous. To define the extent of structural variation in pilins, which polymerize to form pili, the pilin genes (
hifA
) of 26 type a to f and 16 nontypeable strains of
H. influenzae
were amplified by PCR and subjected to restriction fragment length polymorphism (RFLP) analysis with
Alu
I and
Rsa
I. Six different RFLP patterns were identified. Four further RFLP patterns were identified from published
hifA
sequences from five nontypeable
H. influenzae
strains. Two patterns contained only nontypeable isolates; one of these contained
H. influenzae
biotype aegyptius strains F3031 and F3037. Another pattern contained predominantly
H. influenzae
type f strains. All other patterns were displayed by a variety of capsular and noncapsular types. Sequence analysis of selected
hifA
genes confirmed the 10 RFLP patterns and showed strong identity among representatives displaying the same RFLP patterns. In addition, the immunologic reactivity of pili with antipilus antisera correlated with the groupings of strains based on
hifA
RFLP patterns. Those strains that show greater reactivity with antiserum directed against
H. influenzae
type b strain M43 pili tend to fall into one RFLP pattern (pattern 3); while those strains that show equal or greater reactivity with antiserum directed against
H. influenzae
type b strain Eagan pili tend to fall in a different RFLP pattern (pattern 1). Sequence analysis of representative HifA pilins from typeable and nontypeable
H. influenzae
identified several highly conserved regions that play a role in bacterial pilus assembly and other regions with considerable amino acid heterogeneity. These regions of HifA amino acid sequence heterogeneity may explain the immunologic diversity seen in intact pili.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
29 articles.
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