Affiliation:
1. Department of Pediatrics and Communicable Diseases, University of Michigan Medical School,1 and
2. Department of Biology, Eastern Michigan University, Ypsilanti, Michigan 481972
3. Department of Epidemiology, University of Michigan School of Public Health,3 Ann Arbor, Michigan 48109, and
Abstract
ABSTRACT
A subset of nontypeable
Haemophilus influenzae
(NTHI) biotype IV isolates from the human genital tract or from infected newborn infants forms a cryptic genospecies characterized by, among other features, the presence of peritrichous pili. The objective of this study was to determine the similarity of these pili to hemagglutinating, HifA- and HifE-containing pili expressed by respiratory
H. influenzae
isolates. For this analysis, the presence of
hifA
and
hifE
and their gene products in NTHI biotype IV strains was assessed, the binding of
H. influenzae
biotype IV strains to human epithelial cells was characterized, possible genital tissue tropism of these isolates was explored, and the role of HifA- and HifE-possessing pili in the adhesion of NTHI biotype IV strains to human epithelial cells was determined. None of the six biotype IV NTHI isolates tested agglutinated human red blood cells, nor could they be enriched for hemagglutinating variants. Although
hifA
, which encodes the major structural subunit of hemagglutinating pili, and
hifE
, which encodes the tip adhesin of hemagglutinating pili, were detected by PCR from six and five, respectively, of the six biotype IV strains tested, neither HifA nor HifE (the gene products of
hifA
and
hifE
) were detected in any of these strains by Western blot analysis using antisera that recognize HifA and HifE of respiratory strains. Transmission electron microscopy showed no surface pili on the two biotype IV
H. influenzae
isolates examined; strain 4162 containing an insertional mutation in
hifA
also showed no surface pili, whereas strain 1595 containing an insertional mutation in
hifB
showed pilus-like structures that were shorter and thicker than hemagglutinating pili of the respiratory strains AAr176 and M43. In enzyme-linked immunosorbent assays, biotype IV strains adhered to 16HBE14o
−
and HEp-2 cells of respiratory origin as well as to ME180 and HeLa cells of genital origin. This adherence was not pilus specific, however, as GM-1, a known pilus receptor analog, did not inhibit binding of biotype IV strains to ME180, HEp-2, or HeLa cells, and GM-1 inhibition of binding to 16HBE14o
−
cells did not correlate with the presence of
hifE
. While both nonpiliated variants and
hifA
and
hifB
(encoding the pilus chaperone) mutants of respiratory strain AAr176 showed reduced binding (64 to 87% of that of piliated AAr176) to 16HBE14o
−
and ME180 cells,
hifA
and
hifB
mutants of the biotype IV strains showed minimal reduction in binding to these cell lines (91 to 98% of that of wild-type strains). Thus, although biotype IV
H. influenzae
isolates of the cryptic genospecies possess the genes that code for HifA- and HifE-containing hemagglutinating pili, epithelial cell adherence exhibited by these strains is not mediated by expression of hemagglutinating pili.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
6 articles.
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