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Infection and Immunity, November 2001, p. 7010-7019, Vol. 69, No. 11
Department of Pediatrics and Communicable
Diseases, University of Michigan Medical
School,1 and Department of
Epidemiology, University of Michigan School of Public
Health,3 Ann Arbor, Michigan 48109, and
Department of Biology, Eastern Michigan University, Ypsilanti,
Michigan 481972
Received 21 May 2001/Returned for modification 18 July
2001/Accepted 15 August 2001
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
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.11.7010-7019.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Analysis of Pilus Adhesins from Haemophilus
influenzae Biotype IV Strains
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.
*
Corresponding author. Mailing address: Department of
Pediatrics and Communicable Diseases, The University of Michigan, L2224 Women's Hospital Box 0244, Ann Arbor, MI 48109-2029. Phone: (734) 763-2440. Fax: (734) 936-7635. E-mail: gilsdorf{at}umich.edu.
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