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Infection and Immunity, June 1999, p. 3009-3013, Vol. 67, No. 6
Departments of Microbiology and
Immunology1 and of
Medicine,2 University of North Carolina
School of Medicine, Chapel Hill, North Carolina 27599
Received 21 August 1998/Returned for modification 1 December
1998/Accepted 10 March 1999
Many mucosal pathogens, including Neisseria
gonorrhoeae, produce proteases that cleave immunoglobulin A
(IgA), the predominant immunoglobulin class produced at mucosal
surfaces. While considerable circumstantial evidence suggests that IgA1
protease contributes to gonococcal virulence, there is no direct
evidence that N. gonorrhoeae requires IgA1 protease
activity to infect a human host. We constructed a N. gonorrhoeae
iga mutant without introducing new antibiotic resistance markers
into the final mutant strain and used human experimental infection to
test the ability of the mutant to colonize the male urethra and to
cause gonococcal urethritis. Four of the five male volunteers
inoculated with the Iga
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
A Neisseria gonorrhoeae Immunoglobulin
A1 Protease Mutant Is Infectious in the Human Challenge Model of
Urethral Infection

mutant became infected. In every
respect
clinical signs and symptoms, incubation period between
inoculation and infection, and the proportion of volunteers
infected
the outcome of human experimental infection with
FA1090iga was indistinguishable from that previously
reported for a variant of parent strain FA1090 matching the mutant in
expression of Opa proteins, lipooligosaccharide, and pilin. These
results indicate that N. gonorrhoeae does not require IgA1
protease production to cause experimental urethritis in males.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, CB#7290, 804 Mary Ellen Jones Building, University of North Carolina, Chapel Hill, NC 27599. Phone: (919) 966-4774. Fax: (919) 962-8103. E-mail: jgc{at}med.unc.edu.
Present address: Laboratory Corp. of America, Center for Molecular
Biology and Pathology, Research Triangle Park, NC 27709.
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