Previous Article | Next Article ![]()
Infection and Immunity, November 2000, p. 6094-6100, Vol. 68, No. 11
Department of Microbiology, College of
Physicians and Surgeons, Columbia University, New York, New York
10032,1 and Department of Oral Pathology
and Biology, University of Medicine and Dentistry of New Jersey,
Newark, New Jersey 071032
Received 1 June 2000/Returned for modification 12 July
2000/Accepted 2 August 2000
Actinobacillus actinomycetemcomitans, the etiologic
agent for localized juvenile periodontitis and certain other human
infections, such as endocarditis, expresses a leukotoxin that acts on
polymorphonuclear leukocytes and macrophages. Leukotoxin is a member of
the highly conserved repeat toxin (RTX) family of bacterial toxins
expressed by a variety of pathogenic bacteria. While the RTX toxins of
other bacterial species are secreted, the leukotoxin of A. actinomycetemcomitans is thought to remain associated with the
bacterial cell. We have examined leukotoxin production and localization
in rough (adherent) and smooth (nonadherent) strains of A. actinomycetemcomitans. We found that leukotoxin expressed by the
rough, adherent, clinical isolate CU1000N is indeed cell
associated, as expected. However, we were surprised to find that
smooth, nonadherent strains of A. actinomycetemcomitans, including Y4, JP2 (a strain expressing a
high level of toxin), and CU1060N (an isogenic smooth variant of
CU1000N), secrete an abundance of leukotoxin into the culture supernatants during early stages of growth. After longer times of
incubation, leukotoxin disappears from the supernatants, and its loss
is accompanied by the appearance of a number of low-molecular-weight polypeptides. The secreted leukotoxin is active, as evidenced by its ability to kill HL-60 cells in vitro. We found that the growth
phase and initial pH of the growth medium significantly affect the
abundance of secreted leukotoxin, and we have developed a rapid
(<2 h) method to partially purify large amounts of leukotoxin. Remarkably, mutations in the tad genes, which are required
for tight nonspecific adherence of A. actinomycetemcomitans
to surfaces, cause leukotoxin to be released from the bacterial cell.
These studies show that A. actinomycetemcomitans has the
potential to secrete abundant leukotoxin. It is therefore appropriate
to consider a possible role for leukotoxin secretion in the
pathogenesis of A. actinomycetemcomitans.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Secretion of RTX Leukotoxin by Actinobacillus
actinomycetemcomitans
*
Corresponding author. Mailing address: Department of
Microbiology, College of Physicians and Surgeons, Columbia University, 701 W. 168th St., New York, NY 10032. Phone: (212) 305-3425. Fax: (212)
305-1468. E-mail: figurski{at}cuccfa.ccc.columbia.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»