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Infection and Immunity, September 1999, p. 4902-4907, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Use of Genetically Manipulated Strains of Clostridium
perfringens Reveals that Both Alpha-Toxin and Theta-Toxin Are
Required for Vascular Leukostasis To Occur in Experimental Gas
Gangrene
Darren M.
Ellemor,1,*
Rebecca N.
Baird,1
Milena M.
Awad,2
Richard L.
Boyd,1
Julian I.
Rood,2 and
John J.
Emmins1
Department of Pathology and Immunology,
Monash Medical School, Alfred Hospital, Prahran, Victoria
3181,1 and Department of
Microbiology, Monash University, Clayton, Victoria
3168,2 Australia
Received 24 February 1999/Returned for modification 26 April
1999/Accepted 15 June 1999
A hallmark of gas gangrene (clostridial myonecrosis) pathology is a
paucity of leukocytes infiltrating the necrotic tissue. The cause of
this paucity most likely relates to the observation of leukocyte
aggregates at the border of the area of tissue necrosis, often within
the microvasculature itself. Infecting mice with genetically
manipulated strains of Clostridium perfringens type A
(deficient in either alpha-toxin or theta-toxin production) resulted in
significantly reduced leukocyte aggregation when alpha-toxin was absent
and complete abrogation of leukocyte aggregation when theta-toxin was
absent. Thus, both alpha-toxin and theta-toxin are necessary for the
characteristic vascular leukostasis observed in clostridial myonecrosis.
*
Corresponding author. Mailing address: Department of
Pathology and Immunology, Monash University Medical School, Alfred
Hospital, Prahran, Victoria 3181, Australia. Phone: 613 9903 0279. Fax: 613 9903 0731. E-mail:
Darren.Ellemor{at}med.monash.edu.au.
Infection and Immunity, September 1999, p. 4902-4907, Vol. 67, No. 9
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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