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Infect Immun, June 1998, p. 3012-3016, Vol. 66, No. 6
Department of Microbiology and Immunology,
Albert Einstein College of Medicine, Bronx, New York 10461
Received 31 October 1997/Returned for modification 6 January
1998/Accepted 27 March 1998
Nitric oxide (NO) generated by gamma interferon (IFN-
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Clearance of Shigella flexneri Infection
Occurs through a Nitric Oxide-Independent Mechanism
)
activation of macrophages mediates the killing of many intracellular pathogens. IFN-
is essential to innate resistance to Shigella flexneri infection. We demonstrate that NO is produced following S. flexneri infection both in mice and in activated
cells in vitro and that while it is able to kill S. flexneri in a cell-free system, it is not required for clearance
of S. flexneri in either infected mice or in activated
cells in vitro.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Ave., Bronx, NY 10461. Phone: (718) 430-2118. Fax: (718)
430-8711. E-mail: mgoldber{at}aecom.yu.edu.
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