Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/43664
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Type: Journal article
Title: A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence
Author: Stroeher, U.
Kidd, S.
Stafford, S.
Jennings, M.
Paton, J.
McEwan, A.
Citation: Journal of Infectious Diseases, 2007; 196(12):1820-1826
Publisher: Univ Chicago Press
Issue Date: 2007
ISSN: 0022-1899
1537-6613
Statement of
Responsibility: 
Uwe H. Stroeher, Robert S. Kidd, Sian L. Stafford, Michael P. Jennings, James C. Paton and Alastair G. McEwan
Abstract: A transcriptional regulator, NmlR(sp), has been identified in Streptococcus pneumoniae that is required for defense against nitric oxide (NO) stress. The nmlR(sp) gene is cotranscribed with adhC, which encodes an alcohol dehydrogenase that is able to reduce S-nitrosoglutathione (GSNO) with NADH as reductant. nmlR(sp) and adhC mutants exhibited a reduced level of NADH-GSNO oxidoreductase activity and were more susceptible to killing by NO than were wild-type cells. Comparison of the virulence of wild-type and mutant strains by use of a mouse model system showed that NmlR(sp) and AdhC do not play a key role in the adherence of pneumococci to the nasopharynx in vivo. An intraperitoneal challenge experiment revealed that both NmlR(sp) and AdhC were required for survival in blood. These data identify novel components of a NO defense system in pneumococci that are required for systemic infection.
Keywords: Nasopharynx
Respiratory Mucosa
Cell Line
Cell Line, Tumor
Animals
Humans
Mice
Neisseria gonorrhoeae
Streptococcus pneumoniae
Nitric Oxide
NAD
Aldehyde Oxidoreductases
Bacterial Proteins
DNA-Binding Proteins
Phylogeny
Virulence
Transcription, Genetic
Base Sequence
Molecular Sequence Data
Female
Description: Copyright © 2007 by the Infectious Diseases Society of America. All rights reserved.
DOI: 10.1086/523107
Published version: http://dx.doi.org/10.1086/523107
Appears in Collections:Aurora harvest
Molecular and Biomedical Science publications

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