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Infection and Immunity, March 2000, p. 1061-1068, Vol. 68, No. 3
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
A Shift from Oral to Blood pH Is a Stimulus for Adaptive Gene
Expression of Streptococcus gordonii CH1 and Induces
Protection against Oxidative Stress and Enhanced Bacterial Growth
by Expression of msrA
Aldwin J. M.
Vriesema,*
Jacob
Dankert, and
Sebastian A. J.
Zaat
Department of Medical Microbiology, Academic
Medical Center, 1105 AZ Amsterdam, The Netherlands
Received 14 July 1999/Returned for modification 9 September
1999/Accepted 16 November 1999
Viridans group streptococci (VS) from the oral cavity entering the
bloodstream may initiate infective endocarditis (IE). We aimed
to identify genes expressed in response to a pH increase from slightly
acidic (pH 6.2) to neutral (pH 7.3) as encountered by VS entering the
bloodstream from the oral cavity. Using a recently developed
promoter-screening vector, we isolated five promoter fragments from the
genomic DNA of Streptococcus gordonii CH1 responding to
this stimulus. No common regulatory sequences were identified in these
promoter fragments that could account for the coordinate expression of
the corresponding genes. One of the isolated fragments contained the promoter region and 5' end of a gene highly homologous to
the methionine sulfoxide reductase gene (msrA) of
various bacterial and eukaryotic species. This gene has been found to
be activated in S. gordonii strain V288 in a
rabbit model of IE (A. O. Kiliç, M. C. Herzberg,
M. W. Meyer, X. Zhao, and L. Tao, Plasmid 42:67-72, 1999). We
isolated and characterized the msrA gene of S. gordonii CH1 and constructed a chromosomal insertion mutant. This
mutant was more sensitive to hydrogen peroxide, suggesting a role for the streptococcal MsrA in protecting against oxidative stress. Moreover, MsrA appeared to be important for the growth of S. gordonii CH1 under aerobic and anaerobic conditions. Both these
properties of MsrA may contribute to the ability of S. gordonii to cause IE.
*
Corresponding author. Present address: Department of
Biotechnology, NUMICO Research B.V., P. O. Box 7005, 6700 CA
Wageningen, The Netherlands. Phone: 31 317 467 800. Fax: 31 317 466 500. E-mail: Aldwin.vriesema{at}numico-research.nl.
Infection and Immunity, March 2000, p. 1061-1068, Vol. 68, No. 3
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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