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Journal of Clinical Microbiology, June 1999, p. 1876-1880, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Molecular Relationships and Antimicrobial
Susceptibilities of Viridans Group Streptococci Isolated from Blood of
Neutropenic Cancer Patients
H.
Wisplinghoff,1
R. R.
Reinert,2
O.
Cornely,3 and
H.
Seifert1,*
Institute of Medical Microbiology and
Hygiene1 and Department of Internal
Medicine,3 University of Cologne,
Cologne, and National Reference Centre for
Streptococci,2 University Hospital, Aachen,
Germany
Received 15 January 1999/Returned for modification 23 February
1999/Accepted 15 March 1999
From January 1995 to May 1998, 57 episodes of bacteremia due to
viridans group streptococci were identified in 50 febrile neutropenic
patients with hematologic malignancies. Four patients experienced two
separate episodes of streptococcal bacteremia, and one patient had four
separate episodes of streptococcal bacteremia. Strains were identified
to species level as Streptococcus mitis (n = 37), Streptococcus oralis (n = 19), and
Streptococcus salivarius (n = 1).
Epidemiologic relatedness of these strains was studied by using
PCR-based fingerprinting with M13 and ERIC-2 primers and pulsed-field
gel electrophoresis with restriction enzyme SmaI. All
strains that were isolated from different patients exhibited unique
fingerprint patterns, thus suggesting that viridans group streptococcal
bacteremia usually derives from an endogenous source. Cross-transmission of strains between patients could not be
established. Four S. mitis isolates recovered during four
separate bacteremic episodes in a single patient had identical
fingerprint patterns. Susceptibility testing was carried out by broth
microdilution technique according to National Committee for Clinical
Laboratory Standards guidelines. The MICs at which 90% of the isolates
are inhibited were (in milligrams per liter) as follows: 0.5 (penicillin), 0.5 (amoxicillin), 0.25 (cefotaxime), 2 (chloramphenicol), 4 (erythromycin), 0.5 (clindamycin),
32
(tetracycline),
32 (trimethoprim-sulfamethoxazole), 4 (ciprofloxacin), 0.5 (sparfloxacin), 0.5 (vancomycin), 0.25 (teicoplanin), and 1 (quinupristin-dalfopristin). High-level penicillin resistance (MIC,
4 mg/liter) was found in one isolate only, but intermediate penicillin resistance was noted in 11 isolates (19%). Resistance rates to other drugs were as follows: 7% (amoxicillin), 4%
(cefotaxime), 4% (chloramphenicol), 32% (erythromycin), 9% (clindamycin), 39% (tetracycline), 68%
(trimethoprim-sulfamethoxazole), 23% (ciprofloxacin), 0%
(sparfloxacin), 0% (vancomycin), 0% (teicoplanin), and 0%
(quinupristin-dalfopristin).
*
Corresponding author. Mailing address: Institute of
Medical Microbiology and Hygiene, University of Cologne, Goldenfelsstr. 19-21, 50935 Cologne, Germany. Phone: 49 221 4783009. Fax: 49 221 4783081. E-mail: harald.seifert{at}uni-koeln.de.
Journal of Clinical Microbiology, June 1999, p. 1876-1880, Vol. 37, No. 6
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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