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Journal of Clinical Microbiology, September 2001, p. 3147-3155, Vol. 39, No. 9
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.9.3147-3155.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Group G Beta-Hemolytic Streptococcal Bacteremia Characterized
by 16S Ribosomal RNA Gene Sequencing
Patrick C. Y.
Woo,1
Ami M. Y.
Fung,1
Susanna K. P.
Lau,1
Samson S. Y.
Wong,1 and
Kwok-Yung
Yuen1,2,*
Department of Microbiology, The University of
Hong Kong, Queen Mary Hospital,1 and
HKU-Pasteur Research Centre,2 Hong Kong
Received 10 May 2001/Returned for modification 1 July 2001/Accepted 5 July 2001
Little is known about the relative importance of the four species
of Lancefield group G beta-hemolytic streptococci in causing bacteremia
and the factors that determine the outcome for patients with group G
beta-hemolytic streptococcal bacteremia. From 1997 to 2000, 75 group G
beta-hemolytic streptococcal strains were isolated from the blood
cultures of 66 patients. Sequencing of the 16S rRNA genes of the group
G beta-hemolytic streptococci showed that all 75 isolates were
Streptococcus dysgalactiae subspecies equisimilis. The API system (20 STREP) and Vitek system
(GPI) successfully identified 65 (98.5%) and 62 (93.9%) isolates,
respectively, as S. dysgalactiae subspecies
equisimilis with >95% confidence, whereas the ATB
Expression system (ID32 STREP) only successfully identified 49 isolates
(74.2%) as S. dysgalactiae subspecies
equisimilis with >95% confidence. The median age of
the patients was 76 years (range, 33 to 99 years). Fifty-six patients
(85%) were over 60 years old. All patients had underlying diseases. No
source of the bacteremia was identified (primary bacteremia) in 34 patients (52%), whereas 17 (26%) had cellulitis and 8 (12%) had bed
sore or wound infections. Fifty-eight patients (88%) had
community-acquired group G streptococcal bacteremia. Sixty-two patients
(94%) had group G Streptococcus recovered in one blood
culture, whereas 4 patients (6%) had it recovered in multiple blood
cultures. Fifty-nine patients (89%) had group G
Streptococcus as the only bacterium recovered in their
blood cultures, whereas in 7 patients other bacteria were recovered
concomitantly with the group G Streptococcus in the
blood cultures (Staphylococcus aureus in 3, Clostridium perfringens in 2, Citrobacter
freundii in 1, and Bacteroides fragilis in 1).
Overall, 10 patients (15%) died. Male sex, diagnosis other than
cellulitis, hospital-acquired bacteremia, and multiple positive blood
cultures were associated with mortality {P < 0.005 (relative risk [RR] = 7.6), P < 0.05 (RR = 3.7), P < 0.005 (RR = 5.6), and P < 0.05 (RR = 5.6), respectively}. Unlike
group C beta-hemolytic streptococcal bacteremia, group G beta-hemolytic
streptococcal bacteremia is not a zoonotic infection in Hong Kong.
*
Corresponding author. Mailing address: Department of
Microbiology, The University of Hong Kong, University Pathology
Building, Queen Mary Hospital, Hong Kong. Phone: (852) 28554892. Fax:
(852) 28551241. E-mail: hkumicro{at}hkucc.hku.hk.
Journal of Clinical Microbiology, September 2001, p. 3147-3155, Vol. 39, No. 9
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.9.3147-3155.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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