Accuracy of phenotypic and genotypic testing for identification of Streptococcus pneumoniae and description of Streptococcus pseudopneumoniae sp nov.

被引:205
作者
Arbique, JC
Poyart, C
Trieu-Cuot, P
Quesne, G
Carvalho, MDS
Steigerwalt, AG
Morey, RE
Jackson, D
Davidson, RJ
Facklam, RR
机构
[1] Queen Elizabeth II Hlth Sci Ctr, Dept Microbiol, Div Pathol & Lab Med, Halifax, NS B3H 1V8, Canada
[2] Fac Med Necker Enfants Malad, Lab Mixte Pasteur Necker Resh Streptocoques & Str, Paris, France
[3] Fac Med Necker Enfants Malad, INSERM, U570, Paris, France
[4] Ctr Dis Control & Prevent, Natl Ctr Infect Dis, Div Bacterial & Mycot Dis, Atlanta, GA USA
关键词
D O I
10.1128/JCM.42.10.4686-4696.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have identified an unusual group of viridans group streptococci that resemble Streptococcus pneumoniae. DNA-DNA homology studies suggested that a subset of these isolates represent a novel species that may be included in the S. oralis-S. mitis group of viridans group streptococci. We suggest that this novel species be termed Streptococcus pseudopneumoniae. A combination of phenotypic and genetic reactions allows its identification. S. pseudopneumoniae strains do not have pneumococcal capsules, are resistant to optochin (inhibition zones, less than 14 mm) when they are incubated under an atmosphere of increased CO2 but are susceptible to optochin (inhibition zones, >14 mm) when they are incubated in ambient atmospheres, are not soluble in bile, and are positive by the GenProbe AccuProbe Pneumococcus test. The bile solubility test is more specific than the optochin test for identification of S. pneumoniae. Genetic tests for pneumolysin (ply) and manganese-dependent superoxide dismutase (sodA) and identification tests with a commercial probe, AccuProbe Pneumococcus, do not discriminate between the new species and S. pneumoniae.
引用
收藏
页码:4686 / 4696
页数:11
相关论文
共 67 条
[1]  
Advisory Committee on Immunization Practices, 1997, MMWR-MORBID MORTAL W, V46, P1
[2]   IMPORTANCE OF CARBON DIOXIDE IN ISOLATION OF PNEUMOCOCCI [J].
AUSTRIAN, R ;
COLLINS, P .
JOURNAL OF BACTERIOLOGY, 1966, 92 (05) :1281-&
[3]  
BARON EJ, 1990, BAILEY SCOTTS DIAGNO, P334
[4]   Evolving clinical problems with Streptococcus pneumoniae:: Increasing resistance to antimicrobial agents, and failure of traditional optochin identification in Chicago, Illinois, between 1993 and 1996 [J].
Borek, AP ;
Dressel, DC ;
Hussong, J ;
Peterson, LR .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1997, 29 (04) :209-214
[5]   ESCHERICHIA-VULNERIS - A NEW SPECIES OF ENTEROBACTERIACEAE ASSOCIATED WITH HUMAN WOUNDS [J].
BRENNER, DJ ;
MCWHORTER, AC ;
KNUTSON, JKL ;
STEIGERWALT, AG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1982, 15 (06) :1133-1140
[6]   DETECTION OF PNEUMOCOCCI IN BLOOD CULTURES BY LATEX AGGLUTINATION [J].
BROWNE, K ;
MIEGEL, J ;
STOTTMEIER, KD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 19 (05) :649-650
[7]   IDENTIFICATION OF STREPTOCOCCUS-PNEUMONIAE BY THE PHADEBACT COAGGLUTINATION TEST [J].
BURDASH, NM ;
WEST, ME .
JOURNAL OF CLINICAL MICROBIOLOGY, 1982, 15 (03) :391-394
[8]   Comparison of four methods for identifying Streptococcus pneumoniae [J].
Chandler, LJ ;
Reisner, BS ;
Woods, GL ;
Jafri, AK .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2000, 37 (04) :285-287
[9]   Rapid and reliable identification of Streptococcus pneumoniae isolates by pneumolysin-mediated agglutination [J].
Cima-Cabal, MD ;
Vázquez, F ;
de los Toyos, JR ;
Méndez, FJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (06) :1964-1966
[10]   Prospective study to determine clinical relevance of detection of pneumococcal DNA in sera of children by PCR [J].
Dagan, R ;
Shriker, O ;
Hazan, I ;
Leibovitz, E ;
Greenberg, D ;
Schlaeffer, F ;
Levy, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :669-673