Haemolysin-deficient variants of Streptococcus pyogenes and S-dysgalactiae subsp equisimilis may be overlooked as aetiological agents of pharyngitis

被引:20
作者
Dierksen, KP [1 ]
Tagg, JR [1 ]
机构
[1] Univ Otago, Dept Microbiol, Dunedin, New Zealand
关键词
D O I
10.1099/0022-1317-49-9-811
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Variants of large colony beta-haemolytic Lancefield group A, C and G streptococci that are non-haemolytic or alpha-haemolytic on sheep blood agar have been detected in clinical specimens due to their enhanced haemolytic activity when grown on a new selective and differential blood agar medium containing colistin, nalidixic acid and pH 7.5-adjusted PIPES buffer (CNA-P), The large colony Lancefield group C and G isolates mere identified as Streptococcus dysgalactiae subsp, equisimilis by API 20 Strep classification and 165 rDNA profiling, The haemolytic activity of these variants on various blood agar media, including CNA-P, was closely similar to that of known streptolysin S-defective mutants of S, pyogenes and was blocked by addition of cholesterol, a specific inhibitor of the streptolysin O family of haemolysins. As haemolysin variants could be detected in large numbers in cultures from patients with clinical symptoms of pharyngitis it is suggested that they may function as primary pathogens in such infections. The high frequency with which haemolysin variants were isolated from clinical specimens during a 3-month trial (3%, 13% and 10%, respectively, of group A, C and G streptococcal isolates) indicated that a substantial proportion of streptococcal infections may go undetected if only conventional sheep blood agar media are used in clinical laboratories for the detection of beta-haemolytic streptococci. As haemolysin variants have been implicated in the development of serious streptococcal sequelae, further investigation of the full extent of their contribution to streptococcal disease is indicated.
引用
收藏
页码:811 / 816
页数:6
相关论文
共 37 条
[1]   STREPTOCOCCAL TOXINS (STREPTOLYSIN-O, STREPTOLYSIN-S, ERYTHROGENIC TOXIN) [J].
ALOUF, JE .
PHARMACOLOGY & THERAPEUTICS, 1980, 11 (03) :661-717
[2]  
BAUMGARTEN A, 1981, ZBL BAKT-INT J MED M, V249, P460
[3]   Sequencing emm-specific PCR products for routine and accurate typing of group a streptococci [J].
Beall, B ;
Facklam, R ;
Thompson, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :953-958
[4]   INTRAGENERIC STRUCTURE OF STREPTOCOCCUS BASED ON COMPARATIVE-ANALYSIS OF SMALL-SUBUNIT RIBOSOMAL-RNA SEQUENCES [J].
BENTLEY, RW ;
LEIGH, JA ;
COLLINS, MD .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1991, 41 (04) :487-494
[5]   Analysis of a case of recurrent bacteraemia due to group A Streptococcus equisimilis by pulsed-field gel electrophoresis [J].
Bert, F ;
LambertZechovsky, N .
INFECTION, 1997, 25 (04) :250-251
[6]   Differentiation of human and animal strains of Streptococcus dysgalactiae by pulsed-field gel electrophoresis [J].
Bert, F ;
Branger, C ;
Poutrel, B ;
LambertZechovsky, N .
FEMS MICROBIOLOGY LETTERS, 1997, 150 (01) :107-112
[7]   M proteins of group C streptococci isolated from patients with acute pharyngitis [J].
Bisno, AL ;
Collins, CM ;
Turner, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (10) :2511-2515
[8]  
BRADLEY SF, 1991, REV INFECT DIS, V13, P270
[9]   Characterization of blood culture isolates of Streptococcus dysgalactiae subsp equisimilis possessing Lancefield's group A antigen [J].
Brandt, CM ;
Haase, G ;
Schnitzler, N ;
Zbinden, R ;
Lütticken, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (12) :4194-4197
[10]   REPORT OF CASES OF AND TAXONOMIC CONSIDERATIONS FOR LARGE-COLONY-FORMING LANCEFIELD GROUP-C STREPTOCOCCAL BACTEREMIA [J].
CARMELI, Y ;
RUOFF, KL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (08) :2114-2117