Lack of mitogenic activity of speG- and speGdys-positive Streptococcus dysgalactiae subspecies equisimilis isolates from patients with invasive infections

被引:21
作者
Brandt, CM
Schweizer, KG
Holland, R
Lütticken, R
Freyaldenhoven, BS
机构
[1] Goethe Univ Frankfurt, Univ Hosp, Inst Med Microbiol, D-60596 Frankfurt, Germany
[2] Univ Hosp Aachen, Inst Med Microbiol, Aachen, Germany
[3] Univ Hosp Aachen, Natl Reference Ctr Streptococci, Aachen, Germany
关键词
S. dysgalactiae subspecies equisimilis; invasive infections; mitogenicity; superantigen; Emm/emmL;
D O I
10.1016/j.ijmm.2005.07.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In recent years, Streptococcus dysgalactiae subspecies equisimilis has been isolated with an increasing frequency as the cause of invasive streptococcal diseases. For 46 S. dysgalactiae subspecies equisimilis isolates from invasive infections and four isolates from superficial infections, the presence of emm/emmL genes and of genes encoding various different streptococcal superantigens was determined by polymerase chain reaction (PCR). Subsequently, PCR products were identified by DNA sequencing, and the expression of mRNA from superantigen genes was assessed by reverse transcriptase-PCR. The mitogenic activity of S. dysgalactiae subspecies equisimilis was assessed by [3 H]thymidine incorporation into human lymphocytes and compared with that of Streptococcus agalactiae and Streptococcus pyogenes. All S. dysgalactiae subspecies equisimilis isolates studied harbored an emm/emmL gene. Only in six of the S. dysgalactiae subspecies equisimilis isolates from invasive infections, speG was detected by PCR, two of which were further identified as speG(dys) by sequencing of the PCR product. None of the S. dysgalactiae subspecies equisimilis isolates harbored any of the genes speA, speB, speC, speF, speH, speI, speJ, speK, speL, speM, smeZ, or ssa of S. pyogenes. In contrast to S. pyogenes, no expression of speG or speGdys mRNA, respectively, was detected in the reverse transcriptase-PCR assay for any of the speG- or speG(dys)-positive S. dysgalactiae subspecies equisimilis isolates. Moreover, S. dysgalactiae subspecies equisimilis and S. agalactiae revealed no or very low mitogenic activity, while S. pyogenes was a very powerful inducer of proliferative responses. These findings support the hypothesis that the pathogenicity of S. dysgalactiae subspecies equisimilis may be associated in part with the presence of emm/emmL genes, and suggest that the severity of S. dysgalactiae subspecies equisimilis invasive infections is not mediated by superantigen-induced mitogenicity. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:539 / 546
页数:8
相关论文
共 33 条
[21]  
Ojukwu IC, 2001, SCAND J INFECT DIS, V33, P227, DOI 10.1080/00365540151060969
[22]  
OTTEN RA, 1991, J IMMUNOL, V146, P2588
[23]  
PODBIELSKI A, 1991, MED MICROBIOL IMMUN, V180, P213
[24]   3 DIFFERENT TYPES OF ORGANIZATION OF THE VIR REGULON IN GROUP-A STREPTOCOCCI [J].
PODBIELSKI, A .
MOLECULAR & GENERAL GENETICS, 1993, 237 (1-2) :287-300
[25]   Identification and characterization of novel superantigens from Streptococcus pyogenes [J].
Proft, T ;
Moffatt, SL ;
Berkahn, CJ ;
Fraser, JD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (01) :89-101
[26]   Two novel superantigens found in both group A and group C Streptococcus [J].
Proft, T ;
Webb, PD ;
Handley, V ;
Fraser, JD .
INFECTION AND IMMUNITY, 2003, 71 (03) :1361-1369
[27]   Phylogenetic distribution of streptococcal superantigen SSA allelic variants provides evidence for horizontal transfer of ssa within Streptococcus pyogenes [J].
Reda, KB ;
Kapur, V ;
Goela, D ;
Lamphear, JG ;
Musser, JM ;
Rich, RR .
INFECTION AND IMMUNITY, 1996, 64 (04) :1161-1165
[28]   Superantigen-like gene(s) in human pathogenic Streptococcus dysgalactiae, subsp equisimilis:: genomic localisation of the gene encoding streptococcal pyrogenic exotoxin G (speGdys) [J].
Sachse, S ;
Seidel, P ;
Gerlach, D ;
Günther, E ;
Rödel, J ;
Straube, E ;
Schmidt, KH .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 2002, 34 (02) :159-167
[29]   M-PROTEIN OR M-LIKE-PROTEIN GENE POLYMORPHISMS IN HUMAN GROUP-G STREPTOCOCCI [J].
SCHNITZLER, N ;
PODBIELSKI, A ;
BAUMGARTEN, G ;
MIGNON, M ;
KAUFHOLD, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (02) :356-363
[30]  
Stevens D L, 2001, J Infect Chemother, V7, P69, DOI 10.1007/s101560100012