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Bacterial Infections

Inverse Relation between Disease Severity and Expression of the Streptococcal Cysteine Protease, SpeB, among Clonal M1T1 Isolates Recovered from Invasive Group A Streptococcal Infection Cases

Rita G. Kansal, Allison McGeer, Donald E. Low, Anna Norrby-Teglund, Malak Kotb
Rita G. Kansal
Veterans Affairs Medical Center, Research Service, Memphis, Tennessee 38104;
Departments of Surgery and of Microbiology and Immunology, University of Tennessee, Memphis, Tennessee 38163; and
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Allison McGeer
Department of Microbiology, Mount Sinai Hospital, and the University of Toronto, Toronto, Ontario, Canada M5G 1X5
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Donald E. Low
Department of Microbiology, Mount Sinai Hospital, and the University of Toronto, Toronto, Ontario, Canada M5G 1X5
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Anna Norrby-Teglund
Veterans Affairs Medical Center, Research Service, Memphis, Tennessee 38104;
Departments of Surgery and of Microbiology and Immunology, University of Tennessee, Memphis, Tennessee 38163; and
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Malak Kotb
Veterans Affairs Medical Center, Research Service, Memphis, Tennessee 38104;
Departments of Surgery and of Microbiology and Immunology, University of Tennessee, Memphis, Tennessee 38163; and
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DOI: 10.1128/IAI.68.11.6362-6369.2000
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ABSTRACT

The streptococcal cysteine protease (SpeB) is one of the major virulence factors produced by group A streptococci (GAS). In this study we investigated if differences exist in SpeB production by clonally related M1T1 clinical isolates derived from patients with invasive infections. Twenty-nine of these isolates were from nonsevere cases and 48 were from severe cases, including streptococcal toxic shock syndrome (STSS) and necrotizing fasciitis (NF) cases. The expression and amount of the 28-kDa SpeB protein produced were determined by quantitative Western blotting, and protease activity was measured by a fluorescent enzymatic assay. A high degree of variation in SpeB expression was seen among the isolates, and this variation seemed to correlate with the severity and/or clinical manifestation of the invasive infection. The mean amount of 28-kDa SpeB protein and cysteine protease activity produced by isolates from nonsevere cases was significantly higher than that from STSS cases (P = 0.001). This difference was partly due to the fact that 41% of STSS isolates produced little or no SpeB compared to only 14% of isolates recovered in nonsevere cases. Moreover, the cysteine protease activity among those isolates that expressed SpeB was significantly lower for STSS isolates than for isolates from nonsevere cases (P = 0.001). Increased SpeB production was also inversely correlated with intact M protein expression, and inhibition of cysteine protease activity blocked the cleavage of the surface M protein. Together, the data support the existence of both an “on-off” and a posttranslational regulatory mechanism(s) controlling SpeB production, and they suggest that isolates with the speB gene in the “off” state are more likely to spare the surface M protein and to be isolated from cases of severe rather than nonsevere invasive infection. These findings may have important implications for the role of SpeB in host-pathogen interactions via regulation of the expression of GAS virulence genes and the severity of invasive disease.

  • Copyright © 2000 American Society for Microbiology
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Inverse Relation between Disease Severity and Expression of the Streptococcal Cysteine Protease, SpeB, among Clonal M1T1 Isolates Recovered from Invasive Group A Streptococcal Infection Cases
Rita G. Kansal, Allison McGeer, Donald E. Low, Anna Norrby-Teglund, Malak Kotb
Infection and Immunity Nov 2000, 68 (11) 6362-6369; DOI: 10.1128/IAI.68.11.6362-6369.2000

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Inverse Relation between Disease Severity and Expression of the Streptococcal Cysteine Protease, SpeB, among Clonal M1T1 Isolates Recovered from Invasive Group A Streptococcal Infection Cases
Rita G. Kansal, Allison McGeer, Donald E. Low, Anna Norrby-Teglund, Malak Kotb
Infection and Immunity Nov 2000, 68 (11) 6362-6369; DOI: 10.1128/IAI.68.11.6362-6369.2000
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