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PMID: 2050400 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Virulent human strains of group G streptococci express a C5a peptidase enzyme similar to that produced by group A streptococci.

Infection and immunity ·Vol. 59 ·No. 7 ·1991-07-00 ·Pages 2305-10

Cleary PP, Peterson J, Chen C, Nelson C

Abstract

Specific proteolytic destruction of the human chemotaxin, C5a, is a property of group A and B streptococcal pathogens. Here we show that virulent group G streptococci from human sources also express C5a peptidase activity. The enzyme responsible for this activity is approximately the same size as and is antigenically similar to that produced by group A streptococci. On the basis of Southern hybridization analysis with an internal fragment of the group A C5a peptidase gene (scpA) as a probe, a copy of this gene was found in the genome of all group G human isolates tested. Comparison of partial restriction maps of scpA and scpG revealed significant similarity between the two genes. Group G strains isolated from dogs and cows were found to lack C5a peptidase activity and did not hybridize to the scpA-specific probe. The association of this activity with three streptococcal species suggests that elimination of phagocyte chemotactic attractants is a more universal virulence mechanism than originally anticipated.

Related Genes
MeSH Terms
Adhesins, Bacterial Antigens, Bacterial/immunology Blotting, Southern Blotting, Western Chemotaxis, Leukocyte Cross Reactions DNA, Bacterial/genetics Endopeptidases/immunology,metabolism Genes, Bacterial Humans Restriction Mapping Streptococcus/enzymology,genetics,immunology,pathogenicity
Chemicals
Adhesins, Bacterial Antigens, Bacterial DNA, Bacterial Endopeptidases C5a peptidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Cleary P P
Department of Microbiology, University of Minnesota, Minneapolis 55455.
Peterson J
Chen C
Nelson C
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24 references, click to expand
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Article Info
Journal
Infection and immunity
Abbr.
Infect Immun
ISSN
0019-9567
Published
1991-07-00
Pages
2305-10
Language
English
Region
United States
NLM ID
0246127
PMCID
PMC258011
Subset
IM
Grants
NIAID NIH HHS · AI20016 · United States
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