Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1991 May 15;88(10):4481-5.
doi: 10.1073/pnas.88.10.4481.

The major 85-kDa surface antigen of the mammalian-stage forms of Trypanosoma cruzi is a family of sialidases

Affiliations
Comparative Study

The major 85-kDa surface antigen of the mammalian-stage forms of Trypanosoma cruzi is a family of sialidases

S Kahn et al. Proc Natl Acad Sci U S A. .

Abstract

Trypanosoma cruzi, an intracellular protozoan parasite infecting a wide variety of vertebrates, is the agent responsible for Chagas disease in humans. An estimated 15-20 million people in South and Central America are infected with the parasite. Chagas disease often results in severe autoimmune and inflammatory pathology and is the major cause of heart failure in endemic areas. Nevertheless, little is known about the host-parasite interactions that lead to this pathology. We have previously cloned several members of a large gene family (SA85-1) and shown that these genes encode 85-kDa T. cruzi, mammalian-stage-specific, surface antigens. Here we report that members of the SA85-1 family possess sialidase activity and are shed by the parasite. We suggest that the sialidases may contribute to the pathology during T. cruzi infection by cleaving sialic acid from cells of the immune system.

PubMed Disclaimer

References

    1. Mol Biol Med. 1983 Nov;1(4):401-13 - PubMed
    1. Proc Natl Acad Sci U S A. 1982 Nov;79(22):6817-21 - PubMed
    1. Virology. 1985 Aug;145(1):117-22 - PubMed
    1. Eur J Immunol. 1984 May;14(5):392-9 - PubMed
    1. J Cell Biol. 1990 Dec;111(6 Pt 1):2757-64 - PubMed

Publication types

MeSH terms