Cited by 80Trypanosoma species research and implicationsGlycosylation and Glycoproteins ResearchResearch on Leishmaniasis Studies

The trans-sialidase, the major Trypanosoma cruzi virulence factor: Three decades of studies

Freire-de-Lima, L, Fonseca, LM, Oeltmann, T, Mendonça-Previato, L, Previato, JO·2015·Glycobiology

Abstract

Chagas' disease is a potentially life-threatening disease caused by the protozoan parasite Trypanosoma cruzi. Since the description of Chagas'disease in 1909 extensive research has identified important events in the disease in order to understand the biochemical mechanism that modulates T. cruzi-host cell interactions and the ability of the parasite to ensure its survival in the infected host. Exactly 30 years ago, we presented evidence for the first time of a trans-sialidase activity in T. cruzi (T. cruzi-TS). This enzyme transfers sialic acid from the host glycoconjugates to the terminal β-galactopyranosyl residues of mucin-like molecules on the parasite's cell surface. Thenceforth, many articles have provided convincing data showing that T. cruzi-TS is able to govern relevant mechanisms involved in the parasite's survival in the mammalian host, such as invasion, escape from the phagolysosomal vacuole, differentiation, down-modulation of host immune responses, among others. The aim of this review is to cover the history of the discovery of T. cruzi-TS, as well as some well-documented biological effects encompassed by this parasite's virulence factor, an enzyme with potential attributes to become a drug target against Chagas disease.

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Crossref · 10.1093/glycob/cwv057

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97 of 97 references verified0 citation errors · 0 not checkable

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  • Biological roles of glycans

    Varki, A. (2017) · Glycobiology · doi:10.1093/glycob/cww086 · Cited by 2,635 · see citing works

    “These mechanisms range from the simple acquisition of host sialoglycans (997) to the direct transfer of host sialic acids by trans-sialidases (998), to the highly efficient uptake of the small amounts of environmental free sialic acids (999) or even the direct utilization of trace amounts of CMP sialic acid present in…”
    Background

Authors
Freire-de-Lima, L., Fonseca, L., Oeltmann, T., Mendonça-Previato, L., & Previato, J.
Affiliations
Vanderbilt University (US)
Venue
Glycobiology
Published
2015-07-29
Volume
25
Issue
11
Pages
1142-1149
ISSN
  • 0959-6658 (ISSN-L)
  • 1460-2423
OpenAlex
W1832557653
Cited by
80
References
97
Citations by year
2026: 4 · 2025: 5 · 2024: 6 · 2023: 4 · 2022: 5 · 2021: 9 · 2020: 12 · 2019: 12 · 2018: 7 · 2017: 9 · 2016: 6 · 2015: 1
FWCI
1.00
Type
journal article
Language
en
Open access
closed
Locations
  • Glycobiology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Fundação de Apoio à Pesquisa do Estado do Rio de Janeiro (FAPERJ)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Topics
  • Health Sciences › Medicine › Epidemiology › Trypanosoma species research and implications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Research on Leishmaniasis Studies
Keywords
trans-sialidase, Trypanosoma cruzi, Chagas disease, virulence factors, sialic acid transfer, host-parasite interactions, parasite invasion, parasite differentiation, immune evasion, therapeutic target
MeSH terms
Animals, Glycoproteins, Humans, Neuraminidase, Trypanosoma cruzi, Chagas Disease, Protozoan Proteins, Virulence Factors

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