Abstract
The surface of the protozoan parasite Trypanosoma cruzi is covered in mucins, which contribute to parasite protection and to the establishment of a persistent infection. Their importance is highlighted by the fact that the ∼850 mucin-encoding genes comprise ∼1% of the parasite genome and ∼6% of all predicted T. cruzi genes. The coordinate expression of a large repertoire of mucins containing variable regions in the mammal-dwelling stages of the T. cruzi life cycle suggests a possible strategy to thwart the host immune response. Here, we discuss the expression profiling of T. cruzi mucins, the mechanisms leading to the acquisition of mucin diversity and the possible consequences of a mosaic surface coat in the interplay between parasite and host.
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Acknowledgements
We apologize to people whose work was not referenced due to limited space. We thank I.C. Almeida (University of Texas, El Paso, USA) for critical reading of the manuscript and for sharing with us his unpublished results. We also thank J.C. Hafalla (New York University, New York, USA) for critical reading of the manuscript. The experimental work described in this article was carried out with the financial support of the Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT) and the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) of Argentina, an International Research Scholar grant from the Howard Hughes Medical Institute, and a National Institutes of Health grant to A.C.C.F.
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Buscaglia, C., Campo, V., Frasch, A. et al. Trypanosoma cruzi surface mucins: host-dependent coat diversity. Nat Rev Microbiol 4, 229–236 (2006). https://doi.org/10.1038/nrmicro1351
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DOI: https://doi.org/10.1038/nrmicro1351
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