Publication date: Available online 20 August 2016
Source:Microbes and Infection
Author(s): Juan San Francisco, Iván Barría, Bessy Gutiérrez, Ivan Neira, Christian Muñoz, Hernán Sagua, Jorge Araya, Juan Carlos Andrade, Anibal Zailberger, Alejandro Catalán, Francisco Remonsellez, José Luis Vega, Jorge González
Two cell lines derived from a single Trypanosoma cruzi clone by long-term passaging generated a highly virulent (C8C3hvir) and a low virulent (C8C3lvir) cell line. The C8C3hvir cell line was highly infective and lethal to Balb/c mice, and the C8C3lvir cell line was three-to five-fold less infective to mouse cardiomyocytes than C8C3hvir. The highly virulent T. cruzi cell line abundantly expressed the major cysteine proteinase cruzipain (Czp), complement regulatory protein (CRP) and trans-sialidase (TS), all of which are known to act as virulence factors in this parasite. The in vitro invasion capacity and in vivo Balb/c mouse infectiveness of the highly virulent strain was strongly reduced by pre-treatment with antisense oligonucleotides targeting TS or CRP or with E64d. Based on these results, we conclude that decreased levels of TS, CRP and Czp expression could contribute to loss of T.cruzi trypomastigote virulence.
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