Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34330
Title: Correlation between LTR point mutations and proviral load levels among Human T cell Lymphotropic Virus type 1 (HTLV-1) asymptomatic carriers
Authors: Kleine Neto, Walter [UNIFESP]
Da-Costa, Antonio C. [UNIFESP]
Oliveira, Ana Carolina S. de [UNIFESP]
Martinez, Vanessa P. [UNIFESP]
Nukui, Youko
Sabino, Ester C.
Sanabani, Sabri Saeed [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Fundacao Prosangue
São Paulo Inistitute Trop Med
Universidade de São Paulo (USP)
Issue Date: 13-Dec-2011
Publisher: Biomed Central Ltd
Citation: Virology Journal. London: Biomed Central Ltd, v. 8, 7 p., 2011.
Abstract: Background: in vitro studies have demonstrated that deletions and point mutations introduced into each 21 bp imperfect repeat of Tax-responsive element (TRE) of the genuine human T-cell leukemia virus type I (HTLV-1) viral promoter abolishes Tax induction. Given these data, we hypothesized that similar mutations may affect the proliferation of HTLV-1 infected cells and alter the proviral load (PvL). To test this hypothesis, we conducted a cross-sectional genetic analysis to compare the near-complete LTR nucleotide sequences that cover the TRE1 region in a sample of HTLV-1 asymptomatic carriers with different PvL burden.Methods: A total of 94 asymptomatic HTLV-1 carriers with both sequence from the 5' long terminal repeat (LTR) and a PvL for Tax DNA measured using a sensitive SYBR Green real-time PCR were studied. the 94 subjects were divided into three groups based on PvL measurement: 31 low, 29 intermediate, and 34 high. in addition, each group was compared based on sex, age, and viral genotypes. in another analysis, the median PvLs between individuals infected with mutant and wild-type viruses were compared.Results: Using a categorical analysis, a G232A substitution, located in domain A of the TRE-1 motif, was detected in 38.7% (12/31), 27.5% (8/29), and 61.8% (21/34) of subjects with low, intermediate, or high PvLs, respectively. A significant difference in the detection of this mutation was found between subjects with a high or low PvL and between those with a high or intermediate PvL (both p < 0.05), but not between subjects with a low or intermediate PvL (p > 0.05). This result was confirmed by a non-parametric analysis that showed strong evidence for higher PvLs among HTLV-1 positive individuals with the G232A mutation than those without this mutation (p < 0.03). No significant difference was found between the groups in relation to age, sex or viral subtypes (p > 0. 05).Conclusions: the data described here show that changes in domain A of the HTLV-1 TRE-1 motif resulting in the G232A mutation may increase HTLV-1 replication in a majority of infected subjects.
URI: http://repositorio.unifesp.br/handle/11600/34330
ISSN: 1743-422X
Other Identifiers: http://dx.doi.org/10.1186/1743-422X-8-535
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