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Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study

In the present pilot study, massively parallel sequencing (MPS) technology was used to investigate cellular small RNA (sRNA) levels in the peripheral blood mononuclear cells (PBMCs) of human T-lymphotropic virus type I (HTLV–I) infected asymptomatic carriers with monoclonal (ASM) and polyclonal (ASP...

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Autores principales: Valadão de Souza, Daniela Raguer, Pessôa, Rodrigo, Nascimento, Andrezza, Nukui, Youko, Pereira, Juliana, Casseb, Jorge, Penalva de Oliveira, Augusto César, da Silva Duarte, Alberto José, Clissa, Patricia Bianca, Sanabani, Sabri Saeed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400997/
https://www.ncbi.nlm.nih.gov/pubmed/32782548
http://dx.doi.org/10.3892/ol.2020.11803
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author Valadão de Souza, Daniela Raguer
Pessôa, Rodrigo
Nascimento, Andrezza
Nukui, Youko
Pereira, Juliana
Casseb, Jorge
Penalva de Oliveira, Augusto César
da Silva Duarte, Alberto José
Clissa, Patricia Bianca
Sanabani, Sabri Saeed
author_facet Valadão de Souza, Daniela Raguer
Pessôa, Rodrigo
Nascimento, Andrezza
Nukui, Youko
Pereira, Juliana
Casseb, Jorge
Penalva de Oliveira, Augusto César
da Silva Duarte, Alberto José
Clissa, Patricia Bianca
Sanabani, Sabri Saeed
author_sort Valadão de Souza, Daniela Raguer
collection PubMed
description In the present pilot study, massively parallel sequencing (MPS) technology was used to investigate cellular small RNA (sRNA) levels in the peripheral blood mononuclear cells (PBMCs) of human T-lymphotropic virus type I (HTLV–I) infected asymptomatic carriers with monoclonal (ASM) and polyclonal (ASP) T cell receptor (TCR) γ gene. Blood samples from 15 HTLV–I asymptomatic carriers (seven ASM and eight ASP) were tested for the clonal TCR-γ gene and submitted for sRNA library construction together with blood samples of five healthy controls (HCs) using Illumina sequencing platform. The sRNA-sequencing reads were aligned, annotated and profiled using various bioinformatics tools. Based on these results, possible markers were validated in the study samples by performing reverse transcription-quantitative (RT-q)PCR analysis. A total of 76 known sRNAs and 52 putative novel sRNAs were identified. Among them, 44 known and 34 potential novel sRNAs were differentially expressed in the ASM and ASP libraries compared with HCs. In addition, 10 known sRNAs were exclusively dysregulated in the ASM group and one (transfer RNA 65) was significantly upregulated in the ASP group. Homo sapiens (hsa) microRNA (miRNA/mir)-23a-3p, −28-5p, hsa-let-7e-5p and hsa-mir-28-3p and −361-5p were the most abundantly upregulated mature miRNAs and hsa-mir-363-3p, −532-5p, −106a-5p, −25-3p and −30e-5p were significantly downregulated miRNAs (P<0.05) with a >2-fold difference between the ASM and ASP groups compared with HCs. Based on these results, hsa-mir-23a-3p and −363-3p were selected for additional validation. However, the quantification of these two miRNAs using RT-qPCR did not provide any significant differences. While the present study failed to identify predictive sRNA markers to distinguish between ASM and ASP, the MPS results revealed differential sRNA expression profiles in the PBMCs of HTLV-1 asymptomatic carriers (ASM and ASP) compared with HCs.
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spelling pubmed-74009972020-08-10 Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study Valadão de Souza, Daniela Raguer Pessôa, Rodrigo Nascimento, Andrezza Nukui, Youko Pereira, Juliana Casseb, Jorge Penalva de Oliveira, Augusto César da Silva Duarte, Alberto José Clissa, Patricia Bianca Sanabani, Sabri Saeed Oncol Lett Articles In the present pilot study, massively parallel sequencing (MPS) technology was used to investigate cellular small RNA (sRNA) levels in the peripheral blood mononuclear cells (PBMCs) of human T-lymphotropic virus type I (HTLV–I) infected asymptomatic carriers with monoclonal (ASM) and polyclonal (ASP) T cell receptor (TCR) γ gene. Blood samples from 15 HTLV–I asymptomatic carriers (seven ASM and eight ASP) were tested for the clonal TCR-γ gene and submitted for sRNA library construction together with blood samples of five healthy controls (HCs) using Illumina sequencing platform. The sRNA-sequencing reads were aligned, annotated and profiled using various bioinformatics tools. Based on these results, possible markers were validated in the study samples by performing reverse transcription-quantitative (RT-q)PCR analysis. A total of 76 known sRNAs and 52 putative novel sRNAs were identified. Among them, 44 known and 34 potential novel sRNAs were differentially expressed in the ASM and ASP libraries compared with HCs. In addition, 10 known sRNAs were exclusively dysregulated in the ASM group and one (transfer RNA 65) was significantly upregulated in the ASP group. Homo sapiens (hsa) microRNA (miRNA/mir)-23a-3p, −28-5p, hsa-let-7e-5p and hsa-mir-28-3p and −361-5p were the most abundantly upregulated mature miRNAs and hsa-mir-363-3p, −532-5p, −106a-5p, −25-3p and −30e-5p were significantly downregulated miRNAs (P<0.05) with a >2-fold difference between the ASM and ASP groups compared with HCs. Based on these results, hsa-mir-23a-3p and −363-3p were selected for additional validation. However, the quantification of these two miRNAs using RT-qPCR did not provide any significant differences. While the present study failed to identify predictive sRNA markers to distinguish between ASM and ASP, the MPS results revealed differential sRNA expression profiles in the PBMCs of HTLV-1 asymptomatic carriers (ASM and ASP) compared with HCs. D.A. Spandidos 2020-09 2020-07-01 /pmc/articles/PMC7400997/ /pubmed/32782548 http://dx.doi.org/10.3892/ol.2020.11803 Text en Copyright: © Valadão de Souza et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Valadão de Souza, Daniela Raguer
Pessôa, Rodrigo
Nascimento, Andrezza
Nukui, Youko
Pereira, Juliana
Casseb, Jorge
Penalva de Oliveira, Augusto César
da Silva Duarte, Alberto José
Clissa, Patricia Bianca
Sanabani, Sabri Saeed
Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title_full Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title_fullStr Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title_full_unstemmed Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title_short Small RNA profiles of HTLV-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the T-cell antigen receptor γ-chain using massively parallel sequencing: A pilot study
title_sort small rna profiles of htlv-1 asymptomatic carriers with monoclonal and polyclonal rearrangement of the t-cell antigen receptor γ-chain using massively parallel sequencing: a pilot study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400997/
https://www.ncbi.nlm.nih.gov/pubmed/32782548
http://dx.doi.org/10.3892/ol.2020.11803
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