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Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil

Condyloma acuminata (CA), or genital warts, are benign proliferative epidermal or mucous lesions that are caused by infection with human papillomavirus (HPV), mainly the low-risk types 6 and 11. HPV variants are defined as viral sequences that share identity in the nucleotide sequence of the L1 gene...

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Autores principales: Dias, Marina Carrara, Stuqui, Bruna, Provazzi, Paola Jocelan Scarin, Bittar, Cíntia, Candido, Natália Maria, de Matos, Renata Prandini Adum, Badial, Rodolfo Miglioli, do Bonfim, Caroline Measso, Melli, Patricia Pereira dos Santos, Quintana, Silvana Maria, Cordeiro, José Antônio, Rahal, Paula, Calmon, Marilia de Freitas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521423/
https://www.ncbi.nlm.nih.gov/pubmed/31186642
http://dx.doi.org/10.1155/2019/5697573
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author Dias, Marina Carrara
Stuqui, Bruna
Provazzi, Paola Jocelan Scarin
Bittar, Cíntia
Candido, Natália Maria
de Matos, Renata Prandini Adum
Badial, Rodolfo Miglioli
do Bonfim, Caroline Measso
Melli, Patricia Pereira dos Santos
Quintana, Silvana Maria
Cordeiro, José Antônio
Rahal, Paula
Calmon, Marilia de Freitas
author_facet Dias, Marina Carrara
Stuqui, Bruna
Provazzi, Paola Jocelan Scarin
Bittar, Cíntia
Candido, Natália Maria
de Matos, Renata Prandini Adum
Badial, Rodolfo Miglioli
do Bonfim, Caroline Measso
Melli, Patricia Pereira dos Santos
Quintana, Silvana Maria
Cordeiro, José Antônio
Rahal, Paula
Calmon, Marilia de Freitas
author_sort Dias, Marina Carrara
collection PubMed
description Condyloma acuminata (CA), or genital warts, are benign proliferative epidermal or mucous lesions that are caused by infection with human papillomavirus (HPV), mainly the low-risk types 6 and 11. HPV variants are defined as viral sequences that share identity in the nucleotide sequence of the L1 gene greater than 98%. Based on this criterion, HPV6 and 11 variant lineages have been studied, and there are ongoing attempts to correlate these genetic variants with different clinical findings of infection. Therefore, the aims of this study were to detect variants and nucleotide alterations present in the E6 regions of HPV types 6 and 11 found in CA samples, to correlate the HPV presence with the clinical-pathological data of the patients, and to determine phylogenetic relationships with variants from other places in the world. The E6 regions of 25 HPV6 samples and 7 HPV11 samples from CA were amplified using PCR with specific primers. The products were ligated to a cloning vector and five colonies of each sample were sequenced to observe the nucleotide alterations. Twelve samples were identified as the HPV6B3 variant, presenting the mutation (guanine) G474A (adenine), and one of them also showed the mutation (thymine) T369G. The other 13 patients were positive for HPV6B1 without nucleotide alterations. In the analysis of the HPV11 samples, all patients showed the mutations T137C and (cytosine) C380T. One patient also presented the nucleotide alteration T410C. None of the mutations found in the 32 analyzed samples resulted in amino acid changes. Patient age, local occurrence, and HIV infection did not show significant association with HPV infection. Besides, the data found in this study did not show a relationship with the geographical region of isolation when compared to other data from different regions of the world. In this way, despite the nucleotide alterations found, it was not possible to observe amino acid changes and variants grouping according to geographical region.
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spelling pubmed-65214232019-06-11 Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil Dias, Marina Carrara Stuqui, Bruna Provazzi, Paola Jocelan Scarin Bittar, Cíntia Candido, Natália Maria de Matos, Renata Prandini Adum Badial, Rodolfo Miglioli do Bonfim, Caroline Measso Melli, Patricia Pereira dos Santos Quintana, Silvana Maria Cordeiro, José Antônio Rahal, Paula Calmon, Marilia de Freitas Adv Virol Research Article Condyloma acuminata (CA), or genital warts, are benign proliferative epidermal or mucous lesions that are caused by infection with human papillomavirus (HPV), mainly the low-risk types 6 and 11. HPV variants are defined as viral sequences that share identity in the nucleotide sequence of the L1 gene greater than 98%. Based on this criterion, HPV6 and 11 variant lineages have been studied, and there are ongoing attempts to correlate these genetic variants with different clinical findings of infection. Therefore, the aims of this study were to detect variants and nucleotide alterations present in the E6 regions of HPV types 6 and 11 found in CA samples, to correlate the HPV presence with the clinical-pathological data of the patients, and to determine phylogenetic relationships with variants from other places in the world. The E6 regions of 25 HPV6 samples and 7 HPV11 samples from CA were amplified using PCR with specific primers. The products were ligated to a cloning vector and five colonies of each sample were sequenced to observe the nucleotide alterations. Twelve samples were identified as the HPV6B3 variant, presenting the mutation (guanine) G474A (adenine), and one of them also showed the mutation (thymine) T369G. The other 13 patients were positive for HPV6B1 without nucleotide alterations. In the analysis of the HPV11 samples, all patients showed the mutations T137C and (cytosine) C380T. One patient also presented the nucleotide alteration T410C. None of the mutations found in the 32 analyzed samples resulted in amino acid changes. Patient age, local occurrence, and HIV infection did not show significant association with HPV infection. Besides, the data found in this study did not show a relationship with the geographical region of isolation when compared to other data from different regions of the world. In this way, despite the nucleotide alterations found, it was not possible to observe amino acid changes and variants grouping according to geographical region. Hindawi 2019-05-02 /pmc/articles/PMC6521423/ /pubmed/31186642 http://dx.doi.org/10.1155/2019/5697573 Text en Copyright © 2019 Marina Carrara Dias et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dias, Marina Carrara
Stuqui, Bruna
Provazzi, Paola Jocelan Scarin
Bittar, Cíntia
Candido, Natália Maria
de Matos, Renata Prandini Adum
Badial, Rodolfo Miglioli
do Bonfim, Caroline Measso
Melli, Patricia Pereira dos Santos
Quintana, Silvana Maria
Cordeiro, José Antônio
Rahal, Paula
Calmon, Marilia de Freitas
Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title_full Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title_fullStr Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title_full_unstemmed Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title_short Analysis of Nucleotide Alterations in the E6 Genomic Region of Human Papillomavirus Types 6 and 11 in Condyloma Acuminatum Samples from Brazil
title_sort analysis of nucleotide alterations in the e6 genomic region of human papillomavirus types 6 and 11 in condyloma acuminatum samples from brazil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521423/
https://www.ncbi.nlm.nih.gov/pubmed/31186642
http://dx.doi.org/10.1155/2019/5697573
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