巴西尖锐湿疣样本中人类乳头瘤病毒6型和11型E6基因组区核苷酸变化的分析。

IF 1.1 Q4 VIROLOGY
Advances in Virology Pub Date : 2019-05-02 eCollection Date: 2019-01-01 DOI:10.1155/2019/5697573
Marina Carrara Dias, Bruna Stuqui, Paola Jocelan Scarin Provazzi, Cíntia Bittar, Natália Maria Candido, Renata Prandini Adum de Matos, Rodolfo Miglioli Badial, Caroline Measso do Bonfim, Patricia Pereira Dos Santos Melli, Silvana Maria Quintana, José Antônio Cordeiro, Paula Rahal, Marilia de Freitas Calmon
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引用次数: 2

摘要

尖锐湿疣(CA)或生殖器疣是由感染人乳头瘤病毒(HPV)引起的良性增殖性表皮或粘液病变,主要是低风险的6型和11型。HPV变体被定义为在L1基因的核苷酸序列中具有大于98%的同一性的病毒序列。基于这一标准,已经对HPV6和11个变异谱系进行了研究,并正在尝试将这些基因变异与感染的不同临床表现联系起来。因此,本研究的目的是检测CA样本中发现的6型和11型HPV E6区的变异和核苷酸改变,将HPV的存在与患者的临床病理数据相关联,并确定与世界其他地方变异的系统发育关系。用特异性引物对25份来自CA的HPV6样本和7份来自CA样本的HPV11样本的E6区进行了扩增。将产物连接到克隆载体上,并对每个样品的五个菌落进行测序以观察核苷酸的变化。12个样本被鉴定为HPV6B3变体,呈现突变(鸟嘌呤)G474A(腺嘌呤),其中一个样本也呈现突变(胸腺嘧啶)T369G。其他13例患者HPV6B1阳性,无核苷酸改变。在对HPV11样本的分析中,所有患者都显示出T137C和(胞嘧啶)C380T突变。一名患者还出现核苷酸改变T410C。在32个分析样本中发现的突变均未导致氨基酸变化。患者年龄、局部发病率和HIV感染与HPV感染没有显著相关性。此外,与世界不同地区的其他数据相比,这项研究中发现的数据没有显示出与隔离地理区域的关系。通过这种方式,尽管发现了核苷酸的变化,但不可能观察到氨基酸的变化和根据地理区域分组的变体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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 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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