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本文引用的文献

1
Detection of Drug Resistance Mutations in the Reverse Transcriptase Gene of HIV-1-Infected North Indian Population Failing First-Line Antiretroviral Therapy "A Follow-Up Cohort Study".印度北部地区一线抗反转录病毒治疗失败的 HIV-1 感染者体内逆转录酶基因耐药突变的检测:一项随访队列研究。
AIDS Res Hum Retroviruses. 2021 Oct;37(10):796-805. doi: 10.1089/AID.2020.0132. Epub 2021 Feb 24.
2
Transmitted and Acquired HIV-1 Drug Resistance from a Family: A Case Study.一个家庭中传播和获得性HIV-1耐药性:病例研究
Infect Drug Resist. 2020 Oct 22;13:3763-3770. doi: 10.2147/IDR.S272232. eCollection 2020.
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The Genetic Diversity of HIV-1 Quasispecies Within Primary Infected Individuals.初次感染个体体内HIV-1准种的遗传多样性
AIDS Res Hum Retroviruses. 2020 May;36(5):440-449. doi: 10.1089/AID.2019.0242. Epub 2020 Jan 6.
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Signaling Complexity Measured by Shannon Entropy and Its Application in Personalized Medicine.基于香农熵的信号复杂性及其在个性化医疗中的应用
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2019 update of the drug resistance mutations in HIV-1.2019年人类免疫缺陷病毒1型耐药性突变的更新情况。
Top Antivir Med. 2019 Sep;27(3):111-121.
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Simplifying switch to second-line antiretroviral therapy in sub Saharan Africa: predicted effect of using a single viral load to define efavirenz-based first-line failure.简化撒哈拉以南非洲的二线抗逆转录病毒治疗转换:使用单一病毒载量定义依非韦伦为基础的一线治疗失败的预测效果。
AIDS. 2019 Aug 1;33(10):1635-1644. doi: 10.1097/QAD.0000000000002234.
7
HIV drug resistance following a decade of the free antiretroviral therapy programme in India: A review.印度实施免费抗逆转录病毒治疗方案十年后出现的 HIV 耐药性:综述。
Int J Infect Dis. 2018 Jan;66:33-41. doi: 10.1016/j.ijid.2017.10.020. Epub 2017 Nov 8.
8
A step forward understanding HIV-1 diversity.在理解HIV-1多样性方面向前迈进了一步。
Retrovirology. 2016 Apr 19;13:27. doi: 10.1186/s12977-016-0259-8.
9
Proviral DNA as a Target for HIV-1 Resistance Analysis.作为HIV-1耐药性分析靶点的前病毒DNA
Intervirology. 2015;58(3):184-9. doi: 10.1159/000431093. Epub 2015 Jun 27.
10
HIV drug resistance mutations in proviral DNA from a community treatment program.来自社区治疗项目的前病毒DNA中的HIV耐药性突变
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从印度一线抗逆转录病毒治疗患者中分离出的HIV-1 C亚型蛋白酶和逆转录酶基因的基因组特征。

Genomic signatures of protease and reverse transcriptase genes from HIV-1 subtype C isolated from first-line ART patients in India.

作者信息

Barik Sushanta Kumar, Mohanty Keshar Kunja, Patil Shripad A, Tripathy Srikanth Prasad, Singh Dharmendra, Hanna Luke Eilzabeth, Karunaianantham Ramesh, Pattabiraman Sathyamurthi, Singh Tej Pal, Tandon Rekha, Jena Srikanta

机构信息

ICMR-National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Agra, Uttar-Pradesh, India.

ICMR-National Institute for Research in Tuberculosis, Chetpet, Chennai, Tamil Nadu, India.

出版信息

Bioinformation. 2022 Apr 30;18(4):371-380. doi: 10.6026/97320630018371. eCollection 2022.

DOI:10.6026/97320630018371
PMID:36909690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9997500/
Abstract

Genomic signatures of the protease and reverse transcriptase gene of HIV-1 from HIV infected North Indian patients who were under ART from 1 to ≤ 7 years were analyzed. The DNA from plasma samples of 9 patients and RNA from 57 patients were isolated and subjected to amplification for the protease and reverse transcriptase gene of HIV-1 subtype C. Then sequencing was carried out following the WHO dried blood spot protocol. The drug resistance mutation patterns were analyzed using the HIV Drug Resistance Database, Stanford University, USA. Lamivudine-associated drug-resistance mutations such as M184V/M184I, nevirapine-associated drug resistance mutations Y181C and H221Y, and efavirenz-associated drug resistance mutations M230I were observed in reverse transcriptase gene of archived DNA of two HIV-1 infected patients. No mutation was observed in the remaining 7 patients. Various computational tools and websites like viral epidemiological signature pattern analysis (VESPA), hyper mutation, SNAP version 2.1.1, and entropy were utilized for the analysis of the signature pattern of amino acids, hyper mutation, selection pressure, and Shannon entropy in the protease and reverse transcriptase gene sequences of the 9 archived DNA, 56 protease gene and 51 reverse transcriptase gene from the HIV-1 DNA amplified sequences of RNA. The HIV-1 Subtype-C (Gene bank accession number: AB023804) and first isolate HXB2 (Gene bank accession number: K03455.1) was taken as reference sequence. The signature amino acid sequences were identified in the protease and reverse transcriptase gene, no hyper mutation, highest entropy was marked in the amino acid positions and synonymous to non-synonymous nucleotide ratio was calculated in the protease and reverse transcriptase gene of 9 archived DNA sequences, 56 protease and 51 reverse transcriptase gene sequences of HIV-1 Subtype C isolates.

摘要

对来自北印度且接受抗逆转录病毒治疗1至≤7年的HIV感染患者的HIV-1蛋白酶和逆转录酶基因的基因组特征进行了分析。分离了9例患者血浆样本中的DNA和57例患者的RNA,并对HIV-1 C亚型的蛋白酶和逆转录酶基因进行扩增。然后按照世界卫生组织干血斑方案进行测序。使用美国斯坦福大学的HIV耐药数据库分析耐药突变模式。在两名HIV-1感染患者的存档DNA的逆转录酶基因中观察到了拉米夫定相关的耐药突变,如M184V/M184I、奈韦拉平相关的耐药突变Y181C和H221Y,以及依非韦伦相关的耐药突变M230I。其余7例患者未观察到突变。利用各种计算工具和网站,如病毒流行病学特征模式分析(VESPA)、超突变、SNAP 2.1.1版和熵,对9份存档DNA、56个蛋白酶基因和51个逆转录酶基因的HIV-1 DNA扩增RNA序列的蛋白酶和逆转录酶基因序列中的氨基酸特征模式、超突变、选择压力和香农熵进行分析。将HIV-1 C亚型(基因库登录号:AB023804)和首个分离株HXB2(基因库登录号:K03455.1)作为参考序列。在蛋白酶和逆转录酶基因中鉴定出特征氨基酸序列,未发现超突变,在氨基酸位置标记出最高熵,并计算了9份存档DNA序列、HIV-1 C亚型分离株的56个蛋白酶和51个逆转录酶基因序列的蛋白酶和逆转录酶基因中同义核苷酸与非同义核苷酸的比例。