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