Potts K E, Kalish M L, Lott T, Orloff G, Luo C C, Bernard M A, Alves C B, Badaro R, Suleiman J, Ferreira O
Division of HIV/AIDS, Centers for Disease Control and Prevention, Atlanta, Georgia.
AIDS. 1993 Sep;7(9):1191-7. doi: 10.1097/00002030-199309000-00007.
To examine the genetic heterogeneity of the V3 region of HIV-1 gp120 from 22 Brazilian HIV-1 specimens.
Genetic heterogeneity was examined by DNA sequencing of the C2 V3 region of the HIV-1 envelope (env) gene from polymerase chain reaction (PCR)-amplified HIV-1 DNA. Deduced amino-acid sequences were compared to determine the extent of amino-acid conservation among the Brazilian specimens. Genetic similarity among and between the Brazilian specimens and other previously published HIV-1 isolates was analyzed by principal co-ordinate and DNA parsimony methods.
A 282 base pair (bp) region of a 1.5 kilo (k) bp PCR-amplified HIV-1 env fragment was sequenced by a Taq dye-labeled primer cycle sequencing reaction. Nucleotide sequences were used to analyze inter-specimen relationships based on overall nucleotide sequence similarity and DNA parsimony principles.
Amino-acid comparison showed that 15 of the 35 (43%) residues of the V3 loop were conserved among the Brazilian specimens. Nine of the 22 (40%) Brazilian specimens contained the North American-European GPGR tetrapeptide motif, while eight (36%) contained the GWGR motif, previously reported in Japanese isolates. Principal co-ordinate analysis demonstrated that 19 of the 20 examined Brazilian HIV-1 specimens were more similar to North American and Haitian isolates than to African isolates. Similar results were also obtained by DNA parsimony analysis.
The majority of the Brazilian specimens examined are more genetically related to North American and Haitian HIV-1 isolates than to African isolates. This finding and the presence of a GWGR V3 loop motif in some Brazilian isolates may be important for vaccine development.
检测来自22份巴西HIV-1样本的HIV-1 gp120 V3区的基因异质性。
通过对聚合酶链反应(PCR)扩增的HIV-1 DNA中HIV-1包膜(env)基因的C2 V3区进行DNA测序来检测基因异质性。比较推导的氨基酸序列以确定巴西样本中氨基酸保守程度。通过主坐标分析和DNA简约法分析巴西样本与其他先前发表的HIV-1分离株之间以及它们相互之间的遗传相似性。
通过Taq染料标记引物循环测序反应对1.5千碱基(kb)PCR扩增的HIV-1 env片段的282碱基对(bp)区域进行测序。基于总体核苷酸序列相似性和DNA简约原则,利用核苷酸序列分析样本间的关系。
氨基酸比较显示,V3环的35个残基中有15个(43%)在巴西样本中保守。22份巴西样本中有9份(40%)含有北美-欧洲GPGR四肽基序,而8份(36%)含有先前在日本分离株中报道的GWGR基序。主坐标分析表明,20份检测的巴西HIV-1样本中有19份与北美和海地分离株比与非洲分离株更相似。DNA简约分析也得到了类似结果。
所检测的大多数巴西样本在基因上与北美和海地HIV-1分离株的关系比与非洲分离株的关系更密切。这一发现以及一些巴西分离株中存在GWGR V3环基序可能对疫苗开发具有重要意义。