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扎伊尔金沙萨人类免疫缺陷病毒1型毒株的基因多样性。

Genetic diversity of human immunodeficiency virus type 1 strains in Kinshasa, Zaire.

作者信息

Potts K E, Kalish M L, Bandea C I, Orloff G M, St Louis M, Brown C, Malanda N, Kavuka M, Schochetman G, Ou C Y

机构信息

Division of HIV/AIDS, Centers for Disease Control, Atlanta, Georgia 30333.

出版信息

AIDS Res Hum Retroviruses. 1993 Jul;9(7):613-8. doi: 10.1089/aid.1993.9.613.

Abstract

The envelope (env) gene of human immunodeficiency virus type 1 (HIV-1) was amplified by polymerase chain reaction (PCR) from the peripheral blood mononuclear cells (PBMCs) of 14 HIV-1-infected women from Kinshasa, Zaire. Amplified DNA was directly sequenced with a primer specific for the HIV-1 env C2 region. The predicted amino acid sequences for the C2-V3 region for the 14 specimens are presented. The tetrapeptide sequence, GPGQ, located at the crown of the V3 loop, is conserved in all specimens. The same tetrapeptide sequence is present in the Zairian isolate MAL, but not in other published Zairian isolates (Z6, ELI, Z321, JY1, and NDK). Sequence comparison of the env C2-V3 region among the 14 specimens from Kinshasa revealed a 9-25% range of nucleotide divergence, with an average of 16%. Divergence between the 14 specimens and the Zairian isolates MAL, Z6, ELI, Z321, JY1, and NDK ranged from 13 to 31%. A range of 18-28% nucleotide sequence divergence was demonstrated between the 14 Kinshasa specimens and the North American isolate MN. These results demonstrate the importance of examining HIV-1 samples from diverse geographic origins in the development of effective HIV-1 vaccines.

摘要

从扎伊尔金沙萨14名感染人类免疫缺陷病毒1型(HIV-1)的女性外周血单个核细胞(PBMC)中,通过聚合酶链反应(PCR)扩增HIV-1的包膜(env)基因。用针对HIV-1 env C2区域的特异性引物对扩增的DNA进行直接测序。给出了14个样本C2-V3区域的预测氨基酸序列。位于V3环顶部的四肽序列GPGQ在所有样本中均保守。扎伊尔分离株MAL中存在相同的四肽序列,但在其他已发表的扎伊尔分离株(Z6、ELI、Z321、JY1和NDK)中不存在。对金沙萨14个样本的env C2-V3区域进行序列比较,发现核苷酸差异范围为9%-25%,平均为16%。14个样本与扎伊尔分离株MAL、Z6、ELI、Z321、JY1和NDK之间的差异范围为13%-31%。14个金沙萨样本与北美分离株MN之间的核苷酸序列差异范围为18%-28%。这些结果表明,在开发有效的HIV-1疫苗时,检测来自不同地理区域的HIV-1样本非常重要。

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