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Genetic diversity and drug resistance of HIV type 1 circulating recombinant Form_BC among drug users in Guangdong Province.

机译:广东省吸毒人群HIV 1型循环重组Form_BC的遗传多样性和耐药性

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摘要

To study genetic diversity and drug resistance of HIV-1 CRF_BC among drug users in Guangdong Province, 67 circulating recombinant form 07_BC (CRF_07BC) and 32 circulating recombinant form 08_BC(CRF_08BC) HIV-1 pol genes were amplified and sequenced. In the protease gene region (PR), 31 CRF_08BC isolates were amplified and 10 high polymorphism positions were identified. The polymorphisms L19I, M36I, R41K, D60E, L63P, H69K, and I93L were complete substitutions, and were followed by T12S (94%), I15V (90%), and L89M (81%) separately. Five high polymorphisms were found in CRF_07BC isolates; there were E35D (88%), R41K (100%), D60E (96%), L63P (99%), and I93L (91%). Four of the identified polymorphism positions (R41K, D60E, L63P, and I93L) were the same in the PR region of both subtypes. In the reverse transcriptase (RT) region six high polymorphism positions, V35T, E36A, T39D/E/N, S48T, V60I, and V245Q, were identified in both subtypes. E53D (97%), I135V/T/R (81%), S162C (94%), Q207E (100%), and R211K (97%) were primarily in CRF_08BC subtypes and D121Y/H (97%) were primarily in CRF_07BC. The NRTI resistance mutation T69S was 94% (30/32) in CRF_08BC. To now, we have found no related reports concerning such high polymorphisms in the position. Polymorphisms V77M (PI) and K201Q (RT) were not found in the mutation profiles; therefore it may have been a new mutation in HIV-1. This study analyzed the difference between CRF_08BC and 07BC polymorphisms among drug users in Guangdong Province, which may help to guide recommendations for diagnostic assays, vaccine design, and antiretroviral regimen strategies in China.
机译:为了研究广东省吸毒人群HIV-1 CRF_BC的遗传多样性和耐药性,扩增并测序了67个循环重组体07_BC(CRF_07BC)和32个循环重组体08_BC(CRF_08BC)HIV-1 pol基因。在蛋白酶基因区域(PR)中,扩增了31个CRF_08BC分离株,并鉴定了10个高多态性位置。多态性L19I,M36I,R41K,D60E,L63P,H69K和I93L是完全取代,之后分别是T12S(94%),I15V(90%)和L89M(81%)。在CRF_07BC分离物中发现了5个高多态性。有E35D(88%),R41K(100%),D60E(96%),L63P(99%)和I93L(91%)。在两个亚型的PR区域中,四个已鉴定的多态性位置(R41K,D60E,L63P和I93L)相同。在逆转录酶(RT)区域中,在两个亚型中均确定了六个高多态性位点,即V35T,E36A,T39D / E / N,S48T,V60I和V245Q。 E53D(97%),I135V / T / R(81%),S162C(94%),Q207E(100%)和R211K(97%)主要在CRF_08BC亚型中,而D121Y / H(97%)主要在CRF_08BC亚型中。 CRF_07BC。在CRF_08BC中,NRTI抗药性突变T69S为94%(30/32)。到目前为止,我们尚未找到有关该位置如此高的多态性的相关报道。在突变图谱中未发现多态性V77M(PI)和K201Q(RT)。因此它可能是HIV-1的新突变。这项研究分析了广东省吸毒者之间CRF_08BC和07BC多态性的差异,这可能有助于为中国的诊断分析,疫苗设计和抗逆转录病毒疗法策略提供指导。

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