Laboratorio de Biología Celular y Retrovirus-CONICET, Hospital de Pediatría J P Garrahan, Buenos Aires, Argentina.
Infect Genet Evol. 2012 Mar;12(2):443-7. doi: 10.1016/j.meegid.2012.01.003. Epub 2012 Jan 12.
The aim of this work is to characterize the full-length intersubtype recombinant structure of the HIV-1 Circulating Recombinant Form CRF17_BF. A single genome of CRF17_BF was originally described in 2001 as being largely similar to CRF12_BF. Since then, more genomes of CRF17_BF have been sequenced but not adequately described in publications. Here we describe CRF17_BF as a genuine CRF, and analyze its recombination pattern based on bootscan analyses, subtype signature patterns, and phylogenetic reconstruction of subtype-delimited segments. We show that CRF17_BF can be distinguished from CRF12_BF in several regions of the genome, including vpu, pol, env and nef. A complete and accurate characterization and description of recombination breakpoints in CRFs is required for a proper surveillance of HIV-1 genotypes, and important for epidemiological purposes.
本研究旨在对 HIV-1 循环重组形式 CRF17_BF 的全长亚型间重组结构进行特征描述。2001 年首次描述的 CRF17_BF 单基因组与 CRF12_BF 非常相似。此后,已对更多的 CRF17_BF 基因组进行了测序,但在出版物中没有得到充分描述。在这里,我们将 CRF17_BF 描述为一种真正的 CRF,并基于 bootscan 分析、亚型特征模式和亚型限定片段的系统发育重建来分析其重组模式。我们表明,CRF17_BF 可以在基因组的几个区域与 CRF12_BF 区分开来,包括 vpu、pol、env 和 nef。对 CRF 中的重组断点进行完整、准确的特征描述和描述,对于 HIV-1 基因型的正确监测以及流行病学目的都非常重要。