Determination of Human Immunodeficiency Virus Type 1 Subtypes by a Rapid Method Useful for the Routine Diagnostic Laboratory

H. Kessler, D. Deuretzbacher, E. Stelzl, E. Daghofer, B. Santner, E. Marth
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引用次数: 11

Abstract

ABSTRACT The existence of human immunodeficiency virus type 1 (HIV-1) subtypes has many important implications for the global evolution of HIV and for the evaluation of pathogenicity, transmissibility, and candidate HIV vaccines. The aim of this study was to establish a rapid method for determination of HIV-1 subtypes useful for a routine diagnostic laboratory and to investigate the distribution of HIV-1 subtypes in Austrian patients. Samples were tested by a subtyping method based on a 1.3-kb sequence of the polymerase gene generated by a commercially available drug resistance assay. The generated sequence was subtyped by means of an HIV sequence database. Results of 74 routine samples revealed subtype B (71.6%) as the predominant subtype, followed by subtype A (13.5%) and subtype C (6.8%). Subtypes E, F, G, and AE (CM240) were also detected. This subtyping method was found to be very easy to handle, rapid, and inexpensive and has proved suitable for high-throughput routine diagnostic laboratories. The specific polymerase gene sequence, however, must be existent.
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用于常规诊断实验室的快速测定人类免疫缺陷病毒1型亚型的方法
人类免疫缺陷病毒1型(HIV-1)亚型的存在对HIV的全球进化以及对致病性、传播性和候选HIV疫苗的评估具有许多重要意义。本研究的目的是建立一种用于常规诊断实验室的快速测定HIV-1亚型的方法,并调查HIV-1亚型在奥地利患者中的分布。样品采用基于市售耐药试验产生的聚合酶基因1.3 kb序列的分型方法进行检测。生成的序列通过HIV序列数据库进行亚型分型。74份常规标本中,B亚型占71.6%,其次为A亚型(13.5%)和C亚型(6.8%)。还检测到E、F、G和AE亚型(CM240)。这种分型方法易于操作、快速且价格低廉,已被证明适用于高通量常规诊断实验室。然而,特定的聚合酶基因序列必须存在。
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