南非夸祖鲁-纳塔尔一名多药耐药性患者中HIV-1亚型CRF18_cpx的鉴定:流行病学担忧?

IF 1.6 Q4 INFECTIOUS DISEASES
Aabida Khan , Melendhran Pillay , Benjamin Chimukangara , Lilishia Gounder , Sontaga Manyana , Kerri-Lee Francois , Knowledge Chipango
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引用次数: 1

摘要

南非最常见的HIV-1亚型是C亚型,其他亚型的检测很少。我们报告了第一例已知的HIV-1亚型CRF18_cpx病例,该病例通过HIV耐药性基因分型在艾滋病毒流行的中心南非夸祖鲁-纳塔尔发现。这名31岁的女性患者于2017年开始接受固定剂量的联合用药(替诺福韦、恩曲他滨、依非韦伦),但未能实现病毒学抑制。2018年改为二线抗逆转录病毒疗法(替诺福韦、恩曲他滨和利托那韦增强的洛匹那韦)。洛匹那韦引起的腹泻影响了依从性。2020年,她改用齐多夫定、拉米夫定和利托那韦增强的阿他扎那韦。病毒学失败持续存在,2021年4月的HIV耐药性基因分型显示出多药耐药性。Third-line方案(替诺福韦、拉米夫定、多卢替拉韦和利托那韦增强的达芦那韦)于2021年5月开始,并实现了病毒学抑制。顺便说一句,我们从HIV耐药性序列报告中发现,患者感染了HIV-1亚型CRF18_cpx。使用REGA HIV-1亚型工具对HIV序列的分析证实序列亚型分配为HIV-1 CRF 18_cpx(自举置信度=90%)。COMET HIV-1工具、HIV BLAST工具和系统发育分析也证实了亚型。根据我们的偶然发现,CRF18_cpx可能在局部循环,因为患者没有旅行史。由于旅行的增加,预计非C亚型和重组病毒在南非的引入将增加。这突出表明,需要描述南非,特别是夸祖鲁-纳塔尔的亚型多样性,因为艾滋病毒亚型会影响发病机制、治疗反应、耐药性和疫苗开发工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of HIV-1 subtype CRF18_cpx in a patient with multidrug resistance in KwaZulu-Natal, South Africa: An epidemiological worry?

The most common HIV-1 subtype in South Africa is subtype C, and detection of other subtypes is rare. We report the first known case of HIV-1 subtype CRF18_cpx identified in KwaZulu-Natal, South Africa, the epicenter of the HIV epidemic, through HIV drug resistance genotyping.

The 31-year-old female patient was initiated on fixed dose combination (tenofovir, emtricitabine, efavirenz) in 2017, with failure to achieve virologic suppression. Change to second-line antiretroviral therapy (tenofovir, emtricitabine and ritonavir-boosted lopinavir) was made in 2018. Adherence was impacted by lopinavir-induced diarrhoea. In 2020, she was switched to zidovudine, lamivudine and ritonavir-boosted atazanavir. Virologic failure persisted, and HIV drug resistance genotyping in April 2021 showed multidrug resistance. Third-line regimen (tenofovir, lamivudine, dolutegravir and ritonavir-boosted darunavir) was commenced in May 2021 and virologic suppression was achieved.

Co-incidentally we discovered from the HIV drug resistance sequence report that the patient was infected with HIV-1 subtype CRF18_cpx. Analysis of the HIV sequence using REGA HIV-1 Subtyping Tool confirmed sequence subtype assignment as HIV-1 CRF 18_cpx (bootstrap confidence = 90%). Subtyping was also confirmed with the COMET HIV-1 tool, HIV BLAST tool and phylogenetic analysis.

Based on our incidental finding, CRF18_cpx may be circulating locally as the patient had no travel history. Introduction of non-subtype C and recombinant viruses are expected to have increased in South Africa due to increased travel. This highlights the need to characterize subtype diversity in South Africa, particularly in KwaZulu-Natal, as HIV subtype can influence pathogenesis, treatment response, drug resistance and efforts towards vaccine development.

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来源期刊
Journal of clinical virology plus
Journal of clinical virology plus Infectious Diseases
CiteScore
2.20
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66 days
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