尽管暴露于结核分枝杆菌,人类YEATS4变异体仍能对TST和IGRA转化产生耐药性。

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Clément Conil, Jonathan Bohlen, Elouise E Kroon, Marc A Jean-Juste, Jérémy Manry, Matthieu Chaldebas, James M Bean, Kathleen F Walsh, Monica Dallmann-Sauer, Maxime Rotival, Yoann Seeleuthner, Astrid Marchal, Haralambos Mourelatos, Vinicius M Fava, Peng Zhang, Gaspard Kerner, Hanaa Skhoun, Ahmed Abid, Hanane El Ouazzani, Aniss Rafik, Ahmed Aziz Bousfiha, Jamila El Baghdadi, Robert J Wilkinson, Stéphanie Boisson-Dupuis, Daniel W Fitzgerald, Jean W Pape, Marlo Möller, Eileen G Hoal, Jean-Laurent Casanova, Laurent Abel, Erwin Schurr, Aurélie Cobat
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引用次数: 0

摘要

背景:尽管持续暴露于结核分枝杆菌(Mtb),一些个体-所谓的抵抗者-在结核菌素皮肤试验(TST)和干扰素释放试验(IGRAs)中持续呈阴性结果。“对免疫转化的抵抗力”是最著名的与结核杆菌不传播和预防结核病相关的临床指标。我们研究了这种表型的人类遗传基础,假设携带HIV(结核病的主要危险因素)的耐药者会在赋予耐药的基因型中富集。方法:我们招募了两组HIV感染者(PWH),包括来自南非的55名抵抗者和100名对照者(TST和IGRA阳性或有结核病史),以及来自海地的66名抵抗者和57名对照者,这两个地区是结核病高流行地区。所有研究参与者都进行了全基因组测序(WGS)。我们对抗性表型进行了全基因组关联研究(GWAS),重点研究了320,629种常见的蛋白质改变和调节变异。结果:我们在12q15染色体上发现了一组变异,包括rs622656,与南非和海地的抗性表型相关。荟萃分析显示,rs622656的C等位基因与抗性表型相关,优势比(OR)为4.35 (95% CI: 2.44-7.69) (P = 2.47 × 10-7)。组合样品中C等位基因的频率为0.11,4个CC纯合子均为抗性。一致地,我们发现在来自海地、摩洛哥和英国生物银行的hiv阴性结核病患者的三个队列中,rs622656-C耐药相关等位基因的纯合携带者显著减少。硅分析表明,rs622656-C抗性相关等位基因通过抑制上游开放阅读框增加了附近YEATS4基因的翻译。YEATS4已被证明在先天淋巴样细胞分化(一种白细胞亚群)中发挥作用。我们通过实验证实,rs622656-C抗性相关等位基因增加了HEK293T细胞中报告基因的活性。结论:我们在两个PWH群体中报道了12q15染色体上重叠YEATS4基因的一个新的变异簇,与抗性表型密切相关。我们的研究结果有助于理解阻断结核分枝杆菌传播的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A human YEATS4 variant confers resistance to TST and IGRA conversion despite Mycobacterium tuberculosis exposure.

Background: Despite sustained exposure to Mycobacterium tuberculosis (Mtb), some individuals-so-called resisters-have persistently negative results for the tuberculin skin test (TST) and interferon-gamma release assays (IGRAs). "Resistance to immune conversion" is the best-known clinical correlate for absence of Mtb transmission and protection from tuberculosis (TB). We investigated the human genetic basis of this phenotype by hypothesizing that resisters living with HIV, a major risk factor for TB, would be enriched in genotypes conferring resistance.

Methods: We enrolled two cohorts of people living with HIV (PWH), consisting of 55 resisters and 100 controls-either positive for TST and IGRA or with a history of TB-from South Africa, and 66 resisters and 57 controls from Haiti, two regions where TB is hyperendemic. All study participants underwent whole-genome sequencing (WGS). We performed a genome-wide association study (GWAS) of the resister phenotype, focusing on a comprehensive set of 320,629 common protein-altering and regulatory variants.

Results: We identified a cluster of variants on chromosome 12q15, including rs622656, associated with the resister phenotype in both South Africa and Haiti. A meta-analysis revealed that the C allele of rs622656 was associated with the resister phenotype with an odds ratio (OR) of 4.35 (95% CI: 2.44-7.69) (P = 2.47 × 10-7). The frequency of the C allele in the combined sample was 0.11, and all four CC homozygotes in our sample were resisters. Consistently, we found a significant depletion of homozygous carriers of the rs622656-C resistance-associated allele in three cohorts of HIV-negative TB patients from Haiti, Morocco, and the UK Biobank. In silico analysis suggested that the rs622656-C resistance-associated allele increased the translation of the nearby YEATS4 gene by suppressing an upstream open reading frame. YEATS4 has been shown to play a role in innate lymphoid cell differentiation, a leukocyte subset. We confirmed experimentally that the rs622656-C resistance-associated allele increased the activity of the reporter gene in HEK293T cells.

Conclusions: We report a new cluster of variants on chromosome 12q15, overlapping the YEATS4 gene, strongly associated with the resister phenotype in two populations of PWH. Our results contribute to the understanding of the molecular mechanisms that block transmission of Mtb.

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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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