缺乏BDF6严重影响克氏锥虫胞内无尾线虫的发育和传染性

IF 4.5 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2026-10-09 Epub Date: 2026-09-22 DOI:10.1021/acsinfecdis.6c00417
Victoria Boselli Raposo, Virginia Perdomo, Florencia Pacini, Juan A. Cueto, Alejandro Pezza, Patricia S. Romano, Roberto Docampo, Ana Rosa Perez, Esteban Serra
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引用次数: 0

摘要

恰加斯病的病原体克氏锥虫依靠复杂的基因调控机制来适应不同的宿主环境。近年来,表观遗传学通过调控染色质结构在这些机制中起着重要作用。含溴结构域因子(BDFs),以识别组蛋白上的乙酰化赖氨酸而闻名,已成为染色质重塑复合体的关键因子。在克氏t细胞预测的8个bdf中,BDF6是与MRGx和MRGBP的tintin样复合体的一部分,与NuA4/TIP60染色质重塑复合体的组分同源。我们使用CRISPR/ cas9基因编辑技术生成了bdf6基因敲除(KO)寄生虫。BDF6 KO副乳突体形态正常,但大小和生长下降,由此产生的亚环锥乳突体的感染性大大降低。引人注目的是,一旦进入宿主细胞,KO寄生虫分化成无纺丝体,但无法复制。这种细胞内阻滞被BDF6的外源性互补逆转。一致地,KO寄生虫在小鼠中也表现出感染受损,这一缺陷在附加寄生虫系中也得到了修复。我们的研究结果强调了BDF6作为细胞内寄生虫发育的关键调节剂,在附毛线虫以外的阶段起作用,其中表观遗传可塑性对宿主适应至关重要。BDF6 KO的这种惊人的阶段特异性表型强调了其功能的重要性,并强调了表观遗传调节因子在克氏锥虫生命周期中的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BDF6 Deficiency Severely Compromises Intracellular Amastigote Development and Infectivity of Trypanosoma cruzi

Trypanosoma cruzi, the causative agent of Chagas disease, relies on complex gene regulatory mechanisms to adapt to its diverse host environments. In recent years, it has been established that epigenetics plays an essential role in these mechanisms via the regulation of chromatin structure. Bromodomain-containing factors (BDFs), known for recognizing acetylated lysines on histones, have emerged as key factors in chromatin remodeling complexes. Among the eight predicted BDFs in T. cruzi, BDF6 is part of a TINTIN-like complex with MRGx and MRGBP, homologous to components of the NuA4/TIP60 chromatin remodeling complex. We generated knockout (KO) parasites for the bdf6 gene using CRISPR/Cas9 gene editing. BDF6 KO epimastigotes exhibit normal morphology but decreased size and growth, and the resulting metacyclic trypomastigotes displayed drastically reduced infectivity. Strikingly, once inside host cells, KO parasites differentiated into amastigotes but failed to replicate. This intracellular arrest was reversed by episomal complementation of BDF6. Consistently, KO parasites also exhibited impaired infectivity in mice, a defect that was also rescued in the addback parasite lines. Our findings highlight BDF6 as a critical regulator of intracellular parasite development, operating in stages beyond epimastigotes where epigenetic plasticity is essential for host adaptation. This striking stage-specific phenotype of BDF6 KO underscores its functional importance and highlights the relevance of epigenetic regulators along T. cruzi life cycle.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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