Apicomplexan Espionage: Orchestrated Miscommunication at the Host–Parasite Interface

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Vaisak Mohan, Sandeep Reddy Vinjamuri, Parnika Sahoo, Abhinav Hatwar, Sandra S N, Usha Krishna, Vyshnav P V and Kamalakannan Vijayan*, 
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Abstract

Intracellular parasites, including Toxoplasma and Plasmodium, are entirely reliant on the active scavenging of host-derived nutrients to fuel their replicative cycle, as they are confined within a specialized membrane-bound compartment, the parasitophorous vacuole (PV). Initial observations, based on the proximity of host vesicles to the parasitophorous vacuole membrane (PVM), suggested that parasites utilize host vesicles to obtain essential nutrients. However, mounting evidence has now unequivocally demonstrated that intracellular pathogens establish membrane contacts with host organelles, establishing control over host cellular machinery. These intimate interactions enable the parasites to gain unimpeded access to cytosolic resources critical for development while evading host immune responses. This review consolidates the latest advancements in understanding the molecular machinery driving these transkingdom contacts and their functional roles. Further investigation into these processes promises to revolutionize our understanding of organelle communication, with profound implications for identifying new therapeutic targets and strategies.

Abstract Image

顶复合体间谍:寄主-寄主界面上精心安排的错误沟通
细胞内寄生虫,包括弓形虫和疟原虫,完全依赖于主动清除宿主来源的营养物质来为其复制周期提供燃料,因为它们被限制在一个特殊的膜结合腔室,即寄生液泡(PV)中。基于宿主囊泡与寄生物液泡膜(PVM)的接近性,初步观察表明寄生虫利用宿主囊泡获取必需的营养物质。然而,越来越多的证据明确表明,细胞内病原体与宿主细胞器建立了膜接触,建立了对宿主细胞机制的控制。这些密切的相互作用使寄生虫能够不受阻碍地获得对发育至关重要的细胞质资源,同时逃避宿主的免疫反应。本文综述了在分子机制驱动这些跨界接触及其功能作用方面的最新进展。对这些过程的进一步研究有望彻底改变我们对细胞器通信的理解,对确定新的治疗靶点和策略具有深远的意义。
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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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