Molecular mechanisms that govern infection and antifungal resistance in Mucorales.

IF 8 1区 生物学 Q1 MICROBIOLOGY
Microbiology and Molecular Biology Reviews Pub Date : 2024-03-27 Epub Date: 2024-03-06 DOI:10.1128/mmbr.00188-22
Carlos Lax, Francisco E Nicolás, Eusebio Navarro, Victoriano Garre
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Abstract

SUMMARYThe World Health Organization has established a fungal priority pathogens list that includes species critical or highly important to human health. Among them is the order Mucorales, a fungal group comprising at least 39 species responsible for the life-threatening infection known as mucormycosis. Despite the continuous rise in cases and the poor prognosis due to innate resistance to most antifungal drugs used in the clinic, Mucorales has received limited attention, partly because of the difficulties in performing genetic manipulations. The COVID-19 pandemic has further escalated cases, with some patients experiencing the COVID-19-associated mucormycosis, highlighting the urgent need to increase knowledge about these fungi. This review addresses significant challenges in treating the disease, including delayed and poor diagnosis, the lack of accurate global incidence estimation, and the limited treatment options. Furthermore, it focuses on the most recent discoveries regarding the mechanisms and genes involved in the development of the disease, antifungal resistance, and the host defense response. Substantial advancements have been made in identifying key fungal genes responsible for invasion and tissue damage, host receptors exploited by the fungus to invade tissues, and mechanisms of antifungal resistance. This knowledge is expected to pave the way for the development of new antifungals to combat mucormycosis. In addition, we anticipate significant progress in characterizing Mucorales biology, particularly the mechanisms involved in pathogenesis and antifungal resistance, with the possibilities offered by CRISPR-Cas9 technology for genetic manipulation of the previously intractable Mucorales species.

真菌感染和抗真菌耐药性的分子机制。
摘要世界卫生组织制定了一份真菌优先病原体清单,其中包括对人类健康至关重要或高度重要的物种。其中包括粘菌目,这是一个由至少 39 个真菌种类组成的真菌群,可引起被称为粘孢子菌病的危及生命的感染。尽管病例持续增加,而且由于对临床上使用的大多数抗真菌药物具有先天抗药性,预后不佳,但粘孢子菌目受到的关注有限,部分原因是进行基因操作存在困难。COVID-19 的大流行使病例进一步增加,一些患者出现了与 COVID-19 相关的粘孢子菌病,这突出表明迫切需要增加对这些真菌的了解。本综述探讨了治疗该疾病所面临的重大挑战,包括诊断延迟和诊断不准确、缺乏准确的全球发病率估计以及治疗方案有限。此外,它还重点介绍了有关该病发病机制和基因、抗真菌抗药性以及宿主防御反应的最新发现。在确定负责入侵和组织损伤的关键真菌基因、真菌入侵组织时利用的宿主受体以及抗真菌抗性机制方面取得了重大进展。这些知识有望为开发新的抗真菌药物防治粘孢子菌病铺平道路。此外,借助 CRISPR-Cas9 技术对以前难以解决的粘孢子菌物种进行遗传操作的可能性,我们预计粘孢子菌生物学特性的研究将取得重大进展,特别是发病机制和抗真菌抗性机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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