整合细菌病原体和共生菌研究,抗击感染--生态学视角。

IF 20.9 1区 生物学 Q1 INFECTIOUS DISEASES
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引用次数: 0

摘要

抗生素耐药细菌感染的发病率不断上升,而制药业已不再优先开发新的抗生素。基于细菌适应性、竞争和传播等生态学原理的跨学科研究方法可以为抗击耐抗生素感染开辟新的途径。在微生物组和宿主的某些病理状态下,许多兼性细菌病原体利用人体粘膜表面作为其主要贮藏库,并诱发传染病,以帮助它们横向传播到新的宿主生物体。有益的细菌共生体可以取代特定的病原体,从而降低病原体的传播能力并导致严重感染。然而,尽管具有临床意义,人们对共生菌-病原体在其自然栖息地中的相互作用的了解仍然很少。在这篇《个人观点》中,我们将重点介绍在人类微生物组和宿主生物学背景下加强细菌病原体和共生菌之间相互作用研究的方向,从而开发出预防和治疗传染病的创新和可持续方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating research on bacterial pathogens and commensals to fight infections—an ecological perspective

The incidence of antibiotic-resistant bacterial infections is increasing, and development of new antibiotics has been deprioritised by the pharmaceutical industry. Interdisciplinary research approaches, based on the ecological principles of bacterial fitness, competition, and transmission, could open new avenues to combat antibiotic-resistant infections. Many facultative bacterial pathogens use human mucosal surfaces as their major reservoirs and induce infectious diseases to aid their lateral transmission to new host organisms under some pathological states of the microbiome and host. Beneficial bacterial commensals can outcompete specific pathogens, thereby lowering the capacity of the pathogens to spread and cause serious infections. Despite the clinical relevance, however, the understanding of commensal–pathogen interactions in their natural habitats remains poor. In this Personal View, we highlight directions to intensify research on the interactions between bacterial pathogens and commensals in the context of human microbiomes and host biology that can lead to the development of innovative and sustainable ways of preventing and treating infectious diseases.

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来源期刊
Lancet Microbe
Lancet Microbe Multiple-
CiteScore
27.20
自引率
0.80%
发文量
278
审稿时长
6 weeks
期刊介绍: The Lancet Microbe is a gold open access journal committed to publishing content relevant to clinical microbiologists worldwide, with a focus on studies that advance clinical understanding, challenge the status quo, and advocate change in health policy.
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