Complex ecological approach to cystic fibrosis respiratory infections

Q3 Agricultural and Biological Sciences
Dmitriy V. Alekseev, Artem V. Lyamin, Karim A. Kayumov
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引用次数: 0

Abstract

Cystic fibrosis (CF) is one of the most common genetic disorders; resulting in a wide variety of complications, including respiratory infections. Such infections are often ineffectively treated within the framework of a classical paradigm of the infectious process. However, little attention is paid to the unique microecological conditions that are formed in CF respiratory tract. This study aimed to exploring the microecological conditions and to finding out how they may influence the pathogenesis of CF infections. These conditions emerge under the influence of local disruptions in the respiratory functions; inflammatory processes, and complicated relations of the individual microorganisms between each other and between the human bodies as their ecological substrates. As a result, microorganisms that are usually safe for the healthy people become extremely dangerous for CF patients; having adapted to a new ecological niche and having got definite resource advantage, which is attributed to the respiratory tract tissue destruction. Additionally, it is still unknown; how do the anaerobic microbes contribute to CF infections, and whether they collaborate with the traditional CF pathogens or compete with them. In this article, we are analyzing CF respiratory infections from the ecological perspective and proposing in our opinion a more comprehensive picture of their pathogenesis.
囊性纤维化呼吸道感染的复杂生态学方法
囊性纤维化(CF)是最常见的遗传疾病之一,会导致多种并发症,包括呼吸道感染。在经典的感染过程范例框架内,此类感染往往得不到有效治疗。然而,人们很少关注 CF 呼吸道中形成的独特微生态条件。本研究旨在探索微生态条件,并找出它们如何影响 CF 感染的发病机制。这些条件是在呼吸功能局部紊乱、炎症过程以及微生物之间和作为其生态基质的人体之间的复杂关系的影响下出现的。因此,通常对健康人来说是安全的微生物,对 CF 患者来说却变得极其危险;这些微生物已经适应了新的生态位,并获得了明确的资源优势,这归因于呼吸道组织的破坏。此外,厌氧微生物是如何导致 CF 感染的,它们是与传统 CF 病原体合作还是相互竞争,目前仍是未知数。在这篇文章中,我们从生态学的角度分析了 CF 呼吸道感染,并提出了我们认为更全面的发病机制。
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
1.40
自引率
0.00%
发文量
16
审稿时长
4 weeks
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