Dynamic airborne mycobiome in the metropolitan city transit system is driven by seasonality and station type.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Xin Zhou, Da Li, Xiao-Wei Lu, Clement K M Tsui, Supawadee Ingsriswang, Jun-Min Liang, Lei Cai
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引用次数: 0

Abstract

Subway transit systems serve as the primary transportation mode in metropolitan areas. The quality of the airway in transit plays a crucial role in human health as commuters and workers are exposed to microbes transmitted from passengers and circulated within built environments. The diversity and dynamics of bacterial microbiome in these environments have been relatively well studied. However, the fungal communities remain poorly investigated. In this study, we conducted a year-long comprehensive investigation of the mycobiomes within the world's second largest subway system and analyzed the seasonal dynamics of fungal composition across intercity hub stations, urban hub stations, and suburban stations. We found a high diversity of the subway mycobiome that varied seasonally and was influenced by various environmental factors, such as particulate matter (PM2.5) levels and average humidity. Fungal diversity was higher in months with elevated PM2.5 pollution. Autumn exhibited increased diversity and peaks in the distribution of human pathogenic fungi. Furthermore, it was determined that station types exert a significant influence on the diversity of pathogenic fungi, with interchange stations (train and airport transfer stations) showing the highest diversity, while suburban stations showed the lowest. The core taxa of the mycobiome comprised several genera including ubiquitous fungi commonly found in soil and outdoor environments (e.g., Alternaria and Cladosporium), as well as potential plant and human pathogens (e.g., Phoma and Fusarium), indicating a potential risk to public health. Our study demonstrated the seasonal and spatial dynamics of mycobiomes in the Beijing subway system and revealed the factors/mechanisms that shape the indoor fungal communities. Understanding the patterns and processes of mycobiome community is important for infection prevention and public health management.

Importance: Respiratory infections and allergic reactions caused by airborne fungi have received considerable public attention; however, fungal communities remain poorly investigated. This research performed the first year-long investigation of airborne mycobiome in the world's largest subway system. We found that the fungal diversity peaks in autumn and at stations with higher PM2.5 levels. Intercity hubs exhibit the highest diversity of pathogenic fungi and the least seasonal fluctuation. Suburban stations revealed a reduced diversity of human pathogens but an elevated presence of plant pathogens. Core fungal taxa in subways include both common soil fungi (e.g., Alternaria and Cladosporium) and potential plant and human pathogens (e.g., Phoma, Fusarium, and Rhinocladiella) that pose potential health risks. These results are crucial for infection prevention and public health management in city transit systems.

大城市交通系统中空气真菌群落的动态变化受季节和站点类型的影响。
地铁交通系统是大都市区的主要交通方式。由于通勤者和工作人员暴露于乘客传播并在建筑环境中传播的微生物中,运输过程中的气道质量对人类健康起着至关重要的作用。在这些环境中,细菌微生物组的多样性和动态已经得到了较好的研究。然而,真菌群落的研究仍然很少。在这项研究中,我们对世界第二大地铁系统的真菌群落进行了为期一年的全面调查,并分析了城际枢纽站、城市枢纽站和郊区站真菌组成的季节性动态。我们发现地铁真菌群落的高度多样性随季节变化,并受到各种环境因素的影响,如PM2.5水平和平均湿度。在PM2.5污染程度较高的月份,真菌多样性较高。秋季人类病原真菌多样性增加,分布达到高峰。站点类型对病原菌多样性有显著影响,换乘站点(火车和机场转运站)的多样性最高,而城郊站点的多样性最低。真菌群系的核心分类群包括几个属,包括在土壤和室外环境中普遍存在的真菌(如Alternaria和Cladosporium),以及潜在的植物和人类病原体(如Phoma和Fusarium),表明对公众健康存在潜在风险。本研究揭示了北京地铁系统真菌群落的季节和空间动态,揭示了室内真菌群落的形成因素和机制。了解真菌群落的模式和过程对预防感染和公共卫生管理具有重要意义。重要性:空气中真菌引起的呼吸道感染和过敏反应已经引起了公众的广泛关注;然而,真菌群落的研究仍然很少。这项研究对世界上最大的地铁系统进行了为期一年的空气真菌群落调查。我们发现真菌多样性在秋季和PM2.5水平较高的站点达到峰值。城际枢纽区病原菌多样性最高,季节性波动最小。郊区站点显示人类病原体的多样性减少,但植物病原体的存在增加。地铁中的核心真菌类群既包括常见的土壤真菌(例如,交替菌和枝孢菌),也包括潜在的植物和人类病原体(例如,真菌、镰刀菌和鼻枝菌),它们构成潜在的健康风险。这些结果对城市交通系统感染预防和公共卫生管理具有重要意义。
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
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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