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病房医院窗户组件上的存活细菌群落。

Viable bacterial communities on hospital window components in patient rooms.

作者信息

Horve Patrick F, Dietz Leslie G, Ishaq Suzanne L, Kline Jeff, Fretz Mark, Van Den Wymelenberg Kevin G

机构信息

Biology and the Built Environment Center, University of Oregon, Eugene, OR, United States of America.

School of Food and Agriculture, University of Maine, Orono, ME, United States of America.

出版信息

PeerJ. 2020 Jul 27;8:e9580. doi: 10.7717/peerj.9580. eCollection 2020.

DOI:10.7717/peerj.9580
PMID:33194331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7391968/
Abstract

Previous studies demonstrate an exchange of bacteria between hospital room surfaces and patients, and a reduction in survival of microorganisms in dust inside buildings from sunlight exposure. While the transmission of microorganisms between humans and their local environment is a continuous exchange which generally does not raise cause for alarm, in a hospital setting with immunocompromised patients, these building-source microbial reservoirs may pose a risk. Window glass is often neglected during hospital disinfection protocols, and the microbial communities found there have not previously been examined. This pilot study examined whether living bacterial communities, and specifically the pathogens Methicillin-resistant (MRSA) and were present on window components of exterior-facing windows inside patient rooms, and whether relative light exposure (direct or indirect) was associated with changes in bacterial communities on those hospital surfaces. Environmental samples were collected from 30 patient rooms in a single ward at Oregon Health & Science University (OHSU) in Portland, Oregon, USA. Sampling locations within each room included the window glass surface, both sides of the window curtain, two surfaces of the window frame, and the air return grille. Viable bacterial abundances were quantified using qPCR, and community composition was assessed using Illumina MiSeq sequencing of the 16S rRNA gene V3/V4 region. Viable bacteria occupied all sampled locations, but was not associated with a specific hospital surface or relative sunlight exposure. Bacterial communities were similar between window glass and the rest of the room, but had significantly lower Shannon Diversity, theorized to be related to low nutrient density and resistance to bacterial attachment of glass compared to other surface materials. Rooms with windows that were facing west demonstrated a higher abundance of viable bacteria than those facing other directions, potentially because at the time of sampling (morning) west-facing rooms had not yet been exposed to sunlight that day. Viable was not detected and viable MRSA was detected at very low abundance. Bacterial abundance was negatively correlated with distance from the central staff area containing the break room and nursing station. In the present study, it can be assumed that there is more human traffic in the center of the ward, and is likely responsible for the observed gradient of total abundance in rooms along the ward, as healthcare staff both deposit more bacteria during activities and affect microbial transit indoors. Overall, hospital window components possess similar microbial communities to other previously identified room locations known to act as reservoirs for microbial agents of hospital-associated infections.

摘要

先前的研究表明,医院病房表面与患者之间存在细菌交换,并且建筑物内灰尘中的微生物因阳光照射而存活率降低。虽然人类与其局部环境之间的微生物传播是一种持续的交换,通常不会引起警觉,但在有免疫功能低下患者的医院环境中,这些建筑物来源的微生物库可能会带来风险。医院消毒规程中常常忽略窗户玻璃,此前也未曾对其上发现的微生物群落进行过检查。这项初步研究调查了病房内朝向外墙的窗户组件上是否存在有生命的细菌群落,特别是耐甲氧西林金黄色葡萄球菌(MRSA)等病原体,以及相对光照(直接或间接)是否与这些医院表面的细菌群落变化有关。在美国俄勒冈州波特兰市的俄勒冈健康与科学大学(OHSU)的一个病房中,从30个患者房间采集了环境样本。每个房间内的采样位置包括窗户玻璃表面、窗帘两侧、窗框的两个表面以及回风格栅。使用定量聚合酶链反应(qPCR)对活菌丰度进行定量,并使用16S rRNA基因V3/V4区域的Illumina MiSeq测序评估群落组成。活菌占据了所有采样位置,但与特定的医院表面或相对阳光照射无关。窗户玻璃和房间其他地方的细菌群落相似,但香农多样性显著较低,理论上这与低营养密度以及与其他表面材料相比玻璃对细菌附着的抗性有关。朝西的窗户所在房间的活菌丰度高于朝其他方向的房间,这可能是因为在采样时(早晨)朝西的房间当天尚未受到阳光照射。未检测到活菌 ,并且检测到的活菌MRSA丰度非常低。细菌丰度与距离包含休息室和护士站的中央工作人员区域的距离呈负相关。在本研究中,可以假设病房中心的人员流动更多,这可能是导致沿病房房间中观察到的总丰度梯度的原因,因为医护人员在活动期间会沉积更多细菌并影响室内微生物传播。总体而言,医院窗户组件拥有与其他先前确定的已知作为医院相关感染微生物病原体库的房间位置相似的微生物群落。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/05b3f9e0e0e9/peerj-08-9580-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/42b71aa35922/peerj-08-9580-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/3494786b71b7/peerj-08-9580-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/15a6929da1ae/peerj-08-9580-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/5e9d78f9362c/peerj-08-9580-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/05b3f9e0e0e9/peerj-08-9580-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/42b71aa35922/peerj-08-9580-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/3494786b71b7/peerj-08-9580-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/15a6929da1ae/peerj-08-9580-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/5e9d78f9362c/peerj-08-9580-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786c/7391968/05b3f9e0e0e9/peerj-08-9580-g005.jpg

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