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Use of Genome Sequencing to Define Institutional Influenza Outbreaks Toronto Ontario Canada 2014–15

机译:使用基因组测序确定机构性流感爆发加拿大安大略省多伦多市2014-15年

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摘要

Adequacy of the current clinical definition of institutional influenza outbreaks is unclear. We performed a retrospective genome sequencing and epidemiologic analysis of institutional influenza outbreaks that occurred during the 2014–15 influenza season in Toronto, Canada. We sequenced the 2 earliest submitted samples positive for influenza A(H3N2) from each of 38 reported institutional outbreaks in long-term care facilities. Genome sequencing showed most outbreak pairs identified by using the current clinical definition were highly related. Inclusion of surveillance samples demonstrated that outbreak sources were likely introductions from broader circulating lineages. Pairwise distance analysis using majority genome and hemagglutinin-specific genes enabled identification of thresholds for discrimination of within and between outbreak pairs; the area under the curve ranged 0.93–0.95. Routine genome sequencing for defining influenza outbreaks in long-term care facilities is unlikely to add significantly to the current clinical definition. Sequencing may prove most useful for investigating sources of outbreak introductions.
机译:目前尚不清楚机构性流感爆发的当前临床定义是否足够。我们对加拿大多伦多2014-15流感季节期间发生的机构性流感爆发进行了回顾性基因组测序和流行病学分析。我们从长期护理机构中报告的38例机构暴发中的每一种中,对2份最早提交的A型流感(H3N2)呈阳性的样本进行了测序。基因组测序表明,使用当前临床定义确定的大多数暴发对高度相关。包括监测样本表明,暴发源可能是来自更广泛的循环血统的传入。使用多数基因组和血凝素特异性基因进行成对距离分析,能够确定用于区分暴发对内和暴发对的阈值;曲线下面积在0.93-0.95之间。用于确定长期护理机构中流感爆发的常规基因组测序不太可能显着增加当前的临床定义。事实证明,测序对于调查暴发流行源最有用。

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