生物
食源性病原体
巴尔通体
鉴定(生物学)
鼠疫耶尔森菌
人畜共患病
计算生物学
病毒学
医学
遗传学
生态学
毒力
细菌
疾病
病理
单核细胞增生李斯特菌
基因
作者
Xin Lu,Ping Yao,Ying Geng,Haiming Zhao,Xiantao Shen,Dongmei Li,Zhenpeng Li,Liang Lu,Miao Fan,Wenbin Xu,Jin Wang,Lianxu Xia,Zhongbing Zhang,Biao Kan
出处
期刊:China CDC weekly
[Chinese Center for Disease Control and Prevention]
日期:2022-01-01
卷期号:4 (12): 259-263
被引量:2
标识
DOI:10.46234/ccdcw2022.059
摘要
Accurate etiological detection is needed to evaluate the risk of zoonotic diseases. Metagenomic next-generation sequencing (mNGS) can be used to monitor pathogens in animal species and identify potential zoonotic threats. The current sampling model for zoonotic pathogen monitoring in wild animals requires samples to be transferred from the field to a laboratory for further detection.We constructed a zoonotic pathogen survey model using a set of mobile laboratories.The monitoring in this study was preplanned to detect Yersinia pestis, but the mNGS unexpectedly identified Bartonella spp. in the rodent samples, thus exposing the threat of bartonellosis to humans in this region. The co-localization of sampling and sequencing (CLOSS) model we tested required no long-distance transferring of samples and expands the regional coverage of zoonotic surveys by using a mobile laboratory.Using this mNGS technique will enable detection of more zoonotic pathogens beyond the preplanned monitoring targets. This may increase the surveillance efficiency compared with that of the previous workflow and expand the application of the mobile laboratories for infectious diseases identification and surveillance in the field.
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