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冷冻血浆样本的微生物群落揭示了野生鸟类和啮齿动物体内的潜在病原体。

Microbiomes of frozen blood plasma samples reveal potential pathogens in wild birds and rodents.

作者信息

Erickson Cally E, Fair Jeanne M, Bartlow Andrew W

机构信息

Genomics and Bioanalytics, Los Alamos National Laboratory, Mailstop M888, Los Alamos, NM 87545, USA.

出版信息

One Health. 2025 Jun 11;21:101109. doi: 10.1016/j.onehlt.2025.101109. eCollection 2025 Dec.

DOI:10.1016/j.onehlt.2025.101109
PMID:40606019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12221476/
Abstract

The lack of genomic data on pathogens from wildlife severely limits our ability to track transmission patterns and trace the origins of an outbreak. There are currently millions of wildlife samples in biobanks around the world, including blood samples. Blood has traditionally been viewed as a sterile environment in healthy individuals, but recent evidence suggests that this is not the case, especially for wild animals. Our goal was to determine whether frozen plasma samples can be surveyed using 16S sequencing to provide information about potential hosts for pathogens for a more complete understanding of disease systems. We sequenced blood plasma from wild North American deer mice () and American kestrels () that were cryogenically stored for 7 and 13 years, respectively, and compared two DNA extraction kits. The kestrel samples contained a very high number of reads that could not be identified to phylum compared to the mouse samples. The two kits differed in the phyla and genera that were detected, and the Zymo kit, which is optimized for plasma and serum, produced more high-quality reads for both kestrel and mouse samples. We identified several pathogenic genera, including , , and . Sequencing blood samples for pathogens could potentially have broad applications for identifying important reservoir hosts for pathogen transmission and provide a reduced set of species on which to follow up.

摘要

缺乏来自野生动物病原体的基因组数据严重限制了我们追踪传播模式和追溯疫情起源的能力。目前,世界各地的生物样本库中存有数百万份野生动物样本,包括血液样本。传统上,血液在健康个体中被视为无菌环境,但最近的证据表明情况并非如此,尤其是对于野生动物。我们的目标是确定是否可以使用16S测序对冷冻血浆样本进行检测,以提供有关病原体潜在宿主的信息,从而更全面地了解疾病系统。我们对分别冷冻保存了7年和13年的北美野生鹿鼠()和美洲红隼()的血浆进行了测序,并比较了两种DNA提取试剂盒。与小鼠样本相比,红隼样本中含有大量无法鉴定到门的读数。这两种试剂盒在检测到的门和属方面存在差异,而针对血浆和血清优化的Zymo试剂盒为红隼和小鼠样本都产生了更多高质量的读数。我们鉴定出了几个致病属,包括、和。对血液样本进行病原体测序可能在识别病原体传播的重要宿主方面具有广泛应用,并提供一组需要跟进的减少的物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/db02097287fd/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/6e9f7896b3c9/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/875e0d23dcdf/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/e7015679c16e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/cd71ac88647b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/591628088470/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/db02097287fd/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/6e9f7896b3c9/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/875e0d23dcdf/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/e7015679c16e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/cd71ac88647b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/591628088470/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4ed/12221476/db02097287fd/gr5.jpg

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本文引用的文献

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