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Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections
This study provides significant new data on the application of metagenomic next-generation sequencing (mNGS) to clinical diagnostics of central nervous system (CNS) viral infections, which can have high mortality rates and severe sequelae. Conventional diagnostic procedures for identifying viruses c...
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Published in: | Microbiology spectrum 2024-01, Vol.12 (1), p.e0226423-e0226423 |
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description | This study provides significant new data on the application of metagenomic next-generation sequencing (mNGS) to clinical diagnostics of central nervous system (CNS) viral infections, which can have high mortality rates and severe sequelae. Conventional diagnostic procedures for identifying viruses can be inefficient and rely on preconceived assumptions about the pathogen, making mNGS an appealing alternative. However, the effectiveness of mNGS is affected by the presence of human DNA contamination, which can be minimized by using cell-free DNA (cfDNA) instead of whole-cell DNA (wcDNA). This multi-center retrospective study of patients with suspected viral CNS infection found that mNGS using cfDNA had a significantly lower proportion of human DNA and higher sensitivity for detecting viruses than mNGS using wcDNA. Herpesviruses, particularly VZV, were found to be the most common DNA viruses in these patients. Overall, mNGS using cfDNA is a promising complementary diagnostic method for detecting CNS viral infections. |
doi_str_mv | 10.1128/spectrum.02264-23 |
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Conventional diagnostic procedures for identifying viruses can be inefficient and rely on preconceived assumptions about the pathogen, making mNGS an appealing alternative. However, the effectiveness of mNGS is affected by the presence of human DNA contamination, which can be minimized by using cell-free DNA (cfDNA) instead of whole-cell DNA (wcDNA). This multi-center retrospective study of patients with suspected viral CNS infection found that mNGS using cfDNA had a significantly lower proportion of human DNA and higher sensitivity for detecting viruses than mNGS using wcDNA. Herpesviruses, particularly VZV, were found to be the most common DNA viruses in these patients. Overall, mNGS using cfDNA is a promising complementary diagnostic method for detecting CNS viral infections.</description><identifier>ISSN: 2165-0497</identifier><identifier>EISSN: 2165-0497</identifier><identifier>DOI: 10.1128/spectrum.02264-23</identifier><identifier>PMID: 38095471</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>cell-free DNA ; central nervous system infection ; cerebrospinal fluid ; Clinical Microbiology ; herpesvirus ; metagenomic sequencing ; Research Article</subject><ispartof>Microbiology spectrum, 2024-01, Vol.12 (1), p.e0226423-e0226423</ispartof><rights>Copyright © 2023 Lu et al.</rights><rights>Copyright © 2023 Lu et al. 2023 Lu et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a387t-e7dc98ac2426a89ff35154b01b80cbe02d8ed38e4537bbafe1e79c585c147e73</cites><orcidid>0000-0002-3682-6096 ; 0000-0002-9214-7274</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/spectrum.02264-23$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/spectrum.02264-23$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,52726,52727,52728,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38095471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Jhaveri, Tulip A.</contributor><creatorcontrib>Lu, Yuying</creatorcontrib><creatorcontrib>Zhang, Ye</creatorcontrib><creatorcontrib>Lou, Zheng</creatorcontrib><creatorcontrib>He, Xiaomin</creatorcontrib><creatorcontrib>Zhang, Qinghua</creatorcontrib><creatorcontrib>Zhang, Qingxia</creatorcontrib><creatorcontrib>Zhao, Shu</creatorcontrib><creatorcontrib>Chen, Han</creatorcontrib><creatorcontrib>Zhu, Haixia</creatorcontrib><creatorcontrib>Song, Zhi</creatorcontrib><creatorcontrib>Zhang, Ruxu</creatorcontrib><creatorcontrib>Ma, Caiyu</creatorcontrib><creatorcontrib>Liu, Ding</creatorcontrib><title>Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections</title><title>Microbiology spectrum</title><addtitle>Spectrum</addtitle><addtitle>Microbiol Spectr</addtitle><description>This study provides significant new data on the application of metagenomic next-generation sequencing (mNGS) to clinical diagnostics of central nervous system (CNS) viral infections, which can have high mortality rates and severe sequelae. Conventional diagnostic procedures for identifying viruses can be inefficient and rely on preconceived assumptions about the pathogen, making mNGS an appealing alternative. However, the effectiveness of mNGS is affected by the presence of human DNA contamination, which can be minimized by using cell-free DNA (cfDNA) instead of whole-cell DNA (wcDNA). This multi-center retrospective study of patients with suspected viral CNS infection found that mNGS using cfDNA had a significantly lower proportion of human DNA and higher sensitivity for detecting viruses than mNGS using wcDNA. Herpesviruses, particularly VZV, were found to be the most common DNA viruses in these patients. Overall, mNGS using cfDNA is a promising complementary diagnostic method for detecting CNS viral infections.</description><subject>cell-free DNA</subject><subject>central nervous system infection</subject><subject>cerebrospinal fluid</subject><subject>Clinical Microbiology</subject><subject>herpesvirus</subject><subject>metagenomic sequencing</subject><subject>Research Article</subject><issn>2165-0497</issn><issn>2165-0497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9Uktv1DAYjBCIVqU_gAvykUsWP2PnhKryqlTg0rvlOJ-3XiX2Yjur9swfx9vdVu0FX_yamU8zmqZ5T_CKEKo-5S3YkpZ5hSnteEvZq-aUkk60mPfy9bPzSXOe8wZjTAgWVNC3zQlTuBdcktPm708oZg0hzt6iAHelrRdIpvgYUIY_CwTrwxpFhyxMU-sSAPry6wK5mFC5BeRHCMU7bw-Uitv5tGTIyJol76m2ApKZqnraxSWjfJ8LzMgHVw1UTn7XvHFmynB-3M-am29fby5_tNe_v19dXly3hilZWpCj7ZWxlNPOqN45JojgAyaDwnYATEcFI1PABZPDYBwQkL0VSljCJUh21lwdZMdoNnqb_GzSvY7G64eHmNbapOLtBLpzxCoJdTngI2eDGnsuxNhRM3RSmar1-aC1XYYZxqPFF6Ivf4K_1eu40wRLxbBSVeHjUSHFmnIuevZ5H7EJUFPStMe070QveYWSA9SmmHMC9zSHYL3vgn7sgn7ogqasclYHjskz1Zu4pFCj_S_hw3NHTyMeq8L-AVK_xf8</recordid><startdate>20240111</startdate><enddate>20240111</enddate><creator>Lu, Yuying</creator><creator>Zhang, Ye</creator><creator>Lou, Zheng</creator><creator>He, Xiaomin</creator><creator>Zhang, Qinghua</creator><creator>Zhang, Qingxia</creator><creator>Zhao, Shu</creator><creator>Chen, Han</creator><creator>Zhu, Haixia</creator><creator>Song, Zhi</creator><creator>Zhang, Ruxu</creator><creator>Ma, Caiyu</creator><creator>Liu, Ding</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3682-6096</orcidid><orcidid>https://orcid.org/0000-0002-9214-7274</orcidid></search><sort><creationdate>20240111</creationdate><title>Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections</title><author>Lu, Yuying ; Zhang, Ye ; Lou, Zheng ; He, Xiaomin ; Zhang, Qinghua ; Zhang, Qingxia ; Zhao, Shu ; Chen, Han ; Zhu, Haixia ; Song, Zhi ; Zhang, Ruxu ; Ma, Caiyu ; Liu, Ding</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a387t-e7dc98ac2426a89ff35154b01b80cbe02d8ed38e4537bbafe1e79c585c147e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>cell-free DNA</topic><topic>central nervous system infection</topic><topic>cerebrospinal fluid</topic><topic>Clinical Microbiology</topic><topic>herpesvirus</topic><topic>metagenomic sequencing</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Yuying</creatorcontrib><creatorcontrib>Zhang, Ye</creatorcontrib><creatorcontrib>Lou, Zheng</creatorcontrib><creatorcontrib>He, Xiaomin</creatorcontrib><creatorcontrib>Zhang, Qinghua</creatorcontrib><creatorcontrib>Zhang, Qingxia</creatorcontrib><creatorcontrib>Zhao, Shu</creatorcontrib><creatorcontrib>Chen, Han</creatorcontrib><creatorcontrib>Zhu, Haixia</creatorcontrib><creatorcontrib>Song, Zhi</creatorcontrib><creatorcontrib>Zhang, Ruxu</creatorcontrib><creatorcontrib>Ma, Caiyu</creatorcontrib><creatorcontrib>Liu, Ding</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Microbiology spectrum</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Yuying</au><au>Zhang, Ye</au><au>Lou, Zheng</au><au>He, Xiaomin</au><au>Zhang, Qinghua</au><au>Zhang, Qingxia</au><au>Zhao, Shu</au><au>Chen, Han</au><au>Zhu, Haixia</au><au>Song, Zhi</au><au>Zhang, Ruxu</au><au>Ma, Caiyu</au><au>Liu, Ding</au><au>Jhaveri, Tulip A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections</atitle><jtitle>Microbiology spectrum</jtitle><stitle>Spectrum</stitle><addtitle>Microbiol Spectr</addtitle><date>2024-01-11</date><risdate>2024</risdate><volume>12</volume><issue>1</issue><spage>e0226423</spage><epage>e0226423</epage><pages>e0226423-e0226423</pages><issn>2165-0497</issn><eissn>2165-0497</eissn><abstract>This study provides significant new data on the application of metagenomic next-generation sequencing (mNGS) to clinical diagnostics of central nervous system (CNS) viral infections, which can have high mortality rates and severe sequelae. Conventional diagnostic procedures for identifying viruses can be inefficient and rely on preconceived assumptions about the pathogen, making mNGS an appealing alternative. However, the effectiveness of mNGS is affected by the presence of human DNA contamination, which can be minimized by using cell-free DNA (cfDNA) instead of whole-cell DNA (wcDNA). This multi-center retrospective study of patients with suspected viral CNS infection found that mNGS using cfDNA had a significantly lower proportion of human DNA and higher sensitivity for detecting viruses than mNGS using wcDNA. Herpesviruses, particularly VZV, were found to be the most common DNA viruses in these patients. 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subjects | cell-free DNA central nervous system infection cerebrospinal fluid Clinical Microbiology herpesvirus metagenomic sequencing Research Article |
title | Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections |
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