<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Liu Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Rabies is a highly fatal disease. Once symptoms develop, death usually occurs within days. Survivors were occasionally reported in the literatures. Ante-mortem diagnosis remains a challenge in most rabies endemic countries. A novel, accurate diagnostic assay is highly desirable.&lt;h4>Methods&lt;/h4>We used metagenomic next-generation sequencing (mNGS) to examine the cerebrospinal fluid (CSF) samples of a 49-year-old patient with rabies and validated the results by TaqMan PCR and RT-PCR/Sanger sequencing.&lt;h4>Results&lt;/h4>Metagenomic next-generation sequencing identified sequence reads uniquely aligned to the rabies virus (RABV). PCR confirmed the presence of the partial RABV N gene in the CSF. Phylogenetic analysis showed that the RABV grouped as an Asian clade, which is the most broadly distributed clade in China.&lt;h4>Conclusion&lt;/h4>Metagenomic next-generation sequencing may be a useful screening tool for the etiological diagnosis of rabies, especially in the absence of timely rabies laboratory testing or in patients with no exposure history.</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>982290</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9947348</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metagenomic next-generation sequencing for the etiological diagnosis of rabies virus in cerebrospinal fluid.</pubmed_title><pmcid>PMC9947348</pmcid><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Willoughby RE</pubmed_authors><pubmed_authors>Feng Y</pubmed_authors><pubmed_authors>Weng X</pubmed_authors><pubmed_authors>Gao J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Mo X</pubmed_authors><pubmed_authors>Peng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metagenomic next-generation sequencing for the etiological diagnosis of rabies virus in cerebrospinal fluid.</name><description>&lt;h4>Background&lt;/h4>Rabies is a highly fatal disease. Once symptoms develop, death usually occurs within days. Survivors were occasionally reported in the literatures. Ante-mortem diagnosis remains a challenge in most rabies endemic countries. A novel, accurate diagnostic assay is highly desirable.&lt;h4>Methods&lt;/h4>We used metagenomic next-generation sequencing (mNGS) to examine the cerebrospinal fluid (CSF) samples of a 49-year-old patient with rabies and validated the results by TaqMan PCR and RT-PCR/Sanger sequencing.&lt;h4>Results&lt;/h4>Metagenomic next-generation sequencing identified sequence reads uniquely aligned to the rabies virus (RABV). PCR confirmed the presence of the partial RABV N gene in the CSF. Phylogenetic analysis showed that the RABV grouped as an Asian clade, which is the most broadly distributed clade in China.&lt;h4>Conclusion&lt;/h4>Metagenomic next-generation sequencing may be a useful screening tool for the etiological diagnosis of rabies, especially in the absence of timely rabies laboratory testing or in patients with no exposure history.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-06-25T03:24:52.352Z</modification><creation>2025-04-06T19:39:06.41Z</creation></dates><accession>S-EPMC9947348</accession><cross_references><pubmed>36844226</pubmed><doi>10.3389/fmed.2023.982290</doi></cross_references></HashMap>