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Metagenomic search of viral coinfections in herpes simplex encephalitis patients
Little is known about concomitant central nervous system (CNS) infections by more than one virus. Current diagnostics are based on molecular tests for particular pathogens making it difficult to identify multi-viral infections. In the present study, we applied DNA- and RNA-based next-generation sequ...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645616/ https://www.ncbi.nlm.nih.gov/pubmed/37490185 http://dx.doi.org/10.1007/s13365-023-01157-9 |
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author | Perlejewski, Karol Radkowski, Marek Rydzanicz, Małgorzata Dzieciątkowski, Tomasz Silling, Steffi Wieczorek, Magdalena Makowiecki, Michał Horban, Andrzej Laskus, Tomasz |
author_facet | Perlejewski, Karol Radkowski, Marek Rydzanicz, Małgorzata Dzieciątkowski, Tomasz Silling, Steffi Wieczorek, Magdalena Makowiecki, Michał Horban, Andrzej Laskus, Tomasz |
author_sort | Perlejewski, Karol |
collection | PubMed |
description | Little is known about concomitant central nervous system (CNS) infections by more than one virus. Current diagnostics are based on molecular tests for particular pathogens making it difficult to identify multi-viral infections. In the present study, we applied DNA- and RNA-based next-generation sequencing metagenomics (mNGS) to detect viruses in cerebrospinal fluids from 20 patients with herpes simplex encephalitis. Coinfection was detected in one patient: sequences in cerebrospinal fluids matched enterovirus A (2.660 reads; 4% of recovered genome) and enterovirus B (1.571 reads; 13% of recovered genome). Subsequent PCR combined with serotyping allowed to identify human echovirus 6, a representative of enterovirus B. Several other mNGS hits (human pegivirus, Merkel cell polyomavirus, human papillomavirus type 5) were not considered to represent a genuine signal as they could not be confirmed by specific RT-PCR/PCR. HSV DNA, while being detectable by PCR in every patient, was detected by mNGS in only one. In conclusion, contaminations and false signals may complicate mNGS interpretation; however, the method can be useful in diagnostics of viral coinfections in CNS, particularly in the case of rare pathogens. |
format | Online Article Text |
id | pubmed-10645616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-106456162023-11-14 Metagenomic search of viral coinfections in herpes simplex encephalitis patients Perlejewski, Karol Radkowski, Marek Rydzanicz, Małgorzata Dzieciątkowski, Tomasz Silling, Steffi Wieczorek, Magdalena Makowiecki, Michał Horban, Andrzej Laskus, Tomasz J Neurovirol Article Little is known about concomitant central nervous system (CNS) infections by more than one virus. Current diagnostics are based on molecular tests for particular pathogens making it difficult to identify multi-viral infections. In the present study, we applied DNA- and RNA-based next-generation sequencing metagenomics (mNGS) to detect viruses in cerebrospinal fluids from 20 patients with herpes simplex encephalitis. Coinfection was detected in one patient: sequences in cerebrospinal fluids matched enterovirus A (2.660 reads; 4% of recovered genome) and enterovirus B (1.571 reads; 13% of recovered genome). Subsequent PCR combined with serotyping allowed to identify human echovirus 6, a representative of enterovirus B. Several other mNGS hits (human pegivirus, Merkel cell polyomavirus, human papillomavirus type 5) were not considered to represent a genuine signal as they could not be confirmed by specific RT-PCR/PCR. HSV DNA, while being detectable by PCR in every patient, was detected by mNGS in only one. In conclusion, contaminations and false signals may complicate mNGS interpretation; however, the method can be useful in diagnostics of viral coinfections in CNS, particularly in the case of rare pathogens. Springer International Publishing 2023-07-25 2023 /pmc/articles/PMC10645616/ /pubmed/37490185 http://dx.doi.org/10.1007/s13365-023-01157-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Perlejewski, Karol Radkowski, Marek Rydzanicz, Małgorzata Dzieciątkowski, Tomasz Silling, Steffi Wieczorek, Magdalena Makowiecki, Michał Horban, Andrzej Laskus, Tomasz Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title | Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title_full | Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title_fullStr | Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title_full_unstemmed | Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title_short | Metagenomic search of viral coinfections in herpes simplex encephalitis patients |
title_sort | metagenomic search of viral coinfections in herpes simplex encephalitis patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645616/ https://www.ncbi.nlm.nih.gov/pubmed/37490185 http://dx.doi.org/10.1007/s13365-023-01157-9 |
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